On March 12, the CDE website indicated that a new indication for AbbVie's Upadacitinib extended-release tablets is being considered for priority review. The proposed use is for the treatment of non-segmental vitiligo in adults and adolescents aged 12 and above. Upadacitinib is a selective JAK inhibitor and a key product for AbbVie, with global sales reaching $8.304 billion in 2025, a 39.07% increase.
The priority review application pertains to a new indication: non-segmental vitiligo in adults and adolescents aged 12 and above. Regarding this indication, in February of this year, AbbVie announced that it had submitted a new application to the U.S. FDA and the European EMA for the use of Upadacitinib in treating non-segmental vitiligo (NSV) in adults and adolescents.
Comments