drugset / Trial / NCT01570192

Clinical Trials to Reduce the Risk of Antimicrobial Resistance

NCT01570192 ↗

Phase 2 Terminated 43 enrolled University of Florida
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to demonstrate a low rate of emergence of antibiotic resistance in P. aeruginosa and Acinetobacter spp during the treatment of hospitalized patients with pneumonia requiring mechanical ventilation treated with PD optimized meropenem administered as a prolonged infusion in combination with a parenteral aminoglycoside plus tobramycin by inhalation (Group 1) compared to therapy with meropenem alone (Group 2 - control arm).

Timeline

Start
2010-09
Primary completion
2015-04
Completion
2015-04

Outcome

Outcome not reported

Stopped (Enrollment): “NIAID terminated the study due to low subject enrollment”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Amikacin Small molecule 20 mg/kg Intravenous
Subject Gentamicin Small molecule 5 mg/kg Intravenous
Subject Meropenem Small molecule 2 g Intravenous
Subject Tobramycin Unknown 5 mg/kg Intravenous
Subject Tobramycin Unknown 600 mg Intravenous
Background Linezolid Other / unclassified — —
Background Vancomycin Other / unclassified — —

Indications