Updated: Feb 27, 2020

Reglagene is delighted to add Sharon Ayd, PhD, MBA to its Board of Directors. In Dr. Ayd’s 30-year career, she has gained experience commercializing pharmaceuticals from discovery to clinical evaluation, expanded core businesses, and transformed pharmaceutical business operations. Her career began as a research scientist for Baxter International. She went on to serve in a variety of executive positions at companies including Apotex Inc., Hospira (now Pfizer), Fresenius-Kabi, Transcend Therapeutics, Advanced Life Sciences, and Pinnacle Biologics. Dr. Ayd is an industry expert in regulatory strategy and pharmaceutical operations. She has led the regulatory affairs activity for many due diligence projects, resulting in product licensing, mergers and acquisitions, and divestitures. Under her leadership, ~100 drug application approvals (original and supplements) have been obtained. Dr. Ayd holds an MBA from Lewis University and a PhD from the University of Illinois at Chicago in Biopharmaceutical Sciences, and she is an alumnus of Women In Bio’s inaugural class in its Boardroom Ready program, a foundational resource to prepare executive women for service on corporate boards.

Updated: Feb 27, 2020

Glioblastoma Multiforme (GBM) is the most commonly diagnosed brain cancer in adults. It is insidiously aggressive and is the disease that so quickly took the life of Arizona Senator John McCain. Reglagene’s approach to targeting the TERT gene offers new hope for a better therapy. The TERT gene is mutated in 80% of GBM patients. Patients presenting with the mutated gene have a median survival of 10 months, compared with 20 months for patients presenting with the normal gene. The National Institute of Neurological Disorders and Stroke (NINDS) notified Reglagene of a $400,000 STTR small-business award on April 5, 2019, to enable application of its novel TERT gene-targeting technology to discover and develop a new therapy for GBM. Reglagene’s partner in this effort is Dr. Michael Berens, Professor and Director, Cancer and Cell Biology Division at The Translational Genomics Research Institute (TGen). The Principal Investigator on the award is Reglagene’s CSO Dr. Laurence Hurley.

The envisioned therapeutic agent leverages the action of DNA quadruplex structures to selectively attenuate expression of the TERT gene. Distinguishing the GBM program from Reglagene’s effort to apply this same technology to prostate cancer is that the targeted therapeutic agent must access the brain. This difference is substantial and will require a therapeutic agent with unique characteristics. Successful product development will provide a new therapy for GBM, a disease that has seen limited progress in treatment paradigms over the last several years.

Updated: Feb 27, 2020

Reglagene was one of 10 companies selected out of more than 300 applicants to pitch leaders from across Johnson & Johnson Innovation during the 2019 J.P. Morgan Healthcare Conference. JPM Week occurs annually in January and is the largest gathering of the pharma, biotech, and investor sectors. Johnson & Johnson Innovation launched the Quick Pitch to unearth the unseen and brightest innovations in healthcare. During the event on January 9, 2019, Reglagene made a tightly woven and compelling presentation that also served as the basis for conversations with prospective investors and pharmaceutical partners throughout the week. After the presentation, Johnson & Johnson awarded Reglagene a trophy for its participation. Reglagene’s CSO Laurence Hurley and CEO Richard Austin proudly pose with the prize.


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