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COMPLETED Phase 3

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

NCT01318733 · View on ClinicalTrials.gov ↗

Study Summary

A long-term, open-label, non-comparative safety and efficacy study of CD07805/47 gel 0.5% once daily in subjects with moderate to severe facial erythema associated with rosacea.

Conditions Studied

Interventions

  • DRUG CD07805/47 gel 0.5%

Study Locations (20)

North Carolina

  • Metrolina Medical Research — Charlotte
  • Dermatology, Laser & Vein Specialists of the Carolinas — Charlotte
  • Wilmington Medical Research — Wilmington
  • Piedmont Medical Research — Winston-Salem

Tennessee

  • Rivergate Dermatology Clinical Research Center, PLLC — Goodlettsville
  • East Tennessee Medical Research — Johnson City
  • TriCities Medical Research — Kingsport

Colorado

  • Cherry Creek Research, Inc — Denver
  • Longmont Clinical PC — Longmont

Michigan

  • Hamzavi Dermatology — Fort Gratiot
  • Dermcenter PC- Somerset Skin Centre — Troy

California

  • The Laser Institute for Dermatology — Santa Monica

Georgia

  • Gwinnett Clinical Research Center, Inc — Snellville

Indiana

  • Deaconess Clinic — Evansville

Kansas

  • Compliant Clinical Research — Olathe

Trial Details

FieldValue
Enrollment Target 449 participants
Start Date 2011-03
Est. Completion 2012-07
Phase Phase 3

Sponsor

Galderma R&D

49 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01318733

The ClinicalTrials.gov registry entry for NCT01318733 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 449 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 1 intervention — of which CD07805/47 gel 0.5% 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: NCT01318733 reports 20 study locations spanning 13 distinct geographic areas — top geographies include North Carolina, Tennessee, Colorado. 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 NCT01318733 about?

NCT01318733 is a clinical study titled "Study of CD07805/47 Topical Gel in Subjects With Facial Erythema Associated With Rosacea". A long-term, open-label, non-comparative safety and efficacy study of CD07805/47 gel 0.5% once daily in subjects with moderate to severe facial erythema associated with rosacea.

What is the current status of trial NCT01318733?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 449 participants. The study started on 2011-03. Estimated completion is 2012-07.

What conditions does trial NCT01318733 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 NCT01318733?

The interventions under investigation include: CD07805/47 gel 0.5% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01318733?

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 NCT01318733 being conducted?

This trial has 20 study locations across California, Colorado, Georgia, Indiana, Kansas. 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