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Clinical Trial Summary

The purpose of this study is to evaluate the effect of food on pharmacokinetic profile of multiple doses orally administered first-line anti-tuberculosis drugs in subjects with pulmonary tuberculosis.


Clinical Trial Description

This is a single-center, open-label, randomized, two way crossover design, pharmacokinetics study.

1. Treatment A: study agents (Rifater+EMB) will be given approximately 45 minutes prior to breakfast.

2. Treatment B: study agents (Rifater+EMB) will be given approximately 45 minutes after the breakfast is finished. ;


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT00948077
Study type Interventional
Source Taipei Medical University WanFang Hospital
Contact Ming-Chih MC Yu, M.D.
Phone +886-2-29307930
Email yutbc@ms10.hinet.net
Status Recruiting
Phase N/A
Start date July 2009
Completion date December 2011

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