drugset / Trial / NCT04791553

Safety Study of Cenobamate in Subjects With Normal Hepatic Function and Subjects With Severe Hepatic Impairment

NCT04791553

Phase 1 Completed 15 enrolled SK Life Science, Inc.
Non-randomizedParallel-groupOpen-labelOther

Summary

This study is designed investigate the effect of severe hepatic impairment on the pharmacokinetics (PK) of cenobamate.

Timeline

Start
2021-06-17
Primary completion
2022-11-15
Completion
2023-08-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Cenobamate Small molecule 200 mg Oral

Indications

No indication recorded.