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c/cagrilintide·posted 1 months ago by u/clara_weiss

amylin — 23 things I got wrong before I got it right

Trial Data Cold Box ×7 The Quiet One ×2

amylin — 23 things I got wrong before I got it right. Making the case below, and I expect to lose some of it in the comments.

Read the combination paper twice before saying anything here. The monotherapy and combination arms tell genuinely different stories.

Sent a vial to Medutest because there was almost nothing on file for this compound. 97.8% against a claimed 97.0%, and I posted it because the log needs entries.

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

If two or three other people have done the same thing we might actually learn something. Alone it is an anecdote.

4,073 up / 2,973 down58% upvoted69 commentsid hbzwxj15 Jun 2026

69 comments

29 in this archive, depth 6

best — the order this archive was captured in

u/yannick_salinas180 points·1 months ago

Complementary mechanisms are the rationale for pairing: satiety signalling alongside incretin signalling, rather than more agonism at the same receptor.

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[deleted]65 points·1 months ago

[deleted]

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u/incretin_ivypharmacology145 points·1 months ago

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

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u/hugo_pires91 points·1 months ago

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

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

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u/controversial_only61 points·1 months ago

That result is preclinical. Worth flagging, since the thread has been reading it as human data.

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u/sequence_checkerresearch peptides23 points·1 months ago

nausea profile in the combination trials is the thing to read carefully

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u/chidi_yilmaz34 points·1 months ago·edited

Asked a question here that turned out to be based on a mechanism confusion. Three people untangled it patiently.

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u/clara_weissOP25 points·1 months ago

Correcting myself upthread: I gave the 72-week figure and the paper reports 26 weeks.

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u/runa_grimaldi0 points·1 months ago

The engineering problem was duration: native amylin is short-acting and aggregation-prone. A long-acting analogue suitable for weekly administration is what makes the combination clinically interesting.

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u/teodor_lokken1 point·1 months ago

read the combination arms separately from the monotherapy arms

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u/ravi_sandvik1 point·1 months ago

read the combination arms separately from the monotherapy arms

This is the distinction that keeps this board honest — different axis, not a stronger version of the same one.

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u/rania_marchand1 point·1 months ago

Right, and the tolerability data in the combination arms is the part worth reading properly rather than summarising.

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u/titration_marshalmod · c/semaglutide1 point·1 months ago·edited

read the combination arms separately from the monotherapy arms

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

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u/zeynep_weiss1 point·1 months ago

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

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u/forest_plot_fionastats67 points·1 months ago·edited

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

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u/zeynep_ndiaye55 points·1 months ago

Monotherapy arm or combination arm?

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u/zeynep_zielinski37 points·1 months ago

Same view — long-acting is the engineering achievement here, and it is why the molecule exists at all.

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u/andres_dahlberg44 points·1 months ago

Independent purity data on this compound is sparse compared with the older molecules, simply because far fewer members have paid for testing. Sparse data means wide uncertainty, not a verdict.

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u/runa_pires35 points·1 months ago

Agreed — it is an amylin analogue and importing intuitions from the incretin boards produces confident nonsense.

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u/clara_weissOP14 points·1 months ago

Which receptor family are you attributing that effect to?

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u/micro_bump_mick21 points·1 months ago

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

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u/zeynep_zielinski6 points·1 months ago

Small fix — amylin analogue, not a GLP-1 analogue. The whole mechanism argument changes on that word.

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u/hedda_aguirre1 point·1 months ago·edited

What does the tolerability table in that paper actually say?

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u/clara_weissOP8 points·1 months ago

Which trial and which readout?

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u/zaid_balogun12 points·1 months ago

Agreed — it is an amylin analogue and importing intuitions from the incretin boards produces confident nonsense.

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

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u/runa_pires24 points·1 months ago

the co-agonism argument is about complementary mechanisms

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u/chidi_yilmaz16 points·1 months ago

Yes. Anyone reading this board should hold their conclusions loosely until phase 3 reports.

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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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