A Study to Evaluate the Long-term Safety of HS-10380 in Patients With Schizophrenia
2026年8月7日 更新者:Jiangsu Hansoh Pharmaceutical Co., Ltd.
A Multicenter, Open-label, Phase 3 Study to Evaluate the Long-term Safety of HS-10380 in Chinese Adult Patients With Schizophrenia
The primary purpose of this open-label phase 3 study is to evaluate the safety of HS-10380 on the incidence, severity, relationship to investigational product of adverse events (AE), serious adverse events (SAE), and adverse events leading to study drug discontinuationin Chinese adult participants with schizophrenia.
研究概览
详细说明
The study will comprise 3 periods : a Screening Period, an Open-Label Treatment Period during which participants will be treated for 52 weeks and a 14-day Follow-up Period before an End of Study (EOS) Visit.
The total study duration for each participant on this study is 57 weeks.
研究类型
介入性
注册 (估计的)
500
阶段
- 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:Tianmei Si
- 电话号码:010-62723761
- 邮箱:si.tian-mei@163.com
学习地点
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100191
- Peking University Sixth Hospital
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接触:
- Tianmei Si
- 电话号码:010-62723761
- 邮箱:si.tian-mei@163.com
-
-
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
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Participant is aged 18-65 years, inclusive, at screening.
- Body mass index must be ≥18.0 and ≤40.0 kg/m² at screening.
- Participant has a primary diagnosis of schizophrenia established by a comprehensive psychiatric evaluation based on the DSM-5 criteria.
- Willing and able to give informed consent/assent as per local requirements.
- Participants are willing and able to discontinue all antipsychotic medications prior to the baseline visit, as determined by the investigator.
Exclusion Criteria:
- Participant has a current DSM-5 diagnosis or presence of symptoms consistent with a DSM-5 diagnosis other than schizophrenia.
- Judged by the investigator as having treatment-resistant schizophrenia.
- Patients with risk of violent or destructive behavior, or suicidal risk.
- History or presence of clinically significant disease or any other condition that, in the opinion of the investigator, would jeopardize the safety of the subject or the validity of the study results.
- Any surgical condition or medical condition that may significantly affect drug absorption, distribution, metabolism, and excretion, or that may pose a risk to trial participants, such as history of gastrointestinal surgery (gastrectomy, gastroenterostomy, bowel resection, etc.), urinary tract obstruction, or dysuria.
- History of severe allergic reactions.
- Female patients who are pregnant, in puerperium, or lactating at screening or baseline.
- History of drug abuse within 1 year prior to screening.
- History of alcohol abuse within 6 months prior to screening.
- Abnormal physical examination findings、vital signs or 12-lead electrocardiogram (ECG) at screening .
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:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:HS-10380 (1.5-6mg)
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Oral;QD;W1:dose titration; W1-2:dose adjust to optimal level;Week 3-52:stable dose.
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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 |
|---|---|---|
|
Incidence and severity of adverse events (AE)
大体时间:From first dose to end of study (Up to approximately 54 weeks )
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TEAEs are defined as events with an onset date on or after the first dose of HS-10380.
An Adverse Event is any symptom, physical sign, syndrome, or disease that either emerges during the study or, if present at baseline, worsens during the study, regardless of the suspected cause of the event.
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From first dose to end of study (Up to approximately 54 weeks )
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Incidence and severity of serious adverse events (SAE)
大体时间:From first dose to end of study (Up to approximately 52 weeks)
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An SAE is any untoward medical occurrence, in the view of either the investigator or sponsor, that results in death; is life-threatening; results in inpatient hospitalization or prolongation of existing hospitalization ; results in persistent or significant disability/incapacity, and/or; is a congenital anomaly/birth defect.
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From first dose to end of study (Up to approximately 52 weeks)
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Incidence of Treatment-Emergent Adverse Events (TEAE) Leading to Study Drug Discontinuation
大体时间:From first dose to end of study (Up to approximately 54 weeks )
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TEAEs are defined as events with an onset date on or after the first dose of HS-10380.
An Adverse Event is any symptom, physical sign, syndrome, or disease that either emerges during the study or, if present at baseline, worsens during the study, regardless of the suspected cause of the event.
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From first dose to end of study (Up to approximately 54 weeks )
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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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Change From Baseline in Positive and Negative Syndrome Scale (PANSS) Total Score
大体时间:Open-label extension baseline, week 52
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The PANSS rating form contains 7 positive symptom scales, 7 negative system scales, and 16 general psychopathology symptom scales.
Participants are rated from 1 to 7 on each symptom scale.
The positive symptoms in schizophrenia are the excess or distortion of normal function and the negative symptoms are the diminution or loss of normal functions .
PANSS total score is the sum of all 30 items with a minimum score of 30 and a maximum score of 210.
Higher scores indicate more severe symptoms.
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Open-label extension baseline, week 52
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Change from Baseline in Clinical Global Impression-Severity (CGI-S) Score
大体时间:Open-label extension baseline, week 52
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The CGI-S modified asked the clinician 1 question: "Considering your total clinical experience, how mentally ill is the participant at this time?"
The clinician's answer rated on the following 7-point scale: 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 participants.
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Open-label extension baseline, week 52
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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 (估计的)
2026年9月9日
初级完成 (估计的)
2028年7月31日
研究完成 (估计的)
2028年8月31日
研究注册日期
首次提交
2026年8月7日
首先提交符合 QC 标准的
2026年8月7日
首次发布 (实际的)
2026年8月12日
研究记录更新
最后更新发布 (实际的)
2026年8月12日
上次提交的符合 QC 标准的更新
2026年8月7日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- HS-10380-303
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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