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FAST to Advance Gene Therapy Candidate through IND-Enabling Studies Conducted in Partnership with the University of Pennsylvania

The Foundation for Angelman Syndrome Therapeutics (FAST) announced today that the non-profit organization has entered into an exclusive global collaborative research and development agreement with the University of Pennsylvania to develop an investigational adeno-associated virus (AAV) gene therapy for Angelman syndrome (AS).

Angelman syndrome is a rare neurogenetic disorder that is estimated to impact approximately 1 in 15,000 births, or potentially 500,000 individuals world-wide, and is associated with developmental delay, lack of verbal speech, seizures, profound sleep disorder, and motor impairments, among other serious symptoms. There is currently no approved therapy to treat Angelman syndrome in any country making the unmet medical needs for patients significant.

FAST has sponsored preclinical research studies at the Gene Therapy Program (GTP) at the University of Pennsylvania (Penn) since 2017 towards the development of a central nervous system (CNS)-delivered gene therapy for Angelman syndrome. A robust package of preclinical data now support the further advancement of a human clinical candidate through the final investigational new drug application (IND)-enabling studies that are required for first-in-human clinical trials. This updated and expanded collaborative agreement builds upon the original research funding provided by FAST to Penn and enables FAST to work more closely in partnership with the Penn team to further accelerate the advancement of the candidate towards a clinical trial for individuals living with AS.

“We have been working toward this ‘go or no-go decision’ since 2017,” said Allyson Berent, DVM, DACVIM, Chief Science Officer of FAST. “To see the promising results of this robust preclinical data package, based on research that FAST has been so diligently funding for years, is incredibly gratifying. It is our job to ensure that excellent science is always advanced as safely and efficiently as possible, and that we seize every opportunity to potentially benefit those living with Angelman syndrome. Our priorities will never change.”

“Our collaboration with the team at FAST, and the entire Angelman syndrome community, has been incredibly productive and rewarding, since its inception,” said Jim Wilson, MD, PhD, director of the Gene Therapy Program, the Rose H. Weiss Professor and director at the Orphan Disease Center, and a professor of Medicine and Pediatrics in the Perelman School of Medicine at the University of Pennsylvania.  “Our two teams have been both mission and data driven, working closely together to reach this critical inflection point, and FAST and GTP have made an instrumental decision on a promising human clinical candidate to further advance this investigational gene therapy forward quickly and safely for the potential treatment of Angelman syndrome.” 

ABOUT FAST

FAST is the largest research funding organization in the world for Angelman syndrome. Our goal is to bring practical treatments into current medical practice as quickly and safely as possible. It is our hope that programs we fund will lead to additional research support from government agencies, other funding sources and organizations around the globe.

Read the FAQs about this partnership here.

Disclaimer

This website contains information for a broad audience and may include information on current and upcoming programs that are not yet approved or accessible The information provided is for general informational purposes only and is not intended as medical advice, diagnosis, or treatment. While FAST strives to provide accurate and up-to-date information, the content on this site may not always reflect the most current research or clinical guidelines. The inclusion of clinical trial information, treatments or specific healthcare providers does not imply endorsement, recommendation or guarantee of safety, efficacy, or availability. Reliance on any information provided by this website is solely at your own risk. FAST disclaims any liability for any errors or omissions in the information provided or for any decisions made based on this information. For personalized medical advice or specific health concerns including participation in any clinical trial, please consult a qualified healthcare professional.