drugset / Trial / NCT02566967

An Evaluation of the Optimal Dose of Tofacitinib Needed to Achieve Low Disease Activity (LDA) or Clinical Remission in Patients With Active Rheumatoid Arthritis (RA) as Measured From a Clinical and Structural Perspective

NCT02566967

Phase 3 Completed 20 enrolled Norman B. Gaylis, MD
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the optimal dose of tofacitinib needed to achieve low disease activity (LDA) or clinical remission as measured by the CDAI score. Once LDA or clinical remission has been achieved, the structural benefit in reducing erosions, synovitis and bone edema as measured by low field MRI will be determined at the same time period by the use of the OMERACT/RAMRIS scoring system

Timeline

Start
2015-05
Primary completion
2017-12
Completion
2018-03-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Tofacitinib Small molecule 5 mg Oral
Subject Tofacitinib Small molecule 10 mg Oral

Indications