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Completed Phase 3 Interventional Results available

Cantharidin Application in Molluscum Patients

ClinicalTrials.gov ID: NCT03377803

Public ClinicalTrials.gov record NCT03377803. 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 Oct 21, 2026, 6:54 PM 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
NCT03377803
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Verrica Pharmaceuticals Inc.
Industry
Enrollment
262 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
Feb 14, 2018 (Actual)
Primary completion
Sep 26, 2018 (Actual)
Completion
Sep 26, 2018 (Actual)
Last update posted
Dec 14, 2021

2018

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
Bakersfield Dermatology Bakersfield California 93309 —
Rady Children's Hospital San Diego California 92123 —
Redwood Family Dermatology Santa Rosa California 95403 —
Solution Through Advanced Research Jacksonville Florida 32256 —
Lenus Research and Medical Group Sweetwater Florida 33172 —
Northwestern Memorial Hospital Chicago Illinois 60611 —
Dermatology Center of Northwestern Indiana Crown Point Indiana 46307 —
Pedia Research Evansville Indiana 47715 —
Pedia Research Owensboro Kentucky 42301 —
Hamzavi Dermatology Fort Gratiot Michigan 48059 —
Midwest Children's Health-Northwoods Lincoln Nebraska 68505 —
Midwest Children's Health Lincoln Nebraska 68505 —
Tekton Research Austin Texas 78745 —
DCOL Center for Clinical Research Longview Texas 75605 —
The Education and Research Foundation Lynchburg Virginia 24501 —

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 NCT03377803, 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 Dec 14, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03377803 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →