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Roche: priority review in Duchenne myopathy

(CercleFinance.com) - Sarepta Therapeutics announced on Monday that the US FDA haz granted a priority review to its marketing application for SRP-9001, an experimental gene therapy for boys with Duchenne muscular dystrophy that the company is developing in collaboration with Roche.


In its statement, the US biotech said the health agency has set a target date of 29 May 2023 for the product's approval.

In December 2019, Roche entered into a partnership with Sarepta for the moxeparvovec delandistrogen gene therapy (SRP-9001) aimed at accelerating its availability outside the US.


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