FDA批准安进/优时比的抗骨质疏松新药Evenity上市

2019-01-26 MedSci MedSci原创

FDA专家组近日通过投票,批准安进Amgen和优时比UCB联合开发的骨质疏松新药Evenity上市。

FDA专家组近日通过投票,批准安进Amgen和优时比UCB联合开发的骨质疏松新药Evenity上市。

在美国,50%的50岁以上的女性会出现骨质疏松性骨折,但只有20%的骨折女性在第一年就会接受骨质疏松症治疗。

Evenity是一种抗硬化蛋白抗体,从而同时加速骨形成并减少骨吸收。骨硬化蛋白又名硬骨素,是一种分泌性糖蛋白。体内研究证明,骨硬化蛋白特异性地表达于骨细胞(osteocyte)中,并抑制成骨细胞的骨形成。通过拮抗骨硬化蛋白可以缓解骨质疏松的症状。

在ARCH试验中,与现有的骨质疏松药物阿仑膦酸盐相比,Evenity显示出更强的药效,椎骨和非椎骨骨折均减少。但血管副作用的风险要高得多。

Amgen已经在本月早些时候在日本获得了Evenity(romosozumab)的上市批准。Jefferies的分析师最近预测,如果在美国获得批准,该药物每年的销售额能达到5亿美元。

Amgen研发部执行副总裁David Reese提到:"在骨质疏松性骨折后,女性在第一年内再次发生骨折的可能性增加了五倍。如果不治疗,骨折风险会随着时间的推移而持续升高。"

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    2019-07-23 jiyangfei
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    2019-01-28 Eleven17

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