• FDA accepts Sarepta’s NDA for precision medicine Golodirsen pharmaceutical-technology
    February 18, 2019
    US precision medicine company Sarepta Therapeutics has announced the US Food and Drug Administration (FDA) has accepted its new drug application (NDA) for its Duchenne muscular dystrophy (DMD) drug Golodirsen (SRP-4053)....
PharmaSources Customer Service