Coronavirus Breaking News

The coronavirus disease COVID-19 is currently reaching pandemic levels in various countries.

Jan 27, 2021 • 12:25 pm CST

Massachusetts-based Moderna Inc. confirmed on January 27, 2021, that the Company is in discussion with the U.S. government to purchase an additional 100 million doses of the Moderna COVID-19 Vaccine for delivery in the third quarter of 2021.

To date, the U.S. government has agreed to purchase 200 million doses of the Moderna COVID-19 Vaccine. This new purchase would bring the U.S. government’s confirmed order commitment to 300 million doses.

The Moderna COVID-19 Vaccine has been authorized for emergency use by the U.S. Food and Drug Administration (FDA) for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 18 years of age and older.

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Jan 27, 2021 • 10:03 am CST

Reuters reported the Chilean Public Health Institute announced on January 27, 2021, the approval of the AstraZeneca-Oxford COVID-19 vaccine (AZD1222) for emergency use by a unanimous vote of its advisory board. The vaccine approval is for use for Chileans over the age of 18 and without an upper age limit.

The experimental AstraZeneca COVID-19 vaccine is made from a virus (ChAdOx1), a weakened version of a common cold virus (adenovirus). Genetic material has been added to the ChAdOx1 construct, which is used to make proteins from the SARS-CoV-2 coronavirus called Spike glycoprotein.

According to Chile's Department of Statistics and Health Information, in the last 24 hours there were 17 deaths due to causes associated with COVID-19. The total number of deceased amounts to 18,040 in Chile during the COVID-19 pandemic.

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Jan 27, 2021 • 9:30 am CST

The US Centers for Disease Control and Prevention (CDC) confirmed over 286 million RT-PCR diagnostic tests, excluding antibody and antigen tests, have been performed to confirm SARS-CoV-2 virus infections, as of January 26, 2021.

The state of California leads the USA with 34,382,323 coronavirus tests performed, followed by New York (25,937,582), Florida (19,819,234), and Texas (17,759,760).

Overall, the data indicates a COVID-19 infection positivity rate of 9.25% as of January 24, 2021.

Separately, the U.S. FDA announced it had authorized 320 coronavirus diagnostic tests, including 238 molecular tests, 69 antibody tests, and 13 antigen tests during 2020. Furthermore, 32 molecular authorizations can be used with home-collected samples. There is one molecular prescription at-home test, one antigen prescription at-home test, and one over-the-counter at-home antigen test.

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Jan 27, 2021 • 7:44 am CST

France-based Sanofi and Germany-based BioNTech announced they have today entered into an agreement under which Sanofi will support the manufacturing and supply of BioNTech’s Comirnaty COVID-19 vaccine, which is being co-developed with Pfizer.

Sanofi will provide BioNTech access to its established infrastructure and expertise to produce over 125 million doses of the Comirnaty COVID-19 vaccine in Europe. Initial supplies will originate from Sanofi’s production facilities in Frankfurt from the summer of 2021.

Paul Hudson, the CEO of Sanofi, stated in a press release issued on January 27, 2021, “Although vaccination campaigns have started around the world, the ability to get shots into arms is being limited by lower than expected supplies and delayed approval timelines owing to production shortages. We have made the decision to support BioNTech and Pfizer in manufacturing their COVID-19 vaccine in order to help address global needs, given that we have the technology and facilities to do so."

"As always, our top priority is to focus our efforts and capabilities on fighting this global pandemic. First and foremost, we will do this by continuing to develop our own COVID-19 vaccine candidates, in parallel with this industrial cooperation.”

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Jan 26, 2021 • 4:10 pm CST

The Therapeutic Goods Administration (TGA) of Australia granted a two-year provisional approval to Pfizer Australia Pty Ltd on January 25, 2021, for its COVID-19 vaccine, COMIRNATY, the first COVID-19 vaccine to receive regulatory approval in Australia. Following a thorough and independent review of Pfizer's submission, the TGA has decided that this vaccine meets the high safety, efficacy, and quality standards required for use in Australia.

The TGA's press release stated: 'Australians can be confident that the TGA's review process of this vaccine was rigorous and of the highest standard. The decision to provisionally approve the vaccine was also informed by expert advice from the Advisory Committee on Vaccines, an independent committee with expertise in scientific, medical, and clinical fields including consumer representation.'

'The TGA will continue to actively monitor the safety of the Pfizer vaccine both in Australia and overseas and will not hesitate to take action if safety concerns are identified. As an extra check, the TGA laboratories will undertake batch-assessments of the vaccine before it can be supplied in Australia.'

The COMIRNATY vaccine is provisionally approved and included in the Australian Register of Therapeutic Goods (ARTG) for active immunization to prevent COVID-19, caused by SARS-CoV-2, in individuals 16 years of age and older.

During the COVID-19 pandemic, Australia reported 909 fatalities related to the new disease. The vast majority of COVID-19 cases have been reported in Victoria.

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Jan 26, 2021 • 12:34 pm CST

The WHO Strategic Advisory Group of Experts (SAGE) on Immunization issued Interim recommendations on January 26, 2021, for the use of the Moderna mRNA-1273 vaccine against COVID-19.

The new SAGE recommendations included, but are not limited to the following: the Moderna vaccine is safe and effective in people with known medical conditions associated with increased risk of severe diseases, as well as chronic infections that are stable and controlled.

Although further studies are required for immunocompromised persons, people in this category who are part of a group recommended for vaccination may be vaccinated after receiving information and counseling. And known HIV-positive vaccine recipients should be provided with information and counseling.

And, Moderna's vaccine can be offered to a breastfeeding woman who is part of a group recommended for vaccination (e.g., health workers). Discontinuing breastfeeding after vaccination is currently not recommended.

However, SAGE stated, 'While pregnancy puts women at a higher risk of severe COVID-19, the use of the Moderna COVID-19 vaccine in pregnant women is currently not recommended, unless they are at risk of high exposure (e.g., health workers).'

Jan 26, 2021 • 11:00 am CST

New York-based Pfizer's Chief Executive Officer Albert Bourla announced the drugmaker and its German partner BioNTech SE would be able to deliver 200 million Comirnaty vaccine doses to the U.S. well before an earlier July 31, 2021, deadline due to a change in the vaccine’s label that allows an additional dose to be extracted from each vial, for a total of six doses, Bloomberg reported on January 26, 2021.

In total, Pfizer and BioNTech plan to produce 2 billion Comirnaty vaccine doses of 0.3 mL each in 2021, a 50% increase from 2020 estimates.

The Comirnaty (BNT162b2) (Tozinameran) mRNA vaccine was issued the first U.S. Food and Drug Administration (FDA) emergency use authorization on December 11, 2020. However, the experimental Comirnaty COVID-19 vaccine has not been Approved or Licensed by the U.S. FDA.

Jan 26, 2021 • 9:40 am CST

The Ontario government announced on January 25, 2021, it is accelerating the vaccination of residents in long-term care, high-risk retirement, and First Nations elder care homes by a new target date of February 5, 2021.

And to protect access to second doses of the Pfizer-BioNTech Comirnaty vaccine for those who have already received their first dose, Ontario will maintain the maximum interval of 21-27 days for long-term care, retirement, and First Nations elder care home resident groups and up to 42 days between the two doses for all other groups.

As of January 26th, Ontario reported 83,285 total vaccinations completed. And 5,909 COVID-19 related fatalities have been confirmed during the pandemic.

Following notification by the Canadian federal government of reductions in Pfizer-BioNTech vaccine shipments, these vaccination adjustments are being made.

Various media sources reported that Ontario Premier Doug Ford calls on the federal government to increase restrictions for anyone looking to travel into Canada.

“Close down any travel coming into Canada, outside of residents of Canada or citizens of Canada,” Ford said at a press conference on January 26, 2021. “There’s no reason we need people coming in.”

Jan 26, 2021 • 8:30 am CST

New York-based Regeneron Pharmaceuticals announced positive initial results from an ongoing Phase 3 clinical trial evaluating REGEN-COV™ (casirivimab and imdevimab antibody cocktail) used as a passive vaccine for the prevention of COVID-19 in people at high risk of infection.

"In this prevention trial, REGEN-COV was given as injections rather than an infusion, which makes administration much more convenient and efficient for patients and overburdened healthcare providers and facilities," said David Weinreich, M.D., Executive Vice President and Head of Global Clinical Development at Regeneron, in a press statement.

"It's notable that the few infections that did occur after receiving REGEN-COV were all asymptomatic, and associated with markedly lower viral load and duration of viral shedding, potentially further reducing transmission."

The development and manufacturing of REGEN-COV has been funded in part by the Biomedical Advanced Research and Development Authority, part of the U.S. Department of Health and Human Services

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Jan 25, 2021 • 5:50 pm CST

The U.S. NIH announced a worldwide clinical trial found full dose anticoagulation (blood thinner) treatments given to moderately ill patients hospitalized for COVID-19 reduced the requirement of vital organ support—such as the need for ventilation.

Moderately ill patients are those not in intensive care and who did not receive organ support such as mechanical ventilation at trial enrollment, said the NIH in a press statement issued on January 22, 2021.

Three clinical trial platforms spanning five continents in more than 300 hospitals have been working together to test whether there is a greater benefit of full doses of heparin (blood thinners) to treat moderately ill hospitalized adults with COVID-19 compared to the lower heparin dose typically administered to prevent blood clots in hospitalized patients.

Based on the interim results of more than 1,000 moderately ill patients admitted to the hospital, the findings showed that full doses of blood thinners, in addition to being safe, were superior to the doses normally given to prevent blood clots in hospitalized patients. The trial investigators are now working as fast as possible to make the full results of the study available so clinicians can make informed decisions about treating their COVID-19 patients.

Heparin is in a class of medications called anticoagulants ('blood thinners'). It works by decreasing the clotting ability of the blood, says MedlinePlus.

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Jan 25, 2021 • 3:34 pm CST

Lufthansa Group airlines announced on January 22, 2021, they are introducing a requirement to wear a medical protective mask on their flights to and from Germany. Everyday masks are then no longer permitted. The regulation comes into force on February 1, 2021.

From that date, passengers will be required to wear either a surgical mask or an FFP2 mask or mask with the KN95/N95 standard during boarding, while in flight, and when leaving the aircraft. To enable passengers to adapt to the new rules in good time, they will be informed by e-mail and on the airlines' websites and social media channels.

The airlines of the Lufthansa Group had already introduced a requirement to wear a mouth-nose mask on board their flights in May 2020, making them one of the pioneers worldwide. As before, an exemption from the obligation to wear a mouth-nose covering during the flight for medical reasons is only possible if the medical certificate is issued on a form provided by Lufthansa and a negative Covid 19 test is available that is not older than 48 hours at the scheduled start of the journey.

All Lufthansa Group aircraft are equipped with the highest quality air filters, ensuring air quality similar to that in an operating theater. Also, the air circulates vertically instead of being dispersed throughout the cabin.

In principle, infection on board is very unlikely, says the company.

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Jan 25, 2021 • 9:17 am CST

Canadian Blood Services and Canada’s COVID-19 Immunity Task Force (CITF) announced results from their collaborative nine-province SARS-CoV-2 seroprevalence study that suggests that 1.5 % of healthy Canadians had been exposed to SARS-CoV-2, the virus causing COVID-19.

“Although this represents a doubling in comparison to an initial report following the first wave in May and June 2020, the overall seroprevalence – the number of people with antibodies, which suggests a previous COVID-19 infection – remains very low."

"Canada remains a long way from herd immunity,” said CITF Executive Director Tim Evans, in a press release.

This analysis is based on 33,860 blood samples from blood donor centers across Canada (excluding Quebec and the Territories) collected in October and November 2020. Donors aged between 17 and 24 years old had the highest seroprevalence rates (2.97%).

Dr. Catherine Hankins, CITF Co-Chair, added: “However, even using serology to add cases to our count that never came to light through formal diagnostic tests, it is clear that the vast majority of Canadians remain vulnerable to COVID-19. We have no choice but to keep up public health measures until vaccine-induced immunity grows substantially.”

Canadian Blood Services is moving towards using a new assay to test blood samples that will allow them to differentiate between infection-acquired and vaccine-acquired immunity.

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Jan 24, 2021 • 12:54 pm CST

Reuters reported Taiwan would more than double the number of people who have to quarantine at more than 5,000 on January 24, 2021, as the country seeks to contain a rare domestic cluster of COVID-19 cases connected to a local hospital.

The Taoyuan Hospital is located near an international airport, west of Taipei, at the northern end of Taiwan.

Taiwan's Health Minister Chen Shih-chung told local media that they would expand the number of people who have to quarantine at home for 14 days who may have contacted the (15) infected patients from the hospital. These cases include two doctors, four nurses, one migrant caregiver, three family members of two of the nurses, and two hospital patients and their three family members, according to the Central Epidemic Command Center.

Despite this new coronavirus outbreak, Taiwan's 23 million residents have only experienced (7) fatalities related to COVID-19 during the pandemic.

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Jan 23, 2021 • 8:08 pm CST

The UK's Department of Health and Social Care and Government Office for Science published a paper from the New and Emerging Respiratory Virus Threats Advisory Group (NERVTAG) on new coronavirus (COVID-19) variant B.1.1.7. on January 22, 2021.

This NERVTAG paper summarized its recent findings as follows: 'The variant of concern (VOC) B.1.1.7 appears to have substantially increased transmissibility compared to other variants and has grown quickly to become the dominant variant in much of the UK.'

An updated UK matched cohort analysis has reported a death risk ratio for VOC infected individuals compared to non-VOC of 1.65 (95% CI 1.21-2.25). Based on these analyses, there is a real possibility that infection with VOC B.1.1.7 is associated with an increased risk of death than infection with non-VOC viruses.

However, an analysis of CO-CIN data has not identified an increased risk of death in hospitalized VOC B.1.1.7 cases. The analysis found an increased case severity may not necessarily be reflected by increased in-hospital death risk. Furthermore, it should be noted that the absolute risk of death per COVID-19 infection remains low.

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Jan 23, 2021 • 7:51 pm CST

The British Medical Association (BMA) urged England’s chief medical officer on January 23, 2021, to urgently review the U.K.’s current second dose recommendation after 12 weeks. In a BMA statement reported by PBS, the association said there was a growing concern from the medical profession regarding the delay of the second dose of the Pfizer-BioNTech Comirnaty vaccine.

“No other nation has adopted the U.K.’s approach,” Dr. Chaand Nagpaul, chairman of the BMA council, told the BBC. “I do understand the trade-off and the rationale, but if that were the right thing to do, then we would see other nations following suit,” Nagpaul added.

Yvonne Doyle, medical director of Public Health England, defended the decision as “a reasonable scientific balance based on both supply and also protecting the most people.”

On January 5, 2021, the World Health Organization recommended that the second Pfizer-BioNTech Comirnaty vaccine dose could be given up to six weeks after the first but only “in exceptional circumstances.”