Evaluate the Efficacy and Safety of VV913 Capsules in the Treatment of PE
2026年7月19日 更新者:Vigonvita Life Sciences
Phase II Multicenter, Randomized, Double-Blind, Placebo-Controlled Parallel-Group Clinical Trial to Evaluate the Efficacy and Safety of VV913 Capsules in the Treatment of Premature Ejaculation
This trial adopted a multicenter, randomized, double-blind, placebo-controlled design and consisted of two parts: Part Ⅰ and Part Ⅱ.
研究概览
详细说明
Part Ⅰ is a 4-week treatment period and Part Ⅱ is a 12-week treatment period, to evaluate the efficacy, safety, and PK/PD relationships of different doses of VV913 capsules in the treatment of premature ejaculation.
研究类型
介入性
注册 (估计的)
500
阶段
- 阶段2
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:Huaqing Duan
- 电话号码:18061926005
- 邮箱:huaqing.duan@vigonvita.cn
学习地点
-
-
Beijing Municipality
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Beijing、Beijing Municipality、中国、100034
- Peking University First Hospital
-
-
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
接受健康志愿者
不
描述
Inclusion Criteria:
- Male participants aged 18 to 55 years old (inclusive).
- Diagnosed with premature ejaculation (PE) per the definition issued by the International Society for Sexual Medicine (ISSM).
- Participants achieved ≥4 coital ejaculations during the run-in period, with intravaginal ejaculatory latency time (IELT) ≤ 2 min in ≥75% of all sexual intercourse attempts.
- Participants had a Premature Ejaculation Diagnostic Tool (PEDT) total score ≥ 11.
- Participants maintained a stable sexual relationship with the same adult female partner for a minimum of 3 months, and intended to sustain this relationship throughout the study period.
- Participants agreed to complete ≥4 coital ejaculations every 28 days during the double-blind treatment period, and were capable of completing all study visits, examinations, assessments and other trial-related procedures as specified in the protocol.
- Participants fully understood the study procedures, volunteered to participate in this trial, and provided written informed consent.
- Participants must use reliable contraceptive measures from the date of informed consent signature until 3 months after the last study drug administration.
Exclusion Criteria:
- Participants with known hypersensitivity to any components of VV913 capsules or its placebo, or a prior history of hypersensitivity to selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs).
- Participants suffering from erectile dysfunction, defined as a total score ≤21 on the International Index of Erectile Function-5 (IIEF-5).
- Participants who had genitourinary diseases that may impair sexual function (e.g., prostatitis, phimosis, urinary tract infection, etc.) or underwent genitourinary surgery within 28 days prior to screening and during the baseline period.
- Participants or their female partners diagnosed with psychiatric disorders by psychiatrists, such as major depressive disorder, generalized anxiety disorder, bipolar I disorder, bipolar II disorder, panic disorder, obsessive-compulsive disorder, post-traumatic stress disorder, alcohol use disorder, schizophrenia or other psychiatric disorders.
- Participants' female partners who are pregnant, breastfeeding or planning pregnancy, or suffering from gynecological diseases or receiving relevant treatments that restrict sexual activity.
- Participants with diseases that may affect the absorption of oral medications, such as active enteropathy, partial or complete intestinal obstruction, chronic diarrhea, etc.
- Participants with severe cardiovascular diseases judged by investigators to potentially increase trial risks, including heart failure (NYHA Class II-IV), clinically significant conduction abnormalities (e.g., second- or third-degree atrioventricular block, sick sinus syndrome, etc.), severe or unstable coronary artery disease/ischemic heart disease, severe carotid artery stenosis, left ventricular outflow tract obstruction, etc.
- Participants with active malignant tumors, or a medical history of malignant tumors within 5 years before screening (except completely resected and cured cutaneous squamous cell carcinoma).
- Participants with clinically significant liver or renal function abnormalities, i.e., serum ALT and/or AST > 2 times the upper limit of normal (ULN), or serum creatinine > 1.2 times ULN.
- Participants with uncontrolled hypertension (systolic blood pressure >160 mmHg or diastolic blood pressure >95 mmHg) or hypotension (systolic blood pressure <90 mmHg or diastolic blood pressure <60 mmHg).
- Participants who previously discontinued SSRIs or SNRIs due to adverse reactions, or experienced syncope after administration of such drugs.
- Participants who received any anti-premature ejaculation treatment within 28 days before randomization.
- Participants who used monoamine oxidase inhibitors, strong CYP3A4 inhibitors, moderate CYP3A4 inhibitors, strong CYP3A4 inducers or moderate CYP3A4 inducers within 28 days before randomization, or required concomitant use of such agents during the trial.
- Participants who participated in another clinical trial and received investigational medicinal products or medical device treatment within 3 months prior to screening.
- Participants with other conditions deemed ineligible for trial participation by the investigator.
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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安慰剂比较:安慰剂组
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VV913 Placebo Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
|
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实验性的:VV913 2mg group
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VV913 2mg Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
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实验性的:VV913 5mg group
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VV913 5mg Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
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实验性的:VV913 10mg group
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VV913 10mg Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
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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 |
|---|---|---|
|
Mean intravaginal ejaculatory latency time (IELT) over the treatment period
大体时间:Part I: Week 4; Part II: Week 12
|
Assessed was the mean IELT.
IELT is measured with a stopwatch during each sexual intercourse throughout treatment.
|
Part I: Week 4; Part II: Week 12
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Mean IELT after the first dose, Week 4 and Week 8 of treatment
大体时间:Part I: first dose; Part II: first dose, Week 4, Week 8
|
Assessed was the mean IELT after the first dose, Week 4 and Week 8 of treatment.
|
Part I: first dose; Part II: first dose, Week 4, Week 8
|
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Changes from baseline in mean IELT after the treatment period
大体时间:Part I: first dose, Week 4; Part II: first dose, Week 4, Week 8, Week 12
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Assessed was the mean change from baseline in mean IELT after the treatment period.
|
Part I: first dose, Week 4; Part II: first dose, Week 4, Week 8, Week 12
|
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Proportion of participants with a mean IELT increase of >1 min, >2 min, and >3 min
大体时间:Part I: Week 4; Part II: Week 4, Week 8, Week 12
|
Assessed were the proportions of participants whose mean IELT increased by more than 1 min, 2 min, and 3 min.
|
Part I: Week 4; Part II: Week 4, Week 8, Week 12
|
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Geometric mean ratio of mean IELT during the treatment period to baseline mean IELT
大体时间:Part I: Week 4; Part II: Week 4, Week 8, Week 12
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Assessed was the geometric mean ratio of mean IELT during the treatment period to baseline mean IELT.
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Part I: Week 4; Part II: Week 4, Week 8, Week 12
|
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Change from baseline in Premature Ejaculation Diagnostic Tool (PEDT) score
大体时间:Part I: Week 4; Part II: Week 4, Week 8, Week 12
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Assessed was the change from baseline in Premature Ejaculation Diagnostic Tool (PEDT) score.
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Part I: Week 4; Part II: Week 4, Week 8, Week 12
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Changes from baseline in the Index of Premature Ejaculation (IPE) Domains of Ejaculatory Control, Distress and Sexual Satisfaction
大体时间:Part II: Week 4, Week 8, Week 12
|
Assessed were the changes from baseline in the IPE domains of ejaculatory control, distress and sexual satisfaction. Ejaculatory control scores range from 4 to 20 with a higher score indicating greater ejaculatory control. Sexual satisfaction scores range from 4 to 20 with a higher score indicating greater sexual satisfaction. Distress scores range from 2 to 10 with a higher score indicating less distress. |
Part II: Week 4, Week 8, Week 12
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Changes from baseline in Premature Ejaculation Profile (PEP)
大体时间:Part II: Week 4, Week 8, Week 12
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Assessed were the changes from baseline in scores for perceived control over ejaculation, personal distress related to ejaculation, satisfaction with sexual intercourse and interpersonal difficulty related to ejaculation.
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Part II: Week 4, Week 8, Week 12
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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。
调查人员
- 首席研究员:Hui Jiang、Peking University First Hospital
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8月31日
初级完成 (估计的)
2027年12月31日
研究完成 (估计的)
2027年12月31日
研究注册日期
首次提交
2026年7月19日
首先提交符合 QC 标准的
2026年7月19日
首次发布 (实际的)
2026年7月23日
研究记录更新
最后更新发布 (实际的)
2026年7月23日
上次提交的符合 QC 标准的更新
2026年7月19日
最后验证
2026年7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.