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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT02066389

Public ClinicalTrials.gov record NCT02066389. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 11, 2026, 6:57 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Investigate the Safety and Efficacy of ABT-494 With Background Methotrexate (MTX) in Subjects With Active Rheumatoid Arthritis (RA) Who Have Had an Inadequate Response to MTX Alone

Study identification

NCT ID
NCT02066389
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Upadacitinib Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 100 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 25, 2014
Primary completion
Jul 1, 2015
Completion
Jul 1, 2015
Last update posted
Jul 29, 2021

2014 – 2015

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
C.V. Mehta MD, Med Corporation /ID# 126380 Hemet California 92543
Omega Research Consultants, LLC /ID# 125780 DeBary Florida 32713-2260
Lovelace Scientific Resources /ID# 127324 Venice Florida 34292
North Georgia Rheumatology Grp /ID# 125779 Lawrenceville Georgia 30045
PRN Professional Research Network of Kansas, LLC /ID# 126148 Wichita Kansas 67205
The Center for Rheumatology & /ID# 127323 Wheaton Maryland 20902
Summit Medical Group /ID# 125776 Clifton New Jersey 07012
Arthritis and Osteo Assoc /ID# 134994 Las Cruces New Mexico 88011
Altoona Ctr Clinical Res /ID# 125777 Duncansville Pennsylvania 16635
Emkey Arthritis and Osteo Clin /ID# 134716 Wyomissing Pennsylvania 19610
Accurate Clinical Research /ID# 126535 Houston Texas 77034
Mountain State Clinical Resear /ID# 127089 Clarksburg West Virginia 26301

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02066389, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 29, 2021 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02066389 live on ClinicalTrials.gov.

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