MARKET WIRE NEWS

Helus Pharma Appoints Former Pfizer Chief Medical Officer Dr. Freda Lewis-Hall to Board of Directors & Chair of the Scientific Advisory Committee

MWN-AI** Summary

Helus Pharma, a clinical stage pharmaceutical company focused on developing novel serotonergic agonists (NSAs) for mental health conditions, has appointed Dr. Freda Lewis-Hall, former Chief Medical Officer at Pfizer, to its Board of Directors and as Chair of its Scientific Advisory Committee. Dr. Lewis-Hall brings over 40 years of experience in clinical care, research, and corporate leadership, making her a valuable asset to Helus as the company progresses its clinical development strategies and regulatory pathways.

In her new role, Dr. Lewis-Hall will offer strategic guidance for Helus’ NSA portfolio, including key programs targeting major depressive disorder and generalized anxiety disorder. Her extensive background includes significant leadership roles at major biopharmaceutical companies, where she successfully advanced innovative therapies from development to patient care. Notably, she played a crucial role in the establishment and growth of SpringWorks Therapeutics.

Michael Cola, Chief Executive Officer of Helus Pharma, expressed enthusiasm about Dr. Lewis-Hall's appointment, highlighting her expertise in navigating complex regulatory environments and patient engagement initiatives. Dr. Lewis-Hall emphasized her commitment to bridging scientific innovation with effective patient care, aligning with Helus’s mission to address significant unmet needs in mental health treatment.

Dr. Lewis-Hall’s leadership will enhance the company’s research and clinical governance as it seeks to improve outcomes for patients suffering from mental health disorders. Her role will also involve contributing to corporate governance and ensuring that clinical rigor remains central to Helus’ growth strategy.

This appointment comes as Helus Pharma prepares to further develop its proprietary NSAs, which are designed to activate serotonin pathways believed to promote neuroplasticity. As Helus continues its journey in the mental health landscape, Dr. Lewis-Hall's involvement is expected to play a pivotal role in steering the company towards successful commercialization of its innovative therapies.

MWN-AI** Analysis

Helus Pharma’s recent appointment of Dr. Freda Lewis-Hall as Chair of the Scientific Advisory Committee and Board Member is a strategic move that should positively influence the company's trajectory in the pharmaceutical sector. Dr. Lewis-Hall brings over 40 years of extensive experience from her tenures at Pfizer and other leading pharmaceutical companies, where she adeptly guided drug development processes and regulatory engagements. This appointment signals Helus Pharma's commitment to strengthening its innovations in novel serotonergic agonists (NSAs) for mental health conditions, an area marked by significant unmet needs.

Investors should note that Helus Pharma is navigating the competitive landscape of psychiatric medications, especially with its HLP003 and HLP004 products currently in Phase 3 and Phase 2 studies respectively. Dr. Lewis-Hall's insights will be crucial not only in clinical strategy but also in ensuring the effective commercialization of these promising therapies. Her previous experience in advancing therapies through complex regulatory pathways offers a competitive edge that could lead to quicker market entry and potential revenue generation.

Market analysts should consider the broader implications of this strategic leadership change. The increased focus on serious mental health conditions, paired with Dr. Lewis-Hall’s advocacy for patient engagement and equity, may resonate well with healthcare stakeholders and increase the company’s visibility and credibility. Moreover, Helus’s disciplined operational approach aligns with current investor preferences for companies demonstrating both scientific rigor and a clear path to market.

However, potential investors should remain cautious of inherent risks in clinical trials and regulatory approvals. Given the volatility in biotech stocks, a thorough assessment of Helus Pharma’s ongoing trial results and market conditions is advisable. Overall, the company's development in NSAs and the caliber of its new leadership presents a potentially profitable opportunity in the evolving landscape of mental health treatments.

**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.

Source: GlobeNewswire
  • In this role, Dr. Lewis-Hall will guide clinical development strategy, regulatory engagement, and translational rigor across Helus’ novel serotonergic agonist (“NSA”) portfolio

This news release constitutes a “designated news release” for the purpose of the Company’s prospectus supplement dated December 30, 2025, to it short form base shelf prospectus dated September 17, 2025, as amended on December 19, 2025.

NEW YORK and TORONTO, Feb. 24, 2026 (GLOBE NEWSWIRE) -- Helus Pharma™ (Nasdaq: HELP) (Cboe CA: HELP), a clinical stage pharmaceutical company developing NSAs for serious mental health conditions, today announced the appointment of Dr. Freda Lewis-Hall, DFAPA, MFPM, to its Board of Directors. Dr. Lewis-Hall will also serve as Chair of the Company’s Scientific Advisory Committee.

Dr. Lewis-Hall is a pioneering physician and biopharmaceutical executive with more than 40 years of experience spanning clinical care, research, academia, corporate leadership, and public health advocacy. She began her medical career as a practicing psychiatrist, focusing on the impact of mental illness on families and communities.

She later held senior leadership roles across the biopharmaceutical industry, including serving for more than a decade on Pfizer’s Executive Leadership Team as Executive Vice President and Chief Medical Officer. In that role, she led a global medical organization operating in more than 125 countries and supporting a broad portfolio of medicines and vaccines. She subsequently served as Chief Patient Officer, advancing patient engagement, inclusion, and health equity initiatives across the enterprise. During her tenure, she also helped lead the spinout of SpringWorks Therapeutics and served on its Board of Directors, guiding the company through regulatory approvals and its evolution into a commercial-stage organization prior to its acquisition by Merck KGaA for approximately $3.4 billion. Dr. Lewis-Hall has also held senior leadership positions at Vertex Pharmaceuticals, Bristol Myers Squibb, Pharmacia Corporation, and Eli Lilly and Company.

Dr. Lewis-Hall is a Distinguished Fellow of the American Psychiatric Association and previously served as Vice Chairperson and Associate Professor in the Department of Psychiatry at Howard University College of Medicine. She has also advised the National Institute of Mental Health.

“Dr. Lewis-Hall is a highly respected physician and leader whose career has been defined by bringing complex, innovative therapies from development to patients around the world, particularly in areas of serious and underserved mental health need,” said Michael Cola, Chief Executive Officer of the Company. “Her deep experience in clinical strategy, regulatory engagement, and global commercialization will be invaluable as we advance our novel serotonergic agonist programs for psychiatric disorders and continue building a company grounded in scientific rigor, patient impact, and responsible scale. We are honored to welcome her to our Board and as Chair overseeing the Scientific Advisory Committee.”

“Throughout my career, I have focused on ensuring that scientific innovation translates into therapies that make a meaningful difference for patients — and that can be delivered reliably within real-world healthcare systems,” said Dr. Lewis-Hall. “What distinguishes Helus Pharma is its disciplined approach at the intersection of rigorous science, a thoughtfully advancing clinical portfolio, and focused execution in areas of significant unmet need in mental health. I believe the company is building a differentiated development platform that has yet to be fully recognized by the broader market.”

She continues, “Helus Pharma’s commitment to strong clinical design, reproducibility, and regulatory clarity reflects the standards required to earn and sustain trust among patients, providers, and regulators. This work is deeply personal to me, given my early experience on the frontlines of mental health care. I look forward to supporting the company as it advances programs designed to deliver meaningful, durable outcomes for patients and long-term value for stakeholders.”

As Chair of the Scientific Advisory Committee, Dr. Lewis-Hall will provide leadership in scientific, clinical, and regulatory governance across Helus’ portfolio, advising on discovery opportunities, clinical development strategy, and regulatory pathways to support pipeline advancement and progress toward commercialization.

As a member of the Board of Directors, she will contribute to corporate governance and long-term strategic oversight, helping ensure that patient outcomes, clinical rigor, and disciplined decision-making remain central to the Company’s growth strategy.

Dr. Lewis-Hall’s appointment to the Company’s board of directors is subject to approval of Cboe Canada.

About Helus Pharma

Helus Pharma™, the commercial operating name of Cybin Inc. (the “Company” or “Helus Pharma”) is a clinical stage pharmaceutical company committed to helping minds heal by developing proprietary NSAs - novel serotonergic agonists: synthetic molecules designed to activate serotonin pathways that are believed to promote neuroplasticity. The Company’s proprietary NSAs are intended to address the large unmet need for people who suffer from depression, anxiety, and other mental health conditions.

With class leading data, Helus Pharma aims to improve the treatment landscape through the introduction of NSAs that aim to provide durable improvements in mental health. Helus Pharma is currently developing HLP003, a proprietary NSA, in Phase 3 clinical development for the adjunctive treatment of major depressive disorder that has received Breakthrough Therapy Designation from the U.S. Food and Drug Administration and HLP004, also a proprietary NSA in Phase 2 for generalized anxiety disorder. Additionally, Helus Pharma has an extensive research portfolio of investigational NSAs.

The Company operates in Canada, the United States, the United Kingdom, and Ireland. For Company updates and to learn more about Helus Pharma, visit www.helus.com or follow the team on X, LinkedIn, YouTube and Instagram. Helus PharmaTM is a trademark of Cybin Corp.

Cautionary Notes and Forward-Looking Statements

Certain statements in this news release relating to the Company are forward-looking statements or forward-looking information within the meaning of applicable securities laws (collectively, “forward-looking statements”) and are prospective in nature. Forward-looking statements are not based on historical facts, but rather on current expectations and projections about future events and are therefore subject to risks and uncertainties which could cause actual results to differ materially from the future results expressed or implied by the forward-looking statements. These statements generally can be identified by the use of forward-looking words such as “may”, “should”, “could”, “potential”, “possible”, “intend”, “estimate”, “plan”, “anticipate”, “expect”, “believe” or “continue”, or the negative thereof or similar variations. Forward-looking statements in this news release include statements regarding the impact of Freda Lewis-Hall on the Scientific Advisory Committee and Board of Directors, and the Company’s plans to engineer proprietary drug discovery platforms, innovative drug delivery systems, novel formulation approaches and treatment regimens for mental health conditions.

These forward-looking statements are based on reasonable assumptions and estimates of management of the Company at the time such statements were made. Actual future results may differ materially as forward-looking statements involve known and unknown risks, uncertainties, and other factors which may cause the actual results, performance, or achievements of the Company to materially differ from any future results, performance, or achievements expressed or implied by such forward-looking statements. Such factors, among other things, include: fluctuations in general macroeconomic conditions; fluctuations in securities markets; expectations regarding the size of the NSA market; the ability of the Company to successfully achieve its business objectives; plans for growth; political, social and environmental uncertainties; employee relations; the presence of laws and regulations that may impose restrictions in the markets where the Company operates; implications of disease outbreaks on the Company's operations; and the risk factors set out in each of the Company's management's discussion and analysis for the three and nine month periods ended December 31, 2025, and the Company’s annual information form for the year ended March 31, 2025, which are available under the Company's profile on SEDAR+ at www.sedarplus.ca and with the U.S. Securities and Exchange Commission on EDGAR at www.sec.gov/edgar. Although the forward-looking statements contained in this news release are based upon what management of the Company believes, or believed at the time, to be reasonable assumptions, the Company cannot assure shareholders that actual results will be consistent with such forward-looking statements, as there may be other factors that cause results not to be as anticipated, estimated or intended. Readers should not place undue reliance on the forward-looking statements contained in this news release. The Company assumes no obligation to update the forward-looking statements of beliefs, opinions, projections, or other factors, should they change, except as required by law.

The Company makes no medical, treatment or health benefit claims about the Company’s proposed products. The U.S. Food and Drug Administration, Health Canada or other similar regulatory authorities have not evaluated claims regarding NSAs or HLP003, HLP004 and other programs of the Company. The efficacy of such products has not been confirmed by approved research. There is no assurance that the use of NSAs, HLP003, HLP004 or other programs of the Company can diagnose, treat, cure or prevent any disease or condition. Rigorous scientific research and clinical trials are needed. If Helus Pharma cannot obtain the approvals or research necessary to commercialize its business, it may have a material adverse effect on the Company’s performance and operations.

Neither Cboe Canada, nor the Nasdaq Global Market stock exchange, have approved or disapproved the contents of this news release and are not responsible for the adequacy and accuracy of the contents herein.

Investor Contact:
Josh Barer
astr partners
Managing Director
(908) 578-6478
josh.barer@astrpartners.com

George Tziras
Chief Business Officer
Helus Pharma
1-866-292-4601
irteam@helus.com – or – media@helus.com

Media Contact:
Johnny Tokarczyk
RXMD
Public Relations Director
jtokarczyk@rxmedyn.com
(914) 772-7562


FAQ**

How will Dr. Freda Lewis-Hall's extensive experience influence the development strategy for Cybin Inc. HELP's serotonergic agonist portfolio?

Dr. Freda Lewis-Hall's extensive experience in drug development and regulatory processes will enhance Cybin Inc.'s strategy for their serotonergic agonist portfolio by ensuring adherence to industry standards, optimizing clinical pathways, and facilitating strategic partnerships.

What specific regulatory engagement strategies will Cybin Inc. HELP pursue under Dr. Lewis-Hall's leadership to advance their clinical programs?

Under Dr. Lewis-Hall's leadership, Cybin Inc. HELP will adopt proactive regulatory engagement strategies, including early dialogue with regulatory agencies, tailored communication plans, and strategic partnerships to facilitate the advancement of their clinical programs.

How does Cybin Inc. HELP plan to differentiate its NSAs from existing mental health treatments in a competitive market?

Cybin Inc.'s HELP plan aims to differentiate its novel psychedelic-assisted therapies (NSAs) by focusing on personalized treatment protocols, leveraging advanced research in neurobiology, and integrating technology to enhance patient outcomes in the evolving mental health landscape.

What metrics will Cybin Inc. HELP use to measure the success of its drug candidates in clinical trials, especially under Dr. Lewis-Hall's scientific oversight?

Cybin Inc. will measure the success of its drug candidates in clinical trials through key metrics such as efficacy, safety, pharmacokinetics, patient-reported outcomes, and overall tolerability, all under the scientific oversight of Dr. Lewis-Hall.

**MWN-AI FAQ is based on asking OpenAI questions about Contakt World Technologies Corp. (CNQC: HELP:CC).

Contakt World Technologies Corp.

NASDAQ: HELP:CC

HELP:CC Trading

2.63% G/L:

$0.195 Last:

188,988 Volume:

$0.225 Open:

mwn-app Ad 300

HELP:CC Latest News

HELP:CC Stock Data

$436,573,646
48,576,926
N/A
39
15890%
Biotechnology & Life Sciences
Healthcare
CA
Toronto

Subscribe to Our Newsletter

Link Market Wire News to Your X Account

Download The Market Wire News App