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c/trialwatch·posted 2 months ago by u/whois_wanda

[Discussion] TRIUMPH is doing more work than we give it credit for

Discussion Clean Column ×5

TRIUMPH is doing more work than we give it credit for. It is the sort of thing everyone half-believes and nobody writes down.

Spent an evening with the appendix tables and found the subgroup detail that the entire thread had been speculating about.

Quoted a figure here confidently, got asked whether it was ITT, went and checked, and it was not. Learned something.

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

Please do not ask me what dose you should be on. I genuinely do not know and neither does anyone else here.

4,714 up / 4,141 down53% upvoted14 commentsid 14rvad13 May 2026

14 comments

14 in this archive, depth 3

best — the order this archive was captured in

u/cold_chromatogram3154 points·2 months ago

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.

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u/nordic_pricing42 points·2 months ago

Intention-to-treat analyses everybody randomised regardless of what they did afterwards. Completer analyses only those who finished. The second is systematically more flattering and both are legitimate if labelled.

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u/ferran_dahlberg41 points·2 months ago

Cardiovascular outcome trials are powered for events, not for weight, and are typically run in a different population with different inclusion criteria. Reading a weight number out of one is reading a secondary endpoint.

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u/milan_mensah34 points·2 months ago

a press release is not a publication

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u/tb500_tangent9 points·2 months ago

a press release is not a publication

milan_mensah is right about the programme names. They are different populations with different endpoints.

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u/oskar_ibarra22 points·2 months ago

a press release is not a publication

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

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u/nightowl_injector41 points·2 months ago

How to read one of these papers in fifteen minutes, in the order that actually helps.

Start with the registered protocol and check the primary endpoint against what is reported. Then the methods: who was included, what the comparator was, how long the randomised phase ran. Then the discontinuation numbers, which are a tolerability result and are usually in a supplementary table.

Only then the efficacy figure, and read the interval rather than the point estimate. Finish with the limitations section, which is where the authors say what they actually think.

Fifteen minutes, and you will know more than any thread summarising it.

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u/milan_villalobos0 points·2 months ago

A confidence interval is the range of effects compatible with the data. Two trials with overlapping intervals have not disagreed, whatever their point estimates look like next to each other.

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u/iman_castellanos0 points·2 months ago

How long was the randomised phase before any extension?

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u/bastian_ekstrom0 points·2 months ago

A confidence interval is the range of effects compatible with the data.

This is the distinction that would end about half the arguments on this board.

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u/ahmed_iyer14 points·2 months ago

Agreed on comparators. "Superior" means nothing until you know superior to what and at what dose.

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u/whois_wandaOP7 points·2 months ago

Went looking for the registered protocol to see whether the endpoint had changed. It had not, which was reassuring and worth checking.

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Clinical trial reading group. New readouts, protocol amendments, endpoint definitions, dropout handling, and the difference between a press release and a publication. Absolute risk reduction and number-needed-to-treat are house dialect here.

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