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Clinical Trials List

Protocol Number331-10-230

2012-01-05 - 2013-06-30

Phase III

Terminated4

ICD-10F25.9

Schizoaffective disorder, unspecified

ICD-9295.73

Schizo-affective type, subchronic with acute exacerbation

A phase 3, multicenter, randomized, double-blind, placebo-controlled Trial of Fixed-dose OPC-34712 (4,2, and 1 mg/day) in the Treatment of Adults With Acute Schizophrenia

  • Trial Applicant

    IQVIA RDS Taiwan Ltd.

  • Sponsor

    IQVIA Solutions Taiwan Ltd.

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2025/08/20

Investigators and Locations

Principal Investigator Hsien-Yuan Lane Division of Psychiatry

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

17 Terminated

Principal Investigator 陳坤波 Division of Psychiatry

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 周煌智 Division of Psychiatry

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 廖定烈 Division of Psychiatry

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Condition/Disease

Schizophrenia

Objectives

To realize the efficacy of treatment using OPC-34712 (4,2, and 1 mg/day) for adults with acute schizophrenia

Test Drug

OPC-34712

Active Ingredient

OPC-34712

Dosage Form

tablet

Dosage

4, 2, and 1 mg/day

Endpoints

None

Inclution Criteria

Adults with acute schizophrenia

Exclusion Criteria

None

The Estimated Number of Participants

  • Taiwan

    30 participants

  • Global

    660 participants