CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 338 enrolled
Drug / intervention
Upadacitinib +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02955212
NCT02955212Phase 3Completed

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study With Upadacitinib (ABT-494) in Subjects From China and Selected Countries With Moderately to Severely Active Rheumatoid Arthritis Who Have Had an Inadequate Response to Conventional Synthetic Disease-Modifying Anti-Rheumatic Drugs (csDMARDs)

AbbVie·interventional·Posted Nov 4, 2016·Updated Sep 27, 2021

In Brief

A Phase 3 clinical trial evaluating Upadacitinib and Placebo for Rheumatoid Arthritis (RA). Completed, enrolled 338 participants across 43 sites in 3 countries.

Detailed Summary

The study objectives of Period 1 of this study were to compare the efficacy, safety, and tolerability of upadacitinib versus placebo for the treatment of signs and symptoms of subjects from China and selected countries including Brazil and South Korea with moderately to severely active rheumatoid arthritis (RA) who are on a stable dose of csDMARDs and have an inadequate response to csDMARDs. The study objective of Period 2 is to evaluate the long-term safety, tolerability, and efficacy of upadacitinib in subjects with RA who have completed Period 1.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBrazil, China, South Korea
Collaborators--

Timeline

Phase 3CompletedFinished
2017201820192020202120222023202420252026
First PostedNov 4, 2016
Enrollment StartJan 3, 2018
Primary CompletionAug 14, 2019
Study CompletionSep 3, 2020
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 9.7 years ago

Interventions

Upadacitinibdrug

Tablets for oral administration

Placebodrug

Tablets for oral administration