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AbbVie seeks FDA and EMA approval for Rinvoq to treat non-segmental vitiligo, a first-of-its-kind systemic treatment.
AbbVie has submitted applications to the FDA and EMA for expanded approval of Rinvoq to treat non-segmental vitiligo in adults and adolescents.
If approved, it would be the first systemic medication for this chronic autoimmune condition, which causes symmetrical depigmentation.
The drug is already approved for other autoimmune diseases and is projected to generate over $11 billion in revenue by 2027.
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AbbVie solicita la aprobación de la FDA y de la EMA para Rinvoq para tratar el vitiligo no segmental, un tratamiento sistémico de primera clase.