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Confirmatory Study 3 of KPS-0373 in Patients With Spinocerebellar Degeneration

Confirmatory Study 3 of KPS-0373 in Patients With Spinocerebellar Degeneration

Recruiting
18 years and older
All
Phase 3
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Overview

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group, phase III study to evaluate the efficacy and safety of KPS-0373 given once daily after breakfast in 142 patients with spinocerebellar degeneration . This study consists of the 4-week screening period, 24-week treatment period, and 4-week follow-up period.

Eligibility

Inclusion Criteria:

  • Japanese SCD patients with mild to moderate ataxia

Exclusion Criteria:

  • Patients with secondary ataxia
  • Patients with clinically significant hepatic, renal, or cardiovascular dysfunction

Study details
    Spinocerebellar Degeneration

NCT07040137

Kissei Pharmaceutical Co., Ltd.

7 July 2025

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