drugset / Trial / NCT04549168

A Study of Lemborexant in Chinese Participants With Insomnia Disorder

NCT04549168

Phase 3 Completed 194 enrolled Eisai Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to confirm using polysomnography (PSG) that lemborexant 10 milligram (mg) is superior to placebo on objective sleep onset as assessed by latency to persistent sleep (LPS) during the last 2 nights of 1 month of treatment in participants with insomnia disorder.

Timeline

Start
2020-11-06
Primary completion
2023-03-17
Completion
2023-03-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Lemborexant Small molecule 10 mg Oral