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Clinical Trial Summary

The purpose of this study is to evaluate the pharmacokinetics and bioequivalence of Ritonavir tablet 100 mg versus NORVIR 100 mg tablet in healthy Chinese adult participants under fasting or fed condition.


Clinical Trial Description

The study design is an Open-Label Randomized, Single-Dose, 2-way Crossover Bioequivalence Study with a washout period of 6 days. During each session, the subjects will be administered a single dose of 100mg Ritonavir (one Ritonavir Tablet 100mg or one NORVIR Tablet 100mg) under fasting or fed condition. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03302182
Study type Interventional
Source First Affiliated Hospital of Zhejiang University
Contact
Status Completed
Phase Phase 1
Start date September 23, 2017
Completion date December 4, 2017

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