A Study of Lurasidone HCl in Subjects With Schizophrenia

Standard Chem & Pharm

Status and phase

Completed

Phase 4

Conditions

Schizophrenia

Treatments

Drug: Lurasidone

Study type

Interventional

Funder types

Industry

Identifiers

SCPF20L01TW

Details and patient eligibility

About

The study evaluates the effectiveness and safety of Lurasidone in subjects with schizophrenia over a period of 6 weeks.

Enrollment

54 patients

Sex

All

Ages

20 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Males or female aged at 20-75 years old
Subjects who are diagnosed with schizophrenia based on Diagnostic and Statistical Manual of Mental Disorders (DSM-V) criteria
CGI-S≦4 (at both screening and baseline)
Subject is judged by the investigator to have been clinically stable for at least 4 weeks prior to baseline and in need for a switch from their current antipsychotic treatment due to insufficient clinical response or poor tolerability (side effects, metabolic complications, etc.).
If the subject recruits from OPD, the subject should be intolerant to the AE or is insufficient in current antipsychotics treatment by investigator's judgment.
Childbearing potential women who consented to the consistent use of the acceptable contraception (oral contraceptive, contraceptive injection, intrauterine device, double barrier method and contraceptive patch)
Subject is able and agrees to remain off (or stable dosage) prior antipsychotic medication during the study period as defined by this protocol.
In the Investigator's opinion, the ability to understand the nature of the study and any hazards of participation, and to communicate satisfactorily with the investigator and to participate in, and to comply with, the requirements of the entire protocol.
Subject is willing and able to comply with the protocol.

Exclusion criteria

Subject has clinically substantial risk of suicide or violent behavior as judged by the investigator.
Subject with the past history of neuroleptic malignant syndrome, water intoxication, paralytic ileus or dementia related psychosis
Subjects is active pregnancy (must have a negative pregnancy test at screening) or nursing (must not be lactating).
Subject has received treatment with MAO inhibitors within 14 days prior to the screening (Visit 1).
Subject is currently participating, or has participated in, a study with an investigational or marketed compound or device within 1 month prior to signing the informed consent.
Subject is unstable or critical untreated medical illness by the judgment of investigators.
Subject who is otherwise considered ineligible for the study by investigator. For example, subjects experienced serious medical condition including known clinically relevant laboratory abnormalities, and hypersensitivity to Lurasidone.
Subjects who were considered resistance to treatment for psychotic symptoms by the investigator.
Total daily dose of pre-switch antipsychotic was exceeded the equivalent of haloperidol 12 mg/day.
Subjects have received long depot neuroleptics within 4 weeks prior to enrollment. Or, subject was treated with clozapine for refractory psychosis within 1 month of enrollment.
Subject requires treatment with any potent CYP3A4 inhibitors or inducers during the study. Subject requires treatment with a drug that consistently prolongs the QTc interval.