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Rocket Pharmaceuticals withdrew its U.S. gene therapy application for Fanconi anemia to focus on cardiovascular programs and clearer regulatory paths.
Rocket Pharmaceuticals has voluntarily withdrawn its U.S. Biologics License Application for RP-L102, a gene therapy for Fanconi anemia, citing strategic shifts to focus on cardiovascular programs and clearer regulatory paths.
The decision, based on business considerations rather than safety or efficacy, follows the therapy's promising Phase 2 results and prior withdrawal of its European application.
The company ceased internal development, laid off about 30% of staff, and is now prioritizing its Danon disease therapy, RP-A501, after resuming trials post-FDA hold lift.
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Rocket Pharmaceuticals retiró su solicitud de terapia génica de EE. UU. para la anemia de Fanconi para centrarse en programas cardiovasculares y vías regulatorias más claras.