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Completed Phase 3 Interventional Results available

Cantharidin Application in Molluscum Patients-1

ClinicalTrials.gov ID: NCT03377790

Public ClinicalTrials.gov record NCT03377790. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 11:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Pivotal Study to Evaluate the Safety and Efficacy of VP-102 Topical Film-Forming Solution [0.7% (w/v) Cantharidin] in Subjects (2 Years and Older) With Molluscum Contagiosum

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03377790
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Verrica Pharmaceuticals Inc.
Industry
Enrollment
266 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 20, 2018
Primary completion
Nov 25, 2018
Completion
Nov 25, 2018
Last update posted
Jan 10, 2022

2018

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Alabama Clinical Therapeutics Birmingham Alabama 35205
Southeastern Pediatric Associates Dothan Alabama 36305
Applied Research Center of Arkansas Little Rock Arkansas 72212
Study Protocol, Inc., Boynton Beach Florida 33437
Skin Research Institute Coral Gables Florida 33146
ASCLEPES Research Center Spring Hill Florida 34609
Olympian Clinical Research Tampa Florida 33609
Summit Dermatology Oakbrook Terrace Illinois 60181
Clarkston Skin Research Clarkston Michigan 48346
St Louis Children's Hospital St Louis Missouri 63104
Midwest Children's Hospital Lincoln Nebraska 68522
Kings County Hospital Brooklyn New York 11203
University North Carolina Dermatology Center Chapel Hill North Carolina 27516
The Pediatric Associates of Fairfield, Inc Fairfield Ohio 45014
Holston Medical Group Bristol Tennessee 37620
Arlington Research Center Arlington Texas 66011
Center for Skin Research Houston Texas 77056
ACRC Trials Plano Pediatrics Plano Texas 75093

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03377790, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 10, 2022 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03377790 live on ClinicalTrials.gov.

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