Fluphenazine Decanoate for Psoriasis

PHASE2TerminatedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

July 31, 2006

Primary Completion Date

December 31, 2007

Study Completion Date

September 30, 2008

Conditions
Psoriasis
Interventions
DRUG

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."

DRUG

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.

Trial Locations (1)

02111

Tufts-New England Medical Center, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Immune Control

INDUSTRY

lead

Tufts Medical Center

OTHER