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Tivozanib: First Global Approval

机译:Tivozanib:第一个全球批准

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摘要

Abstract Tivozanib (Fotivda ? ) is an oral, potent and highly selective vascular endothelial growth factor receptor (VEGFR) inhibitor that has been approved in the EU, Iceland and Norway for the first-line treatment of adult patients with advanced renal cell carcinoma (RCC) and for adult patients who are VEGFR and mammalian target of rapamycin (mTOR) pathway inhibitor-naive following disease progression after one prior treatment with cytokine therapy for advanced RCC. Tivozanib is at various stages of development in other countries for advanced RCC and advanced solid tumours. This article summarizes the milestones in the development of tivozanib leading to this first global approval in Europe for the treatment of adults with advanced RCC.
机译:摘要Tivozanib(Fotivda?)是口服,有效和高度选择性的血管内皮生长因子受体(VEGFR)抑制剂,在欧盟,冰岛和挪威批准,用于成年肾细胞癌的成人患者的一线治疗(RCC )对于VEGFR和哺乳动物的成年患者,雷帕霉素(MTOR)途径抑制剂抑制剂 - 野生疾病的抑制剂在一次性治疗后的疾病进展后,细胞因子治疗晚期RCC治疗。 Tivozanib是在其他国家的各种发展阶段,用于高级RCC和先进的实体肿瘤。 本文总结了富氮尼的发展中的里程碑,从而导致欧洲第一个全球批准,以治疗具有先进的RCC成人。

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