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Evidence-based GLP-1 & peptide discussion since 2023
ForumsRetatrutide & Triple AgonistsTRIUMPH-2 obesity without diabetes — anyone have experience?

TRIUMPH-2 obesity without diabetes — anyone have experience?

Dr.ObesityLA Wed, Apr 16, 2025 at 8:08 AM 23 replies 1,941 viewsPage 1 of 5
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Dr.ObesityLA
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Apr 16, 2025 at 8:08 AM#1

Read the primary source rather than the write-up and the two do not agree, so here is what is actually in it.

The phase 2 numbers were about 24% mean weight loss at 48 weeks on the top dose, with the curve still descending at the end of the study. A curve that has not flattened is a real finding, but it also means the true plateau is unknown, and phase 2 populations are small and selected.

Where I think it is weakest: the follow-up is short relative to how long people actually take these drugs, so durability is an assumption here rather than a finding.

What I actually want to know is what the phase 2 dropout pattern implies about how the phase 3 tolerability will read. Practical detail welcome, however dull — the duller the better.

Note on sourcing:
Figures above are from the primary publication rather than the press summary. If a number here disagrees with one you have, post yours and we will work out which of us is reading a secondary source.
15 10zoe_NC, Dr.ObesityLA, NurseKim_ATL and 12 others
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LibrarianMeg
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Apr 16, 2025 at 10:34 AM#2
Dr.ObesityLA said:
The phase 2 numbers were about 24% mean weight loss at 48 weeks on the top dose, with the curve still descending at the end of the study.

True, and it depends on a baseline nobody has stated. Without knowing where someone started, the same number can be an excellent result or a disappointing one.

14 9PharmD_Rodriguez, julia.endo, JessicaM_2024 and 11 others
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Dr.SportsMedIN
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Apr 16, 2025 at 1:00 PM#3
Dr.ObesityLA said:
The phase 2 numbers were about 24% mean weight loss at 48 weeks on the top dose, with the curve still descending at the end of the study.

I would rather people stopped quoting the 24% as if it were a licensed outcome. It is a phase 2 result in a few hundred participants with no cardiovascular endpoint and no long-term safety data, and this board has a habit of treating pipeline numbers as settled.

If somebody has the primary source to hand I would rather cite it than paraphrase it.

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LindaRN_retired
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Apr 16, 2025 at 3:26 PM#4

Taking the question as asked, rather than the general version of it. The glucagon component looks paradoxical and is not. Glucagon receptor agonism raises energy expenditure and drives hepatic fatty-acid oxidation, and its hyperglycaemic tendency is offset by the GLP-1 arm's insulin secretagogue effect. Net result: intake down from GLP-1/GIP, expenditure up from glucagon, glycaemia neutral or improved. It is a balancing act, and it is why the liver-fat results are the most interesting part of the dataset.

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paige_pharma
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Apr 17, 2025 at 6:01 AM#5
LibrarianMeg said:
True, and it depends on a baseline nobody has stated.

Can confirm. Same sequence, different timescale.

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