生产力
2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
业务
2019-20冠状病毒爆发
运营管理
管理
医学
工程类
病毒学
内科学
经济
经济增长
疾病
爆发
传染病(医学专业)
作者
Kathy Fernando,Sandeep Menon,Kathrin U. Jansen,Prakash S. Naik,Gianluca Nucci,John Roberts,Shuang Sarah Wu,Mikael Dolsten
标识
DOI:10.1016/j.drudis.2021.12.010
摘要
Over the past decade, Pfizer has focused efforts to improve its research and development (R&D) productivity. By the end of 2020, Pfizer had achieved an industry-leading clinical success rate of 21%, a tenfold increase from 2% in 2010 and well above the industry benchmark of ∼11%. The company had also maintained the quality of innovation, because 75% of its approvals between 2016 and 2020 had at least one expedited regulatory designation (e.g., Breakthrough Therapy). Pfizer's Signs of Clinical Activity (SOCA) paradigm enabled better decision-making and, along with other drivers (biology and modality), contributed to this productivity improvement. These laid a strong foundation for the rapid and effective development of the Coronavirus 2019 (COVID-19) vaccine with BioNTech, as well as the antiviral candidate Paxlovid™, under the company's 'lightspeed' paradigm.
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