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Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder of fatty acid oxidation caused by deficiency of plasma membrane carnitine transport resulting from impairment in the plasma membrane OCTN2 carnitine transporter

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In the Phase 3 trial STEP 1 by Wilding et al., 2021, the authors reported a mean weight change of -14.9 percent versus -2.4 percent on placebo at 68 weeks across n=1961 trial participants

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It reduces scalp irritation and helps create an optimal environment for hair growth

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