KevinCompounds said:The dose-response is real but shallow at the top.
This is exactly what I could not find anywhere else. Adding it to my notes with a link back to this thread.
KevinCompounds said:The dose-response is real but shallow at the top.
This is exactly what I could not find anywhere else. Adding it to my notes with a link back to this thread.
From the other side of the consultation, briefly.
jennifer_SEA said:...but the FDA says semaglutide...
Interesting point. I want to add some regulatory nuance: the FDA labeling reflects the specific clinical trial data submitted for approval. Real-world clinical practice often extends beyond the FDA label based on emerging evidence and clinical judgment.
Example: semaglutide was first approved for diabetes (Ozempic), then obesity (Wegovy). The molecule didn't change — our understanding of its applications expanded. Similarly, semaglutide may evolve as more data accumulates.
jim_asheville said:Steady state is the thing most people miss.
I will push back on the "any working dose is fine" framing. The maintenance evidence sits overwhelmingly at the top studied dose, and the extension data shows regain tracking dose reduction rather than tracking stopping. Holding low is reasonable; pretending it is evidentially equivalent is not.
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