drugset / Trial / NCT06086626
A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Cefiderocol in Hospitalized Neonates and Infants
Non-randomizedSequentialOpen-labelTreatment
Summary
The primary purpose of this study is to understand the pharmacokinetics (PK) of single and multiple doses of cefiderocol in children from birth to less than 3 months of age with suspected or confirmed aerobic Gram-negative bacterial infections.
Timeline
- Start
- 2024-03-14
- Primary completion
- 2025-03-31
- Completion
- 2025-03-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cefiderocol | Small molecule | 60 mg/kg | Intravenous |
| Subject | Cefiderocol | Small molecule | 2000 mg | Intravenous |