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Terminated Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Ustekinumab in the Treatment of Anti-TNF(Alpha) Refractory Participants With Active Radiographic Axial Spondyloarthritis

ClinicalTrials.gov ID: NCT02438787

Public ClinicalTrials.gov record NCT02438787. 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 Oct 19, 2026, 2:31 PM 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 Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Ustekinumab in the Treatment of Anti-TNF(Alpha) Refractory Subjects With Active Radiographic Axial Spondyloarthritis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the efficacy of ustekinumab, in adult anti-TNF(alpha) refractory participants with active radiographic axial spondyloarthritis (AxSpA), as measured by the reduction in signs and symptoms of radiographic AxSpA.

Study identification

NCT ID
NCT02438787
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
315 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Jul 31, 2015 (Actual)
Primary completion
Aug 31, 2017 (Actual)
Completion
Aug 31, 2017 (Actual)
Last update posted
Apr 29, 2025

2015 – 2017

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Not listed Glendale Arizona — —
Not listed Peoria Arizona — —
Not listed Phoenix Arizona — —
Not listed Fremont California — —
Not listed St. Petersburg Florida — —
Not listed Tampa Florida — —
Not listed Boise Idaho — —
Not listed Chicago Illinois — —
Not listed Monroe Louisiana — —
Not listed Eagan Minnesota — —
Not listed Orchard Park New York — —
Not listed Portland Oregon — —
Not listed Duncansville Pennsylvania — —
Not listed Wyomissing Pennsylvania — —
Not listed Jackson Tennessee — —
Not listed Austin Texas — —
Not listed Mesquite Texas — —
Not listed Arlington Virginia — —
Not listed Seattle Washington — —

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 129 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02438787, 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 Apr 29, 2025 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02438787 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →