drugset / Trial / NCT01746680

Efficacy and Safety Study of Tacrobell to Treat Rheumatoid Arthritis

NCT01746680 ↗

Phase 4 Completed 111 enrolled Chong Kun Dang Pharmaceutical
NaSingle-groupOpen-labelTreatment

Summary

The aims of this study are to assess the efficacy and safety of tacrolimus in patients with active rheumatoid arthritis(RA). EULAR(European League Against Rheumatism) response at week 24 compared to baseline will be evaluated to assess the efficacy of Tacrolimus.

Timeline

Start
2012-08
Primary completion
2015-06
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Tacrolimus Small molecule 3 mg Oral
Background Methotrexate Small molecule 20 mg —

Indications