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.
調査の概要
詳細な説明
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.
研究の種類
介入
入学 (推定)
500
段階
- フェーズ2
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Huaqing Duan
- 電話番号:18061926005
- メール:huaqing.duan@vigonvita.cn
研究場所
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100034
- Peking University First Hospital
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
健康ボランティアの受け入れ
いいえ
説明
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.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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プラセボコンパレーター:プラセボ群
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VV913 Placebo Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
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実験的: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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実験的: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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実験的: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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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Mean intravaginal ejaculatory latency time (IELT) over the treatment period
時間枠:Part I: Week 4; Part II: Week 12
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Assessed was the mean IELT.
IELT is measured with a stopwatch during each sexual intercourse throughout treatment.
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Part I: Week 4; Part II: Week 12
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Mean IELT after the first dose, Week 4 and Week 8 of treatment
時間枠:Part I: first dose; Part II: first dose, Week 4, Week 8
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Assessed was the mean IELT after the first dose, Week 4 and Week 8 of treatment.
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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
時間枠: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.
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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
時間枠:Part I: Week 4; Part II: Week 4, Week 8, Week 12
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Assessed were the proportions of participants whose mean IELT increased by more than 1 min, 2 min, and 3 min.
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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
時間枠: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
時間枠: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
時間枠:Part II: Week 4, Week 8, Week 12
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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)
時間枠: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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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者:Hui Jiang、Peking University First Hospital
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年8月31日
一次修了 (推定)
2027年12月31日
研究の完了 (推定)
2027年12月31日
試験登録日
最初に提出
2026年7月19日
QC基準を満たした最初の提出物
2026年7月19日
最初の投稿 (実際)
2026年7月23日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月23日
QC基準を満たした最後の更新が送信されました
2026年7月19日
最終確認日
2026年7月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。