Sarepta Therapeutics, Inc.
Compositions for treating muscular dystrophy
Last updated:
Abstract:
Improved compositions and methods for treating muscular dystrophy by administering antisense molecules capable of binding to a selected target site in the human dystrophin gene to induce exon skipping are described.
Status:
Grant
Type:
Utility
Filling date:
24 May 2017
Issue date:
30 Jul 2019