Palm Beach Atlantic University Gregory School of Pharmacy, FL, USA.
Ann Pharmacother. 2022 Apr;56(4):441-462. doi: 10.1177/10600280211031390. Epub 2021 Jul 14.
To review the spectrum of activity, efficacy, safety, and role in therapy of all antibiotics and related biologics approved by the Food and Drug Administration (FDA) in the last decade.
A literature search was performed using PubMed and Google Scholar (2010 to end May 2021) with the search terms' name of the antibiotic or the biologic. Data were also obtained from the prescribing information, FDA, and ClinicalTrials.gov websites.
All relevant English-language, late phase clinical trials assessing the safety and efficacy of the identified drugs were included. Review articles and references of retrieved articles were evaluated for relevant data.
Antibiotic resistance is a public health crisis, and antibiotic development is imperative to outpace the ability of bacteria to develop resistance. Only 17 new systemic antibiotics and 1 related biologic have been approved by the FDA since 2010. Among these drugs, 14 were approved for common bacterial infections, 1 was approved for infection (CDI), 1 was licensed to prevent CDI recurrence, and 2 were approved for drug-resistant tuberculosis. Very few antibiotics are in clinical development.
The arrival of these new antibiotics was welcomed with great enthusiasm, particularly when they met previously unmet medical needs. Unfortunately, the majority of them represent modifications to existing chemical structures rather than new drug classes. Despite the availability of these antibiotics, managing patients with deep-seated infections and those with extensively resistant gram-negative organisms remains challenging.
The number of new antibiotics and their indications are not keeping up with resistance and the needs of the patients.
回顾过去十年内食品和药物管理局(FDA)批准的所有抗生素和相关生物制剂的作用、疗效、安全性及治疗作用。
通过 PubMed 和 Google Scholar(2010 年至 2021 年 5 月)进行文献检索,检索词为抗生素或生物制剂的名称。还从处方信息、FDA 和 ClinicalTrials.gov 网站获取了数据。
纳入所有评估所鉴定药物安全性和疗效的相关英语、后期临床试验的研究。评估了检索到的文章的综述文章和参考文献,以获取相关数据。
抗生素耐药性是公共卫生危机,开发抗生素对于超越细菌产生耐药性的能力至关重要。自 2010 年以来,FDA 仅批准了 17 种新的全身用抗生素和 1 种相关生物制剂。在这些药物中,有 14 种被批准用于常见细菌感染,1 种用于治疗感染(艰难梭菌感染),1 种被许可用于预防艰难梭菌感染复发,2 种被批准用于治疗耐药结核病。处于临床开发阶段的抗生素非常少。
这些新抗生素的问世受到了极大的欢迎,特别是当它们满足了以前未满足的医疗需求时。不幸的是,它们中的大多数是现有化学结构的改良,而不是新的药物类别。尽管有这些抗生素可用,但管理深部感染患者和那些对广泛耐药革兰阴性菌感染的患者仍然具有挑战性。
新抗生素的数量及其适应证与耐药性和患者的需求并不匹配。