Covid-19 vaccine maker Pfizer Inc. and BioNotech on Friday said they were going to apply for permission to use the vaccine emergency. The companies said that they are doing this to get permission to use the Covid-19 vaccine in the US from December next month.
American pharmaceutical company Pfizer and German company Bioentech have joined hands to provide relief to the entire world affected by the global pandemic Covid-19. Earlier this week, the company claimed that its potential vaccine proved to be up to 95% effective in the final analysis of the trial.
The company said in a statement that the Food and Drug Administration (FDA) may allow vaccine supplements to be given to high-risk populations in the US by the end of December. In their application, the two companies have also attached safety data on about 100 children between the ages of 12 and 15 years.
Pfizer and Bio-Entech made a big announcement about the vaccine on Wednesday. He said that his mRNA-based potential vaccine ‘BNT162B2’ was found to be up to 95% effective in the final analysis of the Phase III trial and that it was effective for people over 65 years of age.
Those in Italy who wish to take vaccine supplements to protect against Covid-19 will probably receive all vaccine doses by September next year. Italy’s Special Commissioner for Virus Emergencies Damonico Arcari gave this information on Thursday. He said that the first dose would be available by January.
Arkari said that Italy is to receive 3.4 million doses of the Pfizer vaccine after the second week of January, which is sufficient to deliver the required two doses to 1.6 million out of Italy’s six million people, under the European Union procurement program. Priority will be given to the elderly and those at higher risk.