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After 30 years, cardiovascular mortality rates for liraglutide 1.2 mg, 1.8 mg, and rosiglitazone reached 69.7%, 68.4%, and 72.5%
The combination of GLP-1, GIP, and glucagon receptor activity produces metabolic and body composition research effects beyond what dual or single-receptor compounds deliver
It just worked quietly in the background
This lipid effect is independent of its glucose action and may complement semaglutide's favorable cardiovascular profile seen in the SUSTAIN-6 trial, where subcutaneous semaglutide reduced major adverse cardiovascular events (MACE) by 26% vs
Bibcode:2004BCons.117..235S
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