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Evaluate the Efficacy and Safety of VV913 Capsules in the Treatment of PE

19 juillet 2026 mis à jour par: 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.

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Estimé)

500

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Beijing Municipality
      • Beijing, Beijing Municipality, Chine, 100034
        • Peking University First Hospital

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  1. Male participants aged 18 to 55 years old (inclusive).
  2. Diagnosed with premature ejaculation (PE) per the definition issued by the International Society for Sexual Medicine (ISSM).
  3. 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.
  4. Participants had a Premature Ejaculation Diagnostic Tool (PEDT) total score ≥ 11.
  5. 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.
  6. 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.
  7. Participants fully understood the study procedures, volunteered to participate in this trial, and provided written informed consent.
  8. Participants must use reliable contraceptive measures from the date of informed consent signature until 3 months after the last study drug administration.

Exclusion Criteria:

  1. 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).
  2. Participants suffering from erectile dysfunction, defined as a total score ≤21 on the International Index of Erectile Function-5 (IIEF-5).
  3. 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.
  4. 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.
  5. Participants' female partners who are pregnant, breastfeeding or planning pregnancy, or suffering from gynecological diseases or receiving relevant treatments that restrict sexual activity.
  6. Participants with diseases that may affect the absorption of oral medications, such as active enteropathy, partial or complete intestinal obstruction, chronic diarrhea, etc.
  7. 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.
  8. 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).
  9. 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.
  10. 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).
  11. Participants who previously discontinued SSRIs or SNRIs due to adverse reactions, or experienced syncope after administration of such drugs.
  12. Participants who received any anti-premature ejaculation treatment within 28 days before randomization.
  13. 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.
  14. Participants who participated in another clinical trial and received investigational medicinal products or medical device treatment within 3 months prior to screening.
  15. Participants with other conditions deemed ineligible for trial participation by the investigator.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur placebo: Groupe placebo
VV913 Placebo Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
Expérimental: VV913 2mg group
VV913 2mg Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
Expérimental: VV913 5mg group
VV913 5mg Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse
Expérimental: VV913 10mg group
VV913 10mg Capsules, taken orally on demand, 0.5-4 hours prior to sexual intercourse

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Mean intravaginal ejaculatory latency time (IELT) over the treatment period
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Mean IELT after the first dose, Week 4 and Week 8 of treatment
Délai: 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
Changes from baseline in mean IELT after the treatment period
Délai: Part I: first dose, Week 4; Part II: first dose, Week 4, Week 8, Week 12
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
Proportion of participants with a mean IELT increase of >1 min, >2 min, and >3 min
Délai: 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
Geometric mean ratio of mean IELT during the treatment period to baseline mean IELT
Délai: Part I: Week 4; Part II: Week 4, Week 8, Week 12
Assessed was the geometric mean ratio of mean IELT during the treatment period to baseline mean IELT.
Part I: Week 4; Part II: Week 4, Week 8, Week 12
Change from baseline in Premature Ejaculation Diagnostic Tool (PEDT) score
Délai: Part I: Week 4; Part II: Week 4, Week 8, Week 12
Assessed was the change from baseline in Premature Ejaculation Diagnostic Tool (PEDT) score.
Part I: Week 4; Part II: Week 4, Week 8, Week 12
Changes from baseline in the Index of Premature Ejaculation (IPE) Domains of Ejaculatory Control, Distress and Sexual Satisfaction
Délai: 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
Changes from baseline in Premature Ejaculation Profile (PEP)
Délai: Part II: Week 4, Week 8, Week 12
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.
Part II: Week 4, Week 8, Week 12

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Hui Jiang, Peking University First Hospital

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

31 août 2026

Achèvement primaire (Estimé)

31 décembre 2027

Achèvement de l'étude (Estimé)

31 décembre 2027

Dates d'inscription aux études

Première soumission

19 juillet 2026

Première soumission répondant aux critères de contrôle qualité

19 juillet 2026

Première publication (Réel)

23 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

23 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 juillet 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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