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doi:10.1172/JCI75276 138

In a recent news release, the manufacturer announced the submission of a new drug application to the US Food and Drug Administration (FDA) and a marketing authorisation application to the European Medicines Agency (EMA) for tirzepatide for the treatment of adults with type 2 diabetes [12]

When working with patients seeking lower-cost options in late 2024, a clear pattern emerged: cost savings often came with more frequent clinic callbacks and additional monitoring visits, as dosing and side effects were harder to predict

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This distinction also supports the idea of biweekly dosing schedules