Eli Lilly's Zepbound/Mounjaro Shows Cardiovascular Benefits In Patients With Obesity-Related Heart Failure
Eli Lilly's Zepbound/Mounjaro Shows Cardiovascular Benefits In Patients With Obesity-Related Heart Failure
On Saturday, Eli Lilly And Co (NYSE:LLY) released detailed results from the SUMMIT Phase 3 trial showing tirzepatide reduced the risk of worsening heart failure events in adults with heart failure with preserved ejection fraction (HFpEF) and obesity.
禮來(NYSE:LLY)在週六公佈了SUMMIt第3期試驗的詳細結果,顯示替雷帕肽降低了攜帶保留射血分數(HFpEF)和肥胖成人患者惡化心力衰竭事件的風險。
The 731-patient SUMMIT study showed that patients treated with tirzepatide also experienced improvements in heart failure symptoms and physical limitations.
731名患者參與的SUMMIt研究表明,接受替雷帕肽治療的患者心力衰竭症狀和體力限制也有所改善。
Also Read: 99% Of Mounjaro/Zepbound Patients Remained Diabetes-Free Even At 3 Years, Eli Lilly's Detailed Phase 3 Data Shows
還閱讀:替雷帕肽3期數據顯示,Mounjaro/Zepbound患者99%在3年後仍保持無糖尿病狀態,詳細數據顯示。
The FDA approved tirzepatide as Mounjaro for adults with type 2 diabetes to improve glycemic control in May 2022 and Zepbound for adults with obesity or those who are overweight who also have at least one weight-related medical problem in November 2023.
FDA已於2022年5月批准Mounjaro作爲替雷帕肽,用於改善2型糖尿病成年患者的血糖控制;2023年11月批准Zepbound用於肥胖或超重患者中至少存在一種與體重相關的醫療問題的成年人。
The results from the SUMMIT trial of tirzepatide in obese patients with heart failure with preserved ejection fraction (HFpEF) showed that Lilly's drug cut the risk of cardiovascular mortality and worsening heart failure events by 38% over a median follow-up of roughly two years.
替雷帕肽在HFpEF患者的SUMMIt試驗結果顯示,禮來的藥物在大約兩年的中位隨訪期間降低了心衰心力衰竭事件的風險和心血管死亡率,降幅達38%。
After a median follow-up of two years and a maximum of three years, cardiovascular death or worsening heart failure events occurred in 9.9% of the tirzepatide group and 15.3% of those taking a placebo.
在兩年的中位隨訪期和最長三年的隨訪期後,心血管死亡或心力衰竭惡化事件發生在替雷帕肽組的9.9%,而安慰劑組的發生率爲15.3%。
Assessing individual endpoints, worsening heart-failure events occurred in 8% of tirzepatide participants and 14.2% of placebo participants, for an HR of 0.54 (95% CI, 0.34-0.85), whereas adjudicated cardiovascular deaths occurred in 2.2% and 1.4% of tirzepatide and placebo participants, respectively.
評估各個終點,替雷帕肽參與者的心力衰竭惡化事件發生率爲8%,安慰劑參與者爲14.2%,相應風險比爲0.54(95% CI爲0.34-0.85)。而心血管死亡發生率分別爲替雷帕肽組的2.2%和安慰劑組的1.4%。
The risk of hospitalization for heart failure was reduced by 56%.
心力衰竭住院風險減少了56%。
In addition, patients taking tirzepatide saw a nearly 25-point improvement in the Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CSS), which measures symptoms and physical limitations associated with heart failure, compared to a 15-point improvement for the placebo group.
此外,接受tirzepatide治療的患者在堪薩斯市心肌病問卷臨床總結評分(KCCQ-CSS,衡量與心力衰竭相關的症狀和身體限制)上看到了近25分的改善,而安慰劑組只有15分的改善。
All key secondary endpoints were also met, with patients treated with tirzepatide demonstrating improved exercise capacity, walking approximately 30 meters farther in six minutes than those on placebo (38.2 meters vs. 7.9 meters).
所有主要的次要終點也都滿足了,接受tirzepatide治療的患者表現出改善的運動能力,在六分鐘內走的距離比安慰劑組要更遠(38.2米對7.9米)。
Additionally, patients treated with tirzepatide saw an average reduction in body weight of 15.7%, compared to 2.2% in the placebo group.
此外,接受tirzepatide治療的患者平均減輕體重15.7%,而安慰劑組僅減輕了2.2%。
Tirzepatide also significantly decreased high-sensitivity C-reactive protein, a key marker of systemic inflammation, by 43.4%, while the placebo group saw a 3.5% decrease.
tirzepatide還顯著降低了高敏C-反應蛋白,這是系統性炎症的一個關鍵標誌,降幅爲43.4%,而安慰劑組降幅爲3.5%。
Lilly said it has already started submitting the SUMMIT data to the FDA and European Medicines Agency regulators for HFpEF and obesity, seeking to extend the labeling for tirzepatide.
禮來表示已開始向FDA和歐洲藥品管理局監管機構提交SUMMIt數據,以尋求擴大tirzepatide的標籤,用於心力衰竭伴隨心衰和肥胖。
Price Action: LLY stock is down 2.54% at $727.27 at last check Monday.
股價表現:LLY股票在週一最後一次檢查時下跌了2.54%,報727.27美元。
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譯文內容由第三人軟體翻譯。