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Clinical Trial Summary

This study will assess the pharmacokinetics of PXL770 after 4 weeks of treatment.


Clinical Trial Description

The study will be performed in subjects with Nonalcoholic Fatty Liver Disease. The primary endpoint will be the assessment of PXL770 exposure in plasma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03950882
Study type Interventional
Source Poxel SA
Contact
Status Completed
Phase Phase 1
Start date August 1, 2019
Completion date March 31, 2020

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