The purpose of this study is to collect data on patients in Canada who are switching from oral antipsychotic therapy to INVEGA® SUSTENNA® to treat schizophrenia.
The goals of the study are:
To look at how treatment with INVEGA SUSTENNA affects patients with schizophrenia.
To understand how long-acting treatments are being used in everyday clinical practice.
19 to 65 years of age
Diagnosed with Schizophrenia
Able and willing to comply with the study protocol
Ambulatory (not chronically hospitalized)
Switching from an oral antipsychotic medication to INVEGA SUSTENNA
Competent to give informed consent
Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers and email addresses are provided for obtaining additional information on specific clinical research trials only. If you have specific questions which require clinical expertise, please call your primary care physician.