drugset / Trial / NCT00922272

Efficacy, Safety, and Tolerability of SPD489 in Adults With Schizophrenia and Predominant Negative Symptoms

NCT00922272

Phase 2 Completed 92 enrolled Shire
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To explore the efficacy of SPD489, as adjunctive therapy to a stable dose of atypical antipsychotic medication, on negative symptoms in adult subjects with clinically stable schizophrenia and predominant negative symptoms, as measured by the Scale for the Assessment of Negative Symptoms (SANS).

Timeline

Start
2009-09-14
Primary completion
2011-01-20
Completion
2011-01-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Lisdexamfetamine Other / unclassified 20 mg Oral
Subject Lisdexamfetamine Other / unclassified 30 mg Oral
Subject Lisdexamfetamine Other / unclassified 40 mg Oral
Subject Lisdexamfetamine Other / unclassified 50 mg Oral
Subject Lisdexamfetamine Other / unclassified 60 mg Oral
Subject Lisdexamfetamine Other / unclassified 70 mg Oral

Indications