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Clinical Trial Summary

This study will evaluate the pharmacokinetics (PK), safety, and tolerability of a single oral dose of Besifovir and its metabolite, LB80331, in participants with normal and impaired renal function


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04249908
Study type Interventional
Source IlDong Pharmaceutical Co Ltd
Contact Kim Min Jung
Phone 8225263179
Email mjkim90@ildong.com
Status Not yet recruiting
Phase Phase 1
Start date February 13, 2020
Completion date April 2021

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