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Completed Phase 2 Interventional Results available

A Study of A-101 Topical Solution Administered Twice a Week in Subjects With Common Warts

ClinicalTrials.gov ID: NCT03278028

Public ClinicalTrials.gov record NCT03278028. 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, 2:32 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 Randomized, Double-Blind, Vehicle-Controlled, Parallel Group Study of A-101 Topical Solution Applied Twice a Week in Subjects With Common Warts

Brief summary

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

The primary objective of this study is to evaluate the effectiveness of A-101 compared to Vehicle when applied to 1 Target common wart on the trunk or extremities twice a week.

Study identification

NCT ID
NCT03278028
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aclaris Therapeutics, Inc.
Industry
Enrollment
159 participants

Conditions and interventions

Eligibility (public fields only)

Age range
8 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
Jul 12, 2017
Primary completion
Feb 28, 2018
Completion
Feb 28, 2018
Last update posted
Apr 8, 2019

2017 – 2018

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Aclaris Investigational Site Glendale Arizona 85308
Aclaris Investigational Site Fort Smith Arkansas 72916
Aclaris Investigational Site Encinitas California 92024
Aclaris Investigational Site Los Angeles California 90045
Aclaris Investigational Site Denver Colorado 80210
Aclaris Investigational Site Omaha Nebraska 68144
Aclaris Investigational Site Albuquerque New Mexico 87106
Aclaris Investigational Site Rochester New York 14623
Aclaris Investigational Site High Point South Carolina 27262
Aclaris Investigational Site Knoxville Tennessee 37922
Aclaris Investigational Site Nashville Tennessee 37215
Aclaris Investigational Site College Station Texas 77845
Aclaris Investigational Site Houston Texas 77004
Aclaris Investigational Site Salt Lake City Utah 84117
Aclaris Investigational Site Lynchburg Virginia 24501
Aclaris Investigational Site Norfolk Virginia 23507

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 NCT03278028, 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 Apr 8, 2019 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03278028 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →