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c/cagrilintide·submitted 7 months ago by u/nz_unfunded

reading REDEFINE threads from 2024 and half of it aged badly

Labbranch of 10 comments

reading REDEFINE threads from 2024 and half of it aged badly. Making the case below, and I expect to lose some of it in the comments. Complementary mechanisms are the rationale for pairing: satiety signalling alongside incretin signalling, rather than more agonism at the same receptor. The engineering problem was…

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10 comments, started 7 months ago
u/rina_sobczak133 points·7 months ago

Cosigning on the thin independent data. Fewer members test this, so the bands are wider and should be treated that way.

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[removed]96 points·7 months ago

[removed by moderator]

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u/zaid_balogun65 points·7 months ago·edited

Monotherapy arm or combination arm?

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u/amara_halonen54 points·7 months ago

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

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u/lucia_bruun113 points·7 months ago

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.

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u/rina_sobczak41 points·7 months ago

independent purity data on this compound is thin

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u/emeka_beaulieu0 points·7 months ago

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

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u/marta_ilunga1 point·7 months ago

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

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u/hugo_pires41 points·7 months ago

This. Complementary mechanisms rather than more of the same is the actual argument for the pairing.

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u/controversial_only23 points·7 months ago

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

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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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