ACTRN12606000447550尚未招募不适用
A Double-Blind, Active-Controlled, Long-Term Safety Extension Study of Optimized Doses of Darusentan in Subjects with Resistant Hypertension Despite Receiving Combination Therapy with Three or More Antihypertensive Drugs, Including a Diuretic, as Compared to Guanfacine (Protocol DAR-312-E)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- Myogen, Inc.
- 入组人数
- 700
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 35 Years 至 80 Years（—）
- 性别
- All
入选标准
- •1) Subjects must be competent to provide written informed consent; 2) Subjects must have completed participation in the DAR-312; 3) Female subjects must be of non-childbearing potential (post menopausal for at least 2 years or surgically sterile).
排除标准
- •1) Subjects who discontinue treatment with study drug prior to the end of the Maintenance Period in DAR-312 due to a study drug-related adverse event (AE); 2) Subjects who experience a study drug-related serious adverse event (SAE) during the DAR-312 study.
研究者
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