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Additional important points represent a source of concern, such as the significantly higher rate of hospitalization for heart failure with saxagliptin reported in the SAVOR-TIMI 53 trial [58], the fact that the research regarding dutogliptininitially considered a promising selective DPP4 inhibitor [146] was abruptly discontinued without giving any reason [63] and the finding of hyperuricemia in patients treated with teneligliptin [129]

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It is metabolized in the liver and it is excreted in the urine, bile and secretions