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Clinical Trial Summary

This study is being conducted in order to assess the need for dose adjustment for elafibranor in participants with renal impairment. Pharmacokinetic parameters of elafibranor and its active metabolite (GFT1007) will be compared in severe renal impaired participants (eGFR<15mL/mn/1.73m^2) versus healthy participants after a single oral administration of elafibranor 120 mg


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03844555
Study type Interventional
Source Genfit
Contact
Status Completed
Phase Phase 1
Start date February 28, 2019
Completion date March 21, 2020

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