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6-K: European Regulatory Authority Adopts a Positive Opinion for an Update of the Wegovy® Label to Reflect Risk Reduction of Major Adverse Cardiovascular Events

6-K: European Regulatory Authority Adopts a Positive Opinion for an Update of the Wegovy® Label to Reflect Risk Reduction of Major Adverse Cardiovascular Events

6-K:欧洲监管机构对更新Wegovy® 标签以反映重大心血管不良事件风险降低情况的积极看法
美股sec公告 ·  07/25 11:48
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On July 25, 2024, Novo Nordisk A/S announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has endorsed a positive opinion for updating the label of its medication Wegovy (semaglutide 2.4 mg). This update reflects the results from the SELECT cardiovascular outcomes trial, which showed a 20% reduction in major adverse cardiovascular events (MACE) for adults with established cardiovascular disease (CVD) and obesity or overweight without diabetes. The trial, which enrolled 17,604 adults across 41 countries, also indicated reductions in cardiovascular death by 15%, death from any cause by 19%, and an 18% reduction in a heart failure composite endpoint. Despite these findings, the superiority in cardiovascular death and the composite heart failure endpoint were not statistically significant based on the prespecified...Show More
On July 25, 2024, Novo Nordisk A/S announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has endorsed a positive opinion for updating the label of its medication Wegovy (semaglutide 2.4 mg). This update reflects the results from the SELECT cardiovascular outcomes trial, which showed a 20% reduction in major adverse cardiovascular events (MACE) for adults with established cardiovascular disease (CVD) and obesity or overweight without diabetes. The trial, which enrolled 17,604 adults across 41 countries, also indicated reductions in cardiovascular death by 15%, death from any cause by 19%, and an 18% reduction in a heart failure composite endpoint. Despite these findings, the superiority in cardiovascular death and the composite heart failure endpoint were not statistically significant based on the prespecified testing hierarchy. Novo Nordisk expects the label update to be implemented within approximately one month following the CHMP's positive opinion. Wegovy is currently indicated for weight management in adults with obesity or overweight in the EU and the US, with additional indications for reducing the risk of MACE in adults with established CVD in the US.
2024年7月25日,诺和诺德公司宣布,欧洲药品管理局人用药品委员会(CHMP)已对其药物Wegovy(2.4毫克盐酸塞格列酮)的标签更新做出积极意见。此次更新反映了来源于SELECt心血管结局试验的结果,该试验显示成人在存在心血管疾病(CVD)和肥胖或超重但没有糖尿病的情况下,主要不良心血管事件(MACE)发生率降低了20%。该试验在41个国家招募了17604名成人,还表明心血管死亡率降低了15%,全因死亡率降低了19%,心衰复合终点降低了18%。尽管发现如此,心血管死亡率和复合心力衰竭终点并非在预先规定的测试层次上具有统计学显著性。诺和诺德公司预计在CHMP的积极意见后约一个月内实施标签更新。Wegovy目前在欧美地区仅适用于治疗肥胖或超重成人及在美国降低已确诊CVD成人的MACE风险。
2024年7月25日,诺和诺德公司宣布,欧洲药品管理局人用药品委员会(CHMP)已对其药物Wegovy(2.4毫克盐酸塞格列酮)的标签更新做出积极意见。此次更新反映了来源于SELECt心血管结局试验的结果,该试验显示成人在存在心血管疾病(CVD)和肥胖或超重但没有糖尿病的情况下,主要不良心血管事件(MACE)发生率降低了20%。该试验在41个国家招募了17604名成人,还表明心血管死亡率降低了15%,全因死亡率降低了19%,心衰复合终点降低了18%。尽管发现如此,心血管死亡率和复合心力衰竭终点并非在预先规定的测试层次上具有统计学显著性。诺和诺德公司预计在CHMP的积极意见后约一个月内实施标签更新。Wegovy目前在欧美地区仅适用于治疗肥胖或超重成人及在美国降低已确诊CVD成人的MACE风险。
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