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COMPLETED Phase 2

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

NCT01174030 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this vehicle controlled study is to evaluate the efficacy and safety of CD07805/47 gel 0.5% applied topically once daily (QD) for 4 weeks, and CD07805/47 gel 0.18% applied topically once daily (QD) or twice daily (BID) for 4 weeks, in subjects with moderate to severe facial erythema associated with rosacea.

Conditions Studied

Interventions

  • DRUG Vehicle Gel
  • DRUG CD07805/47 Gel

Study Locations (20)

North Carolina

  • Dermatology Laser & Vein Specialists — Charlotte
  • Dermatology Consulting Services — High Point

Oregon

  • Oregon Dermatology & Research Center — Portland
  • Oregon Medical Research — Portland

Pennsylvania

  • Philadelphia Institute of Dermatology — Fort Washington
  • DermDox — Hazleton

Texas

  • Arlington Center for Dermatology — Arlington
  • Dermatology Treatment & Research Center — Dallas

Arkansas

  • Burke Pharmaceutical Research — Hot Springs

California

  • University of California at San Francisco — San Francisco

Georgia

  • Meda Phase, Inc — Newnan

Kentucky

  • Dermatology Specialists PC — Louisville

Trial Details

FieldValue
Enrollment Target 269 participants
Start Date 2010-08
Est. Completion 2011-01
Phase Phase 2

Sponsor

Galderma R&D

49 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01174030

The ClinicalTrials.gov registry entry for NCT01174030 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 269 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Galderma R&D, which has 49 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Rosacea appearing as the primary indexed condition, and to 2 interventions — of which Vehicle Gel is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01174030 reports 20 study locations spanning 16 distinct geographic areas — top geographies include North Carolina, Oregon, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01174030 about?

NCT01174030 is a clinical study titled "Efficacy and Safety Study of CD07805/47 Topical Gel in Subjects With Facial Erythema Associated With Rosacea". The purpose of this vehicle controlled study is to evaluate the efficacy and safety of CD07805/47 gel 0.5% applied topically once daily (QD) for 4 weeks, and CD07805/47 gel 0.18% applied topically once daily (QD) or twice daily (BID) for 4 weeks, in subjects with moderate to severe facial erythema a...

What is the current status of trial NCT01174030?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 269 participants. The study started on 2010-08. Estimated completion is 2011-01.

What conditions does trial NCT01174030 study?

This clinical trial studies the following conditions: Rosacea. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01174030?

The interventions under investigation include: Vehicle Gel (DRUG), CD07805/47 Gel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01174030?

This trial is sponsored by Galderma R&D, which has 49 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01174030 being conducted?

This trial has 20 study locations across Arkansas, California, Georgia, Kentucky, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial