30
Participants
Start Date
July 31, 2009
Primary Completion Date
June 30, 2016
Study Completion Date
June 30, 2016
Sodium Nitrite
Subjects assigned to sodium nitrite will receive an initial infusion of 6 nmol/min/kg for 48 hours. After the first six subjects have been enrolled (3 active drug, 3 control) and if there are no dose limiting toxicities, additional cohorts of six subjects each will be randomized to escalating doses of sodium nitrite versus control for a total of 30 subjects.
Johns Hopkins Bayview Medical Center, Baltimore
Johns Hopkins Hospital, Baltimore
University of Massachusetts Medical School, Worcester
Collaborators (1)
Hope Pharmaceuticals
INDUSTRY
Johns Hopkins University
OTHER