The Efficacy And Safety Of Mitizodone Phosphate Tablets In The Treatment of Patient With Major Depressive Disorder
2026年8月20日 更新者:Sunshine Lake Pharma Co., Ltd.
A Phase II/III ,Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, Adaptive Design Study Evaluating the Efficacy And Safety of Mitizodone Phosphate Tablets in the Treatment of Patient With Major Depressive Disorder
This is a phase 2 and 3 adaptive design study for Mitizodone Phosphate,to find out an optimal dose in phase 2 period and confirm the result an efficacy and safety in phase 3 period.Dose-finding will be done after 8 weeks of double-blinded treatment in phase 2 period and will be assessed by both efficacy and safety from 3 dose groups of Mitizodone Phosphate.The dose be found in phase 2 period will be evaluated on efficacy and safety when compared with placebo in phase 3 period with a duration of 8 weeks treatment.The target subjects are patients with MDD.
研究概览
研究类型
介入性
注册 (估计的)
600
阶段
- 阶段2
- 第三阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:gang wang, Ph.D
- 电话号码:86-010-58303236
- 邮箱:gangwangdoc@gmail.com
学习地点
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Guangdong
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Dongguan、Guangdong、中国、523871
- 招聘中
- Sunshine Lake Pharma Co., Ltd.
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接触:
- Li Xue
- 电话号码:+8676985315888
- 邮箱:lixuelc@hec.cn
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 65年 (成人、年长者)
接受健康志愿者
不
描述
Inclusion Criteria:
- 1.a Man or a woman with major depressive disorder(MDD) as the primary diagnosis according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria (classification code 296.22、296.23、296.32、296.33)
- 2.Has a Montgomery Åsberg Depression Rating Scale (MADRS) total score of 26 or greater at Screening and Baseline Visits.
- 3.Has a Clinical Global Impression - Severity of Illness (CGI-S) score of 4 or greater at Screening and Baseline Visits.
Exclusion Criteria:
- 1.has major depressive disorder with psychotic features according to the DSM-5.
- 2.Current or history of: bipolar disorder、schizophrenia、anixety disorder、insomnia、any substance abuse or dependence and other psychiatry disorder as defined in the DSM-5.
- 3.Current or history of a clinically significant neurological disorder (including epilepsy、Alzheimer disease, Parkinson disease, multiple sclerosis, Huntington disease).
- 4. has Serious body disease such as neurological disorders、cardiacvascular disorders、hepatic disorders、 renal disorders, blood system disorders and endocrine disorders.
- 5. Current or history of cancer( except basal cell of the skin and preinvasive carcinoma of cervix uteri).
- 6. Current or history of angle-closure glaucoma.
- 7. has made a suicide behavior in the previous 1 year ,or has a score greater than or equal to 4 on item 10 (suicidal thoughts) of MADRS .
- 8.has taken fluoxetine within 4 weeks prior to initial dosing.
- 9. has taken other antidepressive medications or antipsychotic medications within 2 weeks prior to initial dosing.
- 10.has psychotherap at Screening and/or Baseline Visits.
- 11.has had physiotherapy within 3 months prior to initial dosing.
- 12.Has an alanine aminotransferase, aspartate aminotransferase or total bilirubin level greater than 1.5 times the upper limits of normal.
- 13.Has an alanine aminotransferase, aspartate aminotransferase level greater than 2 times the upper limits of normal;or total bilirubin, direct bilirubin,creatinine level greater than 1.5 times the upper limits of normal;or a thyroid stimulating hormone value outside the normal range.
- 14.Has an abnormal electrocardiogram confirmed as clinically significant by the investigator.
- 15.Has a history of severe allergies.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Mitizodone Phosphate tablet 10mg
Mitizodone Phosphate tablet 10mg ,orally,once daily for 8 weeks, then placebo,orally,once daily for 2 weeks.
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Mitizodone Phosphate tablets will be administered with food.
其他名称:
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实验性的:Mitizodone Phosphate tablet 20mg
Mitizodone Phosphate tablet 10mg ,orally,once daily for 1 weeks, then Mitizodone Phosphate tablet 20mg ,orally,once daily for 7 weeks, then Mitizodone Phosphate tablet 10mg ,orally,once daily for 1 weeks, then placebo,orally,once daily for 1 weeks.
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Mitizodone Phosphate tablets will be administered with food.
其他名称:
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实验性的:Mitizodone Phosphate tablet 40mg
Mitizodone Phosphate tablet 10mg ,orally,once daily for 1 weeks, then Mitizodone Phosphate tablet 20mg ,orally,once daily for 1 weeks, then Mitizodone Phosphate tablet 40mg ,orally,once daily for 6 weeks, then Mitizodone Phosphate tablet 20mg ,orally,once daily for 1 weeks, then Mitizodone Phosphate tablet 10mg ,orally,once daily for 1 weeks.
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Mitizodone Phosphate tablets will be administered with food.
其他名称:
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有源比较器:Placebo
Placebo,tablet,orally,once daily for 10 weeks.
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Placebo will be administered with food.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
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Change From Baseline in the Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score at week 8
大体时间:baseline and week 8
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The MADRS is a depression rating scale consisting of 10 items, each rated 0 (normal) to 6 (most abnormal).
The 10 items represent the core symptoms of depressive illness.
The overall score ranges from 0 (symptoms absent) to 60 (severe depression).
A decrease in the total score or on individual items indicates improvement.
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baseline and week 8
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Percentage of subjects With a MADRS Response at Week 8
大体时间:baseline and week 8
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Response is defined as a subject with a ≥50% decrease in Montgomery Åsberg Depression Rating Scale (MADRS) total score from Baseline.
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baseline and week 8
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Percentage of Participants in MADRS Remission at Week 8
大体时间:week 8
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Remission is defined as a participant with a Montgomery Åsberg Depression Rating Scale (MADRS) total score ≤10.
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week 8
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Change From Baseline in the Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score at week 1、week 2 、week 4、week 6.
大体时间:baseline 、 week 1、week 2 、week 4 and week 6.
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The MADRS is a depression rating scale consisting of 10 items, each rated 0 (normal) to 6 (most abnormal).
The 10 items represent the core symptoms of depressive illness.
The overall score ranges from 0 (symptoms absent) to 60 (severe depression).
A decrease in the total score or on individual items indicates improvement.
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baseline 、 week 1、week 2 、week 4 and week 6.
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Change From Baseline in the Clinical Global Impression - Severity of illness (CGI-S) Total Score at week 1、week 2 、week 4、week 6、week 8.
大体时间:baseline、week 1、week 2 、week 4、week 6 and week 8.
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The Clinical Global Impression-Severity of illness scale assesses the subject's Severity as assessed by the clinician at the moment on a 8-point scale: 0, not assessed ; 1, normal,not at all ill ; 2, borderline mentally ill ; 3, mildly ill ; 4, moderately ill ; 5 , markedly ill ; 6, severely ill;7,among the most extremely ill patients.
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baseline、week 1、week 2 、week 4、week 6 and week 8.
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Clinical Global Impression - Improvement (CGI-I) Score at week 1、week 2 、week 4、week 6、Week 8
大体时间:week 1、week 2 、week 4、week 6 and week 8.
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The Clinical Global Impression- Improvement scale assesses the subject's improvement (or worsening) as assessed by the clinician relative to Baseline on a 8-point scale: 0, not assessed ;1, very much improved; 2, much improved; 3, minimally improved; 4, no change; 5, minimally worse; 6, much worse; or 7, very much worse.
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week 1、week 2 、week 4、week 6 and week 8.
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Change From Baseline in the hamilton anxiety rating scale (HAM-A)Total Score at week 1、week 2 、week 4、week 6、week 8.
大体时间:baseline、week 1、week 2 、week 4、week 6 and week 8.
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the HAM-A is a anxiety rating scale consisting of 14 items, each rated 0 (none) to 4 (very severe).
The 14 items represent the core symptoms of anxiety illness.
The overall score ranges from 0 (symptoms absent) to 56 (severe anxiety).
A decrease in the total score or on individual items indicates improvement.
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baseline、week 1、week 2 、week 4、week 6 and week 8.
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2021年12月14日
初级完成 (估计的)
2027年7月1日
研究完成 (估计的)
2027年11月1日
研究注册日期
首次提交
2021年7月21日
首先提交符合 QC 标准的
2021年7月21日
首次发布 (实际的)
2021年7月30日
研究记录更新
最后更新发布 (实际的)
2026年8月24日
上次提交的符合 QC 标准的更新
2026年8月20日
最后验证
2026年8月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.