Noted, and I have changed what I was going to do on the strength of it.
SURMOUNT-4 and what withdrawal data does and does not tell an individual — one year on posts 121–137
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1 · go to the accepted answer.
Post #119 is right about the mechanism and I think understates the practical bit.
Nausea profile: some people report tirzepatide as less nausea-prone than semaglutide, others report it as more. The trial reported gastrointestinal effects broadly comparable in character. Individual variation is the largest factor.
The evidence for this is thinner than the way I have phrased it suggests.
I had written a reply contradicting post #123 and deleted it. Here is what survived.
One more thing on SURMOUNT-4 that took me far too long to see: the two figures people quote are not measuring the same quantity. Once you notice that, the apparent contradiction disappears.
Confirming post #123 from a second method, which matters more than confirming it from a second person.
Summarising the SURMOUNT-4 thread so far, since it is long and the answer is buried: the first reply has the method, the fourth has the correction to it, and the rest is people agreeing at length.
Weight reduction figures from SURMOUNT-1 are frequently quoted without the trial's duration attached. A mean change at 72 weeks and a mean change at 40 weeks are different numbers and both circulate.
Since SURMOUNT-4 keeps coming up, it should probably be a maintained page rather than a recurring thread. I am happy to draft it if someone with more direct experience will review it.
Where I part company with post #127, and it is a narrow parting.
Taking SURMOUNT-4 seriously for a moment rather than deflecting: the honest position is that the community has observations and no controlled comparison, and those two things support very different sentences.
Categorical response thresholds — the proportion reaching ten, fifteen or twenty per cent reduction — are more persuasive and less informative than the mean. They depend entirely on where the threshold was drawn.
Seconded. It reads as careful rather than confident, which is the right register.
On storage: published stability data covers the licensed formulation at its licensed concentration. A research preparation reconstituted at home in a different diluent at a different concentration is outside every one of those conditions.
Posting it because the silence on this was starting to look like agreement.
Research-use-only tirzepatide is not approved for human use and is not made to pharmaceutical standards. Anyone discussing it here is describing what they did, not recommending it.
Confirming post #133 from a second method, which matters more than confirming it from a second person.
Practical note on SURMOUNT-4: write down what you expect before you look. The number of times I have found what I went looking for is higher than chance would allow.
I had written a reply contradicting post #132 and deleted it. Here is what survived.
Categorical response thresholds — the proportion reaching ten, fifteen or twenty per cent reduction — are more persuasive and less informative than the mean. They depend entirely on where the threshold was drawn.
I would treat the number as indicative rather than as a measurement.
Gastrointestinal effects were comparable in character to the GLP-1 monoagonists across the programme. Individual reports here vary in both directions, which is what you would expect from a between-person difference rather than a between-drug one.
I have deliberately not rounded that, because the rounding is where the argument starts.
This topic was referenced in
- Tirzepatide in obstructive sleep apnoea: reading SURMOUNT-OSACompounds › Tirzepatide · 8 replies
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