129
Participants
Start Date
June 30, 2011
Primary Completion Date
February 29, 2012
Study Completion Date
February 29, 2012
Cariprazine
Patients meeting all study eligibility criteria will be randomized to receive cariprazine (Group 1) 1.5 to 18 mg once daily, administered orally.
Risperidone/Moxifloxacin
Patients randomized to Group 2A will receive double blind placebo for Days 1-5, Moxifloxacin (400mg) on Day 6, Risperidone 4mg once daily Days 7-15, placebo Days 16-20, Risperidone Days 21-29, placebo Days 30-35.
Risperidone/Moxifloxacin
Patients randomized to Group 2B will receive double blind placebo for Days 1-6, Risperidone 4mg once daily Days 7-15, placebo Days 16-20, Risperidone Days 21-29, placebo Days 30-34, Moxifloxacin (400mg) on Day 35.
Forest Investigative Site 003, Houston
Forest Investigative Site 004, Long Beach
Forest Investigative Site 001, Glendale
Forest Investigative Site 002, Willingboro
Lead Sponsor
Forest Laboratories
INDUSTRY