drugset / Trial / NCT02214888

Efficacy, Safety and Pharmacokinetics of BIRB 796 BS Tablets in Patients With Active Rheumatoid Arthritis

NCT02214888 ↗

Phase 2 Terminated 170 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Study to determine the efficacy (including American College of Rheumatology (ACR) 20 response rate), safety, and pharmacokinetics of BIRB 796 BS as monotherapy in patients with moderate to severe rheumatoid arthritis who have failed at least one disease modifying antirheumatic drug (DMARD)

Timeline

Start
2003-05
Primary completion
2004-01
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BIRB 796 BS Unknown 50 mg —
Subject BIRB 796 BS Unknown 70 mg —

Indications