Helus Pharma Appoints Dr. Freda Lewis-Hall to Board and Scientific Advisory Committee Chair
February 24th, 2026 2:45 PM
By: Newsworthy Staff
Helus Pharma has appointed Dr. Freda Lewis-Hall, a veteran biopharmaceutical leader with over 40 years of experience including a decade as Pfizer's chief medical officer, to its board of directors and as chair of its Scientific Advisory Committee, strengthening governance as the company advances novel serotonergic agonist programs targeting serious mental health conditions.

Helus Pharma announced the appointment of Dr. Freda Lewis-Hall, DFAPA, MFPM, to its board of directors, where she will also serve as chair of the company’s Scientific Advisory Committee, subject to approval by Cboe Canada. Dr. Lewis-Hall brings more than 40 years of experience across clinical care, research, academia and senior biopharmaceutical leadership, including more than a decade on Pfizer’s executive leadership team as executive vice president and chief medical officer, as well as leadership roles at Vertex Pharmaceuticals, Bristol Myers Squibb, Pharmacia Corporation and Eli Lilly and Company. A Distinguished Fellow of the American Psychiatric Association and former advisor to the National Institute of Mental Health, she will provide scientific, clinical and regulatory governance across Helus’ portfolio as the company advances its novel serotonergic agonist programs targeting serious mental health conditions.
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.
The appointment of Dr. Lewis-Hall represents a significant strengthening of Helus Pharma’s leadership as it progresses its clinical pipeline. Her extensive experience in both clinical development and regulatory affairs at major pharmaceutical companies provides critical expertise for navigating the complex approval pathways for mental health treatments. This move signals Helus Pharma’s commitment to rigorous scientific oversight as it advances treatments for conditions where current options remain inadequate for many patients. The company’s focus on novel serotonergic agonists represents a distinct approach to mental health treatment that differs from traditional antidepressants, potentially offering new mechanisms of action for patients who don’t respond to existing therapies.
Source Statement
This news article relied primarily on a press release disributed by InvestorBrandNetwork (IBN). You can read the source press release here,
