Synthesis and clinical application of new drugs approved by FDA in 2023

被引:26
作者
Wang, Ya-Tao [1 ]
Yang, Peng-Cheng [2 ]
Zhang, Yan-Feng [3 ]
Sun, Jin-Feng [2 ,4 ]
机构
[1] First Peoples Hosp Shangqiu, Dept Hematol, Shangqiu 476100, Henan, Peoples R China
[2] Yanbian Univ, Coll Pharm, Key Lab Nat Med Changbai Mt, Minist Educ, Yanji 133002, Jilin, Peoples R China
[3] Shangqiu Municipal Hosp, Shangqiu 476100, Henan, Peoples R China
[4] Katholieke Univ Leuven, Rega Inst Med Res, Med Chem, Herestr 49-Box 1041, B-3000 Leuven, Belgium
基金
中国国家自然科学基金;
关键词
FDA; NCEs; Synthesis; Clinical applications; 2023; PROLYL HYDROXYLASE INHIBITOR; RECEPTOR ANTAGONISTS; DISCOVERY; EFFICACY; SAFETY; PHARMACODYNAMICS; TOLERABILITY; ABSORPTION; RESISTANCE; GSK1278863;
D O I
10.1016/j.ejmech.2024.116124
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In 2023, the U.S. Food and Drug Administration (FDA) granted approval to a total of 55 new drugs, comprising 29 new chemical entities (NCEs) and 25 new biological entities (NBEs). These drugs primarily focus on oncology, the central nervous system, anti -infection, hematology, cardiovascular, ophthalmology, immunomodulatory and other therapeutic areas. Out of the 55 drugs, 33 (60 %) underwent an accelerated review process and received approval, while 25 (45 %) were specifically approved for the treatment of rare diseases. The purpose of this review is to provide an overview of the clinical uses and production techniques of 29 newly FDA -approved NCEs in 2023. Our intention is to offer a comprehensive understanding of the synthetic approaches employed in the creation of these drug molecules, with the aim of inspiring the development of novel, efficient, and applicable synthetic methodologies.
引用
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页数:24
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