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The safety and tolerability profile of OW s.c

For treatment of primary systemic carnitine deficiency, a genetic impairment of normal biosynthesis or utilization of levocarnitine from dietary sources, or for the treatment of secondary carnitine deficiency resulting from an inborn error of metabolism such as glutaric aciduria II, methyl malonic aciduria, propionic acidemia, and medium chain fatty acylCoA dehydrogenase deficiency

Understanding potential causes helps patients and healthcare providers determine appropriate next steps

Starting is as simple as 1-2-3 From your first form to your first dose designed to be simple, safe, and supportive every step of the way