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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 Oct 21, 2026, 9:25 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

Brief summary

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

This study will investigate the safety and efficacy of a new formulation of an existing medication for the treatment of papulopustular rosacea. The study will test the active ingredient plus foam against foam alone.

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

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
Dec 2009 (Type not available)
Primary completion
Aug 2010 (Actual)
Completion
Aug 2010 (Actual)
Last update posted
Mar 31, 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 31, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01025635 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →