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This expanding therapeutic landscape re-frames the standard 2.4 mg/week dose as a more modest regimen, further validating our use of a comparable human equivalent dose as a low dose in this preclinical model to specifically isolate and study the drugs weight loss-independent effects

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Maintaining the same batch COA number throughout a study eliminates a potential variable in research data

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Extended-release niacin formulations may cause less glucose elevation than immediate-release products but carry a higher risk of hepatotoxicity