跳至主要内容
临床试验/JPRN-jRCT2080221603
JPRN-jRCT2080221603未知3 期

ong-term study of SYR-322

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点开始时间: 2011年10月4日最近更新:
适应症

试验速览

阶段
3 期
发起方

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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ong-term study of SYR-322 | 临床试验