- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07677384
A Study to Evaluate the Safety of HS-10506 in Chinese Patients With Insomnia Disorder
24 de junho de 2026 atualizado por: 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.
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Intervencional
Inscrição (Estimado)
600
Estágio
- Fase 3
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Contato de estudo
- Nome: Yuping Wang, Principal Investigator
- Número de telefone: 13501186298
- E-mail: wangyuping01@sina.cn
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Não
Descrição
Inclusion Criteria:
- Participants must be 18 to 65 years of age (inclusive 18, not inclusive 65);
- Participants are required to voluntarily sign the informed consent form;
- Body mass index (BMI): BMI (weight/height2 [kg/m2]) must be in the range of 18 to 35 kg/m2 (inclusive);
- 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;
- For new Participants: Participants must meet Diagnostic and Statistical Manual of Mental Disorders (5th edition) (DSM-5) criteria for insomnia disorder;
- For new Participants: Participants must have Insomnia Severity Index (ISI) scores≥15 at screening;
- 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:
- 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;
- 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;
- 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;
- 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;
- Has a history of drug dependency or abuse within the past 1 year or showed positive in urine drug test at screening;
- Has a history of alcohol abuse within the past 1 year or can't obey the rules of alcohol restriction;
- Has a history of smoking≥10 cigars daily within the past 3 months or can't obey the rules of cigar restriction;
- Has a history of caffeine consumption≥600 mg per day or can't obey the rules of caffeine restriction;
- Has been working across 3 or more time zones or shift work within 2 weeks prior to screening;
- Has taken more than 3 naps per week for>1 hour each time within the past 2 weeks prior to screening;
- 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.
- 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;
- 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;
- For Participants completed Study 301: Previously participated in any clinical trial other than HS-10506-301 within 3 months prior to screening;
- 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;
- 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;
- For new Participants: Previously use of HS-10506;
- For new Participants: Previously participated in any clinical trial within 3 months prior to screening.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: HS-10506
Participants will receive HS-10506 tablets, orally, once nightly for 4/24/36/48 consecutive weeks.
|
HS-10506 tablet
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence and severity of adverse events (AE)
Prazo: 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)
Prazo: 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)
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Number of Participants With Clinically Significant Change in hematology
Prazo: 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
Prazo: 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
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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)
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Estimado)
12 de junho de 2026
Conclusão Primária (Estimado)
30 de junho de 2029
Conclusão do estudo (Estimado)
30 de junho de 2029
Datas de inscrição no estudo
Enviado pela primeira vez
8 de junho de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
24 de junho de 2026
Primeira postagem (Real)
30 de junho de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
30 de junho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
24 de junho de 2026
Última verificação
1 de maio de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- HS-10506-303
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .