BriaCell and BriaPro Enter Into Asset Purchase Agreement for Exclusive Soluble CD80 License

BriaCell and BriaPro Enter Into Asset Purchase Agreement for Exclusive Soluble CD80 License




BriaCell and BriaPro Enter Into Asset Purchase Agreement for Exclusive Soluble CD80 License

PHILADELPHIA and VANCOUVER, British Columbia, Feb. 18, 2026 (GLOBE NEWSWIRE) — BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW, BCTXZ, BCTXL) (TSX: BCT) (“BriaCell”), a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care, and its majority-owned subsidiary, BriaPro Therapeutics Corp. (“BriaPro”), are pleased to announce that they have entered into a definitive purchase agreement (the “Purchase Agreement”) pursuant to which BriaPro has agreed to purchase BriaCell’s exclusive license to develop and commercialize Soluble CD80 (“sCD80”) as a biologic agent for the treatment of cancer and other associated assets (the “Transaction”).

Background

BriaCell originally secured the exclusive license from the University of Maryland, Baltimore County (“UMBC”) on August 2, 2022. The novel technology, originally developed by Suzanne Ostrand-Rosenberg, Ph.D., Emeritus Faculty at UMBC, and member of BriaCell’s scientific advisory board, is titled “Soluble CD80 as a Therapeutic to Reverse Immune Suppression in Cancer Patients” and is covered under USPN 8,956,619 B2, USPN 9,650,429 B2, and USPN 10,377,810 B2. In animal models, sCD80 was well-tolerated and stopped tumor growth by potentially restoring natural anti-tumor immunity (see Lucas A Horn, et al. and Samuel T Haile et al. in collaboration with Dr. Ostrand-Rosenberg). Additionally, strong anti-tumor activity of sCD80 has been reported in multiple tumor types (see Lucas A Horn, et al.). Importantly, as demonstrated in the same studies, sCD80’s unique actions may involve both awakening and boosting the immune system to recognize and destroy tumor cells.

The Transaction

Under the terms of the Purchase Agreement, BriaPro gains the worldwide rights to develop and commercialize sCD80 as a therapeutic agent for the treatment of cancer, while UMBC holds all rights, title and interest in the inventions and the patent, except for certain rights retained by the United States Government. BriaPro will pay 2% royalties to UMBC upon the commercialization of the product plus other development costs.

As part of the Transaction, BriaCell will make available to BriaPro up to $3 million to fund research and development efforts (the “Credit Facility”). Each drawdown under the Credit Facility will be subject to BriaCell’s approval regarding the use of funds.

As consideration for the transfer of the exclusive license and the Credit Facility, BriaPro will issue to BriaCell 23,972,589 Common Shares at an aggregate value of approximately C$1.18M, increasing BriaCell’s interest in BriaPro to approximately 78% post-transaction. The Transaction is expected to close on or around March 12, 2026, subject to certain conditions including (i) approval of the disinterested shareholders of BriaPro, and (ii) receipt of a third-party valuation confirming that the Transaction is occurring at fair market value.

Shareholder Approval

In accordance with Multilateral Instrument 61-101 – Protection of Minority Security Holders in Special Transactions (“MI 61-101”), the resolution approving the Purchase Agreement must be approved by a simple majority of votes cast by shareholders, present in person or represented by proxy and entitled to vote at the Meeting, excluding the votes cast by any “interested party” (as defined in MI 61-101). As a 10% shareholder with an interest in the Transaction, BriaCell’s shareholdings in BriaPro will be excluded from voting.

Formal Valuation Requirements

In respect of the formal valuation requirement of MI 61-101, BriaPro intends to rely on the specified markets exemptions set forth in subsection 5.5(b) of MI 61-101, as none of its securities are listed or quoted on a specified senior exchange.

Though a formal valuation is not required under applicable securities laws, as a matter of good governance and best corporate practice, BriaPro intends to obtain a valuation from an independent third-party valuator as a condition to closing, verifying and validating that Transaction is occurring at fair market value.

“Our mission has been to develop safe and effective treatments for cancer patients who do not respond to existing treatments, and a transformational anti-cancer agent such as sCD80 may provide us with such an additional opportunity,” stated Dr. Bill Williams, BriaCell and BriaPro’s President and CEO. “Based on the promising data in animal studies, we plan to explore the potential use of sCD80 technology as a therapeutic agent in combination with our other immunotherapies or on its own. We look forward to accelerating the development of this novel anti-cancer agent to bring hope to patients who need it the most.”

About BriaCell Therapeutics Corp.

BriaCell is a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care. More information is available at https://briacell.com/.

About BriaPro Therapeutics Corp.

BriaPro is a pre-clinical stage immunotherapy company developing binding agents and proteins with the intention to boost the ability of the body’s own cancer-fighting cells to destroy cancerous tumors.

Safe Harbor

This press release contains “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” “will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Examples of forward-looking statements in this news release include, among others, statements that BriaCell and BriaPro make regarding the potential for development and commercialization of sCD80 as a biologic agent for the treatment of cancer, and the possibility that sCD80 may awaken and boost the immune system to recognize and destroy tumor cells. Forward-looking statements are based on BriaCell and BriaPro’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully under the heading “Risks and Uncertainties” in BriaCell and BriaPro’s most recent Management’s Discussion and Analysis, under the heading “Risk Factors” in BriaCell’s most recent Annual Information Form, and under “Risks and Uncertainties” in: (i) BriaCell’s other filings with the Canadian securities regulatory authorities and the U.S. Securities and Exchange Commission, and (ii) BriaPro’s other filings with the Canadian securities regulatory authorities, all of which are available under BriaCell and BriaPro’s profiles on SEDAR+ at www.sedarplus.ca and on BriaCell’s profile on EDGAR at www.sec.gov. Forward-looking statements contained in this announcement are made as of this date. BriaCell Therapeutics Corp. and BriaPro Therapeutics Corp. undertake no duty to update such information except as required under applicable law.

Neither the Toronto Stock Exchange nor its Regulation Services Provider (as that term is defined in the policies of the Toronto Stock Exchange) accepts responsibility for the adequacy or accuracy of this release.

Contact Information

BriaCell and BriaPro Contact:
William V. Williams, MD
President & CEO, BriaCell and BriaPro
1-888-485-6340
info@briacell.com

Investor Relations Contact:
investors@briacell.com

BriaCell and BriaPro Enter Into Asset Purchase Agreement for Exclusive Soluble CD80 License

BriaCell and BriaPro Enter Into Asset Purchase Agreement for Exclusive Soluble CD80 License




BriaCell and BriaPro Enter Into Asset Purchase Agreement for Exclusive Soluble CD80 License

PHILADELPHIA and VANCOUVER, British Columbia, Feb. 18, 2026 (GLOBE NEWSWIRE) — BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW, BCTXZ, BCTXL) (TSX: BCT) (“BriaCell”), a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care, and its majority-owned subsidiary, BriaPro Therapeutics Corp. (“BriaPro”), are pleased to announce that they have entered into a definitive purchase agreement (the “Purchase Agreement”) pursuant to which BriaPro has agreed to purchase BriaCell’s exclusive license to develop and commercialize Soluble CD80 (“sCD80”) as a biologic agent for the treatment of cancer and other associated assets (the “Transaction”).

Background

BriaCell originally secured the exclusive license from the University of Maryland, Baltimore County (“UMBC”) on August 2, 2022. The novel technology, originally developed by Suzanne Ostrand-Rosenberg, Ph.D., Emeritus Faculty at UMBC, and member of BriaCell’s scientific advisory board, is titled “Soluble CD80 as a Therapeutic to Reverse Immune Suppression in Cancer Patients” and is covered under USPN 8,956,619 B2, USPN 9,650,429 B2, and USPN 10,377,810 B2. In animal models, sCD80 was well-tolerated and stopped tumor growth by potentially restoring natural anti-tumor immunity (see Lucas A Horn, et al. and Samuel T Haile et al. in collaboration with Dr. Ostrand-Rosenberg). Additionally, strong anti-tumor activity of sCD80 has been reported in multiple tumor types (see Lucas A Horn, et al.). Importantly, as demonstrated in the same studies, sCD80’s unique actions may involve both awakening and boosting the immune system to recognize and destroy tumor cells.

The Transaction

Under the terms of the Purchase Agreement, BriaPro gains the worldwide rights to develop and commercialize sCD80 as a therapeutic agent for the treatment of cancer, while UMBC holds all rights, title and interest in the inventions and the patent, except for certain rights retained by the United States Government. BriaPro will pay 2% royalties to UMBC upon the commercialization of the product plus other development costs.

As part of the Transaction, BriaCell will make available to BriaPro up to $3 million to fund research and development efforts (the “Credit Facility”). Each drawdown under the Credit Facility will be subject to BriaCell’s approval regarding the use of funds.

As consideration for the transfer of the exclusive license and the Credit Facility, BriaPro will issue to BriaCell 23,972,589 Common Shares at an aggregate value of approximately C$1.18M, increasing BriaCell’s interest in BriaPro to approximately 78% post-transaction. The Transaction is expected to close on or around March 12, 2026, subject to certain conditions including (i) approval of the disinterested shareholders of BriaPro, and (ii) receipt of a third-party valuation confirming that the Transaction is occurring at fair market value.

Shareholder Approval

In accordance with Multilateral Instrument 61-101 – Protection of Minority Security Holders in Special Transactions (“MI 61-101”), the resolution approving the Purchase Agreement must be approved by a simple majority of votes cast by shareholders, present in person or represented by proxy and entitled to vote at the Meeting, excluding the votes cast by any “interested party” (as defined in MI 61-101). As a 10% shareholder with an interest in the Transaction, BriaCell’s shareholdings in BriaPro will be excluded from voting.

Formal Valuation Requirements

In respect of the formal valuation requirement of MI 61-101, BriaPro intends to rely on the specified markets exemptions set forth in subsection 5.5(b) of MI 61-101, as none of its securities are listed or quoted on a specified senior exchange.

Though a formal valuation is not required under applicable securities laws, as a matter of good governance and best corporate practice, BriaPro intends to obtain a valuation from an independent third-party valuator as a condition to closing, verifying and validating that Transaction is occurring at fair market value.

“Our mission has been to develop safe and effective treatments for cancer patients who do not respond to existing treatments, and a transformational anti-cancer agent such as sCD80 may provide us with such an additional opportunity,” stated Dr. Bill Williams, BriaCell and BriaPro’s President and CEO. “Based on the promising data in animal studies, we plan to explore the potential use of sCD80 technology as a therapeutic agent in combination with our other immunotherapies or on its own. We look forward to accelerating the development of this novel anti-cancer agent to bring hope to patients who need it the most.”

About BriaCell Therapeutics Corp.

BriaCell is a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care. More information is available at https://briacell.com/.

About BriaPro Therapeutics Corp.

BriaPro is a pre-clinical stage immunotherapy company developing binding agents and proteins with the intention to boost the ability of the body’s own cancer-fighting cells to destroy cancerous tumors.

Safe Harbor

This press release contains “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” “will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Examples of forward-looking statements in this news release include, among others, statements that BriaCell and BriaPro make regarding the potential for development and commercialization of sCD80 as a biologic agent for the treatment of cancer, and the possibility that sCD80 may awaken and boost the immune system to recognize and destroy tumor cells. Forward-looking statements are based on BriaCell and BriaPro’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully under the heading “Risks and Uncertainties” in BriaCell and BriaPro’s most recent Management’s Discussion and Analysis, under the heading “Risk Factors” in BriaCell’s most recent Annual Information Form, and under “Risks and Uncertainties” in: (i) BriaCell’s other filings with the Canadian securities regulatory authorities and the U.S. Securities and Exchange Commission, and (ii) BriaPro’s other filings with the Canadian securities regulatory authorities, all of which are available under BriaCell and BriaPro’s profiles on SEDAR+ at www.sedarplus.ca and on BriaCell’s profile on EDGAR at www.sec.gov. Forward-looking statements contained in this announcement are made as of this date. BriaCell Therapeutics Corp. and BriaPro Therapeutics Corp. undertake no duty to update such information except as required under applicable law.

Neither the Toronto Stock Exchange nor its Regulation Services Provider (as that term is defined in the policies of the Toronto Stock Exchange) accepts responsibility for the adequacy or accuracy of this release.

Contact Information

BriaCell and BriaPro Contact:
William V. Williams, MD
President & CEO, BriaCell and BriaPro
1-888-485-6340
info@briacell.com

Investor Relations Contact:
investors@briacell.com

Precise Bio to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences Conference

Precise Bio to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences Conference




Precise Bio to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences Conference

GREENSBORO, N.C., Feb. 18, 2026 (GLOBE NEWSWIRE) — Precise Bio, Inc. (“Precise Bio” or the “Company”), a clinical-stage regenerative medicine company pioneering bio-printed tissues and organs with an initial focus on ophthalmology, today announced that Aryeh Batt, Co-Founder and Chief Executive Officer will present at the Oppenheimer 36th Annual Healthcare Life Sciences Conference, which is taking place virtually from February 25-26, 2026. The executive team will also be available for one-on-one meetings with investors throughout the conference.

Format: Company Presentation, Live Webcast

Date/Time: Thursday, February 26, 2026, at 8:00 am ET

About Precise Bio

Precise Bio is a clinical-stage regenerative medicine company pioneering tissue engineering using its proprietary 3D-bio-fabrication platform, which integrates cell biology and biomaterials to produce clinical-grade human tissues under GMP conditions. Its lead program, PB-001, is the world’s first bio-printed corneal implant to enter human clinical trials, with additional ophthalmology and advanced tissue programs in development. For more information, visit www.precise-bio.com.

Contact

Leigh Salvo
New Street Investor Relations
leigh@newstreetir.com

Precise Bio to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences Conference

Precise Bio to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences Conference




Precise Bio to Participate in the Oppenheimer 36th Annual Healthcare Life Sciences Conference

GREENSBORO, N.C., Feb. 18, 2026 (GLOBE NEWSWIRE) — Precise Bio, Inc. (“Precise Bio” or the “Company”), a clinical-stage regenerative medicine company pioneering bio-printed tissues and organs with an initial focus on ophthalmology, today announced that Aryeh Batt, Co-Founder and Chief Executive Officer will present at the Oppenheimer 36th Annual Healthcare Life Sciences Conference, which is taking place virtually from February 25-26, 2026. The executive team will also be available for one-on-one meetings with investors throughout the conference.

Format: Company Presentation, Live Webcast

Date/Time: Thursday, February 26, 2026, at 8:00 am ET

About Precise Bio

Precise Bio is a clinical-stage regenerative medicine company pioneering tissue engineering using its proprietary 3D-bio-fabrication platform, which integrates cell biology and biomaterials to produce clinical-grade human tissues under GMP conditions. Its lead program, PB-001, is the world’s first bio-printed corneal implant to enter human clinical trials, with additional ophthalmology and advanced tissue programs in development. For more information, visit www.precise-bio.com.

Contact

Leigh Salvo
New Street Investor Relations
leigh@newstreetir.com

Teladoc Health Appoints Michael Smith, Experienced Insurance and Financial Services Executive, to Its Board of Directors

Teladoc Health Appoints Michael Smith, Experienced Insurance and Financial Services Executive, to Its Board of Directors




Teladoc Health Appoints Michael Smith, Experienced Insurance and Financial Services Executive, to Its Board of Directors

NEW YORK, Feb. 18, 2026 (GLOBE NEWSWIRE) — Teladoc Health (NYSE: TDOC), the global leader in virtual care, today announced the appointment of Michael Smith to its board of directors. With more than three decades of leadership experience in financial management and strategic transformation, Mr. Smith brings a deep understanding of long-term business sustainability within highly regulated, global markets. He joins the board following the previously announced retirements of Eric Evans and Thomas McKinley and will serve on the board’s audit and nominating and corporate governance committees.

“Michael’s experience leading enterprise transformations makes him a strong addition to the Board,” said Kenneth H. Paulus, the non-executive Chairman of the Teladoc Health board. “As the company continues to scale and innovate, his perspective will be valuable in helping accelerate strategic focus for the company’s next phase of long‑term growth.”

Mr. Smith is the former Vice Chair and Chief Financial Officer of Voya Financial, a leading health, wealth, and investment company, where he played an integral role in the company’s transformation from a traditional insurance business to a market leader in retirement, investment and workplace benefits. He held senior executive roles in Actuarial, Finance, Operations and Risk Management during more than 20 years at Lincoln Financial. He currently serves as Executive Chairman of Talcott Financial Group, an international life insurance and risk management firm with $130 billion in assets under management. Mr. Smith holds an undergraduate degree from the University of Michigan, is a Fellow of the Society of Actuaries, and is a CFA® charterholder.

“Teladoc Health’s mission to transform high‑quality care with technology is more important than ever,” said Smith. “I’m pleased to join the Board and bring my experience leading transformational change and sustainable value creation.”

Teladoc Health will release fourth quarter 2025 results on Wednesday, February 25, 2026, after the market closes. In conjunction, the company will host a conference call to review results at 5:00 p.m. ET on the same day.

About Teladoc Health

Teladoc Health (NYSE: TDOC) is the global leader in virtual care. The company is delivering and orchestrating care across patients, care providers, platforms, and partners — transforming virtual care into a catalyst for how better health happens. Through our relationships with health plans, employers, providers, health systems and consumers, we are enabling more access, driving better outcomes, extending provider capacity and lowering costs. Learn more at teladochealth.com.

Investors:
Michael Minchak
IR@teladochealth.com

Media:
Lou Serio
pr@teladochealth.com

Teladoc Health Appoints Michael Smith, Experienced Insurance and Financial Services Executive, to Its Board of Directors

Teladoc Health Appoints Michael Smith, Experienced Insurance and Financial Services Executive, to Its Board of Directors




Teladoc Health Appoints Michael Smith, Experienced Insurance and Financial Services Executive, to Its Board of Directors

NEW YORK, Feb. 18, 2026 (GLOBE NEWSWIRE) — Teladoc Health (NYSE: TDOC), the global leader in virtual care, today announced the appointment of Michael Smith to its board of directors. With more than three decades of leadership experience in financial management and strategic transformation, Mr. Smith brings a deep understanding of long-term business sustainability within highly regulated, global markets. He joins the board following the previously announced retirements of Eric Evans and Thomas McKinley and will serve on the board’s audit and nominating and corporate governance committees.

“Michael’s experience leading enterprise transformations makes him a strong addition to the Board,” said Kenneth H. Paulus, the non-executive Chairman of the Teladoc Health board. “As the company continues to scale and innovate, his perspective will be valuable in helping accelerate strategic focus for the company’s next phase of long‑term growth.”

Mr. Smith is the former Vice Chair and Chief Financial Officer of Voya Financial, a leading health, wealth, and investment company, where he played an integral role in the company’s transformation from a traditional insurance business to a market leader in retirement, investment and workplace benefits. He held senior executive roles in Actuarial, Finance, Operations and Risk Management during more than 20 years at Lincoln Financial. He currently serves as Executive Chairman of Talcott Financial Group, an international life insurance and risk management firm with $130 billion in assets under management. Mr. Smith holds an undergraduate degree from the University of Michigan, is a Fellow of the Society of Actuaries, and is a CFA® charterholder.

“Teladoc Health’s mission to transform high‑quality care with technology is more important than ever,” said Smith. “I’m pleased to join the Board and bring my experience leading transformational change and sustainable value creation.”

Teladoc Health will release fourth quarter 2025 results on Wednesday, February 25, 2026, after the market closes. In conjunction, the company will host a conference call to review results at 5:00 p.m. ET on the same day.

About Teladoc Health

Teladoc Health (NYSE: TDOC) is the global leader in virtual care. The company is delivering and orchestrating care across patients, care providers, platforms, and partners — transforming virtual care into a catalyst for how better health happens. Through our relationships with health plans, employers, providers, health systems and consumers, we are enabling more access, driving better outcomes, extending provider capacity and lowering costs. Learn more at teladochealth.com.

Investors:
Michael Minchak
IR@teladochealth.com

Media:
Lou Serio
pr@teladochealth.com

XOMA Royalty to Present at Investor Conferences in March

XOMA Royalty to Present at Investor Conferences in March




XOMA Royalty to Present at Investor Conferences in March

EMERYVILLE, Calif., Feb. 18, 2026 (GLOBE NEWSWIRE) — XOMA Royalty Corporation (NASDAQ: XOMA), the biotech royalty aggregator, announced today members of its Executive Team will participate at the following investor conferences in March.  Management will also participate in one-on-one investor meetings.

T.D. Cowen 46th Annual Health Care Conference (March 2-4, 2026)
Format: Fireside chat
Date: Monday, March 2, 2026
Time: 11:50AM ET
Location: Boston, MA
Link: https://bit.ly/3JXiyRJ
   
Leerink 2026 Global Healthcare Conference (March 8-11, 2026)
Format: Fireside chat
Date: Wednesday, March 11, 2026
Time: 11:20AM ET
Location: Miami Beach, FL
Link: https://bit.ly/499Y0Og
   

XOMA’s presentations can also be accessed by visiting the investor relations section of the Company’s website at www.xoma.com.  A replay of each presentation will be available and archived on the site for 90 days after the event.

About XOMA Royalty Corporation
XOMA Royalty is a biotechnology royalty aggregator playing a distinctive role in helping biotech companies achieve their goal of improving human health.  XOMA Royalty acquires the potential future economics associated with pre-commercial and commercial therapeutic candidates that have been licensed to pharmaceutical or biotechnology companies.  When XOMA Royalty acquires the future economics, the seller receives non-dilutive, non-recourse funding they can use to advance their internal drug candidate(s) or for general corporate purposes.  The Company has an extensive and growing portfolio of assets (asset defined as the right to receive potential future economics associated with the advancement of an underlying therapeutic candidate).  For more information about the Company and its portfolio, please visit www.xoma.com or follow XOMA Royalty Corporation on LinkedIn.

XOMA Investor Contact XOMA Media Contact
Juliane Snowden Kathy Vincent
XOMA Royalty  KV Consulting & Management
+1 646-438-9754 kathy@kathyvincent.com
juliane.snowden@xoma.com    

XOMA Royalty to Present at Investor Conferences in March

XOMA Royalty to Present at Investor Conferences in March




XOMA Royalty to Present at Investor Conferences in March

EMERYVILLE, Calif., Feb. 18, 2026 (GLOBE NEWSWIRE) — XOMA Royalty Corporation (NASDAQ: XOMA), the biotech royalty aggregator, announced today members of its Executive Team will participate at the following investor conferences in March.  Management will also participate in one-on-one investor meetings.

T.D. Cowen 46th Annual Health Care Conference (March 2-4, 2026)
Format: Fireside chat
Date: Monday, March 2, 2026
Time: 11:50AM ET
Location: Boston, MA
Link: https://bit.ly/3JXiyRJ
   
Leerink 2026 Global Healthcare Conference (March 8-11, 2026)
Format: Fireside chat
Date: Wednesday, March 11, 2026
Time: 11:20AM ET
Location: Miami Beach, FL
Link: https://bit.ly/499Y0Og
   

XOMA’s presentations can also be accessed by visiting the investor relations section of the Company’s website at www.xoma.com.  A replay of each presentation will be available and archived on the site for 90 days after the event.

About XOMA Royalty Corporation
XOMA Royalty is a biotechnology royalty aggregator playing a distinctive role in helping biotech companies achieve their goal of improving human health.  XOMA Royalty acquires the potential future economics associated with pre-commercial and commercial therapeutic candidates that have been licensed to pharmaceutical or biotechnology companies.  When XOMA Royalty acquires the future economics, the seller receives non-dilutive, non-recourse funding they can use to advance their internal drug candidate(s) or for general corporate purposes.  The Company has an extensive and growing portfolio of assets (asset defined as the right to receive potential future economics associated with the advancement of an underlying therapeutic candidate).  For more information about the Company and its portfolio, please visit www.xoma.com or follow XOMA Royalty Corporation on LinkedIn.

XOMA Investor Contact XOMA Media Contact
Juliane Snowden Kathy Vincent
XOMA Royalty  KV Consulting & Management
+1 646-438-9754 kathy@kathyvincent.com
juliane.snowden@xoma.com    

UPDATE – Health Systems and Strategic Partners Unite to Address Widening Healthcare Gaps in Rural and Underserved Communities

UPDATE – Health Systems and Strategic Partners Unite to Address Widening Healthcare Gaps in Rural and Underserved Communities




UPDATE – Health Systems and Strategic Partners Unite to Address Widening Healthcare Gaps in Rural and Underserved Communities

NEW YORK, Feb. 18, 2026 (GLOBE NEWSWIRE) — The National Specialty Care Access Coalition (NSCAC), a collaboration of more than 20 major US health systems, today announced its launch to address the growing breakdown in access to medical specialists across the United States. The coalition brings together health systems, clinicians, technology partners, and policy stakeholders to advance multispecialty, tech-enabled specialty care models designed to expand access for rural communities and underserved urban neighborhoods. Unlike existing efforts that focus on single specialties, individual technologies, or isolated pilot programs, the NSCAC is a health system coalition designed to align multispecialty care models, policy reform, and real-world implementation at national scale.

The launch comes at a pivotal moment. With the introduction of the Centers for Medicare and Medicaid Services (CMS) Rural Health Transformation initiative and more than $50 billion in new federal and state investment, there is unprecedented momentum to rethink how specialty care is delivered nationwide. Yet access gaps remain severe. Nearly 20 percent of Americans live in rural areas, while only about 9 percent of physicians practice there, leaving many rural hospitals without reliable access to core specialties such as neurology, cardiology, maternal fetal medicine, critical care, dermatology, surgery and pediatrics. Similar shortages affect underserved urban communities, where demand for specialty care continues to far exceed available capacity.

The coalition is convened and chaired by Dr. Chethan Sathya, physician executive and nationally recognized leader in public health innovation, and Dr. Raj Narula, physician and national leader in tech-enabled specialty care access. The NSCAC’s founding 20 plus large health systems collectively deliver care across vast rural regions and high-need urban communities nationwide.

“Access to specialty care should never depend on a patient’s ZIP code, income, or background. Advancing health equity requires coordinated, systemic action. Rutgers Robert Wood Johnson Medical School and Rutgers New Jersey Medical School are proud to stand with the National Specialty Care Access Coalition to dismantle barriers, expand access, and ensure every community receives the expert care it deserves,” says Amy P. Murtha, MD, Dean of Rutgers Robert Wood Johnson Medical School, and Robert L. Johnson, MD, FAAP, Interim Chancellor of Rutgers Health and Dean of Rutgers New Jersey Medical School.

To support the coalition’s policy and infrastructure work, additional thought partners include former CMS leaders, The Children’s Hospital Association, state hospital associations, The Center for Telehealth and eHealth Law, and technology collaborators that work across rural communities such as T-Mobile , Sevaro Health, and Samsung. Participation does not imply endorsement of any single technology platform. Together, the health system coalition brings leaders together around a shared mandate to move beyond fragmented solutions and define scalable, outcomes driven approaches to specialty care access nationwide. 

About the NSCAC

The National Specialty Care Access Coalition will focus on three initial priorities:

  • Standardizing Care Models: Developing scalable, multispecialty care pathways designed for the operational realities of rural hospitals and high-need urban health systems.
  • Advancing Policy Reform: Producing a landmark white paper with unified recommendations for the Centers for Medicare and Medicaid Services and state Medicaid agencies to modernize reimbursement, licensing, and regulatory frameworks for virtual and network-based specialty care.
  • Accelerating Implementation: Sharing real-world learnings on implementation barriers and facilitators, while enabling collaboration among health systems and rural partners to launch pilots across high-impact specialties including neurology, cardiology, maternal fetal medicine, neonatology, critical care, and chronic disease management to inform national standards.

“NSCAC membership affords Dartmouth Health and other members a dynamic opportunity to continue shaping the future of rural healthcare through innovation in technology and telehealth,” said Kevin M. Curtis, MD, MS, Medical Director, Dartmouth Health Connected Care and Center for Telehealth. By collaborating with peer institutions, we can accelerate solutions that overcome longstanding barriers to access, workforce capacity, transportation, cost, and equity. As one of the most rural health systems in the country, Dartmouth Health has long leveraged telehealth to connect patients with the care they need. The advancements generated by NSCAC will be transformative in expanding access and strengthening care delivery across rural communities, including northern New England.”

“We look forward to any opportunity to contribute to sustainability of rural healthcare. This seems like an opportunity that will help us lean into that important part of our mission,” added Adam Hornung, VP Medical Transport-Telehealth-Transfer Centers-Outreach Services, Intermountain Health.

The National Specialty Care Access Coalition will begin formal work in early 2026, with additional health systems invited to submit expressions of interest as the coalition expands.

About the NSCAC

The NSCAC is a national collaborative uniting health systems, clinicians, technology innovators, and policy leaders to confront the widening shortage of medical specialists in rural communities and underserved urban neighborhoods. The coalition focuses on building scalable, tech-enabled multispecialty care models that close persistent access gaps and modernize how specialty care is delivered nationwide.

Founded by leading clinical, public health, and health system experts, NSCAC advances unified standards, policy reform, and multi-system pilots to ensure timely and equitable access to specialty care across the United States.

Press Contact

Info@SpecialtyCareAccess.org

SpecialtyCareAccess.org

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/e1353525-9925-4b30-9bd6-4b0467175d0d

UPDATE – Health Systems and Strategic Partners Unite to Address Widening Healthcare Gaps in Rural and Underserved Communities

UPDATE – Health Systems and Strategic Partners Unite to Address Widening Healthcare Gaps in Rural and Underserved Communities




UPDATE – Health Systems and Strategic Partners Unite to Address Widening Healthcare Gaps in Rural and Underserved Communities

NEW YORK, Feb. 18, 2026 (GLOBE NEWSWIRE) — The National Specialty Care Access Coalition (NSCAC), a collaboration of more than 20 major US health systems, today announced its launch to address the growing breakdown in access to medical specialists across the United States. The coalition brings together health systems, clinicians, technology partners, and policy stakeholders to advance multispecialty, tech-enabled specialty care models designed to expand access for rural communities and underserved urban neighborhoods. Unlike existing efforts that focus on single specialties, individual technologies, or isolated pilot programs, the NSCAC is a health system coalition designed to align multispecialty care models, policy reform, and real-world implementation at national scale.

The launch comes at a pivotal moment. With the introduction of the Centers for Medicare and Medicaid Services (CMS) Rural Health Transformation initiative and more than $50 billion in new federal and state investment, there is unprecedented momentum to rethink how specialty care is delivered nationwide. Yet access gaps remain severe. Nearly 20 percent of Americans live in rural areas, while only about 9 percent of physicians practice there, leaving many rural hospitals without reliable access to core specialties such as neurology, cardiology, maternal fetal medicine, critical care, dermatology, surgery and pediatrics. Similar shortages affect underserved urban communities, where demand for specialty care continues to far exceed available capacity.

The coalition is convened and chaired by Dr. Chethan Sathya, physician executive and nationally recognized leader in public health innovation, and Dr. Raj Narula, physician and national leader in tech-enabled specialty care access. The NSCAC’s founding 20 plus large health systems collectively deliver care across vast rural regions and high-need urban communities nationwide.

“Access to specialty care should never depend on a patient’s ZIP code, income, or background. Advancing health equity requires coordinated, systemic action. Rutgers Robert Wood Johnson Medical School and Rutgers New Jersey Medical School are proud to stand with the National Specialty Care Access Coalition to dismantle barriers, expand access, and ensure every community receives the expert care it deserves,” says Amy P. Murtha, MD, Dean of Rutgers Robert Wood Johnson Medical School, and Robert L. Johnson, MD, FAAP, Interim Chancellor of Rutgers Health and Dean of Rutgers New Jersey Medical School.

To support the coalition’s policy and infrastructure work, additional thought partners include former CMS leaders, The Children’s Hospital Association, state hospital associations, The Center for Telehealth and eHealth Law, and technology collaborators that work across rural communities such as T-Mobile , Sevaro Health, and Samsung. Participation does not imply endorsement of any single technology platform. Together, the health system coalition brings leaders together around a shared mandate to move beyond fragmented solutions and define scalable, outcomes driven approaches to specialty care access nationwide. 

About the NSCAC

The National Specialty Care Access Coalition will focus on three initial priorities:

  • Standardizing Care Models: Developing scalable, multispecialty care pathways designed for the operational realities of rural hospitals and high-need urban health systems.
  • Advancing Policy Reform: Producing a landmark white paper with unified recommendations for the Centers for Medicare and Medicaid Services and state Medicaid agencies to modernize reimbursement, licensing, and regulatory frameworks for virtual and network-based specialty care.
  • Accelerating Implementation: Sharing real-world learnings on implementation barriers and facilitators, while enabling collaboration among health systems and rural partners to launch pilots across high-impact specialties including neurology, cardiology, maternal fetal medicine, neonatology, critical care, and chronic disease management to inform national standards.

“NSCAC membership affords Dartmouth Health and other members a dynamic opportunity to continue shaping the future of rural healthcare through innovation in technology and telehealth,” said Kevin M. Curtis, MD, MS, Medical Director, Dartmouth Health Connected Care and Center for Telehealth. By collaborating with peer institutions, we can accelerate solutions that overcome longstanding barriers to access, workforce capacity, transportation, cost, and equity. As one of the most rural health systems in the country, Dartmouth Health has long leveraged telehealth to connect patients with the care they need. The advancements generated by NSCAC will be transformative in expanding access and strengthening care delivery across rural communities, including northern New England.”

“We look forward to any opportunity to contribute to sustainability of rural healthcare. This seems like an opportunity that will help us lean into that important part of our mission,” added Adam Hornung, VP Medical Transport-Telehealth-Transfer Centers-Outreach Services, Intermountain Health.

The National Specialty Care Access Coalition will begin formal work in early 2026, with additional health systems invited to submit expressions of interest as the coalition expands.

About the NSCAC

The NSCAC is a national collaborative uniting health systems, clinicians, technology innovators, and policy leaders to confront the widening shortage of medical specialists in rural communities and underserved urban neighborhoods. The coalition focuses on building scalable, tech-enabled multispecialty care models that close persistent access gaps and modernize how specialty care is delivered nationwide.

Founded by leading clinical, public health, and health system experts, NSCAC advances unified standards, policy reform, and multi-system pilots to ensure timely and equitable access to specialty care across the United States.

Press Contact

Info@SpecialtyCareAccess.org

SpecialtyCareAccess.org

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/e1353525-9925-4b30-9bd6-4b0467175d0d