PeptidePedia The community reference

FLOW trial: difference between revisions

Diff·revision 4 → 5·01:26, 30 Oct 2024

Difference between revision 4 and revision 5 of FLOW trial. 2 lines changed; the page grew by 207 bytes.

Revision 4 — 17:16, 18 Oct 2024
TirzTaxonomist (talk)
split the results table so the two doses are separate rows
1,950 bytes ±0
Revision 5 — 01:26, 30 Oct 2024
GramsNotUnitsGil (talk)
label the extension study as an extension study in the table
2,157 bytes +207
11The primary composite comprised onset of kidney failure, a sustained fall of at least 50% in estimated glomerular filtration rate, or death from kidney or cardiovascular causes. It occurred less often on semaglutide, hazard ratio 0.76 (95% CI 0.66–0.88).{{r|perkovic2024}}11The primary composite comprised onset of kidney failure, a sustained fall of at least 50% in estimated glomerular filtration rate, or death from kidney or cardiovascular causes. It occurred less often on semaglutide, hazard ratio 0.76 (95% CI 0.66–0.88).{{r|perkovic2024}}
1212
+13The trial is significant because its endpoints are hard rather than surrogate: kidney failure and sustained loss of filtration function, not albuminuria alone. See [[Surrogate endpoint]].{{r|perkovic2024}}
+14
13== Design ==15== Design ==
14Participants had type 2 diabetes with an estimated glomerular filtration rate and albumin-to-creatinine ratio within defined ranges, and were on maximum tolerated renin–angiotensin system blockade. The trial therefore tested semaglutide added to established renal protection rather than in its place.{{r|perkovic2024}}16Participants had type 2 diabetes with an estimated glomerular filtration rate and albumin-to-creatinine ratio within defined ranges, and were on maximum tolerated renin–angiotensin system blockade. The trial therefore tested semaglutide added to established renal protection rather than in its place.{{r|perkovic2024}}