drugset / Trial / NCT00077675

Phase 2 Trial of TD-6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)

NCT00077675

Phase 2 Completed 201 enrolled Cumberland Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

Serious infections caused by resistant bacteria are becoming more of a medical problem throughout the world. This study will measure how well TD-6424 (Telavancin) can control infections and whether the drug is safe to give to patients.

Timeline

Start
2004-02
Primary completion
2004-09
Completion
2004-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Telavancin Other / unclassified 7.5 mg/kg Intravenous
Subject Telavancin Other / unclassified 10 mg/kg Intravenous
Comparator Vancomycin Other / unclassified 1 g Intravenous
Comparator cloxacillin Other / unclassified 0.5 g Intravenous
Comparator cloxacillin Other / unclassified 1 g Intravenous
Comparator nafcillin Small molecule 2 g Intravenous
Comparator oxacillin Small molecule 2 g Intravenous