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

Completed · Phase 2 · Has a placebo group

Conditions studied: Schizophrenia and Predominant Negative Symptoms

In brief

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).

Key facts

Study ID
NCT00922272
Run by
Shire
People needed
92
Starts
2009-09-14
Expected to finish
2011-01-20
Last updated by the study team
2021-06-09

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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