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Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Evaluate the Safety and Efficacy of SB206 in Subjects With Molluscum Contagiosum

ClinicalTrials.gov ID: NCT03436615

Public ClinicalTrials.gov record NCT03436615. 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 4, 2026, 12:01 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 2 Multi-Center, Randomized, Double-Blind, Vehicle-Controlled Ascending Dose Study of SB206 in Subjects With Molluscum Contagiosum

Brief summary

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

This is a phase 2 multi-center, randomized, double-blind, vehicle-controlled ascending dose study to be conducted in non-immunocompromised subjects with molluscum contagiosum.

Study identification

NCT ID
NCT03436615
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novan, Inc.
Industry
Enrollment
256 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
2 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Jan 23, 2018
Primary completion
Nov 2, 2018
Completion
Nov 2, 2018
Last update posted
May 5, 2023

2018

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
Premier Site# 266 Scottsdale Arizona 85255
Premier Site# 260 Santa Ana California 92701
Premier Site# 257 Thornton Colorado 80233
Premier Site# 264 Doral Florida 33172
Premier Site# 116 Newnan Georgia 30263
Premier Site# 251 Indianapolis Indiana 46256
Premier Site# 253 Lenexa Kansas 66215
Premier Site# 117 Louisville Kentucky 40241
Premier Site# 182 Las Vegas Nevada 89129
Premier Site# 252 Norman Oklahoma 73071
Premier Site# 237 Gresham Oregon 97030
Premier Site# 259 Charleston South Carolina 29414
Premier Site# 255 Mt. Pleasant South Carolina 29464
Premier Site# 131 Houston Texas 77004
Premier Site# 167 Houston Texas 77030
Premier Site# 224 San Antonio Texas 78218
Premier Site# 256 Salt Lake City Utah 84124
Premier 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 NCT03436615, 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 May 5, 2023 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03436615 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →