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Adverse Reactions Reported in 1% and More Frequent in EGRIFTAtreated than Placebo Patients during the 26-Week Phase (Combined Studies) In the EGRIFTA clinical trials, mean baseline HbA 1c was 5.3% among patients in both the EGRIFTA and placebo groups

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Non-CYP Phase I and Phase II enzyme profiles mirrored these trends, peaking between Days 15 and 30 (Fig