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Al-Onaizi, Peter Thériault, Sarah Lecordier, Paul Prefontaine, Serge Rivest, Ayman ElAli, Early monocyte modulation by the non-erythropoietic peptide ARA 290 decelerates AD-like pathology progression, Brain, Behavior, and Immunity, Volume 99, 2022, Pages 363-382
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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 (ClinicalTrials, 2021b)
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