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c/cagrilintide·submitted 8 months ago by u/aa_analysis_andy

[Discussion] we are measuring CagriSema at the wrong time and calling it noise

Discussionbranch of 7 comments

we are measuring CagriSema at the wrong time and calling it noise. I have gone back and forth on this for months. Carried an assumption over from the tirzepatide board and was corrected within an hour. Deserved. Dosing intuitions from the GLP-1 boards do not transfer. Different receptor family, different…

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7 comments, started 8 months ago
u/incretin_ivyMOD18 points·8 months ago

Left up. Thin evidence base, honestly labelled, which is the standard here.

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u/georgi_chowdhury4 points·8 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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u/slow_logbook_notes301 point·8 months ago

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

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u/incretin_ivypharmacology5 points·8 months ago

I would not extrapolate the tolerability profile from the monotherapy arm to the combination. The trials report them separately for a reason.

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u/noor_hovland4 points·8 months ago

nothing containing this is approved as a standalone product

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u/liv_dumitru4 points·8 months ago

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

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u/nl_verzekering3 points·8 months ago

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

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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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