Category: Covid-19 Vaccine

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Creation of COVID-19 vaccine creating fears in some people – WRAL.com

May 20, 2020

By Leslie Moreno, WRAL reporter

Chapel Hill, N.C. Researchers are closer to creating a vaccine for COVID-19. The news has been met with both comfort and fear.

A professor at the Carolina Population Center in Chapel Hill says theres a long history of concern when it comes to vaccines. Because of the current rush to find a solution to the coronavirus outbreak, these fears may be intensified.

A lot of companies are throwing every bit of effort they have at producing one, fast,Paul Delamater said.

According to the World Health Organization, more than 70 potential vaccines are currently being developed, all of which are at various stages of development.

I do think people will want to get the vaccine a little more than like the regular vaccine every year, Delamater, said.

But some people are hesitant.

Its way too soon in my opinion," Trenton Lassiter said. "Usually it takes months and years to develop a vaccine for viruses.

Lassiter also said he feels a vaccine is being rushed. He has concerns about long-term side effects and the amount of time in which the vaccine would be created.

Im hearing that the normal procedures arent being followed as far as developing the vaccine, compared to other viruses in the past, because theyre in such a tight schedule. Some things arent being checked off like they would be, so theyre rushing through the process," Lassiter, said.

Delamater said these fears are very common, especially with such a new virus.

The people that refuse to take vaccines tend to do so for a couple of reasons one is concerns about the contents of the vaccine and not wanting it in their body and the other is the state or the nations role, Delamater, said.

According to latest figures from the Johns Hopkins Coronavirus Resource Center, the virus has infected more than 4.5 million people across the world, killing over 300,000.

The FDA can fast-track vaccines, and that would speed up the testing and approval process.

A lot of things have to go right before we can start vaccinating the population, Delamater, said.

According to the World Health Organization, if all goes well, researchers hope to have a vaccine out by the second half of 2021.

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Bharat Biotech and Thomas Jefferson partner on Covid-19 vaccine – Pharmaceutical Technology

May 20, 2020

]]> The new Covid-19 vaccine candidate was created using an existing deactivated rabies vaccine as a vehicle for coronavirus proteins. Credit: pearson0612 from Pixabay.

India-based Bharat Biotech has entered into an exclusive agreement to develop a Covid-19 vaccine candidate created at Thomas Jefferson University in Philadelphia, US.

Infectious Diseases expert professor Matthias Schnells lab created the vaccine candidate in January using an existing deactivated rabies vaccine as a vehicle for coronavirus proteins.

This approach, used as a vehicle or carrier vaccine, is known to generate a strong immune response, authorised for the whole population, including children and pregnant women.

In preliminary tests in animal models, the vaccine demonstrated a strong antibody response in mice. Currently, the researchers are evaluating if vaccinated animals are protected from Covid-19 infection and results are expected to be available next month.

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Schnell noted: Our partnership with Bharat Biotech will accelerate our vaccine candidate through the next phases of development. We will be able to complete animal testing and move to Phase I clinical trial rapidly.

As part of the licence agreement, the company gets exclusive rights to develop, market and deliver Jeffersons vaccine globally, excluding some countries such as the US, Europe and Japan, where Jefferson is seeking partners.

With the Indian governments Department of Biotechnology support, the company intends to advance the vaccine candidate into human trials as early as December this year.

Bharat Biotech CEO Dr Krishna Mohan said: In view of the imminent demand for an effective vaccine, Bharat Biotech is pleased to collaborate with Thomas Jefferson, USA towards developing a new vaccine for Covid-19 using an inactivated rabies vector platform.

Bharat Biotech is committed to global public health and will be involved in an end to end development of the vaccine including comprehensive clinical trials to achieve commercial licensure.

Last month, Bharat Biotech partnered with FluGen and the University of WisconsinMadison (UWMadison) to develop and evaluate a Covid-19 vaccine candidate, CoroFlu.

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Bharat Biotech and Thomas Jefferson partner on Covid-19 vaccine - Pharmaceutical Technology

COVID-19 trial vaccine volunteer thrives after second injection – FOX 5 Atlanta

May 20, 2020

Emory holds COVID-19 vaccine trial

An Atlanta man has received his second injection as part of a COVID-19 vaccine trial by Emory.

ATLANTA - While Norman Hulme shelters in place working from home as a graphic artist for Emory University, he takes comfort knowing the injections, the multiple blood draws and every note in his daily journal could make a big difference in the fight against the COVID-19.

"To be able to participate in a trial vaccine was really important to me. The ultimate goal is to have a vaccine that everybody can use," Hulme told FOX 5's Portia Bruner.

One month and two injections into the 14-month-long Emory COVID-19 vaccine trial, Hulme said he's more than willing to log every step of his journey. Monday, at the Emory Hope Clinic, he received the second of two injections necessary to determine whether participants develop antibodies.

"It's kind of like getting a flu shot they just put it in the arm of your choice and then observe you for an hour afterward to make sure there's no immediate reaction. I have to keep a diary of any other things like pains or headaches or any nausea," said Hulme, who has not experienced any side effects following his two injections.

The 65-year-old Decatur man is one of the first Americans to test this experimental vaccine against the coronavirus. Researchers first gave it to a small group of younger adults in March. The Emory University graphic artist received his first injection in April with other men and women between the ages of 56 and 70.

"I think everybody has to do their part for this because really because it really does impact literally everyone in the world.

Emory, Kaiser Permanente Washington and the Vaccine Research Center at the NIH are testing this experimental vaccine made by the biotech Moderna. The vaccine uses genetic material from that spike protein on the surface of this coronavirus to help the immune system recognize and fight the deadly virus.

"This is really our World War. this is really our moment as people and global citizens and I think everyone needs to do their part wherever they can fit in and this little bit seemed to be what I could do with this point in time," said Hulme has who not contracted coronavirus.

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COVID-19 trial vaccine volunteer thrives after second injection - FOX 5 Atlanta

As we wait for a vaccine, heres a snapshot of potential COVID-19 treatments – Science News

May 20, 2020

Aggressive public health measures tostem the tidal wave of coronavirus infections have left people isolated,unemployed and wondering when it will all end. Life probably wont gocompletely back to normal until vaccines against the virus are available,experts warn.

Researchers are working hard on thatfront. At least six vaccines are currently being tested in people, says EstherKrofah, chief executive of the FasterCures center at the Milken Institute in Washington,D.C. We expect about two dozen more toenter clinical trials by this summer and early fall. That is a huge number,Krofah said at an April 17 briefing. Dozens more are in earlier stages oftesting.

In unpublished, preliminary results of a test of one vaccine, inoculated people made as many antibodies against the coronavirus as people who have recovered from COVID-19 (SN: 5/18/20). The mRNA-based vaccine induces human cells to make one of the viruss proteins, which the immune system then builds antibodies to attack. That study was small, only eight people, but a second phase of safety testing has begun.

But vaccinestake time to test thoroughly (SN: 2/21/20). Even with acceleratedtimelines and talk of emergency use of promising vaccines for health care workersand others at high risk of catching the virus, the general public will likelywait a year or more to be vaccinated.

In the meantime, new treatments may helpsave lives or lessen the severity of disease in people who become ill.Researchers around the world are experimenting with more than 130 drugs to findout if any can help COVID-19 patients, according to atracker maintained by the Milken Institute.

Some of those drugs are aimed atstopping the virus, while others may help calm overactive immune responses thatdamage lungs and other organs. Although researchers are testing a battery ofrepurposed drugs and devising new ones, there is still a great deal ofuncertainty over whether the drugs help, or maybe even hurt.

The wait is frustrating, but theres still much doctors and scientists dont know about how this new coronavirus affects the body. Getting answers will take time, and finding measures to counter the virus that are both safe and effective will take even more. Early results suggest that the antiviral drug remdesivir can modestly speed recovery from COVID-19 (SN: 5/13/20). It is not a cure, but the drug may become the new standard of care as researchers continue to test other therapies.

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Antiviral drugs interfere with a viruss ability to replicate itself, though such drugs are difficult to create. Remdesivir is being tested in half a dozen clinical trials worldwide. The drug mimics a building block of RNA, the genetic material of the coronavirus (SN: 3/10/20). When the virus copies its RNA, remdesivir replaces some of the building blocks, preventing new virus copies from being produced, laboratory studies have shown.

Early results in COVID-19 patients given the drug outside of a clinical trial showed that 68 percent needed less oxygen support after treatment, as reported online April 10 in the New England Journal of Medicine (SN: 4/29/20). The drug went to very sick patients, including those who needed oxygen from a ventilator or through tubes in the nose. Other researchers have disputed those results, questioning the study methods and statistical analyses, which may have given an exaggerated impression of good outcomes. The studys authors say they have reanalyzed the data and still conclude that remdesivir has benefits.

Soon after, the U.S. National Instituteof Allergy and Infectious Diseases announced that hospitalized patients withCOVID-19 who got intravenous remdesivir recoveredmore quickly than those on a placebo: in 11 days versus 15. Those findingshad not been reviewed by other scientists at the time of the announcement. Thedug provides researchers with a baseline for comparing other treatments. Wethink its really opening the door to the fact that we now have the capabilityof treating, Anthony Fauci, director of the NIAID said April 29 in a newsbriefing at the White House.

Antiviral medications used against HIV are also being tested against COVID-19. The combination of lopinavir and ritonavir stops an HIV enzyme called the M protease from cutting viral proteins so that the virus can replicate itself. The SARS-CoV-2 virus produces a similar enzyme. But early results from a small study in China showed that the combination didnt stop viral replication or improve symptoms (SN: 3/19/20), and there were side effects.

For now, the Society of Critical CareMedicine recommendsagainst using the drugs, and the Infectious Diseases Society of Americasays patients should get the drugs onlyas part of a clinical trial. Several large trials may report results soon.

The HIV drugs may not work well against SARS-CoV-2, even though the viruses have similar M proteases: The coronaviruss enzyme lacks a pocket where the drugs fit in the HIV version of the enzyme.

This illustrates why antiviral drugs areso difficult to develop. Designing a drug requires knowing the 3-D structure ofthe viruss proteins, which can take months to years. But researchers arealready getting some close-up views of the new coronavirus. A team in Chinaexamined the structure of the coronaviruss M protease and designed smallmolecules that could block a part of the protein necessary to do its job. Theteam describedtwo such molecules, dubbed 11a and 11b, April 22 in Science.

In test tubes, both molecules stopped the virus from replicating in monkey cells. In mice, 11a stuck around longer in the blood than 11b, so the researchers tested 11a further and found it seemed safe in rats and beagles. More animal tests will probably be needed to show whether it stops the virus, then multiple stages of human tests will have to follow. The drug development and testing process often takes on average 10 years or more, and can fail at any point along the way.

Meanwhile, hundreds of thousands of people worldwide have already recovered from COVID-19, and many are donating blood that might contain virus-fighting antibodies. Clinical trials are under way to test whether antibodies from recovered patients blood plasma can help people fight off the virus (SN: 4/25/20, p. 6). More such trials are planned.

Stopping the virus is only half the problem. In some people seriously ill with COVID-19, their immune system becomes the enemy, unleashing storms of immune chemicals called cytokines. Those cytokines trigger immune cells to join the fight against the virus, but sometimes the cells go too far, causing damaging inflammation.

Some of the drugs used to calm cytokines in cancer patients (SN: 6/27/18, p. 22) may also help people with COVID-19 ride out the storm, says cancer researcher Lee Greenberger, chief scientific officer of Leukemia and Lymphoma Society. Several of those drugs are being tested against the coronavirus now.

Hydroxychloroquine, a drug approved totreat autoimmune disorders such as lupus and rheumatoid arthritis, became ahousehold word after President Trump touted it as a possible COVID-19treatment.

The drug is being tested in numerouslarge clinical trials around the world to see if it might help calm cytokinestorms in COVID-19 patients as well. But so far, there is no solid evidence thatit works either to prevent infection in people or to treat people who alreadyhave the disease.

And in some studies the drug has caused serious side effects, including causing irregular heartbeats, says Raymond Woosley, a pharmacologist at the University of Arizona College of Medicine in Phoenix. People with heart problems, low potassium or low oxygen levels in their blood are at higher risk of these side effects, he says. And those are exactly the kinds of patients who are most vulnerable to COVID-19. So, the very sickest COVID patients are those at most risk for these life-threatening arrhythmias and cardiac effects.

Results of some rigorous clinical trialsof hydroxychloroquine are expected this summer. Meanwhile, the U.S. Food andDrug Administration allows the drug to be used when no other treatment isavailable and patients cant join a clinical trial.

Todays enthusiasm for any drug thatseems promising feels familiar, says Woosley. He remembers the excitement overAZT, the first drug used to fight HIV in the 1980s. It wasnt the best drug tocombat the AIDS epidemic, and better ones came later. Likewise, the firsttreatments for COVID-19 might be better than nothing, but not the best we willultimately get.

Meanwhile, we wait.

With hundreds of clinical trials going on around the world, some answers may come soon. But for now, keeping the coronavirus contained will probably require aggressive testing, tracing and isolating contacts of people who have the virus and continued social distancing.

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As we wait for a vaccine, heres a snapshot of potential COVID-19 treatments - Science News

Head of Trump’s Covid-19 vaccine program to divest more than $10M in Moderna shares after criticism – MedCity News

May 20, 2020

This illustration, created at the Centers for Disease Control and Prevention (CDC), reveals ultrastructural morphology exhibited by coronaviruses

The pharmaceutical executive tapped to lead the Trump administrations program to develop a vaccine for Covid-19 will divest his shares in one of the leading vaccine-development companies after controversy arose surrounding his holdings.

News media reported Monday that Moncef Slaoui who was named last week as head of the administrations Operation Warp Speed effort to rapidly develop Covid-19 vaccines would divest his stock options in Cambridge, Massachusetts-based Moderna, worth more than $10 million. Slaouis 156,000 options in Moderna reportedly increased in value by at least $3 million following the companys announcement Monday of preliminary data from the Phase I study of mRNA-1273, its vaccine against SARS-CoV-2. Slaoui resigned from Modernas board of directors following his appointment to lead Operation Warp Speed.

Shares of Moderna rose 30% on the Nasdaq when markets opened Monday and closed at 20% above their Friday closing price following the announcement of early data from the Phase I study.

Data from the study, which the National Institute of Allergy and Infectious Diseases is sponsoring, showed that among the first eight participants enrolled in the 25- and 100-microgram dosing cohorts, levels of neutralizing antibodies were equivalent or in excess of those seen in patients who have recovered from Covid-19. The study is enrolling 105 participants in total across three dosing cohorts, the third of which is receiving the vaccine at 250 micrograms. However, the company plans to abandon the 250-microgram dose in further testing of the vaccine, with the upcoming placebo-controlled Phase II study using 50- and 100-microgram doses and the Phase III study planned to start in July using a dose somewhere between 25 and 100 micrograms.

The other company in the lead to develop a vaccine against the Covid-19 virus is Tianjin, China-based CanSino Biologics, which has a Phase II study underway in China and plans to develop its adenovirus-based vaccine in Canada as well. Meanwhile, Pfizer and BioNTech recently began dosing participants in the trial of their vaccine, which like Modernas is a messenger RNA vaccine.

Photo: Centers for Disease Control and Prevention

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Head of Trump's Covid-19 vaccine program to divest more than $10M in Moderna shares after criticism - MedCity News

Monkeys infected with COVID-19 develop immunity in studies, a positive sign for vaccines – Reuters

May 20, 2020

CHICAGO (Reuters) - Two studies in monkeys published on Wednesday offer some of the first scientific evidence that surviving COVID-19 may result in immunity from reinfection, a positive sign that vaccines under development may succeed, U.S. researchers said on Wednesday.

FILE PHOTO: A woman holds a small bottle labeled with a "Vaccine COVID-19" sticker and a medical syringe in this illustration taken April 10, 2020. REUTERS/Dado Ruvic/Illustration

Although scientists have assumed that antibodies produced in response to the new coronavirus virus are protective, there has been scant scientifically rigorous evidence to back that up.

In one of the new studies, researchers infected nine monkeys with COVID-19, the illness caused by the novel coronavirus. After they recovered, the team exposed them to the virus again and the animals did not get sick.

The findings suggest that they do develop natural immunity that protects against re-exposure, said Dr. Dan Barouch, a researcher at the Center for Virology and Vaccine Research at Harvards Beth Israel Deaconness Medical Center in Boston, whose studies were published in the journal Science.

Its very good news, Barouch said.

Several research teams have released papers - many of them not reviewed by other scientists - suggesting that a vaccine against the virus would be effective in animals.

In the second study, Barouch and colleagues tested 25 monkeys with six prototype vaccines to see if antibodies produced in response were protective.

They then exposed these monkeys and 10 control animals to SARS-CoV-2, the official name of the novel coronavirus.

All of the control animals showed high degrees of virus in their noses and lungs, but in the vaccinated animals, we saw a substantial degree of protection, Barouch said. Eight of the vaccinated animals were completely protected.

These studies, which have been peer reviewed, do not prove that humans develop immunity or how long it might last, but they are reassuring.

These data will be seen as a welcome scientific advance, Barouch said.

Reporting by Julie Steenhuysen; Editing by Bill Berkrot

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Monkeys infected with COVID-19 develop immunity in studies, a positive sign for vaccines - Reuters

European shares inch lower on doubts over COVID-19 vaccine – Reuters

May 20, 2020

(For a live blog on European stocks, type LIVE/ in an Eikon news window)

May 20 (Reuters) - European shares headed lower on Wednesday after a downbeat session on Wall Street, as doubts over a potential COVID-19 vaccine reignited fears about the slow recovery from a looming global recession.

The pan-European STOXX 600 dropped 0.3% by 0708 GMT in its second day of fall, with banks, telecoms and travel & leisure sector stocks leading the decline.

Wall Street indexes fell more than 1% overnight after a media report questioned the validity of the results of U.S. drugmaker Modernas coronavirus vaccine trial that had sent stock markets soaring on Monday.

In a bright spot, shares of British retailer Marks & Spencer jumped 5.2% after saying that it would accelerate its latest turnaround programme as it dealt with the fallout from the coronavirus crisis and reported a 21% fall in annual profit. (Reporting by Sruthi Shankar in Bengaluru; Editing by Rashmi Aich)

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European shares inch lower on doubts over COVID-19 vaccine - Reuters

Move Over, Moderna: Why Pfizer May Be The Better Bet To Deliver A Vaccine By Fall – Forbes

May 20, 2020

The inside story behind the pandemic, the CEO and a promising, unproven treatment.

In the middle of March, Pfizer chief Albert Bourla beamed into a WebEx video call with the leaders of the American pharmaceutical giants vaccine research and manufacturing groups.The two teams had worked late into the night on a robust development plan for Pfizers experimental Covid-19 vaccine and told Bourla that they aimed to make it available lightning-fast. It could be ready sometime in 2021.

Not good enough, Bourla said. The faces of the researchers tensed up, and conscious of the Herculean effort that had taken place, Bourla made sure to thank them. But he also kept pushing. He asked if people on the call thought the virus might come back in the fall, and what they expected would happen if a vaccine were not available when a new flu season hit at the same time, an issue the federal Centers for Disease Control raised weeks later.

Think in different terms, Bourla told them. Think you have an open checkbook, you dont need to worry about such things. Think that we will do things in parallel, not sequential. Think you need to build manufacturing of a vaccine before you know whats working. If it doesnt, let me worry about it and we will write it off and throw it out.

Says Mikael Dolsten, Pfizers chief scientific officer: He challenged the team to aim for a moon shotlike goalto have millions of doses of vaccine in the hands of vulnerable populations before the end of the year.

On the first Monday of May, Pfizer dosed the initial batch of healthy American volunteers in Baltimore with an experimental Covid-19 vaccine it developed with Germanys Bio-NTech. Bourla was informed immediately. The following day, in an interview from his home in suburban Scarsdale, New York, he pointed out that it normally takes years to accomplish what Pfizer had just done in weeks. How fast we moved is not something you could expect from the big, powerful pharma, he said. This is speed that you would envy in an entrepreneurial founder-based biotech.

A Greek veterinarian who worked his way up the Pfizer corporate ladder for 25 years before becoming CEO in 2019, Bourla says nothing in his career could have prepared him for this moment. But he does believe the massive corporate transformation he has ledsteering a behemoth conglomerate (2019 sales: $51.8 billion) deeper into the high-risk, high-reward game of developing new patented medicines and away from generic drugs and consumer products like Advil and Chapstickhas prepared Pfizer.

Shot of Hope. Volunteers receive injections of Pfizers experimental Covid-19 vaccine in early May at the University of Maryland School of Medicine in Baltimore.

For Bourla, 58, the last four months have been a rollercoaster, an unending series of setbacks and victories. Pfizer is not alone in the race. Most of the worlds biggest pharmaceutical companies, including Johnson & Johnson, Sanofi, AstraZeneca and Roche, are throwing everything they can at Covid-19.

Some experts feel Bourlas timelinea viable vaccine in a matter of a few monthsis simply unrealistic. Undeterred, Bourla has tasked hundreds of researchers to scour Pfizers trove of experimental and existing medicines to look for potential therapies. Early on, he openly authorized having discussions and sharing proprietary information with rival firms, moves unheard of in the secretive world of big pharma. Bourla has made Pfizers manufacturing capabilities available to small biotech concerns and is in talks as well to make large quantities of other companies Covid-19 drug candidates.

Pfizers most prominent effort is its work with Mainz, Germanybased BioNTech, an innovative $120 million (2019 sales) outfit that is mostly known for making cancer medications. The resulting experimental Covid-19 vaccine works with messenger RNA, a bleeding-edge technology that has never resulted in a successful treatment. Pfizer is hoping to get emergency-use authorization from the U.S. government for the vaccine by October. Its unique strategy is to rapidly pit four different mRNA vaccine candidates against one another and double down on the most likely winner.

In preparation, the company is shifting production at four manufacturing plants to make 20 million vaccine doses by the end of the year and hundreds of millions more in 2021. Bourla says Pfizer is willing to spend $1 billion in 2020 to develop and manufacture the vaccine before they know if it will work: Speed is of paramount importance.

While the vaccine effort is getting most of the publics attention, Pfizer is also rushing to start a clinical trial this summer for a new antiviral drug to treat Covid-19. Additionally, its involved in a human study that seeks to repurpose Pfizers big arthritis drug, Xeljanz, for later-stage Covid-19 patients.

Being the CEO of a pharma company that can make a difference or not in a crisis like this is a very heavy weight, Bourla says. Even the way my daughter or son ask me, Do you have something or not? Every person who knows me does the same. You feel if you get it right, you can save the world. And if you dont get it right, you will not.

In January, Uur ahin, the brilliant immunologist who founded BioNTech, read an article about Covid-19 in The Lancet. ahin built BioNTech to hack human cells to go after diseases, particularly cancer, and he thought similar tech might work against the coronavirus. Soon after, ahin spoke to Thomas Strngmann, the German pharma billionaire who for years has backed ahin and his wife, immunologist zlem Treci, in their ventures. He said, This is a big disaster. He said the schools will be closed, that this will be a pandemic, Strngmann says, referring to ahin. He switched most of his team to the vaccine.

A New Reality. Pfizer CEO Albert Bourla under lockdown in his suburban New York home, from which he has directed his troops to make the impossible possible.

In February, ahin (who is also now a billionaire, as BioNTechs stock has soared) called up Kathrin Jansen, who heads vaccine research and development for Pfizer. ahin told Jansen BioNTech had come up with vaccine candidates for Covid-19 and asked if Pfizer would be interested in working with him. Uur, you are asking? Jansen replied. Of course we are interested.

Over the last few years, scientists have become intrigued by the idea of using messenger RNA, the genetic molecule that gives cells protein-making instructions, to develop medicines for cancer, heart disease and even infectious viruses by transforming human cells into drug factories. Because SARS-CoV-2, as the coronavirus is formally known, is an RNA virus, researchers like ahin focused on the idea of giving mRNA the cellular machinery to make proteins that would create virus-protecting antibodies.

An mRNA vaccine has huge advantages over a traditional one. Because it can be made directly from the genetic code of the virus, it can be invented and entered into clinical trials in a matter of weeks, rather than months or years. But theres a big downside: No one has ever successfully made one.

BioNTech is not alone in pursuing an mRNA vaccine. Moderna Therapeutics, a biotech in Cambridge, Massachusetts, also got going in January and has launched a big human trial for its mRNA vaccine, backed by $483 million from the federal government. Moderna is likewise aiming to produce millions of doses per month by the end of the year.

Pfizer was already comfortable with BioNTech. Two years ago, the two companies inked a $425 million deal to develop an mRNA flu vaccine. Pfizer was intrigued by the potential of an mRNA approach to short-circuit the process of developing a vaccine for a new strain of the flu every year. That same flexibility and speed appealed to Bourla when it came to working with a partner on a potential vaccine for Covid-19.

On March 16, Bourla convened Pfizers top executives and informed them that return on investment would not play a role in the companys Covid-19 work. This is not business as usual, Bourla told them. Financial returns should not drive any decisions.

A billion dollars is not going to break us. And I dont plan to lose it. I plan to make sure we use this product.

Pfizer signed a letter of intent with BioNTech the next day. The contract they finalized in April makes no mention of commercialization. Pfizer is bringing its enormous manufacturing, regulatory and research capabilities to the effort. BioNTech is bringing the basic science.

At the same time, Bourla made the decision to spend $1 billion on the project, so if the vaccine works, it can be made available this autumn. Pfizer will also be on the hook to pay BioNTech an additional $563 million if everything goes according to plan. A billion dollars is not going to break us. And, by the way, I dont plan to lose it. I plan to make sure we use this product, Bourla says. You never know until you see the data. So yes, we are going to lose a billion if the vaccine doesnt work.

What makes Pfizers approach unique is that its testing four distinctive vaccinesdifferent mRNA platforms that are supposed to induce a safe immune response. The complex trial will start by testing different dosing levels of the four vaccines in 360 U.S. volunteers and 200 in Germany, eventually expanding to around 8,000 participants.

The U.S. trial was designed to evolve so the company could quickly stop testing any one of the vaccines if immunogenicity data show it is not producing enough antibodies to confer virus protection. The companies are making adjustments on the fly. BioNTech recently realized one of the vaccine candidates should be dosed at a lower level to be safean early fling of a monkey wrench into the plans.

There is considerable skepticism among experts that Pfizers goal of providing millions of doses to vulnerable populations by the fall is possible. Drew Weissmann, whose University of Pennsylvania laboratory has worked with BioNTech on mRNA vaccines for infectious diseases, recently told Forbes it is simply not known if an mRNA vaccine can prevent infectious disease.

First Time. Uur ahin, the Turkish-born CEO of BioNTech. The German outfit was founded 12 years ago, but despite considerable promise it has yet to bring an approved drug to market.

Jansen, Pfizers vaccine research chief, expects that Pfizer and BioNTech will have a better idea around the beginning of July as to which of the four vaccine candidates is the most promising and whether their hyper-accelerated timeframe is feasible. The company will likely move just one or two of the most promising vaccines to more advanced trials.

Its not easy. As a matter of fact, it has never been done beforeI cant give you a probability, Jansen says. An unprecedented crisis, such as the ongoing pandemic, requires unprecedented action. Albert was the first to see that and act on it, and to provide the support and the environment for us to think and act boldly.

W

hen Albert Bourla started his run at the top of Pfizer in January 2019, he removed the bulky brown table from the CEOs conference room and did not replace it, re-arranged the chairs in a circle and put up photographs of patients on the wall. The idea was to promote open discussion and remind people about the real purpose of a pharmaceutical company. Soon after, other Pfizer employees began to put pictures on their desks of patients they know or love.

The unorthodox way Bourla took to the pinnacle of corporate power started in Greeces second-biggest city, Thessaloniki, a northern port city on the Aegean Sea. He grew up middle-classhis father and uncle owned a liquor storeas part of a tiny Jewish minority that survived the German occupation and the Holocaust.

A love of animals and science drove Bourla to become a veterinarian. At Thessalonikis Aristotle University, he was known for playing the guitar and singing, and during the summers worked as a European tour guide. He joined Pfizers Greece office in 1993, working in its animal-health division, beginning an ascent that saw him move his family to eight cities in five countries, including Poland and Belgium.

By 2014, Bourla was a high-level executive at Pfizers Manhattan headquarters on 42nd Street, where, among other things, he ran Pfizers vaccine and cancer divisions. He brought a Mediterranean flair to the buttoned-up conglomerate. His group meetings were boisterous, echoing through the otherwise largely silent corridors. He forced company units to express their metrics in terms of how many patients they were helping, not merely in terms of dollars and cents.

Making It. Pfizer is stockpiling inventory of its existing vaccines and injectable drugs to free up manufacturing capacity to make a Covid-19 vaccine later this year.

Ian Read, Pfizers Scottish-born CEO at the time, had reversed the companys fortunes on Wall Street, where its stock had been badly underperforming, by repurchasing lots of shares and divesting businesses that sold baby formula and animal medicines. Less visibly, Read reinvigorated Pfizers drug pipeline in its core vaccine business and empowered Pfizers researchers to develop targeted therapies, particularly for cancer, as some of its mass-marketed drugs, like the cholesterol-lowering blockbuster Lipitor, went off-patent.

Bourlas last job before ascending to the C-suite was as head of Pfizers innovation group. He approached the position as though he was running a life-sciences venture capital firm. He forced each of his six business units, which included oncology, vaccines and rare diseases, to compete for financing. I was telling all of them, Im your boss, I am private equity, the one who has the better ideas will get the money, he says. A company that has the scale of Pfizer and the mindset of a small biotech was always my dream.

Albert has a sense of urgency, and that is coming out in the way he is marshaling the companys resources behind trying to develop a vaccine or treatment for Covid-19, says Read, his former boss. He is a charismatic people person, energizing groups of people to get the job done.

Bourlas urgency was evident after a difficult weekend in February when he realized that Covid-19 was not going to be just a problem for China. On a call the following Monday morning, Bourla fired off instructions to Pfizers top brass. He told the science executives to make sure the companys labs remained open, and that Pfizer needed to contribute to a medical solution to the pandemic. If not us, then who? Bourla said. He instructed the manufacturing group to make a list of Pfizers drugsincluding those that treat heart failure and opportunistic bacterial infectionsthat would be in high demand in a pandemic and make sure they wouldnt be hampered by production bottlenecks. He then officially informed the board that he was pivoting the company toward Covid-19.

The better ideas will get the money. A company with the scale of Pfizer and the mindset of a small Biotech was always my dream.

One day in the midst of this retooling, Pfizer director Scott Gottlieb, who used run the FDA, left the companys Manhattan headquarters, and within hours his fears were coming to pass: Reports were emerging from California indicating community spread in America. That evening Gottlieb posted a Twitter thread: A long fight could be ahead, one requiring shared sacrifice, he saidbut partly because of Bourlas efforts at Pfizer, he could also say that development of vaccines and therapeutics was already underway.

Albert laid out early why it was so important to put up the enormous resources of Pfizer without an eye toward the business bottom line, Gottlieb says. Coming up with a vaccine could change the course of human history. That is literally whats at stake, and big companies have the ability to scale up manufacturing and run big trials in a way not available to small product developers.

In the middle of March, Bourla decided to publicly release Pfizers plan to share data from its Covid-19 research with rival pharmaceutical companies. He promised to use any excess manufacturing capacity and even shift production at Pfizers facilities away from its own products to make Covid-19 treatments from other companies. You know the saying, Bourla says. Beware [of] what you wish for.

Since then, Pfizer has heard from 340 companies. It has already given technical support to some of them and is on the brink of signing large manufacturing agreements with others. It is also in discussions with additional firms that need financing for their own Covid-19 therapies.

Will my kids go to school next fall? Bourla wonders. Im also part of society. You cannot stay silent.

Quick Kill. Thats how Kathrin Jansen, Pfizers vaccine-research chief, describes its approach to its four vaccine candidates: Terminate any vaccine thats not showing it can produce sufficient neutralizing antibodies.

At a video meeting of Pfizers board of directors in late April, Bourla was asked what would happen if multiple vaccine makers were successful. That would be the best possible outcome, he replied, because enormous amounts of vaccine could be quickly produced.

Beyond the holy grail of a vaccine, Pfizer is also trying to come up with therapeutic solutions. The researchers tasked with combing through Pfizers molecular database became intrigued by several of its antiviral compounds that might attack the virus by stopping it from reproducing. After Pfi-zer got the DNA sequence of the coronavirus in January, researchers figured out which could work best.

Conducting preclinical work on the selected compounds, however, was difficult. Pfizer had trouble finding a lab that could perform the proper assays. The company had scaled down its antiviral research a decade ago and no longer owned a suitable biosafety lab to work with the live virus. At one point, Bourla feared the lack of a lab would delay the clinical-trial process. But a separate government medical agency helped Pfizer find a good one in the Netherlands.

There have been multiple moments of bad news coming to spoil the good news you had three hours earlier, Bourla says. Pfizers laboratory work has since shown one of its protease inhibitors, initially developed to battle SARS, to exhibit antiviral activity against SARS-CoV-2. Pfizer is now aiming to start a human trial for that antiviral, which is administered intravenously, by the end of the summer.

Another Pfizer drug getting attention is Xeljanz, a rheumatoid arthritis pill generating $2.2 billion annually. It is seen as a potential way to tamp down the massive immune response to Covid-19 that overwhelms some infected patients. Pfizer is supporting a Xeljanz trial in Italian Covid-19 patients, as well as another U.S. trial that will test a different arthritis medicine, an experimental drug that targets the Irak-4 protein, against the virus.

While all this is going on, of course, Bourla still needs to run the rest of Pfizer. He recently planned a symbolic visit to a Pfizer plantnone has closedbut after making the arrangements, he was informed that he would not be allowed to enter because he was not deemed essential.

I dont know if I was ever prepared for something like this, Bourla says. But you feel that you need to suck it up and rise to the occasion because thats what you have to do.

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Move Over, Moderna: Why Pfizer May Be The Better Bet To Deliver A Vaccine By Fall - Forbes

Army general to co-lead Operation Warp Speed for COVID-19 vaccine – Theredstonerocket

May 20, 2020

President Donald Trump announced on Friday that Army Gen. Gustave Perna, the commander of Army Materiel Command, will co-lead an effort, dubbed Operation Warp Speed, to find a vaccine for COVID-19 by January 2021.

Defense SecretaryMark Esper said the Defense Department is very excited and committed to partnering with the Department of Health and Human Services, across the government, and in the private sector to accomplish the mission. Winning matters, and we will deliver by the end of this year a vaccine at scale to treat the American people and our partners abroad,he said.

The goal is to produce about 300 million vaccines by January, said Jonathan Rath Hoffman, assistant to the secretary of defense for public affairs, at a Pentagon press briefing on Friday.

Hoffman mentioned that its a goal involving a whole-of-government approach, not just the DOD.

Regarding DOD and the Pentagon, Hoffman said neither has been shut down and daily operations continue, albeit with mitigation steps that include social distancing, face masks, quarantine when necessaryand telework if the situation allows.

As for increasing the number of personnel at the Pentagon, Hoffman said it will be conditions-based and informed by medical experts. The Pentagon, he said, is in consultation with the governments of the District of Columbia, Virginia and Maryland. Policy and decisions are currently under review and are expected to be released in a matter of weeks.

Regarding the hospital ships USNS Comfort and Mercy, Hoffman said they have completed their work in New York City and Los Angeles and are standing by if their services are needed elsewhere.

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Army general to co-lead Operation Warp Speed for COVID-19 vaccine - Theredstonerocket

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