The company expects the trial to support the submission of a biologics license application with the US Food and Drug Administration in 2026.
Regenxbio is pushing its Duchenne muscular dystrophy gene therapy into pivotal development, with a BLA planned for ...
A small trial of an experimental vaccine has shown promising results for patients with the most aggressive type of breast ...
RegenxBio has revealed plans to submit a biologics licence application (BLA) for RGX-202, its investigational gene therapy ...
In mice with muscular dystrophy, the treatment restored large therapeutic muscle proteins to normal levels, the researchers ...
Regenxbio’s investigational gene therapy improved muscle function for patients with Duchenne muscular dystrophy (DMD) in a phase 1/2 study. | Regenxbio’s investigational gene therapy improved muscle ...