drugset / Trial / NCT00686699

Study of Preladenant for the Treatment of Antipsychotic Induced Movement Disorders in Participants With Schizophrenia (Study P04628)

NCT00686699

Phase 2 Terminated 11 enrolled Merck Sharp & Dohme LLC
RandomizedCrossoverQuadruple-blindTreatment

Summary

This study was designed to determine if preladenant (SCH 420814, MK-3814) can reduce drug-induced involuntary movements in participants with schizophrenia or schizoaffective disorder. Participants were to be evaluated for two 14-day treatment periods with a 3-week washout period between treatment periods. The primary outcome measure, Extrapyramidal Symptom Rating Score (ESRS), was to be evaluated frequently during the treatment periods.

Timeline

Start
2006-07-10
Primary completion
2008-03-06
Completion
2008-03-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Preladenant Small molecule 25 mg