Synthesis and Clinical Application of Small‐Molecule Drugs Approved by FDA in 2025

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Authors: Liang Chang, Min Wang, Huijie Zhang, Zhen Li, Zixuan Song, Lijie Zhao, Fengli Jiang, Yi-Xiang Wang, Quan Yuan
Cited by: 1
References: 86

Abstract

In 2025, the U.S. Food and Drug Administration (FDA) continued to advance therapeutic innovation by approving a diverse range of novel drugs. According to the FDA's 2025 Novel Drug Approvals list, 46 new drugs received approval, including both new chemical entities such as Ziftomenib, Sevabertinib, Zoliflodacin, and Gepotidacin, as well as new biologics. These approvals cover a wide range of therapeutic areas, including oncology, rare genetic diseases, infectious diseases, cardiovascular diseases, and immunomodulation. A significant proportion of the approved products navigated accelerated or priority review pathways, reflecting their potential impact on unmet medical needs. This review provides a comprehensive overview of the synthetic routes and clinical applications of FDA-approved small-molecule drugs in 2025, aiming to inspire future development in drug discovery.

Fields of Study & Subjects

Chemical Reactions and Isotopes Protein Degradation and Inhibitors Biochemical and Molecular Research

Publication details

Journal / source
Medicinal Research Reviews
Publisher
Wiley
Volume
46
Issue
6
Pages
1543-1573
Publication date
25 May 2026
Language
EN