drugset / Trial / NCT00124449

Study of Abatacept Versus Placebo to Assess the Prevention of Rheumatoid Arthritis (RA) in Adult Patients

NCT00124449

Phase 2 Completed 56 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blind

Summary

The purpose of this study is to assess if Abatacept given for six months will prevent rheumatoid arthritis (RA) in patients who are at risk for the development of RA in comparison to placebo. High risk patients are defined as those having a positive laboratory test for anti-cyclic citrullinated peptide (anti-CCP2).

Timeline

Start
2005-02
Primary completion
2007-05
Completion
2008-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Abatacept Other / unclassified 500 mg Intravenous
Comparator Abatacept Other / unclassified 750 mg Intravenous
Comparator Abatacept Other / unclassified 1 g Intravenous

Indications