** Shares of drug developer Precision BioSciences DTIL.O rise 6% to $4 premarket
** Co receives the U.S. FDA's clearance to begin testing its experimental therapy, PBGENE‑DMD, for Duchenne muscular dystrophy, a muscle‑wasting condition that weakens the heart
** PBGENE‑DMD aims to fix the underlying genetic error with one‑time treatment; pre-clinical data showed restored muscle protein production and improved muscle function, co says
** The early‑to‑mid‑stage study will enroll boys with common DMD mutations at U.S. sites; initial data expected end‑2026 - Co
** Shares rose ~9% in 2025
(Reporting by Sahil Pandey in Bengaluru)
((Sahil.Pandey@thomsonreuters.com))