Remodulin® to Oral Treprostinil Transition

PHASE2CompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

April 30, 2012

Primary Completion Date

July 31, 2014

Study Completion Date

December 31, 2014

Conditions
Pulmonary Arterial Hypertension
Interventions
DRUG

UT-15C SR

Subjects will transition in the hospital from Remodulin to UT-15C SR within 5 days of the start of the transition. The dose of Remodulin will be decreased as the dose of UT-15C SR is increased over the 5 days. Once subjects have been transitioned from Remodulin, the dose of UT-15C SR will continue to be modified / titrated to the appropriate optimal dose for that subject throughout the rest of the study.

Trial Locations (6)

14642

University of Rochester, Rochester

15213

University of Pittsburgh Medical Center (UPMC), Pittsburgh

43221

The Ohio State University, Columbus

63110

Washington University School of Medicine, St Louis

85013

Arizona Pulmonary Specialists, Phoenix

85724

University of Arizona Clinical and Translational Science (CATS) Research Center, Tucson

Sponsors
All Listed Sponsors
lead

United Therapeutics

INDUSTRY

NCT01588405 - Remodulin® to Oral Treprostinil Transition | Biotech Hunter | Biotech Hunter