Our Vaccine Is Ready - Pfizer

According to alqabas It seems that the "Pfizer" vaccine has become closer than many expected, as the CEO of the company, Albert Burla, announced that Pfizer has collected sufficient safety data on its Corona virus vaccine, and is preparing to apply for an emergency use permit from the US Food and Drug Administration (FDA).

CNN quoted Burla as saying that safety questions in general have been answered, as his safety milestone has already been achieved, and now the company is preparing to submit an application for permission for the emergency use of the vaccine.

The company said - last week - that early clinical trials show that its vaccine is more than 90% effective, and that it is awaiting an application to the US Food and Drug Administration after collecting sufficient data on the safety of the vaccine, before Moderna announces that the preliminary results of its clinical trials It shows that its vaccine is 94.5% effective.

The US Food and Drug Administration (FDA) has set a date for a meeting of the Advisory Committee on Vaccines and Related Biological Products, which is a group of experts, on December 8, 9 and 10, where an informed source confirmed that the administration may take a decision at the end of the December 10 meeting regarding the issuance of emergency use permits. For vaccines.

The source explained that it is logical for the Food and Drug Administration to study both vaccines together, bearing in mind that they both use the same technology, and it appears that they will have very similar results, in terms of safety and efficacy, from large-scale clinical trials of the third phase.

According to the news network, if the US Food and Drug Administration allows the vaccines, they can be distributed immediately. However, no one can be vaccinated until the CDC's advisory committee reviews data, recommends a vaccine, and determines which groups will receive the vaccine first.

Also, in the event that vaccines are approved by the Food and Drug Administration, the CDC's Immunization Practices Advisory Committee will meet within 24 to 48 hours to determine whether everyone should receive the vaccine, or whether some people should be excluded.

 

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