...
首页> 外文期刊>Journal of Medicinal Chemistry >A Decade of FDA-Approved Drugs (2010-2019): Trends and Future Directions
【24h】

A Decade of FDA-Approved Drugs (2010-2019): Trends and Future Directions

机译:十年的FDA批准的药物(2010-2019):趋势和未来的方向

获取原文
获取原文并翻译 | 示例

摘要

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.
机译:2010年至2019年间,美国食品和药物管理局(FDA)共批准了378种新药和27种生物仿制药,根据批准编号、治疗领域、模式、给药途径、一流名称、批准时间和快速审查类别进行了评估。从这篇综述来看,肿瘤学仍然是最主要的治疗领域(25%),其次是感染(15%)和中枢神经系统疾病(11%)。监管激励措施是有效的,孤儿药以及根据《增益法案》批准的抗菌药物的增加就证明了这一点。临床开发时间可能会增加,这可能是孤儿药物适应症增加的结果。小分子仍然主要遵循“5法则”(Ro5)参数,但随着反义寡核苷酸(ASO)、小干扰RNA(siRNA)和抗体导向结合物(ADC)的批准,新模式的创新正在迅速进展。最后,详细讨论了解决未满足临床需求领域的新目标和科学突破。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号