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Completed Phase 3 Interventional Results available

A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participants With Actinic Keratoses

ClinicalTrials.gov ID: NCT02120898

Public ClinicalTrials.gov record NCT02120898. 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 29, 2026, 10:39 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 Multicenter, Randomized, Double-Blind, Vehicle-Controlled, Parallel Group Comparison Study to Determine the Therapeutic Equivalence of Generic Imiquimod Cream, 2.5% and Zyclara® (Imiquimod) Cream, 2.5% in Subjects With Actinic Keratoses

Brief summary

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

The purpose of this study it so compare the safety and efficacy profiles of a generic imiquimod 2.5% cream to the reference listed Zyclara® (imiquimod) cream in the treatment of actinic keratosis (AK).

Study identification

NCT ID
NCT02120898
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Actavis Inc.
Industry
Enrollment
467 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Oct 10, 2013 (Actual)
Primary completion
Apr 30, 2014 (Actual)
Completion
Apr 30, 2014 (Actual)
Last update posted
Dec 13, 2019

2013 – 2014

United States locations

U.S. sites
27
U.S. states
15
U.S. cities
26
Facility City State ZIP Site status
Site 1 Birmingham Alabama 35025 —
Site 10 Fremont California 94538 —
Site 8 Los Angeles California 90045 —
Site 24 Denver Colorado 80220 —
Site 28 Boca Raton Florida 33486 —
Site 26 Brandon Florida 33511 —
Site 27 Brandon Florida 33511 —
Site 21 Boise Idaho 83704 —
Site 3 Arlington Heights Illinois 60005 —
Site 17 Champaign Illinois 61820 —
Site 7 Carmel Indiana 46032 —
Site 15 Indianapolis Indiana 46256 —
Site 22 Plainfield Indiana 46168 —
Site 23 South Bend Indiana 46617 —
Site 16 Clinton Township Michigan 48038 —
Site 13 Fridley Minnesota 55432 —
Site 9 Albuquerque New Mexico 87106 —
Site 4 High Point North Carolina 27262 —
Site 11 Wilmington North Carolina 28403 —
Site 18 Winston-Salem North Carolina 27103 —
Site 25 Portland Oregon 97223 —
Site 20 Fountain Inn South Carolina 29644 —
Site 6 Knoxville Tennessee 37917 —
Site 5 Nashville Tennessee 37203 —
Site 14 Austin Texas 78759 —
Site 12 College Station Texas 77845 —
Site 2 Houston Texas 77056 —

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 NCT02120898, 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 13, 2019 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02120898 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →