Clinical Trial

A Study to Evaluate the Safety of HS-10506 in Chinese Patients With Insomnia Disorder

Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
The primary purpose of this open-label phase Ⅲ study is to evaluate the safety of HS-10506 on the incidence and severity of adverse events (AE), serious adverse events (SAE), adverse events of special interest (AESI) in Chinese adult participants with insomnia disorder.
Trial Details
NCT Number NCT07677384
Lead Sponsor Jiangsu Hansoh Pharmaceutical Co., Ltd.
Conditions Insomnia Disorder
Enrollment 600 participants
Start Date 2026-06-12
Primary Completion 2029-06-30 (estimated)
Study Completion 2029-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-30