drugset / Trial / NCT00079989

Study Evaluating Tigecycline in Selected Serious Infections Due to Resistant Gram-Negative Organisms

NCT00079989

Phase 3 Completed 115 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
Open-labelTreatment

Summary

To evaluate the safety and efficacy of tigecycline in the treatment of subjects with selected serious infections caused by resistant gram-negative bacteria, eg, Acinetobacter baumannii, Enterobacter species, Klebsiella pneumoniae or other resistant gram-negative pathogens, for whom antibiotics have failed or who cannot tolerate other appropriate antimicrobial therapies. The primary efficacy endpoint will be the clinical response.

Timeline

Start
2003-12
Primary completion
2005-11
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Tigecycline Small molecule