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On October 15, 2021, AbbVie announced that the European Medicines Agency (EMA) Committee for Medicines for Human Use (CHMP) recommended to approve risankizumab (trade name Skyrizi) as a single drug or in combination with methotrexate (MTX).
Psoriatic arthritis is a heterogeneous, systemic inflammatory disease with hallmark manifestations in multiple systems (including joints and skin)
Risankizumab is an interleukin-23 (IL-23) inhibitor that selectively blocks IL-23 by binding to its p19 subunit
This positive opinion of CHMP is supported by two pivotal Phase 3 clinical trials
In terms of safety, the most common adverse reactions associated with risankizumab are upper respiratory tract infections, headaches, fatigue, injection site reactions and ringworm infections
Reference materials:
[1] AbbVie Receives CHMP Positive Opinion for Risankizumab (Skyrizi®) for the Treatment of Adults with Active Psoriatic Arthritis in the European Union (EU).
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