High Dose Lurasidone for Patients With Treatment Resistant Schizophrenia

Inclusion Criteria

• •Patients diagnosed with schizophrenia or schizoaffective disorder according to Diagnostic and Statistical Manual IV (DSM-IV) criteria
• •All patients must be capable of giving written informed consent.
• •The criteria for treatment resistance (TR) will be those of Kane et al, (1988) which are:
• •* failure to respond adequately to two or more trials with typical or atypical antipsychotic drugs, of adequate dose and duration (at least 6 weeks) lifetime and at least one such trial within the last two years. No patient with a history of a successful trial of this nature within the last two years will be eligible for inclusion. The minimum doses of antipsychotic drugs permitted in these unsuccessful trials are specified in Table 1.
• •* Patients must have scores of 4 (using a 1-7 scale) or more on at least two of the following Positive and Negative Syndrome Scale (PANSS) items: delusions \[P1\], hallucinations \[P3\] or unusual thought content \[G9\]
• •* Patients must have a total PANSS score of 70 or above
• •* Patients will have had no episodes of good functioning in the previous three years (as defined by current CGI - Severity of moderate to severe, Global Assessment of Functioning (GAF) below 60;
• •* Personal and Social Performance Scale of 60 or below.
• •Requirement for previous exposure to antipsychotic treatment:
• •Patients who meet treatment resistance criteria must have had at least two trials with approved antipsychotic drugs, typical or atypical, in the standard dose range. It is recognized that some treatment resistant patients will have had good responses to antipsychotic drugs before meeting treatment resistant criteria.
• •All patients must have a Clinical Global Impression - Severity (CGI-S) scale score at screening of at least moderate severity, and must have a Personal and Social Performance (PSP) score of 60 or below.
• •Patients may initially be inpatients or outpatients.
• •Females of child bearing potential will be admitted only if they are on stable birth control medication and understand that they should not get pregnant during the course of the study. Pregnancy tests will be done at baseline and at approximately 2 month intervals.
• •All patients must have stable housing at the current time or will be discharged to a stable outpatient setting for housing, if an inpatient.
• •Patients must be willing to remain compliant on oral medication throughout the duration of the trial.