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A Randomized, Double-blind, Placebo-controlled Phase Ⅰb/Ⅱ Study to Investigate the Safety, Tolerability, Pharmacokinetics and Efficacy of HS-10506 in Chinese Adult Participants With Insomnia Disorder

Trial Profile

A Randomized, Double-blind, Placebo-controlled Phase Ⅰb/Ⅱ Study to Investigate the Safety, Tolerability, Pharmacokinetics and Efficacy of HS-10506 in Chinese Adult Participants With Insomnia Disorder

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 05 May 2026

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At a glance

  • Drugs HS 10506 (Primary)
  • Indications Insomnia
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Jiangsu Hansoh Pharmaceutical

Most Recent Events

  • 17 Apr 2026 Primary endpoint has been met. (Change from baseline in the mean LPS measured by PSG on Night 13 and Night 14), according to a Shanghai Hansoh Biomedical media release.
  • 17 Apr 2026 According to a Shanghai Hansoh Biomedical media release, study data evaluating HS-10506 will be presented at the 2026 American Academy of Neurology Annual Meeting (AAN 2026), held on April 18-22 in Chicago.
  • 17 Apr 2026 Results presented in the Shanghai Hansoh Biomedical media Release.

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