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Clinical Trial Summary

The purpose of this study is to evaluate the drug-drug-interaction (DDI), pharmacokinetics (PK) and tolerability of GLS4/RTV combined with TAF in healthy subjects.

Clinical Trial Description

This is a 2-part study with each part is an open-label study in healthy adult subjects. Total 28 subjects will be enrolled into the study and divided into 2 part (Part A and Part B), 14 subjects in each part. With each part, the subject will be receive study drug per the defined treatment periods. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT04551261
Study type Interventional
Source Sunshine Lake Pharma Co., Ltd.
Status Completed
Phase Phase 1
Start date January 10, 2021
Completion date March 12, 2021

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