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Completed Phase 3 Interventional Results available

Phase III Study of BMS-188667 (CTLA4Ig) in Patients With Rheumatoid Arthritis Who Are Currently Failing Anti-TNF Therapy or Who Have Failed Anti-TNF Therapy in the Past.

ClinicalTrials.gov ID: NCT00048581

Public ClinicalTrials.gov record NCT00048581. 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 17, 2026, 4:31 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 Phase III, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of BMS-188667 in Subjects With Active Rheumatoid Arthritis on Background Disease Modifying Anti-Rheumatic Drugs (DMARDS) Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy

Brief summary

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

The purpose of this clinical research study is to determine whether abatacept treatment on a background of Disease Modifying Antirheumatic Drugs (DMARDs) will relieve the symptoms of rheumatoid arthritis (RA) in participants who are currently receiving anti-tumor necrosis factor (TNF) therapy for at least 3 months and are not responding or have taken anti-TNF therapy in the last 3 months and did not respond. The safety of treatment with abatacept will also be evaluated. This study also has a 4.5-year long-term extension beginning 6 months after the start of the study.

Study identification

NCT ID
NCT00048581
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
738 participants

Conditions and interventions

Interventions

Drug

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
Dec 2002 (Type not available)
Primary completion
Sep 2009 (Actual)
Completion
Sep 2009 (Actual)
Last update posted
Nov 21, 2011

2002 – 2009

United States locations

U.S. sites
42
U.S. states
24
U.S. cities
42
Facility City State ZIP Site status
Local Institution Birmingham Alabama — —
Local Institution Mobile Alabama — —
Local Institution Paradise Valley Arizona — —
Local Institution La Jolla California — —
Local Institution Long Beach California — —
Local Institution Palo Alto California — —
Local Institution Rancho Mirage California — —
Local Institution Denver Colorado — —
Local Institution Englewood Colorado — —
Local Institution Bridgeport Connecticut — —
Local Institution Hamden Connecticut — —
Local Institution Clearwater Florida — —
Local Institution Fort Lauderdale Florida — —
Local Institution Largo Florida — —
Local Institution Palm Harbor Florida — —
Local Institution Tampa Florida — —
Local Institution Rome Georgia — —
Local Institution Indianapolis Indiana — —
Local Institution Wichita Kansas — —
Local Institution New Orleans Louisiana — —
Local Institution Boston Massachusetts — —
Local Institution Springfield Massachusetts — —
Local Institution Lincoln Nebraska — —
Local Institution New Brunswick New Jersey — —
Local Institution Albany New York — —
Local Institution Syracuse New York — —
Local Institution Charlotte North Carolina — —
Local Institution Hickory North Carolina — —
Local Institution Bismarck North Dakota — —
Local Institution Cincinnati Ohio — —
Local Institution Oklahoma City Oklahoma — —
Local Institution Eugene Oregon — —
Local Institution Portland Oregon — —
Local Institution Duncansville Pennsylvania — —
Local Institution Norristown Pennsylvania — —
Local Institution Sellersville Pennsylvania — —
Local Institution Willow Grove Pennsylvania — —
Local Institution Charleston South Carolina — —
Local Institution Austin Texas — —
Local Institution Dallas Texas — —
Local Institution Vancouver Washington — —
Local Institution Milwaukee Wisconsin — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00048581, 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 Nov 21, 2011 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00048581 live on ClinicalTrials.gov.

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