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临床试验/JPRN-jRCT2080221242
JPRN-jRCT2080221242已完成2 期

A Phase 2 Randomized Study of LY2541546 versus Placebo in Postmenopausal Women with Low Bone Mineral Density:An Evaluation of the Dose Response Relationship Using Bone Mineral Density

Eli Lilly Japan K.K.0 个研究点开始时间: 2010年9月17日最近更新:
适应症

试验速览

阶段
2 期
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

年龄范围
ot applicable 至 ot applicable(—)
性别
Female

入选标准

  • Have low BMD, defined as a T-score for lumbar spine of between -3.5 and -2.0, inclusive, based on the local DXA report as interpreted by the investigator. The method of determining Tscore values will be based on regional standards. Three of 4 vertebrae, L1 through L4, must be evaluable for BMD scoring, as measure by DXA.

排除标准

  • 未提供

研究者

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