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doi: 10.3350/cmh.2015.21.2.180

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Regulatory agencies, including the US Food and Drug Administration, the European Medicines Agency, and the Pharmaceuticals and Medical Devices Agency, require extensive Phase III clinical trials, immunogenicity assessments, and comprehensive Chemistry, Manufacturing, and Controls data before approving new GLP-1 therapies or label expansions

This is also known as oxidative damage, and it can interfere with normal cellular function and contribute to the development of numerous diseases and aging processes (41)

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