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Patients may start to see results when their initial dose increases a few weeks after the start of their treatment plan, though results will vary

This approach allows assessment of individual response and minimizes the impact of any unexpected sensitivity

The patient experienced a slight weight increase during the 2.5 mg initiation phase, which is expected given that this dose is intended for gastrointestinal tolerability rather than therapeutic weight loss

Intervention Randomly assigned 1:1 to subcutaneous Semaglutide 2.4 mg once-weekly for 52 weeks or placebo Semaglutide treatment was initiated at a dose of 0.25mg once-weekly for the first 4 weeks

In the SUSTAIN-6 trial, no significant difference was observed between semaglutide and placebo groups, with rates of 2.7% and 2.8%, respectively (HR 0.98

It helps grow new blood vessels