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103
c/cagrilintide·posted 14 days ago by u/solene_abubakar

[Discussion] cagri is the most underrated molecule in this space

Discussion

Thinking out loud about this: cagri is the most underrated molecule in this space.

Nothing containing this compound is approved as a standalone product, and research-use-only material is not approved for human use.

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.

Sent a vial to Medutest because there was almost nothing on file for this compound. 97.6% against a claimed 97.0%, and I posted it because the log needs entries.

If somebody has the same thing measured a different way, post it next to mine and we will see whether they agree.

118 up / 15 down89% upvoted12 commentsid epmwli16 Jul 2026

12 comments

12 in this archive, depth 3

best — the order this archive was captured in

u/viktor_nkemelu18 points·13 days ago

Amylin is co-secreted with insulin and acts on satiety and gastric emptying through its own receptor complexes. An amylin analogue is therefore not a variant of an incretin agonist — it is a different signalling axis.

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u/solene_abubakarOP8 points·12 days ago

phase 3 data will change most of what gets said here

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u/titration_marshalmod · c/semaglutide0 points·12 days ago

phase 3 data will change most of what gets said here

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

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u/zaid_grimaldi8 points·13 days ago

Correction: that is the combination programme, not the monotherapy readout. Different arms, different numbers.

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u/ines_ekstrom2 points·12 days ago

Yes. The combination is where the interesting effect sizes are, and the monotherapy arms read very differently.

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u/hana_pereira9 points·12 days ago

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

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u/karim_restrepo11 points·12 days 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/aa_analysis_andy3 points·11 days ago·edited

nothing here is approved as a standalone product and research material is not for human use

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u/solene_abubakarOP4 points·12 days ago

Are you comparing against a GLP-1 monotherapy result? They are not comparable.

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u/tove_vasquez1 point·11 days ago

long-acting amylin is the whole point of the molecule

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u/zaid_balogun7 points·12 days ago·edited

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/bpc_scepticresearch peptides2 points·11 days ago

The tolerability tables were more informative than the headline numbers, which is usually the case and never how it gets summarised.

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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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