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Pfizer, BioNtech To Submit To FDA For Emergency Use Authorisation For Their COVID-19 Vaccine Candidate

In a statement, Pfizer and BioNTech said they expect to produce globally up to 50 million vaccine doses in 2020 and up to 1.3 billion doses by the end of 2021

Pfizer, BioNtech To Submit To FDA For Emergency Use Authorisation For Their COVID-19 Vaccine Candidate
Highlights
  • Pfizer and BioNTech have produced a COVID-19 vaccine candidate BNT162b2
  • Pfizer’s coronavirus vaccine is found to be 95 per cent effective
  • Coronavirus vaccine had no serious side effects on older people: Pfizer

Washington: American drug giant Pfizer and German laboratory BioNTech on Friday (November 20) said that they will be submitting to the US Food and Drug Administration (FDA) for emergency use authorisation for their COVID-19 vaccine candidate. Citing an official statement by the companies, CNN reported that their vaccine candidate, known as BNT162b2, will potentially be available for use in high-risk populations in the United States by the middle to end of December. According to the companies, the vaccine requires two doses a few weeks apart and the protection is achieved 28 days after the first shot.

Also Read: Healthcare Workers, People Aged Above 65 Years Will Be Given COVID Vaccine On Priority: Dr. Harsh Vardhan

The submission to the FDA is based on results from the Phase 3 clinical trial of Pfizer’s vaccine, which began in the United States on July 27 and enrolled more than 43,000 volunteers, CNN reported.

On November 18, Pfizer had said that final results from the late-stage trial of its coronavirus vaccine was found to be 95 per cent effective and had no serious side effects on older people.

The findings are based on two doses given to more than 41,000 people around the world, said the US drugmaker adding that it would apply for emergency US authorisation soon, raising hopes that a working vaccine could soon become a reality.

This comes after Pfizer and its partner German biotechnology firm BioNTech had last week published data that their vaccine offered 90 per cent protection from the infection as compared to placebo saline shot.

In a statement, Pfizer and BioNTech said they expect to produce globally up to 50 million vaccine doses in 2020 and up to 1.3 billion doses by the end of 2021.

Also Read: Pfizer Says COVID-19 Vaccine Trial Complete, Cites Shot Is 95 Per Cent Effective

(Except for the headline, this story has not been edited by NDTV staff and is published from a syndicated feed.)

NDTV – Dettol Banega Swasth India campaign is an extension of the five-year-old Banega Swachh India initiative helmed by Campaign Ambassador Amitabh Bachchan. It aims to spread awareness about critical health issues facing the country. In wake of the current COVID-19 pandemic, the need for WASH (WaterSanitation and Hygiene) is reaffirmed as handwashing is one of the ways to prevent Coronavirus infection and other diseases. The campaign highlights the importance of nutrition and healthcare for women and children to prevent maternal and child mortality, fight malnutrition, stunting, wasting, anaemia and disease prevention through vaccines. Importance of programmes like Public Distribution System (PDS), Mid-day Meal Scheme, POSHAN Abhiyan and the role of Aganwadis and ASHA workers are also covered. Only a Swachh or clean India where toilets are used and open defecation free (ODF) status achieved as part of the Swachh Bharat Abhiyan launched by Prime Minister Narendra Modi in 2014, can eradicate diseases like diahorrea and become a Swasth or healthy India. The campaign will continue to cover issues like air pollutionwaste managementplastic banmanual scavenging and sanitation workers and menstrual hygiene

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