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FDA review of the apitegromab BLA will now proceed solely with the second fill-finish facility after the Catalent Indiana site was removed following an OAI classification. The PDUFA action date remains September 30, 2026, and the company states it is prepared for immediate U.S. launch upon approval.
Scholar Rock Announces FDA Review of Apitegromab Biologics License Application (BLA) for Spinal Muscular Atrophy (SMA) to Progress with Second Fill-Finish Facility; Approval Decision Anticipated by September 30, 2026 Action Date Scholar Rock Announces FDA Review of Apitegromab Biologics License Application (BLA) for Spinal Muscular Atrophy (SMA) to Progress with Second Fill-Finish Facility; Approval Decision Anticipated by September 30, 2026 Action Date Scholar Rock Announces FDA Review of Apitegromab Biologics License Application (BLA) for Spinal Muscular Atrophy (SMA) to Progress with Second Fill-Finish Facility; Approval Decision Anticipated by September 30, 2026 Action Date Today, August 7, 2026, Scholar Rock received customer notification from Catalent Indiana LLC (part of Novo Nor
Scholar Rock: FDA Fast Track + Orphan Drug cho apitegromab trong FSHD