drugset / Trial / NCT01587495

Pharmacokinetics and Safety of Ertapenem in the Postpartum Period

NCT01587495

Phase 1 Terminated 3 enrolled Daniel Benjamin
NaSingle-groupOpen-labelTreatment

Summary

The investigators are doing this study to learn more about the dosing and safety of ertapenem in women with suspected serious infections less than 42 days from the delivery of their infant.

Timeline

Start
2012-03
Primary completion
2014-01
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ertapenem Small molecule 1 g Intravenous

Indications