drugset / Trial / NCT02675426

A Study Comparing Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid Arthritis on a Stable Dose of Conventional Synthetic Disease-Modifying Antirheumatic Drugs (csDMARDs) Who Have an Inadequate Response to csDMARDs Alone

NCT02675426

Phase 3 Completed 661 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objectives of this study are to compare the efficacy, safety, and tolerability of upadacitinib 30 mg once daily (QD) and 15 mg QD versus placebo for the treatment of signs and symptoms of adults with moderately to severely active rheumatoid arthritis who were on a stable dose of csDMARDs and had an inadequate response to csDMARDs.

Timeline

Start
2015-12-17
Primary completion
2017-04-21
Completion
2022-03-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Upadacitinib Small molecule 15 mg Oral
Subject Upadacitinib Small molecule 30 mg Oral

Indications