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Pfizer says its Covid vaccine trial for youths ages 12 to 15 is totally enrolled

Walgreens pharmacist Jessica Sahni will hold the vaccine against Pfizer BioNTech coronavirus disease (COVID-19) at the New Jewish Home in New York on December 21, 2020.

Yuki Iwamura | Reuters

Pfizer said it had fully enrolled its Covid-19 vaccine study in children ages 12-15, an important step before the vaccine could be used in that age group.

The study, an extension of the study used to support the company’s emergency approval for the vaccine in people aged 16 and over, enrolled 2,259 children between the ages of 12 and 15, Pfizer told CNBC on Friday. The entry on a government clinical trial website has been updated to determine that subjects are no longer being recruited.

The vaccine developed with German partner BioNTech was approved in December for people aged 16 and over. Studies in younger age groups are needed to ensure the correct dose as well as safety and effectiveness in these different groups, said Dr. Evan Anderson, a pediatrician at Emory University School of Medicine.

“I am very uncomfortable sending my children back to school where, despite the school’s best efforts, there is a real risk of getting Covid-19,” Anderson told CNBC in October.

While children are less affected by Covid-19 than adults, they still catch the virus and get sick. Some even died. According to a report from the American Academy of Pediatrics and the Children’s Hospital Association, more than 2.5 million cases of Covid-19 in children were reported as of Jan. 14, about 13% of all cases.

“Children can still get sick and die from Covid-19,” said Dr. Paul Offit, director of the Vaccine Education Center and an infectious disease doctor at Philadelphia Children’s Hospital. “In the past year, as many children died of Covid-19 as of influenza. And we recommend an influenza vaccine for children.”

Offit also pointed out that children can suffer from a disease related to Covid-19 called multisystem inflammatory syndrome, “which can be debilitating”.

According to the Centers for Disease Control and Prevention, as of Jan. 8, there were 1,659 cases of the syndrome in children named MIS-C and 26 related deaths. There were a total of 78 deaths from Covid-19 in children under 4 years old and 178 in children between 5 and 17 years old, according to CDC data, although those numbers do not explain all deaths from the United States

Children compete for class at PS 361 on the first day of returning to class during the coronavirus disease (COVID-19) pandemic in the Manhattan neighborhood of New York City, New York, United States, on December 7, 2020.

Carlo Allegri | Reuters

Pfizer declined to say when it expected results from the study, which would depend on the observed infection rate, to compare the rates in the placebo group with those who received the vaccine. With infection rates higher in the US since the fall – the 7-day average of daily cases now stands at 187,500, according to a CNBC analysis of the Johns Hopkins University data – vaccine effectiveness studies have shown their ads are getting faster.

However, enrollment for adolescent studies has been slower than hoped, at least for Moderna’s study in children ages 12-17, Moncef Slaoui, chief advisor to Operation Warp Speed, the Trump administration’s vaccine effort, said at their last meeting on Dec. January.

By then, around 800 children had been included in the study for over a month, of which around 3,000 were needed. Moderna’s vaccine was approved for people aged 18 and over in December, weeks after its teenage study began. Pfizer lowered the age of his trial to 12 years in October.

“While enrollment was lower during the holiday season, we expect an increase in the new year as planned,” said Moderna spokeswoman Colleen Hussey on Friday. “We are on track to provide updated data by mid-2021.”

AstraZeneca, whose vaccine developed by Oxford University is in late-stage trials in the US and approved in the UK, told CNBC Friday that it plans to continue UK trials in a new protocol for children ages 5-18 from the coming months. “”

Johnson & Johnson, whose results are expected in the third phase in adults, said it was in talks with regulators about including pediatric populations in its development plan. The same technology used for the Covid-19 vaccine was found to have been used in vaccines given to more than 200,000 people, including people over 65, infants, children, HIV-positive adults, and pregnant women .

Typically, vaccine trials are conducted in younger age groups after they have been shown to be safe and effective in older groups. The manufacturers of Covid-19 vaccines have indicated that they will follow this plan here as well.

Moderna’s chief executive Stephane Bancel said earlier this month the company is unlikely to have data on children ages 11 and younger who would include a lower dose before next year. He said he expected data for children 12 years and older could be available before September.

U.S. public health officials such as White House Chief Medical Officer Dr. Anthony Fauci, said they hope that by fall 75% to 80% of the US population could be vaccinated so life can return to some form of normal.

About 78% of the US population, or 255 million people, are over 18 years old, according to a CNBC analysis of the census data. Another 25 million people are between 12 and 17 years old.

Fauci did not immediately respond to a query about the need to include children in vaccinations in order to meet his goal of 75% to 80% coverage.

“It is important that all children are vaccinated, and manufacturers cannot conduct these trials fast enough,” Angela Rasmussen, virologist and subsidiary at the Georgetown Center for Global Health Science and Safety, told CNBC on Friday. “The more people of all ages are vaccinated, the better.”

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Pfizer Will Ship Fewer Covid-19 Vaccine Vials to Account for ‘Additional’ Doses

However, the federal health authorities that manage the government’s syringe contracts told the FDA that more than 70 percent of the sites are using more efficient syringes and that more syringes can be bought or made according to another person who is aware of the situation.

Still, Pfizer’s attempts to pressurize the FDA worried some health officials, especially since the company itself originally calculated the vials contained five doses. If an extra dose could be extracted, it would mean the vaccine supply could be stretched, protecting more Americans from the virus. On the other hand, too few specialty syringes would mean the government could pay for wasted doses.

In early January, the debate was resolved after a “standard and customary legal review process,” said an FDA spokeswoman. On January 6, in a change to the emergency approval, the FDA officially changed the vaccine datasheet to specify six doses.

“Syringes and / or needles with low dead volume can be used to extract six doses from a single vial,” says the new US bulletin. It also warned, “If standard syringes and needles are used, there may not be enough volume to extract a sixth dose from a single vial.”

In a statement, an FDA spokeswoman said the agency considered several factors in approving Pfizer’s request, including the availability of the specialty syringes, the fact that other health officials had made a similar decision, and that the change would vaccinate Americans faster.

Pfizer and the federal government have agreed to keep track of which locations receive the syringes and other equipment needed to extract the extra dose, and that the company will not bill the US for six doses per vial for locations without these devices. According to a person familiar with the negotiations who was not allowed to speak because the conversations are confidential.

Beginning next week, the number of Pfizer vaccines the federal government will allocate to each state could be based on the assumption that each vial contains six doses, according to a federal official with no legal capacity to discuss the matter. The CDC and the Department of Health and Human Services did not discuss when they could do the shift until Friday afternoon.

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Pfizer Will Ship Fewer Vaccine Vials to Account for ‘Further’ Doses

In December, pharmacists made the happy discovery that they could squeeze an extra vaccine dose out of Pfizer vials that were supposed to contain only five.

Now, it appears, the bill is due. Pfizer plans to count the surprise sixth dose toward its previous commitment of 200 million doses of Covid vaccine by the end of July and therefore will be providing fewer vials than once expected for the United States.

And yet, pharmacists at some vaccination sites say they are still struggling to reliably extract the extra doses, which require the use of a specialty syringe.

“Now there’s more pressure to make sure that you get that sixth dose out,” said Michael Ganio, the senior director for pharmacy practice and quality at the American Society of Health-System Pharmacists.

For weeks, Pfizer executives pushed officials at the Food and Drug Administration to change the wording of the vaccine’s so-called emergency use authorization so that it formally acknowledged that the vials contained six doses, not five.

The distinction was critical: Pfizer’s contract with the federal government requires that it be paid by the dose.

At one point, Pfizer executives lashed out at the top federal vaccine regulator over the government’s reluctance to budge on the request, according to people familiar with the discussions who were not authorized to discuss them.

On Jan. 6, Pfizer got what it wanted. The F.D.A. changed the language in its fact sheet for doctors to confirm that the vials contain a sixth dose. The change mirrors similar labeling updates by the World Health Organization and the F.D.A.’s counterpart in the European Union.

Company officials, including the chief executive, Dr. Albert Bourla, have said that the sixth dose allows Pfizer to stretch its supply of scarce vaccine even further — it was one factor, for example, in the company’s new estimates that it will be able to manufacture two billion doses for the world this year, instead of the 1.3 billion it had originally planned.

A Pfizer spokeswoman, Amy Rose, said the company would “fulfill our supply commitments in line with our existing agreements — which are based on delivery of doses, not vials.”

When Pfizer first began shipping the vaccines in mid-December, it said that each vial contained enough liquid for five doses. But pharmacists in hospitals across the country soon noticed that the vials held enough for a sixth — and sometimes a seventh — dose. The discovery prompted a flurry of excitement and confusion, with some pharmacists throwing out the extra vaccine because they did not have permission to use it.

But they were soon advised by the F.D.A. that they could use those extra doses, which could be extracted with a so-called low dead volume syringe that is designed to cut down on wasted medication and vaccines.

Suddenly, it seemed as if the 100 million doses of vaccine that Pfizer has promised to the United States by the end of March would stretch to as much as 120 million — a welcome development given the scarcity of Covid-19 vaccines and the coronavirus pandemic’s mounting death toll.

But Pfizer insisted that those doses be counted toward its existing contract. It can now sell vials the United States had been expecting to other countries, or charge the United States for them in future deals. That could threaten the wave of good publicity that the company has enjoyed since developing a highly effective vaccine at record speed.

“Pfizer will make a lot of money from these vaccines, and the U.S. government assumed a lot of the upfront risk in this case, so I’m not sure why Pfizer didn’t just continue to fill their supply as planned, even if it meant oversupplying a little,” said Dr. Aaron S. Kesselheim, a professor of medicine at the Brigham and Women’s Hospital and Harvard Medical School, who studies drug prices.

Covid-19 Vaccines ›

Answers to Your Vaccine Questions

If I live in the U.S., when can I get the vaccine?

While the exact order of vaccine recipients may vary by state, most will likely put medical workers and residents of long-term care facilities first. If you want to understand how this decision is getting made, this article will help.

When can I return to normal life after being vaccinated?

Life will return to normal only when society as a whole gains enough protection against the coronavirus. Once countries authorize a vaccine, they’ll only be able to vaccinate a few percent of their citizens at most in the first couple months. The unvaccinated majority will still remain vulnerable to getting infected. A growing number of coronavirus vaccines are showing robust protection against becoming sick. But it’s also possible for people to spread the virus without even knowing they’re infected because they experience only mild symptoms or none at all. Scientists don’t yet know if the vaccines also block the transmission of the coronavirus. So for the time being, even vaccinated people will need to wear masks, avoid indoor crowds, and so on. Once enough people get vaccinated, it will become very difficult for the coronavirus to find vulnerable people to infect. Depending on how quickly we as a society achieve that goal, life might start approaching something like normal by the fall 2021.

If I’ve been vaccinated, do I still need to wear a mask?

Yes, but not forever. The two vaccines that will potentially get authorized this month clearly protect people from getting sick with Covid-19. But the clinical trials that delivered these results were not designed to determine whether vaccinated people could still spread the coronavirus without developing symptoms. That remains a possibility. We know that people who are naturally infected by the coronavirus can spread it while they’re not experiencing any cough or other symptoms. Researchers will be intensely studying this question as the vaccines roll out. In the meantime, even vaccinated people will need to think of themselves as possible spreaders.

Will it hurt? What are the side effects?

The Pfizer and BioNTech vaccine is delivered as a shot in the arm, like other typical vaccines. The injection won’t be any different from ones you’ve gotten before. Tens of thousands of people have already received the vaccines, and none of them have reported any serious health problems. But some of them have felt short-lived discomfort, including aches and flu-like symptoms that typically last a day. It’s possible that people may need to plan to take a day off work or school after the second shot. While these experiences aren’t pleasant, they are a good sign: they are the result of your own immune system encountering the vaccine and mounting a potent response that will provide long-lasting immunity.

Will mRNA vaccines change my genes?

No. The vaccines from Moderna and Pfizer use a genetic molecule to prime the immune system. That molecule, known as mRNA, is eventually destroyed by the body. The mRNA is packaged in an oily bubble that can fuse to a cell, allowing the molecule to slip in. The cell uses the mRNA to make proteins from the coronavirus, which can stimulate the immune system. At any moment, each of our cells may contain hundreds of thousands of mRNA molecules, which they produce in order to make proteins of their own. Once those proteins are made, our cells then shred the mRNA with special enzymes. The mRNA molecules our cells make can only survive a matter of minutes. The mRNA in vaccines is engineered to withstand the cell’s enzymes a bit longer, so that the cells can make extra virus proteins and prompt a stronger immune response. But the mRNA can only last for a few days at most before they are destroyed.

Pfizer’s accounting for the extra dose is already creating controversy in Europe, where some countries — like Belgium — say they have had to cancel vaccination appointments after discovering that Pfizer is sending them fewer vials. “It’s linked to the sixth dose,” Sabine Stordeur, an official overseeing vaccination efforts in Belgium, told the newspaper Le Soir. “It’s still a private company, so one shouldn’t be surprised.”

The U.S. negotiations come at a particularly harrowing time, as the Biden administration is said to be discussing the purchase of a third round of 100 million doses of Pfizer’s vaccine later in the year. The country is racing to vaccinate as many people as possible before more contagious virus variants become widespread, potentially spurring a wave of new hospitalizations and deaths.

Pfizer’s efforts to capitalize on the discovery were for weeks camouflaged in a bureaucratic language dispute. Before Christmas, Pfizer approached F.D.A. officials requesting a formal change to its fact sheet so that it said each vial contained six doses of vaccine instead of five. But regulators instead suggested the phrase “up to six doses,” depending on what kinds of needles and syringes were used to extract the vaccine.

After the F.D.A. signed a new fact sheet with that more cautious language, Pfizer approached F.D.A. officials again, saying it was crucial to say “six doses.” The company suggested altering the language to indicate that low dead volume syringes should be used. At one point, Pfizer executives lashed out at Dr. Peter Marks, the top vaccine regulator at the F.D.A., according to two people who heard about the exchange but were not authorized to discuss it.

An F.D.A. spokeswoman disputed that characterization of the exchange and said it was “constructive.”

Ms. Rose, the Pfizer spokeswoman, said that “in a situation of limited vaccine supply amidst a public health crisis, our intent with this label change is to provide clarity to health care providers, minimize vaccine wastage, and enable the most efficient use of the vaccine.”

In late December, federal health officials sought to figure out whether there were enough of the specialized syringes to justify the shift. Officials at the Centers for Disease Control and Prevention said they were uncertain whether the supply was sufficient, according to a person familiar with the conversations.

But federal health officials who manage the government’s contracts for syringes told the F.D.A. that more than 70 percent of the sites were using the more efficient syringes and that more could be easily bought or manufactured, according to another person knowledgeable about the situation.

Still, Pfizer’s attempts to pressure the F.D.A. unsettled some health officials, especially since the company itself originally calculated that the vials contained five doses. If an extra dose could be extracted, that would mean the vaccine supply could be stretched, protecting more Americans from the virus. On the other hand, too few of the specialty syringes would mean the government could end up paying for wasted doses.

By early January, the debate was resolved after a “standard and usual legal review process,” an F.D.A. spokeswoman said. On Jan. 6, in an amendment to the emergency authorization, the F.D.A. formally changed the vaccine’s fact sheet to specify six doses.

“Low dead-volume syringes and/or needles can be used to extract six doses from a single vial,” the new U.S. fact sheet read. It also warned, “If standard syringes and needles are used, there may not be sufficient volume to extract a sixth dose from a single vial.”

Pfizer and the federal government have agreed to track which sites are receiving the syringes and other equipment needed to extract the additional dose, and that the company will not charge the United States for six doses per vial at sites that don’t have that equipment, according to a person familiar with the negotiations who was not authorized to speak because the talks are confidential.

Beginning as soon as next week, the number of Pfizer vaccines that the federal government allocates to each state could be based on the assumption that each vial contains six doses, according to a federal official not authorized to discuss the matter. The C.D.C. and the Department of Health and Human Services were discussing as recently as Friday afternoon when they might make the shift.

Pharmacists around the country are still reporting that they don’t have the right supplies to reliably extract extra doses, said Erin Fox, the senior pharmacy director for drug information and support services at the University of Utah.

She said Pfizer deserved credit for developing the vaccine, but “it isn’t fair to people that can’t access the right syringe and needle combination to be able to get that sixth dose out.”

The contracts for low dead volume syringes are managed by the Department of Health and Human Services’ Biomedical Advanced Research and Development Agency. A spokeswoman for the agency said the federal government had procured enough of the syringes for the Pfizer vaccine currently available and was working with the company to “track current inventory and future deliveries of these specific syringes for Pfizer and continually comparing them to projected delivery of doses from Pfizer.”

Dr. Fox said that McKesson, the distribution company that has contracted with the federal government to deliver vaccination supplies, is still sending kits that contain only enough supplies for five doses per vial.

A McKesson spokesman said the company began sending out kits that account for the sixth dose this week.

Jen Psaki, the White House press secretary, said on Thursday that the Biden administration might use the Defense Production Act to accelerate production of the specialized syringes in order to increase supply, suggesting that the federal government is uncertain whether it will have enough in the future.

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CDC modifications Covid vaccine steerage to OK mixing Pfizer and Moderna pictures

Syringe containers for the Covid-19 vaccines from Pfizer BioNtech and Moderna Inc. in Tucson, Arizona, USA, on Friday, January 15, 2021.

Cherry Orr | Bloomberg | Getty Images

The Centers for Disease Control and Prevention have tacitly changed their guidelines for Covid-19 vaccine shots, stating that it is now okay to mix Pfizer and Moderna shots in “exceptional situations” and that it is in Okay, wait up to six weeks to get the second shot. Two-dose immunization from both companies.

While Pfizer and Moderna’s vaccines, both of which use messenger RNA technology, were approved 21 and 28 days apart, the agency now says that under new guidelines, you can get both shots as long as they’re at least apart 28 days administered will be published on its website Thursday.

Although “every effort” should be made to ensure that a patient receives the same vaccine, in rare situations “any available mRNA COVID-19 vaccine can be administered with a minimum of 28 days between doses” – if supply Is limited or the patient does not know what vaccine they originally received, the CDC says in new guidelines.

The CDC says the two products are not interchangeable, admitting that they hadn’t yet investigated whether their new recommendations would alter the safety or effectiveness of either vaccine.

The agency said health care providers should give patients a vaccination card detailing when they received their first shot and what type of shot it was to ensure patients know which shot to receive the second time. The agency also recommends providers to record the patient’s vaccination information on their medical records and on the government vaccination information system.

Both companies need two doses to achieve maximum protection against the coronavirus. While both shots should be administered according to the guidelines originally recommended, the CDC said the second dose of both companies’ vaccine could be delayed for up to six weeks if necessary.

The updated guidelines come as some cities and counties across the country cancel vaccination appointments because they don’t have as many doses as they originally expected.

Wayne County, Michigan, for example, said last week it would be a priority to make sure people who got their first shot get their second shot on time. But the county said it had to cancel nearly 1,400 appointments for people to get their first shot.

“The intent is not to suggest people do something else, but rather to give clinicians flexibility in exceptional circumstances,” said Jason McDonald, a CDC spokesman, in an email to CNBC.

Dr. Nancy Messonnier, director of the CDC’s National Center for Immunization and Respiratory Diseases, was asked on Friday about the interval at which the two shots should be administered.

“The data we have is of a two-dose vaccine on the recommended schedule of 21 or 28 days,” she said at a virtual event hosted by Harvard TH Chan School of Public Health and National Public Radio . “At this point in time, we at CDC agree with what the FDA says, and the FDA has made it very clear that we should be using the approved regimen.”

“It’s firmly ingrained in science and the evidence available, and doing anything else would not follow science and possibly not allow us to really get the full potential of these vaccines,” she added. “For now, from the CDC’s point of view, we think it has to be two doses on the recommended schedule.”

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New York Gov. Cuomo asks to purchase immediately from Pfizer

New York Governor Andrew Cuomo speaks out on Coronavirus Disease (COVID-19) on November 15, 2020 at Riverside Church in Manhattan, New York City, United States.

Andrew Kelly | Reuters

New York Governor Andrew Cuomo asked Pfizer CEO Albert Bourla Monday about the option of purchasing Covid-19 vaccine doses direct from the company. However, a statement from the company said the Department of Health and Human Services must first approve such a model.

The request comes after an alarmingly slow start to national vaccine rollout, with the country falling millions of injections short of original Trump administration projections. By January 15, the US had distributed more than 31 million doses and administered just over 12 million. Health officials had hoped to inject 20 million Americans by the end of 2020.

Cuomo, a Democrat, accused the Trump administration of not sending enough doses of vaccine to his state. This week, he said, New York would receive 250,000 doses – 50,000 fewer than the week before.

In his letter to Bourla, Cuomo suggested that Pfizer should be able to sell directly to his state, bypassing federal agencies, as Pfizer “is not bound by any commitments Moderna made under Operation Warp Speed” .

“The company’s decision to end Operation Warp Speed, which is being redesigned by the Biden Administration, puts it in a unique position that could help save lives here in New York,” Cuomo wrote.

Pfizer said the model would first need to be approved for emergency drug use under the Food and Drug Administration’s approval.

The company said in a statement it was “open to working with HHS on a distribution model that would get as many Americans as possible access to our vaccine as quickly as possible. However, before we could sell directly to state governments, HHS would need to approve it . ” this proposal is based on the EEA granted to Pfizer by the FDA. “

Representatives from HHS did not immediately respond to a request for comment.

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Pfizer to briefly scale back Covid vaccine deliveries to Europe

A picture taken on January 15, 2021 shows a pharmacist holding a vial of undiluted Pfizer BioNTech vaccine for Covid-19 with gloved hands, which is stored at -70 ° in a super freezer at Le Mans hospital in northwestern France became country runs a vaccination campaign to fight the spread of the novel coronavirus.

Jean-Francois Monier | AFP | Getty Images

LONDON – Pfizer will temporarily reduce the number of doses of its coronavirus vaccine shipped to Europe.

The Norwegian Public Health Institute received a message from Pfizer “shortly before 10 a.m.” on Friday, according to a statement by the agency published shortly thereafter. The NIPH statement said supplies of the Pfizer BioNTech vaccine would be reduced from next week “and for an upcoming period”.

“In week 3, Pfizer predicted 43,875 doses of vaccine. Now we appear to be receiving 36,075 doses,” the statement said.

NIPH said the temporary reduction in shipments was “related to an upgrade in production capacity”. “The temporary reduction will affect all European countries,” he added.

Pfizer later confirmed the interruption in supplies in a statement. “As part of normal productivity improvements to increase capacity, we need to make changes to the process and facility that require additional regulatory approvals,” he said.

Pfizer added that while this would “temporarily affect shipments from late January to early February, it will significantly increase the doses available to patients in late February and March”.

Meanwhile, Pfizer said there could be fluctuations in orders and shipping schedules at its facility in Puurs, Belgium, “in the near future”.

Albert Bourla, CEO of Pfizer, told CNBC’s “Squawk Box” on Tuesday that he was confident of “dramatically increasing” production of the vaccine this year, with the goal of producing up to 2 billion doses.

Bourla also said that Pfizer currently has more doses of its vaccine available than are being used.

The European Union announced last week that it was doubling its inventory of Pfizer BioNTech vaccines.

Ursula von der Leyen, President of the European Commission, said the deal would allow the EU to buy an additional 300 million cans on top of its existing inventory. The EU executive has already been criticized for not buying more of the vaccine.

Rollouts have been slow in many EU countries including France, Germany and the Netherlands, and this latest news is likely to weigh on vaccination programs in those countries. Canada has also confirmed that its deliveries will be delayed, but said it was hoped that this would not affect its vaccination program.

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Pfizer Says Its Vaccine Works In opposition to Key Mutation in Contagious Variants

Pfizer and BioNTech announced on Friday that their Covid vaccine is effective against one of the mutations in the new contagious variants in the UK and South Africa.

Independent experts said the results were good news, but warned that each of these coronavirus variants have several different potentially dangerous mutations that have not yet been studied. So it’s possible that one of these mutations could affect the effectiveness of the vaccine.

“It’s the first step in the right direction,” said Dr. John Brooks, the chief medical officer of the Covid-19 emergency department at the Centers for Disease Control. “I hope the additional work that comes out in the future matches this insight.”

The new variant, known as B.1.1.7, first gave cause for concern in December when British researchers found it was rapidly becoming more common in people with Covid-19. Since then, it has appeared in 45 countries.

Subsequent research has confirmed that it has the ability to spread more easily from person to person. On Friday, Public Health England published a new study on B.1.1.7 in which researchers estimated that the variant is 30 to 50 percent more transmissible than other forms of the virus.

The viral line that leads to B.1.1.7 has accumulated 23 mutations. Of particular concern to scientists are eight mutations that affect the gene for a protein called spike on the surface of coronaviruses. That’s because the viruses use the spike protein to capture human cells. It is possible that one or more of them will help B.1.1.7 enter cells more successfully.

One of these mutations, known as N501Y, is of particular concern. Experiments have shown that it allows the virus to bind more tightly to cells. And it has appeared in other lines of the coronavirus as well, including a variant identified in South Africa in December. This variant, named B.1.351, quickly spread across the country and has so far expanded to a dozen other countries.

In the new study, which went online Thursday and has not yet undergone a formal scientific review, researchers from the University of Texas Medical Department conducted an experiment to see if the Pfizer BioNTech vaccine was against viruses with the N501Y mutation works. They found that in cells in the laboratory, the mutated virus could not infect human cells mixed with antibodies from vaccinated people. The antibodies clung to the coronaviruses, preventing them from entering cells. Despite the N501Y mutation, the experiment showed that the antibodies produced by the vaccine were still able to bind to the viruses.

“This indicates that the key N501Y mutation found in the emerging variants in the UK and South Africa does not create resistance to the immune responses induced by the Pfizer BioNTech vaccine,” the companies said in a press release .

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Pfizer nears take care of U.S. authorities for extra doses

The U.S. government is about to sign a deal with Pfizer for up to 100 million additional doses of its coronavirus vaccine, sources told CNBC’s Meg Tirrell on Tuesday.

The deal could be announced on Wednesday, according to a source. The New York Times reported the news first.

Pfizer declined to comment, saying the company “could not comment on confidential discussions that may be taking place with the US government.” The U.S. Department of Health did not immediately respond to a request for comment.

The news comes after Pfizer CEO Dr. Albert Bourla told CNBC last week that the company is negotiating with the federal government to provide an additional 100 million Covid-19 vaccine doses next year.

Pfizer and the US are working out the timing details, Bourla said in an interview with CNBC’s “Squawk Box” on Dec. 14. The company could provide many of these cans in the third quarter of 2021, but the U.S. government is pushing for them in the second quarter, he said.

“We’re working very cooperatively to find a solution and allocate that 100 million [doses] in the second quarter if possible or in many of them, “Bourla said, adding that the company has not yet signed an agreement with the US.

Unlike other drug companies, Pfizer did not accept federal funding to develop or manufacture its vaccine. Pfizer has already signed a contract with the US government to supply 100 million doses of the vaccine as part of Operation Warp Speed, enough to vaccinate 50 million people. Under the agreement, the Americans will receive the vaccine for free.

The initial doses of the Pfizer vaccine are limited as production begins. Officials predict it will be months before everyone in the US who wants to be vaccinated is vaccinated. The U.S. shipped 2.9 million doses of the vaccine last week and plans to ship 2 million doses of that vaccine this week, according to General Gustave Perna, who oversees logistics for Operation Warp Speed.

Earlier this month, the Wall Street Journal reported that Pfizer’s target for vaccine launch of 50 million doses worldwide by the end of the year was only half of its originally planned 100 million. In a statement, Pfizer said there were several factors influencing the number of estimated doses, including increasing the size of a vaccine at an “unprecedented” pace.

The US government has criticized Pfizer in recent weeks, stating that the drug company kept federal officials “at bay” throughout the manufacturing process for its vaccine.

Minister of Health and Human Services Alex Azar told CNBC on Thursday that he would like the federal government’s relationship with Pfizer to change.

“You’re part of Operation Warp Speed, but … it’s a different relationship” than the government deals with Moderna and other federal drug companies that have received federal funding, Azar told CNBC’s Squawk Box in an interview. “We pull together, give [Pfizer] A guaranteed purchase that allows them to make capital investments has a predictable buyer, but we don’t have full visibility into their making because they kept this a bit more on-market. “

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World News

E.U. Company Approves Pfizer Vaccine, Setting Stage for Excessive-Stakes Rollout

BRÜSSEL – Von Stockholm bis Athen und von Lissabon bis Warschau bereiten sich die Regierungen der Europäischen Union darauf vor, später in dieser Woche einen Coronavirus-Impfstoff zu erhalten, auch wenn in einigen Teilen des Kontinents immer mehr Fälle auftreten.

Die Drogenbehörde des Blocks, die Europäische Arzneimittel-Agentur, genehmigte am Montag den Pfizer-BioNTech-Impfstoff und startete einen logistischen Marathon, mit dem sich die meisten Behörden in der Region bisher nicht auseinandersetzen mussten.

Die Operation zum Kauf, zur Genehmigung und zur Verteilung der Schüsse in der gesamten Europäischen Union war komplex und politisch aufgeladen, und die Einsätze könnten nicht höher sein. Die zweite Welle der Pandemie tobt immer noch in Teilen der Region, die meisten Europäer verbringen die Ferien in einer Art Sperrung, und die Volkswirtschaften des Blocks sind in Trümmern.

Um die Sache noch komplizierter zu machen, führte eine hoch ansteckende Variante in England viele europäische Länder am Wochenende dazu, Reisende aus Großbritannien zu blockieren, obwohl Wissenschaftler sagen, dass sie den Kontinent bereits erreicht haben.

Wenn die Impfstoffmission erfolgreich ist, kann sie die Glaubwürdigkeit der Europäischen Union stärken und ihre Verwaltung als eine echte Kraft mit Exekutivbefugnissen und Fähigkeiten etablieren, die wichtige Aufgaben im Namen ihrer Mitglieder übernehmen können. Wenn nicht, kann der Fehler Schärfe und Unzufriedenheit verbreiten.

Die Europäische Arzneimittel-Agentur wurde eingehend auf das Tempo geprüft, mit dem sie den Pfizer-BioNTech-Impfstoff überprüfte. Großbritannien erteilte vor Wochen die Impfstoff-Notfallgenehmigung und begann dann mit der Einführung seines Impfprogramms, wobei die Vereinigten Staaten nicht weit dahinter folgten.

Am Ende beschloss die Europäische Agentur, den Prozess zu beschleunigen und ein für den 29. Dezember angesetztes Zulassungstreffen voranzutreiben. Die Vereinigten Staaten haben auch einen Impfstoff von Moderna zugelassen, aber die Europäische Agentur wird den Antrag auf Zulassung nicht bearbeiten von den Aufnahmen dieser Firma bis zum 6. Januar.

Nachdem die Agentur den Pfizer-BioNTech-Impfstoff zugelassen hat, wird erwartet, dass die Europäische Kommission, die Exekutive der Europäischen Union, die Entscheidung innerhalb von 48 Stunden stempelt. Dies wäre grünes Licht für Pfizer, um Impfstoffe in der Region zu verteilen.

Die Kommission übernimmt die Verantwortung für diese erste Ladung, da die Fracht die Pfizer-Fabriken in Puurs (Belgien) und Mainz (Deutschland) verlässt und höchstwahrscheinlich am Donnerstag in Richtung europäischer Hauptstädte fährt. Das Unternehmen, das sich aus Sicherheitsgründen weigerte, detaillierte Fragen zu Transportplänen zu beantworten, wird in jedem Land eine aktive Rolle beim Transport und der Lagerung von Impfstoffen spielen.

Von diesem Zeitpunkt an wird jede der 27 Mitgliedsregierungen des Blocks dafür verantwortlich sein, den Impfstoff auf eine Weise an die Bevölkerung zu verteilen, die den Bedürfnissen, Prioritäten und Fähigkeiten jedes Landes entspricht.

Die ersten Europäer werden voraussichtlich am 27., 28. und 29. Dezember geimpft.

Der Druck, dies richtig zu machen und dies schnell zu tun, hat zugenommen, als die Europäische Union und ihre Mitglieder einen kollektiven Ansatz in einem kritischen Knotenpunkt im Kampf gegen die Pandemie versuchen. Die meisten Länder waren nationalistischer.

Der europäische Ansatz begann mit der Entscheidung in diesem Sommer, das Verhandlungskapital zu bündeln und die Europäische Kommission und einen Vorstand aus allen Mitgliedsländern zu ermächtigen, Vereinbarungen mit Pharmaunternehmen zu treffen, die an Impfstoffen arbeiten.

Es wurde kritisiert, dass die Europäische Union wie die Vereinigten Staaten nicht genügend Dosen des Pfizer-BioNTech-Impfstoffs bestellt hat, als ihnen eine Chance gegeben wurde. Aus finanzieller Sicht scheint der Ansatz jedoch dem Block zugute gekommen zu sein: Der Pfizer-BioNTech-Impfstoff zahlt weniger als die USA.

In Deutschland, der größten Volkswirtschaft des Blocks und Heimat von BioNTech, wurde die Entscheidung, die Europäische Kommission zur Aushandlung eines Abkommens zu ermächtigen, kritisiert, und einige argumentierten, dass das Land besser dran gewesen wäre, es alleine zu machen. Aber die meisten Blockmitglieder sind mittelgroße Länder oder kleiner, und für sie war der Ansatz sinnvoll. (Wenn die Zeit bis zum Brexit läuft, sehen einige hier möglicherweise auch eine starke politische Botschaft, wobei der Block zeigt, dass die Einheit stark ist.)

Wenn der Prozess bis zu diesem Punkt vereinheitlicht wurde, sieht der Rollout nun von Land zu Land ganz anders aus.

Covid19 Impfungen >

Antworten auf Ihre Impfstofffragen

Mit der Verbreitung eines Coronavirus-Impfstoffs ab den USA finden Sie hier Antworten auf einige Fragen, über die Sie sich möglicherweise wundern:

    • Wenn ich in den USA lebe, wann kann ich den Impfstoff bekommen? Während die genaue Reihenfolge der Impfstoffempfänger von Staat zu Staat unterschiedlich sein kann, werden die meisten Ärzte und Bewohner von Langzeitpflegeeinrichtungen an erster Stelle stehen. Wenn Sie verstehen möchten, wie diese Entscheidung getroffen wird, hilft dieser Artikel.
    • Wann kann ich nach der Impfung wieder zum normalen Leben zurückkehren? Das Leben wird erst wieder normal, wenn die Gesellschaft als Ganzes ausreichend Schutz gegen das Coronavirus erhält. Sobald die Länder einen Impfstoff zugelassen haben, können sie in den ersten Monaten höchstens einige Prozent ihrer Bürger impfen. Die nicht geimpfte Mehrheit bleibt weiterhin anfällig für Infektionen. Eine wachsende Anzahl von Coronavirus-Impfstoffen zeigt einen robusten Schutz vor Krankheit. Es ist aber auch möglich, dass Menschen das Virus verbreiten, ohne zu wissen, dass sie infiziert sind, weil sie nur leichte oder gar keine Symptome haben. Wissenschaftler wissen noch nicht, ob die Impfstoffe auch die Übertragung des Coronavirus blockieren. Selbst geimpfte Menschen müssen vorerst Masken tragen, Menschenmassen in Innenräumen meiden und so weiter. Sobald genügend Menschen geimpft sind, wird es für das Coronavirus sehr schwierig, gefährdete Personen zu finden, die infiziert werden können. Je nachdem, wie schnell wir als Gesellschaft dieses Ziel erreichen, könnte sich das Leben im Herbst 2021 einem normalen Zustand nähern.
    • Muss ich nach der Impfung noch eine Maske tragen? Ja, aber nicht für immer. Hier ist der Grund. Die Coronavirus-Impfstoffe werden tief in die Muskeln injiziert und stimulieren das Immunsystem zur Produktion von Antikörpern. Dies scheint ein ausreichender Schutz zu sein, um die geimpfte Person vor einer Krankheit zu bewahren. Was jedoch nicht klar ist, ist, ob es möglich ist, dass das Virus in der Nase blüht – und geniest oder ausgeatmet wird, um andere zu infizieren -, selbst wenn Antikörper an anderer Stelle im Körper mobilisiert wurden, um zu verhindern, dass die geimpfte Person krank wird. Die klinischen Impfstoffstudien sollten feststellen, ob geimpfte Menschen vor Krankheiten geschützt sind – und nicht herausfinden, ob sie das Coronavirus noch verbreiten können. Basierend auf Studien zu Grippeimpfstoffen und sogar mit Covid-19 infizierten Patienten haben Forscher Grund zu der Hoffnung, dass geimpfte Menschen das Virus nicht verbreiten, aber weitere Forschung ist erforderlich. In der Zwischenzeit müssen sich alle – auch geimpfte Menschen – als mögliche stille Streuer vorstellen und weiterhin eine Maske tragen. Lesen Sie hier mehr.
    • Wird es wehtun? Was sind die Nebenwirkungen? Der Impfstoff gegen Pfizer und BioNTech wird wie andere typische Impfstoffe als Schuss in den Arm abgegeben. Die Injektion in Ihren Arm fühlt sich nicht anders an als bei jedem anderen Impfstoff, aber die Rate kurzlebiger Nebenwirkungen scheint höher zu sein als bei einer Grippeschutzimpfung. Zehntausende Menschen haben die Impfstoffe bereits erhalten, und keiner von ihnen hat ernsthafte gesundheitliche Probleme gemeldet. Die Nebenwirkungen, die den Symptomen von Covid-19 ähneln können, dauern etwa einen Tag und treten nach der zweiten Dosis wahrscheinlicher auf. Frühe Berichte aus Impfstoffversuchen deuten darauf hin, dass einige Menschen möglicherweise einen Tag frei nehmen müssen, weil sie sich nach Erhalt der zweiten Dosis mies fühlen. In der Pfizer-Studie entwickelte etwa die Hälfte Müdigkeit. Andere Nebenwirkungen traten bei mindestens 25 bis 33 Prozent der Patienten auf, manchmal mehr, einschließlich Kopfschmerzen, Schüttelfrost und Muskelschmerzen. Obwohl diese Erfahrungen nicht angenehm sind, sind sie ein gutes Zeichen dafür, dass Ihr eigenes Immunsystem eine starke Reaktion auf den Impfstoff zeigt, die eine dauerhafte Immunität bietet.
    • Werden mRNA-Impfstoffe meine Gene verändern? Nein. Die Impfstoffe von Moderna und Pfizer verwenden ein genetisches Molekül, um das Immunsystem zu stärken. Dieses als mRNA bekannte Molekül wird schließlich vom Körper zerstört. Die mRNA ist in einer öligen Blase verpackt, die mit einer Zelle verschmelzen kann, so dass das Molekül hineinrutschen kann. Die Zelle verwendet die mRNA, um Proteine ​​aus dem Coronavirus herzustellen, die das Immunsystem stimulieren können. Zu jedem Zeitpunkt kann jede unserer Zellen Hunderttausende von mRNA-Molekülen enthalten, die sie produzieren, um eigene Proteine ​​herzustellen. Sobald diese Proteine ​​hergestellt sind, zerkleinern unsere Zellen die mRNA mit speziellen Enzymen. Die mRNA-Moleküle, die unsere Zellen herstellen, können nur wenige Minuten überleben. Die mRNA in Impfstoffen ist so konstruiert, dass sie den Enzymen der Zelle etwas länger standhält, sodass die Zellen zusätzliche Virusproteine ​​bilden und eine stärkere Immunantwort auslösen können. Die mRNA kann jedoch höchstens einige Tage halten, bevor sie zerstört wird.

Deutschland plant, am 27. Dezember mit der Immunisierung von Menschen über 80 Jahren und anderen Personen zu beginnen, die in Pflegeheimen leben, ein oder zwei Tage nach den voraussichtlich 400.000 Dosen, die es bestellt hat. Es ist geplant, die ersten Impfungen von Ärzteteams durchzuführen, die Pflegeheime besuchen. In den ersten Januarwochen werden Hunderte von Impfzentren in Hallen, Turnhallen und Theatern eröffnet.

Für viele Deutsche war es schwierig zu sehen, dass ein von ihren eigenen Bürgern entwickelter Impfstoff die Zulassung erhält und Wochen vor seiner geplanten Ankunft in ihrem eigenen Land in Großbritannien verabreicht wird.

Doch der Gesundheitsminister des Landes, Jens Spahn, hat sich gegen die Kritik gewehrt.

“Es gibt dem Vertrauen und der Verantwortung in ganz Europa viel Glauben, dass wir dies gemeinsam tun”, sagte Spahn letzte Woche gegenüber Reportern. “‘Wir’ sind stärker als ‘Ich'”, sagte er.

Frankreich, die zweitgrößte Volkswirtschaft der Region, wird Ende des Monats ebenfalls mit den Aufnahmen beginnen. Die Behörden dort stehen jedoch vor einer zusätzlichen Herausforderung: der Impfskepsis. Eine kürzlich durchgeführte Umfrage ergab, dass nur 41 Prozent der Befragten die Injektionen planen.

Italien und Spanien, zwei der am stärksten betroffenen europäischen Länder, bewegen sich ebenfalls schnell. Bis Ende dieses Monats finden zumindest einige Impfungen gegen die am stärksten gefährdeten Personen statt. Der Großteil wird im Januar beginnen.

Es ist den Gesundheitsbeamten in ganz Europa nicht entgangen, dass die ersten Impfungen einen übergroßen symbolischen Wert in der Kampagne gegen müde und manchmal skeptische Bevölkerungsgruppen haben könnten.

In Griechenland wurde die Impfaktion von einer Regierung, die darauf aus ist, widerstrebende Bürger für sich zu gewinnen, als Operation Freedom bezeichnet. Eine kürzlich dort durchgeführte Meinungsumfrage ergab, dass drei von zehn Griechen nicht beabsichtigten, sich impfen zu lassen, und Bedenken hinsichtlich Wirksamkeit und Sicherheit äußerten. Weitere drei von zehn Befragten äußerten sich skeptisch.

In Italien sagte Alessio D’Amato, der oberste Gesundheitsbeamte in der Region Latium, zu der auch Rom gehört, der italienischen Zeitung Corriere della Sera, dass die erste Person, die dort geimpft wird, „eine Krankenschwester und eine Frau sein wird – genau wie in New York. “

Bisher hat kein EU-Land Pläne angekündigt, den Impfstoff verbindlich zu machen.

Und obwohl der Druck besteht, die meisten Menschen in kürzester Zeit zu impfen, warnen Experten, dass die Behörden nicht zu schnell vorgehen sollten, insbesondere wenn sie nicht zuversichtlich in die Infrastruktur ihres Landes sind.

“Der beste Ansatz, insbesondere wenn Bedenken hinsichtlich der Logistik bestehen, besteht darin, langsam und stetig vorzugehen”, sagte Prof. Jean-Michel Dogné von der Universität Namur, Belgien, ein Berater der Europäischen Arzneimittel-Agentur.

“Nichts Schlimmeres kann passieren, als jemanden mit einem Impfstoff zu impfen, für den wir die Qualität nicht garantieren können”, sagte er.

Laut Professor Dogné besteht die größte Herausforderung für jedes Land darin, die Temperatur des Pfizer-BioNTech-Impfstoffs auf seinem Weg von der Fabrik bis zur Injektion zu verfolgen.

Die Impfkampagne wird im ersten Quartal 2021 in der Europäischen Union ernsthaft in Gang kommen, und die meisten Regierungen hoffen, dass bis Juni große Teile ihrer Bevölkerung geimpft werden.

Pfizer und die Europäische Kommission geben an, an einem spezifischen Zeitplan für künftige Impfstofflieferungen zu arbeiten, haben jedoch keine Einzelheiten mitgeteilt. Die Steigerung der Produktion ist eine Herausforderung für das Unternehmen, das mehrere Kunden bedient, und die europäischen Regierungen haben Bedenken geäußert, dass das Angebot zu einem Rinnsal werden könnte.

Professor Dogné sagte, dies sei umso mehr ein Grund, es richtig zu machen und sicherzustellen, dass keine der kostbaren Dosen verschwendet werde.

“Dies ist eine beispiellose Operation”, sagte er. “Wir dürfen keinen Tropfen verschwenden.”

Die Berichterstattung wurde von Melissa Eddy aus Berlin beigesteuert; Aurelien Breeden aus Paris; Emma Bubola aus Rom; Monika Pronczuk aus Warschau; Niki Kitsantonis aus Athen; und Raphael Minder aus Madrid.

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Health

Pelosi and McConnell obtain Pfizer Covid vaccine

House spokeswoman Nancy Pelosi (D-CA) will receive a COVID-19 vaccination from Dr Drs on December 18, 2020 in her office on Capitol Hill in Washington. Brian Monahan (R), attending physician for United States Congress, DC.

Ken Cedeno | Getty Images

House Speaker Nancy Pelosi and Senate Majority Leader Mitch McConnell received the Covid vaccine from Pfizer on Friday after the attending physician in Congress asked lawmakers to enroll.

The doctor, Dr. Brian Monahan, cited federal guidelines designed to ensure the U.S. government works during the pandemic.

Senior US government officials have already started receiving the vaccine. Vice President Mike Pence, his wife Karen and Surgeon General Jerome Adams streamed the recording live on national television Friday morning.

However, the general public is not expected to receive the vaccine for months as doses remain limited while Pfizer ramping up production. Moderna’s vaccine could get emergency approval as early as Friday. Congress is currently negotiating an aid package from Covid, which is expected to provide billions of dollars for vaccine distribution.

Monahan, who is also present as a doctor on the Supreme Court, said the National Security Council had told him that Congress, the court and executive agencies would be given a small number of vaccine doses for necessary staff.

“My recommendation to you is absolutely clear: there is no reason why you should postpone receiving this vaccine,” Monahan told Congress in a letter on Thursday. “The benefits far outweigh any small risk.”

Monahan stressed in his letter that “the small number of COVID19 vaccine doses that are being made available to us reflects a fraction of the first batch of vaccines being distributed across the country”. The US logistics plans for the first week of the vaccine rollout include 2.9 million doses for locations in all 50 states.

Monahan administered the vaccine to Pelosi, D-Calif. Friday after the House spokeswoman said she would follow the doctor’s instructions and receive the shot. In a press release on Thursday, she urged President Donald Trump to invoke the Defense Production Act to expedite manufacturing and ensure the equitable distribution of the vaccine to as many Americans as possible.

McConnell, a polio survivor, also received the shot on Friday, calling the vaccine safe and effective. In a statement Thursday, the Kentucky Republican expressed concern that polls show that a quarter of adults in the US are unsure whether they will receive the vaccine when it becomes available.

“As a polio survivor, I know both the fear of disease and the extraordinary promise of hope that vaccines bring,” said McConnell. “I really hope that all Kentuckians and Americans will take this advice and accept this safe and effective vaccine.”

More than 100 members of Congress have either quarantined, tested positive, or been exposed to someone with Covid, according to GovTrack. When the vaccine launches and members of Congress sign up for the shot, they still haven’t reached an agreement on an aid package from Covid that would include billions of dollars to distribute the vaccine. Members of a CDC advisory panel have warned that state and local governments will need more money to administer the vaccines.

The US government and 50 states are rationing the distribution of the vaccine over multiple phases, according to guidelines from the Centers for Disease Control and Prevention. In the first phase, frontline health workers and residents of long-term care facilities, which have about 40% of deaths in Covid, will be given the vaccine. A CDC advisory panel will meet on Sunday to set guidelines on who should get the shot in the next stage of vaccinations.

The New York Times reported on Sunday that the White House had planned to quickly distribute the vaccine to west wing workers who are in close contact with the president. Trump, who contracted the virus and was hospitalized for several days in October, announced hours after the Times report that he had adjusted the plan and that White House workers would receive the vaccine later in the program.

“I don’t plan to take the vaccine, but I look forward to doing so in due course,” the president said in a Twitter post.

At least 52 people linked to Trump and the White House have contracted coronavirus in recent months as senior officials, including the president, violate CDC’s guidelines on social distancing.