An Outpatient Study Of The Efficacy, Safety, And Tolerability Of PF-02545920 In The Adjunctive Treatment Of Sub-Optimally Controlled Symptoms of Schizophrenia
| Status: | Completed |
|---|---|
| Conditions: | Schizophrenia |
| Therapuetic Areas: | Psychiatry / Psychology |
| Healthy: | No |
| Age Range: | 18 - 65 |
| Updated: | 11/8/2014 |
| Start Date: | October 2013 |
| End Date: | November 2014 |
| Contact: | Pfizer CT.gov Call Center |
| Phone: | 1-800-718-1021 |
A 12-Week, Randomized, Phase 2, Double-Blind, Parallel-Group Study Of Two Dose Levels Of PF-02545920 Compared To Placebo In The Adjunctive Treatment Of Outpatients With Sub-Optimally Controlled Symptoms Of Schizophrenia
This study aims to evaluate whether PF-02545920 is safe and effective in the treatment of
sub-optimally controlled symptoms of schizophrenia during a 12-week outpatient treatment
period. The study will use the Positive and Negative Syndrome Scale (PANSS) to measure
change in symptoms for PF-02545920 from baseline compared to placebo.
sub-optimally controlled symptoms of schizophrenia during a 12-week outpatient treatment
period. The study will use the Positive and Negative Syndrome Scale (PANSS) to measure
change in symptoms for PF-02545920 from baseline compared to placebo.
Inclusion Criteria:
- Psychiatrically stable subjects with schizophrenia who have had a suboptimal response
to current treatment
- Evidence of stable schizophrenia symptomatology greater than or equal to 3 months.
- Subjects must be on a stable medication treatment regimen greater than or equal to 2
months, including concomitant psychotropic medications.
Exclusion Criteria:
- History of seizures or of a condition with risk of seizures.
- Subjects with schizophrenia that have not responded at all to current treatment.
- Pregnant or nursing females, and females of child bearing potential.
We found this trial at
41
sites
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