Clinical Trials Directory

Trials / Completed

CompletedNCT01461655

Efficacy and the Tolerability of the Sequential Application of Two Marketed Products in Patients With Acne Vulgaris

Exploratory Study Evaluating the Efficacy and the Tolerability of the Sequential Application of Two Marketed Products in Patients With Acne Vulgaris, Using a Split-Face Model

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (actual)
Sponsor
LEO Pharma · Industry
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Not accepted

Summary

The aim of this proof of principle study is to evaluate efficacy and safety of the sequential application of two marketed products for the treatment of acne vulgaris, using the Split-Face model

Conditions

Interventions

TypeNameDescription
DRUGmarketed topical retinoidonce daily application, 4 weeks
DRUGmarketed topical NSAIDonce daily application, 4 weeks
DRUGvehicle gelonce daily application, 4 weeks
DRUGmarketed topical retinoidonce daily application, 4 weeks

Timeline

Start date
2011-11-01
Primary completion
2012-04-01
Completion
2012-05-01
First posted
2011-10-28
Last updated
2025-03-10
Results posted
2013-12-04

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01461655. Inclusion in this directory is not an endorsement.