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

24 juin 2026 mis à jour par: Jiangsu Hansoh Pharmaceutical Co., Ltd.

A Multicenter, Open-label, Phase 3 Study to Evaluate the Short-term and Long-term Safety of HS-10506 in Chinese Adult Patients With Insomnia Disorder

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.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Intervention / Traitement

Description détaillée

The study will comprise 4 periods : a Screening Period, a Run-in Period, an Open-Label Treatment Period during which participants will be treated for 4, 24, 36, or 48 consecutive weeks and a minimum 7-day Follow-up Period before an End of Study (EOS) Visit. The total study duration for each participant on this study is 2-13 months.

Type d'étude

Interventionnel

Inscription (Estimé)

600

Phase

  • Phase 3

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Yuping Wang, Principal Investigator
  • Numéro de téléphone: 13501186298
  • E-mail: wangyuping01@sina.cn

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  1. Participants must be 18 to 65 years of age (inclusive 18, not inclusive 65);
  2. Participants are required to voluntarily sign the informed consent form;
  3. Body mass index (BMI): BMI (weight/height2 [kg/m2]) must be in the range of 18 to 35 kg/m2 (inclusive);
  4. For Participants completed Study 301: Participants have completed the Study 301, can potentially benefit from extended treatment with HS-10506 and have no major safety risks according to the investigator's clinical judgment;
  5. For new Participants: Participants must meet Diagnostic and Statistical Manual of Mental Disorders (5th edition) (DSM-5) criteria for insomnia disorder;
  6. For new Participants: Participants must have Insomnia Severity Index (ISI) scores≥15 at screening;
  7. For new Participants: Participants must have an sSOL≥30 minutes, sWASO≥30 minutes, and sTST<6.5 hours for at least three nights every week within one month prior to screening; and sSOL≥30 minutes, sWASO≥30 minutes, and sTST<6.5 hours for at least 3 nights from sleep diary in the last 7 consecutive days before the first dose in the open-label treatment period;

Exclusion Criteria:

  1. Has received systemic hypnotherapy, cognitive behavioral therapy (CBT), or other non-pharmacological treatments for insomnia in last 4 weeks or have plans during the study;
  2. Has a risk of suicide according to the Columbia Suicide Severity Rating Scale (C-SSRS), or has a high risk of suicide at the discretion of the investigator;
  3. Has used any medication that may affect the pharmacokinetics of HS-10506 or GLP-1R-related single/multi-target drugs within the past 2 weeks or 5 half-lives of the medication;
  4. Has used any medication that may affect sleep-wake function, or any other prohibited central nervous system active medications within 1 week or 5 half-lives of the medication;
  5. Has a history of drug dependency or abuse within the past 1 year or showed positive in urine drug test at screening;
  6. Has a history of alcohol abuse within the past 1 year or can't obey the rules of alcohol restriction;
  7. Has a history of smoking≥10 cigars daily within the past 3 months or can't obey the rules of cigar restriction;
  8. Has a history of caffeine consumption≥600 mg per day or can't obey the rules of caffeine restriction;
  9. Has been working across 3 or more time zones or shift work within 2 weeks prior to screening;
  10. Has taken more than 3 naps per week for>1 hour each time within the past 2 weeks prior to screening;
  11. Has any circumstances or conditions, which, in the opinion of the investigator, may affect the subject's full participation in the study or compliance with the protocol.
  12. For Participants completed Study 301: Has been diagnosed with a sleep-wake disorders or sleep-related breathing disorders other than insomnia disorder during Study 301, such as restless legs syndrome, periodic limb movement disorder, circadian rhythm disorder, narcolepsy, rapid eye movement sleep phase (REM) behavioral disorders, and obstructive sleep apnea;
  13. For Participants completed Study 301: Has been diagnosed with neurodevelopmental retardation, cognitive impairment, epilepsy, schizophrenia, bipolar disorder, hyperthyroidism, cancer, severe cardio-cerebrovascular diseases or respiratory diseases; or current chronic pain that affects sleep, nocturia resulting in frequent need to get out of bed to use the bathroom during the night; or clinically significant and/or unstable neurological, psychiatric, respiratory, cardiovascular, digestive, immunologic, urologic, endocrine diseases during Study 301; or other systemic diseases that are inappropriate for the study;
  14. For Participants completed Study 301: Previously participated in any clinical trial other than HS-10506-301 within 3 months prior to screening;
  15. For new Participants: Has history of/current sleep-wake disorders or sleep-related breathing disorders other than insomnia disorder, such as restless legs syndrome, periodic limb movement disorder, circadian rhythm disorder, narcolepsy, rapid eye movement sleep phase (REM) behavioral disorders, and obstructive sleep apnea;
  16. For new Participants: Has history of/current neurodevelopmental retardation, cognitive impairment, epilepsy, schizophrenia, bipolar disorder, hyperthyroidism, cancer, severe cardio-cerebrovascular diseases or respiratory diseases; or current chronic pain that affects sleep, nocturia resulting in frequent need to get out of bed to use the bathroom during the night; or clinically significant and/or unstable neurological, psychiatric, respiratory, cardiovascular, digestive, immunologic, urologic, endocrine diseases within the past 3 months prior to screening; or other systemic diseases that are inappropriate for the study;
  17. For new Participants: Previously use of HS-10506;
  18. For new Participants: Previously participated in any clinical trial within 3 months prior to screening.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: HS-10506
Participants will receive HS-10506 tablets, orally, once nightly for 4/24/36/48 consecutive weeks.
HS-10506 tablet

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Incidence and severity of adverse events (AE)
Délai: From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 13 months
An AE is any untoward medical event that occurs in a participant administered an investigational product, and it does not necessarily indicate only events with clear causal relationship with the relevant investigational product.
From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 13 months
Incidence and severity of serious adverse events (SAE)
Délai: From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 13 months
An SAE is any AE that results in: death, persistent or significant disability/incapacity, requires inpatient hospitalization or prolongation of existing hospitalization, is life-threatening experience, is a congenital anomaly/birth defect and may jeopardize participants and/or may require medical or surgical intervention to prevent one of the outcomes listed above.
From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 13 months
Incidence and severity of adverse events of special interest (AESI)
Délai: From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 13 months
An AESI (serious or non-serious) is any medical event specific to the investigational product or clinical trial.
From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 13 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Number of Participants With Clinically Significant Change in hematology
Délai: Baseline, Week 12, Week 24, Week 36, Week 48
Hematology tests will include hemoglobin, hematocrit, red blood cell count, platelets, white blood cell count, count and absolute lymphocytes, neutrophils, basophils, eosinophils, monocytes. Any clinically significant change in hematological values will be determined at the investigator's discretion
Baseline, Week 12, Week 24, Week 36, Week 48
Number of Participants With Clinically Significant Change in clinical chemistry
Délai: Baseline, Week 12, Week 24, Week 36, Week 48
Clinical chemistry tests will include total and direct bilirubin, aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transferase, albumin, total protein, creatinine, glucose, hemoglobin A1c (HbA1c), creatinine kinase. Any clinically significant change in clinical chemistry values will be determined at the investigator's discretion.
Baseline, Week 12, Week 24, Week 36, Week 48
Number of Participants With Clinically Significant Change in urinalysis
Délai: Baseline, Week 12, Week 24, Week 36, Week 48
Urinalysis will include glucose, ketones, urine red blood cells, urine white blood cells. Any clinically significant change in urinalysis values will be determined at the investigator's discretion.
Baseline, Week 12, Week 24, Week 36, Week 48
Withdrawal symptoms by Physician Withdrawal Checklist (PWC-20)
Délai: The day after the last administration and at least 7 days after discontinuation of the medication
The PWC-20 is a 20-item questionnaire and the score of each item ranges from 0-3 (0=not present, 1=mild, 2=moderate, 3=severe) with higher scores indicating greater severity of withdrawal symptoms
The day after the last administration and at least 7 days after discontinuation of the medication
Rebound insomnia by subjective sleep onset latency (sSOL) during the follow-up period
Délai: Baseline, Follow-up Period (7-9 days)
Baseline, Follow-up Period (7-9 days)
Rebound insomnia by subjective wake after sleep onset (sWASO) during the follow-up period
Délai: Baseline, Follow-up Period (7-9 days)
Baseline, Follow-up Period (7-9 days)
Rebound insomnia by subjective total sleep time (sTST) during the follow-up period
Délai: Baseline, Follow-up Period (7-9 days)
Baseline, Follow-up Period (7-9 days)
Change from baseline in subjective sleep onset latency (sSOL) under the treatment of HS-10506
Délai: Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
sSOL: estimated minutes from the time that the participant attempted to sleep until sleep onset as recorded in sleep diary
Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
Change from baseline in subjective sleep efficiency (sSE) under the treatment of HS-10506
Délai: Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
sSE: the ratio of subjective total sleep time (sTST) to subjective time in bed
Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
Change from baseline in subjective wake after sleep onset (sWASO) under the treatment of HS-10506
Délai: Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
sWASO: estimated minutes of wake at night from initial sleep onset to the time when the participant stopped trying to sleep as recorded in sleep diary
Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
Change from baseline in subjective total sleep time (sTST) under the treatment of HS-10506
Délai: Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)
sTST: the total sleep time reported by the participant in sleep diary
Baseline, every 4 weeks during Open-Label Treatment Period (up to 12 months)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

12 juin 2026

Achèvement primaire (Estimé)

30 juin 2029

Achèvement de l'étude (Estimé)

30 juin 2029

Dates d'inscription aux études

Première soumission

8 juin 2026

Première soumission répondant aux critères de contrôle qualité

24 juin 2026

Première publication (Réel)

30 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

24 juin 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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