drugset / Trial / NCT06086626

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

NCT06086626

Phase 2 Completed 30 enrolled Shionogi
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

EvaluationDrugModalityDoseRoute
Subject Cefiderocol Small molecule 60 mg/kg Intravenous
Subject Cefiderocol Small molecule 2000 mg Intravenous