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Efficacy and Safety Study Comparing CD07805/47 Gel 0.5% to Azelaic Acid Gel 15% in Subjects With Erythema of Rosacea
NCT01659853 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to compare the efficacy and assess the safety of CD07805/47 gel 0.5% applied topically once daily versus azelaic acid gel 15% applied topically twice daily in subjects with moderate to severe facial erythema of rosacea.
Interventions
- DRUG CD07805/47 gel 0.5%/CD07805/47 Vehicle
- DRUG azelaic acid gel 15%
Study Locations (4)
Indiana
- Hudson Dermatology — Evansville
Kentucky
- Dermatology Specialists Research, LLC — Louisville
Texas
- DermResearch, Inc — Austin
Virginia
- The Education & Research Foundation, Inc. — Lynchburg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2012-09 |
| Est. Completion | 2012-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01659853
The ClinicalTrials.gov registry entry for NCT01659853 describes a study currently listed as completed. It is categorized as Phase 3, 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 70 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 2 conditions, with Rosacea appearing as the primary indexed condition, and to 2 interventions — of which CD07805/47 gel 0.5%/CD07805/47 Vehicle 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: NCT01659853 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Indiana, Kentucky, Texas. 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 NCT01659853 about?
NCT01659853 is a clinical study titled "Efficacy and Safety Study Comparing CD07805/47 Gel 0.5% to Azelaic Acid Gel 15% in Subjects With Erythema of Rosacea". The purpose of this study is to compare the efficacy and assess the safety of CD07805/47 gel 0.5% applied topically once daily versus azelaic acid gel 15% applied topically twice daily in subjects with moderate to severe facial erythema of rosacea.
What is the current status of trial NCT01659853?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 70 participants. The study started on 2012-09. Estimated completion is 2012-12.
What conditions does trial NCT01659853 study?
This clinical trial studies the following conditions: Rosacea, Erythema. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01659853?
The interventions under investigation include: CD07805/47 gel 0.5%/CD07805/47 Vehicle (DRUG), azelaic acid gel 15% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01659853?
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 NCT01659853 being conducted?
This trial has 4 study locations across Indiana, Kentucky, Texas, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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