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FDA Approves Subcutaneous Induction for Skyrizi in Crohn's Disease
The approval adds an on-body injector option after Phase 3 results showed superior remission and endoscopic response at week 12, the company said.
Summary by pharmexec.com
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4 Articles
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U.S. FDA Approves Subcutaneous Induction Regimen for AbbVie's SKYRIZI® (risankizumab-rzaa) for Adults With Moderately to Severely Active Crohn's Disease
Now with a new route of induction administration, subcutaneous SKYRIZI supports early symptomatic and endoscopic control with an on-body injector (OBI) device throughout the course of treatmentIn the pivotal Phase 3 AFFIRM study, subcutaneous (SC) SKYRIZI® achieved superior clinical remissioni…
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Leaning Left0Leaning Right1Center2Last Updated67% Center
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- 67% of the sources are Center
67% Center
C 67%
R 33%
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