FDA Patient and Care Partner Perspectives on Early Enrollment into Gene Therapy Clinical Trials for Rare Diseases (Catapult’s regulatory round-up – October 2024)
CBER will host a public patient listening meeting to better understand patient and carer perspectives on enrollment of rare disease patients into gene therapy clinical trials in the pre-symptomatic or early symptomatic stages of their disease. The aim of this meeting is to explore what patients, and caregivers of patients in the pre-symptomatic or early stages of disease take into consideration when deciding whether to enroll in a gene therapy clinical trial and potentially receive an investigational gene therapy product. The meeting is on 4th December 2024, Please find further information including how to register here.
Text published on the 5th of November 2024 in Catapult’s Regulatory Round-up – October 2024 (catapult.org.uk).
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adelage (19 novembre 2024). FDA Patient and Care Partner Perspectives on Early Enrollment into Gene Therapy Clinical Trials for Rare Diseases (Catapult’s regulatory round-up – October 2024). ELSIBI. Consulté le 16 janvier 2025 à l’adresse https://doi.org/10.58079/12ps8