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Clinical trial

A Multi-Center, Open-Label, Single Arm and Flexible Dose Study of the Effectiveness and Safety of Oral Use Lurasidone HCl Tablet (LATUDA®) for 40-160 mg/Day in Subjects With Schizophrenia

NCT03393026 is registered in ClinicalTrials.gov with Standard Chem. & Pharm. Co., Ltd. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Multi-Center, Open-Label, Single Arm and Flexible Dose Study of the Effectiveness and Safety of Oral Use Lurasidone HCl Tablet (LATUDA®) for 40-160 mg/Day in Subjects With Schizophrenia
Lead sponsor
Standard Chem. & Pharm. Co., Ltd.
Phase
Phase 4
Overall status
Completed
Start date
January 3, 2018
Completion date
September 17, 2019
Enrollment
54 (actual)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.