Targets U.S. military medical logistics by combining ZenaDrone aircraft with Rattler Medical’s temperature-controlled blood containers; flying prototype and demonstrations planned for summer 2027

VANCOUVER, British Columbia, Nov. 12, 2026 (GLOBE NEWSWIRE) — ZenaTech, Inc. (Nasdaq: ZENA) (FSE: 49Q) (BMV: ZENA) (“ZenaTech” or the “Company”), a technology solution provider specializing in AI-powered drones, Drone as a Service (DaaS), enterprise SaaS and Quantum Computing solutions, announces that its ZenaDrone subsidiary has signed a memorandum of understanding (MOU) with Rattler Medical Inc. (“Rattler Medical”), a developer and manufacturer of temperature-controlled containers for transporting human blood. Under the MOU, the two companies will cooperate to develop and manufacture a drone-driven battlefield blood delivery system designed to move temperature-controlled blood to military medical personnel on the battlefield more quickly and efficiently.

“Getting blood to a wounded service member quickly, and at the right temperature, is one of the most difficult logistics problems in combat medicine,” said Shaun Passley, Ph.D., CEO of ZenaTech. “This MOU pairs ZenaDrone’s cargo drone capability with a container system built by a team that has carried blood in the field. It also sets a defined path to a flying prototype and a demonstration with the U.S. military, extending our defense portfolio into battlefield medical logistics, applications we have long targeted for our drone platforms.”

Keeping blood within a safe temperature range from the supply point to the patient is a central challenge in battlefield medicine. The planned system combines Rattler Medical’s far-forward blood resupply capability with ZenaDrone’s payload delivery capability. The container is expected to be carried as payload beneath a ZenaDrone aircraft and either released from the air or delivered on landing, where medical personnel would detach it. The companies plan to develop and test a prototype to determine the most effective delivery method with the prototype expected to be complete within the next three months.

According to the Business Research Company, the global medical drone delivery services market, which includes blood transfer, is expected to grow from US$510 million in 2026 to US$1.27 billion by 2030, representing a compound annual growth rate of 25.5%.

Drone-based delivery is designed to address several limitations of moving blood by ground. Aircraft can reach medical teams faster than vehicles on contested or damaged roads, and they reduce the need to put personnel at risk on resupply routes. Distributing blood across multiple drones, rather than concentrating it in a single conventional convoy, is intended to ensure safe delivery of blood supply if individual conveyance (aircraft or trucks) is lost. The approach also supports just-in-time delivery, allowing medical units to request blood as casualties occur rather than relying solely on pre-positioned stocks.

Rattler Medical was founded by Donald Young, a U.S. Army combat medic veteran, and its team brings firsthand experience in military medicine along with established relationships across the military medical community. ZenaTech expects those relationships, combined with ZenaDrone’s defense engagement activities, to support the path toward demonstrations and future opportunities with U.S. military services.

“As a combat medic, I saw how much a casualty’s outcome can depend on how fast blood reaches the medic treating them,” said Mr. Young, Rattler Medical CEO. “Pairing our far-forward blood resupply capability with ZenaDrone’s aircraft gives medics a way to receive blood where ground transport cannot reach safely, and to receive it from many aircraft at once instead of a single vehicle. Our goal is to put this capability in front of military users next year.”

The companies plan to develop a flying prototype within the next two to three months. ZenaDrone is currently planning to demonstrate the system at a U.S. military facility in the summer 2027. ZenaTech expects to provide further updates as development milestones are achieved.

About ZenaTech

ZenaTech, Inc. (Nasdaq: ZENA) (FSE: 49Q) (BMV: ZENA) is a technology company that specializes in AI autonomy drone platforms to transform commercial, government, and defense sectors. Its subsidiaries include drone manufacturing through ZenaDrone, a global Drone as a Service (DaaS) business, and an enterprise SaaS division of software brands. The Company is executing an acquisition-led DaaS roll-up strategy to digitize and automate legacy service industries like land surveys and inspections, driving drone-based scalable, recurring revenue growth. With an operating footprint spanning North America, Europe, the Middle East, Asia, and Australia, ZenaTech is advancing AI drones for applications such as agriculture and logistics, as well as ISR, cargo, and counter-UAS for U.S. defense and NATO allies. The company is investing in next-generation technologies, including drone swarms, quantum computing, and advanced AI autonomy to capture long-term opportunities in key markets through its R&D initiatives.

About ZenaDrone

ZenaDrone, a subsidiary of ZenaTech, develops and manufactures AI-powered multifunction autonomous drone solutions integrating machine learning, predictive analytics, and advanced computing technologies, for government, defense, and industrial applications. This includes multifunctional drones for surveying, inspections, logistics, security, and defense applications. Its product portfolio under development includes the ZenaDrone 1000 for ISR defense and specialized cargo, the IQ Nano for indoor inventory management and security, the IQ Square for outdoor inspections and maintenance, the IQ Quad for land surveying, the IQ Aqua, for underwater applications, and the IQ Octo for precision agriculture. ZenaDrone operates three global manufacturing facilities in Arizona, Dubai, and Taiwan, and is advancing counter-UAS maritime interceptor drones and an integrated defense system.

About Rattler Medical

Rattler Medical Inc., based in Boise, Idaho, an award-winning company that develops and manufactures temperature-controlled containers designed to store and transport blood in remote and austere environments. The company was founded by Donald Young, a U.S. Army combat medic veteran, to extend the ability of military and emergency medical personnel to carry blood closer to the patient.

Contacts for more information:

Company, Investors, and Media: Linda Montgomery, ZenaTech, 312-241-1415, investors@zenatech.com

Investors: Michael Mason, CORE IR, investors@zenatech.com

Safe Harbor

This press release and related comments by management of ZenaTech, Inc. include “forward-looking statements” within the meaning of U.S. federal securities laws and applicable Canadian securities laws. These forward-looking statements are subject to the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. This forward-looking information relates to future events or future performance of ZenaTech and reflects management’s expectations and projections regarding ZenaTech’s growth, results of operations, performance, and business prospects and opportunities, including statements about anticipated state transportation contract awards and bids, project timelines, and the integration of drone services into transportation survey work. Such forward-looking statements reflect management’s current beliefs and are based on information currently available to management. In some cases, forward-looking information can be identified by terminology such as “may”, “will”, “should”, “expect”, “plan”, “anticipate”, “aim”, “seek”, “is/are likely to”, “believe”, “estimate”, “predict”, “potential”, “continue” or the negative of these terms or other comparable terminology intended to identify forward-looking statements. Forward-looking information in this document includes, but is not limited to ZenaTech’s expectations regarding its revenue, expenses, production, operations, costs, cash flows, and future growth; expectations with respect to future production costs and capacity; ZenaTech’s ability to deliver products to the market as currently contemplated, including its drone products including ZenaDrone 1000, IQ Square, IQ Nano, IQ Quad, ZenaTech 2000, IQ Glider, IQ Sphere, IQ Aqua and Interceptor P-1; ZenaTech’s ability to develop products for markets as currently contemplated; ZenaTech’s anticipated cash needs and it’s needs for additional financing; ZenaTech’s intention to grow the business and its operations and execution risk; expectations with respect to future operations and costs; the volatility of stock prices and market conditions in the industries in which ZenaTech operates; political, economic, environmental, tax, security, and other risks associated with operating in emerging markets; regulatory risks; unfavorable publicity or consumer perception; difficulty in forecasting industry trends; the ability to hire key personnel; the competitive conditions of the industry and the competitive and business strategies of ZenaTech; ZenaTech’s expected business objectives for the next twelve months; ZenaTech’s ability to obtain additional funds through the sale of equity or debt commitments; investment capital and market share; the ability to complete any contemplated acquisitions; changes in the target markets; market uncertainty; ability to access additional capital, including through the listing of its securities in various jurisdictions; management of growth (plans and timing for expansion); patent infringement; litigation; applicable laws, regulations, and any amendments affecting the business of ZenaTech and other related risks and uncertainties disclosed under the heading “Risk Factors” in the Company’s Form F-1, Form 20-F and other filings filed with the United States Securities and Exchange Commission (the “SEC”) on EDGAR through the SEC’s website at www.sec.gov. The Company undertakes no obligation to update forward-looking information except as required by applicable law. Such forward-looking information represents managements’ best judgment based on information currently available. No forward-looking statement can be guaranteed, and actual future results may vary materially. Accordingly, readers are advised not to place undue reliance on forward-looking statements or information.

Adjusted EBITDA of $0.22 million, improves $1.01 million year-over-year, operating loss narrows by 80%

Proprietary products reach 31% of MyMedi.ca sales, up from 19%; QUIX™ launches with 10 SKUs

TORONTO, Nov. 12, 2026 (GLOBE NEWSWIRE) — Avicanna Inc. (“Avicanna” or the “Company”) (TSX: AVCN) (OTCQB: AVCNF) (FSE: 0NN), a commercial-stage international biopharmaceutical company focused on cannabinoid-based medicines, today reported financial results for the third quarter ended September 30, 2026. The Company achieved adjusted EBITDA positive $0.22 million, an improvement of $1.01 million from Q3 2025 and $0.58 million from Q2 2026. Operating expenses declined 30% year-over-year, and the operating loss narrowed 80% to $0.27 million

Avicanna Reports Positive Q3 2026 Results

Revenue was $5.73 million, up 2% from Q2 2026 and the first sequential increase since the April 2026 Veterans Affairs Canada (“VAC”) reimbursement changes. Proprietary unit sales in Canada rose 16% year-over-year through the first nine months of 2026, and patient retention on MyMedi.ca reached record levels.

“As projected, we achieved positive adjusted EBITDA in the third quarter through disciplined optimization of our operations, enhanced margins and prudent cost management,” said Aras Azadian, Founder and Chief Executive Officer of Avicanna. “This milestone was achieved despite the impact of the VAC reimbursement changes, while we continued to invest in our growth initiatives and advance our research and development pipeline. With the progress of our proprietary product portfolio, including the launch of QUIX™, and the continued evolution of MyMedi.ca, we believe Avicanna is better positioned than ever to scale domestically and pursue international expansion.”

Financial Highlights:

  • Adjusted EBITDA and Operating Expenses: Operating expenses declined 30% year-over-year to $3.19 million, and operating loss narrowed 80% to $0.27 million. Adjusted EBITDA income improved to $0.22 million from a loss of $0.79 million in Q3 2025, a $1.01 million improvement, and from a loss of $0.36 million in Q2 2026, a $0.58 million improvement.
  • Revenue: Third-quarter revenue was $5.73 million, down 10% compared to the third quarter of 2025 following the VAC reimbursement changes in April 2026. Revenue quarter over quarter increased by 2%. Revenue for the nine months ending September 30, 2026, was $18.05 million, down 4% year-over-year, primarily reflecting the impact of the VAC changes.
  • Gross margin: Third-quarter gross profit was $2.92 million, a 51% gross margin, an improvement from 49% a year earlier.
  • Financial position: Working capital improved to a $0.11 million surplus at September 30, 2026, compared with a $1.28 million deficit at December 31, 2025. After quarter-end, the Company completed a $2.0 million non-convertible debenture financing on October 29, 2026.

“We made meaningful progress in improving operating efficiency, expanding margins and strengthening working capital. Together with the additional $2.0 million in financing, these developments provide greater financial flexibility as we pursue our business plan and growth strategy.” Stated Nick Hilborn, Chief Financial Officer at Avicanna.

Portfolio Highlights:

  • Canadian commercial advancements: Avicanna sold 176,694 proprietary finished-product units in Canada during the first nine months of 2026, a 16% increase year-over-year. At quarter-end, its Canadian portfolio comprised 68 commercial SKUs and 178 active listings across channels, up 21% and 3%, respectively, from Q2 2026.
  • QUIX™ Rapid Onset launch: Avicanna introduced 10 initial QUIX™ SKUs, including Rapid Onset Capsules and Soft Chews, with 37 commercial listings at quarter-end. The proprietary nano-emulsion-based technology is designed to support cannabinoid dispersion, faster onset and improved absorption in standardized, accurately dosed, non-combustible formats.

MyMedi.ca Highlights:

  • Proprietary product mix: Avicanna proprietary product sales through the platform increased a further 16%, quarter over quarter and represented 31% of MyMedi.ca sales at quarter-end, compared with 19% in the prior year period.
  • Integrated Healthcare Program: Avicanna launched the MyMedi.ca Integrated Healthcare Program to expand healthcare provider-guided medical cannabis care through hospitals, specialty clinics and healthcare networks. The initiative builds on the platform’s pharmacist-led support, education, formulary and reimbursement capabilities to expand the platform beyond traditional cannabis educated medical institutions.

Research and clinical development:

  • QUIX™ translation from the lab to the market: Company continued translating proprietary research and development into commercial products, including the launch of QUIX™ Rapid Onset capsules and soft chews.
  • Advancements of Clinical programs: Including the MyMedi.ca-supported medical cannabis real-world evidence study, the University of Calgary THC dose-finding (DRATT) study and the University Health Network COPE Phase II osteoarthritis pain pilot study.

Q3 2026 Financial Results Call:

The Company will host a virtual earnings call and corporate update on Thursday, November 12, 2026, at 8:30 a.m. ET. Aras Azadian, Founder and CEO, and Nick Hilborn, CFO, will review quarterly results, discuss strategic priorities and address shareholder questions.

Webcast Details:
Date and time: Thursday, November 12, 2026, 8:30 a.m. ET
Webcast and registration: https://zoom.us/webinar/register/WN_GWCRp7rjRmCasxiwdguUDw

About Avicanna Inc.
Avicanna is a commercial-stage international biopharmaceutical company focused on the advancement and commercialization of cannabinoid-based products and formulations for the global medical and pharmaceutical market segments. Avicanna has an established scientific platform including R&D and clinical development leading to the commercialization of more than fifty proprietary, evidence-based finished products and supporting four commercial-stage business pillars.

  • Medical Cannabis Formulary (RHO Phyto™): The formulary offers a diverse range of proprietary products, including oral, sublingual, topical and transdermal deliveries with varying ratios of cannabinoids, supported by ongoing patient and medical community education. The portfolio has recently expanded with the launch of QUIX™ Rapid Onset, a proprietary nano-emulsion technology-based sub-brand featuring a range of fast-onset products, including capsules and soft chews, designed to provide rapid onset of action and enhanced bioavailability. RHO Phyto is an established brand in Canada, currently available nationwide across several channels and expanding into new international markets.
  • Medical Cannabis Care Platform (MyMedi.ca): MyMedi.ca is a medical cannabis care platform formed with the aim of better serving medical cannabis patients’ needs and enhancing the patient journey. MyMedi.ca is operated by Northern Green Canada Inc. and features a diverse portfolio of products and bilingual pharmacist-led patient support programs. MyMedi.ca also provides specialty services to distinct patient groups such as veterans and collaborates with public and private payers for adjudication and reimbursement. MyMedi.ca provides educational resources to the medical community to facilitate the incorporation of medical cannabis into health care regimens.
  • Pharmaceutical Pipeline: Leveraging Avicanna’s scientific platform, vertical integration and real-world evidence, Avicanna has developed a pipeline of proprietary, indication-specific cannabinoid-based candidates that are in various stages of clinical development. These cannabinoid-based candidates aim to address unmet needs in the areas of dermatology, chronic pain and various neurological disorders.
  • Active Pharmaceutical Ingredients (Aureus Santa Marta™): The Company’s majority-owned subsidiary, Santa Marta Golden Hemp SAS (“SMGH”), is a commercial-stage business dedicated to providing various forms of high-quality CBD, THC and CBG to the Company’s international partners for use in the development and production of food, cosmetics, medical and pharmaceutical products. SMGH also forms part of the Company’s supply chain and is a source of reliable input products for its consumer retail, medical cannabis and pharmaceutical products globally.

SOURCE Avicanna Inc.

Stay Connected

For more information about Avicanna, visit www.avicanna.com or contact Ivana Maric by email at ir@avicanna.com.

Cautionary Note Regarding Forward-Looking Information and Statements

www.sedarplus.ca

This news release contains “forward-looking information” within the meaning of applicable securities laws. Forward-looking information contained in this news release may be identified by the use of words such as “may”, “would”, “could”, “will”, “likely”, “expect”, “anticipate”, “believe”, “intend”, “plan”, “forecast”, “project”, “estimate”, “outlook” and other similar expressions. Forward-looking information contained in this news release includes, without limitation, statements with respect to the Company’s future business operations, including the expansion of its proprietary product portfolio, the scaling of MyMedi.ca and its international commercialization opportunities, the opinions or beliefs of management and future business goals. Although the Company believes that the expectations and assumptions on which such forward-looking information is based are reasonable, undue reliance should not be placed on the forward-looking information because the Company can give no assurance that they will prove to be correct. Actual results and developments may differ materially from those contemplated by these statements. Forward-looking information is subject to a variety of risks and uncertainties that could cause actual events or results to differ materially from those projected in the forward-looking information. Such risks and uncertainties include, but are not limited to, current and future market conditions, including the market price of the common shares of the Company, and the risk factors set out in the Company’s annual information form dated March 31, 2026, filed with the Canadian securities regulators and available under the Company’s profile on SEDAR+ at www.sedarplus.ca. The statements in this news release are made as of the date of this release. The Company disclaims any intent or obligation to update any forward-looking information, whether as a result of new information, future events or results or otherwise, other than as required by applicable securities laws. All financial amounts in this news release are expressed in Canadian dollars unless otherwise indicated. Adjusted EBITDA is a non-IFRS financial measure provided by Management. Refer to the MD&A for a description of the calculation.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/a3f5afb3-1e62-4213-a57d-089152bb1656

AUSTIN, Texas, Nov. 12, 2026 (GLOBE NEWSWIRE) — HydroGraph Clean Power Inc. (CSE: HG) (OTCQB: HGRAF) (“HydroGraph” or the “Company”) today announced that the Supreme Court of British Columbia (the “Court”) has issued a final order dated November 10, 2026 approving the previously announced plan of arrangement under the Business Corporations Act (British Columbia) in connection with the Company’s corporate redomicile transactions (the “Redomicile Transactions”).

The Redomicile Transactions were approved by HydroGraph securityholders at the special meeting held on October 29, 2026. Upon completion of the Redomicile Transactions, HydroGraph will become indirectly owned by HydroGraph Inc., a Delaware corporation, and HydroGraph shareholders will receive one share of common stock of HydroGraph Inc. or, if validly elected and subject to applicable eligibility requirements, one exchangeable share for each HydroGraph common share held immediately prior to completion of the Redomicile Transactions.

“Receipt of the final order is another important milestone in the redomicile process,” said Kjirstin Breure, President and Chief Executive Officer of HydroGraph. “We remain focused on completing the remaining steps required to implement the Redomicile Transactions and align our corporate structure with our growing U.S. operations and long-term strategic objectives.”

Additional details regarding the Redomicile Transactions are included in the Company’s management information circular dated September 16, 2026 (the “Circular”), which is available under HydroGraph’s profile on SEDAR+ at www.sedarplus.ca and on the Company’s website at www.hydrograph.com.

Reminder of Exchangeable Share Election Deadline

HydroGraph reminds eligible holders wishing to receive exchangeable shares of HydroGraph ExchangeCo Ltd. that they must submit a properly completed Letter of Transmittal and Consideration Election Form prior to the extended election deadline of 5:00 p.m. (Vancouver time) on November 15, 2026. Shareholders who hold their HydroGraph common shares through a broker, bank or other intermediary should contact their intermediary immediately, as intermediaries may impose internal deadlines that are earlier than the election deadline. Shareholders who do not make a valid election will receive common stock of HydroGraph Inc. Questions regarding the election process may be directed to Apollo Nora Advisors Ltd. toll-free at 1-888-610-4478 or 647-407-5667, or by email at info@apollo-advisors.ca.

Important Information for Investors and Securityholders

This communication is not intended to and does not constitute an offer to sell, buy or exchange or the solicitation of an offer to sell, buy or exchange any securities or the solicitation of any vote or approval in any jurisdiction, nor shall there be any sale, purchase or exchange of securities in any jurisdiction in contravention of applicable law.

HydroGraph securityholders are urged to read the Circular and all other relevant materials carefully because they contain important information regarding HydroGraph, HydroGraph Inc., the Redomicile Transactions and related matters. Copies of the Circular and related meeting materials are available under HydroGraph’s profile on SEDAR+ at www.sedarplus.ca and on the Company’s website at www.hydrograph.com.

Apollo Nora Advisors Ltd. is acting as HydroGraph’s strategic shareholder advisor, proxy solicitation agent and information agent in connection with the Redomicile Transactions.

About HydroGraph

HydroGraph is a leading producer of pristine synthetic graphene using its proprietary Hyperion Reactor technology, which allows for exceptional purity, low energy use, and identical batches. The quality, performance, and consistency of HydroGraph’s graphene follow the Graphene Council’s Verified Graphene Producer® standards, which very few graphene producers are able to meet. For more information or to learn about the HydroGraph story, visit: https://hydrograph.com/. For company updates, please follow HydroGraph on LinkedIn at https://www.linkedin.com/company/hydrograph/ and X at https://x.com/HydroGraphInc.

Trademarks: HydroGraph™, Fractal Graphene™ and Fractal Graphene Paste™

Forward-Looking Statements

This news release contains certain “forward-looking statements” and certain “forward-looking information” within the meaning of applicable Canadian securities laws (collectively, “forward-looking statements”). Forward-looking statements in this news release include, but are not limited to, statements regarding the Redomicile Transactions; the anticipated timing for completion of the Redomicile Transactions; the election deadline for holders wishing to receive exchangeable shares; the receipt of required regulatory and stock exchange approvals; the satisfaction or waiver of the remaining conditions to completion of the Redomicile Transactions; the anticipated benefits of the Redomicile Transactions; the alignment of the Company’s corporate structure with its growing U.S. operations and long-term strategic objectives; and HydroGraph’s plans, objectives, expectations and business strategy generally. Forward-looking statements can generally be identified by the use of forward-looking terminology such as “may”, “will”, “expect”, “intend”, “estimate”, “anticipate”, “believe”, “continue”, “plan”, “target”, “project”, “potential”, “could”, “would” or similar terminology.

Forward-looking statements are based on management’s current expectations, assumptions and beliefs regarding future events and operations. These assumptions include, among other things, that required regulatory and stock exchange approvals will be obtained on acceptable terms and in a timely manner; that the remaining conditions to completion of the Redomicile Transactions will be satisfied or waived; that the anticipated benefits of the Redomicile Transactions will be realized; and that there will be no material adverse changes in economic, market, regulatory or business conditions.

Forward-looking statements are subject to known and unknown risks, uncertainties and other factors, many of which are beyond HydroGraph’s control, that may cause actual results, performance or achievements to differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation: the failure to obtain required regulatory or stock exchange approvals; delays in obtaining required approvals; the possibility that the Redomicile Transactions may not be completed on the anticipated timeline or at all; the possibility that holders wishing to receive exchangeable shares do not submit a valid election prior to the election deadline; the possibility that HydroGraph may not realize some or all of the anticipated benefits of the Redomicile Transactions; changes in tax laws or the tax consequences of the Redomicile Transactions; costs associated with the Redomicile Transactions; adverse market conditions; changes in applicable laws and regulations; and other risks and uncertainties described in the Circular and HydroGraph’s public disclosure record.

Although HydroGraph believes that the assumptions and expectations reflected in these forward-looking statements are reasonable, there can be no assurance that such assumptions or expectations will prove to be correct. Readers are cautioned not to place undue reliance on forward-looking statements. The forward-looking statements contained herein are made as of the date of this news release and HydroGraph undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by applicable law.

The CSE has neither approved nor disapproved the contents of this news release. Neither the CSE nor its Market Regulator (as that term is defined in the policies of the CSE) accepts responsibility for the adequacy or accuracy of this release.

CONTACTS:

Matt Kreps Senior Vice President of Capital Markets and Investor Relations +1-214-597-8200 matt.kreps@hydrograph.com

‒ Recently announced acquisition of assets of Heron Therapeutics – 

‒ Q3 2026 consolidated revenue of $54.5 million ‒

‒ Q3 2026 net loss of $14.7 million; Adjusted EBITDA of $3.1 million ‒

‒ Company maintains FY 2026 revenue and narrows Adjusted EBITDA guidance ‒

‒ Conference call scheduled for today at 8:30 a.m. Eastern Time ‒

PARSIPPANY, N.J., Nov. 12, 2026 (GLOBE NEWSWIRE) — CorMedix Therapeutics (Nasdaq: CRMD) today announced financial results for the third quarter ended September 30, 2026, and provided an update on its business.

Recent Corporate Highlights:

  • CorMedix and Heron Therapeutics, Inc. (“Heron”) announced on November 9, 2026, that they have entered into a definitive asset purchase agreement under which CorMedix will acquire substantially all of the assets of Heron. CorMedix believes the transaction will be immediately accretive to earnings and free cash flow upon closing, which it anticipates in the first quarter of 2027, subject to approval by Heron’s stockholders, regulatory clearance and other customary closing conditions.
  • CorMedix announces $54.5 million of total revenue and grant income (“consolidated revenue”) for the third quarter of 2026, above street consensus of $51.2 million, reflecting steady third quarter execution in the face of post-TDAPA headwinds for DefenCath. The Company also recognized a net loss of $14.7 million and adjusted EBITDA of $3.1 million (1). Basic and fully diluted earnings per share (EPS) were $(0.19) per share for the quarter.
  • DefenCath® (taurolidine and heparin) sales contributed $17.2 million of net revenue in the third quarter, driven by largely maintaining utilization of DefenCath by large outpatient dialysis customers in the post-TDAPA period, which impacted price, as well as by a $5.0 million favorable change in estimate related to certain sales allowances. The remaining portfolio contributed total revenue and grant income of $37.3 million.
  • CorMedix announced on October 19, 2026, that in collaboration with its global development partner Mundipharma, the FDA accepted for review the submission of the sNDA for an expanded indication of REZZAYO for the prophylaxis of invasive fungal disease. The Company anticipates agency action on the application in the first quarter of 2027.
  • In connection with the Heron asset acquisition, CorMedix entered into a term loan agreement to provide up to $150 million in non-dilutive capital, of which the Company expects to utilize $75 million upon closing. The term loan supports the Company’s financial flexibility to invest in our existing operations as well as in new business development opportunities.
  • The Company maintains full-year 2026 consolidated revenue guidance of $325 to $345 million, narrows full-year adjusted EBITDA guidance to a range of $130 to $140 million from a range of $125 to $140 million, and reduces cash-based OpEx guidance to a range of $140 to $145 million from $145 to $155 million.
  • In light of recently announced changes to the CMS reimbursement framework, the Company believes it is appropriate to suspend any previously issued 2027 DefenCath revenue guidance and defer future guidance until early 2027. This is the estimated timeframe when the Company expects to have better visibility into 2027 utilization and pricing for customers and any potential upside from Medicare Advantage contracting.
  • Cash and short-term investments, excluding restricted cash, at September 30, 2026 totaled $355.2 million.

Joseph Todisco, Chairman & Chief Executive Officer of CorMedix, commented, “CorMedix will be entering 2027 with two meaningful potential growth drivers. First, our pending acquisition of the Heron assets adds four commercial products used in institutional settings of care and is expected to be immediately accretive to earnings and free cash flow upon closing. With an anticipated revenue contribution of between $125 million and $150 million for the full-year 2027, we expect the Heron transaction to effectively double the Company’s non-DefenCath annual product revenue. Second, the FDA granted Priority Review to the REZZAYO prophylaxis sNDA, with a PDUFA date in the first quarter of 2027. If approved, we plan to commence promotional efforts in the second half of 2027. We continue to execute on our strategy to generate value from DefenCath in the post-TDAPA era as well as deploy our capital in a disciplined manner to drive future growth. With a strong current cash position and access to additional non-dilutive capital from Pharmakon, we believe we are well positioned to integrate Heron, prepare for REZZAYO expanded commercialization, and build a more diversified company.”

(1) Adjusted EBITDA is a non-GAAP financial measure and excludes non-cash items such as depreciation, amortization, stock-based compensation, interest and other income and expense, taxes and certain non-recurring items.  See “Non-GAAP Financial Measures” on the following pages for additional information regarding the use of EBITDA and Adjusted EBITDA and a reconciliation to the most comparable GAAP measure.
   

Third Quarter 2026 Financial Highlights

For the third quarter of 2026, CorMedix recorded $54.5 million in consolidated revenue, comprised of $17.2 million in sales of DefenCath and $37.3 million associated with the remainder of the portfolio, a decrease from $104.3 million in total revenue in the comparable period of 2025. DefenCath sales decreased year over year largely due to DefenCath’s transition to the post-TDAPA period on July 1, 2026, which has resulted in lower net pricing. The decrease in DefenCath sales was partially offset by higher revenue from the acquired Melinta portfolio given there was a full quarter of sales in 2026 compared to one month of sales in 2025 after the acquisition of Melinta closed on August 29, 2025.

Total operating expenses in the third quarter of 2026 were $36.6 million, compared with $41.7 million in the third quarter of 2025, a decrease of approximately 12%. The decrease of $5.1 million over the prior period was driven primarily by merger-related and reorganization expenses following the Melinta acquisition in the third quarter of 2025, partially offset by incremental operating expenses from the Melinta acquisition for the full quarter in 2026 relative to only one month of incremental expenses in the prior-year period.

Research and development (R&D) expenses in the third quarter of 2026 were $7.0 million, compared with $5.1 million for the same period in 2025. The increase in R&D was primarily due to an increase in personnel and clinical trial services in support of the ongoing clinical programs.

Selling and marketing expense increased approximately 4% to $11.7 million in the third quarter of 2026 from $11.2 million in the third quarter of 2025. The increase was primarily due to higher personnel cost associated with the larger product portfolio and related marketing programs. This was partially offset by the cost of the overlapping commercial sales teams for one month of the third quarter of 2025, before synergies were realized in 2026.

General and administrative expenses decreased approximately 30% to $17.9 million in the third quarter of 2026 from $25.5 million in the third quarter of 2025. The decrease was primarily attributable to Melinta-related transaction and integration costs incurred in the third quarter of 2025, partially offset by higher costs associated with operating as a combined company following the acquisition, and higher personnel, information technology, legal and facilities costs.  

CorMedix recorded a net loss of $14.7 million, or $(0.19) per basic and diluted share in the third quarter of 2026, compared with net income of $108.6 million, or $1.42 and $1.26 per basic and diluted share, respectively, in the third quarter of 2025. Net loss in the current period was negatively impacted by $11.5 million of non-cash expense from the remeasurement of contingent consideration associated with the Melinta acquisition. Net income in the third quarter of 2025 was positively impacted by a one-time tax benefit of $59.7 million derived from the realization of deferred tax assets associated with the anticipated use of 100% of CorMedix net operation loss carryforwards.

In the third quarter of 2026, CorMedix reported adjusted EBITDA of $3.1 million, compared to adjusted EBITDA of $71.9 million in the third quarter of 2025. Adjusted EBITDA excludes depreciation and amortization, stock-based compensation, interest and other income and expense, changes in contingent consideration, taxes, merger-related costs, and other specified adjustments. The calculation for 2026 also excludes the favorable change in estimate related to sales allowances recorded during the quarter.

The Company reported cash and cash equivalents of $355.2 million at September 30, 2026, excluding restricted cash. For the first nine months of 2026, net cash provided by operating activities was $218.3 million, compared with $80.6 million in the first nine months of 2025. The year-over-year increase reflects the higher year-to-date earnings achieved during the current year relative to 2025, as well as working capital movements, including the timing of certain contractual rebate payments.

The Company believes that it has sufficient resources to fund operations for at least twelve months from the issuance of the Company’s Quarterly Report on Form 10-Q.

Conference Call Information

CorMedix will host a conference call and webcast today, November 12, 2026, at 8:30AM Eastern Time, to discuss recent corporate developments and financial results. Call details and dial-in information are as follows:

Thursday, November 12, 2026 @ 8:30am ET
Domestic: 1-844-676-2922
International: 1-412-634-6840
Webcast: Webcast Link
   

About CorMedix

CorMedix Therapeutics is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of life-threatening conditions and diseases in the United States. CorMedix is focused on selling and marketing products in institutional settings of care in the US and has field based medical and commercial infrastructure deployed in hospitals, clinics and infusion centers. For more information visit: www.cormedix.com.

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 (the “Exchange Act”), that are subject to risks and uncertainties. Forward-looking statements are often identified by the use of words such as, but not limited to, “anticipate,” “believe,” “can,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “project,” “seek,” “should,” “target,” “will,” “would,” and similar expressions or variations intended to identify forward-looking statements. All statements, other than statements of historical facts, regarding management’s expectations, beliefs, goals, plans or CorMedix’s prospects should be considered forward-looking statements including, but not limited to statements regarding financial and business guidance; sales, revenue and operating expense estimates; Adjusted EBITDA estimates; expectations regarding product utilization and sales; the 2027 post-TDAPA Add-on for DefenCath, including the quarterly methodology adopted by CMS, CorMedix’s ability to reach pricing arrangements with dialysis customers that track quarterly Add-on adjustments, and CorMedix’s dependence on a limited number of large dialysis organization customers; CorMedix’s ability to secure separate payment for DefenCath from Medicare Advantage plans; the proposed acquisition of substantially all of the assets of Heron, including the risk that the transaction is not completed on the anticipated timeline or at all, including due to failure to obtain Heron stockholder approval or regulatory clearance, the risk that anticipated revenue contributions, cost synergies and accretion are not realized, and risks relating to integration and the incurrence of indebtedness under the term loan facility; the risk that topline data from CorMedix’s and its partners’ clinical trials, including the ReSPECT study, that CorMedix announces or publishes from time to time may change as more patient data become available or may be interpreted differently if additional data is disclosed; the timing and outcome of FDA review of the REZZAYO sNDA; estimates of total addressable market size; failure to successfully conduct future clinical trials, including due to CorMedix’s or its partners’ potential inability to enroll or retain sufficient patients to conduct and complete the trials, including the Phase 3 TPN study for DefenCath, or generate data necessary for regulatory approval, among other things; development of unexpected safety or efficacy concerns related to CorMedix’s product candidates; expectations and timing regarding clinical trials and development, performance expectations and revenue opportunities of CorMedix’s product pipeline; expectations regarding implementation and perceived benefits of CorMedix’s products; continued pricing pressures and the impact of actions of governmental and private payers affecting pricing of, reimbursement for, and patient access to pharmaceuticals and reporting obligations related thereto; the expiration of intellectual property protection for certain of the company’s products and competition from generic and biosimilar products. Readers are cautioned that actual results may differ materially from projections or estimates due to a variety of important factors, and readers are directed to the Risk Factors identified in CorMedix’s filings with the SEC, including its most recent Annual Report on Form 10-K and its subsequent Quarterly Reports on Form 10-Q, including the Quarterly Report on Form 10-Q for the quarter ended September 30, 2026, copies of which are available free of charge at the SEC’s website at www.sec.gov or upon request from CorMedix. CorMedix may not actually achieve the goals or plans described in its forward-looking statements, and such forward-looking statements speak only as of the date of this press release. In addition, pro forma financial information does not necessarily reflect the actual results that we would have achieved had the pro forma transaction been consummated as of the date indicated nor does it reflect the potential future results of the combined company. Investors should not place undue reliance on these statements. CorMedix assumes no obligation and does not intend to update these forward-looking statements, except as required by law.

Additional Information and Where to Find It

In connection with the proposed acquisition by CorMedix of substantially all of the assets of Heron (the “Proposed Acquisition”), CorMedix has and may file relevant documents with the SEC regarding the Proposed Acquisition. This press release is not a substitute for any other document that CorMedix may file with the SEC. INVESTORS AND STOCKHOLDERS ARE URGED TO READ ANY RELEVANT DOCUMENTS FILED WITH THE SEC, AS WELL AS ANY AMENDMENTS OR SUPPLEMENTS TO THOSE DOCUMENTS, CAREFULLY AND IN THEIR ENTIRETY WHEN THEY BECOME AVAILABLE, BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT THE PROPOSED ACQUISITION. Investors and stockholders may obtain these documents free of charge at the SEC’s website, www.sec.gov, and on the Investors section of CorMedix’s investor relations website at https://cormedix.com/investors/.

Participants in the Solicitation

CorMedix, Heron and their respective directors and executive officers may be deemed to be participants in the solicitation of proxies from Heron’s stockholders in connection with the Proposed Acquisition. Information about the directors and executive officers of Heron, including a description of their direct or indirect interests, by security holdings or otherwise, is set forth in its proxy statement for its 2026 annual meeting of stockholders, filed with the SEC on April 30, 2026, which is available online at https://www.sec.gov/ix?doc=/Archives/edgar/data/818033/000119312526196306/hrtx-20260430.htm, under the headings “Information Concerning the Board of Directors,” “Information Concerning Executive Officers,” “Corporate Governance – 2025 Director Compensation,” “Security Ownership of Certain Beneficial Owners and Management,” “Certain Relationships and Related Person Transactions” and “Executive Compensation,” and information about the directors and executive officers of CorMedix, including a description of their direct or indirect interests, by security holdings or otherwise, is set forth in its proxy statement for its 2026 annual meeting of stockholders, filed with the SEC on April 29, 2026, which is available online at https://www.sec.gov/ix?doc=/Archives/edgar/data/1410098/000121390026049311/ea0286136-05.htm,, under the headings “Proposal No. 1 – Approval of the Director Election Proposal,” “Corporate Governance – Executive Officers,” “Security Ownership of Certain Beneficial Owners and Management,” “Director Compensation,” “Executive Compensation” and “Certain Relationships and Related Transactions,” and, in each case, in subsequently filed Current Reports on Form 8-K, Quarterly Reports on Form 10-Q and Forms 3, 4 and 5. Additional information regarding the interests of such participants will be included in the proxy statement and other relevant materials to be filed with the SEC when they become available.

Other information regarding the participants in the solicitation and a description of their direct and indirect interests, by security holdings or otherwise, will be set forth in Heron’s definitive proxy statement and other relevant materials to be filed with the SEC regarding the Proposed Acquisition when such materials become available. Investors and stockholders should read the proxy statement carefully when it becomes available before making any voting or investment decisions. Copies of these documents may be obtained, free of charge, from the sources indicated above.

No Offer or Solicitation

This press release is for informational purposes only and does not constitute an offer to sell or the solicitation of an offer to buy any securities, or a solicitation of any vote or approval, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. The shares of CorMedix common stock to be issued to Heron in the Proposed Acquisition will be issued in a private placement in reliance on an exemption from the registration requirements of the Securities Act of 1933, as amended, and may not be offered or sold in the United States absent registration or an applicable exemption from registration.

Non-GAAP Financial Measures

This release includes certain non-GAAP financial measures, including EBITDA and adjusted EBITDA, which are intended as supplemental measures of the Company’s performance that are not required by or presented in accordance with GAAP. Management uses these non-GAAP measures internally to evaluate and manage the Company’s operations and to better understand its business because they facilitate a comparative assessment of the Company’s operating performance relative to its performance based on results calculated under GAAP. These non-GAAP measures also isolate the effects of some items that vary from period to period without any correlation to core operating performance and eliminate certain charges that management believes do not reflect the Company’s operations and underlying operational performance.

The Company believes that these non-GAAP measures also provide useful information to investors regarding certain financial and business trends relating to the Company’s financial condition and operating results, which facilitates an evaluation of the financial performance of the Company and its operations on a consistent basis. Providing this information therefore allows investors to make independent assessments of the Company’s financial performance, results of operations and trends while viewing the information through the eyes of management.

These non-GAAP measures are subject to limitations. The non-GAAP measures presented in this release may not be comparable to similarly titled measures used by other companies because other companies may not calculate one or more in the same manner. Additionally, the non-GAAP performance measures exclude significant expenses and income that are required by GAAP to be recorded in the Company’s financial statements; do not reflect changes in, or cash requirements for, working capital needs. Further, our historical adjusted results are not intended to project our adjusted results of operations or financial position for any future period. To compensate for these limitations, management presents and considers these non-GAAP measures in conjunction with the Company’s GAAP results; no non-GAAP measure should be considered in isolation from or as alternatives to any measure determined in accordance with GAAP. Readers should review the reconciliations included below, and should not rely on any single financial measure to evaluate the Company’s business.

Investor Contact:
Dan Ferry
Managing Director
LifeSci Advisors
daniel@lifesciadvisors.com
(617) 430-7576

 
CORMEDIX INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(In Thousands, Except Per Share Data)
(Unaudited)
         
    For the Three Months Ended
September 30,
  For the Nine Months Ended
September 30,
    2026   2025   2026   2025
Revenue and Grant Income:                
Product sales, net   $ 48,622     $ 101,547     $ 264,879     $ 180,365  
Contract revenue     2,642       2,729       10,690       2,729  
Grant income     3,255       –       8,308       –  
Total Revenue and Grant Income   $ 54,519     $ 104,276     $ 283,877     $ 183,094  
Cost of sales (exclusive of amortization of intangibles)     14,215       7,567       40,725       10,922  
Amortization of intangibles     10,300       3,628       30,900       3,732  
Gross profit   $ 30,004     $ 93,081     $ 212,252     $ 168,440  
Operating Expenses:                
Research and development   $ 7,036     $ 5,098     $ 20,932     $ 10,733  
Selling and marketing     11,683       11,186       36,662       22,044  
General and administrative     17,904       25,451       54,709       44,648  
Total Operating Expenses   $ 36,623     $ 41,735     $ 112,303     $ 77,425  
Income (Loss) From Operations   $ (6,619 )   $ 51,346     $ 99,949     $ 91,015  
Other (Expense) Income:                
Unrealized gain on marketable equity security     1,182       3,091       182       3,091  
Change in contingent consideration     (11,543 )     (2,400 )     (22,394 )     (2,400 )
Other non-operating income, net     532       539       193       1,864  
Total Other (Expense) Income     (9,829 )     1,230       (22,019 )     2,555  
Income (loss) before income taxes     (16,448 )     52,576       77,930       93,570  
Tax expense (benefit)     (1,726 )     (55,987 )     28,063       (55,465 )
Net Income (Loss)   $ (14,722 )   $ 108,563     $ 49,867     $ 149,035  
Net Income (Loss) Per Common Share – Basic   $ (0.19 )   $ 1.42     $ 0.63     $ 2.12  
Net Income (Loss) Per Common Share – Diluted   $ (0.19 )   $ 1.26     $ 0.57     $ 1.97  
Weighted Average Common Shares Outstanding – Basic     78,452       75,930       78,814       69,740  
Weighted Average Common Shares Outstanding – Diluted     78,452       86,214       92,659       75,677  
                                 

CORMEDIX INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEET DATA
(In Thousands)
             
    September 30,
  December 31,
    2026   2025
    (Unaudited)
  (Audited)
             
ASSETS            
Cash and cash equivalents   $ 355,150     $ 144,837  
Short-term investments     –       3,694  
Trade receivables, net     76,706       171,233  
Inventories     43,144       29,716  
Goodwill and intangible assets     378,174       409,074  
Deferred tax assets     –       16,276  
Other current and long-term assets     64,571       51,312  
Total Assets   $ 917,745     $ 826,142  
             
Total Liabilities   $ 456,039     $ 420,835  
Stockholders’ Equity     461,706       405,307  
Total Liabilities and Stockholders’ Equity   $ 917,745     $ 826,142  
             

CORMEDIX INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(In Thousands)
(Unaudited)
     
    For the Nine Months Ended
September 30,
    2026   2025
Net income   $ 49,867     $ 149,035  
Net cash provided by operating activities   $ 218,318     $ 80,585  
Net cash (used in) provided by investing activities   $ 491     $ (311,727 )
Net cash (used in) provided by financing activities   $ (8,496 )     239,866  
Net Increase in Cash and Cash Equivalents   $ 210,313     $ 8,725  
Cash, Cash Equivalents and Restricted Cash – Beginning of Period   $ 145,825     $ 40,756  
Cash, Cash Equivalents and Restricted Cash – End of Period   $ 356,138     $ 49,481  
                 

CORMEDIX INC. AND SUBSIDIARIES
Non-GAAP Reconciliations
(In Thousands)
(Unaudited)
         
    For the Three Months Ended
September 30,
  For the Nine Months Ended
September 30,
    2026   2025   2026   2025
Net income (loss)   $ (14,722 )   $ 108,563     $ 49,867     $ 149,035  
Adjusted to add (deduct):                
Interest expense (income)     (578 )     (556 )     (333 )     (1,935 )
Provision for income taxes     (1,726 )     (55,987 )     28,063       (55,465 )
Depreciation and amortization     10,529       3,790       31,613       4,115  
EBITDA (Non-GAAP)   $ (6,497 )   $ 55,810     $ 109,210     $ 95,750  
Adjusted to add (deduct):                
Change in estimate for sales allowances     (5,000 )     –       (13,983 )     –  
Stock-based compensation expense     3,936       4,066       12,602       10,243  
Merger related and reorg costs     300       12,656       1,685       12,510  
Other expense     10,407       (674 )     22,352       (620 )
Adjusted EBITDA (Non-GAAP)   $ 3,146     $ 71,858     $ 131,866     $ 117,883  

VANCOUVER, British Columbia, Nov. 12, 2026 (GLOBE NEWSWIRE) — Cambria Gold Mines Inc. (TSXV: CAMB; OTCQX: CAMVF) (“Cambria” or the “Company”) is pleased to announce new assay results from the ongoing infill drilling program at the Premier Mining Complex (the “Premier Gold Project” or “PGP”), located near Stewart in northwestern British Columbia. Results from eighteen diamond drillholes totalling 2,217 metres are reported herein. Highlight intervals include:

  • 10.32 g/t Au over 7.5 m (incl. 18.01 g/t Au over 2.7 m & 30.60 g/t Au over 0.7 m) in hole P26U-128
  • 6.66 g/t Au over 15.0 m (incl. 28.11 g/t Au over 3.0 m) in hole P26U-127
  • 4.08 g/t Au over 14.6 m (incl. 15.45 g/t Au over 1.1 m & 19.30 g/t Au over 1.1 m) in hole P26-2708

“Development infill drilling has been ongoing at the three major deposits at the Premier Gold Project with emphasis on areas that could be developed during ramp-up of mining while the Red Mountain Gold Deposit is developed. These results continue to demonstrate good continuity of grade and structure.” said Robert McLeod, President and CEO of Cambria Gold Mines. “Additional drill results are expected to continue to be received until Q1 2027. Underground development is expected to commence soon at Premier.”

Infill drilling results from the 2026 program are now fully received from multiple zones of the Premier Deposit, including a 200 by 150 metre area of the “Prew Zone” that has now been infilled to an average 12.5 metre spacing. Infill drilling has focused on areas adjacent to the historic mining areas that were identified by previous operations in the early to mid 1900s. Mineralization consists of visible gold and gold-bearing base metal sulfides that infill and overprint quartz breccia domains, with strong continuity defined on and along section by Cambria’s drilling program.

Assays and geological data will be integrated into internal development planning as the company works toward a restart of the Premier mill and will also help to inform the resource update and Feasibility Study planned for H1 2027. The infill drilling program is anticipated to pause in late November, with assay compilation and modelling updates utilizing over 40,000 metres of new drilling continuing until the end of the year.

A second phase of underground drilling will commence in 2027 upon completion of additional underground access. New underground development will also open exploration opportunities to test potential deposit extensions. The Premier deposit has had limited drilling to test deposit extensions at depth, despite historically producing over two million ounces of gold across multiple operators1.

Two infill holes were also completed from surface into the footwall of the “Northern Light” mineralized structure with encouraging high-grade results in holes P26-2708 and P26-2709 (See Figure 4). These results highlight the potential to continue defining new zones of mineralization within the historic mining areas of the Premier deposit.

The Company is eagerly anticipating additional infill results from approximately 20,000 metres of additional infill drilling, including at the Silver Coin deposit located five kilometres north of Premier along an existing haul road.

  1. Source: Premier & Red Mountain Gold Project Feasibility Study NI 43-101 Technical Report, British Columbia; Effective date April 15, 2020, Report Date May 22, 2020

Plan map of the Premier Deposit showing 2026 infill drilling locations

Figure 1: Plan map of the Premier Deposit showing 2026 infill drilling locations

Plan map of the Premier Deposit showing 2026 infill drilling locations

Figure 2: Plan map of the Prew Zone underground showing 2026 infill drilling locations and previous and newly reported assay results

Plan map of the Prew Zone underground showing 2026 infill drilling locations and previous and newly reported assay results

Figure 3: Cross section A showing underground infill results at the Prew Zone

Cross section A showing underground infill results at the Prew Zone

Figure 4: Cross Section B showing surface infill results and potential extension opportunity in the footwall of the “Northern Light” historic mining zone.

Table 1: Drill Results – Significant Intersections

holeid from
(m)
to
(m)
Interval
(m)
Au
(ppm)
Ag
(ppm)
Zn
(ppm)
Pb
(ppm)
ETW2 Including (>10g/t)
P26-2707 289.0 304.4 15.4 1.47 17.9 15318 2943 91 %  
P26-2708 190.0 194.6 4.6 6.06 7.8 2177 1286 94 % 21.30 g/t Au over 1.1 m
P26-2708 200.3 203.1 2.8 14.51 19.4 6924 4015 94 % 34.60 g/t Au over 1.1 m
P26-2708 209.7 224.4 14.6 4.08 8.6 3575 1556 94 % 15.45 g/t Au over 1.1 m
19.30 g/t Au over 1.1 m
P26-2708 227.8 251.8 23.9 1.53 4.4 1195 760 94 % 24.00 g/t Au over 1.0 m
P26-2709 196.0 200.0 4.0 6.10 11.3 3885 1124 93 %  
P26-2709 209.0 227.0 18.0 1.75 9.6 4591 1503 93 %  
P26-2709 231.0 240.0 9.0 4.26 9.0 3796 1473 93 %  
P26U-0118 77.0 89.0 12.0 1.79 4.7 2165 1059 79 %  
P26U-0122 32.0 45.0 13.0 1.47 4.8 3577 1395 99 %  
P26U-0122 53.0 58.4 5.4 2.08 8.5 5698 2479 99 %  
P26U-0123 48.0 59.0 11.0 1.26 6.7 2948 1814 91 %  
P26U-0125 60.0 70.0 10.0 2.10 9.4 2764 1328 66 %  
P26U-0126 78.0 81.0 3.0 4.76 16.1 4923 2860 75 %  
P26U-0126 86.0 96.0 10.0 3.23 7.3 4469 2170 75 %  
P26U-0127 57.0 72.0 15.0 6.66 10.9 6788 4475 85 % 28.11 g/t Au over 3.0 m
P26U-0128 52.5 67.6 15.1 2.53 7.0 3339 3112 92 % 20.30 g/t Au over 0.7 m
P26U-0128 71.5 79.0 7.5 10.32 22.2 20778 13276 92 % 30.60 g/t Au over 0.7 m
18.01 g/t Au over 2.7 m
P26U-0129 49.0 55.5 6.5 2.19 6.1 1473 865 96 %  
P26U-0129 61.0 68.0 7.0 2.09 3.1 613 419 96 % 13.05 g/t Au over 1 m
P26U-0132 57.0 62.0 5.0 4.71 8.0 3606 2331 97 %  
P26U-0133 33.0 57.0 24.0 1.65 3.7 2190 898 100 %  
                     

1 – ETW = Estimated True Width. All reported intervals are down-hole lengths, with true width estimates ranging from 66-100% of the reported interval. True widths are estimated based on the angle of the drill hole with the interpreted trend of the mineralized zones.

Composite Calculations for Significant Intersections
Composites for significant intersections were calculated using a 1 g/t gold (Au) cut off grade and maximum 3 metres of consecutive internal waste. “Including” results are reported at a 10 g/t Au cut off grade with maximum 3 metres of internal waste.

Table 2: Drill Collar Locations and Hole Orientations

Hole ID UTM East
(m)
UTM North
(m)
Elevation
(masl)
Total Depth
(m)
Azimuth Dip
P26-2707 436831 6212648 550 339 174 73
P26-2708 436895 6212777 542 302 92 52
P26-2709 436895 6212777 542 299 91 45
P26U-0118 437124 6213069 323 90 317 84
P26U-0119 437124 6213069 323 130 317 75
P26U-0122 437198 6212996 331 69.5 136 54
P26U-0123 437198 6212996 331 69.5 135 35
P26U-0124 437198 6212996 331 75 135 21
P26U-0125 437198 6212996 332 83 135 8
P26U-0126 437130 6213043 327 97 311 78
P26U-0127 437130 6213043 327 88.5 269 89
P26U-0128 437131 6213042 327 84 140 83
P26U-0129 437131 6213042 327 68 136 74
P26U-0130 437131 6213041 328 64.5 135 64
P26U-0131 437132 6213041 328 81 135 49
P26U-0132 437154 6213018 330 66.5 135 72
P26U-0133 437154 6213017 330 60.5 135 57
P26U-0134 437154 6213017 330 60 135 42
             

*masl – metres above sea level

Quality Assurance/Quality Control and Sample Preparation

All samples reported in this news release were obtained from NQ and HQ sized drill core. Holes with a P26U Prefix are NQ while holes with a P26 Prefix are HQ. The Company maintains a rigorous sampling and QA/QC procedure for the 2026 drill program. Core samples are prepared at the ALS preparation lab in Terrace, BC. The samples are dried and then crushed to specifications of 70% passing 2mm. Crushed samples are riffle split to 1000g and pulverized to 85% passing 75µm.

Analytical work for all results is completed by ALS Canada Ltd. which maintains an internal quality assurance and quality control (QAQC) program and is ISO:17025 certified for the analytical methods used in this release. Pulp splits are sent directly from the Terrace preparation facility to the ALS Canada Ltd. geochemistry laboratory facility in North Vancouver for analysis. Each sample is analyzed for gold by conventional 50g fire assay with atomic absorption finish (Au-AA26) and multielement analysis by four-acid digest with an ICP finish (ME-ICP61).

Samples over 100ppm gold are re-analyzed by an overlimit 50g fire assay with a gravimetric finish (Au-GRA22). Samples over 100ppm silver are re-analyzed with an ore grade method (ME-OG62) which is a four-acid digest method followed by an ICP-AES finish (up to 1,500ppm). Samples over 1,500ppm silver trigger the overlimit silver fire assay method (Ag-GRA21) which uses a 30g aliquot and gravimetric finish. Sampling and storage activities are conducted at the Company’s secure facility in Stewart, British Columbia.

The Company maintains a QAQC program that includes the submission and review of coarse blank materials to monitor contamination and certified reference materials to assess analytical accuracy. Core duplicates, crush duplicates and pulp duplicates are used to infer sampling precision and nugget effect.

Qualified Person and Technical Information:

The scientific and technical information within this news release was reviewed and approved by Blaine Smit, P.Geo. Vice President Exploration for Cambria Gold Mines Inc. Mr. Smit is a non-independent “Qualified Person” as defined under National Instrument 43-101. To verify the information related to this news release, Mr. Smit visited the 2026 drilling operations to review and discuss logging, sampling, and shipping procedures with responsible site staff, and reviewed and discussed assay and QA/QC results with responsible company personnel.

Investor Relations Engagements:

The Company has also engaged THB Digital Inc. (“THB Digital“) effective April 1, 2026, a corporate communications firm led by Tyler Bowles, Managing Director. THB Digital provides paid advertising set-up & management across Facebook, Instagram, X, Google and YouTube, including strategy, targeting, creative and copy, tracking, optimization, and reporting.

The agreement is continuing on a month to month basis, and may be terminated by either party at any time given 30 days written notice to the other party of its intention to terminate. In consideration for these services, the Company pays THB Digital a fixed monthly cash fee of C$3,500 (plus applicable taxes), with a separate advertising budget of C$5,000 per month, which may fluctuate based on the Company’s desired advertising spend. Changes to the advertising budget will not affect THB Digital’s monthly fee.

As of the date hereof, neither THB Digital nor its principal, Tyler Bowles, holds or has ever held any direct or indirect interest in the Company or its securities, or any right or intent to acquire such an interest. THB Digital operates on an arm’s-length basis to the Company.

The agreement with THB Digital remains subject to the review and final approval of the TSX Venture Exchange.

The Company also entered into an agreement effective March 1, 2026 with Bull Markets Media GmbH (“Bull Markets Media“), a Germany-based financial media company specializing in financial-market information, investor education, and digital financial publishing. All contents/materials distributed / disseminated by Bull Markets Media were reviewed and approved by the issuer.

The engagement is for a fixed term of six (6) months and concluded on August 31, 2026. In consideration for these services, the Company paid Bull Markets Media a total cash consideration of C$65,000 upfront, plus applicable taxes.

Bull Markets Media operates completely at arm’s-length to the Company. As of the date hereof, neither Bull Markets Media nor any of its principals or associates holds any direct or indirect interest in the Company or its securities, or any right or intent to acquire such an interest.

The agreement with Bull Markets Media remains subject to the review and final regulatory acceptance of the TSX Venture Exchange.

The Company has also entered into a corporate communications and marketing services agreement commencing June 1, 2026 with Plutus Invest & Consulting GmbH (“Plutus“), a Germany-based capital markets consultancy and financial media publishing firm.

The agreement is for a fixed term of twelve (12) months and will conclude on May 31, 2027. In consideration for these services, the Company has agreed to allocate a variable media buying and marketing budget ranging from a minimum of €100,000 to a maximum of €250,000. €100,000 was an upfront payment and any additional payment beyond €250,000 will be subject to the prior approval of the TSX Venture Exchange.

Under the terms of the agreement, Plutus is providing consulting on advertorial marketing and public relations strategies and is designing and implementing an advertisement-based investor awareness campaign targeting the European (primarily German-speaking) investment market.

Plutus operates completely at arm’s-length to the Company. As of the date hereof, neither Plutus nor any of its principals or associates holds or had held any direct or indirect interest in the Company or its securities, or any right or intent to acquire such an interest.

The agreement with Plutus and all associated upfront expenditures remains subject to the final regulatory acceptance of the TSX Venture Exchange.

The Company clarifies, further to its news release dated October 18, 2026, that it has paid an upfront, advanced payment of US$250,000 to Native Ads Inc. (“Native Ads”). Any renewal after the 12 months (or after budget exhaustion) will also be subject to TSX Venture Exchange approval. Native Ads continues to operate at arm’s-length to the Company and receives no equity or security-based compensation under the terms of the engagement.

The Company also clarifies further to its news release dated October 19, 2026, Maximus Strategic Consulting Inc. (“Maximus”) and any of its principals do not have and have never had any interest, directly or indirectly, in the Company or its securities and will not receive any securities in the Company as a result of this engagement. The engagement of Maximus is subject to the approval of the TSX Venture Exchange.

About Cambria Gold Mines

Cambria Gold Mines is a Canadian mining company headquartered in Vancouver, British Columbia, and its shares trade on the TSX-V under the ticker CAMB and on the OTCQX Market with the ticker CAMVF. Cambria is the 100% owner of the Premier Project and Red Mountain Gold Project that are located on Nisga’a Nation Treaty Lands, in the prolific Golden Triangle of northwestern British Columbia, as well as the large Mt. Margaret copper-gold porphyry deposit located in Washington State. For more information about the Company, please refer to the Company’s profile on SEDAR+ at www.sedarplus.ca or visit the Company’s web site at www.cambriagold.com.

On behalf of the Board of Directors of Cambria Gold Mines Inc.

Robert McLeod
CEO and Director 

For further information contact:

Cleve Rueckert
VP Corporate Development
Email: crueckert@cambriagold.com

and:

Sam Brezden
VP Communications and Community Engagement
Email: sam.brezden@cambriagold.com
Phone: 236-838-1840

 Or visit:

https://cambriagold.com/

Cautionary Statements:

NEITHER THE TSX VENTURE EXCHANGE NOR ITS REGULATION SERVICES PROVIDER (AS THAT TERM IS DEFINED IN POLICIES OF THE TSX VENTURE EXCHANGE) ACCEPTS RESPONSIBILITY FOR THE ADEQUACY OR ACCURACY OF THIS RELEASE.

Cautionary Statement Regarding Forward-Looking Information

All statements and other information contained in this press release about anticipated future events may constitute forward-looking information under Canadian securities laws (“forward-looking statements”). Forward- looking statements are often, but not always, identified by the use of words such as “seek”, “anticipate”, “believe”, “plan”, “estimate”, “expect”, “targeted”, “outlook”, “on track” and “intend” and statements that an event or result “may”, “will”, “should”, “could”, “would” or “might” occur or be achieved and other similar expressions. All statements, other than statements of historical fact, included herein are forward-looking statements, including statements in respect of the drill results resulting in actual increases of resources and reserves; the timing and certainty of the restart of the Premier mill and mining operations at the Premier and Red Mountain Projects; the timing and outcome of the expansion of the infill drill program and additional assay results; ability of the Company to accomplish its business objectives and the intentions described herein; and future plans, development and operations of the Company. These statements involve known and unknown risks, uncertainties and other factors that may cause actual results or events to differ materially from those anticipated in such forward-looking statements; risks relating to negative operating cash flows of the Company; business and economic conditions in the mining industry generally; fluctuations in commodity prices and currency exchange rates; environmental compliance; risks related to outstanding debt; uncertainty of estimates and projections relating to development, production, costs and expenses, and health, safety and environmental risks; uncertainties relating to interpretation of drill results and the geology, continuity and grade of mineral deposits; the need to obtain additional financing to finance operations and uncertainty as to the availability and terms of future financing; social media and reputation; negative publicity; human rights; business objectives; shortage of personnel; health and safety; the possibility of delay in future plans and uncertainty of meeting anticipated program milestones; claims and legal proceedings; information systems and cyber security; internal controls; violation of anti-bribery or corruption laws; competition; tax considerations; compliance with listing standards; enforcement of civil liabilities; financing requirement risks; market price volatility of the common shares; uncertainty as to timely availability of permits and other governmental approvals; the need for exchange approval, and other regulatory approvals and other risk factors as detailed from time to time in Cambria’s filings with Canadian securities regulators, available on Cambria’s profile on SEDAR+ at www.sedarplus.ca including the Annual Management Discussion and Analysis of the Company for the year ended December 31, 2025 in the section entitled “Risk Factors”. Forward-looking statements are based on assumptions made with regard to: the estimated costs associated with the care and maintenance plans; the tax rate applicable to the Company; future commodity prices; the grade of mineral resources and mineral reserves; labor and materials costs increasing on a basis consistent with the Company’s current expectations, the ability of the Company to convert inferred mineral resources to other categories; the ability of the Company to reduce mining dilution; the ability to reduce capital costs; the ability of the Company to raise additional financing; currency exchange rates being approximately consistent with current levels, compliance with the covenants in Cambria’s credit agreements; exploration plans; and general marketing, political, business and economic conditions. Forward-looking statements are based on estimates and opinions of management at the date the statements are made. Although Cambria believes that the expectations reflected in such forward-looking statements and/or information are reasonable, undue reliance should not be placed on forward-looking statements since Cambria can give no assurance that such expectations will prove to be correct. Cambria does not undertake any obligation to update forward-looking statements, other than as required by applicable laws. The forward-looking information contained in this press release is expressly qualified by this cautionary statement.

Photos accompanying this announcement are available at 
https://www.globenewswire.com/NewsRoom/AttachmentNg/35343c31-9adf-4c9f-8129-870f9994c594
https://www.globenewswire.com/NewsRoom/AttachmentNg/bac3d2dc-8edb-44db-b8ea-57193ce5cbdd
https://www.globenewswire.com/NewsRoom/AttachmentNg/1e06aa5a-707e-4b3d-9e43-d49e2b2a8c89
https://www.globenewswire.com/NewsRoom/AttachmentNg/06562094-f078-48c6-9c0b-aad02e1e6109

LONDON, Nov. 12, 2026 (GLOBE NEWSWIRE) — Central Asia Metals PLC (AIM, TSX: CAML) is pleased to announce that its Chief Executive Officer, Gavin Ferrar, will formally open trading on the Toronto Stock Exchange (TSX) tomorrow in Toronto, to mark the recent listing of CAML’s shares on the TSX.

As detailed in the announcement of 27 October 2026, the TSX listing was associated with CAML’s acquisition of Cygnus Metals Ltd (‘Cygnus’) and its flagship Chibougamau copper-gold project in Québec, which was completed on the same day. The TSX listing gives North American investors, including former shareholders in Cygnus, enhanced access to trading in CAML shares.

Chibougamau project update
CAML’s senior management has just completed a week-long technical workshop at the Chibougamau project with the Chibougamau project team and a number of key consultants, to progress the Group’s strategy for the project and to prioritise the forthcoming work programme.

Main developments

  • Three drilling rigs have been secured to launch a significant exploration programme.
  • One rig is currently on site, with the additional rigs arriving before the end of November which will allow for exploration to take place through the forthcoming winter by facilitating timely construction of ice pads.
  • The focus during H1 2027 will be on exploration drilling at the Corner Bay, Golden Eye and Cedar Bay deposits, with the focus in H2 2027 shifting to infill drilling for resource upgrading from inferred to indicated at Corner Bay, Golden Eye, Cedar Bay and Devlin.
  • In Q2 2027 a fourth drilling rig will join the campaign to focus on geotechnical studies and metallurgical test work to support a future Definitive Feasibility Study (DFS).
  • The total drilling programme is expected to comprise up to 70,000 metres through to the end of 2027.
  • During winter, CAML plans to undertake an electromagnetic geophysical programme over the frozen lakes in its licence area.
  • The Chibougamau project also includes other deposits, including Gwillim, where Cygnus announced some significant gold intersections in August of this year, and the historically producing Joe Mann, which will be prioritised for additional exploration as appropriate.
  • Baseline environmental work is to continue, along with preparatory work for the project’s environmental and social impact assessment, in order to advance the permitting process as far as possible.
  • Site clearance and restoration work is planned in readiness for the rehabilitation and modernisation of the brownfields Copper Rand site in future.

Upcoming catalysts

  • The results from the above-mentioned exploration drilling will be included in an updated Mineral Resource Estimate (MRE), scheduled for completion in Q3 2027. The previous MRE, published by Cygnus in late 2025, comprised 6.4 million tonnes Measured and Indicated, at 2.3% copper, 0.8 g/t gold and 7.6 g/t silver, and 8.5 million tonnes Inferred, at 2.1% copper, 1.7 g/t gold and 7.9 g/t silver1.
  • The infill drilling described above is designed to upgrade the confidence in the resource estimate to support a future DFS.
  • Building on previous work commenced by the Chibougamau team, CAML is undertaking a Preliminary Economic Assessment (PEA) featuring an expanded scope, and has retained Ausenco to lead a team of international consultants to assist.
  • The PEA, which will be based on the current MRE, is expected to be completed in mid-2027.

Gavin Ferrar, Chief Executive Officer of CAML, commented:

“I am delighted to be opening the TSX tomorrow to welcome new shareholders to CAML, and to introduce the Group to the North American market. This ceremony is timely in that I have just spent a week at our newly-acquired Chibougamau project, where CAML’s senior management has worked with the project team to plan what I believe will be an exciting path for the project and the wider CAML Group.

“I was particularly impressed with the quality of the project team and the work completed to date, a great foundation on which we will build. Detailed discussions over the past week have reinforced the quality of the Chibougamau project and the exploration potential of the surrounding camp. I was also encouraged by the positive reception we have received from local stakeholders whom we met, including the Mayor of Chibougamau and representatives of the Oujé-Bougoumou Cree Nation. We look forward to working with all stakeholders to build long-term value through the project.”

For further information contact:  
   
Central Asia Metals
Gavin Ferrar
CEO
Tel: +44 (0) 20 7898 9001
   
Louise Wrathall
CFO
 
   
Richard Morgan
Investor Relations Manager
richard.morgan@centralasiametals.com
   
Peel Hunt (Nominated Adviser and joint broker)
Ross Allister
David McKeown
Emily Bhasin
Tel: +44 (0) 20 7418 8900
   
BMO Capital Markets (joint broker)
Thomas Rider
Pascal Lussier Duquette
Tel: +44 (0) 20 7236 1010
   
BlytheRay (PR advisers)
Megan Ray
Rachael Brooks
Tel: +44 (0) 20 7138 3204
CentralAsiaMetals@BlytheRay.com
   

Note to editors:

Central Asia Metals, an AIM-quoted UK company based in London, owns 100% of the Kounrad SX-EW copper operation in central Kazakhstan, 100% of the Sasa zinc-lead mine in North Macedonia and 100% of the Chibougamau copper-gold project in Québec. The Company also owns an 80% interest in CAML Exploration and 100% in CAML XD, two subsidiaries formed to progress early-stage exploration opportunities in Kazakhstan, and a 38.9% interest in Aberdeen Minerals Ltd, a privately-owned UK company focused on the exploration and development of base metals opportunities in northeast Scotland.

For further information, please visit www.centralasiametals.com and follow CAML on X at @CamlMetals and on LinkedIn at Central Asia Metals PLC.

Cautionary Statement Regarding Forward-Looking Information

This press release includes certain statements that may constitute or be deemed to be ‘forward-looking statements’ or ‘forward-looking information’ within the meaning of applicable Canadian securities legislation. All statements in this press release, other than statements of historical facts, that address future objectives, financial or operating performance of CAML and its subsidiaries and mineral projects, estimates of mineral resources and mineral reserves, exploration drilling, exploration activities, expenditures, development and production activities and events or developments that CAML expects, including but not limited to plans related to: the arrival of additional rigs; infill drilling to upgrade resources; geotechnical studies; metallurgical test work; drilling and electromagnetic geophysical programmes; environmental and social impact assessment work; and anticipated timing for completion of the PEA, an updated MRE and a DFS, are forward-looking statements.

Often, but not always, forward-looking information can be identified by the use of words such as ‘plans’, ‘expects’, ‘is expected’, ‘scheduled’, ‘anticipates’, ‘believes’, ‘estimates’, ‘forecasts’ or ‘intends’, or variations (including negative variations) of such words and phrases or statements that certain actions, events or results ‘may’, ‘could’, ‘would’, ‘might’ or ‘will’ be taken, occur or be achieved. Forward-looking statements are based on the opinions and estimates of management as of the date such statements are made and are based on various assumptions and are subject to known and unknown risks, uncertainties and other factors . Although CAML believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, readers are cautioned that such statements are not guarantees of future performance and actual results or developments may differ materially from those implied or contained in the forward-looking statements. Factors that could cause actual results to differ materially from those in forward-looking statements include, among others, market prices, exploitation and exploration successes, continued availability of capital and financing, political and social uncertainties, changes to project parameters and/or economic assessments, variations of mineral grade or recovery rates, actual costs exceeding estimated costs, other risks related to the mining industry and general economic, market or business conditions. All of the forward-looking statements made in this press release are made as of the date of this press release and are expressly qualified by these cautionary statements. There can be no assurance that forward-looking statements will prove to be accurate and as such, readers should not place undue reliance on forward-looking statements. CAML disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information, future events or otherwise, except to the extent required by applicable law.

www.centralasiametals.com X: @CamlMetals Instagram: Central Asia Metals Plc


1Refer to Cygnus’ ASX announcement dated 17 September 2025 and subsequent technical report dated 31 October 2025 titled ‘NI 43-101 Technical Report Chibougamau Hub and Spoke Complex, Québec, Canada’ prepared in accordance with National Instrument 43-101 Standards of Disclosure for Mineral Projects (‘NI 43-101’) and the Joint Ore Reserves Committee (JORC) Code (2012 Edition).
The Qualified Person responsible for the technical content of this news release is Graham Greenway, BSc Honours (Geology), PGeo. Mr Greenway, CAML’s Group Geologist, is a Practising Registrant of the Professional Geoscientists of Ontario

 – Collaboration aligns with Immuneering’s expanding strategy to provide a broad population of cancer patients with a wide set of treatment options –

– Represents Immuneering’s fourth agreement with a pharma partner –

– Further expands external partnerships to bring innovative new combinations to patients –

NEW YORK, Nov. 12, 2026 (GLOBE NEWSWIRE) — Immuneering Corporation (Nasdaq: IMRX) today announced it has entered into a clinical trial collaboration and supply agreement with Astellas Pharma Global Development, Inc., a subsidiary of Astellas Pharma Inc. (TSE: 4503). Under the agreement, Immuneering will supply its investigational MEK inhibitor, atebimetinib, for two Astellas-sponsored studies targeting the subset of pancreatic cancer patients whose tumors express CLDN18.2. One trial will evaluate an Astellas investigational CLDN18.2-targeted program added to atebimetinib plus modified gemcitabine/nab-paclitaxel (mGnP) in first-line metastatic pancreatic cancer patients. A second trial will evaluate a chemotherapy-free regimen combining a different Astellas investigational CLDN18.2-targeted program with atebimetinib in previously-treated metastatic pancreatic cancer patients. Further trial details will be forthcoming.

“This collaboration reflects our conviction that atebimetinib has the potential to become an essential backbone therapy in a broad range of combinations across MAPK-driven cancers,” said Ben Zeskind, Immuneering CEO and co-founder. “Atebimetinib’s unique tolerability profile and broad activity make it well suited to combine with a wide range of innovative medicines targeted to specific subsets of patients, including the CLDN18.2-targeted therapies that Astellas is developing.”

“Claudin 18.2 has emerged as a promising target in gastrointestinal cancers,” said Igor Matushansky, MD, PhD, Chief Medical Officer of Immuneering. “By combining CLDN18.2 targeted therapy with atebimetinib, these studies will evaluate the extent to which there is synergy between these distinct yet complementary mechanisms that can benefit patients with CLDN18.2-expressing pancreatic cancer.”

Under the terms of the collaboration, Astellas will sponsor and conduct the planned studies and Immuneering will supply atebimetinib. Immuneering maintains global development and commercialization rights to atebimetinib, and Astellas maintains global development and commercialization rights to its CLDN18.2-targeted programs.

About Immuneering Corporation

Immuneering is a late-stage clinical oncology company dedicated to keeping cancer patients alive and helping them thrive, with an initial focus on patients with RAS, RAF, and other MAPK-driven cancers. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications. The Company is conducting a global randomized pivotal trial, MAPKeeper 301, evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and preclinical stage programs. For more information, please visit www.immuneering.com.

Forward-Looking Statements

This press release contains forward-looking statements, including 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 should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer including modified Gemcitabine/nab-paclitaxel (mGnP), claudin 18.2 targeted agents and other Astellas compounds, the suitability of combining atebimetinib, and its potential to reduce tumor volume and preserve body mass in pancreatic cancer; the timing the timing and number of studies being planned and evaluated under this collaboration; and the potential ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.

These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our 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 following: we are a late-stage clinical oncology company with a limited operating history and have not completed any registrational clinical trials; we have incurred significant losses, are not currently profitable and may never become profitable; limitations on our cash runway and potential increases in expenditures; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and changing regulatory standards, and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including the uncertainty of whether positive preclinical or early clinical efficacy and safety results are confirmed in later-stage trials, potential delays in activation of trial sites or enrollment of trial participants, or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.

These and other important factors discussed under the caption “Risk Factors” in our Quarterly Report on Form 10-Q for the period ended September 30, 2026, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management’s estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.

Investor Contact:
Laurence Watts
New Street Investor Relations
laurence@newstreetir.com

Media Contact:
David Caouette
dcaouette@immuneering.com

RemeGen’s expertise and next generation engineering expand Vor Bio’s leadership in the BAFF/APRIL field

RC298 is a next generation, long-acting dual BAFF/APRIL inhibitor designed to combine high potency and extended half-life for potentially best-in-class efficacy and dosing

RC298 is in IND-enabling development, with an initial regulatory filing anticipated in the first half of 2027 in China

Cash runway reaffirmed into early 2029

BOSTON, Nov. 12, 2026 (GLOBE NEWSWIRE) — Vor Bio (Nasdaq: VOR), a clinical-stage biotechnology company transforming the treatment of autoimmune diseases, today announced an amendment to its existing agreement with RemeGen Co., Ltd (HKEX: 9995, SHA: 688331) to add RC298, a next-generation dual BAFF/APRIL inhibitor, to Vor Bio’s exclusive license for development and commercialization outside of Greater China.

RC298 is an engineered TACI-Fc fusion protein designed to inhibit both BAFF (B cell activating factor) and APRIL (a proliferation-inducing ligand), two key regulators of pathogenic B cell and plasma cell biology. RC298 was engineered to optimize functional potency, pharmacokinetics, and developability with a structural design intended to enable sustained dual pathway inhibition and extended dosing intervals. In preclinical studies, RC298 demonstrated potent inhibition of BAFF and APRIL compared to leading BAFF/APRIL inhibitors, as well as significantly prolonged systemic exposure, supporting its potential for a differentiated, best-in-class efficacy and dosing profile.

Building on telitacicept as the clinical foundation of Vor Bio’s BAFF/APRIL franchise with three ongoing registrational trials advancing across the myasthenia gravis spectrum and Sjögren’s disease, RC298’s differentiated long-acting profile has the potential to expand the franchise into additional autoimmune diseases and treatment settings, extending the therapeutic reach of dual BAFF/APRIL inhibition.

RC298 is currently in IND-enabling development, with an IND submission in China anticipated in the first half of 2027. RemeGen will continue to lead the preclinical and Phase 1 clinical development of RC298 in China, with both companies contributing to development efforts. Following completion of the Phase 1 clinical trial, Vor Bio will assume responsibility for subsequent clinical development, regulatory activities, and commercialization of RC298 outside of greater China.

“Over the past year, our successful execution has established Vor as a leader in the BAFF/APRIL field and RC298 meaningfully strengthens that position,” said Jean-Paul Kress, M.D., Chairman and Chief Executive Officer of Vor Bio. “Our conviction in building this franchise is reinforced by what FcRn therapies have already demonstrated across multiple large autoimmune diseases. We believe BAFF/APRIL can build on that precedent by acting both upstream on B cells and downstream on plasma cells, with the potential for deeper, broader, and more durable disease control.”

Dr. Kress continued, “Telitacicept remains our clinical foundation and near-term priority as we execute on our global Phase 3 programs in myasthenia gravis and Sjögren’s disease. RC298 is the next step in our broader campaign to create opportunities with a long-acting, next generation molecule across new diseases and treatment settings. We are building on a biology we know deeply, alongside a partner with extraordinary clinical and commercial experience in the pathway. With multiple differentiated ways to target BAFF and APRIL, we believe Vor is best positioned to build the leading franchise in this category and deploy each molecule where its profile can create the greatest advantage for patients.”

“Telitacicept is the world’s first approved innovative therapy to target both BAFF and APRIL for the treatment of a range of B cell-mediated autoimmune diseases. It has been approved in China for five indications, and its global multicenter clinical trials are progressing well. The clinical evidence to date has demonstrated the potential benefits of dual BAFF/APRIL inhibition. RC298, our next generation, long-acting dual BAFF/APRIL inhibitor, has shown best-in-class potential,” said Dr. Jianmin Fang, Chief Executive Officer of RemeGen. “This transaction will broaden both companies’ global autoimmune disease portfolios and accelerate the international development of RemeGen’s innovative pipeline. With RC298, we aim to bring an innovative treatment option to patients with autoimmune diseases worldwide while strengthening RemeGen’s brand and expanding its global presence.”

Transaction Terms
Under the terms of the agreement, Vor Bio will provide RemeGen with approximately $56 million in aggregate upfront consideration, consisting of a $10 million upfront cash payment and pre-funded warrants to purchase 2.3 million shares of Vor Bio common stock with an exercise price of $0.0001 per share (representing an approximate value of $46 million based on Vor Bio’s closing share price on November 11). RemeGen will be eligible to receive up to an additional $300 million in development milestone payments, including $20 million payable upon the achievement of initial clinical development and technology transfer milestones. The existing collaboration’s sales milestone and royalty framework will continue to apply on an aggregated basis across all licensed products.

About Telitacicept
Telitacicept is a novel recombinant fusion protein designed to treat autoimmune diseases through dual inhibition of BAFF (also known as BlyS) and APRIL – two cytokines essential to B cell development and plasma cell survival. By inhibiting both pathways, telitacicept has the potential to reduce autoreactive B cells and autoantibody production, targeting key drivers of autoimmune pathology.

Telitacicept is approved in China for systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), generalized myasthenia gravis (gMG), IgA nephropathy (IgAN), and Sjögren’s disease (SjD).

Vor Bio is advancing global development programs across major autoimmune indications, including a global Phase 3 trial in gMG and SjD, to support potential regulatory approvals in the United States, Europe, and Japan.

About Vor Bio
Vor Bio is a clinical-stage biotechnology company transforming the treatment of autoimmune diseases. The Company is focused on rapidly advancing telitacicept, a novel dual-target fusion protein, through Phase 3 clinical development and potential commercialization to address serious autoantibody-driven conditions worldwide. For more information visit www.vorbio.com. Vor Bio routinely posts information that may be important to investors in the “Investors” section of its website. The Company encourages investors to consult that section of its website regularly.

About RemeGen Co., Ltd.

Founded in 2008, RemeGen (9995.HK, SHA: 688331) is a leading biopharmaceutical company in China committed to providing solutions to the unmet clinical needs of patients suffering from life-threatening illnesses. RemeGen has research laboratories and offices in China and the United States. The company is committed to discovering, developing, and commercializing innovative and differentiated biologic drugs of significant clinical value in the key therapeutic areas of autoimmune, oncology, and ophthalmic diseases.

Forward-Looking Statements
This press release contains forward-looking statements. The words “anticipate,” “believe,” “continue,” “could,” “design,” “expect,” “initiate,” “intend,” “may,” “on-track,” “ongoing,” “plan,” “potential,” “project,” “should,” “update,” “will,” “would,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward-looking statements in this press release include Vor Bio’s statements regarding the potential of RC298 as a best-in-class, long-acting dual BAFF/APRIL inhibitor, including its potential potency, efficacy, pharmacokinetics, and dosing profile; the anticipated timing of an IND filing for RC298 in China; the development plans for RC298 and the respective roles of Vor Bio and RemeGen; RC298’s potential to expand Vor Bio’s BAFF/APRIL franchise into additional autoimmune diseases and treatment settings; telitacicept’s potential as a BAFF/APRIL therapy for gMG and SjD; the potential benefits of the dual BAFF and APRIL inhibition; Vor Bio’s ability to build the leading franchise in the BAFF/APRIL category; Vor Bio’s projected cash runway; Vor Bio’s development and commercialization plans for telitacicept, including the pursuit of potential regulatory approvals in the United States, Europe, and Japan, and the conduct and timing of its registrational trials across the MG spectrum and in SjD; and other statements that are not historical fact.

Vor Bio may not actually achieve the plans, intentions, or expectations disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result of various factors, including that RC298 is in an early stage of development, that results of preclinical studies of RC298, including comparisons with other BAFF/APRIL molecules, may not be predictive of clinical results, and that RC298 may not demonstrate a differentiated or best-in-class profile in clinical trials; that the IND for RC298 may not be filed or cleared on the anticipated timeline, or at all; that Vor Bio may not realize the anticipated benefits of the amendment with RemeGen; that results from clinical trials of telitacicept and RC298 that RemeGen has conducted or will conduct solely in China, may not be predictive of results in other populations or in our ongoing or future clinical trials, and that the FDA and other regulators outside China may not accept data generated in China; that results of earlier clinical trials or analyses may not be predictive of future results; the risk of unexpected adverse events or safety findings; our reliance on RemeGen, including for clinical data, the supply of telitacicept, the preclinical and Phase 1 clinical development of RC298 and our ability to maintain our license with RemeGen; competition from other therapies, including other BAFF and/or APRIL inhibitors; that the data for our product candidates may not be sufficient for obtaining regulatory approval to commercialize products; we may not be able to execute our business plans, including meeting our planned clinical and regulatory milestones and timelines; and possible limitations of financial and other resources. The clinical trial results and preclinical data described in this press release are based on information reported by RemeGen; Vor Bio has not independently verified these data. These and other risks are described in greater detail under the caption “Risk Factors” included in Vor Bio’s most recent annual or quarterly report and in other reports it has filed or may file with the Securities and Exchange Commission. Statements regarding Vor Bio’s cash runway do not indicate when or if Vor Bio may access the capital markets.

Any forward-looking statements contained in this press release speak only as of the date hereof, and Vor Bio expressly disclaims any obligation to update any forward-looking statements, whether because of new information, future events or otherwise, except as may be required by law.

CONTACT: Media & Investor Contacts:
Carl Mauch
cmauch@vorbio.com

New 2027 Revenue Guidance $65 Million to $85 Million
$128 Million of 2030 Notes Retired Capturing a 36% Discount
Restructuring Lowers Annual Cost by $8.5 Million

FREMONT, Calif., Nov. 12, 2026 (GLOBE NEWSWIRE) — Enovix Corporation (“Enovix” or the “Company,” Nasdaq: ENVX), a developer and manufacturer of advanced lithium-ion batteries, today reported Q3’26 financial results, including a record non-GAAP gross margin this quarter of 34.5%, up 13.5 points.

Fellow Shareholders:

Our Q3’26 revenue was $11.0 million, up 38% from Q3’25 and 22% from Q2’26, our sixth consecutive quarter of year-over-year revenue growth. The higher gross margin resulted from a richer revenue mix, including smart eyewear revenue and drone and defense revenue. Our Q3’26 non-GAAP net loss per share was $0.15, and we ended the quarter with $512.2 million in cash, cash equivalents, marketable securities and restricted cash ($2.35 per outstanding share), as outlined in the GAAP and non-GAAP financial statements below:

Enovix Q3’26 Revenue & Operating Income Statement1
         
  GAAP2 NON-GAAP3
(in thousands, except per share) Q3 2026 Q3 2025 Q3 2026 Q3 2025
Revenue 11,039 7,990 11,039 7,990
Gross Profit 3,328 1,401 3,803 1,681
Gross Margin (%) 30.1% 17.5% 34.5% 21.0%
Operating Expense 42,622 48,374 33,018 31,506
Stock Comp, Intangibles, Other3 10,079 17,148 — —
Operating Income (loss) (39,294) (46,973) (29,215) (29,825)
Net Loss per Share4 (0.19) (0.27) (0.15) (0.14)
Cash Balance5 512,159 — 512,159 —

1 Q3’26 results are unaudited. See the condensed consolidated financial statements and the reconciliation tables below.
2 GAAP figures are derived from the Company’s unaudited condensed consolidated financial statements; the Company’s Q3’26 GAAP financial statements will be included in its Form 10-Q.
3 Our non-GAAP financials are used to run the company and for the commentary herein. Non-GAAP figures exclude a) stock-based compensation, b) amortization of intangible assets and c) certain other one-time events, summarized in the tables below. Revenue is not adjusted and is the same on a GAAP and non-GAAP basis.
4 Diluted net loss per share attributable to Enovix. Non-GAAP net loss per share also excludes items in the non-GAAP tables below.
5 Cash, cash equivalents and marketable securities, including restricted cash, as of October 4, 2026. Reflects $6.2 million of common stock repurchased during Q3’26 but precedes the October and November 2026 repurchases of 2030 Notes and common stock buyback.

Drone and defense customers again drove the quarter. Our drone, defense and industrial pipeline (identified prospects through design wins) grew 18% to approximately $216 million, up from $183 million in the prior quarter with drones accounting for $150 million of that. The drone pipeline spans the full range of unmanned platforms including – unmanned aerial vehicles (UAV), unmanned underwater vehicles (UUV), electric vertical takeoff and landing (eVTOL) aircraft, and unmanned ground vehicles (UGV) – served by our conventional graphite cells and our higher-energy silicon-blended graphite cells. Our 2027 revenue backlog received a boost with an initial 100,000-battery purchase order from a multinational provider of dual-use drone systems for conventional cells, and we also received an initial production order for our new MX1-B01 high-energy aerial drone cells from a U.S. drone manufacturer following successful field trials – with initial deliveries scheduled in early 2027.

Steve Bakos, newly appointed Chief Revenue Officer and General Manager of Enovix, said, “The 100,000-battery order and the first MX1-B01 production order reflect our ability to convert our pipeline into orders. The MX1-B01 has now been sampled by more than 30 industry-leading aerial drone accounts with very positive feedback. Our customers need high-performance cells from a qualified, non-Chinese source, and they need them in volume next year. My team is focused on meeting that demand and helping define next-generation products.”

Our $19 million expansion to double drone battery capacity at our military-qualified South Korean facility is underway and expected to come online in Q2’27. We will make further Korean capacity investments that track our drone and military demand.

Our restructuring in early November included a 220-position reduction that cut approximately $8.5 million of annual cost and rebalanced our resources toward Korean operations where our near-term revenue opportunities continue to expand. Since quarter end, we have also retired $128 million of our 4.75% Convertible Senior Notes due 2030 (the “2030 Notes”) for approximately $81 million, capturing an approximately $47 million market discount, which will show up as profit in the GAAP, but not non-GAAP statements. We have also launched a warrant dividend designed to retire our 3.00% Convertible Senior Notes due 2028 (the “2028 Notes”). Finally, we are now guiding our fiscal year 2027 revenue at $65 million to $85 million, at the midpoint nearly double our expected 2026 revenue.

In smart eyewear, we brought our year-to-date shipments as of today to approximately 19,000 units against a 50,000-pack backlog that will be completed in the first half of 2027, and we continue to sample AI-2TM units to eyewear customers who need the second-generation energy density.

In smartphones, our AI-1TM cells finally passed cell-level qualification testing internally, while our lead OEM customer is expected to successfully finish its parallel qualification next week. Unfortunately, the qualification was on the pre AI-2 version of our process to get going early and did not meet the latest energy density target of more than 1,000 watt-hrs/liter. As a result, we have decided not to proceed with system-level field testing using the pre AI-2 units and are concentrating our silicon-anode development on smart eyewear, where we already have backlog. Our next energy-density gains, including AI-2, will go first to a group of our 24 smart eyewear customers.

Ryan Benton, Interim CEO, said, “Enovix is aligning its resources and cost structure with our strongest near-term opportunities. We are thus concentrating our silicon-anode development on smart eyewear and restructuring to direct more resources toward our operations in Korea. Our growing backlog and pipeline, coupled with our Korean capacity expansion, support our new outlook. For full-year 2027 revenue, we are guiding $65 million to $85 million, with nearly half the midpoint already in backlog.”

Capital Structure Improvements

We have repurchased $6.2 million of our common stock in Q3’26 and another $15.5 million in October. In addition, we have retired $128.0 million face value of 2030 Notes for approximately $81.4 million – a 36% discount that cut our debt by $46.6 million more than we paid. The remaining 2030 Notes stand at $232.0 million.

We declared a dividend of one warrant for every four shares of common stock to stockholders on October 28, 2026, with a record date of tomorrow, November 13, 2026. Each warrant buys one share at $3.00, payable in cash or in 2028 Notes at full face value and expires April 28, 2028 – or earlier if our stock trades at or above $3.30 for 20 of any 30 consecutive trading days. Holders of 2028 Notes and 2030 Notes on the record date receive warrants on the same terms, without converting, based on the shares into which their notes were convertible. We expect to distribute the warrants on or about November 18, 2026, and begin trading on Nasdaq as ENVXW. We cannot predict whether or when holders will exercise. Shareholders must own the shares at the end of trading on November 13 to gain the benefit. Conversely, anyone who has sold shares they do not own will owe the warrants for those shares to the lender on that date.

T.J. Rodgers, Enovix Executive Chairman, concluded, “In our August press release I promised shareholders to reduce our expenses and to make our reports to investors more candid and transparent. This report is our first effort to move toward those standards.”

Financial Outlook
       
  GUIDANCE1 ACTUAL YoY CHANGE2
($ millions, except per share) Q4’26 Q4’25 Q4’26 vs. Q4’25
Revenue $9.0 – 10.0 $11.3 (20%) – (12%)
Non-GAAP loss from operations3 ($28.0 – 31.0) ($28.9) 3% – (7%)
Non-GAAP net loss per share3 ($0.13 – 0.17) ($0.14) 7% – (21%)
Capital expenditures4 $5.0 – 8.0 $1.0 n/m

  GUIDANCE1 ESTIMATE5 YoY CHANGE2
($ millions) FY’27 FY’26 Est. FY’27 vs. FY’26
Revenue $65.0 – 85.0 $36.7 – 37.7 +75% – +128%

1 Guidance as of November 12, 2026. Non-GAAP loss from operations and non-GAAP net loss per share exclude stock-based compensation, amortization of intangible assets and certain other items. We are not presenting a quantitative reconciliation of our guidance for these measures to their GAAP equivalents, in reliance on the unreasonable efforts exception under Item 10(e)(1)(i)(B) of Regulation S-K; see “Non-GAAP Financial Measures” below.
2 Year-over-year change calculated by comparing each end of the guidance range to the prior-period amount (or, for fiscal year 2027, to the $37.2 million midpoint of the fiscal year 2026 estimate); for loss measures, a positive percentage indicates a smaller loss.
3 Q4’25 amounts are non-GAAP; see the reconciliation available on our website at ir.enovix.com.
4 Capital expenditures reflect cash paid for property and equipment. Our outlook does not include provisions for proposed tax law changes, future asset impairments or pending legal matters other than amounts that are probable and estimable, and excludes items such as investment, derivative and foreign currency gains or losses that cannot be accurately forecast. Actual results may differ materially from the outlook. n/m – not meaningful.
5 Fiscal year 2026 revenue estimate of $36.7 million to $37.7 million reflects year-to-date revenue of $27.7 million plus the Q4’26 revenue guidance range; it is not separate guidance for fiscal year 2026.

Third Quarter 2026 Earnings Call
Enovix will host a live video webcast today, November 12, 2026, at 1:00 p.m. ET / 10:00 a.m. PT, during which T.J. Rodgers, Executive Chairman, Ryan Benton, Interim Chief Executive Officer, Steve Bakos, Chief Revenue Officer and General Manager, and Michael Vyvoda, Chief Operating Officer, will discuss third quarter 2026 results, provide a business update and discuss the warrant distribution. To register for the webcast, please visit https://enovix-q3-2026.open-exchange.net/ or the Events page of the Investor Relations website at https://ir.enovix.com/news-events/investor-calendar. Investors may submit questions on the registration page that they would like management to address on the call.

About Enovix
Enovix develops and manufactures advanced lithium-ion batteries, including proprietary silicon-anode architectures for smartphones, smart eyewear, defense, industrial and emerging edge-AI applications. Its proprietary silicon-anode battery architecture enables higher energy density and performance in space-constrained devices while maintaining safety and reliability, supporting commercialization across consumer and industrial markets.

Enovix is headquartered in Silicon Valley with facilities in India, South Korea and Malaysia, serving customers globally. For more information visit https://enovix.com and follow us on LinkedIn.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements relate to future events or our future financial or operating performance and are identified by words such as anticipate, believe, could, estimate, expect, intend, may, might, plan, possible, potential, predict, project, should, will, would and similar expressions. Forward-looking statements in this press release include, but are not limited to, statements regarding: our Q4’26 guidance, our fiscal year 2026 revenue estimate, our fiscal year 2027 guidance and our future operating results, financial position and growth opportunities; the drone battery purchase orders described in this release, including the quantity and timing of deliveries and our expectation of follow-on orders; our backlog for 2027 delivery and its conversion into revenue; the growth of our drone, defense and industrial pipeline and its conversion into design wins, purchase orders, shipments and revenue at acceptable margins; the timing, cost and benefits of our capacity expansion in South Korea and any further investments in South Korea capacity; the expected timing of completion of our smart eyewear customer order, the effectiveness of the corrective actions we have taken in response to the manufacturing process excursion, the sampling of AI-2 and our ability to obtain additional smart eyewear orders; our smartphone strategy, including our decision not to proceed with system-level field testing of AI-1 with our lead smartphone customer, our reduced AI-1 development spending, the concentration of our silicon-anode development on small cells, the potential application of future energy-density gains to large-format smartphone cells, the timing of any revised smartphone timeline and our ability to re-engage in smartphone qualification; the expected savings, costs and timing of our restructuring plan, including the rebalancing of our resources toward our South Korea operations and the narrowing of our development priorities; the expected benefits of our 2030 Notes repurchases and our warrant dividend, any further repurchases of 2030 Notes or common stock under existing authorizations, the number of warrants that may be exercised, the timing of any early expiration of the warrants and the amount of cash raised or debt retired; the expected performance, capabilities and development of our battery products and technology roadmap; the timing and results of customer testing, certification and qualification; our ability to scale and optimize manufacturing, including improvements in yield, throughput, dicing processes, cost and capital efficiency; our expectations regarding regulatory, certification and government sourcing requirements, including under the NDAA and TAA; the sufficiency and use of our capital resources; and the expected benefits of our recent leadership and organizational changes. These statements are based on the current expectations of our management, are not predictions of actual performance, and actual results may differ materially from the future results, performance or achievements expressed or implied by the forward-looking statements.

Risks, uncertainties and assumptions that could cause actual results to differ materially from the results and events anticipated by such forward-looking statements include, but are not limited to: the possibility that purchase orders or backlog are modified, delayed, reduced or cancelled, that deliveries do not occur on the expected schedule or that customers do not place follow-on orders; the possibility that other opportunities in our pipeline do not convert into purchase orders, or convert later or in smaller amounts than we expect; the possibility that our restructuring does not achieve the expected savings, results in unanticipated costs or disrupts our operations, including through the loss of key personnel; the possibility that the corrective actions we have taken in response to the manufacturing process excursion affecting our smart eyewear shipments prove insufficient, or that similar excursions recur and further delay deliveries; the possibility that few or no warrants are exercised, that the warrant distribution is delayed or modified, or that the cash proceeds received or debt retired differ materially from our expectations; risks related to the outcome of customer testing and qualification activities, including the possibility that our products do not meet required performance thresholds, including energy-density requirements, that pending testing with our lead smartphone customer is not completed successfully, or that such testing is delayed beyond expected time frames; the possibility that concentrating our development resources on small cells does not produce the energy-density gains or customer adoption we expect, or that we are unable to re-engage in the smartphone market on acceptable terms or at all; our ability to successfully develop, manufacture and commercialize our battery products and transition to high-volume production; our ability to scale manufacturing operations and achieve expected production capacity and yields, including bringing expanded South Korea capacity online on schedule; our ability to sustain recent gross margin levels as our revenue mix changes; the level and timing of customer demand, qualification and adoption of our products across end markets; our ability to enter into and expand commercial agreements, including securing design wins, purchase orders and production contracts; our ability to execute on our business strategy and build and scale our sales and commercial capabilities; lengthy and unpredictable customer qualification and sales cycles, safety considerations and contractual terms, particularly in defense and other regulated markets; risks related to battery performance, reliability and safety; customer concentration in the defense sector and certain consumer technology markets, such as smartphones and smart eyewear; challenges in forecasting demand, inventory and manufacturing requirements that may result in additional costs and production delays; our history of losses and expectation of continued losses; risks associated with the development and commercialization of products that remain under development and may not be successfully produced at commercial scale; our ability to effectively integrate and derive benefits from acquired businesses; fluctuations in foreign currency exchange rates and interest rates; operational and safety risks associated with manufacturing equipment; intense competition and our ability to keep up with rapid technological change and evolving standards in the battery industry; our ability to attract and retain qualified personnel, including risks associated with our interim chief executive officer arrangement and other recent leadership and organizational changes; the outcome of litigation, regulatory investigations and other legal matters, including the associated legal and other costs; liquidity constraints, capital availability and our ability to service existing debt; our ability to protect and enforce our intellectual property rights; volatility in the trading price of our common stock and warrants; changes in tax laws or regulations; the impact of cyber and other information technology or security-related incidents on us, our customers or other parties; changes in the political, economic or regulatory environment generally and in the markets in which we operate; and other risks described in the disclosures contained in our filings with the Securities and Exchange Commission (“SEC”), including in the “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” sections of our annual report on Form 10-K and quarterly reports on Form 10-Q and other documents that we have filed, or will file, with the SEC. These documents are available in the SEC Filings section of the Investor Relations page at https://ir.enovix.com and at www.sec.gov. It is not possible for us to predict all risks, nor can we assess the impact of all factors on our business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements we may make. Accordingly, you should not rely on any of the forward-looking statements.

Any forward-looking statements in this press release speak only as of the date on which they are made. We undertake no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

Non-GAAP Financial Measures
This press release includes the use of non-GAAP financial measures, which are intended to provide supplemental information regarding our performance. These non-GAAP measures include non-GAAP cost of revenue, non-GAAP gross profit (loss), non-GAAP gross margin, non-GAAP research and development expense, non-GAAP selling, general and administrative expense, non-GAAP operating expenses, non-GAAP income (loss) from operations, EBITDA, adjusted EBITDA, non-GAAP net loss attributable to Enovix shareholders, non-GAAP earnings (loss) per share, free cash flow, and other non-GAAP measures that are included in this press release.

We use these non-GAAP measures to supplement our financial reporting and to evaluate ongoing operations and results, facilitate internal planning and forecasting, and assess performance against prior periods, industry peers, and the broader market. These non-GAAP measures are not prepared in accordance with generally accepted accounting principles (GAAP) and should not be considered as an alternative to GAAP results. Industry peers and other companies may calculate similar non-GAAP measures differently. Non-GAAP financial measures have limitations, including but not limited to, that they exclude certain expenses that are required under GAAP, which adjustments reflect the exercise of judgment by management. We believe that these non-GAAP measures, when considered together with the GAAP results, provide investors with an additional understanding of our operating performance. Reconciliations of each non-GAAP financial measure to the most directly comparable GAAP financial measure can be found in the tables at the end of this press release.

While Enovix provides fourth quarter 2026 guidance for non-GAAP loss from operations, non-GAAP net loss per share and capital expenditures, we are unable to provide without unreasonable effort a GAAP to non-GAAP reconciliation of these projected non-GAAP measures, and we have not provided a quantitative reconciliation in reliance on the unreasonable efforts exception under Item 10(e)(1)(i)(B) of Regulation S-K. Such reconciliation to the corresponding GAAP financial measure cannot be provided without unreasonable effort because of the inherent difficulty in accurately forecasting the occurrence and financial impact of the various adjustments that have not yet occurred, are out of our control, or cannot be reasonably predicted, including but not limited to change in fair value of common stock warrants, stock-based compensation and related tax effects, legal costs related to shareholder lawsuit, gain on bargain purchase of assets, acquisition-related costs, and restructuring costs. As a result, we are unable to assess the probable significance of the unavailable information, which could have a material impact on our future GAAP financial results.

Note Regarding Customer Pipeline, Design Wins and Backlog
We may refer in this press release and other communications to our “customer pipeline” and “design wins.” Our customer pipeline represents our estimate of the peak annual production value of identified design opportunities for products manufactured in South Korea. A “design win” refers to an opportunity that has been awarded to Enovix but has not yet entered production. Customer pipeline and design win amounts do not represent customer orders, backlog or committed revenue and should not be viewed as forecasts of future revenue. Actual revenue, if any, will depend on a number of factors, including customer qualification, final program awards, production timing, capacity and volumes, and the successful launch and ramp of customer programs. We also refer to our “backlog,” which represents orders we have received for delivery in future periods. Backlog is subject to modification, delay, reduction or cancellation. Customer pipeline, design win and backlog amounts are forward-looking and are subject to the risks and uncertainties described above under “Forward-Looking Statements.”

For media and investor inquiries, please contact:
Investor Contact:
Monica Gould
Blueshirt Group
ir@enovix.com

ENOVIX CORPORATION
THIRD QUARTER 2026 FINANCIAL SUMMARY
(Unaudited; in millions, except per share data and percentages; amounts may not sum due to rounding)
 
               
  GAAP NON-GAAP  
($ millions, except per share) Q3’26 Q3’25 YoY Δ Q3’26 Q3’25 YoY Δ  
Revenue $11.0 $8.0 $3.0 $11.0 $8.0 $3.0  
Gross profit $3.3 $1.4 $1.9 $3.8 $1.7 $2.1  
Gross margin 30.1% 17.5% 12.6pts 34.5% 21.0% 13.5pts  
Operating expenses $42.6 $48.4 $(5.8) $33.0 $31.5 $1.5  
Loss from operations $(39.3) $(47.0) $7.7 $(29.2) $(29.8) $0.6  
Net cash used in operating activities $(29.2) $(25.5) $(3.7) $(29.2) $(25.5) $(3.7)  
Capital expenditures1 $(3.9) $(3.0) $(0.9) $(3.9) $(3.0) $(0.9)  
Free cash flow N/A N/A N/A $(33.1) $(28.5) $(4.6)  
Adjusted EBITDA N/A N/A N/A $(21.1) $(21.4) $0.3  
Net loss per share, basic2 $(0.19) $(0.26) $0.07 $(0.15) $(0.14) $(0.01)  
Weighted average shares, basic3 219.6 206.5 13.1 219.6 206.5 13.1  
Net loss per share, diluted2 $(0.19) $(0.27) $0.08 $(0.15) $(0.14) $(0.01)  
Weighted average shares, diluted3 219.6 206.8 12.8 219.6 206.8 12.8  

(1) Capital expenditures reflect cash paid for property and equipment and is a component of our free cash flow calculation. It excludes one-time cash outflows related to business acquisitions.
(2) Net loss per share attributable to Enovix.
(3) Weighted average shares attributable to Enovix, in millions.


ENOVIX CORPORATION
YEAR-TO-DATE 2026 FINANCIAL SUMMARY
(Unaudited; in millions, except per share data and percentages; amounts may not sum due to rounding)
             
  GAAP NON-GAAP
($ millions, except per share) YTD’26 YTD’25 YoY Δ YTD’26 YTD’25 YoY Δ  
Revenue $27.7 $20.6 $7.1 $27.7 $20.6 $7.1  
Gross profit $6.2 $3.6 $2.6 $7.6 $4.4 $3.2  
Gross margin 22.3% 17.5% 4.8pts 27.4% 21.2% 6.2pts  
Operating expenses $132.7 $136.9 $(4.2) $94.3 $88.7 $5.6  
Loss from operations $(126.5) $(133.3) $6.8 $(86.7) $(84.3) $(2.4)  
Net cash used in operating activities $(84.1) $(68.3) $(15.8) $(84.1) $(68.3) $(15.8)  
Capital expenditures1 $(16.7) $(17.2) $0.5 $(16.7) $(17.2) $0.5  
Free cash flow N/A N/A N/A $(100.8) $(85.5) $(15.3)  
Adjusted EBITDA N/A N/A N/A $(60.3) $(62.3) $2.0  
Net loss per share, basic2 $(0.56) $(0.59) $0.03 $(0.41) $(0.40) $(0.01)  
Weighted average shares, basic3 218.5 204.8 13.7 218.5 204.8 13.7  
Net loss per share, diluted2 $(0.56) $(0.59) $0.03 $(0.41) $(0.40) $(0.01)  
Weighted average shares, diluted3 218.5 204.8 13.7 218.5 204.8 13.7  

(1) Capital expenditures reflect cash paid for property and equipment and is a component of our free cash flow calculation. It excludes one-time cash outflows related to business acquisitions.
(2) Net loss per share attributable to Enovix.
(3) Weighted average shares attributable to Enovix, in millions.


ENOVIX CORPORATION
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited; in thousands, except share and par value amounts)
       
  October 4, December 28,  
  2026 2025  
Assets    
Current assets:    
Cash and cash equivalents $63,225 $106,014  
Short-term investments 342,273 406,026  
Accounts receivable, net 4,277 4,421  
Notes receivable, net — 4,012  
Inventory 19,849 13,617  
Prepaid expenses and other current assets 9,967 8,120  
Total current assets 439,591 542,210  
Property and equipment, net 159,651 170,263  
Long-term investments 104,558 106,810  
Customer relationship intangibles and other intangibles, net 27,979 31,638  
Operating lease, right-of-use assets 7,677 11,682  
Goodwill 12,217 12,217  
Other assets, non-current 3,300 4,155  
Total assets $754,973 $878,975  
Liabilities and Equity    
Current liabilities:    
Accounts payable $12,630 $17,818  
Accrued expenses 9,709 13,992  
Accrued compensation 8,270 6,219  
Short-term debt 11,650 9,865  
Deferred revenue 958 5,015  
Warrant liability — 6,578  
Other liabilities 5,113 5,529  
Total current liabilities 48,330 65,016  
Long-term debt, net 521,873 519,271  
Operating lease liabilities, non-current 5,237 11,244  
Deferred revenue, non-current 300 300  
Deferred tax liability 8,075 9,119  
Other liabilities, non-current 15 14  
Total liabilities 583,830 604,964  
Stockholders’ equity:    
Common stock, $0.0001 par value; authorized shares of 1,000,000,000; issued and outstanding shares of 218,348,968 and 216,556,238 as of October 4, 2026 and December 28, 2025, respectively 23 22  
Additional paid-in capital 1,336,896 1,307,912  
Treasury stock, at cost (64,598) (58,385)  
Accumulated other comprehensive loss (2,156) (508)  
Accumulated deficit (1,101,096) (977,827)  
Total Enovix’s stockholders’ equity 169,069 271,214  
Non-controlling interest 2,074 2,797  
Total equity 171,143 274,011  
Total liabilities and equity $754,973 $878,975  
       


ENOVIX CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited; in thousands, except share and per share amounts)
         
  Fiscal Quarters Ended Fiscal Years-to-Date Ended
 
  October 4,
2026
September 28,
2025
October 4,
2026
September 28,
2025
 
Revenue $11,039 $7,990 $27,663 $20,556  
Cost of revenue 7,711 6,589 21,481 16,952  
Gross profit 3,328 1,401 6,182 3,604  
Operating expenses:        
Research and development 26,812 28,180 77,784 82,257  
Selling, general and administrative 15,810 20,194 54,883 54,613  
Total operating expenses 42,622 48,374 132,667 136,870  
Loss from operations (39,294) (46,973) (126,485) (133,266)  
Other income (expense):        
Change in fair value of common stock warrants — 1,867 6,578 11,778  
Gain on bargain purchase of assets — — — 4,761  
Interest income 4,943 2,540 15,853 7,401  
Interest expense (6,559) (11,765) (20,088) (15,186)  
Other income (expense), net (1,154) 140 173 1,501  
Total other income (expense), net (2,770) (7,218) 2,516 10,255  
Loss before income tax benefit (42,064) (54,191) (123,969) (123,011)  
Income tax benefit (148) (422) (718) (1,445)  
Net loss (41,916) (53,769) (123,251) (121,566)  
Net gain (loss) attributable to non-controlling interest 30 (56) 18 185  
Net loss attributable to Enovix $(41,946) $(53,713) $(123,269) $(121,751)  
Net loss per share attributable to Enovix, basic $(0.19) $(0.26) $(0.56) $(0.59)  
Weighted average shares outstanding, basic 219,623,989 206,458,846 218,465,367 204,758,291  
Net loss per share attributable to Enovix, diluted $(0.19) $(0.27) $(0.56) $(0.59)  
Weighted average shares outstanding, diluted 219,623,989 206,811,315 218,465,367 204,758,291  
           


ENOVIX CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited; in thousands)
     
  Fiscal Years-to-Date Ended
 
  October 4, 2026 September 28, 2025  
Cash flows used in operating activities:      
Net loss $(123,251) $(121,566)  
Adjustments to reconcile net loss to net cash used in operating activities    
Depreciation, accretion and amortization 29,931 26,675  
Stock-based compensation expense 33,256 37,973  
Change in fair value of common stock warrants (6,578) (11,778)  
Gain on bargain purchase of assets — (4,761)  
Interest expense (non-cash) — 9,222  
Others 367 1,312  
Changes in operating assets and liabilities:    
Accounts and notes receivables 4,322 (2,359)  
Inventory (5,752) (7,247)  
Prepaid expenses and other assets (817) 445  
Accounts payable (3,110) 6,539  
Accrued expenses and compensation (3,249) (2,781)  
Deferred revenue (4,171) 702  
Deferred tax liability (1,099) (1,135)  
Other liabilities (3,938) 467  
Net cash used in operating activities (84,089) (68,292)  
Cash flows from investing activities:    
Purchase of property and equipment (16,708) (17,216)  
Payment for business acquisition — (10,000)  
Purchases of investments (342,040) (370,133)  
Maturities of investments 409,172 58,145  
Net cash provided by (used in) investing activities 50,424 (339,204)  
Cash flows from financing activities:    
Proceeds from issuance of convertible senior notes and loan borrowing 2,419 360,000  
Payments of debt issuance costs — (9,900)  
Purchase of Capped Calls — (45,288)  
Proceeds from exercise of the 2025 common stock warrants — 232,106  
Proceeds from issuance of common stock under employee stock purchase plan 938 711  
Payroll tax payments for shares withheld upon vesting of RSUs (4,088) (4,855)  
Repurchase of common stock (6,213) (58,385)  
Purchase of Routejade shares from non-controlling interest (740) —  
Repayment of debt (1,696) (794)  
Proceeds from the exercise of stock options — 3,133  
Payments of issuance costs related to common stock and warrant dividends — (5,995)  
Net cash provided by (used in) financing activities (9,380) 470,733  
Effect of exchange rate changes on cash, cash equivalents and restricted cash 394 (409)  
Change in cash, cash equivalents, and restricted cash (42,651) 62,828  
Cash and cash equivalents and restricted cash, beginning of period 107,979 274,691  
Cash and cash equivalents and restricted cash, end of period $65,328 $337,519  
       


ENOVIX CORPORATION
RECONCILIATION OF NON-GAAP FINANCIAL MEASURES
(Unaudited; in thousands, except share and per share data)
           
    Fiscal Quarters Ended Fiscal Years-to-Date Ended
 
  Note Q3’26 Q3’25 YTD’26 YTD’25  
GAAP loss from operations   $(39,294) $(46,973) $(126,485) $(133,266)  
Stock-based compensation expense A 8,457 11,837 33,256 37,973  
Amortization of intangible assets B 1,188 1,190 3,659 3,568  
Legal cost related to shareholder lawsuit C 434 2,743 2,823 5,394  
2025 warrant issuance cost D — 1,378 — 1,378  
Acquisition cost G — — — 664  
Total non-GAAP adjustments   10,079 17,148 39,738 48,977  
Non-GAAP loss from operations   $(29,215) $(29,825) $(86,747) $(84,289)  

    Fiscal Quarters Ended Fiscal Years-to-Date Ended
 
  Note Q3’26 Q3’25 YTD’26 YTD’25  
GAAP net loss attributable to Enovix   $(41,946) $(53,713) $(123,269) $(121,751)  
Stock-based compensation expense A 8,457 11,837 33,256 37,973  
Amortization of intangible assets B 1,188 1,190 3,659 3,568  
Legal cost related to shareholder lawsuit C 434 2,743 2,823 5,394  
2025 warrant issuance cost D — 1,378 — 1,378  
Change in fair value of common stock warrants E — (1,867) (6,578) (11,778)  
Interest expense related to the 2025 warrant dividend F — 9,223 — 9,223  
Acquisition cost G — — — 664  
Gain on bargain purchase of assets H — — — (4,761)  
Import duty forgiveness I — — — (2,431)  
Total non-GAAP adjustments   10,079 24,504 33,160 39,230  
Non-GAAP net loss attributable to Enovix shareholders   $(31,867) $(29,209) $(90,109) $(82,521)  

    Fiscal Quarters Ended Fiscal Years-to-Date Ended
 
  Note Q3’26 Q3’25 YTD’26 YTD’25  
Net loss attributable to Enovix   $(41,946) $(53,713) $(123,269) $(121,751)  
Interest expense (income), net   1,616 9,225 4,235 7,785  
Income tax benefit   (148) (422) (718) (1,445)  
Depreciation, accretion and amortization   10,525 9,398 29,931 26,675  
EBITDA   (29,953) (35,512) (89,821) (88,736)  
Stock-based compensation expense A 8,457 11,837 33,256 37,973  
Change in fair value of common stock warrants E — (1,867) (6,578) (11,778)  
Legal cost related to shareholder lawsuit C 434 2,743 2,823 5,394  
2025 warrant issuance cost D — 1,378 — 1,378  
Acquisition cost G — — — 664  
Gain on bargain purchase of assets H — — — (4,761)  
Import duty forgiveness I — — — (2,431)  
Adjusted EBITDA   $(21,062) $(21,421) $(60,320) $(62,297)  

      Fiscal Years-to-Date Ended
 
  Note   YTD’26 YTD’25  
Net cash used in operating activities     $(84,089) $(68,292)  
Capital expenditures J   (16,708) (17,216)  
Free cash flow     $(100,797) $(85,508)  

    Fiscal Quarters Ended Fiscal Years-to-Date Ended
 
  Note Q3’26 Q3’25 YTD’26 YTD’25  
GAAP cost of revenue   $7,711 $6,589 $21,481 $16,952  
Stock-based compensation expense A (475) (280) (1,410) (757)  
Non-GAAP cost of revenue   $7,236 $6,309 $20,071 $16,195  
GAAP gross profit   $3,328 $1,401 $6,182 $3,604  
Stock-based compensation expense A 475 280 1,410 757  
Non-GAAP gross profit   $3,803 $1,681 $7,592 $4,361  
GAAP research and development (R&D) expense   $26,812 $28,180 $77,784 $82,257  
Stock-based compensation expense A (4,590) (5,754) (14,280) (19,050)  
Amortization of intangible assets B (415) (416) (1,279) (1,247)  
Non-GAAP R&D expense   $21,807 $22,010 $62,225 $61,960  
GAAP selling, general and administrative (SG&A) expense   $15,810 $20,194 $54,883 $54,613  
Stock-based compensation expense A (3,392) (5,803) (17,566) (18,166)  
Amortization of intangible assets B (773) (774) (2,380) (2,321)  
Legal cost related to shareholder lawsuit C (434) (2,743) (2,823) (5,394)  
2025 warrant issuance cost D — (1,378) — (1,378)  
Acquisition cost G — — — (664)  
Non-GAAP SG&A expense   $11,211 $9,496 $32,114 $26,690  
GAAP operating expenses   $42,622 $48,374 $132,667 $136,870  
Stock-based compensation expense included in R&D expense A (4,590) (5,754) (14,280) (19,050)  
Stock-based compensation expense included in SG&A expense A (3,392) (5,803) (17,566) (18,166)  
Amortization of intangible assets B (1,188) (1,190) (3,659) (3,568)  
Legal cost related to shareholder lawsuit C (434) (2,743) (2,823) (5,394)  
2025 warrant issuance cost D — (1,378) — (1,378)  
Acquisition cost G — — — (664)  
Non-GAAP operating expenses   $33,018 $31,506 $94,339 $88,650  
             


Notes:
(A) Stock-based compensation: non-cash expense related to equity awards granted to employees, directors and consultants.
(B) Amortization of intangible assets: non-cash amortization of intangible assets acquired in the Routejade acquisition.
(C) Legal cost related to shareholder lawsuit: litigation expenses related to the defense of an ongoing securities class action, which management does not consider representative of the Company’s performance.
(D) 2025 warrant issuance cost: costs associated with the July 2025 warrant dividend.
(E) Change in fair value of common stock warrants: non-cash gains or losses from the remeasurement of the Company’s common stock warrants.
(F) Interest expense related to the 2025 warrant dividend: non-cash interest expense recognized in connection with the July 2025 warrant dividend.
(G) Acquisition cost: transaction costs related to a business acquisition completed in 2025.
(H) Gain on bargain purchase of assets: non-cash gain recognized in 2025 where the fair value of net assets acquired exceeded the purchase price.
(I) Import duty forgiveness: one-time benefit recognized in 2025 from the forgiveness of previously accrued import duties.
(J) Capital expenditures: cash paid for property and equipment; excludes one-time cash outflows related to business acquisitions.
EBITDA is defined as net loss attributable to Enovix adjusted for interest income, interest expense, income tax benefit, and depreciation, accretion and amortization expense. Adjusted EBITDA further excludes stock-based compensation expense, change in fair value of common stock warrants, warrant issuance cost, certain legal costs related to the defense of an ongoing securities class action that are outside the ordinary course of business, and other special items that management does not believe to be indicative of underlying business trends.
Free Cash Flow is defined as net cash used in operating activities less capital expenditures, each as derived from the Condensed Consolidated Statements of Cash Flows. Free Cash Flow is not intended as an alternative to cash flows from operations as determined in accordance with GAAP.
These non-GAAP measures may differ from similarly titled measures used by other companies.

ENOVIX CORPORATION
RECONCILIATION OF GAAP NET LOSS PER SHARE TO NON-GAAP NET LOSS PER SHARE
(Unaudited; net loss per share attributable to Enovix)
         
  Fiscal Quarters Ended Fiscal Years-to-Date Ended
  Q3’26 Q3’25 YTD’26 YTD’25
GAAP net loss per share, basic $(0.19) $(0.26) $(0.56) $(0.59)  
Weighted average shares outstanding, basic 219,623,989 206,458,846 218,465,367 204,758,291  
GAAP net loss per share, diluted $(0.19) $(0.27) $(0.56) $(0.59)  
Weighted average shares outstanding, diluted 219,623,989 206,811,315 218,465,367 204,758,291  
Non-GAAP net loss per share, basic $(0.15) $(0.14) $(0.41) $(0.40)  
Non-GAAP net loss per share, diluted $(0.15) $(0.14) $(0.41) $(0.40)  

Note: Q3’26 and year-to-date 2026 basic and diluted amounts are the same because potentially dilutive securities were anti-dilutive.

Source: Enovix Corporation

  • Net Income was positive for the second consecutive quarter, and Adjusted EBITDA1 positive for its third consecutive quarter.
  • Net Revenue of $11.8M increased 18% versus Q2 2026, with German revenue increasing 19% sequentially and 81% year over year
  • OPEX decreased 25% versus Q3 2025 and 11% versus Q2 2026
  • Cash of $10.1M, increased from $9.9M in Q2 2026; the Company remains virtually debt free, with outright ownership of two production facilities appraised at over $15M
  • Management to Host Conference Call / Webcast on November 12th, 2026, at 10:00 am ET

TORONTO, Nov. 12, 2026 (GLOBE NEWSWIRE) — MediPharm Labs Corp. (TSX: LABS) (OTCQB: MEDIF) (FSE: MLZ) (“MediPharm”, “MediPharm Labs” or the “Company”), a pharmaceutical company specialized in precision-based cannabinoids, today announced its financial results for the three and nine months ended September 30, 2026 (“Q3 2026”).

MediPharm Labs generated its third consecutive quarter of positive Adjusted EBITDA and achieved positive net income for the second consecutive quarter. Revenue increased 18% versus the three months ended June 30, 2026 (“Q2 2026”), and revenue, gross profit and Adjusted EBITDA were all higher than in the three months ended September 30, 2025 (“Q3 2025”). More than 80% of revenue for the nine months ended September 30, 2026, was generated through prescription-based medical channels and over 55% of revenue was generated through international channels.

“Q3 demonstrates the progress we are making in building a stronger and more profitable MediPharm,” said Greg Hunter, CEO of MediPharm Labs. “We delivered one of our strongest revenue quarters in recent years, achieved positive net income for the second consecutive quarter and generated our third consecutive quarter of positive Adjusted EBITDA. Importantly, more than 80% of our revenue is now generated through prescription-based medical channels, reflecting MediPharm’s deep experience in global medical and pharmaceutical cannabis. Our differentiated regulatory and manufacturing platform continues to translate into international growth and improved commercial results.”

Financial Highlights

  • Revenue of $11.8 million increased 18% versus Q2 2026, driven by growth in International Medical.
  • Gross profit of $3.8 million, an increase of 27% versus Q3 2025. Gross margin was 32%, compared with 26% in Q3 2025
  • Q3 2026 Adjusted EBITDA1 of $0.4 million, an improvement of $1.5 million versus Q3 2025.
  • Net income improved $2.3 million versus Q3 2025, to positive net income of $112K in Q3 2026.
  • Operating expenses decreased 25% versus Q3 2025 and 11% versus Q2 2026.
  • For the nine months ended September 30, 2026, Adjusted EBITDA was $1.4 million, an improvement of $2.9 million versus the prior-year period.
  Three months ended

  30-Sep-26 30-Jun-26 31-Mar-26 31-Dec-25
  $’000s $’000s $’000s $’000s
Revenue 11,802 9,984 8,963 11,062
Gross profit (c) 3,806 4,312 3,322 4,275
% Sales 32% 43% 37% 39%
Opex (a) (3,585) (4,016) (4,164) (5,800)
Adjusted EBITDA (b) 442 894 103 (144)

(a) Opex includes general administrative expense, marketing and selling expenses and R&D expenses.
(b) Adjusted EBITDA is a non-IFRS financial measure. See “Non-IFRS Measures”.
(c) Comparative figures have been reclassified for a change in the classification of patient education fees and differ from those previously reported.

Operational and Commercial Highlights

International Medical

  • International Medical revenue was $6.9 million, an increase of 20% versus Q2 2026 and 59% of total revenue.
  • In Germany, revenue increased 19% versus Q2 2026 and 81% versus Q3 2025, supported by demand across flower, oil and dronabinol and the expansion of the MediPharm branded portfolios, Beacon Medical and Wildlife.
  • Revenue from other international markets increased to $1.8 million from $0.7 million in Q2 2026, with growth in the UK and in Brazil, where the Company’s products launched through national pharmacy channels.
  • In Australia, the Company refreshed its Beacon Medical portfolio, expanded Wildlife into the value segment and broadened its distribution as the market continues to adjust to changes in prescribing practices and pricing.
  • As previously announced, the Phase II LiBBY trial, which used a proprietary cannabinoid formulation manufactured by MediPharm Labs for agitation in patients with advanced dementia, met its primary endpoint, with statistically significant improvement as early as two weeks. The Company is evaluating potential next steps, including additional clinical development opportunities, regulatory pathways and strategic partnerships.
  • Subsequent to quarter end, MediPharm advanced its international inhaler commercialization program with its first commercial shipment of CBD metered-dose inhalers to Panama. The Company has also received a notified-body opinion for its metered-dose inhaler, a regulatory milestone that supports the pathway toward future commercialization in the UK and European Union.

Canada

  • Canadian Medical Cannabis revenue was stable sequentially at $2.3 million and consistent with Q2 2026. The Company continues to prioritize service levels and product access in the face of Veterans Affairs April 1 reimbursement rate changes. Revenue declined versus Q3 2025, reflecting the 30% reduction (from $8.50 to $6.00 per gram) in the maximum reimbursement rate for Veterans Affairs Canada clients. In addition, Harvest Medicine reached a new high in active Veteran patients during the quarter.
  • In Adult Use and Wellness, the Company launched new Pocket Drops in Ontario and Alberta, with additional line extensions confirmed for Q4 2026, and maintained its number two national brand position in adult use traditional oils3.

Strong Balance Sheet with Cash increasing Sequentially

Cash increased to $10.1 million from $9.9 million in Q2 2026. MediPharm Labs strong balance sheet continues to differentiate the company from many industry peers and provides flexibility to fund both organic growth and selective M&A opportunities as the industry continues to evolve. The Company remains virtually debt free, with outright ownership of two licensed production facilities with a combined appraised value of more than $15M, and is current on excise duties, sales taxes and trade payables.

Q3 2026 Financial Results Conference Call / Webcast

MediPharm Labs will host a conference call and webcast on November 12th, 2026, at 10:00 am (Eastern time) to discuss the Company’s financial results. The conference call dial in details are as follows:

Conference Call Dial in Details:
United States Toll-Free: (833) 461-5787
Canada Toll-Free: (833) 769-6440
International: dial-in numbers are available here.
Meeting ID: 571066887
Participants are asked to dial in approximately 15 minutes before the start of the call. 

Webcast:
A webcast will be available by visiting the following link here.

For those who are unable to participate on the live conference call or webcast, a replay will be available at https://www.medipharmlabs.com/investors approximately one day after completion of the call.

The Company’s unaudited condensed interim consolidated financial statements and management’s discussion and analysis for the three and nine months ended September 30, 2026, are available under the Company’s profile on SEDAR+ at www.sedarplus.ca. Readers should review those documents in full.

About MediPharm Labs

Founded in 2015, MediPharm Labs specializes in the development and manufacture of purified, pharmaceutical-quality cannabis concentrates, active pharmaceutical ingredients (API) and advanced derivative products utilizing a Good Manufacturing Practices certified facility with ISO standard-built clean rooms. MediPharm Labs has invested in an expert, research driven team, state-of-the-art technology, downstream purification methodologies and purpose-built facilities for delivery of pure, trusted and precision-dosed cannabis products for its customers. MediPharm Labs develops, formulates, processes, packages and distributes cannabis and advanced cannabinoid-based products to domestic and international medical markets.

In 2021, MediPharm Labs received a Pharmaceutical Drug Establishment Licence from Health Canada, becoming the only company in North America to hold a commercial-scale domestic Good Manufacturing Practices Licence for the extraction of multiple natural cannabinoids. This GMP licence was the first step in the Company’s current foreign drug manufacturing site registration with the US FDA. MediPharm also has EU-GMP certification, ANVISA GMP certification from Brazil and TGA compliance in Australia.

In 2023, MediPharm acquired VIVO Cannabis Inc. which expanded MediPharm’s reach to medical patients in Canada via Canna Farms medical e-commerce platform, and in Australia and Germany through Beacon Medical PTY and Beacon Medical GmbH. This acquisition also included Harvest Medical Clinics in Canada which provides medical cannabis patients with physician consultations for medical cannabis education and prescriptions.

The Company carries out its operations in compliance with all applicable laws in the countries in which it operates.

Website: www.medipharmlabs.com
SOURCE MediPharm Labs Corp.

For further information, please contact: 
MediPharm Labs Investor Relations, 1 416.913.7425
investors@medipharmlabs.com

Notes and References

1. Adjusted EBITDA is a non-IFRS financial measure. See “Non-IFRS Measures” below for a definition and a reconciliation to net operating income (loss), the most directly comparable IFRS measure.
2. Based on the Company’s reported quarterly Adjusted EBITDA results for Q1 2026, Q2 2026 and Q3 2026. See “Non-IFRS Measures” below.
3. As reported in HiFyre Retail analytics ingestible oils – July to September 2026.

Non-IFRS Measures

This press release contains references to “Adjusted EBITDA” which is a non-IFRS financial measure. Management believes that this supplementary non-IFRS financial measure provides useful additional information related to the operating results of the Company. This non-IFRS financial measure is not recognized under IFRS and, accordingly, users are cautioned that this measure should not be construed as an alternative to net income (loss) and gross profit determined in accordance with IFRS as measures of profitability or as alternatives to the Company’s IFRS-based Financial Statements. The non-IFRS measure presented may not be comparable to similar measures presented by other issuers. Adjusted EBITDA is a measure of the Company’s overall financial performance and is used as an alternative to earnings or income in some circumstances. Adjusted EBITDA is essentially net income (loss) with interest, taxes, depreciation and amortization, non-cash adjustments and other unusual or non-recurring items added back in. Adjusted EBITDA has limitations as an analytical tool as it does not include depreciation and amortization expense, interest income and expense, finance fees, gain in revaluation of derivative liabilities, taxes, government grants including rent and wage subsidies, one-off transactions, impairment losses on inventory and on fixed assets and intangibles, write down of deposits and share-based compensation. Because of these limitations, Adjusted EBITDA should not be considered as the sole measure of the Company’s performance and should not be considered in isolation from, or as a substitute for, analysis of the Company’s results as reported under IFRS. Adjusted EBITDA, as used within the Company’s disclosure, may not be directly comparable to Adjusted EBITDA used by other reporting issuers. Adjusted EBITDA does not have a standardized meaning and the Company’s method of calculating such non-IFRS measure may not be comparable to calculations used by other companies bearing the same description.

The following table reconciles the Company’s net operating income (loss) (as reported), and Adjusted EBITDA for the periods presented:

  Three months ended

  30-Sep-26 30-Jun-26 31-Mar-26 31-Dec-25
  $’000s $’000s $’000s $’000s
Net operating profit/(loss) 79 (34) (912) (2,007)
Adjusted for:        
Share-based compensation expense 103 440 154 211
Depreciation and amortization 339 384 382 396
Restructuring related severance expenses – 23 121 942
Incremental cost of cannabis inventory acquired in a business combination (a) – 116 9 7
Fair value adjustments in gross profit (53) (19) 148 (127)
Miscellaneous (d) (26) (16) 171 138
AGM related proxy fees (b) – – 18 162
Transaction costs (c) – – 12 134
Adjusted EBITDA 442 894 103 (144)

(a) This represents the fair value realized on sale of cannabis inventory acquired in a business combination.
(b) This relates to certain fees and expenses associated with the proxy contest in connection with the Company’s annual shareholder meeting held June 16, 2025, and ongoing legal expenses related to the Apollo Claim.
(c) This includes non-recurring fees, expenses associated with the evaluation of potential mergers and acquisitions, and fees related to reorganization of legal entities.
(d) This relates to unusual, non-recurring transactions that are not reflective of the Company’s ongoing operating performance.

Cautionary Note Regarding Forward-Looking Information

This news release contains “forward-looking information” and “forward-looking statements” (collectively, “forward-looking statements”) within the meaning of the applicable Canadian securities legislation. All statements, other than statements of historical fact, are forward-looking statements and are based on expectations, estimates and projections as at the date of this news release. Any statement that involves discussions with respect to predictions, expectations, beliefs, plans, projections, objectives, assumptions, future events or performance (often but not always using phrases such as “expects”, or “does not expect”, “is expected”, “anticipates” or “does not anticipate”, “plans”, “budget”, “scheduled”, “forecasts”, “estimates”, “believes” or “intends” or variations of such words and phrases or stating that certain actions, events or results “may” or “could”, “would”, “might” or “will” be taken to occur or be achieved) are not statements of historical fact and may be forward-looking statements. In this news release, forward-looking statements relate to, among other things, management’s ability to continue to grow international medical and pharmaceutical and B2B revenue and reduce costs to drive growth and long-term value for the Company; MediPharm’s ability to continue to supply international medical cannabis markets, including Germany, the United Kingdom, Brazil, New Zealand, France and Australia; the regulatory pathway for, and future commercialization of, the Company’s metered-dose inhaler in the United Kingdom, the European Union and Panama; the future of MediPharm’s foreign drug manufacturing site registration; the effects of the Veterans Affairs Canada reimbursement change and management’s mitigation initiatives; the expected annualized savings from restructuring initiatives; the appraised value of the Company’s production facilities; the launch of new product formats, line extensions and provincial listings; product optimization and improvement of production efficiencies; the Company’s evaluation of selective merger and acquisition opportunities; and MediPharm’s path to sustained Adjusted EBITDA and cash flow positive results. Forward-looking statements are necessarily based upon a number of estimates and assumptions that, while considered reasonable, are subject to known and unknown risks, uncertainties, and other factors which may cause the actual results and future events to differ materially from those expressed or implied by such forward-looking statements. Such factors include, but are not limited to: general business, economic, competitive, political and social uncertainties; the inability of MediPharm to obtain adequate financing; the delay or failure to receive regulatory approvals; changes in government reimbursement programs; changes in prescribing behaviour, pricing and regulatory enforcement in the markets in which the Company operates; dependence on a limited number of significant customers; and other factors discussed in MediPharm’s filings, available on the SEDAR+ website at www.sedarplus.ca. There can be no assurance that such statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on the forward-looking statements and information contained in this news release. Except as required by law, MediPharm assumes no obligation to update the forward-looking statements of beliefs, opinions, projections, or other factors, should they change.

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