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The primary endpoint was percent change in body weight from baseline to 24 weeks, which resulted in a 17.5% reduction in the 12 mg (2 mg initial dose) group

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Key highlights from the announcement: In the trial, participants with #obesity or #overweight achieved .% , with benefits extending to cardiometabolic risk factors such as blood pressure and systemic inflammation

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Reference Michael Jack Parente, Balaji Sitharaman, Liquid Chromatography Evaluation of a Novel Graphitic Carbon Stationary Phase Using Glucagon-Like Peptide-1 Analogs , ACS Omega, 2025.