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When this goal was achieved a preliminary analysis of PET data for this dose group showed a very low binding of SAR425899 to the GCCR, suggesting that a dose of 0.12 mg will not provide further significant occupancy data
doi:10.1038/nature11450 118
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Role of glutathione redox status in liver injury
GLP-1 drugs primarily support glucose control and weight loss, while SGLT2 inhibitors offer strong heart and kidney protection
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