跳至主要内容
临床试验/PER-065-03
PER-065-03已完成未知

A DOUBLE-BLIND, RANDOMIZED STUDY CONTROLLED WITH ACTIVE COMPARATOR MK-0767 AND METFFORMINA IN PATIENTS THAT SUFFER FROM DIABETES TYPE 2 INAPPROPRIATE CONTROL OF DIET AND EXERCISES.

MERCK & CO.INC.,0 个研究点目标入组 0 人开始时间: 2003年12月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
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
0 至 0(—)

入选标准

  • Between 21 and 78 years old.
  • Men and women not pregnant.
  • Understanding of the study procedures and agreement to participate in it, providing written informed consent.
  • Compliance with placebo treatment during the transition phase greater than or equal to 75%

排除标准

  • History of type 1 diabetes mellitus and / or history of ketoacidosis, peptide C <0.8 ng / mL (<0.26 nmol / L).
  • Patients requiring lipid-lowering agents, such as HMG-CoA reductase inhibitors (statins) other than open label simvastatin.
  • Patients requiring treatment with doses> 40 mg of simvastatin,> 20 mg / day of atorvastatin or equivalent doses of other HMG-CoA reductase inhibitors.
  • Patients under a regimen of estrogen replacement therapy or SERM (Selective Estrogen Receptor Modulator) who are expected to require significant adjustments of the regimen after Visit 1 / Week 9.

研究者

发起方
MERCK & CO.INC.,

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