18
Participants
Start Date
February 29, 2016
Primary Completion Date
June 30, 2018
Study Completion Date
June 30, 2018
F-652
Participants will receive 10 μg/kg, 30 μg/kg or 45 μg/kg of F-652 on Day 1 and Day 7 via slow intravenous infusion. Three patients will receive 10 μg/kg of F-652. Pharmacokinetic testing will be completed on these subjects. If evaluations demonstrate safety and efficacy signals, the next 3 patients will receive 30 μg/kg. If pharmacokinetic testing demonstrates safety and efficacy signals, the next 3 patients will receive 45 μg/kg.
Mayo Clinic in Rochester, Rochester
Lead Sponsor
Indiana University
OTHER
Virginia Commonwealth University
OTHER
Hennepin County Medical Center, Minneapolis
OTHER
Mayo Clinic
OTHER