FDA Accepts Mesoblast’s Biologics License Application (BLA) for Ryoncil® in Children With Steroid-Refractory Acute Graft-Versus-Host Disease (SR-aGVHD)

July 24, 2024

https://www.globenewswire.com/news-release/2024/07/23/2917127/0/en/FDA-Accepts-Mesoblast-s-Biologics-License-Application-BLA-for-Ryoncil-in-Children-With-Steroid-Refractory-Acute-Graft-Versus-Host-Disease-SR-aGVHD.html

NEW YORK, July 23, 2024 (GLOBE NEWSWIRE) — Mesoblast Limited (Nasdaq:MESO; ASX:MSB), global leader in allogeneic cellular medicines for inflammatory diseases, announced that the United States Food and Drug Administration (FDA) has accepted its Biologics License Application (BLA) resubmission for Ryoncil® (remestemcel-L) in the treatment of children with steroid-refractory acute graft versus host disease (SR-aGVHD). FDA considers the resubmission to be a complete response and Mesoblast anticipates a decision on or before the FDA’s Prescription Drug User Fee Act (PDUFA) goal date of January 7, 2025.

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