drugset / Trial / NCT01462565

Study of a New Thermo Stable Formulation of Epoprostenol Sodium to Treat Pulmonary Arterial Hypertension (PAH)

NCT01462565

Phase 4 Completed 16 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this multicentre, open label, single-arm study in approximately 20 adult patients is to evaluate the Impact on lifestyle of a new thermo stable formulation of epoprostenol sodium in subjects with Pulmonary Arterial Hypertension (PAH).

Timeline

Start
2011-11-01
Primary completion
2012-05-16
Completion
2012-11-08

Drugs

EvaluationDrugModalityDoseRoute
Subject epoprostenol Other / unclassified Intravenous