drugset / Trial / NCT00048568

A Phase III Study of Abatacept (BMS-188667) in Patients With Active Rheumatoid Arthritis and Inadequate Response to Methotrexate

NCT00048568

Phase 3 Completed 1250 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

Short Term: The purpose of this clinical research study is to learn if abatacept (BMS-188667) in combination with methotrexate is better than methotrexate alone in participants that have active rheumatoid arthritis and are not responding to methotrexate. The safety of this treatment will also be studied. Long Term Extension: The purpose of this amendment is to provide participants who have completed the initial 12-month double-blind treatment period the opportunity to receive open label treatment with active drug treatment until abatacept is approved in the local country or until clinical development has been discontinued.

Timeline

Start
2002-12
Primary completion
2009-10
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified 10 mg/kg Intravenous
Subject Abatacept Other / unclassified 500 mg Intravenous
Subject Abatacept Other / unclassified 750 mg Intravenous
Subject Abatacept Other / unclassified 1 g Intravenous
Background Methotrexate Small molecule 15 mg Oral

Indications