drugset / Trial / NCT02889302

An Additional Confirmatory Study of KPS-0373 in Patients With Spinocerebellar Degeneration (SCD)

NCT02889302 ↗

Phase 3 Completed 203 enrolled Kissei Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to investigate the superiority of KPS-0373 to placebo, and evaluate the safety of KPS-0373 in SCD patients.

Timeline

Start
2016-11-15
Primary completion
2018-03
Completion
2018-03

Outcome

Missed primary endpoint

paper The primary endpoint showed no significant difference between rovatirelin and placebo in these two studies. PMID 31937586 ↗

release “脊髄小脳変性症治療薬KPS-0373(一般名:ロバチレリン)の第Ⅲ相臨床試験において、主要評価項目である運動失調を評価するSARA合計スコアの変化量について、プラセボと比べて統計学的に有意な改善が認められなかった” kissei.co.jp ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject rovatirelin Small molecule 2.4 mg —