The US Food and Drug Administration is investigating Pfizer’s vaccine to be 95 percent effective by December 10, after which it would be brought to vaccination sites within 24 hours.

Coronavirus: the second wave, the second closure

Later than expected by many, but in mid-November, the Hungarian government also decided to try to curb the second wave of the coronavirus epidemic by introducing restrictions. At the time of the decision, 5,000 new infections a day had been identified and the number of deaths from the virus was mostly between 50 and 100 in 24 hours. The first step is a partial closure, but how effective it is is questionable. Follow our news!

In the United States, vaccinations against the coronavirus could begin before mid-December, said Moncef Slaoui, one of the leaders of the government-organized vaccination campaign.

Our plan is to deliver the vaccine to the vaccination sites within 24 hours of authorization, which means that the vaccination can start on December 11th or 12th. “

Moncef Slaoui told CNN.

Pfizer’s New York-based company and its German partner, BioNTech, filed an application for authorization with the US Food and Drug Administration (FDA) on Friday. According to the New York Times, the FDA plans to study the application for three weeks, after which it will be reviewed by independent experts, and its meeting is scheduled for December 10.

Pfizer announced Wednesday that it has completed the final phase of clinical testing of its 95 percent efficient ribonucleic acid messenger-based vaccine and expects to produce at least 50 million doses of vaccine this year and 1.3 billion doses in 2021.

In the United States, there were 12,102,101 confirmed infections, 255,953 deaths, and 4,529,700 recoveries on Sunday night, according to a summary from Johns Hopkins University in Baltimore.



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