drugset / Trial / NCT00079976

Study Evaluating Tigecycline in Selected Serious Infections Caused by Vancomycin-Resistant Enterococcus (VRE) or Methicillin-Resistant Staphylococcus Aureus (MRSA)

NCT00079976

Phase 3 Completed 174 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedDouble-blindTreatment

Summary

To evaluate the safety and efficacy of tigecycline in the treatment of selected serious infections caused by VRE. The primary efficacy endpoint will be the clinical response for all subjects.

Timeline

Start
2003-10
Primary completion
2005-06
Completion
2005-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Tigecycline Small molecule