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Completed Phase 3 Interventional Results available

Study of Adalimumab in Patients With Axial Spondyloarthritis

ClinicalTrials.gov ID: NCT00939003

Public ClinicalTrials.gov record NCT00939003. 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 Sep 10, 2026, 3:11 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 Multicenter Study of the Efficacy and Safety of the Human Anti-TNF Monoclonal Antibody Adalimumab in Subjects With Axial Spondyloarthritis

Brief summary

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

This study will evaluate how well adalimumab works in the short and long term in patients with axial spondyloarthritis who are not diagnosed as having either ankylosing spondylitis or psoriatic arthritis.

Study identification

NCT ID
NCT00939003
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
192 participants

Conditions and interventions

Interventions

Biological

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
Jun 30, 2009
Primary completion
Jan 31, 2011
Completion
Jul 31, 2013
Last update posted
Sep 8, 2014

2009 – 2013

United States locations

U.S. sites
9
U.S. states
6
U.S. cities
9
Facility City State ZIP Site status
Site Reference ID/Investigator# 21250 Birmingham Alabama 35205
Site Reference ID/Investigator# 21249 Colorado Springs Colorado 80910
Site Reference ID/Investigator# 21245 Denver Colorado 80230
Site Reference ID/Investigator# 21246 Wheaton Maryland 20902
Site Reference ID/Investigator# 26582 Duncansville Pennsylvania 16635
Site Reference ID/Investigator# 21241 Wyomissing Pennsylvania 19610
Site Reference ID/Investigator# 21243 Dallas Texas 75231
Site Reference ID/Investigator# 21248 Houston Texas 77030
Site Reference ID/Investigator# 21247 Seattle Washington 98122

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 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00939003, 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 Sep 8, 2014 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00939003 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →