Urge the FDA to Say YES to Accelerated Approval For Therapies For Duchenne.

March 7, 2014

We urge the Food and Drug Administration (FDA) to use the Accelerated Approval pathway for approval and access to safe, effective therapies for Duchenne Muscular Dystrophy – the leading genetic killer of children that impacts 1 out of every 3,500 boys born in the United States. It’s time for the FDA to Say Yes and make this the first generation of Duchenne survivors.

Please sign the petition here.

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