CARSON CITY, Nev., Oct. 07, 2026 (GLOBE NEWSWIRE) — American Lithium Minerals Inc. (OTC: AMLM) today announced that Worldwide Diversified Holdings, Inc. (“Worldwide”) has agreed to convert its outstanding note into AMLM common shares. Under the agreed structure, Worldwide will facilitate an initial transfer of one AMLM common share for every ten Worldwide common shares, scheduled to be completed in the fourth quarter, advancing AMLM’s capital-markets strategy.

Transaction Overview

  • Debt-to-Equity Conversion: Worldwide will convert its outstanding note into AMLM common stock, eliminating the associated debt from AMLM’s balance sheet.
  • Shareholder Base Expansion: The conversion and subsequent share distribution will increase AMLM’s shareholder count to more than 500 holders, satisfying a key shareholder-distribution requirement for uplisting to a major national securities exchange.
  • Alignment of Interests: Worldwide’s conversion reflects long-term confidence in AMLM’s operational strategy, governance, and capital-markets trajectory.

Strategic Rationale

  • Strengthened Balance Sheet: The conversion reduces leverage and improves AMLM’s financial profile ahead of planned acquisitions and development initiatives.
  • Uplisting Readiness: Achieving the 500-shareholder threshold is a critical milestone in AMLM’s uplisting roadmap, complementing ongoing audit, governance, and reporting enhancements.
  • Enhanced Market Positioning: A broader shareholder base supports improved liquidity, institutional visibility, and long-term value creation.

Management Commentary

Frank Kristan, the Company’s President commented:

“Worldwide’s decision to convert its note into AMLM common equity is a meaningful endorsement of our strategy and a transformative step in our uplisting preparation. This transaction strengthens our balance sheet, expands our shareholder base, and positions AMLM for the next phase of growth.”

AMLM will coordinate with its legal, audit, and capital-markets advisors to finalize all required filings, complete shareholder updates, and advance the company’s uplisting readiness initiatives.

About American Lithium Minerals, Inc.

American Lithium Minerals, Inc. (OTC: AMLM) is a multi-commodity critical minerals exploration company headquartered in Carson City, Nevada. The Company holds active project interests in gold, silver, copper, lithium, and rare earth elements across Nevada (USA), Chile, British Columbia, Yukon and Quebec (Canada), and Western Australia. AMLM’s portfolio includes 11 active project interests, including the Higginsville gold project in Western Australia, silver and copper exploration in Chile, rare earth interests in Quebec, and lithium properties in Nevada.( www.americanmineralresources.com)

Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Statements other than statements of historical facts included in this press release may constitute forward-looking statements and are not guarantees of future performance or results. Such statements involve a number of risks and uncertainties, including, without limitation, statements regarding the Company’s strategic initiatives, project development plans, expected commodity exposure, anticipated market conditions, the strength of macro tailwinds across critical minerals sectors, and the Company’s ability to advance its multi-commodity portfolio.

Investor Contact

American Lithium Minerals, Inc.
1007 South Street
Carson City, Nevada 89701
Telephone: (775) 587-6137
Email: info@americanmineralresources.com
Website: www.americanmineralresources.com
X / Twitter: American Mineral Resources (OTCID:AMLM) (@AMR_MineralRes) / X
LinkedIn: linkedin.com/company/american-mineral-resources

From left: James Heckman, Roundtable CEO and Founder; Erin Schaefer, Roundtable board member; and Eyal Hertzog, Roundtable co-founder and CTO.

Former head of Global Brand advertising for Google and Global Operations for YouTube unites with Pioneering Veterans, Digital Media Pioneers, James Heckman and Eyal Hertzog, to help bring Roundtable’s transformational AI/DeFi-powered platform to the professional media industry.

SEATTLE, WA, Oct. 07, 2026 (GLOBE NEWSWIRE) — Roundtable (Nasdaq: RTB), an AI/DeFi-powered Enterprise Media OS, today announced that Erin Schaefer has joined its Board of Directors. As a transformative leader in digital innovation, Ms. Schaefer brings a 20-year track record of senior technology leadership, scaling and leading high-stakes, multi-billion-dollar commercial engines for Google, YouTube, and Niantic Games, and more recently, leading General Catalyst ($43B+ AUM) as Chief Operating Officer. Throughout her career, Schaefer has been at the forefront of leading global operations at the frontier of technology.

Ms. Schaefer’s 14-year tenure at Google included serving as Managing Director of Global Operations at YouTube, Managing Director of Global Brand Advertising Strategy, and leading Americas video advertising, where she built the brand commercialization engine from scratch into a $10B+ global revenue business. As COO at General Catalyst, she directed the operating model, capital allocation and Applied AI transformation. As General Manager at Niantic, Erin oversaw US Gaming Studio and Publishing, leading to a multi-billion-dollar exit.

Schaefer’s appointment brings together three pioneering digital media leaders whose careers often intersected as architects and competitors. Before Schaefer led and helped build Google’s brand and YouTube advertising businesses, Heckman architected the landmark Google-MySpace partnership that launched Google’s social advertising marketplace, before his News Corp strategy team architected Hulu’s business model to compete directly with YouTube. Their paths crossed again when Heckman created the world’s largest premium media marketplace, partnering with MSN, Yahoo and AOL – as global media strategy leader at Yahoo – while Schaefer led Google’s directly competing “brand-advertising” business. Earlier still, Roundtable co-founder Eyal Hertzog created MetaCafe, the first social video platform, with tens of millions of users, while inventing the algorithmic personalization feed.

“Partnering with Erin Schaefer brings an extraordinary track record to an already extraordinary team of digital media pioneers,” said Founder James Heckman. “She adds a rare combination of transformational technology leadership and major brand relationships. We’re honored to have Erin help guide our team.”

“My entire career has been about using technology to help passionate voices build sustainable businesses, from YouTube creators to the brands that support them,” said Erin Schaefer. “Professional journalism deserves the same. I believe this elite team of media technology pioneers can give it a brighter future, and James and Eyal Hertzog have built the platform to do it, with the full technology stack of AI, DeFi, and on-chain publishing under one roof.”

Schaefer is uniquely positioned to solidify Roundtable’s elite team, bringing her own major media ecosystem, strategy, and experience and sharing the goal of preserving sovereignty for professional media. Founding team and board members include former Prime Minister and Foreign Minister of Great Britain (hon Liz Truss), inventor of both the social video platform and DeFi technology (Eyal Hertzog), platform engineering head for MSN before leading 6 global platforms (Bill Sornsin), and founder and internet pioneer, James Heckman, responsible for 11 successful digital platforms, including 3 public exits, multiple acquisitions (including 2 to Yahoo, 1 to News Corp), and Publisher of an NFL publishing network.

Ms. Schaefer holds a B.A. in Political Science from Stanford University and an M.B.A. from Harvard Business School. She has served on public, private company, and nonprofit boards, including the Hillsborough Schools Foundation, where she is currently president. The appointment is detailed in the Company’s Current Report on Form 8-K filed with the U.S. Securities and Exchange Commission.

About Roundtable (RTB Digital, Inc.)

Roundtable (NASDAQ: RTB) is an AI/DeFi-powered Enterprise Media Operating System, integrating distribution, publishing, monetization, community, syndication, and DeFi payment operations, powering professional and major media brands. The Web3 platform was developed over years by digital pioneers and co-founders Eyal Hertzog and James Heckman. For more information, visit roundtable.io.

Cautionary Note Regarding Forward-Looking Statements

This press release includes information that constitutes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements are based on the Company’s current beliefs, assumptions, and expectations regarding future events, which in turn are based on information currently available to the Company. Such forward-looking statements include statements that are characterized by future or conditional words such as “may,” “will,” “expect,” “intend,” “anticipate,” “believe,” “estimate,” and “continue” or similar words. You should read statements that contain these words carefully because they discuss future expectations and plans, which contain projections of future results of operations or financial condition or state other forward-looking information. Such forward-looking statements include statements regarding the accretive transactions undertaken in 2026 and future operations and revenues of the company. By their nature, forward-looking statements address matters that are subject to risks and uncertainties. A variety of factors could cause actual events and results to differ materially from those expressed in or contemplated by the forward-looking statements, such as the company being able to maintain its listing on Nasdaq for the common stock, having sufficient capital for its acquisitions, operations and business expansion, and developing its business and capturing users for its services. Annualized and longer period revenue and business estimates are subject to the effect of macroeconomic events, to industry changes, to competitive forces, to client development and retention, to capital availability, and to many other operational factors; therefore, any financial forecasts offered by the Company must take into account the fact that the underlying assumptions may significantly change over time and projected results may substantively increase or decrease. Other risk factors affecting the Company are discussed in detail in the Company’s filings with the U.S. Securities and Exchange Commission. The Company undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except to the extent required by applicable laws.

Press Contact: press@roundtable.io

IR Contact: ir@roundtable.io

WALTHAM, Mass., Oct. 07, 2026 (GLOBE NEWSWIRE) — Akebia Therapeutics®, Inc. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by kidney disease, today announced that John P. Butler, Chief Executive Officer, Dr. Steven Burke, Chief R&D and Medical Officer, and Erik Ostrowski, Chief Financial and Chief Business Officer, will participate in one-on-one meetings at the Virtual U.S. Bancorp I BTIG Kidney Health Forum on October 14, 2026.

During meetings, management will discuss its commercial products and clinical stage, differentiated pipeline assets for rare kidney diseases.

About Akebia Therapeutics
Akebia Therapeutics, Inc. is a fully integrated biopharmaceutical company with the purpose to better the lives of people impacted by kidney disease. Akebia was founded in 2007 and is headquartered in Waltham, Massachusetts. For more information, please visit our website at www.akebia.com, which does not form a part of this release.

Akebia Therapeutics Contact
Mercedes Carrasco
mcarrasco@akebia.com  

ANN ARBOR, Mich., Oct. 07, 2026 (GLOBE NEWSWIRE) — Esperion, a company wholly-owned by ARCHIMED, today announced that it has entered into a settlement agreement with Renata Limited (along with an affiliate). This agreement resolves the patent litigation brought by Esperion against Renata in response to Renata’s Abbreviated New Drug Applications (ANDAs) seeking approval to market generic versions of NEXLETOL and NEXLIZET prior to the expiration of the applicable patents. Pursuant to the agreement, Renata has agreed not to market a generic version of either NEXLETOL or NEXLIZET in the United States prior to April 19, 2040, unless certain limited circumstances customarily included in these types of agreements occur.

The pending patent litigation against the remaining defendants (Aurobindo Pharma Limited (along with an affiliate); MSN Pharmaceuticals Inc. (along with an affiliate); and Sandoz Inc.) is ongoing, and there can be no assurance whether such ongoing patent litigation will allow a generic version of NEXLETOL and/or NEXLIZET, as applicable, to be marketed in the U.S. prior to April 19, 2040.

Esperion Therapeutics
Esperion Therapeutics, Inc. is a commercial-stage biopharmaceutical company dedicated to developing and delivering innovative cardiometabolic and rare/orphan disease therapies. The Company leverages deep domain expertise in ACLY biology to develop and commercialize transformative medicines for patients worldwide. Esperion currently markets two oral, once-daily, non-statin therapies for patients struggling to maintain their low-density lipoprotein cholesterol (LDL-C) levels and are at risk of cardiovascular disease.

With a broad U.S. commercial infrastructure and global approvals across more than 40 countries, Esperion is well positioned to serve as a partner-of-choice for global innovators seeking U.S. market access through acquisition, in-license, co-promotion and revenue share opportunities. In tandem, the Company is advancing its leadership in ACLY biology to build a diversified pipeline of novel product candidates, including treatments for Primary Sclerosing Cholangitis and renal diseases. For more information, visit esperion.com and follow Esperion on LinkedIn and X.

About ARCHIMED
With offices in Europe, North America and Asia, ARCHIMED is a leading investment firm focused exclusively on healthcare industries. Its mix of operational, medical, scientific and financial expertise allows ARCHIMED to serve as both a strategic and financial partner to healthcare businesses. Prioritized areas of focus include Animal & Environmental Health, Biopharma Products, Consumer Health, Diagnostics, Healthcare IT, Life Science Tools & Services, and MedTech. ARCHIMED helps partners internationalize, acquire, innovate and expand their products and services. ARCHIMED manages €9 billion across its various funds. Since inception, ARCHIMED has been a committed Impact investor, both directly and through its EURÊKA Foundation. For more information about ARCHIMED, please visit www.ARCHIMED.group.

Esperion Contact Information:
Media:
Tiffany Aldrich
corporateteam@esperion.com
(616) 443-8438

Earnings Release and Conference Call Scheduled for November 4, 2026

SAN FRANCISCO, Oct. 07, 2026 (GLOBE NEWSWIRE) — Sunrun (Nasdaq: RUN) today announced that it will issue its third quarter 2026 earnings report after the market closes on Wednesday, November 4, 2026. A conference call has been scheduled to discuss these earnings results at 4:30 p.m. Eastern Time / 1:30 p.m. Pacific Time.

The conference call can be accessed live via the Sunrun Investor Relations website at https://investors.sunrun.com. An audio replay will be available following the call on the Sunrun Investor Relations website for approximately one month and a transcript of the conference call will be posted to the Sunrun Investor Relations website the following day.

Event:   Sunrun 3Q 2026 Earnings Call
Date:   Wednesday, November 4, 2026
Call Time:   4:30PM ET / 1:30PM PT
Dial-in (toll-free/toll):   (877) 407-5989 / (201) 689-8434
Webcast / Replay:   https://investors.sunrun.com


About Sunrun

Sunrun Inc. (Nasdaq: RUN) is America’s largest provider of home battery storage, solar, and home-to-grid power plants. As the pioneer of home energy systems offered through a no-upfront-cost subscription model, Sunrun empowers customers nationwide with greater energy control, security, and independence. Sunrun supports the grid by providing on-demand dispatchable power that helps prevent blackouts and lower energy costs. Learn more at www.sunrun.com.

Investor & Analyst Contact:

Patrick Jobin
SVP, Deputy CFO & Investor Relations Officer
investors@sunrun.com

Media Contact:

Wyatt Semanek
Sr. Director, Corporate Communications
press@sunrun.com

PLANO, Texas, Oct. 07, 2026 (GLOBE NEWSWIRE) — Deep Isolation Nuclear, Inc. (OTCQB: DBHL) (“Deep Isolation” or the “Company”), a leading innovator in nuclear waste disposal technology, today announced that CEO Rod Baltzer and CFO Joe Nelson will present at three upcoming investor conferences, offering investors opportunities to learn more about the Company’s technology, commercialization strategy and progress toward deploying deep borehole disposal for nuclear waste.

On Oct. 8 at 11.30 am ET, Baltzer and Nelson will participate in the Small Cap Growth Virtual Conference by OTC Markets, an online investor event designed to connect publicly traded companies directly with individual and institutional investors, advisers and analysts. The live, interactive format will provide investors an opportunity to hear from Company leadership and submit questions in real time. Baltzer and Nelson will also be available for 1×1 meetings with investors and analysts. Link to the conference: Registration.

On Oct. 14 at 3:30 pm ET, Deep Isolation will present at the Precious Metals & Critical Minerals Virtual Conference, also hosted by OTC Markets. Baltzer and Nelson will discuss Deep Isolation’s approach to nuclear waste disposal and the Company’s role in supporting the infrastructure needed for the continued development and deployment of nuclear energy. Investors attending virtually will have an opportunity to hear the presentation and engage with Company leadership in 1×1 meetings. Link to the conference: Registration.

On Oct. 15, Baltzer and Nelson will present in person at the ThinkEquity Conference 2026 in New York, where Deep Isolation plans to engage with investors and discuss the Company’s commercialization activities, technology portfolio and opportunities arising from growing investment in nuclear energy and its supporting infrastructure.

“These conferences provide important opportunities to engage directly with the investment community as Deep Isolation advances toward commercialization,” said Baltzer. “We are looking forward to sharing our progress, discussing the growing need for practical nuclear waste disposal solutions and outlining how we are working to make deep borehole disposal an important part of the nuclear industry’s future.”

About Deep Isolation

Deep Isolation (OTCQB: DBHL) is the first company to undertake development of technologies for nuclear waste disposal in deep boreholes. Deep Isolation’s solution will offer a unique approach to help countries identify, plan for and complete the necessary steps to dispose of their nuclear waste inventories. With over 100 patents issued to date, Deep Isolation’s technology is designed to leverage proven drilling practices to allow safe isolation of waste deep underground in horizontal, vertical, or slanted borehole repositories. Deep Isolation’s Universal Canister System is engineered to support integrated management of spent fuel and high-level radioactive waste from legacy and advanced reactors across storage, transportation, and eventual disposal.  In January 2026, Deep Isolation launched a full-scale, at-depth deep borehole Commercialization Pilot for its solution at Cameron, Texas, in collaboration with the Deep Borehole Demonstration Center, Halliburton (NYSE: HAL), Amentum (NYSE: AMTM), NAC International (TYO: 7004), and Occlusion Nuclear Solutions.

For more information, visit: https://www.deepisolation.com

Media Contact
Sophie McCallum
media@deepisolation.com

Investor Contact
Caldwell Bailey
InvestorRelations@deepisolation.com

Forward-Looking Statements

Statements contained in this news release that are not historical facts are “forward-looking information” or “forward-looking statements” (collectively, “forward-looking statements”) within the meaning of Section 27A of the Securities Act and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements include, but are not limited to, statements regarding our plans, objectives and expectations for our business, the future growth of our business and the nuclear energy and nuclear waste disposal industries as a whole, and future benefits expected to arise from our strategic partnerships. In certain cases, forward-looking statements can be identified by the use of words and phrases or variations of words and phrases or statements such as “may,” “should,” “expect,” “intend,” “plan,” “anticipate,” “believe,” “estimate,” “predict,” “will,” “could,” “project,” “target,” “potential,” “continue” and similar expressions. Forward-looking statements are based on management’s belief and assumptions, including current expectations and projections about future events and trends, and on information currently available to management.

Forward-looking statements in this or any other news release are subject to a number of risks, uncertainties, and assumptions that could cause actual results to be materially different from those expressed or implied by such forward-looking statements. Such risks, uncertainties, and assumptions are subject to a number of factors, including, among others: the failure of a market to develop for our deep borehole disposal solutions as quickly as we expect or at all; a failure of demand for our solution to develop sufficiently; regulatory and legal developments, including issues relating to obtaining regulatory approvals or permissions on the timelines we expect or at all; our lack of profitability; delays or failure in our initiative to complete a full-scale, at-depth demonstration of our Universal Canister System and our deep borehole solution; our failure to enter into contracts with customers or, once we do enter into contracts, to continue such contractual relationships or to receive new contract awards; our dependency on governmental contracts and awards and our ability to finalize negotiations on same; our failure to manage our growth effectively or to execute our business plan; our failure to sustain and expand relationships with governmental entities and strategic partners; a failure in the assumptions or analyses we have used in supporting forecasts or plans; our inability to commercialize our products at scale; the development or deployment of other technologies or solutions supplanting or competing with our technologies; challenges to our intellectual property; failures to protect, maintain, enforce, and enhance our intellectual property, and claims by others of intellectual property infringement; political and public perceptions of nuclear energy, including perceptions as to accidents or other high-profile events involving nuclear power facilities or radioactive materials; our liquidity and ability to raise capital; any inability to control operating and project costs and project delays or other project-related problems; security (including cybersecurity) breaches or disruptions; geopolitical, macroeconomic, domestic events or crises, including supply chain disruptions and other risks and uncertainties outside of our control; weather and effects of climate change; and litigation or legal proceedings that may be brought against us.

The foregoing is not an exhaustive list of all the factors that may cause any forward-looking statements to prove inaccurate or our actual results to differ materially from our expectations and forecasts. Moreover, we operate in a highly regulated environment. New risks emerge from time to time. It is not possible for our management 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. In light of these risks, uncertainties, and assumptions, the future events and trends discussed in this release may not occur and actual results could differ materially and adversely from those anticipated or implied in the forward-looking statements, and we cannot guarantee future results, performance, or achievements. Accordingly, readers should not place undue reliance on forward-looking statements. We undertake no obligation to update any forward-looking statements for any reason after the date of this release or to conform these statements to actual results or revised expectations, except as required by law.

Additional information concerning the factors above and other factors will be found in the Company’s public filings with the Securities and Exchange Commission (the “SEC”), including the sections titled “Forward-Looking Statements” and “Risk Factors” in the Company’s Reports on Form 10-K and 10-Q for the fiscal year ended December 31, 2025 and the quarter ending March 31, 2026, respectively, as filed with the SEC on March 30, 2026, our Form S-1, originally filed August 18, 2025 and subsequently amended, our Proxy Statement for our 2026 Annual Meeting as filed on April 29, 2026, and in filings with the SEC that will be made in the future. The Company’s SEC filings are available free of charge at www.sec.gov or upon written request to Deep Isolation at InvestorRelations@deepisolation.com or CorpSec@deepisolation.com.

Vancouver, BC, Oct. 07, 2026 (GLOBE NEWSWIRE) — Skyharbour Resources Ltd. (TSX-V: SYH) (OTCQX: SYHBF) (Frankfurt: SC1P) (“Skyharbour”, “SYH” or the “Company”) is pleased to announce the commencement of drilling at the Getty East Uranium Joint Venture (“Getty East” or the “Property”) representing the first phase of drilling in 2026 at this newly established property. The 3,105-hectare Getty East Property, comprising one claim, is a part of the broader Russell Lake project area and joint venture with Denison Mines Corp. (“Denison”) (TSX: DML) (NYSE American: DNN). The Russell Lake Joint Ventures are strategically located in the central portion of the eastern Athabasca Basin of northern Saskatchewan adjacent and proximal to Denison’s flagship Wheeler River project. There is also access to significant regional infrastructure, including an exploration camp, provincial highways, and the provincial power grid.

Russell Lake Project Area Location Map:
https://www.skyharbourltd.com/_resources/images/Russell-Project-Map-V2.jpg

The Skyharbour-operated drill program will be funded by Denison pursuant to its earn-in option at Getty East and is expected to consist of approximately 3,600 metres of diamond drilling in ten to twelve drill holes. This drilling will test the Little Man Lake Uranium Zone (“Little Man Zone”) and priority targets along the interpreted extension of the mineralized Middle Lake trend. Getty East is one of four property joint ventures formed following completion of the strategic transaction with Denison in December 2025, which reorganized the former Russell Lake uranium project into four separate properties and joint ventures. Skyharbour currently holds a 70% interest in Getty East and acts as operator, with Denison holding the remaining 30% and additional earn-in rights to acquire up to a 70% interest in the Property through staged exploration spending totalling C$15 million over seven years.

Jordan Trimble, President and CEO of Skyharbour, stated: “The commencement of drilling at Getty East is yet another milestone in the advancement of the broader Russell Lake project area with our strategic JV partner, Denison Mines. There is notable discovery potential across numerous target areas on the Property, underpinned by uranium mineralization in previous drilling at the Little Man Zone as well as high-grade uranium in historical drilling along strike to the south of Getty East. This current drilling at Getty East is part of a larger planned +15,000-metre, multi-phased drill campaign at Russell in 2026, some which has been completed with assays pending in addition to a final phase of drilling commencing soon at the Wheeler North JV.”

Getty East Project Map:
https://www.skyharbourltd.com/_resources/images/Getty-East-Project-Map-V2.jpg

The Getty East Property hosts the Little Man Zone, as well as the interpreted extension of the Middle Lake trend on claims owned by Cameco Corp. to the south, where historical drilling intersected high-grade uranium mineralization in a number of holes including 22.1% U3O8 over 0.9 metres in historical drill hole ML-30. Drill targets have been refined by approximately 36 line-kilometres of modified moving loop time-domain electromagnetic (“MLTDEM”) surveying combined with fixed loop time-domain electromagnetic (“FLTDEM”) surveying on the 108 line-kilometre Middle Lake Extension grid completed earlier this summer, which covered targets on both Getty East and Skyharbour’s neighbouring RL property.

2026 Exploration Overview at Getty East:

The 2026 drill program at Getty East is expected to consist of approximately 3,600 metres in ten to twelve drill holes, with four holes initially planned at the Little Man Zone and six to eight holes on the Middle Lake Extension grid testing EM conductors interpreted to be the extension of the same conductive trend that hosts the high-grade uranium mineralization on the Middle Lake trend. Historical drilling by Uranerz in the 1980’s on this trend, located to the south of Getty East, returned high-grade uranium mineralization in a number of drill holes including 22.1% U3O8 over 0.9 metres in ML-30, 11.9% U3O8 over 1.0 metre in ML-40, and 1.17% U3O8 over 2.5 metres in ML-43.

*The historical drilling results from the Middle Lake trend referenced in this news release, including drill holes ML-30, ML-40 and ML-43, are located on an adjacent property outside of the Getty East Project boundary. Historical uranium assays for these drill holes were reported as % U (Saskatchewan Mineral Assessment Database report 74H04-NE-0076) and have been converted to % U3O8 using a factor of 1.1792, with composite grades length-weighted from individual sample assays. Skyharbour’s Qualified Person has not verified this historical information, and mineralization hosted on adjacent properties is not necessarily indicative of mineralization on the Getty East Project.

In preparation for drilling, Skyharbour completed approximately 36 line-kilometres of modified MLTDEM combined with FLTDEM surveying along six lines on the Middle Lake Extension grid earlier this summer, after establishing a 108 line-kilometre grid. The survey, carried out by EarthEX Geophysical Solutions Inc., covered targets on both Getty East and the neighbouring RL Claims properties, and was designed to better define priority conductive corridors associated with the interpreted extension of the Middle Lake trend. The results of this survey, integrated with historical drilling data, will be used to generate and prioritize targets for the current drill program.

At the Little Man Zone, historical drilling on Skyharbour’s Getty East Property outlined an unconformity-hosted uranium zone associated with an unconformity depression that is 10 to 15 metres thick, 25 to 35 metres wide and defined along a strike length of 500 metres. The last drilling in this area was in 1989, prior to modern uranium exploration models, with historical uranium grades ranging from 0.03% up to 0.10% U3O8 at around 300 metres depth (SMDI 2429). Skyharbour has reviewed existing geological and geophysical data from previous programs to generate follow-up targets, and its interpretation suggests that the mineralization remains open along strike in both directions and that the basement rocks are entirely untested. The 2015 ground resistivity survey identified several resistivity lows at the unconformity interpreted to represent alteration zones, breaches or plumes in the sandstone and basement rocks associated with graphitic fault zones, several of which are prospective targets that will be prioritized in this program.

Summary of Russell Lake Joint Ventures:

The Russell Lake Joint Ventures encompass a large, advanced-stage uranium exploration land package totalling 73,314 hectares in the eastern Athabasca Basin of northern Saskatchewan. The properties are strategically positioned between Cameco’s Key Lake and McArthur River operations and immediately north, east and south of Denison’s Wheeler River Project.

Following the completion of a major strategic transaction with Denison in 2025, the former Russell Lake project was restructured into four separate joint venture uranium properties: RL, Wheeler North, Getty East, and Wheeler River Inliers. Each property is subject to its own joint venture agreement with operatorship divided between the partners. Skyharbour is the operator at the RL Claims and Getty East, and Denison is the operator at Wheeler North and the Wheeler River Inliers. In aggregate, the strategic transaction included total project consideration of up to C$61.5 million with Skyharbour retaining an 80% interest at RL while Denison can earn up-to 70% at each of the other properties.

The Russell Lake Joint Ventures benefit from excellent regional infrastructure, with the northern extension of Highway 914 traversing the western portion of the land package and a high-voltage provincial powerline running parallel to the road. Across the joint ventures, there are numerous high-priority exploration targets including the Grayling, Fork, Little Man, Christie Lake, Fox Lake Trail, Sphinx, Blue Steel, Taylor Bay, South Russell, and Kowalchuk Zones. In addition, more than 35 kilometres of largely untested prospective electromagnetic conductors occur across the joint venture properties, highlighting the substantial discovery potential.

Qualified Person:

The technical information in this news release has been prepared in accordance with the Canadian regulatory requirements set out in National Instrument 43-101 and reviewed and approved by Serdar Donmez, P.Geo., VP of Exploration for Skyharbour, as well as a Qualified Person.

About Skyharbour Resources Ltd.:

Skyharbour holds an extensive portfolio of uranium exploration projects in Canada’s Athabasca Basin and is well positioned to benefit from improving uranium market fundamentals with interest in forty-four projects covering over 682,100 hectares (1.69M acres) of land. Skyharbour owns a 100% interest in the Moore Uranium Project, which is located 15 kilometres east of Denison’s Wheeler River project and 39 kilometres south of Cameco’s McArthur River uranium mine. Moore is an advanced-stage uranium exploration property with high-grade uranium mineralization at the Maverick Zones. Adjacent to Moore, Skyharbour is advancing several uranium properties within the broader Russell Lake project area with its joint venture partner and large strategic shareholder Denison Mines. Collectively these co-flagship projects host multiple zones of high-grade uranium mineralization across a highly prospective land package with significant exploration upside, and the Company is actively working on these assets through exploration and drilling programs.

Skyharbour now has joint ventures with industry-leaders Denison Mines and Orano Canada Inc. at the Russell Lake properties and the Preston project, respectively. The Company also has several active earn-in option partners, including CSE-listed Nexus Uranium Corp. at the Mann Lake Uranium Project; TSX-V listed North Shore Uranium at the Falcon Project; UraEx Resources at the South Dufferin and Bolt Projects; Future Fuels at the Highway Project; CSE-listed Mustang Energy at the 914W Project; CSE-listed Purecore Metals at the Yurchison Project, and TSX-V listed Terra Clean Energy at the South Falcon East Project. In aggregate, Skyharbour has now signed earn-in option agreements with partners that total to potentially over $79 million in partner-funded exploration expenditures and over $52 million in cash and share payments coming into Skyharbour, assuming that these partner companies complete the earn-ins at their respective projects.

Skyharbour’s goal is to maximize shareholder value through new mineral discoveries, committed long-term partnerships, and the advancement of exploration projects in geopolitically favourable jurisdictions.

Skyharbour’s Uranium Project Map in the Athabasca Basin:
https://www.skyharbourltd.com/_resources/images/SKY_SaskProject_Locator_2025-12-16.jpg

To find out more about Skyharbour Resources Ltd. (TSX-V: SYH) visit the Company’s website at www.skyharbourltd.com.

SKYHARBOUR RESOURCES LTD.

“Jordan Trimble”

Jordan Trimble
President and CEO

For further information contact myself or:

Nicholas Coltura
Corporate Communications & Development Manager
Skyharbour Resources Ltd.
Telephone: 604-558-5847
Toll Free: 800-567-8181
Facsimile: 604-687-3119
Email: info@skyharbourltd.com

NEITHER THE TSX VENTURE EXCHANGE NOR ITS REGULATION SERVICES PROVIDER ACCEPTS RESPONSIBILITY FOR THE ADEQUACY OR ACCURACY OF THE CONTENT OF THIS NEWS RELEASE.

Forward-Looking Information:

This news release contains “forward‐looking information or statements” within the meaning of applicable securities laws, which may include, without limitation, completing ongoing and planned work on its projects including drilling and the expected timing of such work programs, other statements relating to the technical, financial and business prospects of the Company, its projects and other matters. All statements in this news release, other than statements of historical facts, that address events or developments that the Company expects to occur, are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance and actual results may differ materially from those in the forward-looking statements. Such statements and information are based on numerous assumptions regarding present and future business strategies and the environment in which the Company will operate in the future, including the price of uranium, the ability to achieve its goals, that general business and economic conditions will not change in a material adverse manner, that financing will be available if and when needed and on reasonable terms. Such forward-looking information reflects the Company’s views with respect to future events and is subject to risks, uncertainties and assumptions, including the risks and uncertainties relating to the interpretation of exploration results, risks related to the inherent uncertainty of exploration and cost estimates and the potential for unexpected costs and expenses, and those filed under the Company’s profile on SEDAR+ at www.sedarplus.ca. Factors that could cause actual results to differ materially from those in forward looking statements include, but are not limited to, continued availability of capital and financing and general economic, market or business conditions, adverse weather or climate conditions, failure to obtain or maintain all necessary government permits, approvals and authorizations, failure to obtain or maintain community acceptance (including First Nations), decrease in the price of uranium and other metals, increase in costs, litigation, and failure of counterparties to perform their contractual obligations. The Company does not undertake to update forward‐looking statements or forward‐looking information, except as required by law.

DALLAS, Oct. 07, 2026 (GLOBE NEWSWIRE) — Texas Capital Bancshares, Inc. (NASDAQ: TCBI), the parent company of Texas Capital Bank, today announced that it expects to issue financial results for the third quarter of 2026 after market on Wednesday, October 21, 2026. Executive management will host a conference call and webcast to discuss third quarter 2026 operating results on Wednesday, October 21, 2026, at 5:00 p.m. EDT.

Participants may pre-register for the call by visiting https://events.q4inc.com/analyst/833292417?pwd=y8YwpoQT and will receive a unique PIN number to be used when dialing in for the call for immediate access.

Alternatively, participants may call 833.461.5787 and use the access code 833 292 417 at least fifteen minutes prior to the call to join through an operator.

The live webcast can be found at https://events.q4inc.com/attendee/833292417. Corresponding presentation slides can be accessed on the company’s investor website at https://investors.texascapitalbank.com.

A webcast replay will be available one hour after the conclusion of the call on the company’s investor website.

ABOUT TEXAS CAPITAL BANCSHARES, INC.
Texas Capital Bancshares, Inc. (NASDAQ®: TCBI), a member of the Russell 2000® Index and the S&P MidCap 400®, is the parent company of Texas Capital Bank (“TCB”). Texas Capital is the collective brand name for TCB and its separate, non-bank affiliates and wholly owned subsidiaries. Texas Capital is a full-service financial services firm that delivers customized solutions to businesses, entrepreneurs and individual customers. Founded in 1998, the institution is headquartered in Dallas with offices in Austin, Fort Worth, Houston, San Antonio, Chicago, Los Angeles and New York City, and has a network of clients across the country. With the ability to service clients through their entire lifecycles, Texas Capital has established commercial banking, consumer banking, corporate and investment banking and wealth management capabilities. All services are subject to applicable laws, regulations and service terms. Deposit and lending products and services are offered by TCB. For deposit products, member FDIC. For more information, please visit texascapital.com.

CONTACT: INVESTOR CONTACT
Jocelyn Kukulka, 469.399.8544
jocelyn.kukulka@texascapital.com

Caregivers say they need clearer pain management plans, earlier education, and practical support on non-opioid options before a loved one undergoes surgery

BRISBANE, Calif., Oct. 07, 2026 (GLOBE NEWSWIRE) — Pacira BioSciences, Inc. (NASDAQ: PCRX), the industry leader in its commitment to deliver innovative, non-opioid pain therapies to transform the lives of patients, and Caregiver Action Network (CAN), the nation’s leading family caregiver organization, today announced findings from Ready, Set, Recover, an initiative examining family caregivers’ experiences with surgery preparation, postsurgical pain management, and recovery at home.

The initiative featured a national survey of 202 responses from CAN’s caregiver network, gathering insights on surgery preparation, postsurgical pain management, and recovery at home. Nearly all respondents reported caring for a loved one recovering from surgery or an outpatient medical procedure. The survey was complemented by an August 2026 roundtable discussion with 10 caregivers, and three one-on-one interviews, which provided additional perspective on practical challenges such as managing medications, monitoring pain and balancing recovery responsibilities at home.

Together, the findings underscore a central challenge during the hospital-to-home transition: caregivers are often responsible for managing pain and recovery, yet many feel they lack practical information and support. Nearly eight in 10 respondents (78%) agreed that caregivers are often expected to manage pain at home without sufficient information.

Caregivers Need More Support at the Hospital-to-Home Handoff
Over three-quarters (76%) of survey respondents expressed concern about managing care at home in the initial days after surgery. Pain medication contributed to those worries: 63% were concerned about administering the correct dose on time, while 60% worried about how to get help if pain continued and potential side effects arose. Notably, 38% reported receiving very little or no information about pain management options prior to the surgery.

These challenges were echoed in a caregiver roundtable, with participants describing the transition from hospital-to-home as a period of uncertainty and rapidly changing responsibilities. Some caregivers received only basic discharge instructions or were excluded from care discussions, while others described having to coordinate medications, monitor pain and side effects, and determine when changing symptoms warranted additional medical attention.

“Family caregivers are often the ones who carry a recovery plan from the hospital into the home, where they may suddenly be responsible for managing medications, monitoring pain, and helping a loved one get back on their feet,” said Marvell Adams Jr., CEO of Caregiver Action Network. “These findings reinforce the importance of preparing caregivers before surgery with clear, practical information they can use once they get home.”

A Clear, Detailed Plan Can Help Families Prepare
Nearly all survey respondents (97%) said understanding all available pain management options before surgery was very or extremely important. To better prepare for recovery, 72% wanted a detailed pain management plan outlining medications, timing, and side effects. Other requested resources included information on alternatives to standard pain medications (64%), pre-procedure education about pain management (58%), and access to a healthcare provider after discharge (53%). Roundtable participants stressed the importance of preparing for both expected and unexpected challenges, such as medication schedules, potential side effects, changes in mobility, and questions that emerge after returning home.

These findings suggest that caregivers are ready to play an active role in pain management conversations when given the opportunity. Nearly nine in 10 said they would feel comfortable asking a healthcare provider about different pain management options, and 82% said their involvement or questions influenced their loved one’s pain management or recovery plan. Roundtable participants added that even proactive caregivers sometimes struggled to know what to ask before surgery.

“I went in [to the pre-surgical meeting] prepared with questions for one thing, but then there are other things you forget. I didn’t understand what pain medication would be allowed alongside all the other medicines [my mother] needed to take after surgery,” said a Roundtable Participant.

Understanding of Pain Management Choices Varies
Before a procedure, 41% said they understood that multiple pain management approaches were available and asked their loved one’s healthcare provider about the options. Another 27% knew options existed, but did not fully understand the differences, while 29% assumed the healthcare provider would decide what was best.

Awareness of non-opioid pain management options also varied. Before surgery, 33% said they were either not aware of non-opioid options or were vaguely familiar with them. At the same time, 72% said they would have been very or somewhat likely to consider or request an alternative if they had received more information about pain management options before surgery. Caregivers at the roundtable similarly described gaps in the way pain management options were presented, with several sharing that non-opioid approaches were not proactively discussed and that families instead had to raise alternatives themselves.

“These findings highlight the need to involve caregivers in postsurgical pain management discussions earlier in the surgical process,” said Brendan Teehan, Chief Commercial Officer at Pacira BioSciences. “Caregivers play a key role in implementing recovery plans at home. Giving families clear, practical information before surgery, including recovery expectations and available pain management options, helps them ask informed questions and feel more prepared for the transition at home.”

Roundtable participants also emphasized that recovery support extends beyond clinical instructions. Caregivers described balancing medication management, appointments and communication with healthcare teams alongside work, childcare and other responsibilities. They also called for resources that recognize caregivers’ own well-being and provide access to peer or community support. Together, these findings point to the importance of preparing caregivers before surgery, providing clear guidance at discharge and offering practical resources they can use once their loved one is home, including CAN’s Family Caregiver Toolbox at https://www.caregiveraction.org/toolbox.

Discussing Postsurgical Pain Management Options
Patients and caregivers should speak with a healthcare provider before surgery about the pain management approaches that may be appropriate for the patient, including non-opioid options. One non-opioid option that may be appropriate for certain patients is EXPAREL® (bupivacaine liposome injectable suspension). EXPAREL is a long-acting local anesthetic administered at the time of surgery to provide targeted pain relief during the first few days after surgery, when discomfort is typically at its worst.

About Ready, Set, Recover
Ready, Set, Recover is a collaborative, educational initiative from Pacira BioSciences, Inc., and Caregiver Action Network designed to elevate caregiver voices and better understand the support and tools family caregivers need as they help loved ones prepare for surgery and navigate recovery at home.

The online survey was conducted through email outreach and social media promotion across Caregiver Action Network’s channels. Responses were collected from June 30 through July 31, 2026, from 202 family caregivers and analyzed to better understand caregiver experiences with postsurgical pain, including preparedness for recovery at home, understanding of pain management options, involvement in provider decision-making, awareness of non-opioid approaches, and caregiver support needs.

To complement the survey findings, a roundtable discussion was hosted on August 18, 2026, comprised of 10 family caregivers, along with three one-on-one interviews. These conversations supported the survey findings through first-hand experiences, offering a deeper insight into the challenges faced and support needed while helping loved ones manage postsurgical pain at home. Results reflect the experiences and opinions of survey respondents and roundtable participants, and are not intended to be representative of all U.S. family caregivers. To download the Ready, Set, Recover initiative report visit: www.pacira.com/ready-set-recover.

About Pacira
Pacira delivers innovative, non-opioid pain therapies to transform the lives of patients. Pacira has two commercial-stage non-opioid treatments: EXPAREL® (bupivacaine liposome injectable suspension), a long-acting local analgesic currently approved for infiltration, fascial plane block, and as an interscalene brachial plexus nerve block, an adductor canal nerve block, and a sciatic nerve block in the popliteal fossa for postsurgical pain management and ZILRETTA® (triamcinolone acetonide extended-release injectable suspension), an extended-release, intra-articular injection indicated for the management of osteoarthritis knee pain. The company is also advancing a pipeline of clinical-stage assets for musculoskeletal pain and adjacencies, its most advanced product candidate, PCRX-201 (enekinragene inzadenovec), a novel locally administered gene therapy, is in Phase 2 clinical development for osteoarthritis of the knee. To learn more about Pacira, visit www.pacira.com.  

About EXPAREL® (bupivacaine liposome injectable suspension)
EXPAREL is indicated to produce postsurgical local analgesia via infiltration in patients aged 6 years and older, and postsurgical regional analgesia via an interscalene brachial plexus block in adults, a sciatic nerve block in the popliteal fossa in adults, and an adductor canal block in adults. The safety and effectiveness of EXPAREL have not been established to produce postsurgical regional analgesia via other nerve blocks besides an interscalene brachial plexus nerve block, a sciatic nerve block in the popliteal fossa, or an adductor canal block. The product combines bupivacaine with multivesicular liposomes, a proven product delivery technology that delivers medication over a desired time period. EXPAREL represents the first and only multivesicular liposome local anesthetic that can be utilized in the peri- or postsurgical setting. By utilizing the multivesicular liposome platform, a single dose of EXPAREL delivers bupivacaine over time, providing significant reductions in cumulative pain scores with up to a 78 percent decrease in opioid consumption; the clinical benefit of the opioid reduction was not demonstrated. Additional information is available at www.EXPAREL.com.

INDICATION 

EXPAREL® (bupivacaine liposome injectable suspension) is indicated to produce postsurgical local analgesia via infiltration in patients aged 6 years and older and regional analgesia in adults via an interscalene brachial plexus nerve block, sciatic nerve block in the popliteal fossa, and an adductor canal block. Safety and efficacy have not been established in other nerve blocks. 

IMPORTANT SAFETY INFORMATION 

EXPAREL should not be used in obstetrical paracervical block anesthesia. 

In studies in adults where EXPAREL was injected into a wound, the most common side effects were nausea, constipation, and vomiting. 

In studies in adults where EXPAREL was injected near a nerve, the most common side effects were nausea, fever, headache, and constipation. 

In the study where EXPAREL was given to children, the most common side effects were nausea, vomiting, constipation, low blood pressure, low number of red blood cells, muscle twitching, blurred vision, itching, and rapid heartbeat. 

EXPAREL can cause a temporary loss of feeling and/or loss of muscle movement. How much and how long the loss of feeling and/or muscle movement depends on where and how much of EXPAREL was injected and may last for up to 5 days. 

EXPAREL is not recommended to be used in patients younger than 6 years old for injection into the wound, for patients younger than 18 years old for injection near a nerve, and/or in pregnant women. 

Tell your health care provider if you or your child has liver disease, since this may affect how the active ingredient (bupivacaine) in EXPAREL is eliminated from the body. 

EXPAREL should not be injected into the spine, joints, or veins. 

The active ingredient in EXPAREL can affect the nervous system and the cardiovascular system; may cause an allergic reaction; may cause damage if injected into the joints; and can cause a rare blood disorder. 

Please refer to the full Prescribing Information. 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

Forward-Looking Statements

Any statements in this press release about Pacira’s future expectations, plans, trends, outlook, Any statements in this press release about Pacira’s future expectations, plans, trends, outlook, projections and prospects, and other statements containing the words “anticipate,” “believe,” “can,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “project,” “should,” “will,” “would,” and similar expressions, constitute forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and the Private Securities Litigation Reform Act of 1995, including, without limitation, statements related to: the ability to realize the anticipated benefits of the divestiture of iovera®°; ‘5×30’, our growth and business strategy, our future outlook, the strength and efficacy of our intellectual property protection and patent terms, our future growth potential and future financial and operating results and trends, our plans, objectives, expectations (financial or otherwise) and intentions, including our plans with respect to the repayment of our indebtedness, anticipated product portfolio and product development programs, strategic alliances, plans with respect to the Non-Opioids Prevent Addiction in the Nation (“NOPAIN”) Act, and any other statements that are not historical facts. For this purpose, any statement that is not a statement of historical fact should be considered a forward-looking statement. We cannot assure you that our estimates, assumptions and expectations will prove to have been correct. Actual results may differ materially from these indicated by such forward-looking statements as a result of various important factors, including risks relating to, among others: risks associated with acquisitions, such as the risk that the acquired businesses and/or assets will not be integrated successfully, that such integration may be more difficult, time-consuming or costly than expected or that the expected benefits of the transaction will not occur; risks associated with divestitures; our manufacturing and supply chain, global and United States economic conditions (including tariffs, inflation and rising interest rates), and our business, including our revenues, financial condition, cash flows and results of operations; the success of our sales and manufacturing efforts in support of the commercialization of EXPAREL and ZILRETTA; the rate and degree of market acceptance of EXPAREL and ZILRETTA; the size and growth of the potential markets for EXPAREL and ZILRETTA and our ability to serve those markets; our plans to expand the use of EXPAREL and ZILRETTA to additional indications and opportunities, and the timing and success of any related clinical trials for EXPAREL, ZILRETTA and any of our other product candidates, including, but not limited to, PCRX-201 and PCRX-2002; the commercial success of EXPAREL and ZILRETTA; the related timing and success of United States Food and Drug Administration supplemental New Drug Applications and premarket notification 510(k)s; the related timing and success of European Medicines Agency Marketing Authorization Applications; our plans to evaluate, develop and pursue additional product candidates utilizing our proprietary high-capacity adenovirus (“HCAd”) vector platform; the approval of the commercialization of our products in other jurisdictions (by either us or our partners); clinical trials in support of an existing or potential HCAd-based product candidate; our commercialization and marketing capabilities; our ability to successfully complete capital projects; the outcome of any litigation; the recoverability of our deferred tax assets; assumptions associated with contingent consideration payments; assumptions used for estimated future cash flows associated with determining the fair value of the Company; the anticipated funding or benefits of our share repurchase program; and factors discussed in the “Risk Factors” of our most recent Annual Report on Form 10-K and in other filings that we periodically make with the Securities and Exchange Commission (the “SEC”). In addition, the forward-looking statements included in this press release represent our views as of the date of this press release. Important factors could cause actual results to differ materially from those indicated or implied by forward-looking statements, and as such we anticipate that subsequent events and developments will cause our views to change. Except as required by applicable law, we undertake no intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, and readers should not rely on these forward-looking statements as representing our views as of any date subsequent to the date of this press release.

These forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to differ materially from those expressed or implied by these statements. These factors include the matters discussed and referenced in the “Risk Factors” of our most recent Annual Report on Form 10-K and in other filings that we periodically make with the SEC.

Investor Contact:
Susan Mesco, (973) 451-4030
susan.mesco@pacira.com                

Media Contact:
Sara Marino, (973)-370-5430
Sara.marino@pacira.com

Full one-year results from the KYSA-8 registrational trial in stiff person syndrome to be reported, demonstrating sustained clinical benefit and a well-tolerated safety profile with no high-grade CRS or ICANS and no cases of IEC-HS 

Updated Phase 1 investigator-initiated trial data to be presented, continuing to highlight encouraging clinical activity and a well-tolerated safety profile in progressive multiple sclerosis

EMERYVILLE, Calif., Oct. 07, 2026 (GLOBE NEWSWIRE) — Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical immunology company pioneering transformative therapies for people with neurologic autoimmune diseases, today announced two abstracts selected for presentation at the MSToronto2026 10th Joint ACTRIMS-ECTRIMS Meeting, taking place from October 21-23, 2026, in Toronto, Canada.

“We are excited to share these data, which demonstrate the sustained clinical benefit achieved following a single dose of miv-cel in our registrational SPS trial, alongside encouraging findings from the updated Phase 1 IIT study in progressive multiple sclerosis,” said Warner Biddle, Chief Executive Officer of Kyverna Therapeutics. “Together, these data, combined with a well-tolerated safety profile, reinforce our confidence in miv-cel’s differentiated profile and potential to redefine the treatment paradigm for neurologic autoimmune diseases. As we advance toward completing our BLA in our initial indication this quarter, we are also laying the groundwork for the commercial launch of miv-cel, which, if approved, could become the first CAR T-cell therapy for autoimmune disease and the first approved treatment for SPS.”

Poster Presentation:
Title: 1-Year Analysis of KYSA-8: the Pivotal, Multicenter, Phase 2 Study of Miv-cel (Mivocabtagene Autoleucel; Formerly KYV-101) CD19 CAR T-Cell Therapy in Stiff Person Syndrome
Presenter: Dr. Amanda Piquet, M.D., FAAN, Director of Autoimmune Neurology at the University of Colorado Anschutz School of Medicine
Poster ID: P0364
Date & Time: Wed., Oct. 21, 2026, 4:30 – 6:30 PM ET

Oral Presentation:
Title: Safety and Preliminary Efficacy of CD-19 Directed CAR T-Cell Therapy in Progressive Multiple Sclerosis: A Phase 1 Study
Presenter: Dr. Jeff Dunn, M.D., Lily Sarafan Director of Neuroimmunology and Clinical Professor & Chief of Neuroimmunology in the Department of Neurology & Neurological Sciences at Stanford University
Date & Time: Friday, Oct. 23,2026, 11:05 – 11:15 AM ET

About Stiff Person Syndrome (SPS)
SPS is a rare, progressive neurologic autoimmune disease characterized by muscle stiffness and painful muscle spasms, impacting mobility and gait. Stiffness, rigidity, and spasms in the torso, arms, and legs lead to progressive disability causing up to 80% of patients to lose mobility, requiring walking aid assistance or wheelchair use1-3. SPS has been shown to lead to permanent disability and increased risk of mortality3. Most patients with SPS have antibodies to glutamic acid decarboxylase 65 (GAD65) or the glycine receptor, which disrupt normal inhibitory neurotransmission, contributing to the hallmark symptoms of SPS. There are currently no FDA-approved treatments for SPS. Current treatment options include symptomatic treatments, off-label immunotherapies, such as intravenous immunoglobulin (IVIg), rituximab and plasmapheresis, as well as supportive care and physical, speech, occupational, and psychiatric therapy; however, the majority of patients have inadequate or no response to these treatment options. An estimated 6,000 patients are diagnosed with SPS in the United States4-5.

About Multiple Sclerosis
Multiple sclerosis is a chronic autoimmune disease causing neurodegeneration, in which patients can experience a range of symptoms including blurred vision, slurred speech, tremors, numbness, extreme fatigue, problems with memory and concentration, and, in severe cases, the inability to walk or stand. B cells play a significant role in MS by producing autoantibodies that attack the protective sheath around nerves, activating T cells, and increasing inflammation. Current disease-modifying treatments for MS aim to reduce the frequency of disease relapses and delay progression of disability, but the disease remains a chronic condition that will progressively worsen for most patients.

About Miv-cel (mivocabtagene autoleucel, KYV-101)
Miv-cel is a fully human, autologous, CD19-targeting CAR T-cell therapy with CD28 co-stimulation. It is uniquely designed for potency and tolerability with the potential to achieve deep B-cell depletion, reset the immune system and deliver durable drug-free, disease-free remission in autoimmune diseases with a single dose. Miv-cel is under investigation for B-cell driven autoimmune diseases and is produced using a well-established, validated manufacturing process. To date, more than 100 patients have been treated with miv-cel across a range of autoimmune diseases, and the clinical data demonstrates a consistent and well-tolerated safety profile.

About Kyverna Therapeutics
Kyverna Therapeutics, Inc. (Nasdaq: KYTX) is a late-stage clinical immunology company pioneering differentiated therapies with curative potential for neurologic autoimmune diseases. Kyverna’s lead autologous CD19-targeting CAR T-cell therapy candidate, miv-cel (mivocabtagene autoleucel, KYV-101), has demonstrated the potential to fundamentally change the treatment paradigm across multiple B-cell-driven autoimmune diseases. Kyverna is advancing its potentially first-in-class neuroimmunology franchise with its recently completed registrational trial in stiff person syndrome (SPS) and an ongoing registrational trial for generalized myasthenia gravis (gMG).

Miv-cel has received three FDA Regenerative Medicine Advanced Therapy (RMAT) designations, in SPS, gMG, and non-active secondary progressive multiple sclerosis (naSPMS) based on compelling clinical data, further reinforcing the therapy’s potential across neuroimmunology. Additionally, the Company continues to advance new innovations that broaden access and choice for patients, expanding its leadership position in the field. For more information, please visit https://kyvernatx.com.

Forward-Looking Statements
Statements in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute “forward-looking statements.” The words, without limitation, “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these or similar identifying words. Forward-looking statements in this press release include, without limitation, those related to: the potential for a single dose of miv-cel to achieve deep B-cell depletion, reset the immune system, and deliver durable drug-free, disease-free remission in autoimmune diseases; the potential for miv-cel to redefine the treatment paradigm for neurologic autoimmune diseases and to fundamentally change the treatment paradigm across multiple B-cell-driven autoimmune diseases; the possibility of a commercial launch of the first CAR T-cell therapy to potentially be approved for autoimmune disease and the first approved treatment for SPS; the anticipated timing of the completion of the rolling BLA submission for miv-cel in SPS; Kyverna’s pipeline opportunities, including in progressive multiple sclerosis; and Kyverna’s potentially first-in-class neuroimmunology franchise. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including: uncertainties related to market conditions; risks related to the timing and outcome of regulatory submissions and interactions with the FDA; the ability to enroll patients in clinical trials on anticipated timelines; the possibility that topline results may change following further analysis or differ from final results; the possibility that results from prior clinical trials, named-patient access activities and preclinical studies may not necessarily be predictive of future results; and other factors discussed in the “Risk Factors” section of Kyverna’s most recent Annual Report on Form 10-K and Quarterly Reports on Form 10-Q that Kyverna has filed or may subsequently file with the U.S. Securities and Exchange Commission. Any forward-looking statements contained in this press release are based on the current expectations of Kyverna’s management team and speak only as of the date hereof, and Kyverna specifically disclaims any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.

Contact:
Investors: InvestorRelations@kyvernatx.com
Media: media@kyvernatx.com

1 Rakocevic G, et al. BMC Neurol. 2019;19:1.
2 Dalakas MC. Nat Rev Neurol. 2024;20(10):587-601.
3 Duddy ME, Baker MR. Front Neurol Neurosci. 2009;26:147-165.
4 Crane PD, et al. Neurology. 2024;103(12):e210078.
5 Analysis of 2024 Komodo U.S. Claims Data.

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