CTRI/2011/12/002235已完成未知
An open-label, randomized, single-dose, crossover studyto evaluate the relative bioavailability of two 150 mgaliskiren MR (modified release) microparticle formulations(capsule) vs. marketed 150mg tablet in healthy adultvolunteers
ovartis Healthcare Private Limited0 个研究点目标入组 42 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 42
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Ba/be
入排标准
入选标准
- •1. Healthy Subjects
- •2. Female subejcts must be of non-child bearing potential
- •3. Subjects must weigh at least 50kg & their BMI 18 to 30 kg/m2 for participation
排除标准
- •1. Smokers
- •2. History of hypersensitivity to any of the study drugs or to drugs of similar chemical classes
- •3. Pregnant or nursing (lactating) women
- •4. Impaired hepatic or relnal function test results
- •5. A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result
研究者
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