Clinical Trial

A Study of HS-10506 in Chinese Patients With Insomnia Disorder

Not Yet Recruiting Phase 3
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Summary
The primary purpose of this phase 3 study is to evaluate the safety and the efficacy of HS-10506 (change versus placebo) on latency to persistent sleep (LPS) and wakefulness after sleep onset (WASO) measured by polysomnography (PSG) in Chinese adult participants with insomnia disorder.
Trial Details
NCT Number NCT07587385
Lead Sponsor Jiangsu Hansoh Pharmaceutical Co., Ltd.
Conditions Insomnia Disorder
Enrollment 732 participants
Start Date 2026-05-29
Primary Completion 2028-06-28 (estimated)
Study Completion 2028-08-12 (estimated)
Updated on ClinicalTrials.gov 2026-05-14