drugset / Trial / NCT01597635

The Safety, Tolerability, PK and PD of GSK2586881 in Patients With Acute Lung Injury

NCT01597635 ↗

Phase 2 Completed 44 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindTreatment

Summary

This is an early phase (phase IIa), randomized, multi-center study in subjects with acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). The purpose of this study is to investigate the safety of GSK2586881 and to determine what effects it has on people with Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS). The study has two parts: Part A will be an open-label investigation in five subjects. Part B will be a double-blind, placebo controlled investigation and will involve approximately 60 subjects.

Timeline

Start
2012-09-01
Primary completion
2014-10-01
Completion
2014-10-06

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK2586881 Protein / enzyme biologic 0.1 mg/kg Intravenous
Subject GSK2586881 Protein / enzyme biologic 0.4 mg/kg Intravenous
Subject GSK2586881 Protein / enzyme biologic 0.8 mg/kg Intravenous

Indications