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Dyne Therapeutics' drug met trial goals for Duchenne muscular dystrophy, boosting dystrophin and paving way for U.S. approval by 2027.
Dyne Therapeutics' stock rose after its drug z-rostudirsen met the primary endpoint in a Phase 1/2 trial for Duchenne muscular dystrophy, showing a 5.46% increase in dystrophin levels and functional improvements.
The company plans to file for U.S. accelerated approval in Q2 2026, with a potential launch in early 2027.
Meanwhile, givinostat was approved in Scotland for children with DMD, marking a major step in treatment access.
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El medicamento de Dyne Therapeutics cumplió con los objetivos de prueba para la distrofia muscular de Duchenne, aumentando la distrofina y allanando el camino para la aprobación de EE. UU. para 2027.