The Safety and Efficacy of Lurasidone With Different Initiation Dose in Chinese Acute Phase Patients With Schizophrenia

NCT ID: NCT05011669

Last Updated: 2024-04-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 200 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-08-16
• Study Completion Date: 2023-06-16

Brief Summary

To evaluate the safety and efficacy of Lurasidone initiated with 40mg and 80mg in treatment with acute phase patients with schizophrenia

Conditions

Schizophrenia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Latuda® 40mg/d

Group Type: EXPERIMENTAL

Lurasidone

Intervention Type: DRUG

Oral administration with a meal or within 30 min after eating in the evening. The dosage could be adjusted from Day 8.

Latuda® 80mg/d

Group Type: EXPERIMENTAL

Lurasidone

Intervention Type: DRUG

Oral administration with a meal or within 30 min after eating in the evening. The dosage could be adjusted from Day 8.

Interventions

Lurasidone

Oral administration with a meal or within 30 min after eating in the evening. The dosage could be adjusted from Day 8.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subjects meet ICD10 criteria for a primary diagnosis of schizophrenia;
• Subjects have a score ≥ 4 on the CGI-S at Screening and Baseline;
• Subjects have a PANSS total score ≥ 70 and ≤ 120 at Screening and Baseline, with a score 4 (moderate) or higher in 2 or more items on the following PANSS items: delusions, conceptual disorganization, hallucinations, unusual thought content and suspiciousness;
• Subjects with acute (including recurrence /relapse and first episode) phase patients with schizophrenia;
• Ability to understand the contents of interview and provide written informed consent (If subject is unable to sign, subject's legal guardian or impartial witness shall sign the informed consent).

Exclusion Criteria

• Subjects with severe or unstable physical diseases (including but not limited to severe or unstable cardiovascular diseases, cerebrovascular diseases, liver and kidney diseases) determined by the investigators;
• Subjects had a history of stomach or intestinal surgery or any other condition that could interfere with absorption, distribution, metabolism, or excretion of medications;
• Based on the judgement of investigators, subject has a history of refractory psychosis and/or subject has been treated with clozapine (for any reason) within 4 months of baseline;
• Subjects has used long-term antipsychotic drugs, e.g. Haloperidol decanoate injection, Fluphenazine decanoate injection, Risperidone microspheres injection, Paliperidone palmitate injection, Paliperidone palmitate injection (3M), in the following time prior to the enrolment;
• Subjects is at risk of suicide or self-mutilation behaviours or the act of endangering others, or other corresponding characteristic behaviour, or a history of suicide;
• Female subjects were pregnant (positive pregnancy test at screening) or breast-feeding or planning pregnancy for the duration of the study, or the partners of male subjects were planning pregnancy for the duration of the study;
• Need to use of disallowed concomitant therapy which is specified in the protocol;
• History of severe allergy or hypersensitivity;
• Currently has severe liver function impairment, or serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) level ≥3 times the upper limit of normal value;
• Creatinine clearance rate < 50mL/min Creatinine clearance rate*100%= Male: (140 - Age) x Weight(kg)/Serum creatinine (mg/dL) x 72 Female: 0.85*(140 - Age) x Weight(kg)/Serum creatinine (mg/dL) x 72
• A history of malignant tumors (including benign pituitary tumors);
• Any chronic organic disease of the central nervous system (excluding schizophrenia), such as CNS related tumors and inflammation, active seizures, vascular disease, Parkinson's disease, Alzheimer's disease, or other forms of dementia, myasthenia gravis, and other degenerative diseases. A history of mental retardation or persistent neurological symptoms caused by severe head injury;
• Subjects received electroconvulsive therapy (ECT) within 90 days prior to screening, or were expected to require ECT during the study;
• A history of neuroleptic malignant syndrome;
• Severe tardive dyskinesia, severe dystonia, or any other severe dyskinesia;
• Angioedema occurred after previous administration of lurasidone;
• The subject is participating in or has participated in other clinical trials, including the use of commercially available drugs or medical devices, within 30 days prior to the signing of the informed consent;
• Patients who had previously participated in a clinical study of lurasidone;
• Any other conditions judged by the investigators that not suitable to participate in this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sumitomo Pharma (Suzhou) Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Peking University Sixth Hospital

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

DSPCLAT-003

Identifier Type: -

Identifier Source: org_study_id