FDA approves Icotyde for moderate-to-severe plaque psoriasis

The U.S. Food and Drug Administration has approved Johnson & Johnson’s Icotyde (icotrokinra), an interleukin-23 (IL-23) receptor antagonist, for the treatment of moderate-to-severe plaque psoriasis in adults and pediatric patients aged 12 years and older.

This article was originally published on MedicalXpress.com

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