drugset / Trial / NCT01445678

Study Comparing the Safety and Efficacy of Intravenous CXA-201 and Intravenous Meropenem in Complicated Intraabdominal Infections

NCT01445678 ↗

Phase 3 Completed 494 enrolled Merck & Co., Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 3, multicenter, prospective, randomized, double-blind, double dummy study of CXA-201 Intravenous (IV) infusions (1500mg q8h) and metronidazole (500mg q8h) versus meropenem (1000mg q8h)for the treatment of adults with Complicated Intraabdominal Infections (cIAI).

Timeline

Start
2011-12-23
Primary completion
2013-10-03
Completion
2013-10-15

Outcome

Met primary endpoint

paper Ceftolozane/tazobactam plus metronidazole was noninferior to meropenem in the primary PMID 25670823 ↗

paper meeting the prespecified noninferiority margin. PMID 25670823 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CXA-201 Unknown 1500 mg Intravenous
Comparator Meropenem Small molecule 1000 mg Intravenous
Subject Metronidazole Small molecule 500 mg Intravenous

Indications

No indication recorded.