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Due to the lack of phenotypic differences in metabolic parameters within the control lines (20), we present data for control mice (aggregate of mice expressing Cre ( Vil1 -Cre for Dpp4 Gut/ and Tie2 -Cre for Dpp4 EC/ ) and Dpp4 fl/fl mice (littermate controls from the corresponding line) versus mice with the 2 different targeted Dpp4 deletions

Those are useful for setting expectations

Whilst injection site pain is well-recognised, reporting helps maintain pharmacovigilance and identifies any emerging safety signals

However, questions remain around affordability, patient adherence, and long-term access in the broader population.

Ask your doctor whether a covered alternative could work for you

A medication timer may be useful, too