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Completed Phase 2 Interventional Results available

Efficacy and Safety Study of CD07805/47 Topical Gel in Subjects With Facial Erythema Associated With Rosacea

ClinicalTrials.gov ID: NCT01174030

Public ClinicalTrials.gov record NCT01174030. 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, 2:01 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 4-week, Randomized, Double-blind, Parallel-group, Vehicle-controlled, Multicenter Study Investigating the Efficacy and Safety of CD07805/47 Gel 0.5% Applied Topically Once Daily (QD), and CD07805/47 Gel 0.18% Applied Topically Once Daily (QD) or Twice Daily (BID), in Subjects With Moderate to Severe Facial Erythema Associated With Rosacea

Study identification

NCT ID
NCT01174030
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Galderma R&D
Industry
Enrollment
269 participants

Conditions and interventions

Conditions

Interventions

  • CD07805/47 Gel Drug
  • Vehicle Gel 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
Jul 31, 2010
Primary completion
Nov 30, 2010
Completion
Dec 31, 2010
Last update posted
Feb 25, 2021

2010 – 2011

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Burke Pharmaceutical Research Hot Springs Arkansas 71913
University of California at San Francisco San Francisco California 94143-0660
Meda Phase, Inc Newnan Georgia 30263
Dermatology Specialists PC Louisville Kentucky 40202
Minnesota Clinical Study Center Fridley Minnesota 55432
Central Dermatology, PC St Louis Missouri 63117
Skin Specialty Group New York New York 10021
Dermatology Laser & Vein Specialists Charlotte North Carolina 28207
Dermatology Consulting Services High Point North Carolina 27262
Oregon Dermatology & Research Center Portland Oregon 97210
Oregon Medical Research Portland Oregon 97223
Philadelphia Institute of Dermatology Fort Washington Pennsylvania 19034
DermDox Hazleton Pennsylvania 18201
Palmetto Clinical Trial Services, LLC Greenville South Carolina 29007
The Skin Wellness Center Knoxville Tennessee 37902
Arlington Center for Dermatology Arlington Texas 76011
Dermatology Treatment & Research Center Dallas Texas 75230
The Education & Research Foundation Lynchburg Virginia 24501
Premier Clinical Research Spokane Washington 99204
Madison Skin & Research 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 NCT01174030, 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 Feb 25, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01174030 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →