Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

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

8. mai 2026 oppdatert av: Jiangsu Hansoh Pharmaceutical Co., Ltd.

A Randomized, Double-Blind, Placebo-Controlled Phase 3 Study to Evaluate the Efficacy and Safety of HS-10506 in Chinese Adult Patients With Insomnia Disorder

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.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Detaljert beskrivelse

The study will comprise 4 periods : a Screening Period, a Run-in Period, a Treatment Period during which participants will be treated for 84 nights (3 month) and a minimum 3-day Follow-up Period before an End of Study (EOS) Visit. The total study duration for each participant on this study is 105-113 days.

Studietype

Intervensjonell

Registrering (Antatt)

732

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: Huan Yu Yu Principal Investigator
  • Telefonnummer: 021-54602182
  • E-post: dr.yuhuan@163.com

Studer Kontakt Backup

  • Navn: Yuping Wang Wang Principal Investigator
  • Telefonnummer: 13501186298
  • E-post: wangyuping01@sina.cn

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

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. Participants must meet Diagnostic and Statistical Manual of Mental Disorders (5th edition) (DSM-5) criteria for insomnia disorder;
  5. Participants must have Insomnia Severity Index (ISI) scores ≥ 15 at screening and run-in period;
  6. Subjective sleep assessment: 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 V2 visit and V3 visit respectively;
  7. PSG: Participants must demonstrate a 2-night mean LPS ≥ 30 minutes with neither night < 20 minutes, a 2-night mean WASO ≥ 30 minutes with neither nigh < 20 minutes, and a 2-night mean TST < 7 hours.

Exclusion Criteria:

  1. 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;
  2. Has a Apnea-Hypopnea Index (AHI) ≥ 10 times/hour or periodic leg movement with arousal index (PLMAI) ≥ 10 times/hour monitored by PSG at V2 visit;
  3. 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;
  4. Has a Hamilton Anxiety Scale (HAM-A) score ≥ 14 or Hamilton Depression Scale (HAM-D-17) score ≥ 18;
  5. 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;
  6. 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;
  7. 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;
  8. Has been working across 3 or more time zones or shift work within 2 weeks prior to screening;
  9. Has taken more than 3 naps per week for > 1 hour each time within the past 2 weeks prior to screening;
  10. 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;
  11. Has a history of drug dependency or abuse within the past 1 year or showed positive in urine drug test at screening;
  12. Has a history of alcohol abuse within the past 1 year or can't obey the rules of alcohol restriction;
  13. Has a history of smoking ≥ 10 cigars daily within the past 3 months or can't obey the rules of cigar restriction;
  14. Has a history of caffeine consumption ≥ 600 mg per day or can't obey the rules of caffeine restriction;
  15. Previously participated in any clinical trial of HS-10506;
  16. Has any circumstances or conditions, which, in the opinion of the investigator, may affect the participant's full participation in the study or compliance with the protocol.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: HS-10506
Participants will receive HS-10506 tablets, orally, once nightly for 84 consecutive nights
HS-10506 tablet
Placebo komparator: Placebo
Participants will receive placebo matched in appearance to HS-10506 tablets, orally, once nightly for 84 consecutive nights
Placebo tablet matched to HS-10506

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change from baseline of mean latency to persistent sleep (LPS) over the last 2 nights of 28 days and 84 days under the treatment of HS-10506
Tidsramme: Baseline, Night 27 and Night 28,Night 83 and Night 84
LPS was defined as the time in minutes from lights off to the first epoch of 20 consecutive epochs of non-wakefulness as measured by polysomnography (PSG)
Baseline, Night 27 and Night 28,Night 83 and Night 84
Change from baseline of mean wakefulness after sleep onset (WASO) over the last 2 nights of 28 days and 84 days under the treatment of HS-10506
Tidsramme: Baseline, Night 27 and Night 28, Night 83 and Night 84
WASO was defined as minutes of wake from the onset of persistent sleep until lights on as measured by PSG
Baseline, Night 27 and Night 28, Night 83 and Night 84

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change from baseline of subjective sleep onset latency (sSOL) under the treatment of HS-10506
Tidsramme: Baseline, Week 4, Week 12
sSOL: estimated minutes from the time that the participant attempted to sleep until sleep onset as recorded in sleep diary
Baseline, Week 4, Week 12
Change from baseline in subjective sleep efficiency (sSE) under the treatment of HS-10506
Tidsramme: Baseline, Week 4, Week 12
sSE: the ratio of subjective total sleep time(sTST) to subjective time in bed, sTST: the total sleep time reported by the participant in sleep diary.
Baseline, Week 4, Week 12
Change from baseline in total sleep time (TST) over the last 2 nights of 28 days and 84 days under the treatment of HS-10506
Tidsramme: Baseline, Night 27 and Night 28, Night 83 and Night 84
TST was defined as the total sleep time in minutes, the total sleep time is the total amount of stages 1, 2, 3 non rapid eye-movement (NREM) and rapid-eye-movement (REM) sleep time, as measured by PSG
Baseline, Night 27 and Night 28, Night 83 and Night 84
Change from baseline in sleep efficiency (SE) over the last 2 nights of 28 days and 84 days under the treatment of HS-10506
Tidsramme: Baseline, Night 27 and Night 28, Night 83 and Night 84
SE was defined as percentage (%) of time spent in bed asleep, calculated as total sleep time (TST) divided by interval from lights off until lights on as measured by PSG multiplied by 100
Baseline, Night 27 and Night 28, Night 83 and Night 84
Change from baseline in subjective wake after sleep onset (sWASO) under the treatment of HS-10506
Tidsramme: Week 4, Week 12
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
Week 4, Week 12
Change from baseline in subjective total sleep time (sTST) under the treatment of HS-10506
Tidsramme: Baseline, Week 4, Week 12
sTST: the total sleep time reported by the participant in sleep diary
Baseline, Week 4, Week 12
Incidence and severity of adverse events (AE)
Tidsramme: From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 4 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 4 months
Incidence and severity of serious adverse events (SAE)
Tidsramme: From date of signing the informed consent until the date of the end-of-study visit or early withdrawal, assessed up to 4 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 4 months
Withdrawal symptoms by Physician Withdrawal Checklist (PWC-20)
Tidsramme: The day after the last administration and at least 3 days after discontinuation of the medication
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 3 days after discontinuation of the medication
Rebound insomnia by sleep diary during the follow-up period
Tidsramme: Baseline, Follow-up Period (3-6 days)
Rebound insomnia is defined as worsened sleep relative to baseline after study drug treatment was completed, rebound insomnia is assessed using the data collected in sleep diary, including estimated minutes from the time that the participant attempted to sleep until sleep onset as recorded in sleep diary (subjective sleep onset latency, sSOL), 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 (subjective wake after sleep onset, sWASO) and the total sleep time reported by the participant in sleep diary ( subjective total sleep time, sTST)
Baseline, Follow-up Period (3-6 days)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

29. mai 2026

Primær fullføring (Antatt)

28. juni 2028

Studiet fullført (Antatt)

12. august 2028

Datoer for studieregistrering

Først innsendt

23. april 2026

Først innsendt som oppfylte QC-kriteriene

8. mai 2026

Først lagt ut (Faktiske)

14. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

14. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. mai 2026

Sist bekreftet

1. april 2026

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere