drugset / Trial / NCT03431077

A Study of LJPC-501 in Pediatric Patients With Hypotension

NCT03431077

Phase 2 Completed 2 enrolled La Jolla Pharmaceutical Company
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to evaluate the effect of LJPC-501 infusion on mean arterial pressure (MAP) or reduction in sum norepinephrine (NE) equivalent dosing, at Hour 2 after the start of LJPC-501, in pediatric patients who remain hypotensive despite receiving fluid therapy and vasopressor therapy. In addition, this study will evaluate the safety and tolerability of LJPC-501 in pediatric patients, the change in MAP over 24 hours after the start of LJPC-501, the change in serum lactate concentrations, and the change in Pediatric Logistic Organ Dysfunction (PELOD) scores.

Timeline

Start
2018-02-11
Primary completion
2018-04-14
Completion
2018-04-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Angiotensin II Peptide Other