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临床试验/jRCT2080224848
jRCT2080224848已完成3 期

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

Taisho Pharmaceutical Co.Ltd1 个研究点目标入组 505 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
505
试验地点
1
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Open-label, Multicenter study
主要目的
Treatment Purpose

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • (1)At visit1(-4 weeks), Subject must be fully informed about the study and must obtain written informed consent from the subject himself.
  • (2)At Visit2(0 week), Subjects must have completed the previous study (TS152-3000-JA or TS152-3001-JA) ,and must have completed all evaluations required at the follow-up visit.

排除标准

  • Subjects who had serious adverse drug reactions in the previous study.
  • At Visit1(-4 weeks) or Visit2 (0 week), Subjects who have not recovered from clinically important adverse events.

结局指标

主要结局

-

safety efficacy ACR20 adverse event,Side effects etc.

次要结局

未报告次要终点

研究者

研究点 (1)

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