- Vaccine will begin to be made available across the UK from next week: PM
- Medicine authority's approval to the vaccine is a global win: PM Johnson
- Britain had ordered 40 million doses of the Pfizer vaccine: PM Johnson
London: Britain approved Pfizer’s COVID-19 vaccine on Wednesday (December 2), jumping ahead of the United States and Europe to become the West’s first country to formally endorse a jab it said should reach the most vulnerable people early next week. Prime Minister Boris Johnson touted the medicine authority’s approval as a global win and a ray of hope amid the gloom of the novel coronavirus which has killed nearly 1.5 million people globally, hammered the world economy and upended normal life.
Also Read: ICMR’s Director General Says The Country May Not Have To Vaccine The Entire Population Against COVID-19
Britain’s Medicines and Healthcare products Regulatory Agency (MHRA) granted emergency use approval to the Pfizer-BioNTech vaccine, which they say is 95% effective in preventing illness, in record time – just 23 days since Pfizer published the first data from its final stage clinical trial.
The world’s big powers have been racing for a vaccine for months to begin the long road to recovery, and getting there first may be seen as a coup for Johnson’s government, which has faced criticism over its handling of the crisis.
“It’s fantastic,” Prime Minister Johnson said.
The vaccine will begin to be made available across the UK from next week. It’s the protection of vaccines that will ultimately allow us to reclaim our lives and get the economy moving again.
The approval of a jab for use almost exactly a year since the novel coronavirus emerged in Wuhan, China, is a triumph for science, Pfizer boss Albert Bourla and his German biotechnology partner BioNTech.
But the breakneck speed at which approval was given drew criticism from Brussels where, in an unusually blunt statement, the European Union’s drugs regulator said its longer procedure to approve vaccines was more appropriate as it was based on more evidence and required more checks.
British leaders said that, while they would love to get a jab themselves, priority had to be given to those most in need – the elderly, those in care homes and health workers.
Also Read: Centre Asks States, Union Territories To Upload Data Of Health Workers On ‘COVIN App’ For COVID-19 Vaccination Drive
‘No Corners Cut’
The U.S. drugmaker said Britain’s emergency use authorization marks a historic moment in the fight against COVID-19. Pfizer announced its vaccine breakthrough on Nov. 9 with stage III clinical trial results.
This authorization is a goal we have been working toward since we first declared that science will win, and we applaud the MHRA for their ability to conduct a careful assessment and take timely action to help protect the people of the UK, said CEO Bourla.
Britain’s medicines regulator approved the vaccine in record time by doing a “rolling” concurrent analysis of data and the manufacturing process while Pfizer raced to conclude trials.
“No corners have been cut,” MHRA chief June Raine said in a televised briefing from Downing Street, adding that the first data on the vaccine had been received in June and undergone a rigorous analysis to international standards.
“Safety is our watchword,” she said. Asked if Britain’s looming exit from the European Union’s orbit on Dec. 31 had any role, Raine said the fast-tracked vaccine approval was done under European law.
With 450 people dying of COVID-19 infection every day in the UK, the benefits of rapid vaccine approval outweigh the potential risks, said Andrew Hill, senior visiting research fellow in the Department of Pharmacology at the University of Liverpool.
The U.S. Food and Drug Administration (FDA) is set to meet on Dec. 10 to discuss whether to recommend emergency use authorization of the Pfizer/BioNTech vaccine and the European Medicines Agency said it could give emergency approval for the shot by Dec. 29.
“The data submitted to regulatory agencies around the world are the result of a scientifically rigorous and highly ethical research and development programme,” said Ugur Sahin, chief executive and co-founder of BioNTech.
Anti-poverty campaigners, meanwhile, warned against rich countries hoarding the vaccine at the expense of poorer ones. “The worst thing we can do at this moment is allow a small number of countries to monopolise access to vaccines like this,” said Romilly Greenhill, UK director of the ONE organisation.
Also Read: Centre Has Plan To Vaccinate Around 30 Crore People For COVID-19 By July-August: Union Health Minister Harsh Vardhan
First In Line?
Britain said it would start vaccinating those most at risk of dying early next week after it gets 800,000 doses from Pfizer’s manufacturing centre in Belgium.
“Age is by far the single most important factor in terms of risk from COVID-19,” said Wei Shen Lim, head of Britain’s COVID-19 vaccine committee. Lim said there had been no suggestion a vaccine would be compulsory.
The speed of the rollout depends on how fast Pfizer can manufacture and deliver the vaccine – and the extreme temperature of -70C (-94F) at which the vaccine must be stored.
PM Johnson said last month that Britain had ordered 40 million doses of the Pfizer vaccine – enough for just under a third of the population as two shots of the jab are needed per person to gain immunity.
Health Secretary Matt Hancock said hospitals were ready to receive the shots and vaccination centres would be set up across the country but he admitted distribution would be a challenge given storage at temperature typical of an Antarctic winter. Pfizer has said the shots can be kept in thermal shipping boxes for up to 30 days, from up to 15 days previously guided. Afterwards, the vaccine can be kept at fridge temperatures for up to five days.
Other frontrunners in the vaccine race include U.S. biotech firm Moderna, which has said its shot is 94% successful in late-stage clinical trials. Moderna and Pfizer have developed their shots using new messenger RNA (mRNA) technology.
AstraZeneca said last month its COVID-19 shot, which is based on traditional vaccine technology, was 70% effective in pivotal trials and could be up to 90 per cent effective.
Also Read: High Storage Cost Of Ultra-Cold COVID-19 Vaccines Should Not Hinder Use: World Health Organisation
(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 (Water, Sanitation 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 pollution, waste management, plastic ban, manual scavenging and sanitation workers and menstrual hygiene.