Patent · US Active

Multiple exon skipping compositions for DMD

US8871918B2 · kind B2 · utility

64Cited by
48References
38Claims
0Family size

Assignee

Inventors

Key dates

Filing dateOct 23, 2009
Grant dateOct 28, 2014
Priority date
Expiry dateMar 23, 2030

Classification

  • Technology area (CPC C)Chemistry; Metallurgy
  • CPC primaryC12N2320/33
  • WIPO fieldBiotechnology
  • WIPO sectorChemistry

Abstract

Provided are antisense molecules capable of binding to a selected target site in the human dystrophin gene to induce exon skipping, and methods of use thereof to treat muscular dystrophy.

Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.