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临床试验/PER-052-04
PER-052-04已完成未知

A MULTICENTER STUDY OF 24 WEEKS OF DURATION, RANDOMIZED, DOUBLE-BLIND AND WITH SIMILAR ASPECT DRUGS, TO COMPARE THE EFFECTIVENESS OF AVANDIA FOR PROLONGED RELEASE (8 MG ONCE PER DAY) AND AVANDIA OF IMMEDIATE RELEASE (8 MG ONCE A DAY ) IN SUBJECTS WITH DIABETES MELLITUS OF TYPE 2.

GLAXOSMITHKLINE BIOLOGICALS,0 个研究点目标入组 0 人开始时间: 2004年8月9日最近更新:
适应症

试验速览

阶段
未知
状态
已完成

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

入选标准

  • Subjects with a clinical diagnosis of type 2 diabetes mellitus according to the ADA.
  • Male or female adults who are between 18 and 75 years of age at the time of selection.
  • Subjects that give their informed consent to participate.

排除标准

  • Any clinically significant abnormality identified in the Screening Visit.
  • The use of any investigational drug within 30 days or 5 half-lives (whichever is longer) before administering the first dose of study medication
  • Anemia, defined by a hemoglobin concentration <11 g / dL for men or <10 g / dL for women.
  • The subject has a hemoglobinopathy.

研究者

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