A Pharmacokinetic Study of Lanifibranor in Healthy Adult Chinese Subjects

Status Completed

Clinical Trial Summary

This will be a randomized, open-label parallel design and single centre study conducted at the 1st hospital affiliated to Jilin University. Approximately 24 healthy Chinese volunteers, male and female will be recruited and divided into two equal groups (12 subjects per dose). The primary objective of this study is to evaluate the pharmacokinetic profile of lanifibranor after single dose and multiple doses 800 and 1200 mg in healthy adult Chinese subjects. The secondary objective is to evaluate the safety of lanifibranor after single dose and multiple doses 800 and 1200 mg in healthy adult Chinese subjects.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Pharmacokinetic

Clinical Trial Details

NCT number	NCT06126562
Study type	Interventional
Source	Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Contact
Status	Completed
Phase	Phase 1
Start date	October 31, 2023
Completion date	December 15, 2023

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