
Capricor and Replimune prep for FDA adcomms, Q2 earnings roll on, Sarepta’s new leader, more
FDA advisory committee meetings are dominating the biopharma landscape, with the agency challenging the trial data for Capricor’s Duchenne muscular dystrophy therapy and questioning the sufficiency of Replimune’s single-arm study for melanoma. Meanwhile, the second-quarter earnings season is underway, highlighted by GS...




















