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Drugs. 2019 Apr;79(5):563-572. doi: 10.1007/s40265-019-01077-1.
Roxadustat (Ai Rui Zhuo in China) is an orally administered, small molecule hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor that is being developed by FibroGen, in collaboration with Astellas and AstraZeneca, for the treatment of anaemia in patients with dialysis-dependent chronic kidney disease (CKD), non-dialysis-dependent CKD and in patients with myelodysplastic syndromes. The drug reversibly binds to and inhibits HIF-prolyl hydroxylase enzymes that are responsible for the degradation of transcription factors in the HIF family under normal oxygen conditions. Inhibition of these enzymes reduces HIF breakdown and promotes HIF activity, leading to an increase in endogenous erythropoietin production, thereby enhancing erythropoiesis. It also reduces the expression of the peptide hormone hepcidin, improves iron availability and increases haemoglobin levels. HIF regulates the expression of genes in response to reduced oxygen levels, including genes required for erythropoiesis and iron metabolism. Roxadustat is approved in China and is under regulatory review in Japan for the treatment of anaemia in patients with dialysis-dependent CKD. Studies are underway to investigate long-term cardiovascular outcomes with roxadustat versus placebo (for non-dialysis-dependent CKD) or standard of care (for dialysis-dependent CKD). This article summarizes the milestones in the development of roxadustat leading to this first approval.
罗沙司他(在中国称为爱瑞卓)是一种口服小分子低氧诱导因子(HIF)脯氨酰羟化酶抑制剂,由 FibroGen 公司与安斯泰来和阿斯利康合作开发,用于治疗透析依赖性慢性肾病(CKD)、非透析依赖性 CKD 和骨髓增生异常综合征患者的贫血。该药物可逆地与 HIF-脯氨酰羟化酶结合并抑制其活性,这些酶在正常氧条件下负责 HIF 家族转录因子的降解。抑制这些酶可减少 HIF 的降解并促进 HIF 活性,从而增加内源性促红细胞生成素的产生,从而增强红细胞生成。它还降低肽激素铁调素的表达,改善铁的可用性并增加血红蛋白水平。HIF 可调节基因表达以应对低氧水平,包括红细胞生成和铁代谢所需的基因。罗沙司他已在中国获得批准,在日本正在接受监管审查,用于治疗透析依赖性 CKD 患者的贫血。正在进行研究以调查罗沙司他与安慰剂(用于非透析依赖性 CKD)或标准治疗(用于透析依赖性 CKD)相比的长期心血管结局。本文总结了导致首次批准的罗沙司他开发过程中的里程碑事件。