Brown Dean G, Wobst Heike J
Jnana Therapeutics, 6 Tide St., Boston, Massachusetts 02210, United States.
J Med Chem. 2021 Mar 11;64(5):2312-2338. doi: 10.1021/acs.jmedchem.0c01516. Epub 2021 Feb 22.
A total of 378 novel drugs and 27 biosimilars approved by the U.S. Food and Drug Administration (FDA) between 2010 and 2019 were evaluated according to approval numbers by year, therapeutic areas, modalities, route of administration, first-in-class designation, approval times, and expedited review categories. From this review, oncology remains the top therapy area (25%), followed by infection (15%) and central nervous system disorders (11%). Regulatory incentives have been effective as evidenced by an increase in orphan drugs as well as antibacterial drugs approved under the GAIN act. Clinical development times may be increasing, perhaps as a result of the increase in orphan drug indications. Small molecules continue to mostly adhere to "Rule of 5" (Ro5) parameters, but innovation in new modalities is rapidly progressing with approvals for antisense oligonucleotides (ASO), small-interfering RNA (siRNAs), and antibody-directed conjugates (ADCs). Finally, novel targets and scientific breakthroughs that address areas of unmet clinical need are discussed in detail.
对2010年至2019年间美国食品药品监督管理局(FDA)批准的378种新型药物和27种生物类似药,按照年度批准数量、治疗领域、剂型、给药途径、同类首创药物指定、批准时间和加速审评类别进行了评估。通过此次审评发现,肿瘤学仍然是首要治疗领域(25%),其次是感染(15%)和中枢神经系统疾病(11%)。孤儿药以及根据《食品药品监管局安全与创新法案》(GAIN)批准的抗菌药物数量增加,证明了监管激励措施是有效的。临床研发时间可能在增加,这或许是孤儿药适应症增加的结果。小分子药物大多仍遵循“五规则”(Ro5)参数,但新剂型的创新正在迅速推进,反义寡核苷酸(ASO)、小干扰RNA(siRNA)和抗体偶联药物(ADC)已获批准。最后,详细讨论了针对未满足临床需求领域的新靶点和科学突破。