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从快速开发的 mRNA COVID-19 疫苗中获得的肿瘤学临床试验的见解。

Insights for Oncology Trials Garnered From the Rapid Development of an mRNA COVID-19 Vaccine.

机构信息

From Moderna, Inc., Cambridge, MA.

出版信息

Cancer J. 2022;28(2):146-150. doi: 10.1097/PPO.0000000000000587.

Abstract

The sudden emergence of the coronavirus disease 2019 (COVID-19) pandemic in early 2020 stimulated unprecedented scientific initiatives to rapidly develop effective treatments and vaccines. One example was the development of vaccines based on messenger RNA platforms, which received emergency use authorization in the United States less than 1 year after the primary sequence of the severe acute respiratory syndrome coronavirus 2 virus was published. Novel practices arose from the collaborative efforts and inclusive clinical studies that facilitated the vaccines' rapid development and clinical testing. I describe insights gained from the experience of mRNA-1273 vaccine development that may be applied to or adapted for oncology research. These insights include clinical study design, diversity and inclusion initiatives, speed, and real-world evidence generation, as well as close partnership among regulatory agencies, government, and pharmaceutical companies.

摘要

2020 年初,2019 冠状病毒病(COVID-19)大流行的突然出现刺激了前所未有的科学举措,以迅速开发有效的治疗方法和疫苗。其中一个例子是基于信使 RNA 平台的疫苗的开发,该疫苗在严重急性呼吸综合征冠状病毒 2 病毒的主要序列发表不到 1 年后,就在美国获得了紧急使用授权。新的实践源于协作努力和包容性临床研究,这促进了疫苗的快速开发和临床测试。我描述了从 mRNA-1273 疫苗开发经验中获得的见解,这些见解可能适用于或适用于肿瘤学研究。这些见解包括临床研究设计、多样性和包容性举措、速度和真实世界证据的产生,以及监管机构、政府和制药公司之间的密切合作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0613/9158734/b983a5c97c60/ppo-28-146-g001.jpg

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