Pfizerhas reportedly submitted an application to the Drugs Controller General of India (DCGI) for an emergency use authorisation (EUA) for its Covid-19 vaccine in India. Pfizer is the first company to seek approval from India’s drug regulator, CNN-News18 reported. NDTV quoted VK Paul, who ...
原文出处:Pfizer and BioNTech Receive First U.S. FDA Emergency Use Authorization of a COVID-19 Vaccine in Children Ages 5 Through 11 Years
同时,该疫苗还被授予EUA,作为单剂加强针:(1)用于已完成2针免疫程序的18岁及以上人群;(2)用于已完成另一种不同COVID-19疫苗免疫程序的18岁及以上人群。 原文出处:Pfizer and BioNTech Receive Expanded U.S. FDA Emergency Use Au...
Pfizer-BioNTech COVID-19 vaccine is used to protect you against coronavirus disease, also known as COVID-19. The vaccine may prevent the illness, or reduce the seriousness of it.Vaccines may not fully protect everyone who receives them. How to use Pfizer-Biont COVID-19 Tris (12Y Up) Vac...
The U.S. is prepared to send out 3.5 million doses of Johnson & Johnson’s COVID-19 vaccine as early as next week should the FDA grant emergency use authorization on Friday.
参考资料: [1] Pfizer and BioNTech Conclude Phase 3 Study of COVID-19 Vaccine Candidate, Meeting All Primary Efficacy Endpoints. Retrieved 2020-11-18, from https://www.businesswire.com/news/home/20201118005595/en
本期看点:Moderna和Pfizer-BioNTech COVID-19疫苗扩大EUA人群;Alnylam的RNAi药物AMVUTTRA™获FDA批准;信达生物信迪利单抗注射液新适应症获NMPA批准;多款药物获药监机构特殊审评认定。 中美双报_FDA IND/NDA/BLA_新药注册-奥来恩医药www.aleonpharma.net ...
Novavax Chief Executive Officer Stanley Erck believes the U.S. Food and Drug Administration could grant Emergency Use Authorization for its COVID-19 vaccine by May.
溃疡性结肠炎是一种炎症性肠病（IBD），会导致消化道发炎并损害结肠内壁。目前IBD的病因和发病机制仍未...
Government Trump Picks Vaccine Critic Weldon to Lead CDC, Makary for FDA Head November 25, 2024 · 2 min read · Tristan Manalac Drug Development BridgeBio Wins FDA Approval for ATTR-CM Drug, Launching Competition With Pfizer November 23, 2024 ...