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Clinical Trial Summary

The purpose of this study is to determine the efficacy, safety, tolerability, and pharmacokinetics (PK) of meropenem-vaborbactam compared to piperacillin/tazobactam for 7 to 14 days in the treatment of hospitalized adults who meet clinical, radiographic, and microbiological criteria for hospital-acquired bacterial pneumonia (HABP) or ventilator-associated bacterial pneumonia (VABP).

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT03006679
Study type Interventional
Source Melinta Therapeutics, Inc.
Status Withdrawn
Phase Phase 3
Start date August 2018
Completion date December 2020

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