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c/retatrutide·posted 7 days ago by u/discount_math_dm

[Trial Data] TRIUMPH timeline — what we actually know vs what gets repeated

Trial Data The Quiet One ×8 Slow Clap ×1

TRIUMPH timeline — what we actually know vs what gets repeated. Change my mind, genuinely — I have no stake in being right about this.

Nothing containing this compound is approved anywhere. Research-use-only material is not approved for human use, and that is a statement of fact rather than a disclaimer.

The phase 2 readout ran to 48 weeks in a few hundred participants with a slow escalation. Both the size and the duration matter when people quote the headline number.

Increases in heart rate have been reported across this receptor class. The magnitude and clinical significance are exactly what phase 3 is powered to establish.

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

1,961 up / 167 down92% upvoted39 commentsid 1kmxs423 Jul 2026

39 comments

30 in this archive, depth 5

best — the order this archive was captured in

u/reta_and_regretMOD321 points·6 days ago

Left up. It reads the phase 2 paper carefully and it is honest about the intervals.

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u/helga_vermeulen433 points·6 days ago

Left up.

Disagree with this specific inference. A 48-week readout does not tell you the shape of the curve after it.

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u/noor_ivaturi349 points·6 days ago

Correction: TRIUMPH is the phase 3 programme. The number you are quoting is from the phase 2 readout, which is a different trial.

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u/discount_math_dmOP-32 points·6 days ago

Correction: TRIUMPH is the phase 3 programme.

Adding the standing caveat: none of this is approved anywhere and research material is not for human use.

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u/yusuf_ramos1 point·5 days ago

not approved anywhere, which is the single most important fact in this board

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u/discount_math_dmOP226 points·6 days ago

Correcting my own comment above: that figure was the 36-week interim, not the 48-week endpoint.

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u/sofia_wikstrom278 points·6 days ago

Small fix — three receptors, not two. GLP-1, GIP and glucagon, and the third one is the reason this compound gets its own board.

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u/viktor_laurent165 points·6 days ago

Not convinced. You are attributing a week of food noise to the glucagon arm when the escalation rate alone would explain it.

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u/yannick_salinas74 points·6 days ago

research-use-only material is not approved for human use, full stop

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u/rosa_almeida50 points·6 days ago

Push back: quoting the phase 2 headline as an expected outcome is not a fair reading of a small trial with wide intervals.

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u/discount_math_dmOP45 points·5 days ago

triple agonist — GLP-1, GIP and glucagon, and the glucagon arm is the new part

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u/nikhil_asante204 points·5 days ago

It is a triple agonist at the GLP-1, GIP and glucagon receptors. The glucagon arm is the genuinely novel component and it is the one with the least human outcome data behind it.

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u/nadia_norgaard121 points·6 days ago

Read the phase 2 paper twice before ordering anything. Recommend that to anyone in this board: the error bars are the interesting part.

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u/emil_agyeman178 points·5 days ago

a lot of the confident posting here is extrapolation

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u/rosa_almeida48 points·5 days ago

small trial, big effect, wide error bars

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u/employer_carveout38 points·5 days ago

the glucagon component is why the metabolic story reads differently

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u/heart_rate_bump92 points·5 days ago

Glucagon receptor agonism is associated with increased energy expenditure and with hepatic effects. That is a mechanistic story with strong preclinical support and limited phase 2 human data.

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u/source_or_silence57 points·5 days ago

What is the source for that figure — the published paper or a summary of it?

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u/injection_site_iris46 points·5 days ago

the TRIUMPH programme is still running, so anything definitive is premature

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u/liver_enzyme_liz22 points·4 days ago

heart rate is the thing people report watching

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u/sena_teixeira63 points·5 days ago

The thing that surprised me was how much of the discussion here is inference rather than measurement.

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u/lane_watchermod · logistics35 points·5 days ago

Kept a log specifically because there is so little published. It is one person and it is not data.

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u/mateusz_mensah13 points·5 days ago

Right, and it bears repeating that nothing here is approved anywhere and research material is not for human use.

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u/andres_sorensen6 points·5 days ago·edited

Right, and it bears repeating that nothing here is approved anywhere and research material is not for human use.

This is the sentence the rest of the board should read first. Phase 2 is not a label.

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u/matias_falk15 points·5 days ago

dose escalation in the trials was slow for a reason

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u/priya_weiss12 points·5 days ago

nothing here is available as a prescription product, so read every thread with that in mind

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u/lurker_for_years23 points·5 days ago

That is body weight change, not fat mass. The trials report the first and people quote it as the second.

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u/freya_baptista15 points·5 days ago·edited

That is body weight change, not fat mass.

Agreed, and the glucagon arm is exactly why the comparison threads do not work.

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u/divya_bakken10 points·5 days ago

Agreed, and the glucagon arm is exactly why the comparison threads do not work.

freya_baptista is right about the escalation being the variable. It explains most of the difficult reports here.

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u/trialwatch_theotrial nerd17 points·5 days ago

Has anyone posted an independent test on this compound recently?

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About c/retatrutide

Retatrutide: GIP/GLP-1/glucagon triple agonism, the TRIUMPH programme, and the fact that most people discussing it are handling research-grade material with no human-use approval anywhere. Dose-response, heart-rate signal, and the unusually steep phase-2 weight curves get argued about here weekly.

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