[2026 update] Does dual agonism explain the effect size, or is it dose? posts 61–64
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1 · go to the accepted answer.
Dual agonism versus dose: how much of tirzepatide's effect is the GIP component and how much is simply achieving higher receptor engagement? The honest answer is that the question is not settled. Some of the effect is surely the GIP component, but the trial design does not decompose it.
Collapsed as off-topic by two members at trust level 3 or above
This follows post #60 rather than contradicting it.
The 2.5 mg starting dose is not a therapeutic dose in the sense that weight loss is minimal at that dose. It is a tolerance-testing dose. Confusing the purpose of a starting dose with the purpose of a maintenance dose leads to false conclusions about efficacy.
I read post #62 twice before replying, because I had assumed the opposite.
Dual agonism versus dose: how much of tirzepatide's effect is the GIP component and how much is simply achieving higher receptor engagement? The honest answer is that the question is not settled. Some of the effect is surely the GIP component, but the trial design does not decompose it.
This topic was referenced in
- About the Tirzepatide categoryCompounds › Tirzepatide · 6 replies
- Comparing tirzepatide and semaglutide is harder than the tables suggestCompounds › Tirzepatide · 2 replies
- Tirzepatide in type 2 diabetes: the SURPASS programme, summarised honestly — the long versionCompounds › Tirzepatide · 90 replies
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