Coronavirus Breaking News

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

Jan 18, 2021 • 6:24 am CST

The National Research Center for Epidemiology and Microbiology and the Russian Direct Investment Fund (RDIF) announced on January 18, 2021, creating an International Scientific Advisory Board on the Sputnik V vaccine. Leading scientists in virology, microbiology, genetics, and biotechnology from Argentina, Croatia, France, Germany, India, Russia, Sweden, UK, and the USA, representing top research and medical centers, have joined the Board, stated a press release.

Kirill Dmitriev, CEO of the RDIF, said: "scientific exchange has become especially in demand in connection with the pandemic of the new coronavirus infection, a global problem that has stimulated the unification of all global research potential. We are grateful to all the experts who accepted our offer to join the Council. International partnership, including the coronavirus vaccine, is the key to ultimate victory and proves once again that the noble goal of saving lives has no boundaries."

The Sputnik V (Gam-COVID-Vac) is an adenoviral-based vaccine against the SARS-CoV-2 coronavirus. Sputnik V uses a weakened virus to deliver small parts of a pathogen and stimulate an immune response.

The Sputnik V vaccine has been registered in Argentina, Bolivia, Serbia, Algeria, Palestine, Venezuela, and Paraguay.

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Jan 18, 2021 • 5:37 am CST

The Republic of Vietnam National Steering Committee for COVID-19 Prevention and Control announced on January 17, 2021, the country had gone 47 days without a single community infection case of COVID-19.

The Committee ordered subordinate levels to control borders to prevent illegal entrants strictly to maintain this pace on January 15th. Those who enter Viet Nam by land must be subject to mandatory quarantine at concentrated camps managed by the Army and shall not be required to pay quarantine accommodation fees. Anyone who detects strange people or those likely to have returned from foreign countries need to report to local authorities.

The country’s patient total stands, 693 are local infections, while the rest are imported cases. And there have been 35 fatalities related to COVID-19 during the year-long pandemic.

On January 12, 2021, volunteers got their first shots of the Nanocovax vaccine candidate 75mcg dose. The phase one clinical trials of Nanocovax is expected to finish in February. Nanocovax is one of the four COVID-19 vaccines under development in Vietnam.

The Institute of Vaccines is developing the other three vaccines and Medical Biologicals, Vaccine, Biological Production Company No. 1 (Vabiotech), and the Center for Research and Production of Vaccines Biologicals (Polyvac), says the government.

Jan 17, 2021 • 6:38 pm CST

Local school district leaders in North Carolina approached faculty from Duke University and the University of North Carolina at Chapel Hill, seeking to understand better the scientific underpinnings of SARS-CoV-2 coronavirus mitigation strategies and further guide policies reopening. In response to this request, faculty at Duke and the University of North Carolina (NC) developed the ABC Science Collaborative and conducted a study.

The American Academy of Pediatrics published an early version of this study on January 16, 2021, that found 'In the first nine weeks of in-person instruction in NC schools during 2020, there was a minimal within-school secondary transmission of the SARS-CoV-2 coronavirus.

These researchers examined eleven school districts in NC, with nearly 100,000 students/staff. Of these, there were 773 community-acquired SARS-CoV-2 infections documented by molecular testing.

North Carolina Health department's staff determined an additional 32 infections were acquired within schools during the nine weeks through contact tracing. Each case was independently adjudicated for community or within-school acquisition by local health departments, said this study.

Jan 17, 2021 • 2:04 pm CST

Moderna, Inc. announced the Swiss Agency for Therapeutic Products, Swissmedic, has authorized the COVID-19 Moderna Vaccine in Switzerland. The authorization is given according to the ordinary approvals procedure. It is based on a rolling submission of data and the totality of scientific evidence shared by the Company, including a data analysis from the pivotal Phase 3 clinical study announced on November 30, 2020.

With this authorization, the Swiss Federal Government will secure 7.5 million doses of the COVID-19 Vaccine Moderna, with the first deliveries are expected to begin in Switzerland in January 2021.

Stéphane Bancel, CEO of Moderna, stated in a press release issued on January 12, 2021, “Switzerland has played a critical role in Moderna’s history since our early days, and it means a lot to us that we can now provide a highly effective vaccine to help protect the citizens of Switzerland.”

Moderna has also received authorization from regulatory authorities in the USA, Canada, Israel, the European Union, and the United Kingdom. Additional regulatory authorizations are currently under review in other countries and by the World Health Organization.

Jan 17, 2021 • 12:47 pm CST

The US Department of Defense (DOD) reported on January 15, 2021, there have been 126,437 coronavirus cases amongst Active Duty personnel since the pandemic began, but only 15 fatalities related to COVID-19.

There is about 1.3 million active-duty personnel, with the Army being the largest U.S. military service, followed by the Navy, Air Force, Marine Corps, Coast Guard, and the Space Force.

As part of Operation Warp Speed's mission to develop and distribute COVID-19 vaccines, the DOD confirmed the Defense Logistics Agency Distribution began shipping the Moderna COVID-19 Vaccine to Defense Department employees outside the continental U.S., the deployed U.S. Navy Fleet and a limited number of locations within the continental U.S.

On December 18, 2020, the U.S. FDA issued an emergency use authorization that enables the experimental Moderna COVID-19 Vaccine to be distributed in the USA. This has not been approved or licensed by the FDA but was authorized for emergency use.

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Jan 16, 2021 • 12:30 pm CST

Pakistan’s Drug Regulatory Authority of Pakistan (DRAP) announced it had “granted emergency use authorization to AstraZeneca-Oxford coronavirus vaccine,” Special Assistant to the Prime Minister on Health, Dr. Faisal Sultan’s office confirmed to Gulf News on January 16, 2021.

The AstraZeneca COVID-19 (AZD1222) coronavirus vaccine is made from a weakened version of a common cold virus (adenovirus) that has been genetically changed so that it can't grow in humans.

Pakistan previously announced it would provide COVID-19 vaccines free of charge to its citizens. Pakistan’s frontline healthcare workers would be at the top of the vaccine priority list, followed by people over 65 years of age.

Additionally, Pakistan has enrolled in the COVAX Global Alliance for vaccine immunization, and expects to receive around 50 million coronavirus vaccines, Dr. Sultan added.

'COVAX is necessary because without it there is a very real risk that the majority of people in the world will go unprotected against SARS-CoV-2, and this would allow the virus and its impact to continue unabated, states GAVI, the Vaccine Alliance.

Jan 16, 2021 • 8:45 am CST

The Drugs Control General of India (DCGI) has given Hyderabad-based Dr. Reddy’s Laboratories Ltd. approval to conduct a randomized, double-blind, parallel-group, placebo-controlled phase 3 study for the Sputnik V vaccine in India.

G V Prasad, Co-chairman and Managing Director, Dr. Reddy’s Laboratories announced in a statement issued on January 15, 2021, “We expect to commence the phase 3 study within this month and will continue to fast-track our efforts to bringing in a safe and efficacious vaccine for the Indian population”.

Earlier, India's Data and Safety Monitoring Board (DSMB) reviewed the safety data from the phase 2 clinical trial of the vaccine and recommended the phase 3 recruitment. The DSMB concluded on January 11, 2021, that no safety concerns were identified and the study met the primary endpoints of safety.

The COVID-19 vaccine Sputnik V (Gam-COVID-Vac) is an adenoviral-based vaccine against the SARS-CoV-2 coronavirus. Sputnik V uses a weakened virus to deliver small parts of a pathogen and stimulate an immune response.

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Jan 15, 2021 • 4:09 pm CST

The U.S. Centers for Disease Prevention and Control (CDC) reported 12,279,180 first-doses vaccines had been administered in the USA as of January 15, 2021. The number of people receiving 2 vaccine doses has reached 1,610,524.

From a productivity perspective, the state of Texas leads with 2,105,600 vaccines distributed, and 1,160,242 administered.

Acting US Defense Secretary Christopher Miller stated: 'On behalf of Operation Warp Speed, I am proud to report that today, 816,900 additional vaccines were distributed to the American people. Today’s great work brings the total number of vaccine doses distributed to 30,303,375.'

The CDC added 'viruses constantly change through mutation, and new variants of a virus are expected to occur over time. Scientists are working to learn more about how easily the new SARS-CoV-2 variants might spread, whether they could cause more severe illness and whether currently authorized vaccines will protect people against them.'

'At this time, there is no evidence that these coronavirus variants cause more severe illness or increased risk of death,' affirmed the CDC.

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Jan 15, 2021 • 3:46 pm CST

The US Centers for Disease Control and Prevention (CDC) reported for Week #1, ending January 9, 2021, the percentage of fatalities due to pneumonia, influenza, and COVID-19 (PIC) increased during the most recent week after declining for three weeks.

Based on death certificate data, the percentage of deaths attributed to PIC was 17.2%.

Nationally, the overall percentage of respiratory specimens testing positive for SARS-CoV-2, the betacoronavirus causing COVID-19, decreased from 15.4% during Week #53 to 14.5% #1. And the percentage of specimens testing positive for SARS-CoV-2 increased in Region 1 [New England] but decreased in the other nine regions in the USA.

In December 2020, the overall weekly hospitalization rate reached its highest point since the COVID-19 pandemic began and remained elevated. Although reported rates have declined in recent weeks, these rates are likely to increase as additional data are reported.

Furthermore, the CDC reported on January 15th, among sampled adults hospitalized during March 1–October 31, 2020, with information on underlying medical conditions, 90.0% had at least one reported underlying medical condition. The most-reported underlying medical conditions were hypertension (56.4%), obesity (48.6%), metabolic disease (41.6%), and cardiovascular disease (32.6%).

Among 971 children hospitalized during March 1–October 31, 2020, with information on underlying conditions, 52.0% had at least one reported underlying medical condition. The most-reported underlying medical conditions were obesity (37.7%), neurologic disease (13.4%), and asthma (11.4%).

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Jan 15, 2021 • 1:49 pm CST

A new study at the University of Alabama at Birmingham (UAB) found the diabetes drug metformin was associated with a threefold decrease in mortality in COVID-19 patients with Type 2 diabetes.

After controlling for other covariates, age, and gender, metformin use reduced fatalities with an odds ratio of 0.33 for Type 2 diabetes subjects, compared with those who did not take metformin, concluded these UAB researchers on January 13, 2021.

“This beneficial effect remained, even after correcting for age, sex, race, obesity, and hypertension or chronic kidney disease and heart failure,” added Anath Shalev, M.D., director of UAB’s Comprehensive Diabetes Center and leader of the study, in a press statement.

Metformin helps control the amount of glucose (sugar) in your blood. It decreases the amount of glucose you absorb from your food and the amount of glucose made by your liver. Metformin also increases your body's response to insulin, a natural substance that controls the amount of glucose in the blood states MedlinePlus.

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Jan 15, 2021 • 1:12 pm CST

The US Centers for Disease Control and Prevention (CDC) reported (76) cases of the SARS-CoV-2 betacornavirus B.1.1.7 lineage in the USA, as of January 13, 2021. The states of California and Florida have reported the most variant cases.

The CDC stated there are multiple SARS-CoV-2 variants currently circulating globally, such as the following:

In the United Kingdom (UK), the variant called B.1.1.7 emerged with an unusually large number of mutations. This variant spreads more easily and quickly than other variants. This variant was first detected in September 2020 and is now highly prevalent in London and southeast England.

In South Africa, another variant called 1.351 has emerged independently of the UK's variant. This variant originally detected in early October 2020, shares some mutations with the UK's variant. There have been cases caused by this variant outside of South Africa, but it has not been detected in the USA.

In Brazil, P.1 emerged and was identified during routine screening at Haneda airport outside Tokyo, Japan. This variant contains additional mutations that may affect its ability to be recognized by antibodies. This variant has not been detected in the USA.

These variants seem to spread more easily and quickly than other variants, leading to more cases of COVID-19. Currently, there is no evidence that these variants cause more severe illness or increased risk of death, said the CDC on January 15, 2021.

Jan 15, 2021 • 12:35 pm CST

The NEJM published a collection of resources on COVID-19 vaccines, including frequently asked questions and commentary written by Paul Sax, M.D., a Professor of Medicine at Harvard Medical School and an infectious disease specialist. Dr. Sax offers concise and engaging answers to clinicians’ questions about COVID-19 vaccinations, and the questions and concerns patients will raise.

A recent FAQ published by the NEJM and written by Dr. Sax on January 11, 2021, asked: Should pregnant or breastfeeding women receive the vaccine?

'Although pregnant and breastfeeding women were not enrolled in the COVID-19 vaccine trials and as a result, there are limited data about safety, the U.S. CDC advised on January 7, 2021, that pregnant and lactating women should be offered the vaccine and may choose to be vaccinated.'

'There is no theoretical reason why mRNA vaccines would be harmful to the mother during pregnancy, to a developing fetus, or a breastfeeding infant. Also, reassuring is that gestating rats receiving the Moderna vaccine did not demonstrate any safety concerns related to fetal or embryonal development, concluded Dr. Sax.

This view was recently shared by the American College of Obstetricians and Gynecologists.

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Jan 15, 2021 • 8:53 am CST

The Norwegian Institute of Public Health (MIPH) released a statement on January 15, 2021, indicating the Pfizer-BioNTech Comirnaty COVID-19 vaccine shipments would be reduced for a period ahead, reported CNBC. The NIPH explained the temporary reduction in vaccine deliveries was “connected with an upgrade of production capacity. Furthermore, the temporary reduction would affect all European countries.

Germany-based BioNTech and New York-based Pfizer developed the Comirnaty (BNT162b2) vaccine to prevent severe COVID-19 disease caused by the SARS-CoV-2 coronavirus. Comirnaty is a nucleoside-modified RNA formulated in lipid nanoparticles and encodes an optimized SARS-CoV-2 full-length spike protein antigen.

The U.S. FDA issued an emergency use authorization for the experimental Comirnaty vaccine on December 11, 2020.

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Jan 14, 2021 • 10:54 am CST

Raffaele Gianotti, a dermatopathologist with the University of Milan, said 'SARS-CoV-2 had been found in the 25-year-old woman’s preserved skin tissue from November 2019. She was misdiagnosed with a rare autoimmune disorder but could now be Italy’s COVID-19 “patient zero”, reported the SCMP on January 13, 2021.

These researchers analyzed skin biopsies of patients from Milan, Italy, in July 2020, with dermatoses and positive PCR swabs for SARS‐CoV‐2 at different infection stages. The test results were compared to skin biopsies of non‐diagnosed COVID-19 patients with dermatoses who were at high‐risk of COVID‐19 infection.

“Our patient could represent the oldest case in the literature of detection of the coronavirus on tissue samples,” Gianotti and his collaborators in a peer-reviewed paper published in the British Journal of Dermatology on January 7, 2021.

A newer paper reported in November 2020 the presence of SARS-CoV-2 receptor-binding domain-specific antibodies in blood samples of asymptomatic Italian individuals enrolled in a prospective lung cancer screening trial between September 2019 and March 2020.

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Jan 14, 2021 • 10:25 am CST

The Russian Direct Investment Fund (RDIF) announced on January 13, 2021, the Ministry of Health of the Bolivarian Republic of Venezuela has registered the Sputnik V Vaccine, which was previously registered in Argentina, Bolivia, Serbia, Algeria, and Palestine.

Venezuela's vaccine supplies will be secured through international partners in India, China, South Korea, and other countries said this RDIF press release.

Additionally, Reuters reported on January 14, 2021, Russia would submit a formal application to the European Union in February to gain approval for Sputnik V.

Sputnik V is a vector vaccine based on adenovirus DNA, in which the SARS-CoV-2 coronavirus gene is integrated. Adenovirus is used as a “container” to deliver the coronavirus gene to cells and start the synthesis of the new coronavirus's envelope proteins, “introducing” the immune system to a potential enemy.