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On April 27, 2026, AbbVie filed a supplemental Biologics License Application (sBLA) with the U.S. FDA for a subcutaneous (SC) induction dosing regimen of its top-selling immunology asset SKYRIZI for adults with moderately to severely active Crohn’s disease (CD), supported by positive Phase 3 AFFIRM
AbbVie Inc. (ABBV) Submits SKYRIZI Subcutaneous Crohn’s Regimen to FDA, But Near-Term Upside Remains Capped By Competitive Risks - Sector Underperform
ABBV - Stock Analysis
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