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The FDA granted full approval to all patients aged 4 and older with a confirmed mutation in the DMD gene, while giving accelerated approval to non-ambulatory patients

Human studies need to be more robust to be able to comment on the safety of the long-term use of these peptides

For semaglutide, small pharmacies had to stop production by April 22, while large compounders have until May 22

Many people may ask themselves

However, the use of semaglutide in this population should be carefully evaluated on a case-by-case basis, taking into account factors such as the type of surgery, time since the procedure, and overall health status