A framework for sponsors and the FDA to discuss ways to extrapolate existing data to support a new cell therapy could cut the time to approval.
The Center for Biologics Evaluation and Research is receptive to the idea of creating a regulatory framework on data extrapolation techniques to support the development of next-generation oncologics, CBER Senior Science Advisor Ingrid Markovic said during a Friends of Cancer Research webinar on 8 March.
Markovic, who is a CMC policy lead in the CBER Office of the Center Director, promised to “take back” a...
In what could amount to a de facto enforcement mechanism, the new draft guidance also “strongly encourages” sponsors to share details about their diversity action plan and enrollment goals with the public.
Long-term follow-up requirements have taken a conservative approach but could be ripe for re-examination and global harmonization given the years of experience with the products, Kite Pharma executive director says; former FDA gene/cell therapy office head Wilson Bryan calls for elimination of the classwide REMS.
Program for collaborative reviews of gene therapy applications is getting under way with the European Medicines Agency. After launch, the pilot could be expanded to earlier discussions around CMC and pharm/tox data requirements, FDA’s Nicole Verdun said.
