CTRI/2012/11/003106已完成1 期
An open label, randomized, three period, six sequence, crossover study to determine the bioavailability of diclofenac potassium soft-gelatin capsule as compared to diclofenac potassium powder for oral solution and diclofenac potassium tablet in healthy subjects
ovartis Healthcare Private Limited0 个研究点目标入组 78 人开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 78
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 male and female subjects
- •2. Subjects must weigh atleast 50 kg and their BMI should be within range of 18-30 kg/m2
- •3. Women of child-bearing potential must use effective contraception during the study.
排除标准
- •1. History of hypersensitivity to any of the study drugs or to drugs of similar chemical classes
- •2. Pregnant or nursing (lactating) women
- •3. History of clinically significant ECG abnormalities, malignancy of any organ system, history of immunodeficiency diseases; of drug or alcohol abuse.
研究者
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