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March 17, 2026

FDA accepts Sun Pharma’s Ilumya sBLA for psoriatic arthritis

The US Food and Drug Administration (FDA) has accepted for review Sun Pharmaceutical’s supplemental biologics licence application (sBLA) submitted for Ilumya (tildrakizumab-asmn) to treat adults with active psoriatic arthritis.

FDA accepts Sun Pharma’s Ilumya sBLA for psoriatic arthritis