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Clinical Trials/EUCTR2006-001999-20-HU
EUCTR2006-001999-20-HUActive, not recruitingNot Applicable

ASSESSMENT OF THE EFFICACY AND SAFETY OF THREE CONCENTRATIONS: 1%, 0.3%, 0.1% OF CD5024 CREAM ONCE DAILY AND CD5024 1% CREAM TWICE DAILY, VERSUS ITS VEHICLE AND VERSUS METRONIDAZOLE 0.75% CREAM (ROZEX®), IN PATIENTS WITH PAPULO-PUSTULAR ROSACEA OVER 12 WEEKS

Galderma Research & Development SNC0 sites270 target enrollmentStarted: June 15, 2006Last updated:
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
270

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Sex
All

Inclusion Criteria

  • Male or female subjects with papulo-pustular rosacea with at least 15 inflammatory facial lesions, at least 18 years old, meeting specific inclusion and exclusion criteria
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • 1. The subject has particular forms of rosacea (rosacea conglobata, rosacea fulminans, and secondary rosacea form, isolated erythrosis, isolated rhinophyma, or isolated pustulosis of the chin),
  • 2. The subject has other dermatological disorders such as peri-oral dermatitis, other forms of demodicidosis, facial keratosis pilaris, actual or history of seborrheic dermatitis, which may confound the study assessments,

Investigators

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