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van Royen ME, Cunha SM, Brink MC, Mattern KA, Nigg AL, Dubbink HJ, et al

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)

This means you can feel more confident in knowing that youre getting the clinically studied key ingredients necessary to help support fat loss, boost metabolism, and increase energy

Take 1 dose 30 minutes before your workout for optimum effectiveness, or in the morning on an empty stomach