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GSK-376501 is an investigational small molecule drug developed by GSK (GlaxoSmithKline) as an oral partial agonist of the peroxisome proliferator–activated receptor gamma (PPARγ). It was studied in phase I clinical trials for the treatment and diagnosis of type 2 diabetes mellitus and also evaluated in healthy overweight and obese subjects. The compound was designed to modulate PPARγ activity, a nuclear receptor involved in glucose metabolism and adipogenesis, but development was discontinued after early-phase studies[1][2][3][4][5].
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