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A Study to Evaluate Efficacy and Safety of Upadacitinib in Adults With Axial Spondyloarthritis

Completed · Phase 3 · NCT04169373

Conditions: Spondyloarthritis

At a glance

Research payments reported, 2025
$21,170
U.S. investigators named
2
Sites paid
1
Planned or actual enrollment
734

About the trial

Sponsor
AbbVie
Tested
Upadacitinib (drug), Placebo (drug)
Dates
Started 2019-11-26; completion 2025-02-28
Results posted
Yes

This protocol includes 2 standalone studies with randomization, data collection, analysis and reporting conducted independently. The main objectives of this protocol are: * To evaluate the efficacy of upadacitinib compared with placebo on reduction of signs and symptoms in adults with active axial spondyloarthritis (axSpA) including biologic disease-modifying antirheumatic drug inadequate responders (bDMARD-IR) ankylosing spondylitis (AS) (Study 1) and non-radiographic axial spondyloarthritis (nr-axSpA) (Study 2). * To assess the safety and tolerability of upadacitinib in adults with active axSpA including bDMARD-IR AS (Study 1) and nr-axSpA (Study 2). * To evaluate the safety and tolerab…

From ClinicalTrials.gov, last updated 2026-02-24. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $21,170 in research payments for this study in 2025 (4 payments).

Products named: Rinvoq

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Clinical Investigation Specialists $21,170

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.