drugset / Trial / NCT04699656

Plazomicin Study in ESRD Patients Receiving IHD

NCT04699656

Phase 1 Completed 6 enrolled Cipla USA Inc.
NaSingle-groupOpen-labelTreatment

Summary

This study is being conducted to directly characterize the pharmacokinetic (PK) profile of plazomicin following administration of a single oral dose before and after IHD in subjects with ESRD. This PK assessment will be used to provide appropriate plazomicin dosing recommendations for patients with ESRD receiving IHD.

Timeline

Start
2021-01-05
Primary completion
2021-03-08
Completion
2021-06-09

Drugs

EvaluationDrugModalityDoseRoute
Subject plazomicin Small molecule 2.5 mg/kg Intravenous