drugset / Trial / NCT04077567

An Extension Study of TS-152 in Subjects With Rheumatoid Arthritis

NCT04077567 ↗

Phase 3 Completed 401 enrolled Taisho Pharmaceutical Co., Ltd.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the long-term safety and efficacy of TS-152 in subjects with Rheumatoid Arthritis who have completed the previous study (TS152-3000-JA study or TS152-3001-JA study).

Timeline

Start
2019-10-01
Primary completion
2023-04-28
Completion
2023-04-28

Drugs

EvaluationDrugModalityDoseRoute
Subject TS-152 Unknown 30 mg Subcutaneous
Subject TS-152 Unknown 80 mg Subcutaneous

Indications