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Muscular dystrophy drugs face new FDA questions

from The Wall Street Journal

Hopes are dimming that the drug industry will be able to quickly deliver a treatment for one of the most keenly researched diseases of recent years — an inherited muscle-wasting disorder called Duchenne muscular dystrophy. Advances in understanding the disease sparked a research and development boom in recent years, and fueled excitement that boosted some small companies’ stock prices. more


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