drugset / Trial / NCT02070757

Safety and Efficacy Study of Ceftolozane/Tazobactam to Treat Ventilated Nosocomial Pneumonia (MK-7625A-008)

NCT02070757 ↗

Phase 3 Completed 726 enrolled Merck & Co., Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase 3, multicenter, prospective, randomized study of intravenous (IV) ceftolozane/tazobactam versus IV meropenem in the treatment of adult participants with either ventilator-associated bacterial pneumonia (VABP) or ventilated hospital-acquired bacterial pneumonia (HABP). The primary objective is to demonstrate the non-inferiority of ceftolozane/tazobactam versus meropenem in adult participants with ventilated nosocomial pneumonia (VNP) based on the difference in Day 28 all-cause mortality rates in the Intent-to-treat (ITT) population using a non-inferiority margin of 10%.

Timeline

Start
2014-09-02
Primary completion
2018-05-15
Completion
2018-06-06

Outcome

Met primary endpoint

paper Ceftolozane-tazobactam was thus non-inferior to meropenem in terms of both 28-day all-cause mortality and clinical cure at test of cure. PMID 31563344 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ceftolozane/tazobactam Small molecule 750 mg Intravenous
Subject Ceftolozane/tazobactam Small molecule 1500 mg Intravenous
Subject Ceftolozane/tazobactam Small molecule 3000 mg Intravenous
Comparator Meropenem Small molecule 1000 mg Intravenous