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A key moment in dulaglutide's commercial lifecycle came in February 2020, when the FDA approved a new indication for the reduction of major adverse cardiovascular events (MACE) in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors, based on data from the REWIND trial
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The Precision Peptide Genetic Test ($298) can personalize therapy by mapping genetic variants affecting blood pressure regulation and peptide response
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