RINVOQ® (upadacitinib) is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC) who have had an inadequate score, lost response or were intolerant to either conventional therapy or a biologic agent.1
▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.
Additional prespecified endpoint,
not controlled for multiplicity.
*Bio-naïve defined as without prior biologic failure and includes patients who had previous exposure to biologics but did not experience treatment failure.
†Bio-failure refers to prior treatment failure to at least 1 biologic therapy.
Deep mucosal healing: ESS of 0 and a Geboes score of <2.1
ESS: endoscopic subscore; QD: once daily.
REFERENCES
- RINVOQ Summary of Product Characteristics.
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[Affiliates to insert local adverse events reporting websites]
ALL-RNQG-220224 Date of preparation: February 2024
Adverse events should also be reported to AbbVie on GBPV@abbvie.com