Antibiotics in the clinical pipeline as of December 2022

被引:131
作者
Butler, Mark S. [1 ]
Henderson, Ian R. [1 ]
Capon, Robert J. [1 ]
Blaskovich, Mark A. T. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Ctr Superbug Solut, Brisbane 4072, Australia
关键词
IN-VITRO ACTIVITY; URINARY-TRACT-INFECTION; KILL MYCOBACTERIUM-TUBERCULOSIS; HELICAL ANTIMICROBIAL PEPTIDES; BETA-LACTAMASE INHIBITOR; RNA SYNTHETASE INHIBITOR; CLOSTRIDIUM-DIFFICILE; STAPHYLOCOCCUS-AUREUS; ANTIBACTERIAL AGENT; VIVO EFFICACY;
D O I
10.1038/s41429-023-00629-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The need for new antibacterial drugs to treat the increasing global prevalence of drug-resistant bacterial infections has clearly attracted global attention, with a range of existing and upcoming funding, policy, and legislative initiatives designed to revive antibacterial R&D. It is essential to assess whether these programs are having any real-world impact and this review continues our systematic analyses that began in 2011. Direct-acting antibacterials (47), non-traditional small molecule antibacterials (5), and beta-lactam/beta-lactamase inhibitor combinations (10) under clinical development as of December 2022 are described, as are the three antibacterial drugs launched since 2020. Encouragingly, the increased number of early-stage clinical candidates observed in the 2019 review increased in 2022, although the number of first-time drug approvals from 2020 to 2022 was disappointingly low. It will be critical to monitor how many Phase-I and -II candidates move into Phase-III and beyond in the next few years. There was also an enhanced presence of novel antibacterial pharmacophores in early-stage trials, and at least 18 of the 26 phase-I candidates were targeted to treat Gram-negative bacteria infections. Despite the promising early-stage antibacterial pipeline, it is essential to maintain funding for antibacterial R&D and to ensure that plans to address late-stage pipeline issues succeed.
引用
收藏
页码:431 / 473
页数:43
相关论文
共 398 条
[1]   In Vitro and In Vivo Activity of Gepotidacin against Drug-Resistant Mycobacterial Infections [J].
Ahmad, Mohammad Naiyaz ;
Garg, Tanu ;
Singh, Shriya ;
Shukla, Richa ;
Malik, Pradip ;
Krishnamurthy, Ramya V. ;
Kaur, Parvinder ;
Chopra, Sidharth ;
Dasgupta, Arunava .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2022, 66 (12)
[2]   Susceptibility of Clinical Mycobacterium tuberculosis Isolates to a Potentially Less Toxic Derivate of Linezolid, PNU-100480 [J].
Alffenaar, J. W. C. ;
van der Laan, T. ;
Simons, S. ;
van der Werf, T. S. ;
van de Kasteele, P. J. ;
de Neeling, H. ;
van Soolingen, D. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (03) :1287-1289
[3]   Role of Bismuth in the Eradication of Helicobacter pylori [J].
Alkim, Huseyin ;
Koksal, Ali Riza ;
Boga, Salih ;
Sen, Ilker ;
Alkim, Canan .
AMERICAN JOURNAL OF THERAPEUTICS, 2017, 24 (06) :e751-e757
[4]   Innovation in Antimicrobial Resistance: The CARB-X Perspective [J].
Alm, Richard A. ;
Gallant, Karen .
ACS INFECTIOUS DISEASES, 2020, 6 (06) :1317-1322
[5]   Comparative Efficacy of the Novel Diarylquinoline TBAJ-876 and Bedaquiline against a Resistant Rv0678 Mutant in a Mouse Model of Tuberculosis [J].
Almeida, Deepak ;
Converse, Paul J. ;
Li, Si-Yang ;
Upton, Anna M. ;
Fotouhi, Nader ;
Nuermberger, Eric L. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2021, 65 (12)
[6]   INCATE: a partnership to boost the antibiotic pipeline [J].
Alt, Silke ;
Haggstrom, Douglas ;
Kessmann, Helmut ;
Kloss, Florian ;
Schneider, Christian Elias ;
Jaeger, Timo ;
Schwede, Torsten ;
Brakhage, Axel ;
Dehio, Christoph .
NATURE REVIEWS DRUG DISCOVERY, 2022, 21 (09) :621-622
[7]  
amazonaws, SPERO THERAPEUTICS A
[8]   A Peptidomimetic Antibiotic Interacts with the Periplasmic Domain of LptD from Pseudomonas aeruginosa [J].
Andolina, Gloria ;
Bencze, Laszlo-Csaba ;
Zerbe, Katja ;
Mueller, Maik ;
Steinmann, Jessica ;
Kocherla, Harsha ;
Mondal, Milon ;
Sobek, Jens ;
Moehle, Kerstin ;
Malojcic, Goran ;
Wollscheid, Bernd ;
Robinson, John A. .
ACS CHEMICAL BIOLOGY, 2018, 13 (03) :666-675
[9]   C difficile-a rose by any other name... [J].
不详 .
LANCET INFECTIOUS DISEASES, 2019, 19 (05) :449-449
[10]  
[Anonymous], DEINOVE ANNOUNCES OP