Overview

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

Status:
Completed
Trial end date:
2011-01-20
Target enrollment:
Participant gender:
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).
Phase:
Phase 2
Details
Lead Sponsor:
Shire
Treatments:
Lisdexamfetamine Dimesylate