drugset / Trial / NCT02202395

Hydroxytriptolide in Active Rheumatoid Arthritis Patients With an Inadequate Response to Methotrexate

NCT02202395 ↗

Phase 1/2 Completed 120 enrolled Shanghai Pharmaceuticals Holding Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to investigate the efficacy and safety of Hydroxytriptolide(LTS) in active rheumatoid arthritis patients with an inadequate response to methotrexate.

Timeline

Start
2014-06
Primary completion
2015-04-30
Completion
2016-12-28

Drugs

EvaluationDrugModalityDoseRoute
Comparator LTS Unknown 0.25 mg —
Comparator LTS Unknown 0.5 mg —
Comparator LTS Unknown 1 mg —

Indications