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Completed Phase 3 Interventional Results available

A Phase 3 Efficacy & Safety of SB206 & Vehicle Gel for the Treatment of MC

ClinicalTrials.gov ID: NCT03927703

Public ClinicalTrials.gov record NCT03927703. 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 3, 2026, 4:27 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 Multi-Center, Randomized, Double-Blind, Vehicle-Controlled, Parallel Group Study Comparing the Efficacy and Safety of SB206 and Vehicle Gel Once Daily in the Treatment of Molluscum Contagiosum

Brief summary

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

This is a Phase 3 multi-center, randomized, double-blind, vehicle-controlled, parallel group study to be conducted in up to approximately 340 subjects ≥6 months of age with MC. Subjects or their caregivers will apply SB206 12% or Vehicle Gel once daily for a minimum of 4 weeks and up to 12 weeks to all lesions identified at Baseline and new treatable lesions that arise during the course of the study.

Study identification

NCT ID
NCT03927703
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novan, Inc.
Industry
Enrollment
355 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Months 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
Jun 12, 2019
Primary completion
Nov 10, 2019
Completion
Feb 2, 2020
Last update posted
Mar 22, 2023

2019 – 2020

United States locations

U.S. sites
27
U.S. states
21
U.S. cities
27
Facility City State ZIP Site status
Site #266 Scottsdale Arizona 85255
Site #101 Hot Springs Arkansas 71913
Site #282 Beverly Hills California 90212
Site #113 San Diego California 92123
Site #257 Thornton Colorado 80233
Site #268 Boynton Beach Florida 33437
Site #292 DeLand Florida 32720
Site #278 Miami Florida 33175
Site #305 Tampa Florida 33613
Site #175 New Albany Indiana 47150
Site #294 Owensboro Kentucky 42301
Site #289 Metairie Louisiana 70006
Site #297 New Orleans Louisiana 70124
Site #275 Largo Maryland 20774
Site #274 Clarkston Michigan 48346
Site #121 Fridley Minnesota 55448
Site #206 Omaha Nebraska 68144
Site #304 Portsmouth New Hampshire 03801
Site #201 Berlin New Jersey 08009
Site #108 Rochester New York 14623
Site #309 Portland Oregon 97223
Site #255 Mt. Pleasant South Carolina 29464
Site #271 Knoxville Tennessee 37938
Site #167 Houston Texas 77030
Site #293 Plano Texas 75024
Site #281 Syracuse Utah 84075
Site #267 Richmond Virginia 23294

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 NCT03927703, 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 Mar 22, 2023 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03927703 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →