drugset / Trial / NCT02066389

A Study Investigating the Efficacy and Safety of Upadacitinib (ABT-494) Given With Methotrexate (MTX) in Adults With Rheumatoid Arthritis Who Have Had an Inadequate Response to MTX Alone

NCT02066389 ↗

Phase 2 Completed 300 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study was to compare the safety and efficacy of multiple doses of upadacitinib versus placebo in adults with moderately to severely active rheumatoid arthritis (RA) on stable background methotrexate therapy who had not shown an adequate response to methotrexate alone.

Timeline

Start
2014-03-26
Primary completion
2015-07-02
Completion
2015-07-02

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Upadacitinib 6 mg BID; p = 0.018; Chi-squared; note: Statistical tests were 1-sided at a significance level of 0.05. NCT02066389 ↗

release “BALANCE-I and BALANCE-II achieved ACR20 at week 12 across all dose levels, except the lowest dose in BALANCE-II.” abbvie.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Upadacitinib Small molecule 3 mg Oral
Subject Upadacitinib Small molecule 6 mg Oral
Subject Upadacitinib Small molecule 12 mg Oral
Subject Upadacitinib Small molecule 18 mg Oral
Subject Upadacitinib Small molecule 24 mg Oral

Indications