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Topic summary

Second pass at: Retatrutide dose escalation in the published trials

This is a generated summary. It shows the 9 most-liked posts from a topic of 126, in their original order, with the accepted answer included where one exists. It is a reading aid and it will miss nuance — the full topic is the record.
B
BuchholzTL2Member14 Jul 2024#1

Second pass at: Retatrutide dose escalation in the published trials — setting out what I have, and where I think it stops being reliable.

I have seen LEADER (N Engl J Med, 2016) cited in support of a claim I do not think it supports, twice this month, so I would like to work through what it actually shows.

My reading is that the trial is sound for its own question and is being stretched to answer a different one. I might be wrong about that, which is why this is a topic rather than a correction.

What I would like from this discussion: someone who disagrees with me to say why, with the section of the paper they are relying on.

48 likes 2y
NK
n.krastevTL2 Moderator16 Jul 2024#14
t.marchetti, post #5: I read post #3 twice before replying, because I had assumed the opposite. Glucagon receptor agonism seems paradoxical in a weight-loss compound because glucagon raises blood glucose. The paradox resolves because glucagon agonism also increases energy expenditure and promotes hepatic fat oxidation, and the incretin components offset the… Go to post

Having read the exchange above, I think I was wrong earlier in this topic and I want to say so plainly rather than quietly editing.

The correction was fair and I had been repeating something I had not checked carefully enough.

32 likes in reply to #5 2y
TV
t.vasquezTL4 Moderator17 Jul 2024#28
ni.kravchenko, post #3: TRIUMPH is phase 3 and it is ongoing. No phase 3 results exist. Nothing should be attributed to TRIUMPH because the trial has not finished. When it does, this page will update. Go to post

post #27 is right about the mechanism and I think understates the practical bit.

Mass and identity: a report on retatrutide should state the mass detected by LC-MS, not assume a theoretical mass. The theoretical mass is not published in peer-reviewed literature for retatrutide at present.

28 likes in reply to #3 2y
RN
r.novakTL2 Moderator18 Jul 2024#32
Buchholz, post #1: Second pass at: Retatrutide dose escalation in the published trials — setting out what I have, and where I think it stops being reliable. I have seen LEADER ( N Engl J Med , 2016) cited in support of a claim I do not think it supports, twice this month, so I would like to work through what it actually shows. My reading is that the trial… Go to post

Two things before anyone answers the substance.

First, the context in the first post is clear and specific. Second, the question is framed so that an answer can actually address it. Both are the norm here and both matter more than they sound.

30 likes in reply to #1 2y
MD
methods_draftTL2Member18 Jul 2024#39
m.rasmussen, post #23: Glucagon receptor agonism seems paradoxical in a weight-loss compound because glucagon raises blood glucose. The paradox resolves because glucagon agonism also increases energy expenditure and promotes hepatic fat oxidation, and the incretin components offset the glycaemic effect. In diabetes trials, HbA1c improved rather than worsened. Go to post

post #38 is right about the mechanism and I think understates the practical bit.

Phase 2 sample sizes are not adequate for safety characterisation of a novel triple agonist. Phase 3 is where that question gets answered. Using phase 2 results to make claims about safety profile is using the trial for a purpose it was not designed for.

29 likes in reply to #23 2y
SA
s.antonsenTL2 Moderator19 Jul 2024 · edited#44

The phase 2 obesity paper reported dose-dependent weight reduction of a magnitude that attracted attention. It also reported dose-dependent heart-rate increases. The heart-rate signal is the reason phase 3 exists rather than something assumed negligible based on phase 2.

31 likes 2y
GH
g.haalandTL3Regular23 Jul 2024#101

Thank you for the correction. I have edited my earlier post with a note rather than silently, so the thread still makes sense to read. The error was mine and it was the kind that comes from remembering a figure instead of looking it up.

32 likes 2y
VB
v.baptistaTL2 Moderator24 Jul 2024#115
compounding_ruth, post #26: I disagree with the reply above, and I think the disagreement is substantive rather than terminological. The distinction being drawn does not survive when you look at the published data for this specific question. I would be glad to be shown wrong on this, because the version I am arguing against is more convenient. Go to post

Having read the exchange above, I think I was wrong earlier in this topic and I want to say so plainly rather than quietly editing.

The correction was fair and I had been repeating something I had not checked carefully enough.

30 likes in reply to #26 2y
KB
k.brandl_deTL3Translator · DE24 Jul 2024#122
two_year_line, post #10: Picking up post #7: that is the part I would want checked first. Triple agonism: is the effect additive, synergistic, or neither? A phase 2 comparison of tirzepatide (dual) to retatrutide (triple) would answer that question. The published data does not include such a direct comparison. Go to post

Dose escalation in the published trials: the protocols started at lower doses and escalated by defined steps. The step sizes are documented and they may or may not match what someone self-prescribing would choose.

29 likes in reply to #10 2y

Read the full topic (126 posts)

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