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Larimar Therapeutics doses first patient in nomlabofusp study
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Larimar Therapeutics doses first patient in nomlabofusp study

Larimar Therapeutics announced dosing of the first patient in an open label extension, or OLE, study evaluating 25 mg daily subcutaneous injections of nomlabofusp in participants with Friedreich’s ataxia, or FA. Nomlabofusp is a novel protein replacement therapy designed to address the root cause of Friedreich’s ataxia by delivering frataxin to mitochondria.

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