Study Phase
3
Additional Information:
Please note: individual participant-level data are not available for this trial. Only the synoptic report is available.
An Open-label Study of the Efficacy and Safety of RISPERDAL Long-acting Microspheres (RISPERDAL CONSTA) Administered Once Monthly in Adults With Schizophrenia or Schizoaffective Disorder
CSR Summary
Not Yet Available
Data Specification
Not Available
Annotated CRF
Not Available
Trial Information
Generic Name
Risperidone
Product Name
RISPERDAL CONSTA®
Therapeutic Area
Behaviors and Mental Disorders
Enrollment
86
% Female
14.3%
% White
N/A
Product Class
Atypical Antipsychotics
Sponsor Protocol Number
RIS-USA-305
Data Partner
Johnson & Johnson
Condition Studied
Schizophrenia
Mean/Median Age (Years)
35.0
Supporting Documentation
Clinical Study Report
APPROVED DATA REQUESTS ASSOCIATED WITH THIS TRIAL
Disclaimer
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