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临床试验/JPRN-jRCT2080220992
JPRN-jRCT2080220992未知3 期

A phase III, double-blind, comparative study of NE-58095 (once-monthly formulation)

Takeda Pharmaceutical Company Limited0 个研究点开始时间: 2010年2月1日最近更新:

试验速览

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
>= 50age old 至 ot applicable(—)
性别
All

入选标准

  • [Main inclusion criteria]
  • -Aged 50 years or older at the time of obtaining consent
  • -Female subjects must be at least 2 years postmenopausal (i.e., at least 2 years since last menstrual period)

排除标准

  • [Main exclusion criteria]
  • -Secondary osteoporosis
  • -Presence of any disease that can decrease bone mass, except secondary osteoporosis
  • -Findings that can affect DXA measurements of mean lumbar spine bone mineral density
  • -Prior radiotherapy to the lumbar spine or pelvic region
  • -Planned dental extraction or other dental surgical procedures (including dental implants) to be performed during the study period

研究者

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