Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT07465432
PHASE4

Pharmacokinetic Analysis of Cefiderocol in Patients With Acute Burn Injuries

Sponsor: University of Tennessee

View on ClinicalTrials.gov

Summary

Cefiderocol is a powerful, broad spectrum antibiotic approved to treat hospital-acquired or ventilator associated pneumonia and urinary tract infections. Although cefiderocol has labeled dosing recommendations, including augmented renal clearance, patients with burn injury remain an unstudied population at high risk for MDR pathogens. The primary objective of this study is to evaluate the pharmacokinetic principles of cefiderocol in patients after acute burn injury. Findings from this study will determine the dose and interval necessary to maintain therapeutic concentrations of cefiderocol in patients after burn injury for adequate bactericidal activity, prevention of resistance, and treatment outcomes.

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2026-02-16

Completion Date

2027-02-28

Last Updated

2026-03-12

Healthy Volunteers

No

Interventions

DRUG

Cefiderocol

Cefiderocol will be prescribed according to indication and estimated renal function as either 2g over 3 hours dosed either every 6 or 8 hours.

Locations (1)

Regional One Health

Memphis, Tennessee, United States