FDA nod for Regeneron’s Pasatru for ultra-rare genetic disorder FOP
The US Food and Drug Administration (FDA) has granted approval for Regeneron Pharmaceuticals’ (Nasdaq: REGN) Pasatru (garetosmab-grts) to reduce formation of new heterotopic ossification (HO) lesions and clinician-assessed flare-ups in adults with fibrodysplasia ossificans progressiva (FOP).
The company’s shares closed up 3.8% at $840.84 following the announcement yesterday.
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