Coronavirus Breaking News

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

Nov 30, 2020 • 7:22 am CST

Moderna Inc. announced today that the U.S. FDA’s Vaccines and Related Biological Products Advisory Committee meeting to review the safety and efficacy data package for mRNA-1273 will likely be scheduled for December 17, 2020.

The Company anticipates that the shipping of the mRNA-1273 vaccine to designated distribution points throughout the U.S. will occur shortly after an Emergency Use Authorization is granted. By the end of 2020, the Company expects to have approximately 20 million doses of mRNA-1273 available in the U.S. and remains on track to manufacture 500 million to 1 billion doses globally in 2021.

Nov 30, 2020 • 2:15 am CST

Moderna, Inc. announced an expanded agreement with the UK government for an additional 2 million doses of the experimental mRNA-1273 vaccine, beginning in March 2021. In total, the UK government has now secured 7 million doses of mRNA-1273.

“We appreciate the collaboration with the UK government as with many other governments and other key partners around the world,” said Stéphane Bancel, Chief Executive Officer of Moderna, in a press release. “For almost a decade, Moderna has invested in creating and developing a novel platform for designing and manufacturing a new class of mRNA-based vaccines.

Nov 30, 2020 • 1:43 am CST

Hadassah-University Medical Center and Sheba Medical Center reported that they had completed administering the BriLife coronavirus vaccine candidate to 80 volunteers, thus completing the Phase I clinical trial, reported JPost on November 27, 2020.

“We are pleased to announce that the first phase of the clinical research trial of the coronavirus vaccine was a success,” said the director of the clinical research unit at Hadassah, Prof. Yossi Karko.

Nov 30, 2020 • 1:05 am CST

The COVID-19 vaccine development landscape includes innovative platforms such as nucleic acid (DNA and RNA), virus-like particle, peptide, viral vector, recombinant protein, live attenuated virus, and inactivated virus approaches.

The goal of these vaccine candidates is to prevent SARS-CoV-2, the coronavirus that causes COVID-19, from getting into cells, replicating itself, which then infects a person, says the U.S. FDA.

As of November 30, 2020, the FDA has not authorized any of these experimental coronavirus vaccine candidates.

Nov 29, 2020 • 9:35 am CST

Los Angeles Mayor Eric Garcetti announced on November 24, 2020, that all travelers entering the City from another state or country will be required to fill out an online form to acknowledge and spread awareness of California’s recommended 14-day quarantine upon arrival.

And starting in early December, passengers arriving at LAX and Van Nuys Airport will see signs and messages reminding them to fill out the required form.

Mayor Eric Garcetti in a press statement, “Our new form delivers a clear message: if you travel to our city, we want you to be informed of guidelines that will save lives and keep all of us healthy and safe.”

Nov 29, 2020 • 2:58 am CST

About 187 million diagnostic tests, excluding antibody, and antigen tests have been performed during 2020 to confirm if a person has a SARS-CoV-2 virus infection. Overall, the U.S. CDC data indicates a COVID-19 infection positivity rate of 7.83%, as of November 28, 2020.

The state of California leads the USA with 20,318,880 coronavirus tests performed, followed by New York (17,440,570), Florida (13,658,216), and Texas (11,364,558).

On November 16, 2020, the U.S. FDA stated it 'has been working around the clock to help increase the availability of critical medical products, including diagnostic tests, to fight the COVID-19 pandemic. And the FDA published a patient and consumer overview of COVID-19 testing which offers plain language information about both diagnostic and antibody testing for COVID-19.'

Nov 28, 2020 • 2:35 pm CST

The Spanish Agency for Medicines and Health Products authorized a phase III of the clinical trial in Spain of the Janssen (a Johnson & Johnson company) Ad26.COV2-S vaccine candidate. This is the first phase III clinical trial for a vaccine against COVID-19 of this type authorized in Spain.

This coronavirus vaccine study will be conducted in 9 hospitals in Spain that will begin to recruit eligible volunteers, which include both people without any chronic diseases and people with concurrent illnesses.

Known as Ad26.COV2.S, this vaccine is based on a soundly documented technology with a non-replicative recombinant adenovirus, to generate an immunological response to one of the coronavirus proteins known as protein S (from spike, proteína espiga in Spanish).

Nov 28, 2020 • 11:45 am CST

Brazil's 38th President Jair Bolsonaro announced on November 28, 2020, that 'he would refuse a coronavirus vaccine. I'm telling you, I'm not going to take it. It's my right,' reported Voice of America.

Previous, during July 2020, Bolsonaro announced on Twitter that his diagnostic test results for the SARS-CoV-2 coronavirus came back positive.

Nov 28, 2020 • 5:45 am CST

United announced today it is expanding its customer COVID-19 testing efforts to include flights out of Houston to select destinations in Latin America and the Caribbean. Starting December 7, 2020, United customers in Houston will have the option to take a self-collected, mail-in SARS-CoV-2 virus test that meets local entry requirements.

"Widespread testing is key to unlocking international borders and safely reopening global travel," said Toby Enqvist, chief customer officer for United, in a press statement issued on November 23, 2020. "United was the first to offer free tests on flights across the Atlantic – and we'll look at new, innovative ways to make the travel experience even safer."

Nov 28, 2020 • 4:52 am CST

United Airlines began charter flights on November 27, 2020, bringing Germany-based BioNTech's COVID-19 vaccine candidate BNT162 to the USA. In a statement to The Hill, 'As a result of the historic pace of vaccine development through Operation Warp Speed and careful logistics planning, the Federal Aviation Administration is supporting the first mass air shipment of a vaccine.'

"The FAA established the 'FAA COVID-19 Vaccine Air Transport Team' in October to ensure safe, expeditious, and efficient transportation of vaccines. Several vaccines need continued cold temperatures during transport, which, in some circumstances, require dry ice, a hazardous material," the FAA statement added.

Nov 27, 2020 • 4:51 pm CST

Hyderabad-based Hetero Labs Limited announced it has agreed to produce 100 million doses of the Sputnik V vaccine in 2021. This manufacturing agreement is with the Russian Direct Investment Fund (RDIF).

The RDIF stated in a press statement issued on November 27, 2020, 'When the Sputnik V vaccine is used, the coronavirus itself does not enter the body as the vaccine only contains genetic information about part of its outer protein coat, the so-called "spikes" forming its crown. This completely eliminates the possibility of getting infected as a result of vaccination while also causing the body's stable immune response.'

B. Murali Krishna Reddy, Director, Hetero Labs Limited commented: “While we look forward to the clinical trial results in India, we believe that manufacturing the product locally is crucial to enable swift access to patients. This collaboration is another step towards our commitment in the battle against Covid-19 and realizing the objective of ‘Make-in-India’ campaign as envisioned by our Hon’ble Prime Minister of India.”

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Nov 27, 2020 • 3:18 pm CST

The president of the Japan Medical Association, Nakagawa Toshio, M.D., expressed a strong sense of alarm on November 25, 2020, concerned that Japan's medical care systems were at capacity in many parts of Japan, reported JapanTimes.

About 140,000 Japanese have tested positive for the SARS-CoV-2 virus since the outbreak began, with the related COVID-19 fatalities approaching 2,000.

In response to the expanding COVID-19 outbreak, Japan's capital city of Tokyo is set to open its second medical facility dedicated specifically for COVID-19 patients with mild or moderate symptoms, reported local media. Located in Fuchu City, this hospital will begin operations on December 16, 2020, as part of the Tokyo Metropolitan Tama Medical Center.

Nov 27, 2020 • 11:45 am CST

BioNTech SE and Shanghai Fosun Pharmaceutical (Group) Co., Ltd jointly announced on November 25, 2020, that their lead mRNA COVID-19 vaccine candidate BNT162b2 will be evaluated in a Phase 2 clinical trial in Taizhou and Lianshui, Jiangsu Province, China.

The recruitment of 960 healthy participants, aged between 18 and 85, to assess the safety and immunogenicity of the vaccine candidate and to support future Biologic License Application in China, is scheduled to start soon.

Dr. Aimin Hui, President of Global Research and Development and Chief Medical Officer of Fosun Pharma in China, said in a press release, “As an important part of global research and development, the Phase 2 clinical study with BNT162b2 in China will not only provide key data for the launch of the vaccine in China but also may play a positive role in the widespread promotion and use of the vaccine throughout Asia and around the world.”

Nov 27, 2020 • 11:32 am CST

The University Medical Center (UMC) of El Paso, Texas gave the local TV station KFOX14 an inside look on November 26, 2020, at the cold-chain freezers that are required to store certain COVID-19 vaccines, such as the Pfizer - BioNTech’s BNT162 vaccine.

Positioned in UMC's pharmacy, the freezers have emergency power back-up, commented the Director of Pharmacy at UMC Myron Lewis. “The freezer is an ultra-code freezer... 80 degrees centigrade."

The U.S. FDA previously announced the agency has scheduled a vaccine committee review meeting for December 10, 2020, and could issue emergency authorizations for experimental COVID-19 vaccine candidates.

Nov 27, 2020 • 7:57 am CST

The U.S. Department of Health and Human Services and the U.S. Department of Defense announced on November 23, 2020, they have jointly awarded an $11.6 million contract to Puritan Medical Products Company, LLC, to expand the domestic production capacity of Cue Sample Wands, the nasal swabs used exclusively with the COVID-19 cartridge-based molecular testing system developed and manufactured by Cue Health, Inc.

This new coronavirus test generates results in about 20 minutes at the point-of-care.

The Cue COVID-19 Test received Emergency Use Authorization from the U.S. FDA on June 10, 2020.