Condition: Spinocerebellar Degeneration · Sponsor: Kissei Pharmaceutical Co., Ltd.
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.
This description comes directly from the study's public registry record.
Kissei Pharmaceutical Co., Ltd Kissei Pharmaceutical Co., Ltd · Email only · rinsyousiken@pharm.kissei.co.jp
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| Research Site | Multiple Locations, Japan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07040137