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Moderna asks FDA to authorize 5 further doses per Covid vaccine vial to hurry distribution, supply tells CNBC

A health care worker holds a vial of the Moderna COVID-19 vaccine at a pop-up vaccination station operated by SOMOS Community Care during the coronavirus disease (COVID-19) pandemic in New York on January 29, 2021 .

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Moderna has asked the U.S. Food and Drug Administration for permission to fill their Covid-19 vaccine bottles with up to five additional doses to help clear a manufacturing bottleneck, according to a person familiar with the matter.

The change would allow Moderna to fill 15 cans into vials of the same size, now cleared for 10, which eases the pressure on the manufacturing process known as filling / finishing, said the person who refused to named because the application is not public yet.

The availability of Covid-19 vaccines has caused frustration since their approval in the US in mid-December. While the pace of administration has increased to an average of more than 1 million a day, the limited supply has hampered states’ ability to operate mass vaccination centers. By Friday, the US had distributed 49.2 million doses and 27.9 million had been given, according to the Centers for Disease Control and Prevention.

“We have problems making these mRNA vaccines,” said Dr. Paul Offit, director of the Vaccine Education Center and a physician at Philadelphia Children’s Hospital. “We have up to 1.2 million doses a day when we need 3 million doses a day.”

The FDA declined to comment and asked questions to the company. Moderna did not immediately respond to a request for comment.

The move from Moderna came after Pfizer requested and received a change in emergency approval from the FDA to specify that the Covid-19 vaccine bottles contain six doses instead of five after pharmacists determined that it had a bonus dose the correct syringes could be extracted. Pfizer then said it would ship fewer vials to the US, but the same number of doses specified in its contracts.

Moderna vials have also been found to contain a bonus dose, but a policy change is being sought to add volume to the vials.

The bottleneck is not the vials themselves, but the manufacturing capacity to fill the vials. The manufacturing filling / finishing process must be performed under aseptic conditions to ensure contamination does not occur and the capacity is high.

Companies have begun to form manufacturing partnerships that focus on this step in the process to increase production. Novartis announced on Friday that it has signed an initial vial fill agreement for BioNTech, Pfizer’s partner in Europe, for the Covid-19 vaccine.

“We expect this to be the first in a series of such agreements,” said Steffen Lang, head of technical operations at Novartis.

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Pfizer sending fewer Covid vaccine vials to account for additional doses

Dr. Scott Gottlieb, who sits on Pfizer’s board of directors, on Monday defended the company’s move to send fewer vials of its Covid-19 vaccine and count six doses per vial instead of five. This is the best way to ensure the extra dose is used.

When the company started shipping vaccine bottles last month, pharmacists found that they could often extract an extra dose from each vial, which on paper only held five doses. That discovery meant the United States could actually receive more doses of the vaccine than the $ 200 million the Department of Defense bought under its deal with Pfizer.

“The bottom line is that this is a very scarce resource. We have to make sure that every dose is used,” Gottlieb said Monday in CNBC’s “Squawk Box”. “The only way to do this is to market this as a six-dose vial and have the right equipment ready to extract that sixth dose, which is what Pfizer is actually doing.”

The New York Times reported Friday that Pfizer executives in recent weeks have successfully urged Food and Drug Administration officials to revise the wording of the vaccine’s emergency approval to officially include the sixth dose for the federal treaty.

Some pharmacists were confused by the extra doses or didn’t have the correct syringes to extract them and threw them away.

“During this pandemic that is killing many people around the world, it is important that we use all available vaccines and vaccinate as many people as possible. To keep an extra dose in each vial that could be used to vaccinate more people would be one Tragedy, “said company spokeswoman Amy Rose.

Gottlieb said Monday the move will help the US speed up the distribution of vaccine doses, adding that Pfizer can now deliver 120 million doses of the vaccine in the first quarter of 2021, up from 100 million before the labeling change.

However, the move puts pressure on U.S. pharmacists to extract six doses from each vial, which requires some special syringes called low dead space syringes. The US government, which ships kits of syringes and vaccine doses, has signed a contract with syringe manufacturers such as Becton Dickinson, the world’s largest syringe maker, to ensure supplies to local authorities.

However, Becton Dickinson is unable to significantly increase the US supply of syringes, Reuters reported earlier Monday, doubting how many vials the US can extract six doses from.

Gottlieb said the vaccines will only qualify as six-dose vials, which will also give local authorities the correct syringes to extract the final dose.

Gottlieb noted that when Pfizer applied for approval of his emergency vaccine, he knew that six doses could be taken from each vial, but revising the wording of the application would have delayed approval of the vaccine. The company therefore applied for approval with the intention of revising the wording later to reflect the six-dose vials.

He added that it took the U.S. FDA longer than regulators in other countries to make the change. Authorities in the UK, Switzerland and Israel have already revised the wording of their approvals for the Pfizer vaccine to take into account that each vial contains six doses.

Gottlieb, the former head of the FDA, clarified that the change should not be applied retrospectively, which means that all vials previously shipped will be counted as containing five doses.

But “at some point you had to set up the accommodation to properly account for the doses,” said Gottlieb.

Disclosure: Scott Gottlieb is a CNBC employee and a member of the boards of directors of Pfizer, genetic testing startup Tempus, health technology company Aetion Inc., and biotech company Illumina. He is also co-chair of the Healthy Sail Panel of Norwegian Cruise Line Holdings and Royal Caribbean.

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Pfizer to provide as much as 40 million Covid vaccine doses to Covax international program

A nurse prepares the Pfizer BioNTech Covid-19 vaccine on January 10, 2021 at a vaccination center in Sarcelles near Paris.

ALAIN JOCARD | AFP | Getty Images

Pfizer will deliver up to 40 million doses of its coronavirus vaccine to a global alliance that aims to provide coronavirus vaccines to poor nations, the head of the World Health Organization said on Friday.

The agreement will enable Covax – together with the WHO – to deliver vaccine doses to the participating countries from February, said WHO Director General Tedros Adhanom Ghebreyesus during a press conference. Tedros added that until an emergency is approved, the program expects 150 million doses of AstraZeneca’s vaccine to be available for distribution in the first quarter of this year.

The Covax program aims to provide 2 billion doses of Covid-19 vaccines to participating countries, which include low- to middle-income countries, by the end of this year. The Pfizer BioNTech vaccine requires two vaccinations spaced weeks apart, suggesting the deal would only cover 20 million people.

Tedros said the deal would allow other countries with supplies of Pfizer’s vaccine to donate them to the program. The WHO chief criticized wealthy nations for signing supply agreements with drug manufacturers for their starting doses of Covid-19 vaccines to stockpile supplies from poorer nations.

“This is not only important for COVAX, it is also an important step forward for equitable access to vaccines and an essential part of the global effort to fight this pandemic. We will only be safe everywhere if we are safe everywhere,” so Dr. Seth Berkley, CEO of Gavi, the Vaccine Alliance, said in a statement.

Albert Bourla, CEO of Pfizer, said during the press conference that the company will make the vaccine doses available to Covax and poorer countries for a fee. Pfizer was the first company to receive a global list of emergency uses for its vaccine from the WHO, allowing other countries to expedite their regulatory approval processes to begin administering the vaccine.

Bourla said the company will help ship the cans, which require ultra-cold storage and special handling, to low-income countries. UNICEF, which is helping with the dispensing of the cans, previously warned that some of the world’s poorest countries could face the challenge of storing and managing the shots upon arrival.

The program’s contract with Pfizer increases supply agreements to a total of just over 2 billion doses, but negotiations for an additional supply continue. The goal, according to Covax, is to immunize healthcare and other frontline workers as well as some high-risk individuals from the first quarter of this year.

The agreement follows the United States’ decision to remain a member of WHO under President Joe Biden. The new administration will also join the Covax program, a move the Trump administration opposed last year.

“I couldn’t escape the temptation to say that I’m very happy that this press conference is taking place on the day the United States rejoins the WHO organization. I think it’s a symbolic, great day for us,” Pfizer boss Bourla said at the meeting.

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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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Releasing most vaccine doses will not trigger scarcity

Boxes containing the Moderna COVID-19 vaccine are prepared for shipment at the McKesson distribution center in Olive Branch, Mississippi, United States, on December 20, 2020.

Paul Sancya | Reuters

The Biden government’s plan to release virtually every available dose of Pfizer and Moderna’s coronavirus vaccines to states shouldn’t cause supply problems later, a member of President-elect Joe Biden’s Covid-19 advisory board said Thursday.

The advisory team has had numerous discussions with vaccine manufacturers Pfizer, Moderna, and Johnson & Johnson, including about supply issues, said Dr. Celine Gounder, who sits on the panel and is an infectious disease specialist at NYU’s Grossman School of Medicine.

Aside from unforeseen “Snafu products”, the Biden government is “confident” that there will be no problem getting people to get their second shots on time, she said.

“We’re not too worried about that,” Gounder told the Johns Hopkins Bloomberg School of Public Health during a webcast on Thursday afternoon. “If you look at the production schedule, they’re going to be releasing more and more doses over time, so things really open up significantly.”

Gounder’s comment comes hours before Biden announces his plan to vaccinate the U.S. population and end the pandemic that killed at least 385,503 Americans in almost a year. Criticizing the Trump administration’s strategy of introducing vaccines, Biden said at the current pace, “It will be years, not months, for the American people to be vaccinated.”

The pace of vaccination in the US is much slower than officials had hoped. As of 9:00 a.m. ET on Wednesday, more than 29.3 million vaccine doses had been distributed in the United States, but just over 10.2 million vaccinations had been given, according to the Centers for Disease Control and Prevention. The number is a far cry from the federal government’s goal of vaccinating 20 million Americans by the end of 2020 and 50 million Americans by the end of this month.

Some state governors, including New York Governor Andrew Cuomo, have complained about the availability of vaccines, stating that the lack of doses has affected their ability to vaccinate people.

The Trump administration on Tuesday passed Biden’s plan to release most of the doses it had withheld for the second round of recording of Pfizer’s and Moderna’s two-dose vaccines.

General Gustave Perna, who oversees the logistics for President Donald Trump’s vaccination program, Operation Warp Speed, had previously said the provision of replacement doses of Covid was “good planning for the Army Officer General” to ensure the right people are available can get the shots if necessary.

To speed up the pace of vaccinations, the Trump administration also changed the way vaccine doses are assigned to states, and the CDC expanded vaccination eligibility to include anyone aged 65 and over, as well as those with comorbid conditions such as diabetes and heart disease.

Some public health experts have questioned whether companies can make more cans before people need their second shots.

Gounder said Thursday that the government still plans to hold “a small buffer” of cans in reserve.

“We’ll publish almost all of them [doses] with a little buffer left because we want to speed up the pace of vaccinations, “she said.” This is really a decision on how to manage care. It is not a recommendation about vaccine dose or schedule. “

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EU broadcasts 300 million extra doses of Pfizer-BioNTech covid vaccine

European Commission President Ursula von der Leyen holds a press conference in Brussels, Belgium on December 13, 2020 after speaking to British Prime Minister Boris Johnson on the phone.

Olivier Hoslet | Reuters

LONDON – The European Union doubles its inventory of Pfizer BioNTech coronavirus vaccines as concerns about adoption mount across 27 member states.

The vaccine developed with German biotechnology was the first to be approved by European regulatory authorities. It has been administered across the region since December 27th. However, the rollout was inconsistent and the European Commission was criticized for not buying more vaccine.

The Commission has argued that, at the request of Member States, it has a diversified portfolio of vaccination contracts, totaling up to 2.3 billion doses of “the most promising candidates”.

“As you know, we currently have access to 300 million doses of the BioNTech-Pfizer vaccine. Now the good news is: we have now agreed with BioNTech-Pfizer to renew this contract. With the new agreement, we could buy more in total another 300 million cans, “said the President of the Commission, Ursula von der Leyen, at a press conference on Friday.

This would mean the EU is on track to receive 600 million doses of this vaccine. Speaking to CNBC in December, Pfizer’s CEO pledged to produce a total of 1.3 billion cans in 2021, which would mean Europe would get almost half of its annual output.

75 million cans of the new order will be available in the second quarter of 2021. The rest will be delivered in the third and fourth quarters.

The Netherlands only started vaccinating its citizens this week and the bureaucracy has reportedly made France one of the biggest stragglers in distributing the shock.

According to the European Center for Disease Prevention and Control, more than 15 million cases of coronavirus have been reported in the region to date.

European regulators approved a second coronavirus vaccine on Wednesday. Moderna’s candidate is expected to be available to European citizens in the coming days.

“Europe will have more than enough vaccines within a reliable timeframe, and this shows that the path that we have taken in the European Union is the right one,” said von der Leyen on Friday, rejecting the criticism.

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A pharmacist accused of sabotaging vaccine doses is a conspiracy theorist, the police say.

A pharmacist arrested for deliberately sabotaging more than 500 doses of the Covid-19 vaccine in a Wisconsin hospital was “a licensed conspiracy theorist” who believed the vaccine could harm people and “alter their DNA”, so the police in Grafton, Wisconsin, where the man was employed.

Police said Steven Brandenburg, 46, who worked the night shift at Aurora Medical Center in Grafton, twice removed a box of Moderna vaccine from the refrigerator for 12 hours, rendering it “unusable.” .

“Brandenburg admitted to having done this on purpose, knowing that it would reduce the effectiveness of the vaccine,” said police.

The attempt to destroy valuable doses of the vaccine came over the holidays as the state worked to quickly deliver vaccines to the health front. As of Saturday, the state had received 159,800 doses of vaccines and administered 64,657, according to the Centers for Disease Control and Prevention. Although the Moderna product is sometimes described as a “genetic” vaccine, it does not alter a person’s genes in any way.

The vials, which held 570 doses of vaccine and were valued at $ 8,000 to $ 12,000 according to prosecutors, were discovered on Dec. 26. Five days later, Mr Brandenburg was arrested for crimes of reckless endangerment and property damage, although prosecutors said Monday the charges could be dropped on a single misdemeanor if the vials, which have yet to be tested, are still usable.

Prosecutor Adam Gerol said Mr. Brandenburg was “quite cooperative and admitted everything he did”. He said that, according to employees, Mr. Brandenburg had already brought a gun to work twice.

In a decision signed on Monday, a family court temporarily granted his wife Gretchen Brandenburg sole custody of the two daughters of Mr Brandenburg and determined that the children were in “immediate danger of physical or mental harm”.

Ms. Brandenburg filed for divorce last June. At a hearing in July, her lawyer testified that his client was afraid of Mr. Brandenburg’s temper.

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Moderna will increase minimal 2021 Covid vaccine manufacturing by 20% to 600 million doses

A health worker holds a Moderna COVID-19 vaccine bottle on the first day Orange County residents 65 and older can be vaccinated on December 29, 2020 at a drive through at the Orange County Convention Center in Orlando, Florida.

Paul Hennessy | NurPhoto | Getty Images

Moderna is increasing its Covid-19 vaccine production this year, increasing the expected minimum dose by 20% to 600 million, the company said on Monday.

The company says it is working to produce up to 1 billion doses of its Covid vaccine this year. The U.S. is well on its way to securing 100 million shots of Moderna’s vaccine by the end of March and an additional 100 million by June, the Massachusetts-based company said in a statement.

The U.S. Food and Drug Administration granted Moderna’s emergency coronavirus vaccine approval to anyone age 18 and older in the U.S. in December and started the drug’s first launch.

The federal government has agreed to buy 200 million doses of Moderna’s vaccine, with an option to secure an additional 300 million, the company said.

Moderna’s Covid-19 vaccine, which uses the new mRNA technology and requires two doses four weeks apart, has also been approved in Canada for people aged 18 and over. The company has agreed to supply this country with 40 million doses of its vaccine, with the option to provide an additional 16 million.

“Our effectiveness in delivering early supplies to the US and Canadian governments, as well as our ability to increase baseline production estimates for 2021, are both signals that our increase in mRNA vaccine production is a success,” said Juan Andres, director made a statement to Moderna’s technical department.

The U.S. government, under the Trump administration’s Operation Warp Speed, said it would distribute close to 6 million doses of Moderna’s vaccine in an emergency once FDA approved.

The introduction of the vaccine in the nation has been slower than originally planned. So far, the US has only distributed more than 13 million doses of vaccine, but given only 4.2 million “shots in the arms,” ​​according to data from the US Centers for Disease Control and Prevention, last updated on Saturday. By the end of December, officials wanted to vaccinate 20 million people with Pfizers and Moderna’s two-dose vaccines against Covid-19.

Minister of Health and Human Services Alex Azar defended the operation’s vaccine distribution Monday on ABC’s Good Morning America. He said there was a delay in getting the cans first made available, ordered by the states, and then delivered, all of which was slowed down by the holidays.

However, the US has seen a “rapid uptake” of vaccines in the past few days, Azar said.

“We said our goal is to actually have 20 million first doses available by December. Those are available,” said Azar. It is unclear what Azar meant when he said the cans were “available” as only 13 million were distributed in the US on Saturday morning.

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U.S. may ramp up sluggish Covid vaccinations by giving two half doses of Moderna shot

A FDNY EMS Fire Department employee receives a COVID-19 Moderna vaccine amid the coronavirus disease (COVID-19) pandemic in the Manhattan neighborhood of New York City, New York, United States. December 23, 2020.

Carlo Allegri | Reuters

The head of the federal government’s Covid-19 vaccination program said Sunday that health officials are considering the idea of ​​giving a large group of Americans half-volume doses of a vaccine to speed up adoption.

Moncef Slaoui, head of Operation Warp Speed, said on CBS’s “Face the Nation” that one way to speed up immunization against Covid-19 is to give some people two half-volume doses of the Moderna vaccine.

“We know that for the Moderna vaccine, half the dose is given to people between the ages of 18 and 55 – two doses, half the dose, which is exactly the goal of getting twice the number of people using the doses immunize that we have – we know it induces an identical immune response to the 100 microgram dose, “Slaoui said.

“And that’s why we’re in talks with Moderna and the FDA – of course it will ultimately be a decision of the FDA – to accelerate the injection of half the volume,” he added.

Moncef Slaoui, a former executive director of GlaxoSmithKline, speaks to President Donald J. Trump during a vaccine development event in the Rose Garden of the White House on Friday, May 15, 2020 in Washington, DC.

Jabin Botsford | The Washington Post | Getty Images

The comments came in response to why the US is not adopting the strategy of giving all available vaccine doses now, even though the approved vaccines require a second round of firing to be fully effective. The UK has taken this approach in the hope that continued production will enable the second recordings in the future.

Slaoui said it was a mistake to make a decision that was not supported by the experimental data. White House Health Advisor Dr. Anthony Fauci, commented similarly on NBC’s Meet the Press on Sunday, said the strategy “goes against science” and would not solve the problems with the US launch.

“The idea of ​​expanding it so you can get more people is when you don’t have enough vaccine and a lot of people are waiting in line to wait for a vaccine,” Fauci said. “That’s not our problem now. We have a vaccine. We have to get it into people’s arms. It really is the right solution to the wrong problem.”

The FDA and Moderna did not immediately respond to requests for comment.

The dispute over different vaccination approaches stems from the fact that the introduction of the vaccine in the US did not achieve the goals of Operation Warp Speed ​​and the pandemic continues to devastate the country. President Donald Trump has blamed states for the slow adoption as the number of vaccinations given lags behind the number of vaccines sent and delivered.

Health officials wanted to inject a vaccine to 20 million Americans by the end of the year. However, according to the Centers for Disease Control and Prevention, only about 4.2 million people had received gunfire by January 2.

The last 7-day average for new cases of the coronavirus in the US is 205,093, according to John Hopkins University. That number has grown by 8% week-to-week, although tests and reports tended to be inconsistent during the holiday season. According to Johns Hopkins, the nation has an average of more than 2,600 deaths a day attributed to the virus.