An Important Dose-response study for tirzepatide, a novel dual (GIP and GLP-1) Agonist (https://doi.org/10.1111/dom.13979)

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Abstract

There is considerable interest and anticipation in the metabolic profile of novel dual agonists currently in clinical development, especially Lilly's tirzepatide which is administered once weekly by subcutaneous injection. Dual agonists may be clinically useful both as anti-obesity and glucose-lowering agents. This phase II study of tirzepatide was conducted over 12-weeks in >100 patients with type 2 diabetes to evaluate different dose-escalation regimens using a placebo-controlled randomised design. The primary endpoint of the trial was HbA1c lowering after once-weekly tirzepatide vs placebo. Baseline HbA1c and BMI were 8.4% and 31.9, respectively. The authors report clinically significant HbA1c reductions with tirzepatide, and found that a lower starting dose, combined with smaller dose increments, resulted in better tolerability.

新型双(GIP和GLP-1)激动剂替西帕肽的重要剂量反应研究(https://doi.org/10.1111/dom.13979)
人们对目前正在临床开发的新型双激动剂的代谢谱有相当大的兴趣和预期,尤其是礼来的替西帕肽,它每周皮下注射一次。双重激动剂可能在临床上既可用作抗肥胖剂又可用作降血糖剂。该替西帕肽的II期研究在>;100名2型糖尿病患者使用安慰剂对照随机设计评估不同的剂量递增方案。试验的主要终点是与安慰剂相比,每周一次替西帕肽后HbA1c降低。基线HbA1c和BMI分别为8.4%和31.9。作者报告了替西帕肽在临床上显著降低HbA1c的情况,并发现较低的起始剂量加上较小的剂量增量,可产生更好的耐受性。
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