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Sarepta options Duke's CRISPR/Cas9 IP for DMD
03 Nov 2017
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
- Pharmaceuticals
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Biotechnology
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Drug Discovery Tools
- Genomics-Proteomics
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Drug Discovery Tools
Deal Status
- Final
Deal Type
-
Alliance
- R&D and Marketing (Licensing)
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