美国食品和药物管理局将在2022年批准生物制品
Alexander C Martins1, Fernando Albericio2,3, Beatriz G de la Torre4
1School of Health Sciences, UAM, Universidade Anhembi-Morumbi, São Paulo 03101-001, Brazil.
Biomedicines
|May 27, 2023
概括
2022年,美国食品和药物管理局 (FDA) 的生物批准仍然强,单克隆抗体领先于新药授权,主要用于癌症和自身免疫性疾病.
科学领域:
- 生物制药的发展.
- 药物监管事务 药物监管事务
- 瘤学和免疫学治疗药物治疗学
背景情况:
- 在2022年控制COVID-19大流行并没有阻碍生物药物开发.
- 美国食品和药物管理局 (FDA) 看到药物批准总体下降,主要是小分子.
- 生物批准保持稳定,有15种新分子获得批准.
研究的目的:
- 分析2022年FDA授权的生物制剂.
- 为了比较新批准的生物药物的疗效与前几年的疗效.
- 检查生物药物开发的趋势,包括孤儿药物和特定的治疗领域.
主要方法:
- 在2022年对FDA批准的生物制品进行定量分析.
- 根据化学结构对生物制剂进行分类 (单克隆抗体,抗体-药物联合体,蛋白质/酶).
- 对2022年生物制剂与历史数据进行比较的疗效评估.
主要成果:
- 单克隆抗体 (mAbs) 在生物批准中占主导地位.
- 癌症和自身免疫性疾病是新生物制剂的主要目标.
- 观察到两种特定生物的批准 (四) 显著增加.
- 2022年没有批准任何抗微生物生物药物.
结论:
- 生物药物批准在2022年仍然强,主要是由单克隆抗体推动.
- 针对癌症和自身免疫性疾病的趋势继续下去.
- 双特异生物制剂的增加意味着一种不断进步的治疗策略.
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