FDA grants Acceleron’s ACE-031 orphan designation for treatment of DMD

Acceleron Pharma, Inc., a biopharmaceutical company developing novel therapeutics that modulate the growth of cells and tissues including , bone, fat, red blood cells and the vasculature, today announced the United States Food and Administration (FDA) granted orphan designation for ACE-031 for the treatment of Duchenne Muscular Dystrophy (DMD), a fatal neuromuscular disease in which patients experience a progressive loss of mass and strength. ACE-031 is an investigational therapeutic being developed to increase mass and strength.


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