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Clinical Trial Summary

This is a Phase 1, single center, single dose, open-label clinical study to evaluate the pharmacokinetics, safety and tolerability of SHR6390 under fasting conditions in healthy caucasian volunteers


Clinical Trial Description

The objective of this study is to determine the comparative pharmacokinetics, safety and tolerability of single oral dose of reformulated SHR6390 in healthy volunteers under fasting conditions. Each subject will receive a single dose of SHR6390, blood samples will be collected before dosing and at various time points up to 144 hours after drug administration, safety and the statistical analysis of the pharmacokinetic data will be obtained from this study ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04301804
Study type Interventional
Source Atridia Pty Ltd.
Contact
Status Completed
Phase Phase 1
Start date March 12, 2020
Completion date September 28, 2020

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