drugset / Trial / NCT00902486

INCB028050 Compared to Background Therapy in Patients With Active Rheumatoid Arthritis (RA) With Inadequate Response to Disease Modifying Anti-Rheumatic Drugs

NCT00902486 ↗

Phase 2 Completed 127 enrolled Incyte Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

This was a randomized, double blind, placebo controlled, dose ranging, parallel group study. Participants who had active rheumatoid arthritis (RA) who had inadequate response to any disease modifying anti-rheumatic drug (DMARD) therapy including biologics were enrolled. Screening evaluations were performed within approximately 28 days of randomization. The duration of the study was 6 months with the primary endpoint assessed at 3 months. Eligible participants were randomly assigned to one of three doses (4, 7 or 10 mg QD) of INCB028050 (Baricitinib) or placebo.

Timeline

Start
2009-05
Primary completion
2010-06
Completion
2010-07

Outcome

Missed primary endpoint

registry analysis (superiority or other test); Placebo vs INCB028050 4 mg QD vs INCB028050 7 mg QD vs INCB028050 10 mg QD; p = 0.0619; Odds Ratio (OR) 2.17 (95% CI 0.77 to 6.15); Cochran-Armitage trend test NCT00902486 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Baricitinib Small molecule 4 mg Oral
Subject Baricitinib Small molecule 7 mg Oral
Subject Baricitinib Small molecule 10 mg Oral

Indications