Study to Evaluate the Potential Effects of KH-001 on Intravaginal Ejaculatory Latency Time (IELT), Patient-Reported Outcomes, and Safety in Men With Lifelong Premature Ejaculation (LPE)

Recruiting Phase 2 Interventional Study
Premature Ejaculation
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 65
Sex
Male
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
40 (estimated)
Sponsor
Kadence Bio · Industry
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About This Trial

This is a Phase 2a, double-blind, placebo-controlled, crossover study evaluating the efficacy, safety, and patient-reported outcomes of KH-001 in men with lifelong premature ejaculation (LPE). Approximately 40 participants will receive KH-001 or placebo in two 4-week treatment periods separated by a washout.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Male participants aged 18 to 65 years (inclusive) at the time of informed consent. 2. In a stable (≥6 months) monogamous heterosexual relationship. 3. Self-reported lifelong premature ejaculation (LPE), meeting the ISSM definition. 4. Intravaginal Ejaculatory Latency Time (IE…
Contacts

Maya Worth

0395096166

mayaworth@emeritusresearch.com

CONTACT