Condition: Premature Ejaculation · Sponsor: Kadence Bio
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.
This description comes directly from the study's public registry record.
Maya Worth · 0395096166 · mayaworth@emeritusresearch.com
Always discuss trial participation with your own doctor first.
| Emeritus Research Sydney | Botany, New South Wales, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07434271