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Clinical Trial Summary

This study is designed to estimate the drug interaction between RIF and ABT. This will be a single-center, open-label, parallel study in healthy adult subjects.


Clinical Trial Description

The purpose of this study is to describe and compare RIF and ABT pharmacokinetics following administration of 320mg ABT and 600mg RIF.12 subjects will receive 320mg ABT on Days 1、2、3、8 (Treatment 1). And 12 subjects will receive 600mg RIF daily for 16 days from Day 1 to 16, and receive 320mg ABT on Days 7、8、9 and 14 (Treatment 2). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04006353
Study type Interventional
Source Shanghai Public Health Clinical Center
Contact
Status Completed
Phase Phase 4
Start date July 11, 2019
Completion date December 3, 2019

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