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AbbVie has sought approval from the European Medicines Agency (EMA) for risankizumab (Skyrizi, 600 mg intravenous (IV) induction and 360 mg subcutaneous (SC) maintenance therapy), to treat patients who are 16 years and above suffering with moderate to...
Phase III trial data shows more than half of patients with moderate to severe Crohn’s disease treated with risankizumab (Skyrizi®) 360mg achieved clinical remission in a year.