Patient and care partner perspectives on safety considerations for approved gene therapy treatments for rare diseases (from Catapult’s regulatory round-up for November 2024)
The FDA Center for Biologics Evaluation and Research (CBER) hosted a public patient listening meeting on the 20th September 2024 and opened a docket to better understand patient and care partner perspectives on safety considerations and long term follow-up for approved gene therapy treatments for rare diseases. The video recording of this meeting is available here.
Published on the 3rd of december 2024. Read the entire Regulatory Round-up – November 2024 here.
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adelage (12 février 2025). Patient and care partner perspectives on safety considerations for approved gene therapy treatments for rare diseases (from Catapult’s regulatory round-up for November 2024). ELSIBI. Consulté le 18 mars 2025 à l’adresse https://doi.org/10.58079/13axm