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Safety and Tolerability of Rapid Dose Titration of Subcutaneous Remodulin® Therapy in PAH Subjects (RAPID) — RAPID  

Pulmonary Arterial Hypertension Clinical Trial

Official title:
A 16 Week, Open Label, Multi-centre, Study to Evaluate the Safety, Tolerability and Pharmacodynamic Effects of a Rapid Dose Titration Regimen of Subcutaneous Remodulin® Therapy in Subjects With Pulmonary Arterial Hypertension (PAH)

Clinical Trial Summary

The purpose of the study is to evaluate the safety and tolerability of a rapid dose titration regimen of subcutaneous Remodulin® therapy in patients with PAH.

Clinical Trial Description

This is an open label, single territory, multi-centre study in subjects with pulmonary arterial.

hypertension (PAH). Subjects were treatment naïve or receiving an approved endothelin receptor antagonist (ERA) and / or phosphodiesterase (PDE)-5 inhibitor for at least 60 days prior to screening and maintained on a stable dose for at least 30 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02847260
Study type Interventional
Source United Therapeutics
Contact
Status Completed
Phase Phase 4
Start date April 2012
Completion date March 2014
View Details
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