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Clinical Trial Summary

The objective of this study is to determine the mass balance and routes of excretion of total radioactivity after a single oral 30mg (100µCi) dose of [14C] HQP1351 given as a suspension. For further clinical development, human mass balance data are required to elucidate the absorption, metabolism, and excretion of HQP1351.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04126707
Study type Interventional
Source Ascentage Pharma Group Inc.
Contact
Status Completed
Phase Phase 1
Start date November 19, 2019
Completion date January 13, 2020

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