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If a patient experiences side effects, the provider may slow down the increase, keep the dose steady longer, or adjust the plan to support comfort and safety

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Supplementary Materials Data Availability Statement The datasets generated for the current trials will be shared on a specialised SAS data platform in a de-identified/anonymised format with bona fide researchers submitting a research proposal requesting access to data for use as approved by the Independent Review Board (IRB) according to the IRB Charter (see novonordisk-trials.com)