A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Cefiderocol in Hospitalized Neonates and Infants

PHASE2CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

March 14, 2024

Primary Completion Date

March 31, 2025

Study Completion Date

March 31, 2025

Conditions
Gram-Negative Bacterial Infections
Interventions
DRUG

Cefiderocol

Administered via intravenous (IV) infusion

DRUG

Standard of Care

Antibiotics selected by the investigator based on the participant's symptoms, in accordance with local standards

Trial Locations (4)

333

Chang Gung Memorial Hospital, Linkou Department of Pediatrics, Taoyuan

8000

Tygerberg Hospital, Cape Town

27705

Duke University, Durham

72202

Arkansas Children's Hospital, Little Rock

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Shionogi

INDUSTRY