drugset / Trial / NCT00989235

Substudy - Low Dose of Abatacept in Subjects With Rheumatoid Arthritis

NCT00989235

Phase 3 Completed 108 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this exploratory sub-study was to evaluate from a clinical perspective the impact on disease activity of lowering the dose of abatacept from 10 mg/kg to 5 mg/kg in subjects who had achieved remission (Disease Activity Score 28 \[DAS 28\]-erythrocyte sedimentation rate \[ESR\] \< 2.6) at Day 701 of study IM101023.

Timeline

Start
2007-04
Primary completion
2009-10
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Abatacept Other / unclassified 5 mg/kg Intravenous
Comparator Abatacept Other / unclassified 10 mg/kg Intravenous

Indications