跳至主要内容
临床试验/JPRN-jRCT2080221859
JPRN-jRCT2080221859未知3 期

A Multi-center, Open Label Study for Evaluation of the Safety, Tolerability and Efficacy of 8-week Treatment With LCZ696 in Japanese Patients With Severe Hypertension

ovartis Pharma K.K.0 个研究点目标入组 34 人开始时间: 2012年7月23日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
34

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • *Satisfy office msSBP>=180 mmHg or office msDBP>=110 mmHg at baseline.

排除标准

  • *Patients show msSBP >=220 mmHg and/or msDBP >=120 mmHg.
  • *History of angioedema, drug-related or otherwise, as reported by the patient.
  • *Patients unwilling or not able to discontinue safely the use of current antihypertensive medications during the study, as required by the protocol.
  • *Patients have significant cardiovascular co-morbidities.
  • *Patients who previously entered a LCZ696 study and had been randomized or enrolled into the active drug treatment epoch.
  • Other protocol defined inclusion/exclusion criteria may apply.

研究者

发起方
ovartis Pharma K.K.

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