drugset / Trial / NCT01175135

An Inpatient Study Of The Efficacy, Safety, And Tolerability Of PF-02545920 In The Treatment Of Acute Exacerbation Of Schizophrenia

NCT01175135

Phase 2 Completed 259 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

This study aims to evaluate whether PF-02545920 is safe and effective in the treatment of acute exacerbation of schizophrenia during a 4-week inpatient treatment period. The study will use the Positive and Negative Syndrome Scale (PANSS) to measure change in symptoms for PF-02545920 compared to risperidone and placebo treatment.

Timeline

Start
2010-10
Primary completion
2011-08
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject MARDEPODECT Small molecule 5 mg
Subject MARDEPODECT Small molecule 15 mg
Comparator Risperidone Other / unclassified 3 mg

Indications