Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder
Start Date
8/27/2021
Completion Date
12/31/2027
Summary
This is a study of the efficacy and safety of BXCL501 in children and adolescents with acute agitation and either bipolar disorder or schizophrenia.
Detailed Description
The study will enroll approximately 140 subjects randomized to dose regimens of 80 µg or 120 µg BCXL501 or placebo (Group one), or 60 µg BCXL501 or placebo (Group two; Europe only). Subjects with acute agitation will include male and female children and adolescents who are either newly admitted to a hospital setting or already admitted and experiencing acute agitation. Subjects will be domiciled in a clinical research setting or hospitalized to remain under medical supervision while undergoing screening procedures to assess eligibility. Efficacy and safety assessments will be conducted periodically before and after dosing.
Eligibility Criteria
Age Range: 10 years to 17 years
Interventions
BXCL501 80 Micrograms
Placebo Film
BXCL501 120 Micrograms
BXCL501 60 Micrograms
Conditions
Locations
BioXcel Clinical Research Site
Anaheim, California 92805
United States
Bioxcel Clinical Research Site
Hialeah, Florida 33016
United States
BioXcel Clinical Research Site
Atlanta, Georgia 30331
United States
Bioxcel Clinical Research Site
Decatur, Georgia 30030
United States
BioXcel Clinical Research Site
DeSoto, Texas 75115
United States