UAE approves RINVOQ for vitiligo
Analysis based on 11 articles · First reported Aug 17, 2026 · Last updated Aug 17, 2026
The approval expands AbbVie's market for RINVOQ into a new indication, potentially boosting sales and reinforcing its position in immunology. It also enhances the UAE's reputation as a hub for pharmaceutical innovation, which may attract further industry investment.
The United Arab Emirates — Emirates Drug Establishment (EDE) of the United Arab Emirates has approved the expanded use of RINVOQ (upadacitinib), an oral JAK inhibitor developed by AbbVie, for the treatment of non-segmental vitiligo in adults and adolescents aged 12 years and older whose condition requires systemic therapy. This approval makes the UAE the first country in the world to license an oral treatment for this indication, and RINVOQ becomes the first licensed oral therapy for this patient group. The decision reflects the UAE's advanced regulatory framework and commitment to accelerating access to innovative therapies. Vitiligo is a chronic autoimmune skin condition causing loss of pigmentation, affecting 0.5-1% of the global population. The approval provides a new once-daily oral option for eligible patients, complementing existing topical, phototherapy, and laser treatments.
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