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Efficacy, Safety, and Tolerability of TD1414 2% Cream in Impetigo and Secondarily Infected Traumatic Lesions (SITL)

Impetigo Clinical Trial

Official title:
Efficacy, Safety and Tolerability of TD1414 2% Cream in Impetigo and Secondarily Infected Traumatic Lesions (SITL)

Clinical Trial Summary

An international, multi-centre, prospective three arm parallel-group, phase II proof of concept study comparing the efficacy and safety of two dosage regimens (BID 7 days and TID 7 days) of TD1414 2% cream and one dosage regimen (BID 7 days) of Bactroban® (mupirocin) 2% cream in adults and children down to 2 years of age with impetigo or SITL. Furthermore an evaluation of the pharmacokinetics of TD1414 2% cream TID for 7 days will be performed. A total of 664 patients will be enrolled in a stepwise manner according to age groups starting with the oldest age group.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Impetigo
  • Secondarily Infected Traumatic Lesions
Clinical Trial Details
NCT number NCT00626795
Study type Interventional
Source LEO Pharma
Contact
Status Completed
Phase Phase 2
Start date February 2008
Completion date June 2009
View Details
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