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In the Phase 3 randomized, double-blind, multicenter, placebo-controlled REDEFINE 1 (NCT05567796) and REDEFINE 2 (NCT05394519) medical trials, carried out over 68 weeks, CagriSema (Novo Nordisk)—a once-weekly mixture remedy of semaglutide and cagrilintide, an amylin analog—demonstrated vital weight reduction and metabolic enhancements in contrast with placebo.1,2
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REDEFINE 1 evaluated the efficacy and security of once-weekly CagriSema in people with obese or weight problems over 68 weeks. Baseline traits included a imply physique weight of 106.9 kg, a imply physique mass index of 37.9 kg/mÇ, a waist circumference of 114.7 cm, and a hemoglobin A1c (HbA1c) of 5.5%. Primary endpoints included relative physique weight change at 68 weeks and the proportion of members attaining 5% or extra weight reduction.1,2
CagriSema produced clinically significant and sustained weight reduction in contrast with semaglutide alone, cagrilintide alone, or placebo. Participants receiving CagriSema have been extra more likely to obtain 5% or larger, 20% or larger, and 30% or larger weight discount and skilled enhancements in blood stress, glycemic management, and lipid profiles.1
REDEFINE 2 targeted on people with obese or weight problems and sort 2 diabetes. Findings confirmed that CagriSema led to vital and clinically related weight reduction, glycemic enhancements (together with HbA1c and steady glucose monitor metrics), and near-normoglycemic management. Participants additionally confirmed enhancements in cardiovascular danger markers and bodily perform.1
“These are spectacular results,” presenter Louis J. Aronne, MD, FACP, DABOM, stated. “I keep hearing people talk about best in class. This is now right there as best in class.”1
In the Phase 3, multinational, double-blind, randomized STRIDE medical trial, semaglutide (Ozempic, Rybelsus, Wegovy; Novo Nordisk), a glucagon-like peptide-1 receptor agonist, confirmed potential in managing peripheral arterial illness (PAD) amongst people with kind 2 diabetes (T2D).
A complete of 792 people (median age 68 years; 25% feminine) with T2D and PAD presenting with intermittent claudication have been randomly assigned to obtain both semaglutide (n = 396) or placebo (n = 396) over 52 weeks.1,2
The outcomes demonstrated that semaglutide considerably improved strolling outcomes, enhanced high quality of life, and diminished the chance of illness development by 54%. At week 52, the estimated median ratio to baseline in most strolling distance was 1.21 within the semaglutide group vs 1.08 within the placebo group.1,2
Importantly, advantages have been noticed independently of baseline hemoglobin A1C ranges, diabetes length, therapy depth, physique mass index, or concurrent use of sodium-glucose cotransporter-2 (SGLT2) inhibitors.1,2
This web page was created programmatically, to learn the article in its authentic location you may go to the hyperlink bellow:
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This web page was created programmatically, to learn the article in its authentic location you…
This web page was created programmatically, to learn the article in its unique location you…
This web page was created programmatically, to learn the article in its unique location you…
This web page was created programmatically, to learn the article in its authentic location you…
This web page was created programmatically, to learn the article in its unique location you…
This web page was created programmatically, to learn the article in its authentic location you'll…