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临床试验/NCT00847821
NCT00847821终止不适用

RNA Expression Analysis Of Endometrial Biopsies Comparing Placebo, Bazedoxifene/ Conjugated Estrogens And Raloxifene

Wyeth is now a wholly owned subsidiary of Pfizer1 个研究点 分布在 1 个国家目标入组 185 人开始时间: 2009年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
发起方
入组人数
185
试验地点
1
主要终点
Endometrial gene regulation at the level of mRNA expression in placebo, Bazedoxifene/CE, and raloxifene treated groups

研究概览

简要总结

This study is an observational study analyzing the biopsy samples collected from subjects that participated in Study 3115A1-303 (NCT00675688). These endometrial biopsy samples will be de-identified at an anatomical laboratory and then sent to a molecular biology lab where an RNA extraction and analysis will be performed. The purpose of this study is to compare specific endometrial gene regulation at the level of mRNA expression in samples from placebo, bazedoxifene/conjugated estrogens, and raloxifene treated groups with a known set of genes that have been previously identified to be associated with estrogenization, endometrial hyperplasia, and endometrial cancer.

详细描述

The termination date was June 23, 2010. The study was terminated because the endometrial biopsy blocks from the 3115A1-303 study that were to be used for this study need to be retained and accessible in case of a regulatory inspection of the 303 protocol. Additionally, the Brazilian sites were not likely not to receive national IRB (CONEP) approval, and enrollment could not be met without the inclusion of these subjects. The study was not terminated due to safety concerns.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Each subject must have participated in study 3115A1-303 and must have satisfied all of the following criteria:
  • Has completed 24 months of treatment.
  • Was at least 80% compliant with study drug administration.

排除标准

  • Endometrial biopsy at baseline, month 6 or month 24 that were technically unacceptable
  • Did not have an endometrial biopsy at all of the required timepoints (baseline, month 6, month 24)

研究组 & 干预措施

Bazedoxifene 10 mg/CE 0.625 mg

干预措施: Bazedoxifene 10 mg/CE 0.625 mg (Drug)

Bazedoxifene 20 mg/CE 0.625 mg

干预措施: Bazedoxifene 20 mg/CE 0.625 mg (Drug)

Bazedoxifene 40 mg/CE 0.625 mg

干预措施: Bazedoxifene 40 mg/CE 0.625 mg (Drug)

Bazedoxifene 10 mg/CE 0.45 mg

干预措施: Bazedoxifene 10 mg/CE 0.45 mg (Drug)

Bazedoxifene 20 mg/CE 0.45 mg

干预措施: Bazedoxifene 20 mg/CE 0.45 mg (Drug)

Bazedoxifene 40 mg/CE 0.45 mg

干预措施: Bazedoxifene 40 mg/CE 0.45 mg (Drug)

Raloxifene 60 mg

干预措施: Raloxifene 60 mg (Drug)

Placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Endometrial gene regulation at the level of mRNA expression in placebo, Bazedoxifene/CE, and raloxifene treated groups

时间窗: Baseline, 6 months and 24 months

次要结局

未报告次要终点

研究者

发起方
Wyeth is now a wholly owned subsidiary of Pfizer
申办方类型
Industry

研究点 (1)

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