EP3662912A1 — Improved dosages of eteplirsen for treating duchenne muscular dystrophy
Assigned to Sarepta Therapeutics Inc · Expires 2020-06-10 · 6y expired
What this patent protects
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.
USPTO 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.
Drugs covered by this patent
- Exondys 51 (ETEPLIRSEN) · Sarepta
Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.
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