Agreement leverages Ubiquigent’s DUB-focused drug discovery platform to support the development of novel therapeutic candidates for multiple disease targets selected by Nanna Therapeutics.
FDA’s Peter Marks overrode reviewers’ call to reject Sarepta’s new Duchenne gene therapy
Peter Marks, the senior FDA official who oversees the regulation of gene therapies, overrode agency reviewers’ decision to reject Sarepta Therapeutics’ Duchenne muscular dystrophy gene