drugset / Trial / NCT02706873

A Study to Compare Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Monotherapy in Adults With Rheumatoid Arthritis (RA) Who Have Not Previously Taken Methotrexate

NCT02706873

Phase 3 Completed 1002 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objectives of Period 1 were the following: * To compare the safety and efficacy of upadacitinib 7.5 mg once daily (QD) monotherapy (for participants in Japan only), 15 mg QD monotherapy, and 30 mg QD monotherapy versus weekly methotrexate monotherapy for the treatment of signs and symptoms of RA in methotrexate-naïve adults with moderately to severely active RA; * To compare the efficacy of upadacitinib 15 mg QD monotherapy and upadacitinib 30 mg QD monotherapy versus weekly methotrexate monotherapy for prevention of structural progression in methotrexate-naïve adults with moderately to severely active RA. The objective of Period 2 is to evaluate the long-term safety, tolerability, and efficacy of upadacitinib 7.5 mg QD (for participants in Japan only), 15 mg QD, and 30 mg QD in adults with RA who have completed Period 1.

Timeline

Start
2016-02-23
Primary completion
2018-03-15
Completion
2022-11-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Methotrexate Small molecule 7.5 mg Oral
Comparator Methotrexate Small molecule 10 mg Oral
Subject Upadacitinib Small molecule 7.5 mg Oral
Subject Upadacitinib Small molecule 15 mg Oral
Subject Upadacitinib Small molecule 30 mg Oral

Indications