JPRN-jRCT2080222646已完成3 期
An open-label, multi-center, roll-over study to assess long term safety in patients with endogenous Cushing's syndrome who have completed a prior Novartis-sponsored osilodrostat (LCI699) study and are judged by the investigator to benefit from continued treatment with osilodrostat
未提供0 个研究点目标入组 137 人开始时间: 2014年11月6日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 137
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
- >= 18age old 至 <= 75age old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- 未提供
研究者
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