AbbVie says EU CHMP backs Rinvoq approval for non-segmental vitiligo

AbbVie, Inc.

AbbVie, Inc.

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  • AbbVie won a positive CHMP opinion backing EU approval of Rinvoq (upadacitinib) 15 mg for adults, adolescents with non-segmental vitiligo.
  • EU Commission decision expected in coming months; clearance would position Rinvoq as the first systemic medicine for the condition.
  • Phase 3 Viti-Up studies met co-primary endpoints at week 48: T-VASI 50 total-body repigmentation, F-VASI 75 facial repigmentation.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. AbbVie Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: 202606290300PR_NEWS_USPR_____CG93459) on June 29, 2026, and is solely responsible for the information contained therein.

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