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