Start Date
November 30, 2013
Primary Completion Date
December 31, 2015
Study Completion Date
December 31, 2015
Remodulin
Subcutaneous (SQ) remodulin will be initiated at 1.25 ng/kg/min, and increased by 2-6 ng/kg/min weekly to a target dose of 40 ng/kg/min. If the initial infusion rate cannot be tolerated it will be reduced to 0.625 ng/kg/min. If subjects cannot tolerate the SQ therapy, we will attempt to switch to IV therapy.
Ohio State University/Nationwide Children's Hospital, Columbus
UCLA Medical Center, Los Angeles
Collaborators (1)
United Therapeutics
INDUSTRY
University of California, Los Angeles
OTHER