Semaglutide formulation: what is in the licensed product besides the peptide — setting out what I have, and where I think it stops being reliable.
Comparing LEADER (N Engl J Med, 2016) with SURMOUNT-1 (N Engl J Med, 2022) and finding the comparison harder than it looks.
Different populations, different durations, different endpoints defined slightly differently, and in one case a different estimand. People compare the headline percentages anyway, including me until recently.
Is there a defensible way to put these side by side, or is the honest answer that there is not and we should stop?