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10.1096/fj.201801595RR [DOI] [PubMed] [Google Scholar] 117.Labus J, Hackel S, Lucka L, Danker K
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The phase II of the MOXIe trial to assess the safety and efficacy of 150 mg of Omav in genetically diagnosed FRDA patients was also reported to have met its primary endpoint which is a significant change from baseline in mFARS score at 48 weeks (FARA, 2023b)
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