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Priovant nabs first FDA approval for targeted tablet in dermatomyositis

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FDA approves Priovant's Lisraya for rare inflammatory disorder dermatomyositis

The FDA approved Roivant Sciences subsidiary Priovant Therapeutics' Lisraya as a once-daily pill treatment for dermatomyositis, a rare inflammatory disorder. The drug was licensed from Pfizer.

Aug 28, 2026·3 sourcesFDA drug approval
FDA approves Priovant's Lisraya for rare inflammatory disorder dermatomyositis
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Other sources for this story

BioPharma Dive

FDA green lights Priovant drug for rare skin disease

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FDA Nod for Inflammation Drug Notches Wins for Rare Disease Patients, Roivant’s Biz Strategy - MedCity News

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