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Completed Phase 2 Interventional Results available

Safety and Efficacy of Azelaic Acid Foam, 15% in Papulopustular Rosacea

ClinicalTrials.gov ID: NCT01025635

Public ClinicalTrials.gov record NCT01025635. 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 22, 2026, 10:27 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

Randomized, Double-blind, Vehicle-controlled, Multicenter, Parallel-group Study to Investigate Safety and Efficacy of Azelaic Acid Foam, 15% Topically Applied Twice Daily in Subjects With Papulopustular Rosacea

Study identification

NCT ID
NCT01025635
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
LEO Pharma
Industry
Enrollment
401 participants

Conditions and interventions

Interventions

  • Azelaic acid foam 15% Drug
  • Vehicle foam 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
Nov 30, 2009
Primary completion
Jul 31, 2010
Completion
Jul 31, 2010
Last update posted
Mar 30, 2020

2009 – 2010

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Not listed Birmingham Alabama 35209
Not listed Birmingham Alabama 35233
Not listed Fremont California 94538
Not listed Santa Monica California 90404
Not listed Miami Florida 33175
Not listed Miramar Florida 33027
Not listed Omaha Nebraska 68144
Not listed Albuquerque New Mexico 87106
Not listed High Point North Carolina 27262
Not listed Wilmington North Carolina 28401
Not listed Winston-Salem North Carolina 27103
Not listed Portland Oregon 97210
Not listed Johnston Rhode Island 02919
Not listed Simpsonville South Carolina 29681
Not listed Knoxville Tennessee 37922
Not listed Nashville Tennessee 37215
Not listed Austin Texas 78759
Not listed Plano Texas 75093
Not listed Salt Lake City Utah 84124
Not listed Madison Wisconsin 53719

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 NCT01025635, 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 Mar 30, 2020 · Synced Jul 22, 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 NCT01025635 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →