drugset / Trial / NCT03377790

Cantharidin Application in Molluscum Patients-1

NCT03377790 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is a Phase 3, randomized, double-blind, placebo-controlled, pivotal study to evaluate the safety and efficacy of VP-102 topical film-forming solution in subjects with Molluscum Contagiosum. VP-102 will be applied once every 21 days for up to 4 applications, to treatable molluscum contagiosum (molluscum) lesions on subjects 2 years and older. Efficacy will be assessed as the proportion of subjects achieving complete clearance of all treatable molluscum lesions (baseline and new) on the Day 84 visit.

Timeline

Start
2018-03-21
Primary completion
2018-11-26
Completion
2018-11-26

Outcome

Met primary endpoint

registry analysis (superiority test); VP-102 vs Placebo; p <0.0001 NCT03377790 ↗

paper Complete clearance of all molluscum lesions at day 84 occurred in 50% of VP-102 participants and 15.6% of vehicle recipients (p < 0.0001). PMID 33599960 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Cantharidin Small molecule 0.7 % Topical

Indications