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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 Oct 19, 2026, 4:22 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 24, 2018 (Actual)
Primary completion
Nov 3, 2018 (Actual)
Completion
Nov 3, 2018 (Actual)
Last update posted
May 6, 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 6, 2023 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03436615 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →