Skip to main content
Donate

Voice of the Patient Report Submitted: A Powerful Milestone for the Angelman Syndrome Community

We are proud to announce that the Voice of the Patient Report from the Externally-Led Patient-Focused Drug Development (EL-PFDD) Meeting on Angelman Syndrome has been officially submitted to the U.S. Food and Drug Administration (FDA).

Hosted by ASF and FAST, this meeting brought together hundreds of families, caregivers, researchers, clinicians, FDA representatives, and industry partners to spotlight the urgent, unmet needs of people living with Angelman syndrome. This powerful report captures the lived experiences of individuals with Angelman syndrome and their families.

This milestone reflects the strength of the Angelman syndrome community—a community that continues to drive science forward and ensure decision makers have the knowledge needed to bring meaningful treatments to life.

Read the full Voice of the Patient Report

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.