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Monday, January 4, 2021

New York finds first case of more contagious, 'UK' strain of coronavirus

 New York Governor Andrew Cuomo says his state has found its first case of the more contagious, "UK" strain of the coronavirus, raising concerns about threats to hospital capacity should it spread rapidly in the state.

Cuomo says on Monday that a man in his 60s living in a town north of Albany has the new strain. The man, who is recovering, had not traveled recently, suggesting community spread is taking place. New York has carried out 5,000 tests for the new strain - and so far has only found the one case. Cuomo says it could be a "game changer" if the new strain increases hospitalizations and forces regions to close down.

https://www.marketscreener.com/news/latest/New-York-finds-first-case-of-more-contagious-UK-strain-of-coronavirus--32118789/

Genmab in Phase 3 Trial of Tisotumab Vedotin in Cervical Cancer

Genmab announced today the initiation of innovaTV 301 trial, a global phase 3 study to evaluate the efficacy of tisotumab vedotin compared to chemotherapy in patients with recurrent or metastatic cervical cancer who have received one or two prior lines of systemic therapy. The innovaTV 301 trial is a global, randomized phase 3 trial in which tisotumab vedotin will be compared with physician’s choice single agent chemotherapy.

“Currently, there is no established standard of care for women with recurrent or metastatic cervical cancer, who have disease progression after first or second line of therapy. There is a need for a novel, safe and effective treatment option that can improve the clinical outcome for these patients,” said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab. “We look forward to the innovaTV 301 trial which is designed to support potential regulatory applications for marketing approval globally and serve as a confirmatory trial for a potential accelerated approval in the US for patients with metastatic or recurrent cervical cancer.”

https://www.globenewswire.com/news-release/2021/01/04/2152892/0/en/Genmab-Announces-Phase-3-Trial-of-Tisotumab-Vedotin-in-Recurrent-or-Metastatic-Cervical-Cancer.html

Provention Files Application, Priority Review for Teplizumab for Delay, Prevention of Type 1 Diabetes

 Provention Bio, Inc. (Nasdaq: PRVB), a biopharmaceutical company dedicated to intercepting and preventing immune-mediated disease, today announced that the Biologics License Application (BLA) for teplizumab for the delay or prevention of clinical type 1 diabetes (T1D) in at-risk individuals has been filed by the U.S. Food and Drug Administration (FDA). The FDA also granted Provention's request for Priority Review and assigned a user fee goal date of July 2, 2021, under the Prescription Drug User-Fee Act (PDUFA).

"The FDA's acceptance of our BLA represents a significant achievement for Provention Bio in our mission to deliver the first potential disease-modifying T1D therapy and drive a paradigm shift in how individuals at risk of developing the disease are treated," stated Ashleigh Palmer, CEO and Co-Founder, Provention Bio. "We intend to work closely with the FDA to support their review while also preparing for a potential product launch in the third quarter of 2021."

In its acceptance letter, the FDA stated that it is currently planning to hold an advisory committee meeting, tentatively scheduled for May 27, 2021.

https://www.prnewswire.com/news-releases/provention-bio-announces-us-fda-filing-of-a-biologics-license-application-bla-and-priority-review-for-teplizumab-for-the-delay-or-prevention-of-clinical-type-1-diabetes-in-at-risk-individuals-301199992.html

Chinese cancer biotech Gracell Biotechnologies sets terms for $150M IPO

Gracell Biotechnologies, a Phase 1 Chinese biotech developing CAR-T cell therapies for cancer, announced terms for its US IPO on Monday.


The Suzhou, China-based company plans to raise $150 million by offering 8.8 million ADSs at a price range of $16 to $18. At the midpoint of the proposed range, Gracell Biotechnologies would command a fully diluted market value of $1.1 billion.

The company aims to disrupt conventional approaches to CAR-T cell therapies with its two proprietary technology platforms, FasTCAR and TruUCAR. Its lead FasTCAR-enabled candidate, GC012F, has achieved multiple minimal residual disease, negative stringent complete responses in relapsed or refractory multiple myeloma patients in an ongoing investigator-initiated Phase 1 trial in China. Its lead TruUCAR-enabled allogeneic product candidate, GC027, has achieved multiple complete responses in relapsed or refractory T cell acute lymphoblastic leukemia patients in an ongoing investigator-initiated Phase 1 trial also being performed in China.

Gracell Biotechnologies was founded in 2017 and plans to list on the Nasdaq under the symbol GRCL. Citi, Jefferies, Piper Sandler and Wells Fargo Securities are the joint bookrunners on the deal. It is expected to price during the week of January 4, 2021.

Amazon-Berkshire-JPMorgan venture to disrupt healthcare is disbanding

 Haven, the joint venture formed by three of America’s most powerful companies to lower costs and improve outcomes in health care, is disbanding after three years, CNBC has learned exclusively.

The company began informing employees Monday that it will shut down by the end of next month, according to people with direct knowledge of the matter.

Many of the Boston-based firm’s 57 workers are expected to be placed at AmazonBerkshire Hathaway or JPMorgan Chase as the firms each individually push forward in their efforts, and the three companies are still expected to collaborate informally on healthcare projects, the people said.

The announcement three years ago that the CEOs of Amazon, Berkshire Hathaway and JPMorgan Chase had teamed up to tackle one of the biggest problems facing corporate America – high and rising costs for employee health care  – sent shock waves throughout the world of medicine. Shares of healthcare companies tumbled on fears about how the combined might of leaders in technology and finance could wring costs out of the system.

The move to shutter Haven may be a sign of how difficult it is to improve American health care, a complicated and entrenched system of doctors, insurers, drug makers and middle men that costs the country $3.5 trillion every year. Last year, Berkshire CEO Warren Buffett seemed to indicate as much, saying that were was no guarantee that Haven would succeed in improving health care.

Brooke Thurston, a spokeswoman for Haven, confirmed the company’s plans to close and gave this statement:

The Haven team made good progress exploring a wide range of healthcare solutions, as well as piloting new ways to make primary care easier to access, insurance benefits simpler to understand and easier to use, and prescription drugs more affordable,” Thurston said in an email.

“Moving forward, Amazon, Berkshire Hathaway, and JPMorgan Chase & Co. will leverage these insights and continue to collaborate informally to design programs tailored to address the specific needs of our individual employee populations and locations,” she said.

https://www.cnbc.com/2021/01/04/haven-the-amazon-berkshire-jpmorgan-venture-to-disrupt-healthcare-is-disbanding-after-3-years.html

Britain takes a gamble with Covid-19 vaccines, upping stakes for others

 


In an extraordinary time, British health authorities are taking extraordinary measures to beat back Covid-19. But some experts say that, in doing so, they are also taking a serious gamble.

In recent days, the British have said they will stretch out the interval between the administration of the two doses required for Covid-19 vaccines already in use — potentially to as long as three months, instead of the recommended three or four weeks. And they have said they will permit the first dose and second dose for any one person to be from different vaccine manufacturers, if the matching vaccine is not available.

The moves are borne of a desire to begin vaccinating as many people as quickly as possible, particularly with Britain facing high levels of transmission of an apparently more infectious form of SARS-CoV-2, the virus that causes Covid-19.

But they are also effectively turning that country into a living laboratory. The moves are based on small slices of evidence mined from “subsets of subsets” of participants in clinical trials, as one expert described it for STAT, and on general principles of vaccinology rather than on actual research into the specific vaccines being used. If the efforts succeed, the world will have learned a great deal. If they fail, the world will also have gained important information, though some fear it could come at a high cost.

American health officials have dismissed the possibility that the U.S. would follow Britain’s lead, with Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, saying the vaccines in use — one made by Moderna, the other by the Pfizer and BioNTech partnership — will be deployed here using the schedules that were tested in Phase 3 trials that generated the evidence on which the Food and Drug Administration authorized the vaccines for emergency use.

While data from both suggest the vaccines start to protect about 10 or 12 days after the first dose, it’s not known how long that initial protection lasts. In clinical trials, levels of neutralizing antibodies, which are thought to play a critical role in protecting against infection, were not substantial after the first dose of vaccine for the Pfizer vaccine.

“While we think that single shot could give protection for more than four weeks, we just don’t know that. We don’t know when it’s going to drop off,” said John Mascola, director of NIAID’s Vaccine Research Center. Mascola said Operation Warp Speed, the federal government’s project to fast-track Covid vaccines, ruled out the possibility of altering vaccination schedules before Britain decided to do so.

Paul Bieniasz of Rockefeller University is one of those who is watching the evolving situation in Britain with dread. A retrovirologist who turned from HIV research to work on SARS-2, Bieniasz is studying how the virus acquires mutations that allow it to evade the protective antibodies people develop when they have contracted Covid-19, or when they have been vaccinated against it. 

Bieniasz believes Britain is replicating in people the experiments he’s been doing in his lab — and could be fostering vaccine-resistant forms of the virus. 

On New Year’s Day he posted a short, sarcastic treatise — “Musings of an anonymous, pissed off virologist”— on Twitter outlining how one could go about rendering Covid vaccines “impotent,” if that was one’s goal. Giving millions of people who are at daily risk of contracting the disease incomplete protection by delaying the second dose of vaccine was key, he suggested. 

“My concern, as a virologist, is that if you wanted to make a vaccine-resistant strain, what you would do is to build a cohort of partially immunized individuals in the teeth of a highly prevalent viral infection,” Bieniasz told STAT. Even rolling out the vaccine at all when there is so much transmission occurring is far from ideal, he said, suggesting it would have been safer to beat down the amount of virus in circulation before beginning the vaccine deployment.

“You are essentially maximizing the opportunity for the virus to learn about the human immune system. Learn about antibodies. Learn how to evade them,” he said.

Isabella Eckerle, a coronavirus researcher at the Geneva Center for Emerging Viral Diseases, shares Bieniasz’s concern that Britain is increasing the potential for so-called escape mutants. She understands the public health imperative behind its approach, but worries about having large numbers of partially protected people for several months at a stretch. Britain is vaccinating its oldest citizens first. The immune systems of the elderly don’t function as well as those of younger adults; some will inevitably contract Covid while waiting for their second dose of vaccine, she said.

Reports of partially vaccinated people contracting Covid may also erode confidence in the vaccines, Eckerle said: “If we fail to use this vaccine in a good way, it will damage the whole field of vaccinology for many, many years, I think.”

Stephen Goldstein, a virologist at the University of Utah who specializes in coronaviruses, said that taking Britain’s approach at a time of limited supply of vaccine could create other problems. 

“If we vaccinate everybody with one dose and … six weeks later, the efficacy is now like 30% and we don’t have the doses to boost them at that point because we’ve used up their second doses on another round of first doses, it’s a disaster potentially,” he said.

Not everyone agrees there is a disaster in the making. Some believe it makes sense, given Britain’s surge in cases and the rapid spread there of the B.1.1.7 variant, which studies suggest may be 50% more transmissible than the viruses it is quickly replacing.

“At the core of my being, I really wish that we could adhere to the original schedule of vaccines, because that’s the safest thing to do,” said Akiko Iwasaki, a virologist and immunologist at Yale University who tweeted about her support for the British approach. “But seeing what’s happening in the world and just sort of looking at the situation of poor rollout and distribution, I’m feeling frustrated that we need to come up with some other options.”

(Iwasaki was dismayed, though, to realize Britain’s instructions to clinicians that they could use a non-matching second dose of vaccine if that is their only option was not going to be done in the context of a clinical trial. While there is reason to believe boosting with a different type of vaccine might actually be useful in some cases — particularly if the first dose is a vaccine like the AstraZeneca vaccine that uses a harmless virus onto which genetic material from SARS-2 has been fused — the approach has not been studied at all in clinical trials. 

“They’re kind of wasting the opportunity if they’re just sort of randomly doing it and not even following up on the effectiveness of that combination,” Iwasaki said. “So yeah, I’m a lot more comfortable if it was a trial of some sort.”)

Rajeev Venkayya, president of global vaccines for Takeda Pharmaceuticals, also believes Britain’s decision to stretch out the interval between vaccine doses is “justifiable.” 

“Of course we would all want to see vaccines used exactly as they were tested in Phase 3 efficacy trials. I don’t think there’s any debate about that. The question is: Do you have evidence to support flexibility? And here, I do think that — and this is specific to the AstraZeneca vaccine — it does appear that there is additional evidence that can support a modified recommendation,” said Venkayya, who served as special assistant to President George W. Bush and senior director for biodefense. In that role, Venkayya was the White House point person for pandemic preparedness efforts triggered by the spread of H5N1 bird flu.

While the U.S.-based trial of the AstraZeneca vaccine is testing two doses given four weeks apart, studies the company conducted elsewhere gave some participants the two doses at intervals of six to eight weeks, or nine to 11 weeks, and some received the doses at an interval greater than 12 weeks.

The Pfizer and Moderna vaccines are the first using mRNA technology, and the companies did not study those extended dosing schedules. Pfizer has objected to the proposal that the vaccine be used with a longer interval between vaccinations.

Venkayya, whose thinking is influenced by his years in the White House, said sometimes policy has to be made without perfect data. 

“I think that to take the standards that we typically apply to the body of evidence we require before reaching decisions and recommendations on how to use vaccines, that by necessity has to change in the midst of a crisis like this,” he said. “I think there is the way we do medicine and public health in peacetime … where we have the luxury of taking the time we need and investing the resources and effort to collect enough data to reach a conclusion. You just don’t have that luxury in the midst of a crisis.”

https://www.statnews.com/2021/01/04/britain-takes-a-gamble-with-covid-19-vaccines-upping-the-stakes-for-the-rest-of-us/

5 key milestones in the Covid-19 pandemic anticipated in 2021

On the first day of fall, STAT published its best guesses of 30 moments to come in the pandemic that could mark a change in its course or serve as a time to reflect on how Covid-19 had reshaped our lives.

In reality, some of the turning points have turned out better than they could have. Schools, particularly for younger children, seem to be safer than initially feared, although many students continue to be stuck with virtual classes. Separately, the vaccine regulatory reviews rebuffed potential political interference, with the candidates going through the process of obtaining emergency authorization with the regular rigor.

At the same time, the U.S. epidemic has grown even more dire. We knew the fall would be bad, but with new records of infections, hospitalizations, and deaths regularly being set, and many states not implementing intensive strategies in response (to say nothing about any sort of federal initiative to rein in transmission), the outlook continues to worsen. As an example, we had speculated the country would hit 250,000 deaths from Covid-19 in late November. Instead, the country crossed that mark in mid-November, a sign of how transmission accelerated.

Now, we’re taking another look ahead, to milestones in the next year that we’ll be watching to see if and how they redirect the pandemic and what they signal about the progress in the fight against the coronavirus.

If 2020 was defined by the explosion of the SARS-CoV-2 virus, 2021 could be about its dwindling. But how many people will fall ill, and die, as that happens is dependent on our leaders, individuals, vaccine makers, and public campaigns to encourage people to get the Covid-19 shots developed with unprecedented speed.

As always when making forecasts, some of these moments could take place in different ways or at different times than charted out below.

Jan. 20 — Inauguration of Joe Biden

With the president-elect’s team already telling people to stay home for the inauguration, the formal start of the Biden administration won’t look like past transition-of-power ceremonies. The absence of throngs of people on the National Mall will be a stark reminder that the top job for President Biden will be Covid-19.

His administration will take over the vaccine rollout, ensuring that the logistical web of distributing hundreds of millions of doses continues apace and that Americans get the shots as they become available. But Biden will also likely be inheriting an out-of-control viral outbreak in some places. He won’t be able to snap his fingers and put the country on a new path immediately, but there could be a more forceful federal campaign to rally the country to slow transmission.

Biden has been modeling the precautionary behavior experts say can put a drag on spread, and has urged Americans to wear masks. His advisers have previewed that a Biden administration will get more involved in efforts like procuring testing supplies and PPE. And he’ll need to chart the country’s recovery from the ongoing economic fallout.

Biden has stressed that he’ll let science lead the U.S. Covid-19 strategy. Expect to see more briefings from career government employees. Biden’s health officials will become leaders of agencies that to varying levels have been subject to intervention from the Trump White House and suffered reputational blows. Restoring credibility and independence will take time, but the task for the Biden administration starts on this day.

Late January — 400,000 deaths

The country hit 300,000 deaths from Covid-19 in the middle of December, so it seems unbelievable that another 100,000 could be dead by the end of January. But with more than 2,000 or even 3,000 people dying some days, that’s how quickly the toll goes up. Given the number of people currently infected, transmission at the levels it is, and the resistance to the most extreme interventions in many places, the ball is already rolling.

A cognitive dissonance will pervade early 2021. Based on the number of hospitalizations and deaths, the U.S. epidemic could be at its worst point yet. At the same time, more and more people will be getting vaccinated. The disconnect shows how deep of a hole the country is in, and how it will take months for enough people to get immunized to noticeably reduce the number of new symptomatic cases.

Care for Covid-19 has improved over the months, and people are now more likely to survive an infection than in March (that is, as long as hospitals aren’t overwhelmed). But that progress has come in the absence of groundbreaking treatments cooked up for Covid-19. U.S. regulators approved the antiviral remdesivir to treat hospitalized patients, but it’s just been shown to speed recovery, not to save lives. Monoclonal antibodies can help people with mild illness from progressing to more serious disease, but they have run into issues reaching patients. It’s still not clear whether convalescent plasma is effective for Covid-19. In fact, the most important therapy for the pandemic has been an old, cheap steroid called dexamethasone, which has been shown to reduce deaths in people with the most severe cases.

Scientists far outpaced expectations as they developed vaccines in record time, but they have not had the same success with therapies. That could change in 2021, however, with oral antivirals from Atea Pharmaceuticals and Merck/Ridgeback Biotherapeutics, for example, among a number of possible treatments moving through clinical trials.

End of June — Status update on vaccinations

There are various estimates for when vaccines will be widely available to Americans. But during the first half of the year, supplies from Moderna and Pfizer/BioNTech will grow, and the U.S. could also see the arrival of shots from such companies as Johnson & Johnson, AstraZeneca, and Novavax, depending on clinical trial data and regulatory authorization.

Let’s say (hope?) that, broadly, Americans will have the opportunity to get immunized in the first half of the year (at least adults — vaccines for children might not be available until later). The question then becomes, how many will do so? Polling data has indicated a warming toward the shots among people who had been hesitant about the vaccines, and experts think that seeing millions of people get what trials have shown to be highly effective vaccines will reassure some who might have otherwise been nervous.

But as scientists are quick to say, even the best vaccines won’t do much unless lots of people get them. The purpose of the vaccine campaign is to get as much uptake as possible — the way to get to herd immunity, and an end to the pandemic. By the start of the summer, we should have a good idea of whether the campaign is finding success in connecting with target communities — including people of color and those who don’t have access to regular medical care — and what portion of people are willing to roll up their sleeves.

July 23 — The Olympics begin in Japan

The games, originally scheduled for 2020, will begin in Japan after more than a year when big gatherings were verboten in many places and international travel evaporated. What will this Olympiad look like? Will fans be streamed in virtually like in the NBA bubble? What kind of testing and quarantine steps will athletes, coaches, and trainers have to pass through? It might be jarring for competitors from places that have successfully contained the virus to endure such a rigmarole that’s required because other countries haven’t put a lid on their epidemics.

But we’re not just interested in the Olympics to see how organizers pull off such a massive event. By the time the starter’s pistol fires for this ultimate expression of international goodwill, there could be a massive global divide in vaccine coverage. Wealthy countries have been trying to scoop up as many millions of doses as possible for themselves, while experts have warned that immunizations won’t be more widely available in some low- and middle-income countries until 2022. Depending on the success of campaigns to broaden vaccine access, it’s possible that by the summer, countries will still be competing for vials, not just for medals.

November and December — The holidays

The holidays in 2020 were a lonely stretch for some, and the source of infection for others who didn’t heed warnings not to travel nor to celebrate with people outside their households. A year later, the festivities should be much safer, and jollier to boot.

But what an end to a pandemic looks like remains abstract. It won’t just happen one day, like waking up on Christmas morning. Experts describe a gradual easing of restrictions and strategies, as more activities we’ve spurned become safe again as the virus recedes. SARS-2 likely won’t be eradicated, and cases could crop up if not enough people get vaccinated. But if all goes to plan, the holidays — at least in the U.S. — should be a time to celebrate making it through, and perhaps to consider all that was lost.

Still, we won’t be free of the ghost of Covid past. The effects of the pandemic will be felt for years to come. At a minimum, scientists will still be studying the long-term protection and effects from vaccines, which will affect how frequently people will need booster shots. They’ll also be on the lookout for significant mutations to the virus, like those that emerged recently in the U.K., that could potentially allow it to evade the protection afforded by the vaccines — and for other pathogens that could ignite the next pandemic.

https://www.statnews.com/2021/01/04/five-key-milestones-in-the-covid19-pandemic-2021/