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Sarepta options Duke's CRISPR/Cas9 IP for DMD

Executive Summary

Sarepta Therapeutics Inc. is working with Duke University to develop a treatment for Duchenne muscular dystrophy (DMD) and gains an option to exclusively license the university’s CRISPR/Cas9 gene editing technology in this indication. DMD is a rare muscle-wasting disease caused by a mutation in the dystrophin gene (an essential protein involved in muscular function).
Deal Industry
  • Biotechnology
    • Drug Discovery Tools
      • Genomics-Proteomics
  • Pharmaceuticals
Deal Status
  • Final
Deal Type
  • Alliance
    • R+D and Marketing-Licensing

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