The FDA’s Oncologic Drugs Advisory Committee will meet on Thursday, August 13, to
review and discuss Mesoblast Limited’s (
MESO +5.9%) marketing application for Ryoncil (remestemcel-L) for the treatment of children with steroid-refractory acute graft versus host disease (GvHD).
Under Priority Review status, the agency’s action date is September 30.
Ryoncil is an allogeneic mesenchymal stem cell product derived from bone marrow.
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