Overview

A Study to Assess the Pharmacodynamics of Lemborexant in Korean Participants With Insomnia Disorder

Status:
Not yet recruiting
Trial end date:
2024-01-26
Target enrollment:
Participant gender:
Summary
The primary purpose of the study is to evaluate the treatment difference between lemborexant 5 milligram (mg) (LEM5) and placebo (PBO) on latency to persistent sleep (LPS) using polysomnography (PSG) on Day 30.
Phase:
Phase 2
Details
Lead Sponsor:
Eisai Co., Ltd.
Treatments:
Lemborexant