10
Participants
Start Date
July 31, 2006
Primary Completion Date
December 31, 2007
Study Completion Date
September 30, 2008
Fluphenazine Decanoate
"Fluphenazine decanoate marketed by APP Pharmaceuticals (25 mg/mL, 5 mL vial) was used in this study. This was an ascending dose study with the first cohort of 5 subjects dosed at 10 µg/mL, followed by 5 subject dosed in the second cohort at 100 µg/mL. Note: APP Pharmaceuticals is the name of the pharmaceutical company; APP is not an acronym."
Placebo
The sterile placebo (sesame oil with 1.2% (w/v) benzyl alcohol) was prepared at the University of Iowa, Division of Pharmaceutical Services, a FDA registered pharmaceutical manufacturing facility.
Tufts-New England Medical Center, Boston
Collaborators (1)
Immune Control
INDUSTRY
Tufts Medical Center
OTHER