Omaveloxolone for the treatment of Friedreich ataxia: clinical trial results and practical considerations

被引:11
作者
Lynch, David R. [1 ,4 ]
Perlman, Susan [2 ]
Schadt, Kim [3 ]
机构
[1] Childrens Hosp Philadelphia, Friedrech Ataxia Program, Div Neurol, Philadelphia, PA USA
[2] David Geffen UCLA Sch Med, Dept Neurol, Los Angeles, CA USA
[3] Childrens Hosp Philadelphia, Friedreich Ataxia Program, Div Neurol, Philadelphia, PA USA
[4] Childrens Hosp Philadelphia, Friedrech Ataxia Program, Div Neurol, 502 Abramson, Philadelphia, PA 19104 USA
关键词
Antioxidant; KEAP1; clinical trial; ferritin; mFARS; Friedrech ataxia; TRITERPENOID RTA 408; TOPICAL APPLICATION; DOUBLE-BLIND; NRF2; PHARMACODYNAMICS; FRATAXIN; PHARMACOKINETICS; PROGRESSION; THERAPY; SAFETY;
D O I
10.1080/14737175.2024.2310617
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Omavaloxolone, an NRF2 activator, recently became the first drug approved specifically for the treatment of Friedreich ataxia (FRDA). This landmark achievement provides a background for a review of the detailed data leading to the approval. Areas covered: The authors review the data from the 4 major articles on FRDA in the context of the authors' considerable (>1000 patients) experience in treating individuals with FRDA. The data is presented in the context not only of its scientific meaning but also in the practical context of therapy in FRDA. Expert opinion: Omaveloxolone provides a significant advance in the treatment of FRDA that is likely to be beneficial in a majority of the FRDA population. The data suggesting a benefit is consistent, and adverse issues are relatively modest. The major remaining questions are the subgroups that are most responsive and how long the beneficial effects will remain significant in FRDA patients.
引用
收藏
页码:251 / 258
页数:8
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