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Melbourne-based biotech, Mesoblast Limited MESO announced the FDA acceptance of the resubmission of its biological license application (BLA) for remestemcel-L for the treatment of pediatric steroid-refractory acute graft versus host disease (SR-aGVHD). The FDA considered the resubmission of a complete response and granted priority review designation to the BLA. The FDAâs decision is expected on Aug 2, 2023. Shares of the company were up 24% on Wednesday, following the news.
In the past yea...
>>> Read more: Mesoblast's (MESO) GVHD Drug BLA Gets FDA Priority Tag, Stock Up
In the past yea...
>>> Read more: Mesoblast's (MESO) GVHD Drug BLA Gets FDA Priority Tag, Stock Up