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c/cagrilintide·posted 4 months ago by u/forest_plot_fiona

satiety: the version I wish someone had shown me in week 1

Trial Data Cold Box ×8 Clean Column ×3

satiety: the version I wish someone had shown me in week 1. Numbers below. Ask me the boring questions, they are the useful ones.

Kept a log purely because so few people are logging this one. It is one person and it is not data.

Why this compound is not simply another agonist, which is how it gets described everywhere else.

Amylin is co-secreted with insulin and signals satiety through its own receptor complexes. It is a different axis from the incretin system, not a parallel version of it. That is why the combination story is interesting: two mechanisms that address appetite differently, rather than more agonism at one receptor.

It is also why the dosing intuitions people bring from the semaglutide and tirzepatide boards do not transfer. Different receptors, different exposure-response, and no published schedule anybody here can reason from.

I will update this if the picture changes rather than quietly leaving it up.

2,033 up / 42 down98% upvoted22 commentsid 1agxc929 Mar 2026

22 comments

14 in this archive, depth 4

best — the order this archive was captured in

u/niels_norgaard373 points·4 months ago

Dosing intuitions from the GLP-1 boards do not transfer. Different receptor family, different exposure-response, and no published schedule for members to reason from.

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u/noor_hovland108 points·4 months ago

Dosing intuitions from the GLP-1 boards do not transfer.

Agreed, and the combination arms are where the interesting numbers actually live.

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u/ice_pack_auditcold chain0 points·4 months ago

Agreed, and the combination arms are where the interesting numbers actually live.

noor_hovland is right that the evidence base here is thin. Conclusions should be held loosely.

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u/lucia_bruun0 points·4 months ago

noor_hovland is right that the evidence base here is thin.

Adding the standing caveat — nothing here is approved standalone and research material is not for human use.

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u/yannick_petrov36 points·4 months ago

Push back: the evidence base here is thin enough that a confident ranking against the established compounds is not supportable.

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u/zeynep_zielinski203 points·4 months ago

do not assume the dosing intuitions from the GLP-1 boards transfer

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u/aa_analysis_andy65 points·4 months ago

amylin and GLP-1 are not redundant pathways

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u/rt_shift_reggie140 points·4 months ago

Combination and monotherapy arms must be read separately. Efficacy and tolerability both differ substantially between them and summaries routinely blur the two.

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u/noor_hovland48 points·4 months ago

Went looking for independent results on this and found a handful across the whole site. That is the honest state of the evidence.

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u/rafael_krastev60 points·4 months ago

independent purity data on this compound is thin

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[removed]34 points·4 months ago

[removed by moderator]

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u/ms_fragmenter31 points·4 months ago

That is preclinical work and the thread is treating it as a human finding.

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u/throwaway_44b1131 points·4 months ago

Is there any independent purity data on this compound that you have seen?

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u/forest_plot_fionaOPstats78 points·4 months ago

Which trial and which readout?

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About c/cagrilintide

Amylin analog pharmacology and the CagriSema combination: why amylin and GLP-1 co-agonism produces a different satiety profile, the REDEFINE readouts, and the very limited pool of people handling cagrilintide as research material.

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