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Completed Phase 3 Interventional Results available

A Study to Evaluate the Safety and Clinical Study of Azelaic Acid Gel 15% in Patients With Moderate Facial Rosacea

ClinicalTrials.gov ID: NCT02120924

Public ClinicalTrials.gov record NCT02120924. 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 Jul 21, 2026, 10:17 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, Double-blind, Randomized, Parallel-group, Vehicle-Controlled Study to Evaluate the Safety and Clinical Equivalence of a Generic Azelaic Acid Gel, 15% and the Reference Listed Finacea® (Azelaic Acid) Gel, 15% in Patients With Moderate Facial Rosacea.

Study identification

NCT ID
NCT02120924
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Actavis Inc.
Industry
Enrollment
1,009 participants

Conditions and interventions

Conditions

Interventions

  • Azelaic acid Drug
  • Vehicle Drug
  • Finacea Drug

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
Jun 30, 2013
Primary completion
Aug 31, 2014
Completion
Aug 31, 2014
Last update posted
Jun 1, 2020

2013 – 2014

United States locations

U.S. sites
30
U.S. states
16
U.S. cities
29
Facility City State ZIP Site status
Site 24 Fremont California
Site 22 Santa Monica California
Site 1 Brandon Florida
Site 3 Fort Myers Florida
Site 27 Jacksonville Florida
Site 19 Miami Florida
Site 9 Miami Florida
Site 29 Miramar Florida
Site 2 Tampa Florida
Site 15 Chicago Illinois
Site 4 Plainfield Indiana
Site 14 Lake Charles Louisiana
Site 17 Glenn Dale Maryland
Site 6 Bay City Michigan
Site 30 Clinton Township Michigan
Site 16 Las Vegas Nevada
Site 11 Raleigh North Carolina
Site 23 Winston-Salem North Carolina
Site 26 Philadelphia Pennsylvania
Site 12 Warwick Rhode Island
Site 28 Simpsonville South Carolina
Site 20 Nashville Tennessee
Site 21 College Station Texas
Site 5 Dallas Texas
Site 8 El Paso Texas
Site 13 Houston Texas
Site 7 Katy Texas
Site 18 Salt Lake City Utah
Site 10 Norfolk Virginia
Site 25 University Place Virginia

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 NCT02120924, 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 Jun 1, 2020 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02120924 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →