Friedreich’s Ataxia (FA) is a rare, progressive, and debilitating genetic disorder with no approved treatments. Kidney function was assessed in patients with Friedreich’s ataxia in Part 2 of MOXIe, a Phase 2 international, multicenter, double-blind, randomized, placebo-controlled study of omaveloxolone in FA.
KIDNEYCODE is a sponsored, no-charge genetic testing program to facilitate a personalized, precision medicine-based approach to CKD diagnosis, and contribute to the global understanding of genetic causes of CKD.
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