Department of Pharmacology, Faculty of Pharmacy, Ankara University, Ankara, Turkey.
Department of Pharmacology, Faculty of Pharmacy, Izmir Katip Celebi University, Izmir, Turkey.
Naunyn Schmiedebergs Arch Pharmacol. 2023 Aug;396(8):1619-1632. doi: 10.1007/s00210-023-02465-x. Epub 2023 Mar 23.
While new drug approvals by the U.S. Food and Drug Administration (FDA) had remained stable or even increased in the first 2 years of the COVID-19 pandemic, the 37 newly approved drugs in 2022 are considerably less than the 53 and 50 new drugs approved in 2020 and 2021, respectively, and less than the rolling 10-year average of 43. As in previous years of this annual review, we assign these new drugs to one of three levels of innovation: first drug against a condition ("first-in-indication"), first drug using a novel molecular mechanism ("first-in-class"), and "next-in-class," i.e., a drug using an already exploited molecular mechanism. We identify two "first-in-indication" (ganaxolon and teplizumab), 20 (54%) "first-in-class," and 17 (46%) "next-in-class" drugs. By treatment area, rare diseases and cancer drugs were once again the most prevalent (partly overlapping) therapeutic areas. Other continuing trends were the use of accelerated regulatory approval pathways and the reliance on biopharmaceuticals (biologics).
尽管美国食品和药物管理局 (FDA) 在 COVID-19 大流行的头 2 年新药批准数量保持稳定甚至有所增加,但 2022 年新批准的 37 种药物明显少于 2020 年和 2021 年分别批准的 53 种和 50 种新药,也少于滚动 10 年平均每年批准的 43 种。与本年度审查的前几年一样,我们将这些新药分为三个创新水平之一:针对某种疾病的第一种药物(“适应证首创”)、使用新分子机制的第一种药物(“同类首创”)和“同类中下一梯队”,即使用已开发分子机制的药物。我们确定了两种“适应证首创”(加那洛隆和替普利珠单抗)、20 种(54%)“同类首创”和 17 种(46%)“同类中下一梯队”药物。按治疗领域划分,罕见病和癌症药物再次成为最常见(部分重叠)的治疗领域。其他持续的趋势包括加速监管审批途径的使用和对生物制药(生物制剂)的依赖。