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2021 年的批准情况:悬而未决的加速批准、药物剂量、新批准及未来展望

英文原题:Approvals in 2021: dangling Accelerated Approvals, drug dosing, new approvals and beyond.

查看英文原题

Approvals in 2021: dangling Accelerated Approvals, drug dosing, new approvals and beyond.

PubMed 2022/04/01(内容时间) Nat Rev Clin Oncol Q1 · IF 94.6(JCR 2025)

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中文摘要

2021年,FDA肿瘤学关注的政策领域包括加速批准计划、扩大资格标准、剂量优化和患者报告结局。FDA继续积极批准新药和补充申请,包括三种新的CAR-T 细胞产品、两种抗体-药物偶联物和几种新的靶向药物。

展开英文摘要原文

In 2021, policy areas of focus for FDA Oncology included the Accelerated Approval programme, expanding eligibility criteria, dose optimization and patient-reported outcomes. The FDA continued to be active with approvals of both new drugs and supplementary applications, including three new chimeric antigen receptor T cell products, two antibody–drug conjugates and several new targeted agents.

论文信息

作者
Lemery S、Pazdur R
单位
Office of Oncologic Diseases, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA. Steven.Lemery@fda.hhs.gov.United States
期刊
Nature reviews. Clinical oncology2022 Apr
原文标识
PubMed 35136230 · DOI 10.1038/s41571-022-00605-5