跳至主要内容
临床试验/JPRN-UMIN000042554
JPRN-UMIN000042554已完成未知

A Multi-Center Retrospective Study to Describe Clinical Characteristics and Outcomes of Early EVENITY Users, Transitioning to Antiresorptive Agents in Japan - A Multi-Center Retrospective Study to Describe Clinical Characteristics and Outcomes of Early EVENITY Users, Transitioning to Antiresorptive Agents in Japan

Amgen K.K. Medical Affairs Japan0 个研究点目标入组 1,027 人开始时间: 2020年11月26日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
1,027

研究概览

简要总结

There was a total of 1027 patients in this study of which >=90% were female. The mean age at the initiation of EVENITY for all patients was 77.0 years. A percentage of 54.9% of patients had previous OP medications within 6 months before EVENITY initiation. At 12 and 18 months of treatment, the mean percent change in BMD from baseline was 13.4% and 13.8% for the LS, 4.0% and 4.8% for TH, and 3.6% and 4.5% for FN in the FAS.

研究设计

研究类型
Observational

入排标准

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

入选标准

  • 未提供

排除标准

  • Conditions specified as contraindication in Japanese package insert: - Patients with a history of hypersensitivity to any of the ingredients of EVENITY - Patients with hypocalcemia

研究者

发起方
Amgen K.K. Medical Affairs Japan

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