Pulmonary Tuberculosis Clinical Trial
Official title:
A Single-Center, Open-Label, Randomized, Crossover Design Study to Evaluate the Effect of Dietary Status on Pharmacokinetic Profile of Orally Administered First-Line Anti-TB Drugs in Subjects With Pulmonary Tuberculosis
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.
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.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label
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