NCT05525637已完成3 期
A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter, Phase 3 Clinical Study to Evaluate the Efficacy and Safety of YZJ-1139 Tablets in the Treatment of Insomnia Disorder
Shanghai Haiyan Pharmaceutical Technology Co., Ltd.103 个研究点 分布在 1 个国家目标入组 1,037 人开始时间: 2021年12月17日最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 1,037
- 试验地点
- 103
- 主要终点
- Change from baseline in the subjective sleep efficiency (sSE) after 14 days of treatment
研究概览
简要总结
The main purpose of this study is to assess efficacy and safety of YZJ-1139 in adult subjects with insomnia disorder. Efficacy will be evaluated on objective and subjective sleep parameters.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •- Subjects who meet all of the following criteria may be enrolled in the study:
- •Aged ≥ 18 to < 65 years.
- •Meet the clinical diagnostic criteria for insomnia disorder as defined in International Classification of Sleep Disorders, 3rd Edition (ICSD-3) criteria.
- •sTSO ≥ 30 min for at least 3 nights per week and/or sWASO ≥ 60 min for at least 3 nights per week within 28 days (4 weeks) prior to screening.
- •During the run-in period or on Day 1 of the treatment period, sTSO ≥ 30 min for at least 3 nights in the last 7 sleep diaries and/or sWASO ≥ 60 min for at least 3 nights out of 7 nights as confirmed by the sleep diary prior to Polysomnography (PSG) monitoring.
- •PSG results for 2 consecutive nights during the run-in period should meet the following conditions:
- •The mean LPS of 2 nights is ≥ 30 min, with the LPS ≥ 20 min for any night;
- •And/or the mean WASO of 2 nights is ≥ 60 min, with neither night < 45 min;
- •The mean SE of 2 nights is ≤ 85%, with the SE ≤ 87.5% for both nights.
- •ISI score ≥ 15 at screening and on Day 1 of the treatment period.
- •Agree to follow the habitual bedtime between 9 p.m. and 1 a.m., wake up between 5 a.m. and 10 a.m. every day, and stay in bed for 6.5 to 9 hours per night during the study.
- •Have a bedtime between 9 p.m. and 1 a.m., wake up between 5 a.m. and 10 a.m., and stay in bed for 6.5 to 9 hours for at least 5 days in the last 7 sleep diaries as confirmed by the sleep diary prior to PSG monitoring during the run-in period or on Day 1 of the treatment period.
- •Female subjects are confirmed to be non-pregnant at screening; both men of reproductive potential and women of childbearing potential should agree to use medically acceptable and effective contraception throughout the study and within 3 months after the end of the study.
- •Understand the study procedures and contents, voluntarily participate in the clinical study and sign the written Informed Consent Form (ICF), have good compliance during participation in the study, and are willing to attend the visits.
排除标准
- •Subjects who meet any of the following criteria should be excluded from this study:
- •Depression: Hamilton Depression Scale (HAMD) score ≥ 18; anxiety: Hamilton Anxiety Scale (HAMA) score ≥
- •Suicidal ideation with or without plan at screening or within 6 months prior to screening (score ≥ 3 on item 3 [suicide] of HAMD, or select "Yes" on item 3, 4 or 5 of suicidal ideation subscale of Columbia-Suicide Severity Rating Scale (C-SSRS)), or have any suicidal behavior in the past 10 years (as assessed by the suicidal ideation subscale of C-SSRS).
- •Apnea-hypopnea index (AHI) and/or periodic limb movement index (PLMI) > 10 times/hour detected by PSG monitoring during the run-in period.
- •Repeat electrocardiogram (ECG) at screening shows QTcF interval prolongation (QTcF > 450 ms) (the ECG should be repeated 2 more times only if the initial ECG shows QTcF interval > 450 ms).
- •Have serious endocrine diseases, hematological diseases, cardiovascular and cerebrovascular diseases, gastrointestinal diseases, liver and kidney diseases, autoimmune diseases, impaired respiratory function or other related diseases, or have other medical history that may affect the safety of the subjects or interfere with the study assessments in the opinion of the investigator.
- •Have insomnia disorder due to other causes such as chronic pain, headache, eczema, neurodermatitis, allergic rhinitis, and serious dermatitis (difficulty sleeping due to physical reasons, difficulty falling asleep due to medical reasons).
- •Previous history of nervous system disorders such as epilepsy, schizophrenia, bipolar mental disorder, neurodevelopmental retardation, and cognitive disorder, or previous history of other mental illness that may affect the safety of the subjects or interfere with the study assessments in the opinion of the investigator.
- •Previous history of sleep-related respiratory disorders including obstructive sleep apnea (with or without continuous positive airway pressure (CPAP) therapy), periodic limb movement disorder, restless legs syndrome, circadian rhythm sleep disturbances, narcolepsy or other sleep disorders: subjects with restless legs syndrome which is diagnosed by relevant diagnostic and treatment guidelines should be excluded.
- •Have previous complex sleep behaviors, such as sleep driving, sleep eating, and sleep phone calls.
- •Plan to undergo surgery during the study.
- •Have received any hypnotics, antidepressants, antipsychotic drugs, anticholinergics, memory-enhancing drugs, antihistamines, centrally acting analgesics, centrally acting muscle relaxants, central nervous system stimulants, cytochrome P450 3A (CYP3A) inducers, CYP3A inhibitors, traditional Chinese medicines and traditional Chinese medicinal products with sleep-improving effects, or any other therapies for insomnia disorder within 1 week prior to the run-in period or within 5 half-lives of the investigational product, whichever is longer.
- •History of drug taking or addiction, which is known through questioning.
- •Have any lifestyle that interferes with the study process or may interfere with sleep: for example, there will be travels across 3 or more time zones (mainland China is considered as 1 time zone) within the next 2 weeks or during the study period, or there will be shift work (night and daytime shift).
- •Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 2 × the upper limit of normal (ULN), or Creatinine (Cr) > 1.5 × ULN.
- •Hyperthyroidism.
- •History of alcohol abuse (defined as regular daily alcohol consumption exceeding the following criteria: approximately 720 mL of beer, or 240 mL of wine, or 60 mL of liquor) within the past 2 years.
- •History of drug abuse within the past 2 years, or positive urine drug screening for any indicator.
- •Regular daily consumption of excessive tea and coffee drinks (defined as consumption of > 4 cups of caffeinated beverages or > 400 mg of caffeine per day), or daily habituation to drinking caffeinated beverages beyond 18:
- •Have nocturia increased caused by urinary tract infection, urinary tract injury or prostatic disorder.
- •Have positive infectious disease screening for hepatitis B surface antigen (HBsAg), hepatitis C antibody (HCVAb) and human immunodeficiency virus (HIV) antibody at screening.
- •Unable to avoid vaccination within 1 month prior to screening or during the first treatment phase.
- •Have participated in clinical studies of other drugs within the past 1 month or 5 half-lives (whichever is longer), or plan to participate in other studies simultaneously during participation in this study.
- •Pregnant or lactating women.
- •History of allergy to the investigational product or its components.
- •Have prior participation in clinical studies of YZJ-1139 Tablets.
- •Have other conditions that make the subject unsuitable for participation in the clinical study in the opinion of the investigator.
研究组 & 干预措施
Placebo
Placebo Comparator
干预措施: Placebo (Drug)
YZJ-1139 40mg
Experimental
干预措施: YZJ-1139 40mg (Drug)
YZJ-1139 20mg
Experimental
干预措施: YZJ-1139 20mg (Drug)
结局指标
主要结局
Change from baseline in the subjective sleep efficiency (sSE) after 14 days of treatment
时间窗: from baseline to week 2
Subjective Sleep efficiency variation assessed by the sleep diary questionnaire at 14 days of treatment from baseline. A positive change from baseline indicates an increase in the subjective Sleep efficiency. A negative change from baseline indicates a decrease in subjective Sleep efficiency
Change from baseline in the sleep efficiency (SE) after 14 days of treatment
时间窗: from baseline to day 14
Sleep efficiency variation assessed by polysomnography at 14 days of treatment from baseline. A positive change from baseline indicates an increase in the Sleep efficiency. A negative change from baseline indicates a decrease in Sleep efficiency
次要结局
- Changes from baseline in the Subjective wake after sleep onset (sWASO) after 14 days of treatment for subjects entering the second treatment phase(Baseline, week 1, week 2)
- Latency to persistent sleep (LPS) after 2 and 14 days of treatment(Baseline, Day1/Day2, Day13/Day14)
- Wake after sleep onset (WASO) after 2 and 14 days of treatment(Baseline, Day1/Day2, Day13/Day14)
- Total sleep time (TST) after 2 and 14 days of treatment(Baseline, Day1/Day2, Day13/Day14)
- Changes from baseline in the Subjective time to sleep onset (sTSO) after 14 days of treatment for subjects entering the second treatment phase(Baseline, week 1, week 2)
- Changes from baseline in the SE after 2 days of treatment(Baseline, Day1/Day2)
- Sleep structure (wakefulness, N1, N2, N3, rapid eye movement sleep [REM], non-rapid eye movement sleep [NREM], REM latency, number of awakenings [NAW], arousal index for REM and NREM) after 2 and 14 days of treatment(Baseline, Day1/Day2, Day13/Day14)
- Changes from baseline in the sTSO after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
- Changes from baseline in the sNAW after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
- Percentage of Participants who enter the second treatment phase on each scale of Patient Global Impressions - ImprovementGlobal Impression of Insomnia (PGI-I) each Item at 30, 90 and 180 days of treatment(Day 30, Day 90, and Day 180)
- Changes from baseline in the Subjective total sleep time (sTST) after 14 days of treatment for subjects entering the second treatment phase(Baseline, week 1, week 2)
- Change from baseline in the subjective sleep efficiency (sSE) after 7 days of treatment(Baseline, week 1)
- Changes from baseline in the Subjective number of awakenings (sNAW) after 14 days of treatment for subjects entering the second treatment phase(Baseline, week 1, week 2)
- Change from baseline in the mean subjective sleep quality score after 7 and 14 days of treatment for subjects(Baseline, Week 1, Week 2)
- Percentage of Participants on each scale of Global Impression of Insomnia (PGI-I) each Item at 14 days of treatment(Day 14)
- Changes from baseline in the sSE after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
- Changes from baseline in the sTST after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
- Change from baseline in the Insomnia Severity Index (ISI) score after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
- Changes from baseline in the sWASO after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
- Change from baseline in the mean subjective sleep quality score after 30, 90 and 180 days of treatment for subjects entering the second treatment phase(Baseline, Day 30, Day 90, and Day 180)
研究者
研究点 (103)
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