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Virus World provides a daily blog of the latest news in the Virology field and the COVID-19 pandemic. News on new antiviral drugs, vaccines, diagnostic tests, viral outbreaks, novel viruses and milestone discoveries are curated by expert virologists. Highlighted news include trending and most cited scientific articles in these fields with links to the original publications. Stay up-to-date with the most exciting discoveries in the virus world and the last therapies for COVID-19 without spending hours browsing news and scientific publications. Additional comments by experts on the topics are available in Linkedin (https://www.linkedin.com/in/juanlama/detail/recent-activity/)
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Coronavirus: India Approves Vaccines from Bharat Biotech and Oxford/AstraZeneca

Coronavirus: India Approves Vaccines from Bharat Biotech and Oxford/AstraZeneca | Virus World | Scoop.it

It aims to inoculate some 300m people this year in one of the world's largest vaccination campaigns. The drugs regulatory authority gave the green light to the jabs developed by AstraZeneca with Oxford University and by local firm Bharat Biotech. Prime Minister Narendra Modi called it "a decisive turning point". India plans to inoculate some 300 million people on a priority list this year. It has recorded the second-highest number of infections in the world, with more than 10.3 million confirmed cases to date. Nearly 150,000 people have died. On Saturday India held nationwide drills to prepare more than 90,000 health care workers to administer vaccines across the country, which has a population of 1.3 billion people.  The Drugs Controller General of India said both manufacturers had submitted data showing their vaccines were safe to use. However, opposition politicians and some doctors have criticised a lack of transparency in the approval process.

 

Dr Swapneil Parikh, an infectious diseases researcher based in Mumbai, told the BBC doctors were in a difficult position. "I understand there is a need to go through the process quickly, remove regulatory hurdles," he said. "However... [governments and regulators] have a duty to be transparent about the data they have reviewed and the process involved in making the decision to authorise a vaccine, because if they don't do this, it can affect the public's faith in the process." The Oxford/AstraZeneca vaccine is being manufactured locally by the Serum Institute of India, the world's largest vaccine manufacturer. It says it is producing more than 50 million doses a month.  Adar Poonawalla, the company's CEO, told the BBC in November that he aimed to ramp up production to 100 million doses a month after receiving regulatory approval. The jab, which is known as Covishield in India, is administered in two doses given between four and 12 weeks apart. It can be safely stored at temperatures of 2C to 8C, about the same as a domestic fridge, and can be delivered in existing health care settings such as doctors' surgeries. This makes it easier to distribute than some of the other vaccines. The jab developed by Pfizer/BioNTech - which is currently being administered in several countries - must be stored at -70C and can only be moved a limited number of times - a particular challenge in India, where summer temperatures can reach 50C.

 

The local vaccine, however, was approved despite the absence of data on how efficient it can be. It has yet to go through large-scale trials. The Drugs Controller General, V.G. Somani, said Bharat Biotech's Covaxin was "safe and provides a robust immune response". Mr Somani said it had been approved "in public interest as an abundant precaution, in clinical trial mode, to have more options for vaccinations, especially in case of infection by mutant strains". India, which makes about 60% of vaccines globally, plans to immunise about 300 million people by July 2021. It will prioritise health care workers, the emergency services, and those who are clinically vulnerable because of age or pre-existing conditions. India's existing vaccination programme already reaches about 55 million people a year, administering 390 million free jabs against a dozen diseases. It stocks and tracks the vaccines through a well-oiled electronic system.

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AstraZeneca Vaccine Not Ready for Quick European Approval, Watchdog Official Says | Reuters

AstraZeneca Vaccine Not Ready for Quick European Approval, Watchdog Official Says | Reuters | Virus World | Scoop.it

The European Medicines Authority (EMA) will most likely not be able to approve the COVID-19 vaccine developed by drug maker AstraZeneca and the University of Oxford in January, the watchdog's Deputy Executive Director Noel Wathion said. 

 

AMSTERDAM (Reuters) - The European Medicines Authority (EMA) will most likely not be able to approve the COVID-19 vaccine developed by drug maker AstraZeneca and the University of Oxford in January, the watchdog’s Deputy Executive Director Noel Wathion said. “They have not even filed an application with us yet”, Wathion said in an interview with Belgian newspaper Het Nieuwsblad published on Tuesday. European regulators have only received some information about the vaccine, Wathion said. “Not even enough to warrant a conditional marketing licence”, he said. “We need additional data about the quality of the vaccine. And after that, the company has to formally apply.” This made it “improbable” that an approval could already be granted next month, Wathion said. The EMA could not be reached for comment.  AstraZeneca told Reuters last week that its COVID-19 vaccine should be effective against the new coronavirus variant, adding that studies were under way to fully probe the impact of the mutation. It has submitted a full data package about its vaccine to the British medicines regulator, British health minister Matt Hancock said.

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Covid-19: Oxford-AstraZeneca Vaccine Approved for Use in UK

Covid-19: Oxford-AstraZeneca Vaccine Approved for Use in UK | Virus World | Scoop.it

The first doses are due to be given on Monday, amid concern over rising coronavirus cases.  The UK has ordered 100 million doses - enough to vaccinate 50 million people. This would cover the entire population when combined with the full order of the Pfizer-BioNTech jab, Health Secretary Matt Hancock said. It comes as millions more people in England are expected to be the toughest tier four restrictions. Vaccination centres will now start inviting patients to come and get the jab from next week. Priority groups for immunisation have already been identified, starting with care home residents, the over-80s, and health and care workers. Eventually all over 50s and younger adults with health conditions will be offered a jab in the first phase of rollout - more than 25 million people in total. It is hoped that about two million patients a week could soon be vaccinated with two vaccines now approved.

 

On Tuesday, 53,135 new Covid cases were recorded in the UK - the highest single day rise since mass testing began - as well as 414 more deaths within 28 days of a positive test.  The Medicines and Healthcare products Regulatory Agency (MHRA) has authorised two full doses of the Oxford vaccine, with the second dose to be given four to 12 weeks after the first. The immunisation campaign will now shift to giving as many people as possible their first dose of vaccine with a second dose following within that period.  When the Pfizer-BioNTech jab rollout began, the aim was to give the second dose after three weeks. But based on advice from the Joint Committee on Vaccination and Immunisation, the aim now is to give as many vulnerable people some protection from Covid-19, irrespective of the jab they are given. The Oxford vaccine is easier to store and distribute, as it can be kept at normal fridge temperature unlike the Pfizer-BioNTech jab that has to be kept at -70C. There is also more confidence about supply as it is UK-made, whereas the Pfizer-BioNTech jab has to be shipped in from Belgium.  Pregnant and breastfeeding women can now take either of the two approved coronavirus vaccines "when the potential benefits outweigh the risks", experts said at an MHRA news conference. The Pfizer/BioNTech vaccine can also now be administered to people with a wide range of food and medicine allergies, but people allergic to ingredients in the vaccine should not take it. Dr June Raine, chief executive of the MHRA, told the briefing that "no corners have been cut" in assessing the safety and effectiveness of the Oxford-AstraZeneca jab....

 

AstraZeneca Official Release (Dec. 30, 2020):

https://www.astrazeneca.com/media-centre/press-releases/2020/astrazenecas-covid-19-vaccine-authorised-in-uk.html

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