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c/survodutide·posted 14 days ago by u/cato_girard

[Caution] hepatic endpoints need biopsy data, not an ALT screenshot

Caution Sourced ×6

Something I keep coming back to: hepatic endpoints need biopsy data, not an ALT screenshot.

Sent a vial to Janoshik because there was nothing on file. 98.4% against a claimed 97.5%. First entry for this compound in my own log.

The escalation schedules in the published protocols are slow and deliberate, and the tolerability tables show why. That is a description of the trials rather than a suggestion for anybody.

Read the phase 2 hepatic paper properly and the endpoint definitions were more interesting than the headline response rate.

Research-use-only material is not approved for human use and nothing here should be read as a recommendation to use it.

311 up / 45 down87% upvoted18 commentsid 19q60116 Jul 2026

18 comments

9 in this archive, depth 4

best — the order this archive was captured in

u/refund_ledger44 points·12 days ago

Nothing containing this compound is approved anywhere. Research-use-only material is not approved for human use.

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u/incretin_ivypharmacology37 points·12 days ago

Independent purity results for this compound are very sparse across the whole site, which means any impression about consistency is built on almost nothing.

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u/endotoxin_elliemicro8 points·12 days ago

That figure is from the obesity programme, and this thread is about the hepatic one.

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u/rania_marchand18 points·13 days ago

How fast was the escalation in that protocol?

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u/incretin_ivyMOD11 points·13 days ago

Independent result logged. There are almost none for this compound, so it is genuinely valuable.

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u/cato_batista8 points·12 days ago

the weight numbers are secondary to what this is being developed for

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[deleted]7 points·12 days ago

[deleted]

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u/elin_tamm3 points·12 days ago

research material is not approved for human use, which is why the clinical record here is thin

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u/whois_wanda16 points·12 days ago

Went slowly because everything published describes a deliberate escalation. That is the extent of what I will say about it.

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About c/survodutide

Survodutide-specific discussion: glucagon-receptor co-agonism, the hepatic fat and MASH resolution data, and how the side-effect profile compares with GIP-based dual agonism. Small community, high signal.

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