Drug Profile

Research programme: gene therapies - CANbridge Pharmaceuticals/University of Washington School of Medicine

Latest Information Update: 28 Dec 2025

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At a glance

Orphan Drug Status

Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

No
New Molecular Entity No

28 Dec 2025 No recent reports of development identified for research development in Duchenne muscular dystrophy in USA (Parenteral)
22 Mar 2022 CANbridge Pharmaceuticals intends to announce pre-clinical lead candidate in Duchenne muscular dystrophy, in 2023
01 Nov 2021 CANbridge Pharmaceuticals and University of Washington School of Medicine agree to develop gene therapies for Duchenne muscular dystrophy

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