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临床试验/JPRN-jRCT2080221694
JPRN-jRCT2080221694未知3 期

Study of combination therapy with SYR-322

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点目标入组 179 人开始时间: 2012年1月20日最近更新:

试验速览

阶段
3 期
发起方
入组人数
179

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 1. The subject is an outpatient.
  • 2. The subject signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures.

排除标准

  • 1. The subject has any serious cardiac disease, serious cerebrovascular disorder, or any serious pancreatic or hematological disease.
  • 2. The subject is considered ineligible for the study for any other reason by the investigator or subinvestigator.

研究者

发起方
TAKEDA PHARMACEUTICAL COMPANY LTD.

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Study of combination therapy with SYR-322 | 临床试验