A Study to Learn About the Effects and Safety of RTA 408 (Omaveloxolone) in People Aged 16 to 40 With Friedreich's Ataxia
2期
已完成
NCT02255435
| 适应症 | Friedreich Ataxia |
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| 分期 | 2期 |
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| 申办方 | Biogen |
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| 状态 | 已完成 |
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| 受试者人数 | 172 人 |
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| 干预（药物） | Omaveloxolone Capsules, 2.5 mg, Omaveloxolone Capsules, 5 mg, Omaveloxolone Capsules, 10 mg, Omaveloxolone Capsules, 20 mg, Omaveloxolone Capsules, 40 mg |
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| 开始日期 | 2015年1月31日 |
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| 完成日期 | 2019年10月31日 |
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| 结果公布日 | 2022年11月29日 |
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摘要
In this study, researchers are learning more about RTA 408, also known as omaveloxolone, BIIB141, or SKYCLARYS®. The main goal of this study is to learn more about the safety of RTA 408 and how it affects physical effort, movement, coordination, and how participants feel in daily life. The main questions researchers want to answer in this study are: * How much physical effort can a participant produce during a cycling test after 12 weeks of treatment? * How do scores on the modified Friedreich's Ataxia Rating Scale (mFARS) change after 48 weeks? Researchers will use the modified Friedreich's Ataxia Rating Scale (mFARS) to measure how FA affects the nervous system. The mFARS looks at movement ability, balance, coordination, speech, and how well the arms and legs work. They will also use a cycling test to measure physical effort, along with questionnaires to learn how participants feel and function in daily life. Safety will also be tested using physical exams, vital sign checks, echocardiograms (ECHO), electrocardiograms (ECG), and blood and urine tests. The study will be done in 2 main parts, followed by an optional Extension period: * In Part 1, participants will be randomly assig
Change From Baseline in Peak Work (in Watts/kg) During Exercise Testing at Week 12 in Part 1
Baseline through 12 weeks after participant receives the first dose in Part 1. · W/kg
| Part 1 Omaveloxolone Capsules 2.5 and 5 mg | 0.14 W/kg |
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| Part 1 Omaveloxolone Capsules 10 mg | 0.07 W/kg |
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| Part 1 Omaveloxolone Capsules 20 mg | -0.09 W/kg |
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| Part 1 Omaveloxolone Capsules 40 mg | 0.06 W/kg |
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| Part 1 Omaveloxolone Capsules 80 mg | 0 W/kg |
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| Part 1 Omaveloxolone Capsules 160 mg | 0.02 W/kg |
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| p-value | 0.1524 |
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| LS Mean difference (Net) | 0.10 (95% CI -0.04–0.23) |
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Change in the Modified Friedreich's Ataxia Rating Scale (mFARS) at Week 48 in Part 2
48 weeks after participant receives the first dose in Part 2 · score on a scale
| Part 2 Placebo Capsules | 0.85 ± 0.640 score on a scale |
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| Part 2 Omaveloxolone Capsules 150 mg | -1.55 ± 0.689 score on a scale |
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| p-value | 0.0141 |
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| LS Mean difference (Net) | -2.40 (95% CI -4.31–-0.50) |
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本页整理自 ClinicalTrials.gov 的公开数据，不构成医疗建议，也不构成投资建议。请务必咨询专业医师。