SAN MATEO, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — Oportun (Nasdaq: OPRT), a mission-driven financial services company, today announced that it will participate in the upcoming Stephens NASH2026 Annual Investor Conference.

Oportun’s Chief Financial Officer, Bill Franklin, will participate in a fireside chat and in investor meetings at the conference. The fireside chat will begin at 8:00 am CT / 9:00 am ET on November 17th and can be accessed live at this link.

A link to the presentation webcast will also be accessible in the “IR calendar” section of Oportun’s Investor Relations website under “News & Events” at https://investor.oportun.com. A replay will be available for an additional 90 days via the same link following the conference.

About Oportun 
Oportun (Nasdaq: OPRT) is a mission-driven financial services company that puts its members’ financial goals within reach. With intelligent borrowing, savings, and budgeting capabilities, Oportun empowers members with the confidence to build a better financial future. Since inception, Oportun has provided more than $23.3 billion in responsible and affordable credit, saved its members more than $2.5 billion in interest and fees, and helped its members set aside an average of more than $1,800 annually. For more information, visit Oportun.com.

Investor Contact
Dorian Hare
(650) 590-4323
ir@oportun.com

Media Contact
Michael Azzano
Cosmo PR for Oportun
michael@cosmo-pr.com
(415) 596-1978

SARATOGA, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — CapsoVision, Inc. (NASDAQ: CV), a commercial-stage medical technology company developing advanced imaging and AI-enabled capsule endoscopy solutions, today reported financial results and provided a business update for its third quarter ended September 30, 2026.

Recent Highlights

  • Reported third quarter 2026 revenue of $3.6 million, compared with $3.5 million in the third quarter 2025.
  • CapsoCam Plus® used by more than 184,000 patients worldwide as of September 30, 2026, compared with 151,000 a year earlier.
  • Received FDA clearance for AI Highlights™, the Company’s AI-assisted reading tool for CapsoCam Plus®, on September 25, 2026, followed by its U.S. commercial launch on November 2, 2026. Available for both adults and pediatric patients aged two and older, AI Highlights supports physician review through both local computer and cloud-based platforms. The Company expects the addition of AI Highlights to accelerate CapsoCam Plus sales growth, with the full commercial impact anticipated in 2027.
  • Completed enrollment and clinical data collection for the second-generation CapsoCam Colon™ study, including physician review of capsule videos both with and without AI assistance. FDA 510(k) submission remains on track for year-end 2026.
  • Continued expanding the clinical footprint of the CapsoCam UGI study for pancreatic cancer detection. Building on two active community-based clinical sites, the Company has executed a clinical trial agreement with a third site and is in various stages of contracting and feasibility discussions with more than a dozen larger medical centers with expertise in pancreatic ductal adenocarcinoma (PDAC), which the Company expects will help accelerate patient enrollment.
  • Completed an $18 million registered direct offering with existing shareholders in September 2026, generating approximately $17.8 million in net proceeds.
  • Raised approximately $1.7 million in net proceeds through the at-the-market offering program during the third quarter of 2026.
  • Appointed David S. Shields, M.D., to the Board of Directors effective July 1, 2026.

Management Commentary

“The FDA clearance and subsequent U.S. launch of AI Highlights marks an important step forward for CapsoVision,” said Johnny Wang, President and Chief Executive Officer. “Our four-camera, 360-degree panoramic capsule already provides physicians with a differentiated view of the small bowel. By combining that imaging capability with AI-assisted review, we believe we can reduce reading time, improve detection accuracy compared with manual review, and give physicians an additional level of diagnostic confidence. We believe the combination of panoramic imaging and FDA-cleared AI-assisted review, approved for use in patients two years and older is a meaningful differentiator for CapsoCam Plus.

At the same time, completing enrollment in our colon clinical study brings us closer to our planned FDA submission by year end, which we believe represents a substantially larger market opportunity. With the support of our existing shareholders through our recent financing, we are focused on translating these milestones into broader adoption and long-term growth,” concluded Wang.

Third Quarter 2026 Financial Results

Total revenue was $3.6 million compared to $3.5 million in the third quarter of 2025. Average selling price was stable year over year. The Company expects the addition of AI Highlights, launched on November 2, 2026, following FDA clearance, to accelerate CapsoCam Plus sales growth, with the full commercial impact anticipated in 2027.

Gross profit was $1.8 million, compared with $1.9 million in the third quarter of 2025. Gross margin was 49%, compared to 54% in the third quarter of 2025. The decline primarily reflected higher material costs associated with increased flash memory prices, a one-time inventory obsolescence charge, and higher stock-based compensation expense.

Operating expenses decreased to $9.1 million, from $9.9 million in the third quarter of 2025, reflecting continued expense management while supporting clinical and development programs, including the CapsoCam Colon pivotal study. With the study now complete, the Company expects related clinical expenses to decline while it continues advancing its development pipeline.

Net loss was $7.3 million, or $0.15 per share, compared with a net loss of $7.9 million, or $0.17 per share, in the third quarter of 2025.

Cash and cash equivalents totaled $21.8 million as of September 30, 2026. During September, the Company completed an $18 million registered direct offering with existing shareholders, generating approximately $17.8 million in net proceeds. The Company also sold 276,446 shares through its at-the-market offering program during the quarter for approximately $1.7 million in net proceeds.

Conference Call and Webcast

CapsoVision will host a conference call today, November 12, 2026, at 4:30 p.m. ET to discuss its third quarter financial results. Individuals interested in listening to the conference call may do so by dialing (800) 715-9871 for domestic callers or (646) 307-1963 for international callers and referencing conference ID 2841803, or from the webcast link on the Events page in the investor relations section of the company’s website at www.capsovision.com.

To access the replay, please register via the webcast link on the Events page. The webcast will be available for one year following the completion of the call.

About CapsoVision

CapsoVision is a commercial-stage medical technology company focused on developing advanced imaging and AI-enabled solutions to transform the detection and screening of gastrointestinal diseases. Its flagship product, CapsoCam Plus®, is a wire-free, panoramic capsule endoscope that enables high-resolution visualization of the small bowel and supports cloud-based or direct capsule video review. The Company’s next pipeline product, CapsoCam Colon™ with enhanced AI, is designed to enable non-invasive colon imaging and polyp detection. With a proprietary platform targeted to expand across multiple GI indications, including esophageal and pancreatic disorders, CapsoVision is advancing a new era in capsule-based diagnostics. For more information on CapsoVision, please visit www.capsovision.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. In this context, forward-looking statements mean statements related to future events, which may impact our expected future business and financial performance, and often contain words such as “expected”, “positioned”, “on track”, “anticipate(s)”, “intend(s)”, “plan(s)”, “believe(s)”, “potential”, “will”, “should”, “could”, “would”, “may”, “continue”, “remain”, “advancing”, “approach(ing)”, “planned”, “look forward”, or “target(ed)” and other words of similar meaning. Examples of these forward-looking statements include, but are not limited to, statements concerning possible or assumed future results of operations and financial position, including the Company’s expectations regarding sales growth of CapsoCam Plus® and the timing thereof, the Company’s expectations regarding clinical and other operating expenses, the Company’s product and clinical development efforts, the timing and receipt of regulatory submissions and approvals , the Company’s plans, strategies and timing for its pipeline development (including the commercialization, physician adoption and anticipated benefits of AI Highlights™, the continued development and anticipated 510(k) submission for CapsoCam Colon™, and the market opportunity for CapsoCam Colon™, the clinical study for CapsoCam® UGI in pancreatic cancer detection) and the success of the Company’s plans and strategies. These forward-looking statements are based on the Company’s current expectations and inherently involve significant risks and uncertainties, including those beyond the Company’s control. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, market conditions (including competition in the capsule endoscopy market, including from competitors with FDA-cleared AI products), the Company’s financial condition and the availability of cash and financing (including through the Company’s at-the-market equity offering program), the success of the Company’s product and clinical development efforts, the failure to receive regulatory clearance or approval, changes in U.S. trade policies, tariffs or other government regulations that could increase the Company’s costs or affect the Company’s supply chain, and the failure to adapt the Company’s products for new indications. These and other risks and uncertainties are described more fully in the Company’s filings with the Securities and Exchange Commission (“SEC”), including the “Risk Factors” section of the Company’s most recent Form 10-K and Form 10-Q. Forward-looking statements speak only as of the date of this press release, and the Company undertakes no obligation to update or revise these statements, except as required by law.

Investor Relations Contact
Leigh Salvo
New Street Investor Relations
Investors@CapsoVision.com

Media Contact
Leslie Strickler and Paul Spicer
Être Communications
leslies@etrecommunications.com | (804) 240-0807
pauls@etrecommunications.com | (804) 503-9231

       
CAPSOVISION, INC.
CONDENSED BALANCE SHEETS (UNAUDITED)
(in thousands, except par value and share amounts)
       
  September 30, 2026   December 31, 2025
ASSETS      
Current Assets      
Cash and cash equivalents $ 21,757   $ 10,112
Accounts receivable, net   2,456     2,498
Inventory   4,747     2,987
Prepaid expenses and other current assets   2,086     1,072
Total current assets   31,046     16,669
Property and equipment, net   508     611
Operating lease right-of-use assets   747     843
Other long-term assets   451     41
TOTAL ASSETS $ 32,752   $ 18,164
       
LIABILITIES AND STOCKHOLDERS’ EQUITY      
Current Liabilities      
Accounts payable $ 1,102   $ 1,143
Accrued expenses and other current liabilities   4,355     2,697
Deferred revenue   146     177
Operating lease liabilities – current   521     410
Total current liabilities   6,124     4,427
       
Operating lease liabilities – long-term   259     477
Total liabilities   6,383     4,904
       
Commitments and contingencies – Note 8      

Stockholders’ Equity      
Preferred stock, $0.001 par value: 10,000,000 shares authorized and none issued and outstanding as of September 30, 2026; 10,000,000 shares authorized and none issued and outstanding as of December 31, 2025   —       —  
Common stock, $0.001 par value: 300,000,000 shares authorized as of September 30, 2026; 53,569,896 and 46,865,051 issued and outstanding as of September 30, 2026 and December 31, 2025, respectively   54       47  
Additional paid-in capital   203,833       168,878  
Accumulated deficit   (177,518 )     (155,665 )
Total stockholders’ equity   26,369       13,260  
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY $ 32,752     $ 18,164  

       
CAPSOVISION, INC.
CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (UNAUDITED)
(in thousands, except share and per-share amounts)
       
  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
               
Net revenue $ 3,568     $ 3,538     $ 10,003     $ 9,636  
               
Costs of revenue   1,804       1,624       5,039       4,417  
               
Gross profit   1,764       1,914       4,964       5,219  
               
OPERATING EXPENSES              
Selling and marketing   2,060       1,773       6,087       5,581  
Research and development   4,803       6,090       14,547       12,589  
General and administrative   2,285       2,070       6,387       5,101  
Total operating expenses   9,148       9,933       27,021       23,271  
               
Operating loss   (7,384 )     (8,019 )     (22,057 )     (18,052 )
               
NON-OPERATING INCOME              
Interest income, net   46       132       187       175  
Other non-operating income (expense), net   (1 )     (34 )     17       (44 )
Total non-operating income, net   45       98       204       131  
               
Loss before income taxes   (7,339 )     (7,921 )     (21,853 )     (17,921 )
               
Provision for income taxes   —       —       —       —  
               
Net loss and comprehensive loss $ (7,339 )   $ (7,921 )   $ (21,853 )   $ (17,921 )
               
Net loss per share – basic and diluted $ (0.15 )   $ (0.17 )   $ (0.44 )   $ (1.05 )
               
Weighted average common shares outstanding – basic and diluted   50,568,141       46,217,127       49,332,254       17,049,671  

   
CAPSOVISION, INC.
CONDENSED STATEMENTS OF CASH FLOWS (UNAUDITED)
(in thousands)
   
  Nine Months Ended September 30,
    2026       2025  
CASH FLOWS FROM OPERATING ACTIVITIES      
Net loss $ (21,853 )   $ (17,921 )
Adjustments to reconcile net loss to net cash used in operating activities:      
Depreciation and amortization   173       161  
Loss on disposal of property and equipment   —       1  
Amortization of operating lease right-of-use assets   307       260  
Unrealized foreign exchange losses (gains)   57       (170 )
Stock in lieu of debt repayment   —       31  
Stock-based compensation   1,863       629  
Bad debt expense   10       11  
Changes in operating assets and liabilities:      
Accounts receivable   10       151  
Inventory   (1,760 )     (558 )
Prepaid expenses and other current assets   (1,014 )     (303 )
Other long-term assets   (410 )     —  
Accounts payable   (203 )     596  
Accrued expenses and other current liabilities   1,658       2,220  
Deferred revenue   (31 )     (26 )
Operating lease liabilities   (318 )     (260 )
Net cash used in operating activities $ (21,511 )   $ (15,178 )
       
CASH FLOWS FROM INVESTING ACTIVITIES      
Purchases of property and equipment   (70 )     (82 )
Net cash used in investing activities $ (70 )   $ (82 )
       
CASH FLOWS FROM FINANCING ACTIVITIES      
Proceeds from IPO, net of commissions   —       26,557  
Payment of IPO offering costs   —       (3,184 )
Repayment of promissory note   —       (1,000 )
Proceeds from Private Placement   14,000       —  
Payment of Private Placement issuance costs   (601 )     —  
Proceeds from ATM Program, net of issuance costs   1,710       —  
Proceeds from Securities Purchase Agreement   18,000       —  
Payment of constructive dividend   (12 )     —  
Proceeds from promissory note issuance   —       1,000  
Proceeds from exercises of options on common stock and warrants   164       216  
Net cash provided by financing activities $ 33,261     $ 23,589  
       
Net increase in cash and cash equivalents   11,680       8,329  
Effect of exchange rate changes on cash and cash equivalents   (35 )     139  
Cash and cash equivalents at beginning of period   10,112       9,319  
Cash and cash equivalents at end of period $ 21,757     $ 17,787  
       
SUPPLEMENTAL CASH FLOW DISCLOSURES      
Cash paid for income taxes $ 10     $ 7  
Cash paid for interest   —       15  
NON-CASH FINANCING AND INVESTING ACTIVITIES      
Obtaining a right-of-use asset in exchange for a lease liability   211       —  
Underwriters warrants issued in connection with the IPO   —       519  
Conversion of convertible preferred stock into common stock upon initial public offering   —       143,625  
Securities Purchase Agreement issuance costs in accounts payable   162       —  
       

Surging demand for high-speed inference fuels growth from new and existing customers

  • Record GAAP revenue of $210.8 million
  • Record Core revenue of $230.9 million
  • GAAP cloud revenue grew 265% from a year ago
  • Core cloud revenue $144.9 million, up 272% from a year ago
  • Commercial wins with two new hyperscalers
  • 700 megawatts of data center capacity now under contract
  • First to deliver production scale heterogeneous disaggregated inference offering

SUNNYVALE, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — Cerebras Systems (NASDAQ: CBRS), maker of the world’s fastest AI infrastructure, today announced financial results for the third quarter ended September 30, 2026.

“Cerebras’ technology remains the undisputed champion of speed,” said Andrew Feldman, co-founder and CEO of Cerebras. “We’re giving customers more ways to access our technology and scale with us be it through direct system sales, Cerebras Cloud or third-party cloud providers. I’m proud of our team for delivering the performance and speed customers need to build entirely new applications and expand what AI can do. That progress energizes us to do even more as we push the limits of innovation and expect to triple revenue in 2027.”

“We exceeded our guidance across the board for the third quarter in a row and delivered sequential improvements on all core financial metrics,” said Bob Komin, CFO of Cerebras. “We won new marquee customers, including hyperscalers, neoclouds and large enterprises. And we saw our pipeline for high-speed AI inference increase by more than 10x in the quarter.”

Q3 2026 Financial Highlights

GAAP Financial Results

  • GAAP cloud and other services revenue: Record $141.9 million, up 265% year-over-year
  • GAAP total revenue: Record $210.8 million, up 55% year-over-year
  • GAAP gross margin: 20% up sequentially
  • GAAP operating margin: (106%)

Core Financial Results (Non-GAAP)

Core results exclude the impacts of non-cash amortization of customer warrants and stock-based compensation, data center pass-through revenues and costs, and certain other items.

  • Core cloud and other services revenue: $144.9 million, up 272% year-over-year
  • Core total revenue: $230.9 million, up 70% year-over-year
  • Core gross margin: 41% up both sequentially and year-over-year
  • Core operating margin: (14%)

Fourth Quarter 2026 Financial Outlook

  • Core Non-GAAP Financial Outlook:
    • Core revenue of approximately $310 to $330 million
    • Core gross margin in the range of 47% – 49%
    • Core operating margins in the range of (1%) to 1%

Full Year 2026 Financial Outlook

  • Core Non-GAAP Financial Outlook:
    • Core revenue of $940 to $960 million
    • Core gross margin in the range of 42% – 44%
    • Core operating margins in the range of (10%) to (8%)

Liquidity

  • Strong liquidity with cash, cash equivalents, restricted cash, and short-term investments of $7.8 billion and debt capacity of $850 million.

Business Highlights: General

  • $26.1 billion in remaining performance obligations as of September 30, 2026.

Business Highlights: Customers

Cerebras is rapidly expanding its customer base, broadening its reach and diversifying its revenue.

  • Oracle is integrating Cerebras’ fast inference into Oracle Cloud Infrastructure. With the fastest AI inference, AI labs, enterprises and developers that rely on Oracle will now have the performance required to build robust agents and applications that are hyper responsive and execute complicated tasks in a shorter period of time. Cerebras will be available in Oracle Cloud Infrastructure in 2027.
  • Today, Cerebras announced an important cloud deal with a top three hyperscaler. More will be shared next year.
  • Expanded reach through a variety of neoclouds, diversifying routes to market and giving customers more ways to access Cerebras’ high-speed inference.
  • Cerebras high-speed inference will power the new Bilt Neighborhood OS platform and Bilt Concierge AI assistant to deliver faster, seamless interactions between the platform and the eight million consumers and 50,000 businesses it serves.

Business Highlights: Capacity

Global data center capacity and manufacturing capacity continue to grow.

  • Secured 700 gross megawatts of data center capacity for delivery by the end of 2027, increasing pipeline of opportunities to gigawatt scale. Cerebras Cloud is now among the largest non-hyperscaler AI clouds.
  • Signed contracts for additional capacity in Norway and Finland. This expands Cerebras’ European capacity and supports long-term cloud inference demand.
  • Scaling manufacturing capacity with Flex and Sanmina; expects to exit 2026 with more than 10x manufacturing capacity versus beginning of the year.
  • Plans in place to add factories and further increase capacity in 2027 to support substantial growth.
  • Cerebras disaggregated inference expands capacity by increasing up to 5x the number of tokens that data centers can deliver. More superfast tokens per MW means each data center produces more revenue.

Business Highlights: Capabilities

Cerebras is advancing capabilities on every front: new systems and processors, improved software, advanced manufacturing techniques, and partnerships that deliver best-in-industry solutions.

  • Cerebras is the first in the market to deliver production-scale heterogeneous disaggregated inference, which is expected to become a default offering in major clouds. Disaggregated inference delivers substantially more high-speed tokens for the same power, resulting in more profit per MW for cloud owners and lower cost per token for AI users.
  • This August, Cerebras unveiled its next-generation systems, setting new standards for ultra-fast AI inference performance, efficiency and scalability:
    • At Supernova 2026, Cerebras introduced CS-4, the world’s fastest AI accelerator, delivering up to 30x faster inference. CS-4 will soon be in full production.
    • At Hot Chips 2026, Cerebras previewed its next-generation system the CS-5, targeted for early Summer 2027, designed to deliver up to 10,000 tokens per second per user.
    • Cerebras’ next-generation processor, the Wafer Scale Engine 5 to be deployed in CS-5, is back from the fab, completed bring up and is in system testing. From tape out to in system test in less than 5 months.
  • Cerebras was a day-zero launch partner for Kimi K3.1, Moonshot AI’s 2.8 trillion-parameter frontier class open-weight model. Kimi 3.1 on Cerebras is the fastest in the industry, running up to 2,000 tokens per second.

Upcoming Investor Events

Cerebras will participate in the following events with the financial community:

TomorrowX Summit, Austin, TX
Tuesday, November 17, 2026

Barclays Global Technology Conference, San Francisco, CA
Wednesday, December 9, 2026

Earnings Webcast and Conference Call

Cerebras Systems will host a conference call to review its financial results for the third quarter of 2026 and to discuss our financial outlook today at 2 p.m. PT (5 p.m. ET). Interested parties may join the conference call via the webcast and can be accessed at the Cerebras website at https://investors.cerebras.ai/. The webcast will be recorded and available for replay on the same website following the conclusion of the conference call.

About Cerebras Systems

Cerebras Systems (NASDAQ: CBRS) builds the world’s fastest AI infrastructure. The Cerebras team of pioneering computer architects, computer scientists, AI researchers, and engineers of all types came together to make AI blisteringly fast through innovation and invention. Cerebras believes that when AI is fast, it will change the world. Leading global corporations, research institutes, and governments choose Cerebras to run their AI workloads. Cerebras solutions are available on premises and in the cloud. For more information, visit cerebras.ai

Contacts

Investor Relations
Sean Dorsey
investors@cerebras.ai

Media & Analyst Relations
Kriselle Laran
pr@cerebras.ai

Cerebras Disclosure Information

Cerebras uses its blog (cerebras.ai/blog), its investor relations page (investors.cerebras.ai), its X account (@cerebras), and its LinkedIn page (linkedin.com/company/cerebras-systems/) to disclose material nonpublic information and for complying with its disclosure obligations under Regulation FD. Accordingly, investors should monitor these channels, in addition to following Cerebras’ press releases, Securities and Exchange Commission (SEC) filings, public conference calls and public webcasts.

Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of applicable securities laws. All statements other than statements of historical fact could be deemed to be forward-looking, including, but not limited to, statements about: demand for high-speed AI inference and long-term growth; the fourth quarter and full year 2026 financial outlook; tripling revenue in 2027; data center capacity and the timing of delivery; the Mikkeli, Finland data center; expanding data center geographic and infrastructure reach across Europe and Canada, and establishing first presence in South America; the performance, efficiency and scalability of CS-4 and CS-5, and the targeted timing of the CS-5 AI accelerator; the timing and expected benefits of customer and partner relationships, including the partnership with hyperscalers, availability in Oracle Cloud Infrastructure in 2027, expanding access of high-speed inference to European customers, powering the new Bilt Neighborhood OS platform and Bilt Concierge AI assistant to deliver faster, seamless interactions between the platform, consumers and businesses; and any assumptions relating to the foregoing. The words “may,” “will,” “shall,” “should,” “expects,” “plans,” “anticipates,” “could,” “intends,” “target,” “projects,” “contemplates,” “believes,” “estimates,” “predicts,” “potential,” “objective,” or “continue,” or the negative of these words or other similar terms or expressions that concern our expectations, strategy, plans, or intentions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. These forward-looking statements are subject to a number of risks and uncertainties, many of which involve factors or circumstances that are beyond Cerebras’ control. These risks and uncertainties include, but are not limited to: Cerebras’ ability to sustain and manage its growth, access borrowings and other sources of capital on acceptable terms, and deploy available capital to support growth; its history of net losses and ability to achieve and maintain profitability; its limited operating history at its current scale and ability to accurately forecast revenue and appropriately budget and manage expenses; its dependence on a limited number of significant customers, and the potential impact of any reduction in demand from, material adverse development in its relationships with, or failure to meet its obligations to, such customers, including under its Master Relationship Agreement with OpenAI; the timing, execution and expected benefits of its strategic customer, partner and financing arrangements; its historical reliance on sales of hardware systems and the early-stage, rapidly evolving market for its cloud-based offerings and AI infrastructure; its ability to secure sufficient data center capacity and capital to support its cloud-based offerings; its ability to launch new offerings and add new product capabilities; and its ability to compete effectively in the rapidly evolving and competitive market for AI computing solutions.

Cerebras’ actual results or outcomes could differ materially from those stated or implied in forward-looking statements due to a number of factors. Accordingly, undue reliance should not be placed on such statements. These forward-looking statements are made as of the date they were first issued and are based on information available to Cerebras together with Cerebras’ expectations, estimates, forecasts, projections, beliefs, and assumptions as of such date. These forward-looking statements should not be relied upon as representing Cerebras’ views as of any date subsequent to the date of this press release. Past performance is not necessarily indicative of future results. Cerebras undertakes no intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise, except as required by law.

Further information on potential risks that could affect actual results is included in Cerebras’ most recent filings with the SEC, copies of which may be obtained by visiting Cerebras’ Investor Relations website at investors.cerebras.ai or the SEC’s website at www.sec.gov.

CEREBRAS SYSTEMS INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited)
(in thousands, except per share amounts)
 
  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
Revenue              
Hardware $ 68,881     $ 96,794     $ 233,592     $ 236,763  
Cloud and other services   141,928       38,920       350,732       101,785  
Total revenue   210,809       135,714       584,324       338,548  
Cost of revenue              
Hardware   61,290       47,969       179,362       143,028  
Cloud and other services   107,425       32,610       251,135       66,682  
Total cost of revenue   168,715       80,579       430,497       209,710  
Gross profit   42,094       55,135       153,827       128,838  
Operating expenses              
Research and development   177,842       57,257       573,488       170,775  
Sales and marketing   32,813       20,834       134,483       49,388  
General and administrative   55,588       3,513       162,277       20,796  
Total operating expenses   266,243       81,604       870,248       240,959  
Loss from operations   (224,149 )     (26,469 )     (716,421 )     (112,121 )
Other income, net   63,900       5,787       93,409       380,431  
Income (loss) before income taxes   (160,249 )     (20,682 )     (623,012 )     268,310  
Income tax expense   969       1,519       2,740       4,866  
Net income (loss) $ (161,218 )   $ (22,201 )   $ (625,752 )   $ 263,444  
               
Net income (loss) attributable to common shareholders              
Basic $ (161,218 )   $ (22,201 )   $ (625,752 )   $ 101,685  
Diluted $ (161,218 )   $ (22,201 )   $ (625,752 )   $ 263,444  
Net income (loss) per share attributable to common shareholders              
Basic $ (0.67 )   $ (0.41 )   $ (4.13 )   $ 1.92  
Diluted $ (0.67 )   $ (0.41 )   $ (4.13 )   $ 1.61  
Weighted average shares outstanding              
Basic   238,885       53,983       151,532       52,909  
Diluted   238,885       53,983       151,532       163,677  
                               

CEREBRAS SYSTEMS INC.
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME (LOSS)
(unaudited)
(in thousands)
 
  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
Net income (loss) $ (161,218 )   $ (22,201 )   $ (625,752 )   $ 263,444  
Change in foreign currency translation adjustments, net of tax   (53 )     (615 )     585       297  
Available-for-sale investments:              
Change in net unrealized gain (loss) on debt securities, net of tax   (8,938 )     (397 )     (5,110 )     (1,204 )
Comprehensive income (loss) $ (170,209 )   $ (23,213 )   $ (630,277 )   $ 262,537  
                               

CEREBRAS SYSTEMS INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(unaudited)
(in thousands)
 
  September 30, 2026   December 31, 2025
ASSETS      
Current assets:      
Cash and cash equivalents $ 3,074,752     $ 701,706  
Restricted cash   444,042       228,672  
Investments   4,286,026       406,531  
Accounts receivable, net   231,762       50,423  
Inventories   146,100       63,626  
Customer warrants   140,174       60,906  
Prepaid expenses and other current assets   542,805       31,782  
Total current assets   8,865,661       1,543,646  
Property and equipment, net   1,507,797       437,396  
Customer warrants, net of current portion   951,800       91,447  
Operating lease right-of-use assets   571,237       248,950  
Other non-current assets   41,917       4,598  
Total assets $ 11,938,412     $ 2,326,037  
       
LIABILITIES, REDEEMABLE CONVERTIBLE PREFERRED STOCK, AND STOCKHOLDERS’ EQUITY (DEFICIT)      
Current liabilities:      
Accounts payable $ 236,981     $ 48,630  
Deferred revenue   234,309       131,049  
Operating lease liability   98,368       45,865  
Customer deposits   108,715       354,460  
Working capital loan   706,518       —  
Accrued and other current liabilities   295,980       139,536  
Total current liabilities   1,680,871       719,540  
Deferred revenue, net of current portion   453,293       35,847  
Operating lease liability, net of current portion   522,771       215,957  
Working capital loan, net of current portion   122,564       —  
Total liabilities   2,779,499       971,344  
       
Redeemable convertible preferred stock   —       1,933,348  
Stockholders’ equity (deficit)      
Class A common stock   2       1  
Class B common stock   1       —  
Class N common stock   —       —  
Treasury stock   (21,456 )     (21,456 )
Additional paid-in capital   10,714,672       346,829  
Accumulated other comprehensive income   (3,224 )     1,301  
Accumulated deficit   (1,531,082 )     (905,330 )
Total stockholders’ equity (deficit)   9,158,913       (578,655 )
Total liabilities, redeemable convertible preferred stock, and stockholders’ equity (deficit) $ 11,938,412     $ 2,326,037  
               

CEREBRAS SYSTEMS INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited)
(in thousands)
 
  Nine Months Ended September 30,
    2026       2025  
Cash flows from operating activities:      
Net income (loss) $ (625,752 )   $ 263,444  
Adjustments to reconcile net income (loss) to net cash flows used in operating activities:      
Stock-based compensation   541,706       33,781  
Amortization of customer warrants   82,739       —  
Depreciation and amortization   72,342       17,941  
Non-cash lease expense   61,826       13,729  
Non-cash interest expense   57,170       —  
Provision for product warranties   10,830       14,348  
Extinguishment of forward contract liability   —       (363,336 )
Other   (14,974 )     (1,453 )
Changes in operating assets and liabilities:      
Accounts receivable   (181,338 )     102,797  
Inventories   (101,124 )     58,798  
Prepaid expenses and other assets   (546,038 )     894  
Accounts payable   134,529       14,327  
Deferred revenue   288,047       26,532  
Customer deposits   (245,745 )     (334,034 )
Other liabilities   76,888       18,016  
Net cash flows used in operating activities $ (388,894 )   $ (134,216 )
Cash flows from investing activities:      
Purchases of property and equipment $ (1,046,059 )   $ (301,139 )
Purchases of investments   (5,120,232 )     (20,175 )
Maturities and sales of investments   1,274,091       138,590  
Net cash flows used in investing activities $ (4,892,200 )   $ (182,724 )
Cash flows from financing activities:      
Proceeds from initial public offering, net of underwriting discounts and commissions $ 6,232,511     $ —  
Proceeds from sale of shares of Series G redeemable convertible preferred stock   —       1,074,999  
Costs incurred in connection with the sale of shares of Series G redeemable convertible preferred stock   —       (16,718 )
Proceeds from sale of shares of Series H redeemable convertible preferred stock   1,014,249       —  
Costs incurred in connection with a debt facility and an equity sale   (4,019 )     —  
Proceeds from Working Capital Loan   1,004,571       —  
Proceeds from exercise of stock options, net of repurchases of early exercised stock options   39,507       10,531  
Proceeds from issuance of shares of Class N common stock   15,035       —  
Tax withholding from tender offer and initial public offering   (416,659 )     —  
Payments of deferred offering costs and other financing activities   (15,774 )     —  
Net cash flows provided by financing activities $ 7,869,421     $ 1,068,812  
Effect of exchange rate on cash   89       297  
Increase (decrease) in cash, cash equivalents, and restricted cash $ 2,588,416     $ 752,169  
Cash, cash equivalents, and restricted cash beginning of period   930,378       581,965  
Cash, cash equivalents, and restricted cash end of period $ 3,518,794     $ 1,334,134  
               


CEREBRAS SYSTEMS INC.
RECONCILIATION OF GAAP TO NON-GAAP MEASURES
(unaudited)
(in thousands)
 
Reconciliation of GAAP Revenue to Core Revenue:
    Three Months Ended September 30,
      2026       2025
    Total   Hardware   Cloud and Other Services   Total   Hardware   Cloud and Other Services
GAAP revenue   $ 210,809     $ 68,881   $ 141,928     $ 135,714   $ 96,794   $ 38,920
Less: Pass-through revenue     (16,360 )     —     (16,360 )     —     —     —
Add: Amortization of customer warrant assets     36,424       17,078     19,346       —     —     —
Core revenue   $ 230,873     $ 85,959   $ 144,914     $ 135,714   $ 96,794   $ 38,920

    Nine Months Ended September 30,
      2026       2025
    Total   Hardware   Cloud and Other Services   Total   Hardware   Cloud and Other Services
GAAP revenue   $  584,324      $  233,592    $  350,732      $  338,548    $  236,763    $  101,785 
Less: Pass-through revenue      (34,974 )      —       (34,974 )      —       —       — 
Add: Amortization of customer warrant assets      82,739         46,068       36,671         —       —       — 
Core revenue   $  632,089      $  279,660    $  352,429      $  338,548    $  236,763    $  101,785 
                                         

Reconciliation of GAAP Gross Profit to Core Gross Profit:

    Three Months Ended September 30,
      2026       2025
    Total   Hardware   Cloud and Other Services   Total   Hardware   Cloud and Other Services
GAAP gross profit   $ 42,094     $ 7,591   $ 34,503     $ 55,135   $ 48,825   $ 6,310
Less: Pass-through revenue and related data center costs, net     (488 )     —     (488 )     —     —     —
Add: Amortization of customer warrant assets     36,424       17,078     19,346       —     —     —
Add: Stock-based compensation expense     16,545       2,003     14,542       161     40     121
Core gross profit   $ 94,575     $ 26,672   $ 67,903     $ 55,296   $ 48,865   $ 6,431

    Nine Months Ended September 30,
      2026       2025
    Total   Hardware   Cloud and Other Services   Total   Hardware   Cloud and Other Services
GAAP gross profit   $ 153,827     $ 54,230   $ 99,597     $ 128,838   $ 93,735   $ 35,103
Less: Pass-through revenue and related data center costs, net     (1,037 )     —     (1,037 )     —     —     —
Add: Amortization of customer warrant assets     82,739       46,068     36,671       —     —     —
Add: Stock-based compensation expense     32,848       5,000     27,848       674     169     505
Add: Employer payroll tax related to stock-based compensation from IPO     471       118     353       —     —     —
Core gross profit   $ 268,848     $ 105,416   $ 163,432     $ 129,512   $ 93,904   $ 35,608
                                         

Reconciliation of GAAP Gross Margin to Core Gross Margin:

    Three Months Ended September 30,
    2026     2025  
    Total   Hardware   Cloud and Other Services   Total   Hardware   Cloud and Other Services
GAAP gross margin   20.0 %   11.0 %   24.3 %   40.6 %   50.4 %   16.2 %
Non-GAAP adjustments   21.0     20.0     22.6     0.1     0.1     0.3  
Core gross margin   41.0 %   31.0 %   46.9 %   40.7 %   50.5 %   16.5 %

    Nine Months Ended September 30,
    2026     2025  
    Total   Hardware   Cloud and Other Services   Total   Hardware   Cloud and Other Services
GAAP gross margin   26.3 %   23.2 %   28.4 %   38.1 %   39.6 %   34.5 %
Non-GAAP adjustments   16.2     14.5     18.0     0.2     0.1     0.5  
Core gross margin   42.5 %   37.7 %   46.4 %   38.3 %   39.7 %   35.0 %
                                     

Reconciliation of GAAP Operating Expenses to Core Operating Expenses:

    Three Months Ended September 30,
      2026       2025  
    Total   Research and Development   Sales and Marketing   General and Administrative   Total   Research and Development   Sales and Marketing   General and Administrative
GAAP operating expenses   $ 266,243     $ 177,842     $ 32,813     $ 55,588     $ 81,604     $ 57,257     $ 20,834     $ 3,513  
Less: Stock-based compensation expense     (138,560 )     (80,999 )     (20,915 )     (36,646 )     (11,185 )     (8,619 )     (1,502 )     (1,064 )
Core operating expenses   $ 127,683     $ 96,843     $ 11,898     $ 18,942     $ 70,419     $ 48,638     $ 19,332     $ 2,449  

    Nine Months Ended September 30,
      2026       2025  
    Total   Research and Development   Sales and Marketing   General and Administrative   Total   Research and Development   Sales and Marketing   General and Administrative
GAAP operating expenses   $ 870,248     $ 573,488     $ 134,483     $ 162,277     $ 240,959     $ 170,775     $ 49,388     $ 20,796  
Less: Stock-based compensation expense     (508,858 )     (308,845 )     (93,762 )     (106,251 )     (33,107 )     (23,631 )     (4,984 )     (4,492 )
Less: Employer payroll tax related to stock-based compensation from IPO     (22,307 )     (16,491 )     (3,907 )     (1,909 )     —       —       —       —  
Core operating expenses   $ 339,083     $ 248,152     $ 36,814     $ 54,117     $ 207,852     $ 147,144     $ 44,404     $ 16,304  
                                                                 

Reconciliation of GAAP Loss from Operations to Core Operating Loss:

  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
GAAP loss from operations $ (224,149 )   $ (26,469 )   $ (716,421 )   $ (112,121 )
Less: Pass-through revenue and related data center costs, net   (488 )     —       (1,037 )     —  
Add: Stock-based compensation expense   155,105       11,346       541,706       33,781  
Add: Amortization of customer warrant assets   36,424       —       82,739       —  
Add: Employer payroll tax related to stock-based compensation from IPO   —       —       22,778       —  
Core operating loss $ (33,108 )   $ (15,123 )   $ (70,235 )   $ (78,340 )
                               

Reconciliation of GAAP Operating Margin to Core Operating Margin:

  Three Months Ended September 30,   Nine Months Ended September 30,
  2026     2025     2026     2025  
GAAP operating margin (106.3 %)   (19.5 %)   (122.6 %)   (33.1 %)
Non-GAAP adjustments 92.0     8.4     111.5     10.0  
Core operating margin (14.3 %)   (11.1 %)   (11.1 %)   (23.1 %)
                       

Reconciliation of GAAP Loss from Operations to Core Adjusted EBITDA:

  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
GAAP loss from operations $ (224,149 )   $ (26,469 )   $ (716,421 )   $ (112,121 )
Less: Pass-through revenue and related data center costs, net   (488 )     —       (1,037 )     —  
Add: Stock-based compensation expense   155,105       11,346       541,706       33,781  
Add: Amortization of customer warrant assets   36,424       —       82,739       —  
Add: Depreciation and amortization   29,794       8,625       72,342       17,941  
Add: Employer payroll tax related to stock-based compensation from IPO   —       —       22,778       —  
Core Adjusted EBITDA $ (3,314 )   $ (6,498 )   $ 2,107     $ (60,399 )
                               

Reconciliation of GAAP Net Income (Loss) to Core Net Income (Loss):

  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
GAAP net income (loss) $ (161,218 )   $ (22,201 )   $ (625,752 )   $ 263,444  
Less: Pass-through revenue and related data center costs, net   (488 )     —       (1,037 )     —  
Less: Change in fair value (extinguishment) of forward contract liability   —       —       —       (363,336 )
Add: Stock-based compensation expense   155,105       11,346       541,706       33,781  
Add: Amortization of customer warrant assets   36,424       —       82,739       —  
Add: Employer payroll tax related to stock-based compensation from IPO   —       —       22,778       —  
Core net income (loss) $ 29,823     $ (10,855 )   $ 20,434     $ (66,111 )
                               

Discussion of Non-GAAP Financial Measures

Use of non-GAAP financial measures

We use certain non-GAAP financial measures to supplement the performance measures in our consolidated financial statements, which are presented in accordance with GAAP. These non-GAAP financial measures include core total revenue, core hardware revenue, core cloud and other services revenue, core gross profit, core hardware gross profit, core cloud and other services gross profit, core gross margin, core hardware gross margin, core cloud and other services gross margin, core operating loss, core operating margin, core net income (loss), and core adjusted earnings before interest, income tax, depreciation and amortization (“Core Adjusted EBITDA”). We use these non-GAAP financial measures for financial and operational decision-making and as a means to assist us in evaluating period-to-period comparisons.

Reconciliations of each of these non-GAAP financial measures to their most directly comparable GAAP measures for this quarter and prior periods are included in the tables below or elsewhere in the materials accompanying this press release.

Usefulness of non-GAAP financial measures to investors

By excluding certain items that may not be indicative of our recurring operating results from our core technology and service offerings and stock-based compensation from grants of equity awards, we believe that the non-GAAP metrics described below provide meaningful supplemental information regarding our performance. Accordingly, we believe these non-GAAP financial measures are useful to investors and others because they allow additional information with respect to financial measures used by management in its financial and operational decision-making and may be useful to our institutional investors and the analyst community to help them analyze the health of our business. Disclosure of these non-GAAP financial measures also facilitates the comparisons of Cerebras’ operating performance with the performance of other companies in the same industry that supplement their GAAP results with non-GAAP financial measures that may be calculated in a manner comparable to their core operations.

Economic substance of and material limitations associated with non-GAAP financial measures used by Cerebras

Core revenue, core hardware revenue, core cloud and other services revenue, core gross profit, core hardware gross profit, core cloud and other services gross profit, core gross margin, core hardware gross margin, core cloud and other services gross margin, core operating loss, core operating margin, Core Adjusted EBITDA and core net income (loss) are adjusted, as applicable, to: (i) exclude non-cash stock-based compensation; (ii) exclude pass-through revenues and costs that are not part of our core technology and services offering; and (iii) add back non-cash amortization from customer warrants that is recorded as a reduction in revenues; (iv) exclude from core net income (loss) the effect of the change in fair value (extinguishment) of the forward contract liability; and (v) present employer payroll tax related to stock-based compensation from IPO as an offset to the stock-based compensation adjustment in calculating core net income (loss). Core adjusted EBITDA also excludes the impacts of depreciation and amortization.

Core gross margin, core hardware margin, and core cloud and other services margin represent core gross profit, core hardware gross profit, and core cloud and other services gross profit, respectively, expressed as a percentage of their corresponding core revenue.

More specifically, Cerebras makes the adjustments described above for the following reasons:

  • Stock-based compensation expense consists of equity awards granted based on the estimated fair value of those awards at the grant date. Although stock-based compensation is a key incentive offered to employees, Cerebras excludes these charges for the purpose of calculating these non-GAAP measures, primarily because they are non-cash expenses, and the Company’s internal benchmarking analyses evidence that many industry participants and peers present non-GAAP financial measures excluding stock-based compensation expense.
  • Amortization of customer warrants consists of equity granted to customers and recorded as contra-revenue. We exclude the impact of amortization of customer warrant assets recorded as contra‑revenue from our non‑GAAP results because it represents a non‑cash, valuation‑driven adjustment associated with equity instruments issued to customers. The amount and timing of this amortization may be influenced by factors outside our operational performance, including the timing of customer capacity deployment decisions and product delivery schedules, which are at the discretion of the customer. This adjustment does not reflect the underlying economics of our core revenue‑generating activities, including pricing, volume, or cost of delivering our products and services, and therefore may not be indicative of our ongoing operating performance.
  • Pass-through revenue and associated pass-through cost of revenue relate to non-recurring data center start-up and recurring data center costs that are incurred on behalf of specific customers. We exclude pass‑through revenue and the associated pass-through cost of revenue from our non‑GAAP financial measures because such amounts are incurred on behalf of specific customers and do not reflect the underlying economics of our core hardware technology and services offerings and generally generate fixed minimal gross margins. These pass-through revenues and costs are dependent on the pace of customer data center build-outs, deployment schedules, and customer deployment choices and approval of associated billings. Accordingly, these amounts may fluctuate significantly between reporting periods and can obscure comparisons of our operating performance results and trends in our core business.
  • The change in fair value (extinguishment) of the forward contract liability reflects the impact recognized in connection with the forward contract liability. We exclude this item from core net income (loss) because it arose from the forward contract liability rather than from the operating performance of our core technology and services offerings.
  • Employer payroll tax related to stock-based compensation from IPO is presented as an adjustment in calculating core net income (loss). This treatment presents the employer payroll tax separately from the non-cash stock-based compensation excluded from core net income (loss).

There are a number of limitations related to the use of non-GAAP financial measures, and these non-GAAP measures should be considered in addition to, not as a substitute for or in isolation from, our financial results prepared in accordance with GAAP. Other companies, including companies in our industry, may calculate these non-GAAP financial measures differently or not at all, which reduces their usefulness as comparative measures. No reconciliation is provided with respect to certain forward-looking non-GAAP financial measures as the GAAP measures are not accessible on a forward-looking basis. We cannot reliably predict all necessary components or their impact to reconcile such financial measures without unreasonable effort. The events necessitating a non-GAAP adjustment are inherently unpredictable and may have a significant impact on our future GAAP financial results. Cerebras compensates for these limitations on the use of non-GAAP financial measures by relying primarily on its GAAP results and using non-GAAP financial measures only as a supplement. Cerebras also provides a reconciliation of each non-GAAP financial measure to its most directly comparable GAAP financial measure for this quarter and prior periods within this press release, and Cerebras encourages investors to review those reconciliations carefully.

First participant dosed in Phase 1 clinical trial of EQ504, proof-of-mechanism data expected in Q2 2027

Cash equivalents of $53.3 million as of September 30, 2026; pro forma cash balance of approximately $72.0 million after the net effect of $20 million in gross financing received in October 2026

Cash runway expected into 2029

LA JOLLA, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — Equillium, Inc. (Nasdaq: EQ), a clinical-stage biotechnology innovator developing novel therapies to treat serious autoimmune and inflammatory disorders, today reported financial results for the third quarter ended September 30, 2026, and provided a corporate update highlighting recent progress with EQ504, its novel small-molecule aryl hydrocarbon receptor (AhR) modulator.

“We continue to make important progress advancing EQ504, with the recent initiation of clinical development marking a significant milestone for the program,” said Bruce Steel, Chief Executive Officer of Equillium. “We believe EQ504’s differentiated immunoregulatory mechanism of action, without broad immune suppression, has the potential to address key epithelial and immune pathways involved in inflammatory disease. We look forward to reporting proof-of-mechanism data in the second quarter of 2027, which we expect will inform our planned proof-of-concept study in ulcerative colitis that we expect to initiate in the second half of 2027. Supported by our strong financial position, we remain focused on advancing EQ504 to patients while continuing to evaluate its broader therapeutic potential.”

Recent Corporate and Clinical Highlights:

Initiated Phase 1 clinical trial of EQ504
In October 2026, Equillium initiated a first-in-human, randomized, double-blind, placebo-controlled study in Australia evaluating single and multiple ascending doses of EQ504 in approximately 70 healthy participants. The trial is designed to characterize safety, tolerability, pharmacokinetics and pharmacodynamics, and establish proof of mechanism of EQ504. The multiple ascending dose portion will include longitudinal gastrointestinal mucosal biopsies, including measurement of CYP1A1 expression, to assess AhR target engagement and localized biological activity in the gastrointestinal tract. Equillium expects to report topline data, including proof-of-mechanism assessments, in the second quarter of 2027. Subject to supportive results, Equillium plans to initiate a placebo-controlled proof-of-concept study in patients with moderately to severely active ulcerative colitis in the second half of 2027.

Milestone Closing of $20 Million Financing
On October 26, 2026, concurrent with the first patient dosed in the Phase 1 clinical trial, Equillium closed the second tranche of the Company’s previously announced August 2025 equity private placement agreement, resulting in aggregate gross proceeds of approximately $20 million.

Presented new nonclinical data further characterizing EQ504’s effects on epithelial barrier repair and immune regulation
Data presented at the 7th International AHR Conference demonstrated EQ504’s activity across complementary epithelial and immune pathways relevant to intestinal inflammation, including effects on barrier integrity, inflammatory chemokine production and immune regulation. Additional data presented at the 50th Anniversary La Jolla Immunology Conference further characterized coordinated AhR signaling across epithelial and immune compartments, supporting the potential of EQ504 to restore intestinal homeostasis through a differentiated, non-immunosuppressive mechanism of action.

Third Quarter 2026 Financial Results:

Cash and cash equivalents totaled $53.3 million as of September 30, 2026, compared to $33.1 million as of September 30, 2025. In October 2026, first participant dosing in the Phase 1 clinical trial of EQ504 triggered the second tranche of the Company’s previously announced August 2025 private placement agreement, resulting in approximately $20 million in additional funding. On a pro forma basis, after giving effect to the estimated net proceeds from this subsequent funding as if received on September 30, 2026, cash and cash equivalents would have been approximately $72.0 million. The pro forma amount is presented for supplemental informational purposes only and does not reflect cash used after September 30, 2026. Equillium believes that its cash and cash equivalents on the balance sheet as of September 30, 2026, together with the additional funding received in October 2026, are sufficient to fund its currently planned operations into 2029.  

Research and development (R&D) expenses for the third quarter of 2026 were $2.5 million, compared with $1.3 million for the same period in 2025.

General and administrative (G&A) expenses for the third quarter of 2026 were $2.6 million, compared with $3.3 million for the same period in 2025.

Net loss for the third quarter of 2026 was $4.6 million, or $(0.04) per basic and diluted share, compared with a net loss of $4.2 million, or $(0.06) per basic and diluted share for the same period in 2025.

About EQ504
EQ504 is an investigational potent and selective aryl hydrocarbon receptor (AhR) modulator with a multi-modal immunoregulatory mechanism of action without broad immune suppression, designed to be complementary to other inflammation and immunology agents. AhR is critical to barrier organ tissue physiology and immunology, maintaining barrier function and promoting tissue repair and regeneration, while regulating resident immune cells with anti-inflammatory responses. For ulcerative colitis, EQ504 is formulated as an oral, colon-targeted delayed-release drug product. Equillium is also evaluating the potential of EQ504 for additional indications, including inflammatory lung diseases through inhaled formulations.

About Equillium
Equillium is a biotechnology innovator with a mission to develop highly impactful therapies to treat serious autoimmune and inflammatory disorders. For more information, visit www.equilliumbio.com.

Forward Looking Statements
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words such as “anticipate”, “believe”, “could”, “continue”, “expect”, “estimate”, “may”, “plan”, “outlook”, “future”, “potential”, “will”, “designed to” and “project” and other similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These statements include, but are not limited to, statements regarding Equillium’s plans and strategies with respect to developing EQ504, including the initiation of clinical studies and the reporting of data therefrom; the expected timeline for reporting data from the Phase 1 study of EQ504; the potential benefits of EQ504, including its potential ability to address key epithelial and immune pathways involved in inflammatory disease; the anticipated initiation of a placebo-controlled proof-of-concept study, or the expected timeline for initiating such study, in patients with ulcerative colitis; the expected use of proceeds from the Milestone Closing; and Equillium’s expectations that its financial position and cash runway is sufficient to fund its currently planned operations into 2029. Because such statements are subject to risks and uncertainties, many of which are outside of Equillium’s control, actual results may differ materially from those expressed or implied by such forward-looking statements. Risks that contribute to the uncertain nature of the forward-looking statements include: Equillium’s ability to execute its plans and strategies; risks related to performing clinical and nonclinical studies; risks associated with relying on pro forma financial information; whether the results from clinical and nonclinical studies will validate and support the safety and efficacy of Equillium’s product candidates; changes in the competitive landscape; and Equillium’s ability to raise sufficient financing, which may not be available on acceptable terms or at all, to advance EQ504 and fund Equillium’s strategic plans. These and other risks and uncertainties are described more fully under the caption “Risk Factors” and elsewhere in Equillium’s filings and reports, which may be accessed for free by visiting the Securities and Exchange Commission’s website and on Equillium’s website under the heading “Investors.” Investors should take such risks into account and should not rely on forward-looking statements when making investment decisions. All forward-looking statements contained in this press release speak only as of the date on which they were made. Equillium undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.

Investor Contact
PJ Kelleher
LifeSci Advisors, LLC
+1-617-430-7579
pkelleher@lifesciadvisors.com

Equillium, Inc.
Condensed Consolidated Balance Sheets
(In thousands)
(unaudited)
   
    September 30,     December 31,
    2026     2025
Assets          
Cash and cash equivalents   $ 53,322     $ 30,277
Prepaid expenses and other assets   1,818     952
Operating lease right-of-use assets   671     658
Total assets   $ 55,811     $ 31,887
Current liabilities          
Accounts payable and other current liabilities   $ 2,819     $ 2,934
Total current liabilities   2,819     2,934
Long-term operating lease liabilities   313     356
Total liabilities   3,132     3,290
Total stockholders’ equity   52,679     28,597
Total liabilities and stockholders’ equity   $ 55,811     $ 31,887

Equillium, Inc.
Condensed Consolidated Statements of Operations
(In thousands, except share and per share data)
(unaudited)
                           
  Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
  2026       2025     2026       2025  
Operating expenses:                          
Research and development $ 2,488       $ 1,301     $ 8,228       $ 11,307  
General and administrative 2,560       3,274     7,585       8,365  
Total operating expenses 5,048       4,575     15,813       19,672  
Loss from operations   (5,048 )       (4,575 )     (15,813 )       (19,672 )
Total other income, net 465       345     1,226       1,049  
Net loss $ (4,583 )     $ (4,230 )   $ (14,587 )     $ (18,623 )
Net loss per share, basic and diluted $ (0.04 )      $ (0.06 )   $ (0.14 )     $ (0.41 )
Weighted-average number of common shares outstanding, basic and diluted 111,923,380       65,322,753     106,726,715       45,651,900  

Hearing request stays any suspension or delisting action; ordinary shares continue to trade on the Nasdaq Capital Market pending the Hearings Panel’s decision

TEL AVIV, Israel, Nov. 12, 2026 (GLOBE NEWSWIRE) — PRF Technologies Ltd. (Nasdaq: PRFX) (“PRF” or the “Company”) today announced that on November 9, 2026, it received a letter from the Listing Qualifications Department of The Nasdaq Stock Market LLC (“Nasdaq”) notifying the Company that the closing bid price of its ordinary shares had been below US$1.00 per share for 30 consecutive business days, from September 24, 2026 through November 4, 2026, and that the Company therefore does not meet the minimum bid price requirement of Nasdaq Listing Rule 5550(a)(2).

Companies that do not meet the minimum bid price requirement are normally given a 180-calendar day period to regain compliance. Because the Company effected a 1-for-5 reverse share split on February 6, 2026, within the prior one-year period, Nasdaq Listing Rule 5810(c)(3)(A)(iv) provides that the Company is not eligible for that compliance period, and Nasdaq staff has issued a determination to delist the Company’s securities from the Nasdaq Capital Market.

Under the terms of the letter, the Company had until 4:00 p.m. Eastern Time on November 16, 2026 to request a hearing before a Nasdaq Hearings Panel (the “Panel”). The Company has timely requested a hearing. As set forth in the letter, the hearing request stays the suspension and delisting of the Company’s securities pending the Panel’s decision, and the Company’s ordinary shares will continue to trade on the Nasdaq Capital Market under the symbol “PRFX” during that time.

At the hearing, the Company intends to present a plan to regain compliance with the minimum bid price requirement, which may include, if necessary, a reverse share split. The Panel has the discretion to grant the Company an exception of up to 180 days from the date of the delisting determination, or until May 8, 2027, to regain compliance. There can be no assurance that the Panel will grant the Company’s request for continued listing.

Efraim Cohen-Arazi, Interim Chief Executive Officer of PRF Technologies, commented, “The notice does not affect our current business operations. We had approximately US$11.0 million in cash and short-term deposits as of September 30, 2026, based on preliminary unaudited information, and our majority-owned subsidiary LayerBio expects to begin enrolling patients in the Phase 2 trial of OcuRing™-K before year-end 2026. We are also working toward completing the proposed GridFeed transaction with Dotz, which is subject to a non-binding term sheet and the negotiation and execution of definitive agreements. We intend to present the Panel with a plan to regain compliance, which we believe will support our request for continued listing on Nasdaq.”

This announcement is made in accordance with Nasdaq Listing Rule 5810(b), which requires prompt public disclosure of receipt of the letter.

About PRF Technologies

PRF Technologies (Nasdaq: PRFX) is a company focused on the reformulation of established therapeutics, and a developer of AI-driven energy optimization technologies through its DeepSolar platform. The Company’s pharmaceutical programs leverage a proprietary extended-release drug-delivery system intended to provide prolonged post-surgical pain relief while minimizing the need for repeated dosing and reducing reliance on opioids. Through DeepSolar and GridFeed, PRF also develops advanced software solutions that enable both consumers and enterprises to monitor, forecast, trade and optimize energy – particularly in solar-integrated environments. This dual business model reflects PRF’s strategic commitment to applying precision technology across high-impact sectors including healthcare and sustainable energy. For more information, please visit www.prf-tech.com.

Notice Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, about PRF’s expectations, beliefs and intentions, including statements regarding the Company’s ability to continue to remain listed on Nasdaq and the Company’s ability to successfully appeal the Nasdaq staff’s delisting determination; the Company’s hearing before the Nasdaq Hearings Panel; the Company’s plan to regain compliance with Nasdaq’s minimum bid price requirement, including any reverse share split; the continued listing and trading of the Company’s ordinary shares on the Nasdaq Capital Market; the completion of the proposed transaction with Dotz Nano Limited; the expected commencement of patient enrollment in the Phase 2 clinical trial of OcuRing™-K before year-end 2026; and the Company’s cash resources. Forward-looking statements can be identified by the use of forward-looking words such as “believe”, “expect”, “intend”, “plan”, “may”, “should”, “could”, “might”, “seek”, “target”, “will”, “project”, “forecast”, “continue” or “anticipate” or their negatives or variations of these words or other comparable words or by the fact that these statements do not relate strictly to historical matters. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties, many of which are outside of the Company’s control. Many factors could cause the Company’s actual activities or results to differ materially from the activities and results anticipated in forward-looking statements, including, but not limited to, the following: the possibility that the Panel will not grant the Company’s request for continued listing or will impose conditions the Company is unable to meet; the Company’s ability to regain and maintain compliance with Nasdaq’s continued listing requirements; the delisting of the Company’s ordinary shares from Nasdaq, including the resulting adverse effects on liquidity, market price, analyst coverage and the Company’s ability to raise capital; the Company’s ability to obtain shareholder approval for, and the timing of, any reverse share split, and the possibility that any reverse share split will not result in sustained compliance with the minimum bid price requirement or will cause the Company to fail other continued listing requirements; the effect of any reverse share split on the market price and liquidity of the Company’s ordinary shares; the non-binding nature of the term sheet with Dotz and the possibility that definitive agreements will not be negotiated or executed, or that the proposed transaction will not be completed; the preliminary and unaudited nature of the cash information included in this press release; the Company’s ability to continue as a going concern, the Company’s history of significant losses, its need to raise additional capital and its ability to obtain additional capital on acceptable terms, or at all; the Company’s dependence on the success of its product candidates, PRF-110 and OcuRing™-K; the ability of LayerBio to commence patient enrollment in the Phase 2 trial of OcuRing™-K on the anticipated timeline, including obtaining required regulatory and site approvals; the outcomes of preclinical studies and clinical trials; the Company’s reliance on third parties; the impact of competition and new technologies; the Company’s ability to comply with regulatory requirements; the overall global economic environment; and the impact of the political and security situation in Israel on the Company’s business. More detailed information about the risks and uncertainties affecting the Company are contained under the heading “Risk Factors” included in the Company’s most recent Annual Report on Form 20-F and in other filings that the Company has made and may make with the Securities and Exchange Commission in the future. Forward-looking statements in this press release are made as of the date of this press release, and the Company undertakes no duty to update or revise any such statements, whether as a result of new information, future events or otherwise.

Contact:

Crescendo Communications, LLC
Tel: 212-671-1020
Email: prfx@crescendo-ir.com

Dr. Ehud Geller, Chairman
PRF Technologies Ltd.
Tel: +972-54-4236711
Email: egeller@medicavp.com

CULVER CITY, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — Snail, Inc. (Nasdaq: SNAL) (“Snail Games” or the “Company”), a leading global independent developer and publisher of interactive digital entertainment, today announced financial results for the third quarter ended September 30, 2026.

Third Quarter 2026 and Recent Operational Highlights

ARK Franchise Updates:

  • ARK: Survival Evolved (“ASE”):
    • Units sold were approximately 559,000 for the third quarter of 2026
    • During the third quarter of 2026, average daily active users (“DAU”) were approximately 99,000 and peak DAU was approximately 126,000
  • ARK: Survival Ascended (“ASA”):
    • Units sold were approximately 1.2 million for the third quarter of 2026
    • During the third quarter of 2026, average DAU was approximately 121,000 and peak DAU was approximately 184,000
    • Launched ARK: Genesis Part 1 Ascended, ARK: Tides of Fortune, and shadow-dropped ARK: Dragontopia
    • Released ARK: Dragontopia content updates in July and September 2026
    • Released the Cerberax fantastic tame under the ARK: Fantastic Tames Season 1 Pack
    • Released a major update for the ARK: Astraeos downloadable content (“DLC”)
    • Upcoming tames and content releases planned for ARK: Fantastic Tames Season 1 and ARK: Dragontopia in November and December 2026
  • ARK: Ultimate Mobile Edition (“ARK Mobile”)
    • Approximately 14.5 million downloads as of September 30, 2026
    • During the third quarter of 2026, average DAU was approximately 134,000
  • Other ARK IPs
    • Released PixARK: Terracrypt DLC
    • Debuted the first public demo of ARK: Survival of the Fittest during ChinaJoy 2026

Game Portfolio and Business Updates:

  • AAA Game Pipeline
    • Officially unveiled 9 Yin Sutra: Immortal at ChinaJoy 2026, revealing a new trailer and Steam page
    • Publicly debuted 9 Yin Sutra: Wuxia at Gamescom 2026, revealing a new trailer and Steam page
    • Showcased For The Stars at Gamescom 2026, releasing a new gameplay trailer and exclusive demos for attending media
    • Showcased 9 Yin Sutra: Immortal and For The Stars during the IGN Fan Fest event
  • Launched Honeycomb: The World Beyond across Steam, Epic Games Store, PlayStation 5, and Xbox Series X|S
  • Showcased a new playable demo of Bellwright at Gamescom 2026, previewing its highly requested traversal update planned for the end of 2026
  • Launched Stoneguard on Steam Early Access and achieved a “Mostly Positive” rating from Steam users to date
  • Launched The Fame Game II: LA Heartbreaker, receiving an “Overwhelmingly Positive” Steam rating to date with more than 500 reviews
  • Launched Dead Party on Steam
  • Released new demos for Dead Party, Whispers of West Grove, and Veil of Madness during Steam Next Fest

Business and Operational Updates

  • Egofold, the Company’s subsidiary, publicly debuted the AI Ranch initiative and Non-Human Player™ (NHP), an AI gaming companion for consumers, at the Ai4 2026 conference
  • As of September 30, 2026, SaltyTV released 350+ short film dramas

ARK Content Pipeline

Title Platforms Type Release Schedule
ARK Dragontopia Steam, Xbox, PlayStation DLC Content Update
(new map)
December 2026
ARK Maker Steam, Xbox, PlayStation ASA Content Creation Tool 2027
ARK Survival of the Fittest Steam, Xbox, PlayStation ASA Game Mode 2027
PixARK Worlds Steam, Xbox, PlayStation, Nintendo Switch 2 New Title 2027
ARK Atlantis Steam, Xbox, PlayStation ASA DLC 2027
ARK Galaxy Wars Steam, Xbox, PlayStation ASA DLC 2027
ARK Legacy of Santiago Steam, Xbox, PlayStation ASA DLC 2027
       

Diversified Content Pipeline

Title Platforms Type Release Schedule
       
Bellwright Steam, Xbox, PlayStation Game Content Update 2026
Veil of Madness Steam Indie Title 2026/2027
Whispers of West Grove Steam Indie Title 2027
Gobby Gang Steam Indie Title 2027
For The Stars Steam AAA Title TBD
9 Yin Sutra: Immortal Steam AAA Title TBD
9 Yin Sutra: Wuxia Steam AAA Title TBD
       

Management Commentary

“Our third quarter results reflected the continued execution of our ARK content pipeline, which extends through 2027 and remains a key driver of engagement and monetization across ASA,” said Snail CEO Hai Shi. “The release of three ASA DLCs at the beginning of the quarter provided a strong foundation for our performance, demonstrating the importance of our ongoing content strategy to expand the franchise’s reach and longevity.

“Beyond our revenue-generating ARK content, the past several months have provided valuable opportunities to showcase the breadth and progress of our broader development portfolio. We unveiled and publicly debuted our two 9 Yin Sutra titles at ChinaJoy and Gamescom, supported by new trailers and the official launch of their respective Steam pages. These milestones mark important steps in building early awareness and engagement, particularly among the IP’s established fan base in China. We also featured For The Stars at Gamescom, where we released a new gameplay trailer and offered exclusive demos to attending media, and again at IGN Fan Fest. The positive reception and continued development progress across these projects reinforce our confidence in the commercial potential of our AAA pipeline. As these highly anticipated titles continue advancing toward launch, industry events and community engagement initiatives remain important platforms to build momentum and provide players with greater visibility into our development progress.

“Looking ahead, we are encouraged by the opportunities in front of us. We expect our recently released titles, together with the anticipated ARK: Dragontopia skyworld map in December, to support fourth quarter performance. More importantly, our visibility beyond the current year remains strong. With an established ARK content roadmap extending throughout 2027 and multiple AAA titles continuing to make solid development progress toward key milestones, we believe we are well positioned to build on the momentum generated this year. Our focus remains on disciplined execution, consistent content delivery, and advancing our high-conviction development initiatives.”

Third Quarter 2026 Financial Highlights

Net revenues increased 139.2% to $33.1 million compared to $13.8 million in the same period last year. The increase was primarily due to a $13.9 million change in deferred revenue, a $4.9 million increase in ASA sales, which was primarily driven by the base game and the release of ARK: Tides of Fortune and ARK: Dragontopia, a $1.0 million increase in Bellwright sales, and a $0.4 million increase in Honeycomb: The World Beyond sales, partially offset by a decrease of $0.5 million in ASE sales, a decrease of $0.2 million in ARK Mobile sales, and a decrease of $0.2 million in SaltyTV sales.

Total units sold increased 73.3% to 2.0 million units compared to 1.1 million units in the same period last year, primarily driven by increased sales of ASA by 0.7 million units and an increase in sales of Bellwright of 0.1 million units.

Net income improved to $6.7 million compared to a net loss of $(7.9) million in the same period last year. The increase was primarily due to an increase in gross profit of $17.6 million, partially offset by an increase in the provision for income taxes of $2.0 million, an increase in total operating expenses of $0.6 million, and an increase in total other expense of $0.5 million.

Bookings increased 30.4% to $23.0 million compared to $17.6 million in the same period last year. The increase was primarily due to higher sales of ASA and Bellwright, partially offset by a decrease in bookings from ASE.

EBITDA improved to $7.2 million compared to $(9.7) million in the same period last year. The increase was primarily driven by the $14.5 million increase in net income, a decrease in interest income and interest income – related parties of $0.4 million, and an increase in the provision of income taxes of $2.0 million.

Nine Months 2026 Financial Highlights

Net revenues increased 42.6% to $80.0 million compared to $56.1 million in the same period last year. The increase was primarily due to the change in deferred revenue of $19.2 million, an increase in ASA sales of $4.8 million, which was primarily driven by the sales of the base game, ARK: Bob’s Tall Tales, ARK: Lost Colony, and the newly released ARK: Tides of Fortune and ARK: Dragontopia, an increase of $4.6 million in Bellwright sales, and an increase of $0.4 million in Honeycomb: The World Beyond sales. The increase in revenue was partially offset by a decrease in ASE revenue of $3.2 million, a decrease in ARK Mobile revenue of $1.5 million, and a decrease in SaltyTV application revenue of $0.4 million.

Total units sold increased 28.0% to 6.2 million units compared to 4.8 million units in the same period last year, primarily due to an increase in ASA sales of 1.7 million units and an increase in Bellwright sales of 0.3 million units, partially offset by a decrease in ASE sales of 0.8 million units.

Net income improved to $5.8 million compared to a net loss of $(26.4) million in the same period last year. The improvement was primarily due to an increase in revenue of $23.9 million, a decrease in the provision of income taxes of $10.4 million, and a decrease in cost of revenue of $0.3 million, partially offset by an increase in total operating expenses of $1.9 million and total other expense of $0.6 million.

Bookings increased 7.0% to $71.7 million compared to $67.0 million in the same period last year. The increase was primarily due to higher sales of ASA and Bellwright, which benefited from promotional pricing during the period, offset by ASE as the title continued to mature and consumer demand shifted toward ASA and its related downloadable content.

EBITDA improved to $6.5 million compared to $(15.6) million in the same period last year. The increase was primarily due to an increase in net income of $32.1 million, partially offset by a decrease in provision for income taxes of $10.4 million.

As of September 30, 2026, unrestricted cash was $12.1 million compared to $8.6 million as of December 31, 2025.

Use of Non-GAAP Financial Measures

In addition to the financial results determined in accordance with U.S. generally accepted accounting principles, or GAAP, Snail believes EBITDA, as a non-GAAP measure, and Bookings as a key operating metric, are useful in evaluating its operating performance. Bookings and EBITDA are non-GAAP and key operating financial measures that are presented as supplemental disclosures and should not be construed as alternatives to net income (loss) or revenue as indicators of operating performance, nor as alternatives to cash flow provided by operating activities as measures of liquidity, both as determined in accordance with GAAP. Snail supplementally presents Bookings and EBITDA because they are key operating measures used by management to assess financial performance. Bookings adjusts for the impact of deferrals and, Snail believes, provides a useful indicator of sales in a given period. Management believes Bookings and EBITDA are useful to investors and analysts in highlighting trends in Snail’s operating performance. At the same time, other measures can differ significantly depending on long-term strategic decisions regarding capital structure, the tax jurisdictions in which Snail operates, and capital investments.

Bookings is defined as the net amount of products and services sold digitally or physically in the period. Bookings is equal to revenues, excluding the impact from deferrals. Below is a reconciliation of total net revenue to Bookings, the closest GAAP financial measure.

    Three Months Ended
September 30,
Nine Months Ended
September 30,
    2026     2025     2026     2025
    (in millions)     (in millions)
Total net revenue   $ 33.1     $ 13.8     $ 80.0     $ 56.1
Change in deferred net revenue     (10.1 )     3.8       (8.3 )     10.9
Bookings   $ 23.0     $ 17.6     $ 71.7     $ 67.0
                               

We define EBITDA as net income (loss) before (i) interest expense, (ii) interest income, (iii) provision for (benefit from) income taxes and (iv) depreciation expense. The following table provides a reconciliation from net income (loss) to EBITDA:

    Three Months Ended
September 30,
Nine Months Ended
September 30,
    2026     2025     2026     2025  
    (in millions)     (in millions)
Net income (loss)   $ 6.7     $ (7.9 )   $ 5.8     $ (26.4 )
Interest income and interest income – related parties     (0.1 )     (0.5 )     (0.2 )     (0.6 )
Interest expense     0.2       0.2       0.5       0.4  
(Benefit from) provision for income taxes     0.4       (1.6 )     0.4       10.8  
Depreciation expense     —       0.1       —       0.2  
EBITDA   $ 7.2     $ (9.7 )   $ 6.5     $ (15.6 )
                                 

Webcast Details

The Company will host a webcast at 4:30 PM ET today to discuss its third quarter 2026 financial and operational results. Participants may access the live webcast and replay via the link here or on the Company’s investor relations website at https://investor.snail.com/.

About Snail, Inc.

Snail, Inc. (Nasdaq: SNAL) is a leading, global independent developer and publisher of interactive digital entertainment for consumers around the world, with a premier portfolio of premium games designed for use on a variety of platforms, including consoles, PCs, and mobile devices. For more information, please visit: https://snail.com/.

Forward-Looking Statements

This press release contains statements that constitute forward-looking statements. Many of the forward-looking statements contained in this press release can be identified by the use of forward-looking words such as “anticipate,” “believe,” “could,” “expect,” “should,” “plan,” “intend,” “may,” “predict,” “continue,” “estimate” and “potential,” or the negative of these terms or other similar expressions. Forward-looking statements appear in a number of places in this press release and include, but are not limited to, statements regarding Snail’s intent, belief or current expectations. These forward-looking statements include information about possible or assumed future results of Snail’s business, financial condition, results of operations, liquidity, plans and objectives. The statements Snail makes regarding the following matters are forward-looking by their nature: upcoming tames and content releases for ARK: Fantastic Tames Season 1 and ARK: Dragontopia in November and December 2026; the further development of Bellwright, including the traversal update planned for the end of 2026; the commercial potential of Snail’s AAA pipeline; Snail’s ARK content pipeline extending through 2027 and Snail’s ongoing content strategy to expand the franchise’s reach and longevity; Snail’s recently released titles, together with the anticipated ARK: Dragontopia skyworld map in December supporting fourth quarter performance; and being well positioned to build on the momentum generated this year.
Any forward-looking statements included herein reflect our current views, and they involve certain risks and uncertainties, including, among others, acceptance of our titles in the marketplace and the successful development, marketing or sale of our titles and our ability to retain our key employees or maintain our Nasdaq listing. These risks should not be construed as exhaustive and should be read together with the other cautionary statement included in our Annual Report on Form 10-K for the year ended December 31, 2025, subsequent Quarterly Reports on Form 10-Q and current reports on Form 8-K filed with the Securities and Exchange Commission. Any forward-looking statement speaks only as of the date on which it was initially made. We undertake no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, changed circumstances or otherwise, unless required by law.

Investor Contact:

John Yi and Steven Shinmachi
Gateway Group, Inc.
949-574-3860
SNAL@gateway-grp.com


Snail, Inc. and Subsidiaries
Condensed Consolidated Balance Sheets as of September 30, 2026 and December 31, 2025 (Unaudited)
             
    September 30,
2026
    December 31,
2025
 
             
ASSETS                
                 
Current Assets:                
Cash and cash equivalents   $ 12,104,332     $ 8,568,164  
Restricted cash and cash equivalents     562,000       187,000  
Accounts receivable, net of allowances for credit losses of $523,500 as of September 30, 2026 and December 31, 2025     7,052,196       12,528,347  
Loan and interest receivable – related party     109,255       107,759  
Prepaid expenses – related party     3,339,620       2,700,474  
Prepaid expenses and other current assets     2,677,154       2,232,485  
Prepaid taxes     611,871       4,734,007  
Total current assets     26,456,428       31,058,236  
                 
Restricted cash and cash equivalents, net of current portion     1,748,000       1,748,000  
Prepaid expenses – related party, net of current portion     5,582,500       8,282,974  
Property and equipment, net     4,107,573       4,146,175  
Intangible assets, net     3,763,110       3,827,927  
Intangible assets, net – related party     4,166,667       4,916,667  
                 
Other noncurrent assets, net     1,130,406       604,793  
Operating lease right-of-use assets, net     4,537,349       4,722,366  
Total assets   $ 51,492,033     $ 59,307,138  
                 
LIABILITIES, NONCONTROLLING INTERESTS AND STOCKHOLDERS’ DEFICIT                
                 
Current Liabilities:                
Accounts payable   $ 5,432,378     $ 5,506,332  
Accounts payable – related parties     16,556,305       20,067,013  
Accrued expenses and other liabilities     3,577,183       3,364,150  
Interest payable – related parties     527,770       527,770  
Convertible notes at fair value     —       3,842,189  
Current portion of long-term debt     1,350,071       1,305,880  
Current portion of deferred revenue     17,305,342       14,799,840  
Current portion of operating lease liabilities     485,905       393,448  
Total current liabilities     45,234,954       49,806,622  
                 
Accrued expenses     625,354       468,106  
Revolving loan     2,500,000       5,000,000  
Long-term debt, net of current portion     3,356,578       4,292,538  
Deferred revenue, net of current portion     5,326,512       17,282,685  
Operating lease liabilities, net of current portion     4,188,089       4,336,240  
Total liabilities     61,231,487       81,186,191  
                 
Commitments and contingencies                
                 
Stockholders’ Deficit:                
Class A common stock, $0.0001 par value, 500,000,000 shares authorized; 3,485,979 shares issued and 3,205,095 shares outstanding as of September 30, 2026, and 2,076,467 shares issued and 1,806,412 shares outstanding as of December 31, 2025     348       208  
Class B common stock, $0.0001 par value, 100,000,000 shares authorized; 5,749,716 shares issued and outstanding as of September 30, 2026 and December 31, 2025     575       575  
                 
                 
Additional paid-in capital     33,341,655       26,926,245  
Accumulated other comprehensive loss     (315,197 )     (275,049 )
Accumulated deficit     (33,587,550 )     (39,352,510 )
Treasury stock at cost (270,055 shares as of September 30, 2026 and December 31, 2025)     (3,671,806 )     (3,671,806 )
Total Snail, Inc. deficit     (4,231,975 )     (16,372,337 )
Noncontrolling interests     (5,507,479 )     (5,506,716 )
Total stockholders’ deficit     (9,739,454 )     (21,879,053 )
Total liabilities, noncontrolling interests and stockholders’ deficit   $ 51,492,033     $ 59,307,138  

Snail, Inc. and Subsidiaries
Condensed Consolidated Statements of Operations and Comprehensive Income (Loss) for the Three and Nine Months Ended September 30, 2026 and 2025 (Unaudited)
             
    Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
    2026     2025     2026     2025  
                         
Revenues, net   $ 33,061,435     $ 13,819,527     $ 80,032,536     $ 56,116,149  
Cost of revenues     15,418,013       13,805,121       43,044,890       43,299,471  
                                 
Gross profit     17,643,422       14,406       36,987,646       12,816,678  
                                 
Operating expenses:                                
General and administrative     4,911,867       4,844,261       14,537,874       13,283,701  
Research and development     4,619,542       3,731,441       13,087,364       10,634,595  
Advertising and marketing     901,768       884,914       2,585,262       3,711,480  
Depreciation     13,034       67,915       38,602       203,579  
Impairment of film assets     24,250       336,134       190,237       751,853  
Total operating expenses     10,470,461       9,864,665       30,439,339       28,585,208  
                                 
Income (loss) from operations     7,172,961       (9,850,259 )     6,548,307       (15,768,530 )
                                 
Other income (expense):                                
Interest income     55,718       492,088       155,799       553,966  
Interest income – related party     504       504       1,496       1,496  
Interest expense     (188,873 )     (194,189 )     (547,044 )     (444,304 )
Other (expense) income     56,060       130,529       (3,971 )     192,323  
Foreign currency transaction gain (loss)     10,436       (8,519 )     18,695       (76,697 )
Total other (expense) income, net     (66,155 )     420,413       (375,025 )     226,784  
                                 
Income (loss) before provision for (benefit from) income taxes     7,106,806       (9,429,846 )     6,173,282       (15,541,746 )
                                 
Provision for (benefit from) income taxes     435,891       (1,564,152 )     409,086       10,833,616  
                                 
Net income (loss)     6,670,915       (7,865,694 )     5,764,196       (26,375,362 )
                                 
Net loss attributable to non-controlling interests     (88 )     (1,153 )     (763 )     (2,391 )
                                 
Net income (loss) attributable to Snail, Inc.     6,671,003       (7,864,541 )     5,764,959       (26,372,971 )
                                 
Comprehensive income (loss) statement:                                
                                 
Net income (loss)     6,670,915       (7,865,694 )     5,764,196       (26,375,362 )
                                 
Other comprehensive income (loss) related to foreign currency translation adjustments, net of tax     (19,619 )     4,462       (45,458 )     68,282  
Other comprehensive income related to credit adjustments, net of tax     —       997       5,310       23,020  
                                 
Total comprehensive income (loss)   $ 6,651,296     $ (7,860,235 )   $ 5,724,048     $ (26,284,060 )
                                 
Net income (loss) attributable to Class A common stockholders:                                
Basic   $ 2,377,869     $ (1,847,559 )   $ 1,790,950     $ (6,066,325 )
Diluted   $ 2,377,869     $ (1,847,559 )   $ 1,792,798     $ (6,066,325 )
                                 
Net income (loss) attributable to Class B common stockholders:                                
Basic   $ 4,293,134     $ (6,016,982 )   $ 3,974,009     $ (20,306,646 )
Diluted   $ 4,293,134     $ (6,174,656 )   $ 3,974,009     $ (20,585,138 )
                                 
Income (loss) per share attributable to Class A common stockholders:                                
Basic   $ 0.75     $ (1.05 )   $ 0.69     $ (3.53 )
Diluted   $ 0.75     $ (1.05 )   $ 0.68     $ (3.53 )
                                 
Income (loss) per share attributable to Class B common stockholders:                                
Basic   $ 0.75     $ (1.05 )   $ 0.69     $ (3.53 )
Diluted   $ 0.75     $ (1.07 )   $ 0.69     $ (3.58 )
                                 
Weighted-average shares used to compute income (loss) per share attributable to Class A common stockholders:                                
Basic     3,184,637       1,765,493       2,591,200       1,717,647  
Diluted     3,184,637       1,765,493       2,619,768       1,717,647  
                                 
Weighted-average shares used to compute income (loss) per share attributable to Class B common stockholders:                                
Basic     5,749,716       5,749,716       5,749,716       5,749,716  
Diluted     5,749,716       5,749,716       5,749,716       5,749,716  

Snail, Inc. and Subsidiaries
Condensed Consolidated Statements of Cash Flows for the Nine Months Ended September 30, 2026 and 2025 (Unaudited)
             
    2026     2025  
             
Cash flows from operating activities:                
Net income (loss)   $ 5,764,196     $ (26,375,362 )
Adjustments to reconcile net income (loss) to net cash provided by operating activities:                
Amortization – intangible assets, net     505,070       190,981  
Amortization – intangible assets, net – related party     750,000       —  
Amortization – film assets     271,054       1,025,201  
Amortization – loan origination fees and debt discounts     6,915       (16,073 )
Loss on change in fair value of convertible notes     154,669       268,220  
Gain on change in fair value of warrant liabilities     (76,423 )     (481,825 )
Depreciation – property and equipment     38,602       203,579  
Impairment of film assets     190,237       751,853  
Gain on remeasurement of previously held equity interest     —       (7,857 )
Gain on lease termination     (1,799 )     —  
Stock-based compensation expense     146,130       325,941  
Gain on sale of fixed assets     (22,200 )     —  
Deferred taxes, net     —       10,808,885  
                 
Changes in assets and liabilities, net of business acquisitions:                
Accounts receivable     5,476,151       2,351,251  
Accounts receivable – related party     —       3,836,866  
Prepaid expenses – related party     2,061,328       (2,692,532 )
Prepaid expenses and other current assets     (444,669 )     514,921  
Prepaid taxes     4,122,136       2,893,867  
Other noncurrent assets, net     (986,317 )     (1,152,434 )
Accounts payable     (113,954 )     581,910  
Accounts payable – related parties     (3,510,708 )     (325,322 )
Accrued expenses and other liabilities     1,053,244       791,258  
Loan and interest receivable – related party     (1,496 )     (1,496 )
Lease liabilities     131,122       (243,095 )
Deferred revenue     (9,450,671 )     10,901,655  
Net cash provided by operating activities     6,062,617       4,150,392  
                 
Cash flows from investing activities:                
Acquisition of software     —       (290,000 )
Acquisition of software licenses     (400,253 )     (2,989,026 )
Investments in software     —       (849,138 )
Net cash paid for acquisition of Matrioshka     —       (9,719 )
Acquisition of fixed assets     —       (9,109 )
Proceeds from sale of fixed assets     22,200       —  
Net cash used in investing activities     (378,053 )     (4,146,992 )
                 
Cash flows from financing activities:                
Proceeds from at-the-market offering, net of issuance costs     4,796,702       —  
Repayments on promissory note     —       (64,419 )
Repayments on notes payable     (891,769 )     (271,658 )
Repayments on convertible notes     (3,125,298 )     (1,414,705 )
Repayments on revolving loan     (2,500,000 )     —  
Borrowings on term loan     —       3,500,000  
Cash proceeds from exercise of warrants     —       159,000  
Proceeds from issuance of convertible notes     —       3,000,000  
Cash paid in lieu of fractional shares     (73 )     —  
Payments of loan origination fees     (7,500 )     —  
Net cash (used in) provided by financing activities     (1,727,938 )     4,908,218  
                 
Effect of foreign currency translation on cash and cash equivalents     (45,458 )     69,113  
                 
Net increase in cash and cash equivalents, and restricted cash and cash equivalents     3,911,168       4,980,731  
                 
Cash and cash equivalents, and restricted cash and cash equivalents – beginning of the period     10,503,164       8,238,944  
                 
Cash and cash equivalents, and restricted cash and cash equivalents – end of the period   $ 14,414,332     $ 13,219,675  
                 
Supplemental disclosures of cash flow information                
Cash paid during the period for:                
Interest   $ 443,069     $ 477,157  
Income taxes   $ 182,428     $ 612,007  
Noncash transactions during the period for:                
Liabilities converted to equity upon exercise of warrants   $ 606,541     $ 323,113  
Acquisition of film licenses in accounts payable   $ —     $ 1,050  
Acquisition of software and software licenses in accounts payable   $ 40,000     $ 2,000  
Change in fair value of notes recorded in accumulated other comprehensive income   $ 5,310     $ 18,568  
Right-of-use assets obtained in exchange for lease liability   $ (288,229 )   $ (124,214 )
Net assets acquired in a business combination   $ —     $ 5,461  
Debt converted to equity   $ 866,250     $ 231,000  

Reports revenue of $19.3 million for the third quarter of 2026, company reiterates full-year revenue guidance

Shared new advances in RNA therapeutic manufacturing at TIDES Europe

Entered into a $60 million term loan facility with Trinity Capital; initial tranche used to refinance current debt

REDWOOD CITY, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — Codexis, Inc. (NASDAQ: CDXS), a leading provider of enzymatic solutions for efficient and scalable manufacturing of complex therapeutics, today announced financial results for the third quarter ended September 30, 2026, and provided a business update.

“I am pleased with our outstanding progress in 2026, through both innovation and technical achievements, that has garnered attention from leading innovators in the siRNA field,” stated Alison Moore, PhD, President and Chief Executive Officer of Codexis. “Last week we presented new data at the TIDES Europe annual meeting showing successful scale-up of the ECO Synthesis® Manufacturing Platform at 100-gram scale with high product quality, and including improved process performance with reduced cycle time. In addition, we significantly strengthened our balance sheet with an equity raise of approximately $25 million in net proceeds, completed in July. This was followed by a $60 million term loan agreement which we closed earlier this month, of which $42.5 million was used to refinance our existing debt. We have made significant progress in industrializing our technology while simultaneously increasing our revenue base, managing expenses, and improving the financial stability of our company.”

Third Quarter and Recent Business Highlights

  • In November, the company completed a $60 million senior secured loan agreement with Trinity Capital. The first tranche of $42.5 million was used to replace the existing agreement the company had with Innovatus Life Sciences Lending Fund I, LP. The remainder of the facility is available for future drawdown, subject to certain conditions.
  • In November, Codexis hosted key presentations at the 2026 TIDES Europe annual meeting. These presentations demonstrated successful production of 100 grams of high-quality oligonucleotide. The company also showed greater potency of stereo-defined siRNA as compared to chemically synthesized material. These presentations have continued to expand industry-wide interest in the ECO Synthesis Manufacturing Platform.
  • In October, Codexis announced a feasibility study with a pioneer company in the siRNA field, where Codexis will use its ECO Synthesis technology to synthesize stereo-defined fragments. This innovator uses a fragment synthesis and ligation strategy and is seeking a method to increase the purity of fragments above what can be attained using standard solid phase chemistry techniques.
  • The company successfully completed an equity financing in July that raised a total of approximately $25 million in net proceeds.

Upcoming Milestones

  • Advance its partnerships with drug innovators toward clinical stage manufacturing agreements.
  • Codexis expects to begin retrofit construction for its ECO GMP Manufacturing Center in the new year, with the facility being operational by the end of 2027. The purpose of this facility is to provide siRNA material for preclinical investigations and Phase 1 and 2 clinical trials.
  • Expand relationships with existing and future CDMO partners with a goal of commencing a strategic partner agreement.

Third Quarter 2026 Financial Highlights

  • Total revenues were $19.3 million for the third quarter of 2026 compared to $8.6 million in the third quarter of 2025. The increase was primarily due to higher product revenue, driven by the approval and launch of new products by our customers with higher margins compared to more established products.
  • Product gross margin was 74.5% for the third quarter of 2026, compared to 64% in the third quarter of 2025. The increase in gross margin was largely due to a shift in sales toward more profitable products, and declines in less profitable, established products.
  • Research and Development expenses for the third quarter of 2026 were $12.6 million compared to $13.9 million in the third quarter of 2025. The decrease was primarily due to lower employee-related costs, reduced spending on outside services and lower lab supplies, partially offset by higher allocable costs.
  • Selling, General & Administrative expenses for the third quarter of 2026 were $10.1 million compared to $11.2 million in the third quarter of 2025. The decrease was primarily due to lower employee-related costs associated with reduced headcount, lower stock-based compensation expenses, and lower allocable costs, partially offset by higher facility-related expenses.
  • The net loss for the third quarter of 2026 was $8.1 million, or $0.08 per share, compared to a net loss of $19.6 million, or $0.22 per share, for the third quarter of 2025.
  • As of September 30, 2026, Codexis had $72.7 million in cash, cash equivalents, and short-term investments. During the third quarter, Codexis successfully completed an equity financing that raised a total of approximately $25 million in net proceeds. In addition, after the close of the third quarter Codexis entered into a $60 million term loan facility with a $42.5 million drawdown at closing, which was used to retire existing debt.

2026 Financial Revenue Guidance Reiterated, Gross Margin Estimate Increased

Codexis reiterated and updated its full-year 2026 financial guidance as follows:

  • Total revenues are expected to be in the range of $72 million to $76 million. Gross margin for the year 2026 is expected to be in the low 70% range.
  • Codexis expects that its existing cash, cash equivalents, and short-term investments will be sufficient to fund its planned operations through the end of 2028. The financial guidance and cash runway projections include the expenses associated with the build out of the GMP production facility.

Conference Call and Webcast

Codexis will hold a conference call and webcast today beginning at 4:30 pm ET. A live webcast will be available on the Investors section of the Company website at ir.codexis.com. The conference call dial-in numbers are 877-705-2976 for domestic callers and 201-689-8798 for international callers.

A webcast replay will be available on the Investors section of the Company website, beginning approximately two hours after the completion of the call.

About Codexis

Codexis® is a leading provider of high-performance enzymatic solutions for efficient and scalable therapeutics manufacturing. The company is currently developing its proprietary ECO Synthesis® Manufacturing Platform, an aqueous enzymatic process that may offer a scalable alternative to traditional solid phase organic synthesis of oligonucleotide manufacturing. Initially, Codexis is applying its technology to address the rapidly growing demand for RNAi therapeutics. Codexis’ unique enzymes can drive improvements such as higher yields, increased purity, reduced energy usage and waste generation, stereoisomer control of siRNA, and improved overall capacity in manufacturing at substantially lower capital requirements, all of which may lead to greater efficiency and reduced costs. In addition, the company supplies high-performance enzymes through its BioCatalysis business that are used in the manufacture of multiple commercially available small molecule therapeutics. For additional information, please visit https://www.codexis.com.

Forward Looking Statements

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. In some cases, you can identify forward-looking statements by terminology such as “aim,” “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “design,” “due,” “estimate,” “expect,” “goal,” “intend,” “may,” “objective,” “plan,” “positioned,” “potential,” “predict,” “forecast,” “guidance,” “look forward to,” “milestone,” “on track,” “outlook,” “project,” “runway,” “seek,” “should,” “suggest,” “target,” “will,” “would” and other similar expressions that are predictions of or indicate future events and future trends, or the negative of these terms or other comparable terminology. To the extent that statements contained in this press release are not descriptions of historical facts, they are forward-looking statements reflecting the current beliefs and expectations of management. These forward-looking statements include, but are not limited to, statements regarding anticipated milestones, including technical milestones, data releases and public announcements related thereto; Codexis’ expectation that its existing cash, cash equivalents and short-term investments will be sufficient to fund its planned operations, including the expenses associated with the build out of its GMP production facility; Codexis’ financial guidance; the receipt of required permits and approvals for, and the timing, cost and completion of, the retrofit construction of Codexis’ ECO GMP Manufacturing Center, the anticipated timing of the commencement of retrofit construction and the facility being operational, and the intended use of the facility to supply siRNA material for preclinical investigations and clinical trials; Codexis’ ability to advance partnerships with drug innovators toward clinical stage manufacturing agreements; Codexis’ ability to expand relationships with CDMO partners and to commence a strategic partner agreement; the availability of the remainder of Codexis’ loan facility for future drawdown, subject to certain conditions; Codexis’ feasibility study; and the anticipated benefits, performance, sustainability and commercial potential of Codexis’ ECO Synthesis® Manufacturing Platform and the anticipated level of customer interest in and adoption of Codexis’ technology. The forward-looking statements in this press release are subject to the safe harbor created by these sections, speak only as of the date of this press release, and are qualified by the cautionary statements set forth below. You should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties and other factors that are, in some cases, beyond Codexis’ control and that could materially affect actual results. Factors that could materially affect actual results include, among others: Codexis’ dependence on its licensees and collaborators and the risk that collaborators may terminate their development programs under their respective license agreements with Codexis; Codexis’ dependence on a limited number of products and customers, and potential adverse effects to Codexis’ business if its customers’ products are not received well in the markets; Codexis’ ability to successfully develop and commercialize new technology and products for its target markets, including its ECO Synthesis® Manufacturing Platform; the risk that competitors and potential competitors who have greater resources and experience than Codexis may develop products and technologies that make Codexis’ products and technologies obsolete; Codexis’ ability to advance partnerships with drug innovators toward clinical stage manufacturing agreements and to establish strategic partnerships with CDMOs; the timing, cost and successful completion of the retrofit construction of Codexis’ GMP facility and the risk that the facility may not achieve operational readiness on the anticipated timeline; the risk that the FDA or other regulatory authorities may not accept enzymatically synthesized oligonucleotides or that the regulatory pathway for ECO Synthesis-derived products may be longer or more uncertain than anticipated; risks relating to Codexis’ dependence on its GMP facility, and the risk of delays or cost overruns; the concentration of Codexis’ revenue in a limited number of contracts and milestones; Codexis’ potential need for additional capital in the future in order to expand its business and the risk that additional capital may not be available on acceptable terms or at all; Codexis’ ability to comply with debt covenants under its loan facility and to satisfy scheduled principal and interest payment obligations, and the effect of the terms of that facility on Codexis’ liquidity and operating flexibility; risks relating to Codexis’ ability to obtain, maintain, defend and enforce patents, trade secrets and other intellectual property rights covering its technologies, and the risk of intellectual property infringement claims by third parties; Codexis’ dependence on key personnel and its ability to attract and retain qualified employees; Codexis’ reliance on third-party suppliers; risks relating to cybersecurity incidents and data integrity; volatility in the market price of Codexis’ common stock and its ability to maintain compliance with Nasdaq listing requirements; Codexis’ ability to accurately forecast financial and operational performance; the impact of market, political and economic conditions on Codexis’ business, financial condition and share price; and the impact of international trade policies, including tariffs, sanctions and trade barriers, on Codexis’ business. Additional information about factors that could materially affect actual results can be found in Codexis’ Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC) on March 11, 2026, and in Codexis’ Quarterly Report on Form 10-Q for the quarterly period ended September 30, 2026, to be filed with the SEC, in each case including under the caption “Risk Factors,” and in Codexis’ other filings with the SEC. Codexis expressly disclaims any intent or obligation to update these forward-looking statements, except as required by law. Codexis’ results presented in this press release are not necessarily indicative of Codexis’ operating results for any future periods.

For More Information
Investor Contact
Georgia Erbez
(650) 421-8100
ir@codexis.com

       
Codexis, Inc.
Condensed Consolidated Statements of Operations
(Unaudited)
(In Thousands, Except Per Share Amounts)
       
  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
Revenues:              
Product revenue $ 15,740     $ 6,807     $ 36,149     $ 20,246  
Research and development revenue   3,522       1,794       13,277       11,226  
Total revenues   19,262       8,601       49,426       31,472  
Costs and operating expenses:              
Cost of product revenue   4,014       2,465       9,590       7,295  
Research and development   12,587       13,868       35,741       40,586  
Selling, general and administrative   10,097       11,217       30,803       35,889  
Total costs and operating expenses   26,698       27,550       76,134       83,770  
Loss from operations   (7,436 )     (18,949 )     (26,708 )     (52,298 )
Interest income   658       634       1,859       1,969  
Interest and other expense, net   (1,341 )     (1,292 )     (3,933 )     (3,217 )
Loss before income taxes   (8,119 )     (19,607 )     (28,782 )     (53,546 )
Provision for income taxes   9       8       55       29  
Net loss $ (8,128 )   $ (19,615 )   $ (28,837 )   $ (53,575 )
               
Net loss per share, basic and diluted $ (0.08 )   $ (0.22 )   $ (0.30 )   $ (0.62 )
Weighted average common stock shares used in computing net loss per share, basic and diluted   107,259       90,251       96,507       86,045  
                               

Codexis, Inc.
Condensed Consolidated Statements of Comprehensive Loss
(Unaudited)
(In Thousands)
       
  Three Months Ended September 30,   Nine Months Ended September 30,
    2026       2025       2026       2025  
Net loss $  (8,128 )   $  (19,615 )   $  (28,837 )   $  (53,575 )
Other comprehensive income (loss):              
Unrealized income (loss) on available-for-sale short-term investments, net of tax    (42 )      15         (63 )      (40 )
Comprehensive loss $  (8,170 )   $  (19,600 )   $  (28,900 )   $  (53,615 )
               

Codexis, Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
(In Thousands)
       
       
  September 30, 2026   December 31, 2025
Assets      
Current assets:      
Cash and cash equivalents $ 29,213     $ 50,793  
Restricted cash, current   —       478  
Short-term investments   43,446       27,416  
Financial assets:      
Accounts receivable   6,499       8,757  
Contract assets   8,590       492  
Unbilled receivables   604       1,480  
Total financial assets   15,693       10,729  
Less: allowances   (43 )     (43 )
Total financial assets, net   15,650       10,686  
Inventories   2,096       1,817  
Prepaid expenses and other current assets   5,360       5,626  
Total current assets   95,765       96,816  
Restricted cash   1,612       1,612  
Investment in non-marketable equity securities   2,498       2,498  
Right-of-use assets – Operating leases, net   27,659       30,501  
Property and equipment, net   13,329       13,024  
Goodwill   2,463       2,463  
Other non-current assets   895       883  
Total assets $ 144,221     $ 147,797  
Liabilities and Stockholders’ Equity      
Current liabilities:      
Accounts payable $ 5,760     $ 1,554  
Accrued compensation   8,751       11,042  
Other accrued liabilities   4,105       2,768  
Current portion of lease obligations – Operating leases   2,946       2,944  
Current portion of long-term debt   11,793       —  
Deferred revenue   735       7,009  
Total current liabilities   34,090       25,317  
Deferred revenue, net of current portion   —       360  
Long-term lease obligations – Operating leases   28,043       30,159  
Long-term debt   29,485       40,105  
Other long-term liabilities   1,365       1,327  
Total liabilities   92,983       97,268  
       
Stockholders’ equity:      
Common stock   11       9  
Additional paid-in capital   686,899       657,292  
Accumulated other comprehensive income (loss)   (55 )     8  
Accumulated deficit   (635,617 )     (606,780 )
Total stockholders’ equity   51,238       50,529  
Total liabilities and stockholders’ equity $ 144,221     $ 147,797  
       

REMAIN-1 Pivotal Cohort met its six-month co-primary endpoint with high statistical significance (p=0.0023); Revita® participants retained approximately 80% of GLP-1-induced weight loss versus 67% for sham

Planned FDA De Novo submission in late Q4 2026; topline 12-month data from the REMAIN-1 Pivotal Cohort anticipated in Q1 2027

Sharpened focus on Revita, with a workforce reduction of approximately 45% and discontinuation of internal Rejuva development

Cash runway into Q2 2027, through planned De Novo submission and anticipated 12-month pivotal data; quarterly operating cash spending expected to be reduced by approximately 50%, to approximately $8 million, by the end of Q2 2027

Conference call today at 4:30 p.m. ET

BURLINGTON, Mass., Nov. 12, 2026 (GLOBE NEWSWIRE) — Fractyl Health, Inc. (Nasdaq: GUTS) (the Company or Fractyl), a clinical-stage metabolic therapeutics company focused on pioneering novel approaches to treat obesity and type 2 diabetes (T2D), today announced third quarter 2026 financial results and provided business updates. The Company also reiterated its anticipated Revita® milestones, including a planned U.S. Food and Drug Administration (FDA) De Novo marketing application submission in late Q4 2026 and topline 12-month data from the REMAIN-1 Pivotal Cohort in Q1 2027, and its cash runway guidance into Q2 2027.

“There are approximately 1 million Americans discontinuing GLP-1s each month, and these individuals are at high risk of weight and metabolic rebound. In this context, we believe the positive pivotal results from REMAIN-1 represent a defining moment for Fractyl. In the most rigorous stress test we could conceive, a single Revita procedure met its six-month co-primary endpoint with high statistical significance,” said Harith Rajagopalan, M.D., Ph.D., Co-Founder, President and Chief Executive Officer of Fractyl. “Armed with positive data, we have focused the Company around Revita’s post-GLP-1 weight maintenance opportunity. We expect the capital we have today to be sufficient to fund our planned De Novo submission and upcoming 12-month pivotal data and. Our goal is for Revita to potentially establish an entirely new therapeutic category of post-GLP-1 weight maintenance by aiming to reverse years of diet-induced damage to the gut.”

Select Recent Revita Clinical Highlights

Fractyl is studying Revita in the REMAIN-1 weight maintenance program, which is designed to evaluate Revita’s potential to maintain weight loss following GLP-1 based therapy discontinuation. The REMAIN-1 program includes three distinct participant cohorts that are conducted under a single IDE: the REVEAL-1 Cohort, the REMAIN-1 Midpoint Cohort and the REMAIN-1 Pivotal Cohort.

  • In October 2026, Fractyl reported positive topline six-month results from the REMAIN-1 Pivotal Cohort, a 308-participant, multicenter, randomized, double-blind, sham-controlled study of Revita for weight maintenance in adults with obesity following discontinuation of GLP-1 therapy. REMAIN-1 met its pre-specified six-month co-primary endpoint of weight loss retention, as patients treated with a single Revita procedure demonstrated a highly statistically significant reduction in weight regain compared to sham (p=0.0023).
    • Six-month co-primary endpoint met: In the modified intention-to-treat (mITT) population (N=308), Revita participants maintained approximately 80% of their GLP-1-induced weight loss after a single treatment at six months with high statistical significance versus sham (p=0.0023). 32% of Revita participants were either weight stable or had further weight loss at six months post GLP-1 discontinuation (<2% regain or incremental loss) versus 18% for sham (post hoc; nominal p=0.020).
    • Dose-dependent effect observed: In a post hoc analysis by ablation length, participants who received 12 to 18 cm of duodenal ablation had 43% less regain than sham (observed mean weight regain of 4.7% versus 8.2%; n=107 versus 74). Participants who received 20 cm or more had 53% less regain than sham (mean regain of 3.8%; n=47).
    • Treatment effect grew over time: The difference in weight regain between Revita and sham widened at each assessment, nearly doubling from Month 3 to Month 6.
    • Favorable interim safety data: There have been no device- or procedure-related serious adverse events, no deaths, and no unanticipated adverse device effects observed as of the September 24, 2026, data cut-off date. Related adverse events were predominantly mild and peri-procedural, with 94% occurring within seven days of the procedure.
  • The second co-primary endpoint, the proportion of Revita participants maintaining at least 5% total body weight loss relative to their pre-tirzepatide weight at one year, will be assessed against an FDA-mandated pre-specified performance goal of greater than 50%.

Commercial Readiness and Market Access

  • In September 2026, Fractyl hosted a Commercial Investor Day outlining the potential path to commercializing Revita in post-GLP-1 weight maintenance. The Company’s launch plan focuses on the top 100 to 200 of approximately 1,000 accredited bariatric centers in the United States, beginning with 30 to 50 centers in the first year.
  • In October 2026, the American Medical Association published Category III CPT code 1122T, a dedicated code for the Revita procedure, which takes effect January 1, 2027, well ahead of a potential U.S. launch in early 2028.
  • The Centers for Medicare & Medicaid Services (CMS) has proposed RAPID, a pathway that could align Medicare coverage with FDA authorization for breakthrough devices. More than 160 comments were filed during the comment period, nearly all supporting an on-ramp for devices with pivotal trials already underway, including comments from ASGE and ASMBS that cited Revita. Fractyl expects to learn whether CMS adopts such an on-ramp in early January 2027.
  • In October 2026, Fractyl announced findings from company-sponsored market research highlighting strong patient interest in a one-time procedural approach to weight maintenance following GLP-1 therapy. Among nearly 300 current or recent GLP-1 users surveyed, 33% preferred stopping GLP-1 therapy and receiving a hypothetical endoscopic procedure.
  • In October 2026, Fractyl announced additions to its U.S. patent portfolio for Revita. The U.S. Patent and Trademark Office issued U.S. Patent No. 12,740,821, covering features of the Revita single-use catheter, with a term extending to November 28, 2042, and issued a Notice of Allowance for a patent application directed to Revita’s thermal dosing method. Fractyl’s intellectual property portfolio includes 39 granted U.S. patents, approximately 40 pending U.S. applications and more than 50 issued patents outside the United States.

Sharpened Focus on Revita

On October 21, 2026, Fractyl adopted a plan to sharpen its strategic focus on its Revita program in connection with a strategic reprioritization, concentrating its financial and operational resources on advancing Revita toward potential FDA marketing authorization and commercialization in post-GLP-1 weight maintenance.

  • Workforce Reduction: The Company is reducing its workforce by approximately 45%, with the reduction expected to be completed during the fourth quarter of 2026. The Company estimates that it will incur charges of approximately $2 million for severance and other employee termination-related costs, with the majority of such costs to be incurred in the fourth quarter of 2026.
  • Reduced Quarterly Operating Cash Spending: As cost reductions take effect and REMAIN-1 Pivotal Cohort expenditures decline, the Company expects quarterly operating cash spending to be reduced by approximately 50%, to approximately $8 million, by the end of Q2 2027.
  • Rejuva Strategic Alternatives: The Company is discontinuing internal development of its Rejuva gene therapy program and is seeking strategic alternatives to maximize the value of the program. There can be no assurance that the Company’s review of strategic alternatives for Rejuva will result in any transaction, and the Company does not intend to disclose further developments unless and until it determines that disclosure is appropriate or required.

Appointment of Michael Wartell as Independent Director

  • On November 6, 2026, the Company announced that effective November 2, 2026, the Board of Directors (the “Board”) increased the size of the Board from nine to ten and appointed Michael Wartell as a Class III director, with a term expiring at the Company’s 2027 annual meeting of stockholders and until his successor is duly elected and qualified or until his earlier resignation or removal. Mr. Wartell is the President of Bluerose Associates LLC and has extensive experience serving as an independent director for both public and private corporations, specializing in guiding companies through complex situations.

Fractyl Forward: Advancing Revita Toward a New Therapeutic Category in Obesity Care

The Company continues to anticipate the following milestones:

  • Late Q4 2026: Planned FDA De Novo submission for Revita in post-GLP-1 weight maintenance.
  • January 1, 2027: Category III CPT code 1122T for the Revita procedure takes effect.
  • Q1 2027: Anticipated topline 12-month data from the REMAIN-1 Pivotal Cohort, including the second co-primary endpoint.
  • Late 2027: Potential FDA marketing authorization.
  • Early 2028: Potential U.S. commercial launch.

As in all applications, the FDA indicated that final pathway determinations will be made following review of the complete safety dataset, which the Company intends to include in its potential De Novo submission.

Third Quarter 2026 Financial Results

  • Research and Development Expenses: R&D expenses were $12.5 million for the quarter ended September 30, 2026, compared to $17.5 million for the same period in 2025. The decrease of $5.0 million was primarily related to reduced spending on Fractyl’s Revita and Rejuva programs, as well as lower personnel-related expenses.
  • Selling, General and Administrative Expenses: SG&A expenses were $6.2 million for the quarter ended September 30, 2026, compared to $5.2 million for the same period in 2025. The increase of $1.0 million was primarily driven by higher personnel-related expenses and stock compensation expenses, partially offset by decreased professional service fees.
  • Net Loss: For the quarter ended September 30, 2026, Fractyl reported a net loss of $14.2 million, compared to a net loss of $45.6 million for the same period in 2025. The decrease in net loss of $31.5 million was driven by a $4.0 million reduction in operating expenses, a $25.7 million favorable non-cash change in the fair value of warrant liabilities, $1.6 million lower non-cash loss from change in fair value of debt, and $0.1 million higher interest income.
  • Adjusted EBITDA: Adjusted EBITDA was negative $16.0 million for the quarter ended September 30, 2026, compared to negative $20.8 million for the same period in 2025. The decrease in the non-GAAP adjusted loss of $4.8 million was primarily due to reduced operating expenses excluding stock compensation expenses.
  • Cash Position: As of September 30, 2026, Fractyl had approximately $31.5 million in cash and cash equivalents. Based on current business plans, the Company believes its cash position will fund operations into the second quarter of 2027, through the planned De Novo submission and anticipated 12-month REMAIN-1 Pivotal Cohort data, subject to compliance with the minimum liquidity covenant under the Company’s credit agreement, as discussed further in the “Liquidity and Capital Resources” section of our Quarterly Report on Form 10-Q.

Webcast and Conference Call Information
Fractyl will host a conference call to discuss its third quarter financial results and provide business updates on Thursday, November 12, 2026, at 4:30 p.m. ET. A live webcast of the conference call can be accessed in the “Events” section of Fractyl’s website at ir.fractyl.com. The webcast will be archived and available for replay for at least 30 days after the event.

Ahead of the call, Fractyl invited all shareholders to submit and vote on questions for management through Say by Robinhood by visiting: https://app.saytechnologies.com/fractyl-health-2026-q3. Management will address a selection of the most-voted shareholder questions during the call.

About Fractyl Health

Fractyl is a clinical-stage metabolic therapeutics company focused on pioneering novel approaches to treat obesity and type 2 diabetes. The Company’s lead product candidate, Revita, is an endoscopic procedural therapy in pivotal development for post-GLP-1 weight maintenance. Fractyl’s goal is to change the course of metabolic disease, advancing treatment from chronic management toward prevention and reversal of disease. Fractyl is headquartered in Burlington, Massachusetts.

About Revita

The Revita® DMR System is Fractyl’s lead product candidate, designed to remodel the duodenal lining via a single, minimally invasive endoscopic procedure intended to restore healthy nutrient sensing and signaling disrupted by chronic metabolic disease. By targeting duodenal dysfunction, Revita is designed to address an underlying driver of obesity and enable durable weight maintenance following GLP-1 discontinuation. Revita has received FDA Breakthrough Device Designation for weight maintenance in people with obesity who discontinue GLP-1 therapies. Revita is for investigational use only in the United States and is CE marked in the European Union and United Kingdom.

Non-GAAP Financial Measures

This press release contains certain financial information that is not presented in conformity with U.S. generally accepted accounting principles (GAAP), including Adjusted EBITDA, which is a non-GAAP financial measure as defined in Regulation G promulgated under the Securities Exchange Act of 1934. This non-GAAP financial measure is provided as supplemental information to Fractyl’s financial measures presented in this press release in accordance with GAAP.

The Company defines Adjusted EBITDA as net loss adjusted to exclude (i) interest income, net, (ii) depreciation expense, (iii) stock-based compensation expense, (iv) change in fair value of notes payable and (v) change in fair value of warrant liabilities.

Management believes Adjusted EBITDA provides useful supplemental information to investors regarding the Company’s core operating performance and facilitates period-to-period comparisons by excluding items that are non-cash or non-operational in nature and may vary in magnitude. Adjusted EBITDA is also used by management in evaluating the Company’s operating performance and in planning and forecasting activities.

The non-GAAP financial measures used by Fractyl may not be the same or calculated in the same manner as those used and calculated by other companies. Non-GAAP financial measures have limitations as analytical tools and should not be considered in isolation or as a substitute for Fractyl’s financial results prepared and reported in accordance with GAAP. This non-GAAP measure should not be construed as an inference that the Company’s future results will be unaffected by unusual or non-recurring items. A reconciliation of Adjusted EBITDA reported in this press release to the most comparable GAAP measure for the respective periods appears in the table captioned “Reconciliation of GAAP Net Loss to Adjusted EBITDA” later in this press release.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact are forward-looking statements. These statements may be identified by words such as “aims,” “anticipates,” “believes,” “could,” “estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,” “seeks,” “will” and variations of these words or similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these words. Forward-looking statements in this press release include, without limitation, statements regarding: the potential benefits of Fractyl’s sharpened strategic focus and reprioritization, including the workforce reduction and its anticipated impact on Fractyl’s expenditures and financial runway; Fractyl’s anticipated financial performance, including cash and cash equivalents, for any period of time; Fractyl’s expected quarterly operating cash spending and cash runway, including the period over which its existing cash and cash equivalents will be sufficient to satisfy the minimum liquidity covenant under its credit agreement; Fractyl’s ability to continue as a going concern; the promise and potential impact of Fractyl’s clinical trial data and product candidates, including Revita’s potential for maintaining weight loss after GLP-1 based therapy discontinuation; the design, initiation, timing and results of clinical studies or readouts, including readouts from the REMAIN-1 Pivotal Cohort, including anticipated 12-month data from the REMAIN-1 Pivotal Cohort and the second co-primary endpoint; the potential launch or commercialization of any of Fractyl’s product candidates or products; Fractyl’s commercial readiness activities and launch plans; coding, coverage and payment for Revita, including the effectiveness and use of Category III CPT code 1122T, the timing and outcome of any CMS rulemaking, including RAPID, and eligibility for or timing of Medicare transitional pass-through payment or other coverage, which are subject to AMA and CMS review and are not assured; Fractyl’s regulatory strategy, including the timing of any potential De Novo marketing application submission and the potential use and benefits of the De Novo pathway (FDA pre-submission feedback is advisory and non-binding, and there is no assurance that FDA will accept a De Novo marketing application submission or that the Revita DMR System will receive marketing authorization, or as to the timing of any such authorization); the potential treatment population or benefits for any of Fractyl’s product candidates or products; Fractyl’s exploration of strategic alternatives for Rejuva and the potential benefits thereof; Fractyl’s strategic and product development objectives and goals; and the timing of any of the foregoing. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause Fractyl’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the risks that are discussed more fully in Fractyl’s filings with the Securities and Exchange Commission (the SEC) including the “Risk Factors” section of Fractyl’s Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on March 24, 2026, and other documents Fractyl subsequently files with or furnishes to the SEC, including Fractyl’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2026, filed with the SEC on November 12, 2026. These forward-looking statements are based on management’s current estimates and expectations. While Fractyl may elect to update such forward-looking statements at some point in the future, Fractyl disclaims any obligation to do so, even if subsequent events cause Fractyl’s views to change.

Contact

Brian Luque, Head of Investor Relations and Corporate Development
IR@fractyl.com, 951.206.1200

Fractyl Health, Inc.
Selected Consolidated Balance Sheet Data
(in thousands)
(unaudited)
 
  September 30,
2026
    December 31,
2025
 
Cash and cash equivalents $ 31,515     $ 81,540  
Restricted cash   4,255       4,255  
Working capital (1)   16,989       69,247  
Total assets   65,925       121,402  
Notes payable, long-term   29,234       30,586  
Total liabilities   79,141       111,944  
Total stockholders’ equity (deficit)   (13,216 )     9,458  
 

(1) Working capital is defined as total current assets less total current liabilities.

Fractyl Health, Inc.
Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except for share and per share information)
(unaudited)
 
  Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
  2026     2025     2026     2025  
Operating expenses:                      
Research and development $ 12,454     $ 17,457     $ 41,864     $ 58,043  
Selling, general and administrative   6,195       5,237       16,701       15,489  
Total operating expenses   18,649       22,694       58,565       73,532  
Loss from operations   (18,649 )     (22,694 )     (58,565 )     (73,532 )
Other income (expense), net:                      
Interest income, net   297       166       1,321       895  
Change in fair value of notes payable   (284 )     (1,868 )     (2,276 )     (3,824 )
Change in fair value of warrant liabilities   4,499       (21,201 )     29,070       (20,724 )
Other expense, net   (13 )     (6 )     (20 )     (42 )
Total other income (expense), net   4,499       (22,909 )     28,095       (23,695 )
Net loss and comprehensive loss $ (14,150 )   $ (45,603 )   $ (30,470 )   $ (97,227 )
Net loss per share, basic and diluted (2) $ (1.07 )   $ (8.46 )   $ (2.30 )   $ (21.51 )
Weighted-average number of common shares outstanding, basic and diluted (2)   13,250,080       5,387,747       13,226,323       4,520,293  
 

(2) All share and per share information has been retroactively adjusted to reflect the 1-for-12 reverse stock split effected on October 2, 2026. Refer to Quarterly Report on Form 10-Q for details.

Fractyl Health, Inc.
Reconciliation of GAAP Net Loss to Adjusted EBITDA
(in thousands)
(unaudited)
 
  Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
  2026     2025     2026     2025  
Net loss $ (14,150 )   $ (45,603 )   $ (30,470 )   $ (97,227 )
Interest income, net   (297 )     (166 )     (1,321 )     (895 )
Depreciation   276       290       835       850  
EBITDA   (14,171 )     (45,479 )     (30,956 )     (97,272 )
Stock-based compensation expense   2,386       1,638       7,413       4,829  
Change in fair value of notes payable   284       1,868       2,276       3,824  
Change in fair value of warrant liabilities   (4,499 )     21,201       (29,070 )     20,724  
Adjusted EBITDA $ (16,000 )   $ (20,772 )   $ (50,337 )   $ (67,895 )

FAIRFAX, Va., Nov. 12, 2026 (GLOBE NEWSWIRE) — WidePoint Corporation (NYSE American: WYY), a leading provider of Secure Mobility Management solutions, reported results for the third quarter ended September 30, 2026.

Third Quarter 2026 and Recent Operational Highlights:

  • 37th consecutive quarter of positive Adjusted EBITDA
  • 12th consecutive quarter of positive free cash flow
  • Awarded 40 new and replacement task orders with a total value of approximately $33.7 million during the third quarter under the U.S. Department of Homeland Security’s (“DHS”) Cellular Wireless Managed Services (“CWMS”) 2.5 bridge contract
  • Awarded the CWMS 2.5 bridge contract, a 6-month IDIQ with a ceiling value of approximately $113 million

Third Quarter 2026 Financial Highlights:

  • Revenues were $45.1 million, an increase of $9.5 million from the same quarter last year
  • Gross margin was 14%, and gross margin excluding carrier services revenue was 30%
  • Net loss was $(192,000) or $(0.02) per share, compared to a net loss of $(559,000) or a loss of $(0.06) per share in the same quarter last year
  • Adjusted EBITDA1, a non-GAAP financial measure, was $338,000 compared to $344,000 in the same quarter last year
  • Free cash flow1, a non-GAAP financial measure, was $338,000 compared to $324,000 in the same quarter last year
  • As of September 30, 2026, unrestricted cash was $10.1 million with no bank debt
  • As of September 30, 2026, federal contract backlog was approximately $209 million

Nine Months 2026 Financial Highlights:

  • Revenues were $123.6 million, an increase of $17.3 million from the same period last year
  • Gross margin was 14%, and gross margin excluding carrier services revenue was 33%
  • Net loss was $(49,000) or $(0.00) per share, compared to a net loss of $(1.9) million or a loss of $(0.20) per share in the same period last year
  • Adjusted EBITDA1, a non-GAAP financial measure, was $1.7 million, a 178% increase from the same period last year
  • Free cash flow1, a non-GAAP financial measure, was $1.6 million, a 242% increase from the same period last year

1 Free cash flow and Adjusted EBITDA are non-GAAP financial measures. See below for the definition of such measures and a reconciliation to GAAP.

Management Commentary
WidePoint CEO, Jin Kang commented: “The decision by the Government Accountability Office (“GAO”) to sustain the protest related to the CWMS 3.0 award has undoubtedly created near-term disruption; however, we believe the issues are temporary in nature. While sustained protests are not unprecedented in federal procurement, we recognize this was an unexpected setback. With respect to the pending CWMS 3.0 procurement, DHS has requested revised proposals, and WidePoint has submitted a revised proposal for evaluation by DHS. We await DHS’s announcement of the results of its evaluation and the resulting award decision. We will have no further comment on the status of the CWMS 3.0 procurement at this time.

“Importantly, operations continue uninterrupted under the CWMS 2.5 bridge contract. In the third quarter alone, we received 40 new and replacement task orders valued at approximately $33.7 million and we continue to receive additional task orders in the fourth quarter. We also hold CWMS 2.0 task orders extending into 2027, providing a meaningful runway as the CWMS 3.0 award process moves towards resolution.

“Beyond CWMS, integration efforts under the ATV contract continue to advance, and we remain on track for our targeted year-end go-live. We also recently received a letter of authorization from CDW as we work toward potentially becoming the official subcontractor supporting CDW’s role as the Official IT Equipment and Solutions Provider for the LA28 Olympic and Paralympic Games and Team USA. In addition, we strengthened our federal growth initiative through the hiring a professional with extensive experience in federal government acquisitions, IDIQ contracts, and the implementation of a Program Management Office (PMO) model similar to that of the DHS PMO model to maximize opportunities under the NASA SEWP VI contract vehicle. Together, these developments reinforce our confidence in WidePoint’s long-term growth prospects and execution against multiple strategic opportunities.”

  Third Quarter 2026 Financial Summary      
         
    THREE MONTHS ENDED
    SEPTEMBER 30,
  (In millions except per share amounts)   2026       2025  
      (Unaudited)  
  REVENUES $ 45.1     $ 35.5  
  GROSS PROFIT   6.2       5.3  
  GROSS PROFIT %   14 %     15 %
  OPERATING EXPENSES   6.4       5.7  
  NET LOSS   (0.19 )     (0.56 )
  LOSS PER SHARE BASIC AND DILUTED $ (0.02 )   $ (0.06 )
  EBITDA   0.23       0.19  
  ADJUSTED EBITDA   0.34       0.34  
  FREE CASHFLOW   0.34       0.32  

Nine Months 2026 Financial Summary   NINE MONTHS ENDED
    SEPTEMBER 30,
(In millions except per share amounts)     2026       2025  
      (Unaudited)  
REVENUES   $ 123.6     $ 106.3  
GROSS PROFIT     17.6       15.2  
GROSS PROFIT %     14 %     14 %
OPERATING EXPENSES     17.9       17.2  
NET LOSS     (0.05 )     (1.90 )
LOSS PER SHARE BASIC AND DILUTED   $ (0.00 )   $ (0.20 )
EBITDA     1.19       0.10  
ADJUSTED EBITDA     1.73       0.62  
FREE CASHFLOW     1.64       0.48  


Conference Call
WidePoint’s management will host the conference call today (November 12, 2026) at 4:30 p.m. Eastern time (1:30 p.m. Pacific time) to discuss these results.

U.S. dial-in number: 888-506-0062
International number: 973-528-0011
Access Code: 633294

Please call the conference telephone number 5-10 minutes prior to the start time. An operator will register your name and organization. If you have any difficulty connecting with the conference call, please contact Gateway Group at (949) 574-3860.

The conference call will be broadcast live and available for replay here and via the investor relations section of the company’s website.

A replay of the conference call will be available after 7:30 p.m. Eastern time on the same day through Thursday, November 26, 2026.

Toll-free replay number: 877-481-4010
International replay number: 919-882-2331
Replay ID: 54625

About WidePoint
WidePoint Corporation (NYSE American: WYY) is a leading technology Managed Solution Provider (MSP) dedicated to securing and protecting the mobile workforce and enterprise landscape. WidePoint is recognized for pioneering technology solutions that include Identity & Access Management (IAM), Mobility Managed Services (MMS), Telecom Management, Information Technology as a Service, Cloud Security, and Analytics & Billing as a Service (ABaaS). To learn more, visit https://www.widepoint.com .

Non-GAAP Financial Measures
WidePoint uses a variety of operational and financial metrics, including non-GAAP financial measures such as EBITDA, Adjusted EBITDA, and Free cashflow, to enable it to analyze its performance and financial condition. The presentation of non-GAAP financial information should not be considered in isolation or as a substitute for, or superior to, the financial information prepared and presented in accordance with GAAP. A reconciliation of GAAP Net income to EBITDA and Adjusted EBITDA and Free cashflow is provided below:

        THREE MONTHS ENDED   NINE MONTHS ENDED
        SEPTEMBER 30,   SEPTEMBER 30,
          2026       2025       2026       2025  
Other adjustments to reconcile net loss to adjusted EBITDA and free cashflow (Unaudited)   (Unaudited)
                     
NET LOSS $ (192,000 )   $ (559,200 )   $ (48,600 )   $ (1,901,700 )
Adjustments to reconcile net income to EBITDA:              
  Depreciation and amortization   432,800       650,400       1,395,000       2,085,600  
  Income tax provision (benefit)   13,000       134,400       (28,600 )     (12,000 )
  Interest income   (68,200 )     (83,400 )     (257,400 )     (226,200 )
  Interest expense   42,500       47,600       131,300       155,100  
                     
EBITDA     228,100       189,800       1,191,700     $ 100,800  
                     
  Stock-based compensation expense   110,200       154,100       533,900       519,000  
                     
Adjusted EBITDA $ 338,300     $ 343,900     $ 1,725,600     $ 619,800  
  Capital expenditures   –       (20,031 )     (85,537 )     (140,918 )
Free cashflow $ 338,300     $ 323,869     $ 1,640,063     $ 478,882  

WidePoint uses EBITDA, Adjusted EBITDA and Free cashflow as supplemental non-GAAP measure of performance. WidePoint defines EBITDA as net income excluding (i) interest expense, (ii) provision for or benefit from income taxes, (iii) depreciation and amortization, and (iv) Impairment charges. Adjusted EBITDA excludes certain amounts included in EBITDA such as stock-based compensation expense. WidePoint defined Free cashflow as Adjusted EBITDA less capital expenditures. Management believes that adjustments for certain non-cash or other items and the exclusion of certain pass-through revenue and expenses should enhance stockholders’ ability to evaluate the Company’s performance, as such measures provide additional insights into the factors and trends affecting its business. Therefore, the Company excludes these items from its GAAP financial measures to calculate these unaudited non-GAAP measures. These unaudited non-GAAP measures may not be comparable to similarly titled measures reported by other companies and should be considered in addition to, and not as a substitute for GAAP.

Safe Harbor Statement
This press release contains forward-looking statements concerning our business, operations and financial performance and condition as well as our plans, objectives and expectations for our business operations and financial performance and condition that are subject to risks and uncertainties. All statements other than statements of historical fact included herein are forward-looking statements. You can identify these statements by words such as “aim,” “anticipate,” “assume,” “believe,” “could,” “due,” “estimate,” “expect,” “goal,” “intend,” “may,” “objective,” “plan,” “potential,” “positioned,” “predict,” “should,” “target,” “will,” “would” and other similar expressions that are predictions of or indicate future events and future trends. These forward-looking statements are based on current expectations, estimates, forecasts and projections about our business and the industry in which we operate and our management’s beliefs and assumptions. These statements are not guarantees of future performance or development and involve known and unknown risks, uncertainties and other factors that are in some cases beyond our control. All forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those that we expected, including, the impact of supply chain issues; our ability to successfully execute our strategy; our ability to sustain profitability and positive cash flows; our ability to access sufficient financing on acceptable terms given the tightening credit markets due to the current banking environment; our ability to gain market acceptance for our products; our ability to win new contracts, execute contract extensions and expand scope of services on existing contracts; our ability to compete with companies that have greater resources than us; our ability to penetrate the commercial sector to expand our business; our ability to identify potential acquisition targets and close such acquisitions; our ability to successfully integrate acquired businesses with our existing operations; our ability to maintain a sufficient level of inventory necessary to meet our customers demand due to supply shortage and pricing; our ability to retain key personnel; our ability to mitigate the impact of increases in interest rates; the impact of increasingly volatile public equity markets on our market capitalization; the impact and outcome of negotiations around the Federal debt ceiling; our ability to mitigate the impact of inflation; and the risk factors set forth in our Form 10-Q for the quarter ended September 30, 2026 filed with the SEC on November 12, 2026.

The forward-looking statements included herein are made only as of the date hereof. We undertake no obligation to publicly update or revise any forward-looking statement as a result of new information, future events or otherwise, except as otherwise required by law.

WidePoint Investor Relations:
Gateway Group, Inc.
Matt Glover or John Yi
949-574-3860
WYY@gateway-grp.com

WIDEPOINT CORPORATION AND SUBSIDIARIES
CONDENSED CONSOLIDATED UNAUDITED BALANCE SHEETS
         
         
         
  SEPTEMBER 30,   DECEMBER 31,
    2026       2025    
ASSETS (Unaudited)  
CURRENT ASSETS        
Cash and cash equivalents $ 10,103,515     $ 9,818,503    
Restricted cash   1,042,925       2,647,990    
Accounts receivable, net of allowance for credit losses        
of $134,996 and $57,454, respectively   13,926,953       15,002,571    
Unbilled accounts receivable   46,456,528       33,548,228    
Other current assets   16,173,725       5,196,613    
         
Total current assets   87,703,646       66,213,905    
         
NONCURRENT ASSETS        
Property and equipment, net   331,649       480,082    
Lease right of use asset   3,325,968       3,904,479    
Intangible assets, net   2,554,282       3,352,296    
Goodwill   5,811,578       5,811,578    
Deferred tax assets, net   –       1,123    
Other long-term assets   874,257       48,822    
         
Total assets $ 100,601,380     $ 79,812,285    
         
LIABILITIES AND STOCKHOLDERS’ EQUITY  
         
CURRENT LIABILITIES        
Accounts payable $ 24,814,711     $ 25,891,150    
Accrued expenses   43,572,673       31,159,173    
Current portion of deferred revenue   15,835,046       6,114,402    
Current portion of lease liabilities   771,493       751,233    
         
Total current liabilities   84,993,923       63,915,958    
         
NONCURRENT LIABILITIES        
Lease liabilities, net of current portion   3,337,801       3,930,495    
Deferred revenue, net of current portion   800,045       435,151    
Deferred tax liabilities, net   15,496       –    
         
Total liabilities   89,147,265       68,281,604    
         
Commitments and contingencies (Note 16)   –       –    
         
STOCKHOLDERS’ EQUITY        
Preferred stock, $0.001 par value; 10,000,000 shares        
authorized; 2,045,714 shares issued and none outstanding   –       –    
Common stock, $0.001 par value; 30,000,000 shares        
  authorized; 10,028,316 and 9,892,565 shares        
issued and outstanding, respectively   10,029       9,894    
Additional paid-in capital   103,715,779       103,733,790    
Accumulated other comprehensive loss   (389,726 )     (379,665 )  
Accumulated deficit   (91,881,967 )     (91,833,338 )  
         
Total stockholders’ equity   11,454,115       11,530,681    
         
Total liabilities and stockholders’ equity $ 100,601,380     $ 79,812,285    
         

WIDEPOINT CORPORATION AND SUBSIDIARIES
CONDENSED CONSOLIDATED UNAUDITED STATEMENTS OF OPERATIONS
                 
                       
                       
        THREE MONTHS ENDED   NINE MONTHS ENDED  
        SEPTEMBER 30,   SEPTEMBER 30,  
          2026       2025       2026       2025    
        (Unaudited)  
REVENUES $ 45,066,908     $ 35,526,949     $ 123,642,520     $ 106,320,797    
COST OF REVENUES (including amortization and depreciation of                
$261,479, $424,411, $813,530, and $1,402,836, respectively)   38,881,325       30,251,637       106,012,455       91,149,722    
                       
GROSS PROFIT   6,185,583       5,275,312       17,630,065       15,171,075    
                       
OPERATING EXPENSES                
Sales and marketing   646,723       677,618       1,908,155       1,986,897    
General and administrative expenses (including share-based                
compensation of $110,241, $154,111, $533,892 and $518,988, respectively)   5,572,106       4,832,422       15,393,752       14,486,853    
Depreciation and amortization   171,382       225,908       580,768       682,718    
                       
Total operating expenses   6,390,211       5,735,948       17,882,675       17,156,468    
                       
LOSS FROM OPERATIONS   (204,628 )     (460,636 )     (252,610 )     (1,985,393 )  
                       
OTHER INCOME (EXPENSE)                
Interest income   68,191       83,439       257,350       226,209    
Interest expense   (42,445 )     (47,671 )     (131,277 )     (155,126 )  
Other income (expense), net   (70 )     93       49,358       590    
                       
Total other income (expense), net   25,676       35,861       175,431       71,673    
                       
LOSS BEFORE INCOME TAX PROVISION (BENEFIT)   (178,952 )     (424,775 )     (77,179 )     (1,913,720 )  
INCOME TAX PROVISION (BENEFIT)   13,057       134,410       (28,551 )     (12,013 )  
                       
NET LOSS $ (192,009 )   $ (559,185 )   $ (48,628 )   $ (1,901,707 )  
                       
EARNINGS PER SHARE, BASIC AND DILUTED $ (0.02 )   $ (0.06 )   $ (0.00 )   $ (0.20 )  
                       
WEIGHTED-AVERAGE SHARES OUTSTANDING, BASIC AND DILUTED   10,018,287       9,655,173       9,928,651       9,598,478    
                       

WIDEPOINT CORPORATION AND SUBSIDIARIES
CONDENSED CONSOLIDATED UNAUDITED STATEMENTS OF CASH FLOWS
             
             
             
        NINE MONTHS ENDED
        SEPTEMBER 30,
          2026       2025  
        (Unaudited)
CASH FLOWS FROM OPERATING ACTIVITIES      
Net loss $ (48,628 )   $ (1,901,707 )
Adjustments to reconcile net income (loss) to net cash provided by      
(used in) operating activities:      
Deferred income tax expense   10,200       50,200  
Depreciation expense   597,013       699,768  
Provision for credit losses   96,043       38,694  
Amortization of intangibles   798,015       1,385,786  
Share-based compensation expense   533,892       518,988  
Non-cash lease expense   213,288       164,883  
(Gain) loss on disposal of fixed assets   (49,043 )     8,161  
Changes in assets and liabilities:      
Accounts receivable and unbilled receivables   (11,942,864 )     6,784,375  
Inventories   (8,459,836 )     (712,121 )
Other current assets   (2,520,191 )     (1,542,224 )
Other assets   (825,435 )     161,150  
Accounts payable and accrued expenses   11,383,901       (1,124,995 )
Income tax payable   (76,746 )     (55,111 )
Deferred revenue and other liabilities   10,098,943       1,556,822  
Other liabilities   (198,896 )     (152,483 )
             
Net cash (used in) provided by operating activities   (390,344 )     5,880,186  
             
CASH FLOWS FROM INVESTING ACTIVITIES      
Purchases of property and equipment   (85,537 )     (140,918 )
Proceeds from the sale of property and equipment   49,043       –  
             
Net cash used in investing activities   (36,494 )     (140,918 )
             
CASH FLOWS FROM FINANCING ACTIVITIES      
Advances on bank line of credit   –       2,800,000  
Repayments of bank line of credit advances   –       (2,800,000 )
Principal repayments under finance lease obligations   (353,521 )     (412,299 )
Withholding taxes paid on behalf of employees on net settled equity awards   (551,768 )     (130,745 )
             
Net cash used in financing activities   (905,289 )     (543,044 )
             
Net effect of exchange rate on cash   12,074       (52,334 )
             
NET (DECREASE) INCREASE IN CASH, CASH EQUIVALENTS, AND RESTRICTED CASH   (1,320,053 )     5,143,890  
             
CASH, CASH EQUIVALENTS, AND RESTRICTED CASH, beginning of period   12,466,493       7,817,395  
             
CASH, CASH EQUIVALENTS, AND RESTRICTED CASH, end of period $ 11,146,440     $ 12,961,285  
             
CASH, CASH EQUIVALENTS, AND RESTRICTED CASH CONSISTED OF THE FOLLOWING:  
Cash and cash equivalents $ 10,103,515     $ 12,128,422  
Restricted cash   1,042,925       832,863  
             
        $ 11,146,440     $ 12,961,285  
             

Third Quarter 2026 Product Revenues Grew 15.7% Year-over-Year to $5.5 Million; Appellee Brief Filed with the Federal Circuit in Support of the $78 Million Final Judgment; Shares Repurchased Under $5.0 Million Program

CORSICANA, Texas, Nov. 12, 2026 (GLOBE NEWSWIRE) — Birchtech Corp. (NYSE American: BCHT) (TSX: BCHT) (“Birchtech” or the “Company”), a leader in specialty activated carbon technologies for sustainable air and water treatment, today reported financial results for the third quarter ended September 30, 2026.

Key Third Quarter 2026 & Subsequent Operational Highlights

  • Filed the Company’s appellee brief with the U.S. Court of Appeals for the Federal Circuit on October 22, 2026, asking the court to affirm in full the jury’s verdict and the approximately $78 million final judgment entered in favor of Birchtech against the CERT defendants by the U.S. District Court for the District of Delaware; post-judgment interest continues to accrue while the appeal is pending.
  • Commenced an initial repurchase of shares in the open market in September 2026 under the Company’s previously authorized $5.0 million share repurchase program, buying back 103,864 shares of common stock during the third quarter funded from available cash.
  • Entered into an agreement with an industry partner for the supply of high-grade granular activated carbon (GAC), under which the Company expects to begin supplying water treatment customers in early 2027, starting at 2,000 tons per year; the Company believes the agreement will provide a faster, more capital-efficient route into the water treatment market without requiring capital expenditures to establish its initial supply capabilities.
  • Appointed Charlie Cooper as Business Development Manager, effective October 1, 2026, to expand Birchtech’s relationships with municipalities, public service districts and utility operators, with a focus on rural and small water systems; Mr. Cooper brings 21 years of water treatment experience, including five years overseeing the West Virginia Rural Water Association’s Emerging Contaminants Program.
  • Advanced the Company’s ongoing efforts to develop its first Carbon Rejuvenation® reactivation facility, which is intended to provide water utilities with a lower-cost, more sustainable alternative to replacing spent GAC with virgin media; the Company’s thermally rejuvenated GAC has demonstrated PFAS removal performance comparable to virgin carbon.
  • Presented Birchtech’s air and water platforms to institutional investors at the H.C. Wainwright Global Investment Conference, Gabelli Funds’ PFAS Symposium, Noble Capital Markets’ Emerging Growth Conference, and Lake Street Capital Markets’ Best Ideas Growth Conference.

Management Commentary

Richard MacPherson, Birchtech President and Chief Executive Officer, commented: “Our third quarter results reflect the underlying strength of our core business. Product revenues grew 15.7% year-over-year to $5.5 million, driven by stronger demand in our mercury emissions business and sales to the water treatment market, while SG&A expenses declined 35% largely reflecting significantly lower legal costs associated with prior-year licensing activity. In October, we filed our appellee brief with the Federal Circuit, which details the evidence and the law supporting the jury’s findings on inducement, contributory infringement and damages and asks the court to affirm the approximately $78 million final judgment in full. The appeal does not pause the accrual of post-judgment interest, and we remain committed to collecting the judgment in full while continuing to turn former users of our patented SEA® technology into licensed, long-term product supply customers.

“In water, we continued to build the commercial foundation required to scale. Our ongoing efforts to develop our first Carbon Rejuvenation® reactivation facility advanced during the quarter, and we believe this capacity will offer utilities a more affordable and sustainable path to PFAS compliance. Our new GAC agreement with an industry partner should accelerate the growth of our water business, and give us a faster path to revenue starting in early 2027, with no capital spending on our part to establish an initial supply. Combined with the expanded capabilities of our Analytical Design Centers, which help smaller systems identify the most cost-effective path to compliance before committing capital, these steps should strengthen our ability to support utilities from initial testing through treatment and media reuse.

“Looking ahead, our priorities as we close out 2026 and move into 2027 are clear: convert licensed coal-fired utilities into recurring SEA® supply customers, advance offtake discussions with prospective utility partners for our first planned Carbon Rejuvenation® facility, and expand our presence across the water treatment market through our Design Centers. With $10.8 million in cash and no debt, we have the financial flexibility to execute on these priorities, while our air business continues to serve as a self-funding engine for the growth of our water platform,” concluded MacPherson.

Third Quarter 2026 Financial Results

Revenues totaled $5.5 million in the third quarter of 2026, as compared to $7.4 million in the same year-ago quarter. Product revenues increased 15.7% to $5.5 million, as compared to $4.7 million in the same year-ago quarter, primarily due to the mix of plants running and increased demand for coal in connection with the Company’s mercury emissions business, driven by more extreme weather conditions and higher natural gas prices. Additionally, sales were recognized for the water treatment market in 2026 compared to none in the comparable period of 2025. The change in total revenues was primarily due to $2.6 million in one-time up-front license fees recognized in the third quarter of 2025, for which there were no comparable transactions in the third quarter of 2026.

Gross profit totaled $1.6 million, or 29.9% of total revenues, as compared to $4.0 million, or 54.8% of total revenues, in the same year-ago quarter. The change in gross profit was primarily driven by a shift in revenue mix, as the Company recognized higher-margin licensing revenues in the prior-year period compared to no licensing revenues in the third quarter of 2026. The impact of the decrease in licensing revenue was partially offset by greater product sales in the third quarter of 2026 compared to the prior year period.

SG&A expenses decreased 35% to $1.8 million in the third quarter of 2026, as compared to $2.7 million in the same year-ago quarter. The decrease in expenses was primarily due to lower professional fees, as the prior-year period included significantly higher legal fees associated with licensing activities that generated revenues during that period.

R&D expenses remained approximately flat at $0.5 million in the third quarter of 2026, comparable to $0.5 million in the same year-ago quarter. R&D expenses relate to research conducted to develop water treatment products utilizing new sorbent technologies.

Net loss for the third quarter of 2026 totaled $0.3 million, or $0.01 per basic and diluted share, as compared to net income of $0.8 million, or $0.04 per basic and diluted share, in the same year-ago quarter.

Adjusted EBITDA totaled a loss of ($0.5) million for the three months ended September 30, 2026, as compared to a positive $1.0 million during the three months ended September 30, 2025.

Cash as of September 30, 2026, totaled $10.8 million, with no debt, as compared to $2.2 million as of December 31, 2025.

Third Quarter 2026 Earnings Conference Call

Management will host an investor conference call at 5:00 p.m. Eastern time today, Thursday, November 12, 2026, to discuss Birchtech’s third quarter 2026 financial results and provide a corporate update. To participate, please use the following information:

Third Quarter 2026 Earnings Conference Call
Date: Thursday, November 12, 2026
Time: 5:00 p.m. Eastern time
U.S./Canada Dial-in: 1-877-407-0792
International Dial-in: 1-201-689-8263
Conference ID: 13762817
Webcast: BCHT Q3 2026 Earnings Conference Call

Please dial in at least 10 minutes before the start of the call to ensure timely participation.

A telephone playback of the call will be available through Thursday, December 3, 2026. To listen, call 1-844-512-2921 within the United States and Canada or 1-412-317-6671 when calling internationally, using replay pin number 13762817. A webcast replay will be available for one year, using the webcast link above.

About Birchtech Corp.

Birchtech Corp. (NYSE American: BCHT) (TSX: BCHT) is a leader in specialty activated carbon technologies delivering innovative solutions for air and water purification to support a cleaner, more sustainable future. The Company provides patented SEA® sorbent technologies for mercury emissions capture for the coal-fired utility sector and SEA disruptive water purification technologies with a specialization on removing contaminants, including ‘forever chemicals’ such as PFAS, from potable water and industrial wastewater. Backed by a strong intellectual property portfolio and a team of activated carbon experts, Birchtech provides cleaner air to North American communities and is applying this expertise to a novel approach in water purification. To learn more, please visit www.birchtech.com.

Non-GAAP Financial Measures

To supplement our consolidated financial statements presented in accordance with GAAP and to provide investors with additional information regarding our financial results, we consider and are including herein Adjusted EBITDA, a Non-GAAP financial measure. We view Adjusted EBITDA as an operating performance measure and, as such, we believe that the GAAP financial measure most directly comparable to it is net income (loss). We define Adjusted EBITDA as net income adjusted for interest and financing fees, income taxes, depreciation, amortization, stock-based compensation, and other non-cash income and expenses. We believe that Adjusted EBITDA provides us an important measure of operating performance because it allows management, investors, debtholders and others to evaluate and compare ongoing operating results from period to period by removing the impact of our asset base, any asset disposals or impairments, stock-based compensation and other non-cash income and expense items.

Our use of Adjusted EBITDA has limitations as an analytical tool, and this measure should not be considered in isolation or as a substitute for an analysis of our results as reported under GAAP, as the excluded items may have significant effects on our operating results and financial condition. Additionally, our measure of Adjusted EBITDA may differ from other companies’ measure of Adjusted EBITDA. When evaluating our performance, Adjusted EBITDA should be considered with other financial performance measures, including various cash flow metrics, net income and other GAAP results. In the future, we may disclose different non-GAAP financial measures in order to help our investors and others more meaningfully evaluate and compare our future results of operations to our previously reported results of operations.

The following table shows our reconciliation of net income (loss) to Adjusted EBITDA for the three months ended September 30, 2026, and 2025, respectively:

    For the Three Months Ended      
    September 30,     September 30,      
    2026     2025      
    (In thousands)      
                 
Net income (loss)   $ (275 )   $ 788      
                     
Non-GAAP adjustments:                    
Depreciation and amortization     117       107      
Change in fair value of profit share     (252 )     39      
Interest     (88 )     (15 )    
Income taxes     –       1      
Stock based compensation     –       20      
                     
Adjusted EBITDA   $ (498 )   $ 940      
                     

Safe Harbor Statement

With the exception of historical information contained in this press release, content herein may contain “forward-looking statements” that are made pursuant to the Safe Harbor Provisions of the U.S. Private Securities Litigation Reform Act of 1995 or forward-looking information under applicable Canadian securities laws (collectively, “forward-looking statements”). Forward-looking statements are generally identified by using words such as “anticipate,” “believe,” “plan,” “expect,” “intend,” “will,” and similar expressions, but these words are not the exclusive means of identifying forward-looking statements. Forward-looking statements in this release include, without limitation, statements relating to expected developments and growth in Birchtech’s business, the development of the Company’s Carbon Rejuvenation™ capacity, the timing, volumes, revenues and benefits expected under the agreement with an industry partner for the supply of GAC, the enforcement and collection of the Company’s final judgment, the appellate process and its outcome, the timing, and amount or likelihood of any recovery under the judgment, and the accrual and potential recovery of post-judgment interest, and the timing, amount and extent of any future repurchases of the Company’s common stock under its share repurchase program. These statements are based on management’s current expectations and are subject to uncertainty and changes in circumstances. Investors are cautioned that forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from the statements made. In addition, this release contains time-sensitive information that reflects management’s best analysis only as of the date of this release. Birchtech does not undertake any obligation to publicly update or revise any forward-looking statements to reflect future events, information or circumstances that arise after the date of this release. Further information concerning issues that could materially affect financial performance or other forward-looking statements contained in this release can be found in Birchtech’s periodic filings with the Securities and Exchange Commission or Canadian securities regulators.

Investor Relations Contact:

Lucas A. Zimmerman
Managing Director
MZ Group – MZ North America
(949) 259-4987
BCHT@mzgroup.us
www.mzgroup.us

Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.