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临床试验/JPRN-jRCT2080221847
JPRN-jRCT2080221847未知3 期

A long-term clinical study of OPC-262 in patients with type 2 diabetes (Extension study from Study 262-09-001)

Otsuka Pharmaceutical Co., Ltd.0 个研究点目标入组 175 人开始时间: 2012年7月3日最近更新:
适应症

试验速览

阶段
3 期
入组人数
175

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
>= 20age old 至 <= 74age old(—)
性别
All

入选标准

  • (1) Patients who completed Study 262-09-001 (patients who visited the hospital at visit Week 24)
  • (2) Patients who are capable of giving informed consent prior to participating in this clinical study
  • (3) Patients who are able to take contraceptive measures to avoid pregnancy of the patient or the patient's partner

排除标准

  • (1) Patients who withdrew fyom Study 262-09-001
  • (2) Patients who experienced serious adverse events that the relationship with the study drug was not denied in Study 262-09-001
  • (3) Patients who experienced serious adverse events that the relationship with the study drug are denied in Study 262-09-001 and whose symptoms are still emerged at the time of initiation of this study
  • (4) Patients who met the exclusion criteria of Study 262-09-001 during the study period of Study 262-09-001
  • (5) Female patients who wish to become pregnant during the study period of Study 262-09-002 or within 4 weeks after the study
  • (6) Patients other wise judged by the investigator or subinvestigator to be inappropriate for inclusion in the study

研究者

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