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Lixisenatide: difference between revisions

Diff·revision 3 → 4·00:06, 10 Nov 2024

Difference between revision 3 and revision 4 of Lixisenatide. 2 lines changed; the page grew by 276 bytes.

Revision 3 — 01:50, 19 Oct 2024
AnalyticalAnnie (talk)
convert the substitution list to a table so the analogues line up
1,771 bytes ±0
Revision 4 — 00:06, 10 Nov 2024
DulaglutideDug (talk)
add the peptide length to the infobox
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11Its pharmacological profile emphasises postprandial glycaemic control through pronounced delay of [[Gastric emptying|gastric emptying]], an effect that does not attenuate as it does with continuously present long-acting agonists.{{r|drucker2018}}11Its pharmacological profile emphasises postprandial glycaemic control through pronounced delay of [[Gastric emptying|gastric emptying]], an effect that does not attenuate as it does with continuously present long-acting agonists.{{r|drucker2018}}
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+13The ELIXA trial randomised people with type 2 diabetes and a recent acute coronary syndrome and reported no difference in cardiovascular outcomes. That neutral result is one of the principal reasons cardiovascular benefit is not treated as a class property.{{r|pfeffer2015}}
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13== Pharmacology ==15== Pharmacology ==
14Like exenatide, lixisenatide carries glycine at position 2 of the exendin scaffold and is therefore not a substrate for [[Dipeptidyl peptidase-4|DPP-4]]. Its half-life of about three hours nonetheless requires daily dosing, since renal clearance dominates once proteolysis is removed.{{r|drucker2018}}16Like exenatide, lixisenatide carries glycine at position 2 of the exendin scaffold and is therefore not a substrate for [[Dipeptidyl peptidase-4|DPP-4]]. Its half-life of about three hours nonetheless requires daily dosing, since renal clearance dominates once proteolysis is removed.{{r|drucker2018}}