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Ilumya FDA Approval History

FDA Approved: Yes (First approved March 20, 2018)
Brand name: Ilumya
Generic name: tildrakizumab-asmn
Dosage form: Injection
Company: Sun Pharmaceutical Industries Inc.
Treatment for: Plaque Psoriasis

Ilumya (tildrakizumab-asmn) is a humanized, anti-IL-23p19 monoclonal antibody for the treatment of moderate-to-severe plaque psoriasis.

Development timeline for Ilumya

Mar 21, 2018Approval FDA Approves Ilumya (tildrakizumab-asmn) for the Treatment of Moderate-to-Severe Plaque Psoriasis
May 24, 2017Sun Pharma Announces US FDA Filing Acceptance of Biologics License Application (BLA) For Tildrakizumab

Further information

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