drugset / Trial / NCT02452047

Efficacy and Safety of Imipenem+Cilastatin/Relebactam (MK-7655A) Versus Colistimethate Sodium+Imipenem+Cilastatin in Imipenem-Resistant Bacterial Infection (MK-7655A-013)

NCT02452047 ↗

Phase 3 Completed 50 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The study will evaluate the efficacy and safety of imipenem+cilastatin/relebactam (MK-7655A) versus colistimethate sodium+imipenem+cilastatin in the treatment of imipenem-resistant bacterial infections. Infections evaluated in the study will be hospital-acquired bacterial pneumonia (HABP), ventilator-associated bacterial pneumonia (VABP), complicated intra-abdominal infection (cIAI), and complicated urinary tract infection (cUTI).

Timeline

Start
2015-08-21
Primary completion
2017-09-18
Completion
2017-09-18

Outcome

Met primary endpoint

release “demonstrated a favorable overall response in the treatment of certain imipenem–non-susceptible bacterial infections, the primary endpoint” merck.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Cilastatin Small molecule 200 mg Intravenous
Subject Cilastatin Small molecule 500 mg Intravenous
Comparator Colistimethate sodium Unknown 180 mg Intravenous
Comparator Colistimethate sodium Unknown 360 mg Intravenous
Subject IMIPENEM ANHYDROUS Small molecule 200 mg Intravenous
Subject IMIPENEM ANHYDROUS Small molecule 500 mg Intravenous
Subject Relebactam Small molecule 100 mg Intravenous
Subject Relebactam Small molecule 250 mg Intravenous