Santhera to discontinue Phase 3 SIDEROS study and development of Puldysa® in Duchenne Muscular Dystrophy (DMD) and focus on vamorolone. Original Press Release > Pratteln, Switzerland, October [...]
Pfizer receives FDA fast track designation for Duchenne muscular dystrophy (DMD) investigational gene therapy. Official press release > NEW YORK–(BUSINESS WIRE) Pfizer Inc. announced [...]