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c/trialwatch·posted 3 months ago by u/adaeze_weiss

[Discussion] the endpoint advice in here is 3 years out of date

Discussion Cold Box ×3

The title is the argument: the endpoint advice in here is 3 years out of date. Here is the rest of it.

To save the first four comments: 3 years.

On means, which this board treats as targets and which are nothing of the sort.

A reported mean body weight change is the centre of a distribution that in these trials is very wide. Substantial numbers of participants did much better, and substantial numbers did considerably worse while remaining on the drug and in the analysis.

Quoting the mean as an expectation therefore misleads in both directions: it makes ordinary results look like failures and it makes exceptional results look normal. If a paper publishes the distribution — and several do, in the appendix — look at that instead. It is far more informative than the number in the abstract.

Why comparing across trials almost never works, with the specific failure modes.

Different populations: an obesity programme and a diabetes programme enrol different people with different baseline characteristics. Different endpoints: body weight change, glycaemic control and cardiovascular events are not convertible. Different durations: 68 weeks and 72 weeks are not the same, and the curves have not flattened by either.

Different analysis populations: one paper reports intention-to-treat, another emphasises completers. Different support: some trial designs include structured lifestyle contact that no member of this board receives.

Stack those and the "X beats Y" tables that circulate here are comparing five things at once and attributing the difference to the molecule.

Not medical advice, obviously, and nothing here is approved for human use. One person with a spreadsheet.

537 up / 120 down82% upvoted19 commentsid 14hvoo24 Apr 2026

19 comments

18 in this archive, depth 4

best — the order this archive was captured in

u/rina_sobczak28 points·3 months ago

The registered protocol is public. Comparing the registered primary endpoint with the reported one is a two-minute check and it is how outcome switching gets caught.

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u/emil_agyeman7 points·3 months ago

read the endpoint before you read the headline

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u/ines_boateng18 points·3 months ago

Agreed. Half the arguments on this site are two people quoting different trials at each other without noticing.

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u/heart_rate_bump26 points·3 months ago

Small fix — that was the cardiovascular outcomes trial, so weight was a secondary endpoint and the population was different.

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u/adaeze_weissOP14 points·3 months ago·edited

Read a press release and the publication three months apart. The hedging in the second one was substantial.

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u/rulebook_rachaelmod · c/meta8 points·3 months ago

the appendix is where the interesting tables live

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u/hugo_norgaard10 points·3 months ago

discontinuation rate is a result, not a footnote

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u/hugo_norgaard18 points·3 months ago

SURPASS is the diabetes programme and reports glycaemic endpoints

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u/hamza_weiss8 points·3 months ago

Same. A press release is a claim about a result; the publication is the result.

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u/tove_ogunleye2 points·3 months ago

Is that intention-to-treat or completers?

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u/kaia_cabrera5 points·3 months ago

Yes. The appendix tables are where the subgroup and the adverse event detail actually live.

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u/joaquin_trevino2 points·3 months ago

Yes.

Agreed. And the interval, not the point estimate, is what the trial actually established.

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u/adaeze_weissOP1 point·3 months ago

open-label extensions are not the same evidence as the randomised phase

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u/anders_karlsen-18 points·3 months ago

How long was the randomised phase before any extension?

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u/tove_ogunleye5 points·3 months ago

Yes — the interval is the finding. A point estimate with a wide interval is a hypothesis in a nice font.

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u/adaeze_weissOP2 points·3 months ago

Absolute or relative risk reduction?

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