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Sarepta resumes shipments of Duchenne treatment Elevidys for walking patients after FDA review.
Sarepta Therapeutics has been permitted by the FDA to resume shipments of its Duchenne muscular dystrophy treatment, Elevidys, for patients who can still walk.
The company had paused shipments following the deaths of two teenagers, but the FDA concluded that an 8-year-old's recent death was unrelated to the treatment.
Sarepta will continue to work with the FDA on safety measures for patients who cannot walk.
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Sarepta reanuda los envíos del tratamiento de Duchenne Elevidys para pacientes caminantes después de la revisión de la FDA.