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Clinical Trial Summary

The primary objective of this study is to compare all-cause mortality at Day 14 in participants receiving cefiderocol with participants receiving the comparator, meropenem, in adults with hospital-acquired bacterial pneumonia (HABP), ventilator-associated bacterial pneumonia (VABP), or healthcare-associated bacterial pneumonia (HCABP) caused by Gram-negative pathogens.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03032380
Study type Interventional
Source Shionogi Inc.
Contact
Status Completed
Phase Phase 3
Start date October 24, 2017
Completion date April 1, 2019

See also
  Status Clinical Trial Phase
Completed NCT02714595 - Study of Cefiderocol (S-649266) or Best Available Therapy for the Treatment of Severe Infections Caused by Carbapenem-resistant Gram-negative Pathogens Phase 3
Completed NCT01782755 - Probiotics: Prevention of Severe Pneumonia and Endotracheal Colonization Trial (PROSPECT): A Feasibility Clinical Trial Phase 2
Completed NCT02440828 - Addition of Tobramycin Inhalation in the Treatment of Ventilator Associated Pneumonia Phase 4
Terminated NCT02652247 - Serial, Non-invasive Analysis of Exhaled Breath Condensate in Ventilated Trauma Patients N/A
Active, not recruiting NCT05792501 - Pulmonary Infections and Barotrauma Associated With MV IN PICU