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To save his brother's life, Harvard graduates tailored gene therapy for him

 Last Update: 2022-09-09
 Source: Internet
 Author: User

▎ WuXi AppTec content team editor

On August 9, 2022, Cure Rare Disease (CRD), a Boston-based nonprofit organization, announced that the FDA had approved its IND application for a CRISPR gene-edited therapy called CRD-TMH-001 for the treatment of Duchenne muscular dystrophy (DMD

Richard Hogan (Image source: Cure Rare Disease official website)

In 2019, he teamed up with the University of Massachusetts School of Medicine, Yale University, and other institutions to build a team

Terry's condition was also caused

Image credit: 123RF

To reduce the body's response to the virus, Terry also needs to take immunosuppressants

As WuXi AppTec's CTDMO focused on cell and gene therapies, WuXi Biotech is committed to accelerating and transforming the development, testing, production and commercialization of gene and cell therapies and other high-end therapies

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