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Those are different trials, so they are not perfectly apples-to-apples

Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)

I take 120 mg of lurasidone daily, which is an antipsychotic medication that will be targeted by Kennedys commission

It can feel impossible to lose weight in the face of obstacles like genetics, comorbid medical conditions, and difficult diets

If your plan currently denies coverage, talk to your doctor about your options whether thats appealing the decision, switching to a covered medication, or exploring patient assistance programs