Schizophrenia Clinical Trial
Official title:
A Randomized, Open-Label, Parallel-Group Study to Assess the Relative Bioavailability of LY03004 and Risperdal® Consta® at 25 mg Following Multiple Intramuscular Injections in Stable Patients With Schizophrenia or Schizoaffective Disorder
This study is to assess the bioavailability of LY03004 compared to Risperdal Consta as well as the evaluate the safety and tolerability and preliminary efficacy of LY03004 with repeat injections
- To assess the relative bioavailability of LY03004 compared to Risperdal® Consta® at 25
mg following multiple intramuscular injections at steady-state;
- To evaluate the safety and tolerability of LY03004 following repeated intramuscular
injections
- To evaluate the preliminary efficacy of LY03004 following repeated intramuscular
injections
;
Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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