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SURPASS trial programme: difference between revisions

Diff·revision 6 → 7·19:05, 21 Sep 2024

Difference between revision 6 and revision 7 of SURPASS trial programme. 3 lines changed; the page grew by 330 bytes.

Revision 6 — 00:53, 3 Sep 2024
CagriCass (talk)
fix a dangling clause
2,281 bytes +288
Revision 7 — 19:05, 21 Sep 2024
PioneerPerdita (talk)
the trial was open-label; the article implied blinding
2,611 bytes +330
24SURPASS-CVOT is unusual among cardiovascular outcome trials in using an active comparator with an established benefit rather than placebo, which changes what a non-inferiority result means: non-inferiority to an agent that itself reduced events is a stronger statement than non-inferiority to placebo.{{r|frias2021}}24SURPASS-CVOT is unusual among cardiovascular outcome trials in using an active comparator with an established benefit rather than placebo, which changes what a non-inferiority result means: non-inferiority to an agent that itself reduced events is a stronger statement than non-inferiority to placebo.{{r|frias2021}}
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+26Open-label design in SURPASS-2 is a limitation for subjective endpoints and adverse-event reporting, though less so for glycated haemoglobin, which is a laboratory measurement.{{r|ich_e9}}
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26== References ==28== References ==
27{{reflist}}29{{reflist}}
28<ref name="frias2021">Frías JP, Davies MJ, Rosenstock J, et al. "Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes." ''New England Journal of Medicine'' 385(6):503–515 (2021). DOI:10.1056/NEJMoa2107519. PMID 34170647.</ref>30<ref name="frias2021">Frías JP, Davies MJ, Rosenstock J, et al. "Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes." ''New England Journal of Medicine'' 385(6):503–515 (2021). DOI:10.1056/NEJMoa2107519. PMID 34170647.</ref>
+31<ref name="ich_e9">International Council for Harmonisation, ''E9(R1): Estimands and Sensitivity Analysis in Clinical Trials'' (2019).</ref>
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30{{DEFAULTSORT:SURPASS trial programme}}33{{DEFAULTSORT:SURPASS trial programme}}