Han-Bo Seng, Yi-Ru Bai, Dan-Dan Shen, Chun-Li Wang, Yan-Xia Xu, Hong Zhang, Ying Xu, Hong-Min Liu, Dong-Jie Seng
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引用次数: 0
Abstract
In 2025, the U.S. FDA approved 46 new drug applications, including 34 new molecular entities and 12 biologics license applications. The new molecular entities include 31 small-molecule drugs and 3 oligonucleotides, while the biological license applications cover monoclonal antibodies, bispecific antibodies, antibody-drug conjugates, and fusion proteins. These newly approved molecules not only feature favorable skeletal structures but also embody the comprehensive achievements of multiple fields, including modern drug discovery, drug synthesis, and the study of pathogenesis. In this review, we comprehensively summarize the clinical indications, mechanisms of action, and synthetic routes of the 31 newly approved small-molecule drugs in 2025, providing a reference for follow‑up drug‑discovery practice.
期刊介绍:
Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.