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
| Type | Name | Description |
|---|---|---|
| DRUG | SB-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.