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GLP-1 Lozenges dissolve slowly under the tongue, allowing semaglutide to be absorbed steadily through the oral mucosa
Congenital lactase deficiency or hereditary alactasia This is a rare disorder caused by a mutation in the LCT gene which results in the absence of lactase and hence the inability of affected infants to break down the lactose present in breastmilk or formula, this can lead to severe diarrhoea and subsequent dehydration and weight loss if lactose is not excluded 1,4
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A realistic earliest FDA decision window, assuming Phase 3 confirms the Phase 2 findings, is 2028
It takes weeks, which is exactly why the clinical protocols build in four-week intervals between dose increases
