A Phase III Study of BMS-188667 in Children and Adolescents with Juvenile Rheumatoid Arthritis

Registry ID
EUCTR2005-000443-28
Source registry
EUCTR
Phase
PHASE3
Sponsor
Bristol Myers Squibb International Corporation
Last update
2026-08-16

Conditions

Summary

The study will compare the clinical efficacy of BMS-188667 versus placebo in children and adolescents with JRA/JIA in whom a response had been initially induced by 4 months of open-label therapy. Following 6 months of double-blind treatment, clinical efficacy will be measured by the time to occurrence of JRA/JIA disease flare during the double-blind treatment period.

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