A year in pharmacology: new drugs approved by the US Food and Drug Administration in 2021

被引:13
|
作者
Kayki-Mutlu, Gizem [1 ]
Aksoyalp, Zinnet Sevval [2 ]
Wojnowski, Leszek [3 ]
Michel, Martin C. [3 ]
机构
[1] Ankara Univ, Dept Pharmacol, Fac Pharm, Ankara, Turkey
[2] Izmir Katip Celebi Univ, Dept Pharmacol, Fac Pharm, Izmir, Turkey
[3] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Pharmacol, Langenbeckstr 1, D-55118 Mainz, Germany
关键词
FDA; New drugs; First-in-indication; First-in-class; Next-in-class; CABOTEGRAVIR PLUS RILPIVIRINE; PREVIOUSLY TREATED RECURRENT; VILOXAZINE EXTENDED-RELEASE; PLACEBO-CONTROLLED TRIAL; RENAL-CELL CARCINOMA; PARALLEL-GROUP TRIAL; DOUBLE-BLIND; OPEN-LABEL; AMIVANTAMAB JNJ-61186372; MELPHALAN FLUFENAMIDE;
D O I
10.1007/s00210-022-02250-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The second year of the COVID-19 pandemic had no adverse effect on the number of new drug approvals by the US Food and Drug Administration (FDA). Quite the contrary, with a total of 50 new drugs, 2021 belongs to the most successful FDA years. We assign these new drugs to one of three levels of innovation: (1) first drug against a condition ("first-in-indication"), (2) first drug using a novel molecular mechanism ("first-in-class"), and (3) "next-in-class", i.e., a drug using an already exploited molecular mechanism. We identify 21 first-in-class, 28 next-in-class, and only one first-in-indication drugs. By treatment area, the largest group is once again cancer drugs, many of which target specific genetic alterations. Every second drug approved in 2021 targets an orphan disease, half of them being cancers. Small molecules continue to dominate new drug approvals, followed by antibodies and non-antibody biopharmaceuticals. In 2021, the FDA continued to approve drugs without strong evidence of clinical effects, best exemplified by the aducanumab controversy.
引用
收藏
页码:867 / 885
页数:19
相关论文
共 50 条
  • [32] RE: Magnitude of Clinical Benefit of Cancer Drugs Approved by the US Food and Drug Administration Response
    Pierce, John P.
    Leas, Eric C.
    Benmarhnia, Tarik
    Strong, David R.
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2018, 110 (10)
  • [33] Communication of Survival Data in US Food and Drug Administration-Approved Labeling of Cancer Drugs
    Naci, Huseyin
    Guan, Xiaodong
    Woloshin, Steven
    Xu, Ziyue
    Wagner, Anita K.
    [J]. JAMA INTERNAL MEDICINE, 2021, 181 (11) : 1521 - 1522
  • [34] Ultimate Fate of Oncology Drugs Approved by the US Food and Drug Administration Without a Randomized Trial
    Tsimberidou, Apostolia-Maria
    Braiteh, Fadi
    Stewart, David J.
    Kurzrock, Razelle
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) : 6243 - 6250
  • [36] Missing Companion Diagnostic for US Food and Drug Administration-Approved Hematological and Oncological Drugs
    Jorgensen, Jan Trost
    [J]. JCO PRECISION ONCOLOGY, 2022, 6
  • [37] Application of physiologically based pharmacokinetic modeling of novel drugs approved by the US food and drug administration
    Sun, Zexu
    Zhao, Nan
    Zhao, Xia
    Wang, Ziyang
    Liu, Zhaoqian
    Cui, Yimin
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2024, 200
  • [38] Innovation in Development of Dermatologic Drugs Approved by the US Food and Drug Administration Between 2012 and 2022
    Kamat, Samir
    Ungar, Benjamin
    Agarwal, Aneesh
    Wan, Joy
    Ross, Joseph S.
    Gupta, Ravi
    [J]. JAMA DERMATOLOGY, 2024, 160 (02) : 226 - 229
  • [39] NON-APPROVED USE OF FOOD-AND-DRUG-ADMINISTRATION APPROVED DRUGS
    MINDEL, JS
    GOLDSTEIN, JI
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1979, 88 (03) : 626 - 628
  • [40] Integrating New Effectiveness Data Into US Food and Drug Administration-Approved Drug Labeling
    Gyawali, Bishal
    Darrow, Jonathan J.
    Kesselheim, Aaron S.
    [J]. JAMA INTERNAL MEDICINE, 2021, 181 (07) : 897 - 898