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The dual Glucagon/GLP-1 agonist survodutide was also evaluated at different doses, with weekly subcutaneous injection in MASH patients without cirrhosis, with 39% of patients having T2DM
Most studies reported diabetic neuropathy as one of the endpoints, rather than classifying it into peripheral neuropathy and autonomic neuropathy
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Food and Drug Administration (FDA) for these medications, which reflect the companys commitment to address chronic health conditions through innovative therapies
