• Amy Rock, Ph.D., appointed Chief Regulatory and Quality Officer, bringing extensive experience in global regulatory strategy, clinical development, and with approvals of novel immunotherapies
  • Dae Gon Ha, Ph.D., appointed Senior Vice President, Corporate Development, bringing expertise in biopharmaceutical capital markets strategy and business development
  • Chief Operating Officer Timothy Keutzer to retire after eleven years of leadership and instrumental contributions to Utebzi (tebipenem pivoxil), Spero’s legacy program out licensed to GSK

CAMBRIDGE, Mass., Oct. 26, 2026 (GLOBE NEWSWIRE) — Spero Therapeutics, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on advancing next-generation medicines for patients with serious immune-mediated diseases, today announced the appointments of Amy Rock, Ph.D., as Chief Regulatory and Quality Officer and Dae Gon Ha, Ph.D., as Senior Vice President, Corporate Development. The Company also announced that Timothy Keutzer, Chief Operating Officer, will retire from Spero effective December 31, 2026.

Dr. Rock will lead Spero’s global regulatory strategy, quality, and pharmacovigilance functions, including engagement with global health authorities to support SP001’s clinical development in IgG4-related disease and potential additional indications. Dr. Ha will lead investor relations strategy and business development, including engagement with the investment community and evaluating opportunities to expand the Company’s immunology pipeline.

“These appointments represent another important step to bolster our leadership team, as we execute on Spero’s immunology-focused strategy, advancing SP001 and evaluating opportunities to expand our pipeline of therapies for immune-mediated diseases,” said Esther Rajavelu, President and Chief Executive Officer of Spero Therapeutics. “Amy brings a strong track record of navigating complex regulatory pathways for innovative therapies, including biologics, and will be instrumental in shaping an efficient global development strategy for SP001. Dae Gon brings a distinctive combination of scientific expertise and deep knowledge of biopharma markets. Together with the recent appointment of Dr. Debra Zack as Chief Medical Officer, these appointments significantly strengthen our ability to advance SP001 and execute our long-term strategy.”

Dr. Rock brings more than 25 years of biopharmaceutical experience spanning regulatory affairs, clinical development and quality-related functions. Most recently, she served as Senior Vice President, Regulatory Sciences at Vir Biotechnology, where she led global regulatory activities for multiple development programs, including GSK-partnered sotrovimab, a monoclonal antibody that received regulatory authorizations and approvals across multiple markets. She also supported programs that received FDA Fast Track and Breakthrough Therapy designations, as well as EMA PRIME and Orphan Drug designations. Previously, Dr. Rock held senior regulatory and clinical development leadership roles at ImmunityBio, Altor BioScience and Cumberland Pharmaceuticals, where she contributed to the development and regulatory advancement of novel immunotherapies and other pharmaceutical products. Dr. Rock holds a Ph.D. in immunology from the University of Kentucky, an MBA from Vanderbilt University and a B.A. in economics from Washington University in St. Louis.

Dr. Ha brings more than nine years of experience in biopharmaceutical equities research and subsequent business development experience. Most recently, he served as Senior Vice President, Head of Strategy and Business Development at Fulcrum Therapeutics, where he was a member of the executive team and led strategic planning, in-licensing and out-licensing initiatives across rare disease programs. Previously, Dr. Ha held biotechnology equity research positions at Stifel, BTIG, and Leerink Partners, advising institutional investors through his coverage of small- and mid-cap biotechnology companies.

Chief Operating Officer Retirement

Spero also announced that Timothy Keutzer will retire as Chief Operating Officer after 11 years of service to the Company, effective December 31, 2026. During his tenure, Mr. Keutzer was instrumental in building Spero’s operational capabilities and played a pivotal role in Spero’s growth and development, including leading the Utebzi (tebipenem pivoxil) development program through important clinical and regulatory milestones.

“On behalf of the Board and the entire Spero team, I want to express my deepest appreciation to Tim for his extraordinary dedication and contributions over the past 11 years,” said Ms. Rajavelu. “Tim has been an invaluable partner and trusted colleague throughout some of the most consequential chapters in Spero’s history. His leadership was central to the advancement of Utebzi, its successful FDA approval and our partnership with GSK, achievements that have helped establish the foundation for Spero’s growth. We are deeply grateful for his lasting contributions to Spero and wish him every happiness in his well-deserved retirement.”

Following Mr. Keutzer’s retirement, his responsibilities will be assumed by other members of Spero’s executive leadership team.

About Spero Therapeutics
Spero Therapeutics is a clinical-stage biopharmaceutical company focused on advancing next-generation medicines for patients with serious immune-mediated diseases. The company’s lead program, SP001, is a third-generation, Fc-silent anti-CD40L monoclonal antibody being advanced first in IgG4-related disease, with potential for development in additional immunological & inflammatory diseases. For more information, visit www.sperotx.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements include, but are not limited to, statements relating to Spero’s plans to advance SP001 and execute its long-term strategy; and Spero’s plans to evaluate opportunities to expand its pipeline of therapies for immune-mediated diseases. Forward-looking statements are based on Spero’s current expectations and assumptions and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include, among others, risks related to the completion and integration of the Innovent transaction; Spero’s ability to successfully develop SP001; the timing and outcome of clinical trials and regulatory interactions; the ability to obtain and maintain regulatory approvals; potential safety, efficacy, manufacturing, supply, intellectual property, financing, competitive, and market risks; and other risks described in Spero’s filings with the Securities and Exchange Commission. Spero undertakes no obligation to update any forward-looking statements, except as required by law.

Investor Relations Contact:
Shai Biran, Ph.D.
Spero Therapeutics
IR@Sperotx.com

Media Inquiries:
media@sperotx.com

HALIFAX, Nova Scotia, Oct. 26, 2026 (GLOBE NEWSWIRE) — Morien Resources Corp. (“Morien” or the “Company”) (TSX-V: MOX) is pleased to announce that it has entered into a non-binding term sheet with Rife Royalties Ltd. (“Rife”) to establish a strategic alliance focused on acquiring royalties on construction aggregate production in the United States and Canada.

Strategic Alliance

Rife is wholly owned by one of Canada’s largest single-employer pension funds and ranks among North America’s largest private energy and mining investment companies.

Under the proposed alliance, Morien will identify, evaluate and introduce qualifying royalty acquisition opportunities, Rife will provide the acquisition capital, and Morien will earn a direct beneficial interest alongside Rife in each royalty successfully acquired through the alliance.

Construction aggregates are essential to infrastructure and construction, with relatively inelastic demand and reserve lives that commonly span decades. The alliance is intended to build a diversified portfolio of aggregate royalties across the United States and Canada, increasing the scale and geographic reach of Morien’s existing aggregate royalty portfolio.

Alliance Structure and Economics

Following execution of a definitive agreement, the arrangement is expected to begin with a 12-month trial period. Leveraging Morien’s established network, the Company will identify, evaluate and introduce qualifying opportunities to Rife. Morien may earn up to an 8% beneficial interest in each royalty acquired through the alliance, without contributing acquisition capital. For each introduction that results in a successful acquisition, Morien will earn at closing a beneficial interest equal to 4% of the acquired royalty, on the same economic terms as Rife’s acquired interest, and may earn a further 4% if the royalty meets certain performance criteria.

If the alliance achieves certain acquisition thresholds during the trial period, the arrangement will automatically extend for a further 24 months. The parties may also agree to extend the alliance regardless of whether those thresholds are achieved.

During the trial period, Morien and Rife will share agreed sourcing and evaluation costs on a 50/50 basis, subject to an approved budget.

The term sheet is non-binding, other than certain provisions including confidentiality, termination and general provisions, and remains subject to the negotiation and execution of a definitive agreement. There can be no assurance that a definitive agreement will be executed, that any identified opportunity will result in an acquisition, or that Morien will earn any royalty interest under the proposed alliance.

About Morien

Morien is a Nova Scotia-based royalty and mining development company focused on building long-duration royalty exposure through disciplined, capital-efficient partnerships. Its primary assets include royalties on the Donkin Mine in Cape Breton and the Lazy Head and Black Point aggregate projects in Guysborough County, Nova Scotia. The proposed Rife alliance has the potential to expand Morien’s royalty portfolio through sourcing and evaluation work rather than direct acquisition capital, consistent with the Company’s partner-driven business model. Management and the Board remain focused on disciplined capital allocation and long-term per-share value creation. Morien has 60,180,889 issued and outstanding common shares and 62,330,889 common shares on a fully diluted basis. Further information is available at www.MorienRes.com.

Forward-Looking Statements

Some of the statements in this news release may constitute “forward-looking information” as defined under applicable securities laws. These statements reflect Morien’s current expectations of future revenues and business prospects and opportunities and are based on information currently available to Morien. Morien cautions that actual performance will be affected by a number of factors, many of which are beyond its control, and that future events and results may vary substantially from what Morien currently foresees. Factors that could cause actual results to differ materially from those in forward-looking statements include risks and uncertainties described in documents filed by Morien with the Canadian securities regulators on SEDAR+ (www.sedarplus.ca) from time to time. Morien cautions that its royalty revenue will be based on production by third party property owners and operators who will be responsible for determining the manner and timing for the properties forming part of Morien’s royalty portfolio. These third party owners and operators are also subject to risk factors that could cause actual results to differ materially from those predicted herein including: volatility in financial markets or general economic conditions; capital requirements and the need for additional financing; fluctuations in the rates of exchange for the currencies of Canada and the United States; prices for commodities including coal and aggregate; unanticipated changes in production, mineral reserves and mineral resources, metallurgical recoveries and/or exploration results; changes in regulations and unpredictable political or economic developments; loss of key personnel; labour disputes; and ineffective title to mineral claims or property. There are other business risks and hazards associated with mineral exploration, development and mining. Although Morien believes that the forward-looking information contained herein is based on reasonable assumptions (including assumptions relating to economic, market and political conditions, the Company’s working capital requirements and the accuracy of information supplied by the operators of the properties in which the Company has a royalty interest), readers cannot be assured that actual results will be consistent with such statements. Morien expressly disclaims any intention or obligation to update or revise any forward-looking information in this news release, whether as a result of new information, events or otherwise, except in accordance with applicable securities laws. All dollar values discussed herein are in Canadian dollars. Any financial outlook or future-oriented financial information in this news release, as defined by applicable securities laws, has been approved by management of Morien as of the date of this news release. Such financial outlook or future-oriented financial information is provided for the purpose of providing information about management’s current expectations and plans relating to the future. Readers are cautioned that such outlook or information should not be used for purposes other than for which it is disclosed in this news release.

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

For more information, please contact:

Dawson Brisco, President & CEO
Phone: (902) 403-3149
dbrisco@MorienRes.com
or
John P.A. Budreski, Executive Chairman
Phone: (416) 930-0914
www.MorienRes.com

CARSON CITY, Nev., Oct. 26, 2026 (GLOBE NEWSWIRE) — BioVie Inc. (NASDAQ: BIVI) (“BioVie” or the “Company”), a clinical-stage company developing innovative drug therapies for neurological and neurodegenerative diseases, today announced the Company has been invited to present at the 2026 RECOVER–Treating Long COVID (RECOVER-TLC) Hybrid Workshop, hosted by the National Institute of Allergy and Infectious Diseases (NIAID) and the Foundation for the National Institutes of Health (FNIH) from November 4–5, 2026, in Bethesda, Maryland.

Dr. Penelope Markham, BioVie’s Senior Vice President and Program Lead for Long COVID, will share results from the Company’s Phase 2 ADDRESS-LC trial evaluating bezisterim for the treatment of the neurological symptoms of Long COVID at the “Recent Insights from Long COVID Clinical Trials” Panel Discussion on Thursday, November 5, being held from 9:10 –10:10 a.m. ET. The 2026 RECOVER-TLC hybrid workshop will provide updates on RECOVER-TLC clinical trials and emerging discoveries in Long COVID research. The event will also provide opportunities for community members to help inform future research priorities for RECOVER-TLC clinical trials.

The RECOVER-TLC Initiative was launched to accelerate the development of treatments for Long COVID, recognizing that millions of people continue to experience persistent symptoms following COVID-19 infection and that no therapies have yet been approved. To date, RECOVER-TLC has advanced four therapeutic candidates into clinical testing and continues to evaluate additional promising interventions for this underserved patient population.

The ADDRESS-LC trial showed treatment with bezisterim showed a consistent trend toward improvement across most patient-reported and objective efficacy measures compared with placebo. Patients with more severe baseline fatigue, post-exertional malaise (PEM), or objective cognitive impairment – symptoms affecting approximately 78% of trial participants in at least one domain – experienced the greatest benefits with bezisterim, including statistically significant improvements in multiple measures corresponding to their most pronounced symptoms. Bezisterim’s safety and tolerability profile in the trial was similar to placebo.

“We observed a consistent and clinically coherent pattern of improvement across measures of fatigue, post-exertional malaise, clinician- and patient-reported outcomes, and objective measures of cognitive function among patients with greater baseline symptom burden,” said Dr. Penelope Markham. “These findings provide valuable insights into which patients may benefit most from bezisterim and provide an important foundation for the design of a confirmatory Phase 3 study.”

About Long COVID

An estimated 17-20 million U.S. adults reported to be living with Long COVID,1 with 3.8 million experiencing significant limitation to their daily lives.2 Almost 50 percent of those with Long COVID develop persistent or intermittent symptoms.3 The neurological and neuropsychiatric symptoms are among the most common and disabling manifestations of the condition and include fatigue, PEM, sleep disturbance, and persistent sense of difficulty with thinking and memory.4 Chronic innate inflammation accompanied by ongoing immune dysregulation is among the leading hypotheses proposed to explain the symptoms in Long COVID, with numerous investigators describing findings in Long COVID that appear to be supportive of the intended biological targets of bezisterim. Currently, there are no FDA-approved treatment options for Long-COVID.

About the ADDRESS-LC trial

The Phase 2 ADDRESS-LC study (NCT06847191), which is fully funded by a grant from the U.S. Department of War (DoW), is a randomized (1:1), placebo-controlled, signal-finding proof-of-concept, multicenter trial evaluating the efficacy, safety and tolerability of bezisterim in adult participants with Long COVID who have cognitive impairment sequelae and fatigue. The study compared bezisterim, administered as a 20 mg oral capsule twice daily, with a matching placebo to assess its effects on neurocognitive and fatigue-related symptoms. The trial evaluated 22 clinical outcome measures, with no single endpoint pre-specified as the primary determinant of study success. Endpoints include assessing changes in overall clinical benefit, subjective and objective cognitive function, fatigue, sleep disturbance, Quality of Life and PEM. As a signal-finding study, the trial was designed to identify efficacy signals, measure treatment effect magnitude, and identify patient subgroups most likely to benefit, to inform the design of future Phase 3 trials.

About Bezisterim

Bezisterim (NE3107) is an investigational oral drug that crosses the blood-brain barrier and works to reduce inflammation and improve insulin sensitivity without suppressing the immune system and with a low risk of drug-drug interactions. By modulating key pathways involved in neuroinflammation (ERK, NFκB, TNFα), bezisterim may have therapeutic potential in several disease indications, including Parkinson’s disease (PD), Long COVID (LC), and Alzheimer’s disease (AD).

In PD, BioVie completed the SUNRISE-PD trial, which enrolled 57 patients to establish proof of mechanism and proof of concept in individuals with early-stage disease who had not previously been treated with carbidopa/levodopa. Topline results showed that patients treated with bezisterim experienced improvements with blood-based markers of inflammation, as well as a broad range of biomarkers associated with cellular health and neuronal integrity. Clinically, patients treated with bezisterim showed numerically greater improvement than those receiving placebo across multiple measures of daily functioning, motor symptoms, and non-motor symptoms.

For LC, the ADDRESS-LC trial enrolled approximately 200 patients to evaluate whether bezisterim may help reduce brain fog, fatigue, and other lingering neurological symptoms associated with LC. The hypothesis being studied is that these symptoms may be triggered by persistent circulation of spike protein fragments that trigger inflammation via NFκB activation (which bezisterim has been shown to modulate).

In AD, BioVie has conducted Phase 2 and Phase 3 trials. Preliminary data from these trials suggest improvements in cognition and biomarkers, supporting further trials to evaluate its potential as a therapy for the six million Americans living with AD.

Terms of the U.S. Department of War (DoW) Award

The Long COVID study is supported by the Assistant Secretary of War for Health Affairs and endorsed by the DoW by a fully funded award in the amount of $13.13 million through the Peer-Reviewed Medical Research Program (PRMRP) under Award No. HT9425-24-1-0113. Opinions, interpretations, conclusions and recommendations in this press release are those of the author and are not necessarily endorsed by the Assistant Secretary of War for Health Affairs or the DoW.

About BioVie Inc.

BioVie Inc. (NASDAQ: BIVI) is a clinical-stage biopharmaceutical company focused on developing therapies for neurological disorders and advanced liver disease. Its lead investigational drug candidate, bezisterim (NE3107), targets neuroinflammation and insulin resistance, which are believed to be key drivers of Alzheimer’s and Parkinson’s disease. Bezisterim is also being studied for Long COVID, where persistent inflammation is thought to underlie symptoms such as brain fog and fatigue.

In liver disease, BioVie is advancing BIV201, a continuous infusion of terlipressin treatment that has received FDA Orphan and Fast Track designations. The active agent is approved in the U.S. and in about 40 countries for related complications of advanced liver cirrhosis, and the Company plans to study BIV201 in a Phase 3 trial for the reduction of further decompensation in patients with cirrhosis and ascites. For more information, visit www.bioviepharma.com.

Forward-Looking Statements

This press release contains forward-looking statements, which may be identified by words such as “expect,” “look forward to,” “anticipate,” “intend,” “plan,” “believe,” “seek,” “estimate,” “will,” “project,” “potential,” “may,” or words of similar meaning. Forward-looking statements in this release include, but are not limited to, statements regarding: the potential for bezisterim to address unmet clinical needs in Long COVID and Parkinson’s disease; the design and conduct of future clinical trials, including a potentially pivotal Phase 3 trial; the potential clinical significance of subgroup analyses and biomarker observations; and the Company’s ability to advance bezisterim through clinical development. The clinical endpoints reported in this release are exploratory in nature. The Phase 2 ADDRESS-LC trial did not achieve statistical significance on any endpoint in the overall intent-to-treat population; statistically significant results were observed only in pre-specified subgroup analyses. Subgroup analyses are hypothesis-generating and may not be replicated in future trials. Changes in biomarkers may not correlate with clinical benefit or support regulatory approval. The FDA has not validated these endpoints as surrogate endpoints for Long COVID. Although BioVie Inc. believes such forward-looking statements are based on reasonable assumptions, it can give no assurance that its expectations will be attained. Actual results may vary materially from those expressed or implied by the statements herein due to risks related to the early stage of development of bezisterim and other product candidates, the possibility that results observed in this Phase 2 study of 203 patients may not be replicated in larger or longer-duration trials, the exploratory nature of subgroup analyses, the Company’s ability to successfully raise sufficient capital on reasonable terms or at all, available cash on hand and contractual and statutory limitations that could impair our ability to pay future dividends, our ability to complete our pre-clinical or clinical studies and to obtain approval for our product candidates, the possibility that clinical trial results may not be indicative of results in subsequent or larger trials, our ability to successfully defend potential future litigation, changes in local or national economic conditions as well as various additional risks, many of which are now unknown and generally out of the Company’s control, and which are detailed from time to time in reports filed by the Company with the SEC, including quarterly reports on Form 10-Q, reports on Form 8-K and annual reports on Form 10-K. BioVie Inc. does not undertake any duty to update any statements contained herein (including any forward-looking statements), except as required by law.

For Investor Relations Inquiries:

Contact:
Chuck Padala
Managing Director, LifeSci Advisors, LLC
chuck@lifesciadvisors.com

For Media Inquiries:

Contact:
Melyssa Weible
Managing Partner, Elixir Health Public Relations
mweible@elixirhealthpr.com

_________________________________
1  U.S. Department of Health and Human Services (https://www.hhs.gov/longcovid/index.html)
2  Bonuck et al. Commun Med. 2026;6:177. doi:10.1038/s43856-026-01516-7.
3  Thaweethai et al. Nat Commun. 2025;16(1):9557. doi:10.1038/s41467-025-65239-4.
4  Geng et al. JAMA. 2025 Feb 25;333(8):694-700. doi: 10.1001/jama.2024.24184.

As market conditions allow, facility provides access to incremental capital to support XRP acquisitions, product development in the XRP ecosystem and general corporate purposes

Evernorth Holdings, Inc.

SAN FRANCISCO, Oct. 26, 2026 (GLOBE NEWSWIRE) — Evernorth Holdings, Inc. (Nasdaq: XRPN) (“Evernorth”), a digital asset treasury company building institutional access to the XRP economy at scale, today announced that it has entered into a common stock purchase agreement with CF Principal Investments LLC (“Cantor”) to establish a committed equity facility for up to 5,218,935 Shares of Class A Common Stock. Assuming the closing stock price of XRPN on October 22, 2026, if fully executed the facility would generate aggregate gross proceeds of approximately $80 million.

As market conditions present themselves, Evernorth intends to use some proceeds for general corporate purposes, including the acquisition of XRP and product development in the XRP ecosystem. Evernorth will continue to consider further capital raising transactions to execute its strategy, including additional committed equity facilities and other equity and equity-linked transactions, in the future.

“This represents our first step in putting facilities in place to help grow and manage our treasury in an accretive manner for shareholders,” said Matt Frymier, Chief Financial Officer of Evernorth.

The facility follows a period of rapid execution for Evernorth. The company recently announced the completion of its business combination with Armada Acquisition Corp. II, began trading on Nasdaq under the ticker XRPN, appointed Hugo Jeadesboz as Chief Investment Officer, announced its inaugural execution partners, and rang the Nasdaq Closing Bell. The committed equity facility adds a flexible source of capital as Evernorth moves into its next phase as a public company.

About Evernorth

Evernorth Holdings Inc. (Nasdaq: XRPN) is a publicly traded digital asset treasury company that provides investors with exposure to XRP through a regulated, liquid, and transparent structure. Evernorth holds one of the largest XRP treasuries of any public company and intends to put that XRP to work, pursuing strategies designed to grow XRP per share over time through institutional and DeFi yield strategies, ecosystem participation, and capital markets activities. To learn more, visit www.evernorth.xyz.

Forward-Looking Statements

This press release contains forward-looking statements, including statements about Evernorth’s treasury strategy, XRP Ledger developments, market opportunities, and the expected contributions of its Chief Investment Officer. They are based on current expectations and are not guarantees of future performance. Actual results may differ materially due to factors including the volatility of XRP and other digital assets, changes in laws and regulations, Evernorth’s ability to execute its strategies, and the other risks described under “Risk Factors” in Evernorth’s filings with the SEC. Evernorth undertakes no obligation to update these statements except as required by law.

Media Contact
Prosek Partners for Evernorth
pro-evernorth@prosek.com

Investor Relations
ir@evernorth.xyz

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/da9306df-57da-442d-bb07-367284944444

New wholly owned subsidiary, led by Adrian Jones, to expand the Company’s network of clinics and pharmacies across Australia

VANCOUVER, British Columbia, Oct. 26, 2026 (GLOBE NEWSWIRE) — Optimi Health Corp. (Nasdaq: OPTH, CSE: OPTI, FSE: 8BN) (the “Company” or “Optimi“), a commercial-stage pharmaceutical developer and manufacturer of regulated psychedelic drug products, today announced the establishment of Optimi Australia Pty Ltd (“Optimi Australia“), a wholly owned subsidiary responsible for distribution and business development in Australia, and the appointment of Adrian Jones as Director of Australian Operations.

Optimi Australia will handle the Company’s sales, distribution, and prescriber relationships across the country. It will sell Optimi’s finished drug products, 5mg naturally derived psilocybin capsules and 40mg and 60mg MDMA capsules, to clinics and pharmacies under Australia’s Authorised Prescriber Scheme. All products are manufactured at the Company’s Health Canada-licensed GMP facility in Princeton, British Columbia.

Mr. Jones joins Optimi after more than 15 years at Bristol Myers Squibb, most recently as Associate Director, Head of Sales and Marketing for its Australian oncology and cardiovascular portfolios, where he led national commercial teams and served as launch lead for first-in-class therapies including Opdivo and Camzyos. His early career includes psychiatry roles with Eli Lilly and Hospira.

“Australia is our first commercial market and we believe demand from authorized prescribers there continues to grow,” said Dane Stevens, Chief Executive Officer of Optimi. “Optimi Australia puts our team on the ground, and in Adrian we have a leader with extensive experience launching new therapies in this market.”

“My immediate focus is to understand the needs of the clinician and to help them deliver therapy as efficiently and effectively as possible,” said Adrian Jones, Director of Australian Operations.

Authorised prescribers, clinics, and pharmacies seeking product information or account setup can contact Adrian Jones at adrian@optimihealth.ca or visit the Company’s Australian website, www.optimi.com.au.

About Optimi Health Corp.

Optimi Health Corp. (Nasdaq: OPTH, CSE: OPTI, FSE: 8BN) is a commercial-stage pharmaceutical company focused on developing, manufacturing, and distributing GMP-grade psychedelic drug products for mental health therapies. As a Health Canada-licensed pharmaceutical manufacturer, Optimi produces validated MDMA and botanical psilocybin drug products at its GMP-compliant facility in British Columbia, Canada.

Optimi supplies both active pharmaceutical ingredients and finished dosage forms to regulated clinical and therapeutic programs internationally, with products currently prescribed to patients in Australia under the country’s Authorised Prescriber Scheme and accessible in Canada through the Special Access Program. The Company plans to advance a Health Canada-approved Phase 2 clinical trial evaluating psilocybin-assisted therapy for major depressive disorder and a proposed Phase 3 clinical trial evaluating MDMA-assisted therapy for post-traumatic stress disorder.

Learn more at www.optimi.net.

Company Contact:

Dane Stevens, Chief Executive Officer
Telephone: (778) 761-4551
investors@optimi.net

Australian Inquiries:

Adrian Jones
Director of Australian Operations
Optimi Australia Pty Ltd
E. adrian@optimihealth.ca
M. +61 (0) 408 117 700
W. www.optimi.com.au

Forward-Looking Statements

This news release contains forward-looking statements and forward-looking information within the meaning of applicable Canadian and United States securities legislation (collectively, “forward-looking statements”). All statements other than statements of historical fact contained in this news release, including statements regarding the anticipated role, responsibilities, and operations of Optimi Australia Pty Ltd, the expansion of the Company’s clinic and pharmacy network in Australia, anticipated demand for the Company’s products in Australia, the expected contributions of Mr. Jones, the results of the Company’s clinical trials, the Company’s growth objectives, and the Company’s business plans and commercial strategy, are forward-looking statements. Forward-looking statements are necessarily based upon a number of material assumptions, including that the Authorised Prescriber Scheme will remain in place on substantially current terms, that authorised prescribers will continue to prescribe the Company’s products, and that the Company will have sufficient capital to fund its Australian operations. While considered reasonable by management, these assumptions are inherently subject to significant business, economic, regulatory and competitive uncertainties and contingencies. Such statements involve known and unknown risks, uncertainties, and other factors that may cause actual results or events to differ materially from those anticipated in such statements, including risks related to changes in the Australian regulatory framework for psilocybin and MDMA, the number of authorised prescribers, controlled substance import, export, and permitting requirements, the Company’s ability to maintain its licences, the commercialization of the Company’s products, the results and timing of clinical trials, foreign operations, the Company’s ability to obtain financing, and general market conditions, as well as the risks described under “Risk Factors” in the Company’s most recent filings available on SEDAR+ at www.sedarplus.ca and on EDGAR at www.sec.gov. Readers are cautioned not to place undue reliance on forward-looking statements, which speak only as of the date of this news release. The Company undertakes no obligation to update or revise any forward-looking statements except as required by applicable law.

Neither the Canadian Securities Exchange nor the Canadian Investment Regulatory Organization accepts responsibility for the adequacy or accuracy of this release.

Phase 1 plant now in stable operation following commissioning; first liquid helium in storage ahead of initial deliveries to contracted offtakers

DALLAS, Oct. 26, 2026 (GLOBE NEWSWIRE) — ASP Isotopes Inc. (NASDAQ: ASPI) (“ASP Isotopes” or the “Company”), an advanced materials company focused on developing technologies and processes for the production of critical materials used in multiple industries, today announced that Tetra4 Proprietary Limited (“Tetra4”), a subsidiary of Renergen Limited (“Renergen”), has completed commissioning and achieved stable production of liquid helium. Liquid helium is now accumulating in Tetra4’s cryogenic storage ahead of initial deliveries under existing offtake agreements. The Virginia Gas Project holds South Africa’s first onshore petroleum production right and is the country’s first integrated producer of both liquid helium and liquefied natural gas (“LNG”).

“Stable helium production at the Virginia Gas Project is a defining milestone for Renergen and for ASP Isotopes,” said Paul Mann, Executive Chairman and Chief Executive Officer of ASP Isotopes, and Chief Executive Officer of Renergen. “With global helium supply under significant pressure, a new, independent source matters more than ever, and our offtake partners have been waiting for exactly this. We are now ramping towards nameplate capacity, which we expect to reach during the fourth quarter of 2026, and we are finalising logistics with our offtakers for first deliveries.”  

Phase 1 is expected to produce approximately 2,500 GJ/day of LNG and approximately 70 Mcf/day of liquid helium.

About ASP Isotopes Inc.

ASP Isotopes Inc. is an advanced materials company focused on developing technologies and processes for the production of critical materials used in multiple industries, including nuclear medicine, electronics and nuclear energy. The Company’s proprietary Aerodynamic Separation Process (“ASP technology”) and Quantum Enrichment (“QE technology”) are designed to enable the production of isotopes for a range of industrial and advanced technology applications. The Company operates isotope enrichment facilities in Pretoria, South Africa, focused on low atomic mass elements, or light isotopes, and a gas production facility in Free State Province, South Africa, focused on liquid natural gas and liquid helium. For more information, please visit www.aspisotopes.com.

About Renergen

Renergen Limited, a subsidiary of ASP Isotopes Inc., is a company incorporated under the laws of the Republic of South Africa whose principal asset is its 94.5% equity interest in Tetra4 Proprietary Limited, which owns an onshore petroleum production right and is engaged in the exploration and production of natural gas and the processing of natural gas into liquid natural gas and liquid helium in Free State Province, South Africa.

Important Additional Information and Where to Find It 

This press release relates to the proposed merger and related transactions (the “Proposed Transactions”) involving ENDRA Life Sciences Inc. (“ENDRA”), ASP Isotopes, Renergen and Noble Africa LLC, a subsidiary of ASP Isotopes and future holding company for Renergen (“Noble Africa”), and may be deemed to be solicitation material in respect of the Proposed Transactions. In connection with the Proposed Transactions, ENDRA has filed relevant materials with the SEC, including a registration statement on Form S-4 (the “Form S-4”) that contains a proxy statement (the “Proxy Statement”) and prospectus. This press release is not a substitute for the Form S-4, the Proxy Statement or for any other document that ENDRA may file with the SEC and/or send to its stockholders in connection with the Proposed Transactions. INVESTORS AND STOCKHOLDERS OF ENDRA ARE URGED TO READ THE FORM S-4, THE PROXY STATEMENT AND ANY OTHER RELEVANT DOCUMENTS THAT MAY BE FILED WITH THE SEC, AS WELL AS ANY AMENDMENTS OR SUPPLEMENTS TO THESE DOCUMENTS, CAREFULLY AND IN THEIR ENTIRETY IF AND WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT ENDRA, ASP ISOTOPES, RENERGEN, NOBLE AFRICA, THE PROPOSED TRANSACTIONS AND RELATED MATTERS.

Investors and stockholders will be able to obtain free copies of the Form S-4, the Proxy Statement and other documents filed by ENDRA and ASP Isotopes with the SEC (when they become available) through the website maintained by the SEC at www.sec.gov. ENDRA’S Internet website address is www.endrainc.com. ENDRA’s Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form 8-K, including exhibits, and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Exchange Act are available free of charge through the investor relations page of its Internet website as soon as reasonably practicable after it electronically files such material with, or furnishes such material to, the SEC.

Participants in the Solicitation

ENDRA, ASP Isotopes, Renergen, Noble Africa, and their respective directors and managers and certain of their executive officers and other members of management may be deemed to be participants in the solicitation of proxies from ENDRA’s stockholders in connection with the Proposed Transactions under the rules of the SEC. Information about ENDRA’s directors and executive officers, including a description of their interests in ENDRA, is included in ENDRA’s most recent Annual Report on Form 10-K for the year ended December 31, 2025. Information about ASP Isotopes’ directors and executive officers, including a description of their interests in ASP Isotopes, is included in ASP Isotopes’ most recent Annual Report on Form 10-K for the year ended December 31, 2025. Additional information regarding the persons who may be deemed participants in the proxy solicitations, including the directors and executive officers of Renergen, and a description of their direct and indirect interests, by security holdings or otherwise, are also included in the Form S-4 and the Proxy Statement and may be included in other relevant materials filed with the SEC. These documents can be obtained free of charge from the sources indicated above.

No Offer or Solicitation

This press release is not intended to and does not constitute a solicitation of a proxy, consent or approval with respect to any securities or in respect of the Proposed Transactions or an offer to sell or the solicitation of an offer to subscribe for or buy or an invitation to purchase or subscribe for any securities pursuant to the Proposed Transactions or otherwise, nor shall there be any sale, issuance or transfer of securities in any jurisdiction in contravention of applicable law. No offering of securities shall be made except by means of a prospectus meeting the requirements of Section 10 of the Securities Act of 1933, as amended, and otherwise in accordance with applicable law, or an exemption therefrom. Subject to certain exceptions to be approved by the relevant regulators or certain facts to be ascertained, the public offer will not be made directly or indirectly, in or into any jurisdiction where to do so would constitute a violation of the laws of such jurisdiction, or by use of the mails or by any means or instrumentality (including without limitation, facsimile transmission, telephone and the internet) of interstate or foreign commerce, or any facility of a national securities exchange, of any such jurisdiction.

Cautionary Statement Regarding Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on our current beliefs, expectations, and assumptions regarding the future of our business, future plans and strategies, projections, anticipated events and trends, the economy, and other future conditions. Forward-looking statements can be identified by words such as “anticipates,” “believes,” “could,” “estimates,” “expects,” “intends,” “may,” “might,” “plans,” “projects,” “will,” and words of a similar nature. Examples of forward-looking statements include, but are not limited to, statements relating to the expected production quantities of LNG and liquid helium, Renergen’s expected revenues, the Proposed Transactions; the expected structure, timing and the completion of the Proposed Merger, the Proposed Transactions and the expected effects, perceived benefits or opportunities of the Proposed Transactions; the combined company’s listing on Nasdaq after the closing of the Proposed Transactions; expectations regarding the structure, timing and completion of the Proposed Transactions, including investment amounts from investors, timing of closing of the Proposed Transactions, expected proceeds, expectations regarding the use of proceeds, and impact on ownership structure; the anticipated timing of the closing of the Proposed Transaction; the expected executive officers and directors of the combined company; each company’s and the combined company’s expected cash position at the closing of the Proposed Transactions and cash runway of the combined company following the Proposed Transactions; the future operations and pipeline, estimates of financial position, competitive landscape, addressable market and strategic and financial initiatives of the combined company; the nature, strategy and focus of the combined company; statements regarding the continuation of Renergen’s Virginia Gas Project and its funding timeline and other statements that are not historical fact.

Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks, and changes in circumstances that are difficult to predict, many of which are outside our control. Actual results, financial condition, and events may differ materially from those indicated in the forward-looking statements based upon a number of factors. Forward-looking statements are not a guarantee of future performance or developments. You are strongly cautioned that reliance on any forward-looking statements involves known and unknown risks and uncertainties. Therefore, you should not rely on any of these forward-looking statements. There are many important factors that could cause actual results and financial condition to differ materially from those indicated in the forward-looking statements, including, but not limited to: the outcomes of various strategies and projects undertaken by Renergen; the potential impact of laws or government regulations or policies in South Africa or elsewhere; Renergen’s future capital requirements and sources and uses of cash; Renergen’s ability to obtain funding for its operations and future growth, including debt funding for Phase 2 of the Virginia Gas Project; Renergen’s reliance on the efforts of third parties; Renergen’s ability to complete Phase 1 and 2 of the Virginia Gas Project; the financial terms of any current and future commercial arrangements; Renergen’s ability to complete certain transactions and realize anticipated benefits from acquisitions and contracts; Renergen’s ability to comply with the terms of the loan and credit facilities of Renergen’s subsidiary Tetra4; the ability of Renergen and its subsidiaries to retain and hire key personnel; the volatility of LNG and liquid helium prices; Renergen’s success in discovering, estimating and developing natural gas and helium reserves; actions of competitors or regulators; limitations in the availability of, and costs of, supplies, materials, contractors and services that may delay the drilling or completion of wells or make such wells more expensive; the amount and timing of future development costs; uncertainties inherent in estimating quantities of natural gas and helium reserves and projecting future rates of production and timing of development activities; risks relating to the lack of capital available on acceptable terms to finance the Renergen’s continued growth; the competitive nature of Renergen’s industry; the risk that the conditions to the closing or consummation of the Proposed Transactions are not satisfied, including the failure to timely obtain approval of the Proposed Merger from ENDRA stockholders, if at all; the risk that the proposed financings are not completed in a timely manner, if at all; uncertainties as to the timing of the consummation of the Proposed Transactions and the ability of each of ENDRA and Noble Africa to consummate the Proposed Transactions; risks related to ENDRA’s continued listing on Nasdaq until closing of the Proposed Transactions and the combined company’s ability to remain listed following the closing of the Proposed Transactions; the ability to obtain debt financing on terms that are favorable, or at all; the risk that Renergen does not receive funding from the U.S. DFC or Standard Bank SA or that such funding is delayed; risks related to ENDRA’s ability to correctly estimate its respective operating expenses and its respective expenses associated with the Proposed Transactions, as applicable, pending the closing of the Proposed Transactions, as well as uncertainties regarding the impact any delay in the closing would have on the anticipated cash resources of ENDRA, and other events and unanticipated spending and costs that could reduce ENDRA’s cash resources; risks related to the failure or delay in obtaining required approvals from any governmental or quasi-governmental entity necessary to consummate the Proposed Transactions; the occurrence of any event, change or other circumstance or condition that could give rise to the termination of the merger agreement; the effect of the announcement or pendency of the Proposed Merger on ENDRA’s or Renergen’s business relationships, operating results and business generally; costs related to the Proposed Merger; risks related to the market price of ENDRA’s common stock relative to the value suggested by the Proposed Merger; the outcome of any legal proceedings that may be instituted against ENDRA, Noble or any of their respective directors, managers, or officers related to the Proposed Transactions; costs of the Proposed Transactions and unexpected costs, charges or expenses resulting from the Proposed Transactions; changes in regulatory requirements and government incentives; risks associated with the possible failure to realize, or that it may take longer to realize than expected, certain anticipated benefits of the Proposed Transactions, including with respect to future financial and operating results, legislative, regulatory, political and economic developments, and those uncertainties and factors; and the risk of involvement in litigation, including securities class action litigation, that could divert the attention of the management of ENDRA or the combined company, harm the combined company’s business and may not be sufficient for insurance coverage to cover all costs and damages, and the other risks and uncertainties described in ENDRA’s SEC reports, and under the heading “Risk Factors” in its most recent Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, the factors disclosed in Part I, Item 1A. “Risk Factors” of ASP Isotopes’ Annual Report on Form 10-K for the fiscal year ended December 31, 2025 (as amended) and in ASP Isotopes’ subsequent reports filed with the SEC, each of which are available at www.sec.gov, and in other filings that ENDRA and ASP Isotopes have made and will make with the SEC in connection with the Proposed Transactions, including the Form S-4 and Proxy Statement described above under “Additional Information and Where to Find It”. Any forward-looking statement made by the parties in this press release is based only on information currently available to the parties and speaks only as of the date on which it is made. The parties undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments or otherwise. No information in this press release should be interpreted as an indication of future success, revenues, results of operations, or stock price. All forward-looking statements herein are qualified by reference to the cautionary statements set forth herein and should not be relied upon.

Contact
IR@ASPIsotopes.com

Significantly Deeper Well Will Test Additional Oil and Potential Natural Gas-Bearing Formations Identified Through 3-D Seismic Program

JAKARTA, INDONESIA AND DANVILLE, CA, Oct. 26, 2026 (GLOBE NEWSWIRE) — Indonesia Energy Corporation (NYSE American: INDO) (“IEC”), an oil and gas exploration and production company focused on Indonesia, today announced that drilling operations commenced on October 21, 2026, at its WK-5 well, marking another important milestone in IEC’’s ongoing development program at the Kruh Block in Sumatra, Indonesia.

WK-5 is planned to reach a total depth of approximately 5,200 feet, significantly deeper than the recently completed K-29 well, which was drilled to approximately 3,400 feet. The deeper drilling program is designed to evaluate additional formations identified through IEC’s previous extensive 3-D seismic program, including a potentially natural gas-bearing formation. Both wells are located within IEC’s approximately 63,000-acre Kruh Block.

A video featuring oil production from K-29 and a recent visit by IEC’s delegation to the WK-5 wellsite can be viewed at the following link:

https://www.youtube.com/watch?v=uW2igiI9p4U

Frank Ingriselli, President of IEC, commented: “We are pleased to have commenced drilling WK-5 on schedule, following my visit to the Kruh Block earlier this month. This well represents an exciting opportunity for IEC as we drill significantly deeper than K-29 to evaluate additional formations identified by our previously announced 3-D seismic program. We believe these formations offer meaningful potential to expand the resource base and create long-term value for our shareholders.

“If successful, production from WK-5 would complement our ongoing production from K-29 and our other producing wells, with oil production sold to Pertamina, Indonesia’s state-owned oil and gas company. We are also working to secure the necessary Indonesian government approval to publicly disclose individual well production rates and look forward to providing additional information once the required approvals are obtained.

“The successful commencement of WK-5 drilling, together with the recent initiation of oil production from K-29, demonstrates our team’s continued progress in executing our Kruh Block development strategy. We remain focused on increasing production, evaluating new opportunities, and unlocking the long-term potential of our assets in Indonesia,” concluded Mr. Ingriselli.

About Indonesia Energy Corporation Limited

Indonesia Energy Corporation Limited (NYSE American: INDO) is a publicly traded energy company engaged in the acquisition and development of strategic, high growth energy projects in Indonesia. IEC’s principal assets are its Kruh Block (63,000 acres) located onshore on the Island of Sumatra in Indonesia and its Citarum Block (195,000 acres) located onshore on the Island of Java in Indonesia. IEC is headquartered in Jakarta, Indonesia and has a representative office in Danville, California. For more information on IEC, please visit www.indo-energy.com.

Cautionary Statement Regarding Forward-Looking Statements

All statements in this press release, the YouTube videos described herein and related statements of Indonesia Energy Corporation Limited (“IEC”) and its representatives and partners that are not based on historical fact are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 and the provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Acts”). In particular, the words “explore,” “could,” “estimates,” “seek,” “believes,” “hopes,” “understand,” “expects,” “intends,” “on-track”, “plans,” “anticipates,” “aim,” “goal,” “may” and similar conditional expressions related to the future are intended to identify forward-looking statements within the meaning of the Acts and are subject to the safe harbor created by the Acts. Any statements made in this news release, other than those of historical fact, about an action, event or development, are forward-looking statements. In this press release, forward-looking statements include, without limitation those related to the timing for, and results of, 2026 and other drilling activities at IEC’s Kruh Block as well as the price of oil, which changes daily and could lower over time. While management has based any forward-looking statements contained herein on its current expectations, the information on which such expectations were based may change. These forward-looking statements rely on a number of assumptions concerning future events and are subject to a number of significant risks, uncertainties, and other factors, many of which are outside of the IEC’s control, that could cause actual results to materially and adversely differ from such statements. Such risks, uncertainties, and other factors include, but are not necessarily limited to, those set forth in the Risk Factors section of IEC’s annual report on Form 20-F for the fiscal year ended December 31, 2025, filed on April 29, 2026, and other filings with the Securities and Exchange Commission (SEC). Copies are of such documents are available on the SEC’s website, www.sec.gov and IEC’s website at https://ir.indo-energy.com/sec-filings/. IEC undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.

Company Contact:
Frank C. Ingriselli
President, Indonesia Energy Corporation Limited
Frank.Ingriselli@Indo-Energy.com

Larger resource base strengthens potential to extend mine life

SYDNEY, Oct. 26, 2026 (GLOBE NEWSWIRE) — Brazilian Rare Earths Limited (ASX: BRE / OTCQX: BRELY) (‘BRE’) announces a major Mineral Resource Estimate (MRE) upgrade for the flagship Monte Alto deposit in Bahia, Brazil, delivering a 41% increase in Indicated ultra-high-grade resource tonnes to 3.5 Mt at 10.7% TREO.

Total ultra-high grade resource tonnes, comprising Indicated and Inferred material, have increased by 29% to 4.4 Mt at 9.9% TREO, reported above a cut-off grade of 1% TREO. Indicated resources now account for 87% of contained TREO within the ultra-high-grade resource.1

HIGHLIGHTS

  • Major expansion of ultra-high grade resource: Updated Mineral Resource Estimate (MRE) expands Monte Alto Indicated Resource tonnes by 41% to 3.5 Mt at 10.7% TREO.1
  • Monte Alto southern extension drives growth: Indicated resource tonnes at Monte Alto South have increased by approximately 200% to 1.9 Mt1, supported by repeated intersections of thick, stacked mineralised horizons.
  • Improved geological confidence: Indicated resources now account for 87% of contained TREO1 within the resource, providing a strong foundation for upcoming feasibility-level mine planning and economic studies.
  • Extensive drilling foundation: Over 43,000 m of diamond drilling across 255 drillholes underpins a high-quality MRE and a more detailed understanding of the deposit’s geology and heavy rare earth rich mineralisation.
  • Further resource growth targeted: Mineralisation remains open in all directions and further significant regional upside across the district. A 5,000 m drilling programme is underway to extend recent high-grade additions.
  • Monte Alto Concentrate Sales Feasibility Study: The expanded MRE directly underpins mine planning for a fast-tracked, low-capex Monte Alto development producing a high-grade concentrate for export markets. Fast-tracked concentrate exports could generate cash flow before the downstream Camaçari refinery development.2
FIGURE 1: 3D VIEW OF UPDATED MONTE ALTO MINERAL RESOURCE


FIGURE 1: 3D VIEW OF UPDATED MONTE ALTO MINERAL RESOURCE

Bernardo da Veiga, CEO & Managing Director commented:

“This major resource upgrade strengthens the foundation for a longer-life Monte Alto operation and a staged, low-capex development route to first production and exports. The Monte Alto concentrate sales feasibility study will assess an initial rare-earth concentrate export business, with the opportunity to commit capital in stages and generate cash flow ahead of Camaçari’s refinery construction and commissioning.

This simple mineral concentrate operation would draw on Monte Alto’s ultra-high grades and ore-sorting performance to produce a direct-ship export product through conventional mining and dry processing. By establishing this operation ahead of the Camaçari refinery, we aim to generate early cash flow to fund downstream development and reduce our reliance on external capital.

We are advancing this development work while continuing to explore the full limits of Monte Alto’s scale. Mineralisation remains open to the south, and drilling beyond the current resource boundary offers further scope to increase the resource available for a longer-life project.”

A link to the full announcement can be found here.

Contacts

Bernardo Da Veiga
Managing Director and CEO

investors@brazilianrareearths.com
www.brazilianrareearths.com

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/6180e4aa-38a3-4f5a-8869-7e29414fe0d9

__________________________________
1   Inferred Mineral Resources comprise 20% of the tonnes and 13% of the contained TREO of the updated Mineral Resource. There is a low level of geological confidence associated with Inferred Mineral Resources and there is no certainty that further exploration work will result in the determination of Indicated Mineral Resources.
2   See BRE’s ASX announcement dated 18 August 2026, which described a potential staged, low-capex development pathway to generate earlier cash flow from Monte Alto concentrate sales. Preliminary and indicative only, not based on a completed feasibility study, and subject to further work and approvals.

PALM BEACH, Florida, Oct. 26, 2026 (GLOBE NEWSWIRE) — Gabelli is hosting the 8th Annual Healthcare Symposium in conjunction with Columbia Business School on Friday, November 13, 2026, at the Paley Center in New York. The symposium brings together leading companies and organizations from across the healthcare ecosystem, with an emphasis on industry dynamics, current trends, and business fundamentals.

This year’s program will cover the pace of oncology innovation, drug access in the specialty and GLP-1 era, and the role of artificial intelligence in care delivery.

For additional information and to register, please visit our website. Space is limited, so please register as soon as possible. For those who cannot attend in person, the symposium will also be available via live webcast.

Program:
Opening Remarks & Welcome Address (8:45 – 8:50 AM)

Cancer’s Breakthrough Year: Can Care Keep Pace? (8:50 – 9:50 AM)
Moderated by Rebecca Stern, PhD, SVP, Gabelli
Richard Barakat, MD, MBA (CBS ’14), Physician-in-Chief & Executive Director, Northwell Cancer Institute
Alan Bash, MBA (CBS ’99), President of CARVYKTI®, Legend Biotech (NASDAQ: LEGN)
Christophe Griolet, PharmD, MBA, VP & General Manager, US Commercial Organization, Kite, a Gilead Company (NASDAQ: GILD)
Mohit Manrao, MBA, SVP, Head of US Oncology, AstraZeneca (NYSE: AZN)

Drug Access in the Specialty and GLP-1 Era (10:05 – 11:05 AM)
Moderated by Daniel Barasa, MBA, Portfolio Manager, Gabelli
Natalie Bedford, SVP, US Pharmaceutical Distribution Services, McKesson (NYSE: MCK)
Marko Blagojevic, PharmD, SVP, Pharmacy, Gravie
Leonard Glass, MD, FACE, SVP, Cardiometabolic Health, Global Medical Affairs, Eli Lilly and Company (NYSE: LLY)
David Senior, MPH, President & SVP, Strategic Global Sourcing and Policy Economics, Cencora (NYSE: COR)

Leveraging AI to Improve Care Delivery (11:20 AM – 12:20 PM)
Moderated by Carri Chan, PhD, Cain Brothers and Company Professor of Healthcare Management and Faculty Director, Columbia Business School
Anil Jain, MD, Chief Innovation Officer, Provider Digital Transformation, Innovaccer
Kevin Larsen, MD, SVP, Clinical Innovation, Optum (NYSE: UNH)
Dave Ross, Chief Technology Officer, Teladoc Health (NYSE: TDOC)
Paul Taheri, MD, MBA, Chief Medical Officer, InnovAge (NASDAQ: INNV)

Closing Remarks (12:20 – 12:30 PM)
Breakfast and networking begin at 8:00 AM. Participants are subject to change.

8th Annual Healthcare Symposium

Click here to register for the 8th Annual Healthcare Symposium or scan the QR code.

Contact

Patricio Salem
P: 914-921-5117
E: PSalem@gabelli.com

Gabelli Funds, LLC is a registered investment adviser with the Securities and Exchange Commission and is a wholly owned subsidiary of GAMCO Investors, Inc.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/226ab686-f6e1-4cef-8a44-50c82b754e9a

Companies to combine OPT’s PowerBuoy® platforms and patent portfolio with Stratum’s GPU infrastructure to advance edge AI inference powered by wave, wind, and solar energy

MONROE TOWNSHIP, NJ and CELEBRATION, FL, Oct. 26, 2026 (GLOBE NEWSWIRE) — Ocean Power Technologies, Inc. (NYSE American: OPTT) (“OPT”) and Stratum Holdings Corp. (NASDAQ: SRTM) (“Stratum”) today announced that they have entered into a non-binding letter of intent (the “LOI”) for a proposed strategic collaboration to demonstrate offshore data center assets powered by renewable wave, wind, and solar energy.

The LOI contemplates that OPT and Stratum negotiate definitive agreements pursuant to which OPT would grant Stratum a limited, non-exclusive license to certain of its PowerBuoy® patents for use in the demonstration program and make available certain prototype PowerBuoy® assets currently on hand, and Stratum would make available certain GPU assets, including its latest generation NVIDIA B300 GPUs, and related integration expertise. Stratum would also pay OPT a monthly retainer under the terms of the definitive agreements. The proposed strategic collaboration would focus on integrating OPT’s PowerBuoy® platforms with Stratum’s high-performance compute hardware to validate the technical feasibility of hosting edge AI inference and related workloads on systems powered primarily by onboard renewable generation, without a power umbilical to shore.

OPT holds more than 60 issued patents worldwide relating to its PowerBuoy® technology, including  more than 15 in the U.S., covering buoy architecture, energy conversion, power take-off, control systems, mooring and anchoring, autonomous charging interfaces, communications, and related systems. These patents form the foundation of the PowerBuoy® platform, which is designed to deliver persistent, renewable power and real-time communications in remote marine environments.

Cooling accounts for a significant portion of power consumption in conventional data centers. OPT and Stratum believe that positioning PowerBuoy®-based systems in cooler regions of the ocean could reduce this cooling-related power demand, although this has not yet been demonstrated and will be among the matters tested in the proposed demonstration program.

“This proposed strategic collaboration aligns with OPT’s mission to deliver persistent renewable power and technology integration for critical offshore applications,” said Tracy Pagliara, Acting President and Chief Executive Officer of Ocean Power Technologies. “By combining our patented PowerBuoy® technology with Stratum’s GPU assets, we aim to demonstrate a practical path toward self-powered edge AI infrastructure that operates independently of shore-based power.”

“Stratum is focused on expanding high-performance compute capacity in new environments,” said Nicholas H. Adler, Chief Executive Officer of Stratum Holdings. “Partnering with OPT allows us to explore the potential of renewable-powered offshore platforms combined with our GPU assets for edge AI inference, where local processing can reduce bandwidth requirements and leverage the natural cooling advantages of the marine environment.”

The proposed strategic collaboration’s initial efforts are expected to center on system integration, performance validation, and data collection from demonstration deployments. Results from the program, if any, may inform potential future commercial applications in maritime domain awareness, offshore energy monitoring, scientific sensing, and other remote edge-compute use cases.

About Ocean Power Technologies

Ocean Power Technologies, Inc. (NYSE American: OPTT) provides intelligent maritime systems and services for defense and security, offshore energy, science and research, and offshore wind. Its PowerBuoy® platforms deliver clean, renewable power and real-time data communications for remote maritime and subsea applications. The company also offers the WAM-V® autonomous surface vehicle and Merrows™ software for multi-domain awareness. For more information, visit www.oceanpowertechnologies.com.

About Stratum Holdings

Stratum Holdings Corp. (NASDAQ: SRTM) is an AI infrastructure company focused on GPU leasing and high-performance compute capacity. The company is transitioning from legacy real estate operations to provide scalable compute solutions supporting artificial intelligence workloads. For more information, visit www.stratumholdingscorp.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements involve risks and uncertainties that could cause actual results to differ materially from those anticipated, including the risk that the parties do not negotiate or execute definitive agreements on the terms described or at all; the non-binding nature of the LOI and the ability of either party to terminate discussions; the failure to obtain required board, regulatory, or stockholder approvals; the potential dilution to Stratum stockholders from any issuance of shares as payment of the retainer; the value and liquidity of potential Stratum common stock received by OPT, including restrictions on resale pending registration; the parties’ ability to fund and complete the demonstration program on the anticipated timeline or at all; risks related to the successful integration of technologies, technical performance of demonstration systems, regulatory approvals, and market adoption; and other factors described in the companies’ filings with the Securities and Exchange Commission, including their most recent Annual Reports on Form 10-K and Quarterly Reports on Form 10-Q. Neither company undertakes any obligation to update these forward-looking statements, except as required by law.

Media Contacts

Ocean Power Technologies
Investors: 609-730-0400 x401
InvestorRelations@oceanpowertech.com 

Media: 609-730-0400 x402 
MediaRelations@oceanpowertech.com 

Stratum Holdings
Crescendo Communications, LLC
(212) 671-1020
srtm@crescendo-ir.com 

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