Clinical Trials Directory

Trials / Completed

CompletedNCT00133874

Topical SB-275833 Ointment, 1% For The Treatment Of Impetigo

An Observer-blind, Multicenter, Non-inferiority, Comparative Study of the Safety and Efficacy of Topical 1% SB-275833 Ointment, Applied Twice Daily for 5 Days, Versus Topical 2% Fusidic Acid Cream Applied Three Times Daily for 7 Days in the Treatment Adult and Paediatric Subjects With Impetigo

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
520 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
9 Months
Healthy volunteers
Not accepted

Summary

The goal of this study is to determine if topical SB-275833 ointment, 1% is as safe and effective as topical sodium fusidate ointment, 2% for the treatment of impetigo in adults and children as young as 9 months of age.

Detailed description

A Randomised, Observer-blind, Multicentre, Non-inferiority, Comparative, Phase III Study of the Safety and Efficacy of Topical 1% SB-275833 Ointment, Applied Twice Daily for 5 Days, versus Topical 2% Sodium Fusidate Ointment Applied Three Times Daily for 7 Days in the Treatment of Adult and Paediatric Subjects with Impetigo.

Conditions

Interventions

TypeNameDescription
DRUGSB-275833 ointment, 1%

Timeline

Start date
2005-04-01
Primary completion
2005-09-01
Completion
2005-09-01
First posted
2005-08-24
Last updated
2017-01-23

Locations

69 sites across 10 countries: Canada, Costa Rica, France, Germany, India, Mexico, Netherlands, Peru, Poland, South Africa

Source: ClinicalTrials.gov record NCT00133874. Inclusion in this directory is not an endorsement.