Category: Covid-19 Vaccine

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China Says It Will Have Covid-19 Vaccine Ready This Year – The Wall Street Journal

July 24, 2020

One of the first Chinese projects to start testing its Covid-19 vaccine candidates overseas said it would have a vaccine ready for the public before the end of the year.

Liu Jingzhen, chairman of state-owned China National Pharmaceutical Group, also known as Sinopharm, said on state broadcaster CCTV on Tuesday that clinical trials that began in Abu Dhabi last week should be completed in roughly three months, paving the way for a vaccine to go to the market this year.

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China Says It Will Have Covid-19 Vaccine Ready This Year - The Wall Street Journal

COVID-19 vaccine trials underway in the Valley – ABC15 Arizona

July 24, 2020

Clinical trials for a number of coronavirus vaccines are underway, and the hope is to have one available for the public by 2021, but many are pushing to make sure speed and safety go hand-in-hand.

Patients are asking me, 'How effective is it going to be?' and, 'Is it safe for me to get? Is it safe for children? Is it safe for pregnant women? Is it safe for elderly seniors?' said Dr. Andrew Carroll.

Dr. Carroll expects these questions to continue as the world creeps closer to a vaccine to fight the coronavirus.

He says transparency from all the players, the drug companies, the FDA and CDC is crucial.

And that means the good -- is it 50 percent effective? Is it 90 percent effective? Will it require one shot or two shots? Thats another question, that being answered right now, and what are the side effects, said Dr. Carroll.

These are questions that look to be answered as three vaccines enter phase three of clinical trials.

Theres no use having a vaccine thats effective if no one wants to take it, said FDA Commissioner Dr. Stephen Hahn.

He says while the timeline for a vaccine has been compressed significantly, its still facing the same rigorous process.

We will not cut corners, we realize that the American people put their faith in the FDA, we have the world's best experts looking at this, said Dr. Hahn.

He says manufacturers are already making the vaccines in huge quantities.

So that if, not when, but if the FDA decides a vaccine based upon the data and science is safe and effective, they can have vaccine ready to go, said Dr. Hahn.

Moderna, in partnership with the Hope Research Institute, is lining up volunteers from across Arizona for their phase three trial.

Weve had several thousand people reach out to us, said Hope Research Institute CEO Dr. Nathan Alderson.

Dr. Alderson says they hope to enroll as many local participants as they can for the Moderna trial.

We do need more people that are at higher risk, so healthcare workers, first responders, grocery store clerks, explained Dr. Alderson.

They also need more volunteers from minority communities.

Enrollment continues until August, and they hope to inject their first volunteer next week.

Both Pfizer and AstraZeneca are expected to begin their own phase three vaccine trials in the state within the next few weeks.

To volunteer for the clinical trial visit http://HRIAZ.com/COVID or call 602-288-HOPE

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COVID-19 vaccine trials underway in the Valley - ABC15 Arizona

Confusion spreads over selection of priority groups for Covid-19 vaccines – STAT

July 24, 2020

As manufacturers around the world race to develop Covid-19 vaccines, a parallel effort has begun to figure out who in the United States should get them first and how those doses should be distributed.

But already the effort is being complicated by tensions over who gets to make those critical decisions, with some groups feeling sidelined and multiple new actors crowding the stage.

On Tuesday, the National Academy of Medicine, tasked by top U.S. health officials, named an expert panel to develop a framework to determine who should be vaccinated first, when available doses are expected to be scarce. But that panel is ostensibly encroaching on the role of the Advisory Committee on Immunization Practices, a panel that has made recommendations on vaccination policy to the Centers for Disease Control and Prevention for decades, including drawing up the vaccination priority list during the 2009 H1N1 flu pandemic.

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There is also the matter of Operation Warp Speed, the governments vaccine fast-tracking program that has claimed authority over, among other things, distribution decisions when it comes to Covid-19 vaccines.

Amid so many players, public health experts are expressing concern and confusion.

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It seems to me like weve just assigned four different air traffic control towers to land the same plane, said Michael Osterholm, director of the University of Minnesotas Center for Infectious Diseases Research and Policy. Between ACIP, and this new committee, the group working within Operation Warp Speed and just in terms of input from the general community, its not clear to me who will make the final decision and how that process will unfold.

The health of untold numbers could hang in the balance, given that initial batches of vaccine are likely to be available only for a sliver of the population. Additionally, most vaccines will probably be given in two-dose regimens, meaning any figure of available doses would have to be divided in half to see how many people could be vaccinated.

There is no doubt that health care workers will be offered vaccines first. But after that, tough decisions will have to be made about the order in which other frontline workers which? how many? are offered priority access to vaccine and who will follow, in what order.

Normally, such decisions would fall to ACIP, which months ago set up a working group to monitor the evolving science on Covid-19 and the vaccines being developed to protect against it. But its not clear what task ACIP will be handed here.

We havent been given a firm answer as to what our role will be. We are continuing with our routine planning and discussion, and we will come up with what we think are appropriate guidelines for prioritization. But that weve not been given assurances that we will actually be contributing to that, said Jos Romero, the panels chairman.

Romero told STAT he even had applied to be on the National Academys panel after the academy urged people who were interested to nominate themselves. Romero said he never heard back. The agenda for the first public meeting of the panel, scheduled for Friday, states Romero has been invited to speak to the kickoff session. He said late Monday he hadnt received an invitation.

ACIP member Beth Bell, who chairs its Covid-19 vaccines work group, is also concerned about the National Academy panel working on vaccination priorities before ACIP.

Hopefully it wont be a parallel process and itll be something which can complement the work of the ACIP, said Bell, a professor of global health at the University of Washington and a former director of the CDCs national center for emerging and zoonotic infectious diseases.

She seemed to take some solace from the fact that former CDC director Bill Foege one of the architects of the smallpox eradication program and a revered figure in public health circles has been named co-chair of the new panel.

Foege will share chairing duties with Helene Gayle, president and CEO of Chicago Community Trust. Gayle previously worked at the CDC for 20 years on HIV/AIDS and at the Bill and Melinda Gates Foundation. In addition to the co-chairs, the 15 panelists include vaccine experts, ethicists, experts in vaccine hesitancy, global health, health policy, risk communications, and the delivery of health care to low-income populations.

Francis Collins, director of the National Institutes of Health, first asked National Academy of Medicine President Victor Dzau to create the new panel, even though setting vaccination priorities is a public health role traditionally on the CDCs turf, not the NIHs. Later a letter formally requesting that the panel be struck came from Collins and Robert Redfield, the CDC director.

In an interview, Collins seemed puzzled as to why ACIP members might be concerned about the creation of the expert panel. He said the decision-making framework the panel designs will make their job, I think, a lot more straightforward and less likely to be attacked as being capricious.

This is a discussion which is potentially going to be contentious and we want to try to minimize that, Collins told STAT.

There are certainly parts of society that are suspicious of what the government is doing, no matter what it is, he added. And this takes it out of that framework and provides an opportunity for whose sort of wisest big thinkers to gather and make this kind of a judgment about what those priorities ought to look like, he said.

Whats not to love about this? he said.

Some vaccine developers have embraced the idea of the National Academys involvement, which the body suggests will set a priorities framework that can be used in the United States and beyond.

It is the CDCs responsibility, the ACIP that makes decisions about allocation, but in this very special case, I have personally and I think many of us have called for the National Academy of Medicine to create a mechanism to look at health equity and make sure that the allocation is fair, Julie Gerberding, the chief patient officer at Merck, told a House subcommittee on Tuesday.

Others acknowledge there is confusion about who is doing what and most importantly, who will make the final decisions.

Osterholm, the University of Minnesota expert, called the composition of the National Academy panel outstanding. They couldnt find two better chairs than Bill and Helene.

But the excellence of the panel doesnt negate the fact there isnt much clarity about roles, he said.

Ultimately the administration in power when vaccine is approved for use will likely dictate who stands where in the vaccine priority line. The current administrations past decisions about distribution of desperately needed protective equipment for health workers and scarce supplies of the antiviral drug remdesivir dont instill confidence that the painstakingly crafted recommendations of the National Academy group, or of the ACIP, will be followed to the letter.

In the end it will be decided by the U.S. government, Osterholm said. Look at how the remdesivir situation unfolded nationally. That was a terrible situation.

The task of setting priority groups wont be an easy one.

Older adults are most at risk of dying if they become infected. But essential workers in food production and distribution may be at higher risk of contracting the virus. Who should move to the front of the line? Should the vaccination program prioritize people of color, who have contracted and died from Covid-19 in disproportion numbers? At the June meeting of the ACIP, at least one member suggested that should be considered. One of the charges to the National Academy panel is to advise on how communities of color can be assured equitable access to the vaccines.

Other questions asked of the National Academy panel include what criteria should be used to set priorities for equitable allocation of vaccines for example, how to weigh individual risk, due to age, underlying health conditions, or occupation, versus group risks posed by being in prison, being homeless or being a resident of a long-term care facility. The panel is also being asked to provide input on how to communicate vaccine priority decisions to the wider public, and how to address vaccine hesitancy, especially in high-risk populations.

Collins said the panel has been asked to come up with interim recommendations by Labor Day, which would then be subject to a short period of public comment. Dzau, the academy president, said last week that the final recommendations would probably take about three months to deliver, which would mean early October.

Dzau strenuously refuted the idea that the new panel might be driving in someone elses lane. The group will create scenarios, he said, of how to deal with the variety of circumstances the country might face, for instance starting to vaccinate with 10 million doses, or 60 million, or 100 million.

I think our job will be to look at the evidence and the strategy of who should get what and how. Some kind of priority list and the rationale for that, Dzau said.

The time frame he and Collins envisage may leave the ACIP with little time to fine-tune the framework the National Academy panel devises. Some of the most aggressive manufacturers have stated they may have enough evidence to support the issuance of an emergency use authorization from the Food and Drug Administration by October.

Beyond questions of priority-setting, there are also concerns about how vaccines will be distributed.

Those concerns were first triggered by the press release announcing the formation of Operation Warp Speed, which claimed distribution as one of the projects responsibilities.

Four organizations representing professionals who make up the last mile of a vaccines journey into arms in the United States wrote to the leaders of Operation Warp Speed on June 23, asking if the project intended to use existing vaccine delivery infrastructure to get Covid-19 vaccines into Americans. They still havent received a reply.

If your job is logistics and you dont know that theres a system out there already, it might be easy for you to start planning things down a different path, said Claire Hannan, executive director of the Association of Immunization Managers, one of the groups. And we dont want that to happen.

Another group that signed the letter, the Association of State and Territorial Health Officials, has since had a discussion with Lt. Gen. Paul Ostrowski, from Operation Warp Speed, said Jim Blumenstock, the organizations chief program officer for health security. Blumenstock said that after the conversation, he felt more confident that traditional vaccine distribution networks would play a part in the roll out of Covid-19 vaccines.

The proof is always in the pudding, he said, recounting that Ostrowski told him that micro-planning for vaccine distribution would start in the next two to three weeks.

STAT asked Operation Warp Speed for interviews about these issues. The requests were neither turned down nor granted they were merely acknowledged.

Hannan, who hadnt heard anything from Operation Warp Speed as of Monday, remains unsettled.

I am still very concerned about how distribution will be carried out and about the lack of planning with state and local public health agencies, she told STAT. We have received no assurance that existing vaccine allocation, distribution, and tracking systems will be used.

Damian Garde contributed reporting

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Confusion spreads over selection of priority groups for Covid-19 vaccines - STAT

ClinEdge and BTC Networks Contribute to COVID-19 Vaccine Programs with Sites Selected for Three Different Large Programs – BioSpace

July 24, 2020

ClinEdge, BTC Network and GuideStar Research, portfolio companies of ClinX, provide consulting, financial, marketing, advertising, enrollment, patient travel, and trial management solutions to the clinical research industry.

BOSTON--(BUSINESS WIRE)-- ClinEdge and BTC Network, portfolio companies of ClinX, announce today over twenty of its experienced vaccine centers of excellence have been selected for several of the major pharmaceutical company programs for COVID-19 vaccines initiating this summer and fall. In addition, a number of the ClinEdge & BTC Network sites are being considered for dozens of upcoming vaccine programs preparing study start-up activities.

Site selection is critical in any study but more critical than ever to ensure COVID studies meet historical records of approvals and require vaccine centers of excellence. Our dedicated research health and research facilities have proven staff, policies and processes around hybrid study structures in order to achieve enrollment and safety said Christian Burns, President of ClinEdge & BTC.

ClinEdge & BTC Network sites are in high demand during this time because of our facilities' significant vaccine experience, having contributed to more than 45 large programs within the past two years across a range of vaccine programs (which includes 17 different sponsors in the past year). During the pandemic, the networks combined expertise to launch a new offering specific for COVID-19 vaccine studies. This offering enables dedicated biotech and pharmaceutical companies to have an integrated solution that can fast track site start-up and enrollment at our sites. Together, the networks provide access to hundreds of thousands of potential volunteers to test vaccines against the pandemic.

ClinEdge & BTC integrate and centralize operations while implementing patient education and recruitment services. This allows the sites to focus on enrolling subjects quickly while maintaining an emphasis on patient safety and data quality. ClinEdge and BTC also have the ability to conduct hybrid clinical trial offerings, including support for home health care and remote monitoring. These services help ensure sites are able to reach as many potential subjects as possible.

Site Network Services & Opportunities for COVID Vaccine Pharmaceutical & Biotech Studies:

All of the network sites have access to ClinEdge & BTCs Risk Mitigation and Recovery Plans to ensure the successful execution of clinical trials under FDA guidelines. In present studies, our sites have over 100% of volunteers pre-identified prior to First Patient First Visit (FPFV). Prior centralized vaccine studies in addition to COVID-19 include Influenza, Shingles, C. difficile, Meningitis, Herpes Zoster, Pneumococcal, RSV, HPV, Cholera, Ebola, and Smallbox.

ClinEdge and BTC Network highly recommend the centralization of COVID-19 study conduct into an experienced network to maximize speed and quality of data. By managing the trials centrally, goals can be exceeded and the enhanced infrastructure enables process accommodations and risk mitigation to be implemented on a rolling basis as the ebbs and flows of the current environment continue to shift.

ClinX and its portfolio companies, ClinEdge, BTC Network and GuideStar Research, provide a full suite of clinical and outsourced business services to clinical research institutions, pharmaceutical companies, and CROs. The companies include: two global networks of research clinics, marketing and creative design, patient recruitment and retention, patient travel services, and consulting and financial services to both private site and hospital-based research institutions. With extensive experience in medical indications representing all therapeutic areas, the three companies have helped clients successfully conduct thousands of clinical studies by maximizing clinical research operations, minimizing enrollment times, and improving overall business performance. To learn more about ClinX and its portfolio companies visit http://www.Clin-X.com

View source version on businesswire.com: https://www.businesswire.com/news/home/20200724005011/en/

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ClinEdge and BTC Networks Contribute to COVID-19 Vaccine Programs with Sites Selected for Three Different Large Programs - BioSpace

Moderna Analyst Says Odds Are Good For COVID-19 Vaccine Approval, But Valuation Overcooked – Yahoo Finance

July 24, 2020

Moderna Inc's (NASDAQ: MRNA) coronavirus vaccine in development mRNA-1273 continues to inspire confidence among sell-side analysts.

The Moderna Analyst: SVB Leerink analyst Mani Foroohar initiated coverage of Moderna with a Market Perform rating and $65 price target.

The Moderna Thesis: The intense unmet need and the political will to get one or more vaccines approved are likely to sway regulators into showing substantial flexibility for vaccine candidates against SARS-CoV-2, the virus that causes COVID-19, Foroohar said in a Thursday initiation note. (See his track record here.)

"As a result, odds of approval for MRNA-1273 and competing therapies are high, even if pivotal clinical datasets show some inadequacies or inconsistencies," the analyst said.

Initial demand for the vaccine should be robust, he said.

SVB Leerink's base case estimates are modestly above the consensus for2021.

Medium- and long-term expectations are unlikely to be met unless Moderna shows a best-in-class profile, Foroohar said.

This is an unlikely proposition for Moderna, given its many competitors, including big biopharma players pursuing mRNA strategies similar to Moderna's, the analyst said.

SVB Leerink also sees commoditization risk even in the face of excellent data, as many companies are entering the market in a short time and considering the early price point implied by Pfizer Inc. (NYSE: PFE)/BioNTech SE's ADR supply agreement with the U.S. government.

This scenario impliesa price target of $19 per share attributable to Moderna's vaccine program, Foroohar said.

While being optimistic aboutModerna's mRNA-1273, the analyst said he's uncomfortable with Moderna's valuation,even after ascribing value to a dozen programs, many of which are quite early.

"Without major pipeline catalysts to counterbalance competitive risk to MRNA-1273, we view risk/reward as unappealing at this valuation."

MRNA Price Target: Moderna shares were trading down 3.17% at $80.59 at last check Thursday.

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Moderna Analyst Says Odds Are Good For COVID-19 Vaccine Approval, But Valuation Overcooked - Yahoo Finance

Southern Research collaborating on COVID-19 vaccine tests – AL.com

July 24, 2020

Birminghams Southern Research is collaborating with a company to study responses to the virus that causes COVID-19 as part of a broader program to develop a vaccine.

Southern Research, an independent nonprofit scientific research organization, announced today an expansion of an existing collaboration with Tonix Pharmaceuticals Holding Corp. The two back in February began developing and conducting testing of Tonixs TNX-1800, a potential vaccine designed to protect against COVID-19. Results from this testing are expected in the fourth quarter of this year, followed by human trials.

In addition, the two groups will focus specifically on T cell immune responses by volunteers who have recovered from the disease or who remain asymptomatic after exposure to COVID-19. T cells are a central part of the immune system. Raj Kalkeri, a senior scientist with Southern Researchs Infectious Disease Research Group, said the most successful vaccines mimic how the immune system responds to an invader.

By collecting data from recovered or asymptomatic volunteers, researchers hope to provide the same type of protection for those who take the vaccine as those who have actually recovered from COVID-19.

Tonix CEO and President Seth Lederman said TNX-1800 is designed to elicit a predominant T cell response, along with some antibody response. Three other early candidates in the companys vaccine portfolio are designed to elicit an almost pure T cell response.

We are looking forward to a timely completion of this study, utilizing readouts from a variety of assays that can provide information about TH1 or other types of immunity, Kalkeri said.

As of today, more than 15 million people have been infected with COVID-19, with more than 618,000 deaths.

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Southern Research collaborating on COVID-19 vaccine tests - AL.com

When a COVID-19 vaccine is approved, how long will protection last? – WLWT Cincinnati

July 22, 2020

The race to develop an effective COVID-19 vaccine is speeding ahead as new, promising data comes from human trials.But when a vaccine is finally given the green light, how will it work and how long will it last?WLWT talked with a local infectious diseases doctor about what he foresees.University of Cincinnati Health is set to take part in a third-phase Moderna vaccine trial soon.Doctors predict there will be a need for several vaccines to be produced globally."I think that will be very hard for one vaccine company to cover the entire world," Dr. Carl Fichtenbaum said.Fichtenbaum is leading studies at UC Health to fight COVID-19, including the upcoming Moderna vaccine trial.Participants will get two injections of the vaccine or a placebo, officials said."We won't know how long the vaccine is effective, so we'll have to figure out whether or not people need boosters, does it need to be annual or not," Fichtenbaum said.The spotlight is now on new data showing candidate vaccines from BioNTech SE and Pfizer, and Astra-Zeneca appearing to be safe, having minor to moderate side effects and stimulating t-cell and antibody responses.Scientists said the Astra-Zeneca, Oxford University candidate produced a response lasting at least two months.Moderna reported promising early results last week.Fichtenbaum believes several vaccines by different companies will be needed around the world to make them widely available."In doctor's offices, pharmacies, hospitals and, you know, there might even be school campaigns," Fichtenbaum said.He said it's not clear if multiple doses will be required or if vaccines will need to be retooled yearly like the flu vaccine, but he hopes people will follow science and get a shot when the time comes."As a society, we have to take that on because if too few of us do it, there will continue to be outbreaks," Fichtenbaum said.He said the 500-patient Moderna vaccine trial at UC Health is not open yet, but start-up calls are underway and the first national sites for the study are set to open later this month.Doctors said there are more than two-dozen vaccines being developed across the country.If you're interested in the Phase 3 clinical trial at UC Health, there are qualifications to be eligible.Officials said those eligible include adults 18 years or older with no known history of COVID-19, but are at risk of being infected.Read more from UC Health about the eligibiltiy requirements and the study here.For more information, call 513-245-3417 or email UCCovidResearch@UCHealth.com.

The race to develop an effective COVID-19 vaccine is speeding ahead as new, promising data comes from human trials.

But when a vaccine is finally given the green light, how will it work and how long will it last?

WLWT talked with a local infectious diseases doctor about what he foresees.

University of Cincinnati Health is set to take part in a third-phase Moderna vaccine trial soon.

Doctors predict there will be a need for several vaccines to be produced globally.

"I think that will be very hard for one vaccine company to cover the entire world," Dr. Carl Fichtenbaum said.

Fichtenbaum is leading studies at UC Health to fight COVID-19, including the upcoming Moderna vaccine trial.

Participants will get two injections of the vaccine or a placebo, officials said.

"We won't know how long the vaccine is effective, so we'll have to figure out whether or not people need boosters, does it need to be annual or not," Fichtenbaum said.

The spotlight is now on new data showing candidate vaccines from BioNTech SE and Pfizer, and Astra-Zeneca appearing to be safe, having minor to moderate side effects and stimulating t-cell and antibody responses.

Scientists said the Astra-Zeneca, Oxford University candidate produced a response lasting at least two months.

Moderna reported promising early results last week.

Fichtenbaum believes several vaccines by different companies will be needed around the world to make them widely available.

"In doctor's offices, pharmacies, hospitals and, you know, there might even be school campaigns," Fichtenbaum said.

He said it's not clear if multiple doses will be required or if vaccines will need to be retooled yearly like the flu vaccine, but he hopes people will follow science and get a shot when the time comes.

"As a society, we have to take that on because if too few of us do it, there will continue to be outbreaks," Fichtenbaum said.

He said the 500-patient Moderna vaccine trial at UC Health is not open yet, but start-up calls are underway and the first national sites for the study are set to open later this month.

Doctors said there are more than two-dozen vaccines being developed across the country.

If you're interested in the Phase 3 clinical trial at UC Health, there are qualifications to be eligible.

Officials said those eligible include adults 18 years or older with no known history of COVID-19, but are at risk of being infected.

Read more from UC Health about the eligibiltiy requirements and the study here.

For more information, call 513-245-3417 or email UCCovidResearch@UCHealth.com.

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When a COVID-19 vaccine is approved, how long will protection last? - WLWT Cincinnati

How to get a COVID-19 vaccine faster | TheHill – The Hill

July 22, 2020

A "New York Times:articlehighlights that 22 states are experiencing rapid increases in COVID-19 cases while reopening their economies. Although Texas, Florida, and Arizona have beenparticularly affected, the Center for Infectious Disease Research and Policy at the University of Minnesota finds most of the country is in asimilar situation.

Escalating new cases have prompted many to prepare for future outbreaks. Restaurants across Phoenix, Ariz., arereclosingto prevent COVID-19 exposure. The Arizona Department of Health Services recently directed hospitalsto activate emergency plans, expandinghospital-bedcapacity for COVID-19 patients.

Others believe more drastic actions are required. Columbia University virologist Dr. Angela Rasmussenrecentlysaidthat "at least 4 states are going to need to reinstitute stay-home orders this weeklike NOWto stop upward case trajectories."

New York may soon become one of those states. New York Gov. Andrew CuomoAndrew CuomoVisitors from 31 states now required to quarantine when visiting New York, New Jersey, Connecticut Watch live: NY Gov. Andrew Cuomo holds press briefing Ice cream store manager in NY says he was fired for not serving customer coughing without mask MORE recently threatened to reinstate a lockdown for Manhattan and the Hamptons if citizens continued to (allegedly)violatesocial-distancing rules. In his ownwords, "Im not going to allow situations to existthat we know have a high likelihood of causing an increase in the virus.

Unfortunately, the only ways to end the pandemic are herd immunity, prolonged lockdowns, or the development of avaccine. Each option comes with its own downsides.

Herd immunity would likely require70 to 90 percentof the population to contract COVID-19,endangeringthe lives ofmillions withpreexisting conditions. Reinstituting widespread lockdowns would likely extenddepression-likeeconomic hardship and themental tollof prolonged isolation.

Developing avaccine, although much less invasive than the other options, will requirepioneering medical breakthroughs at record speed.

Hoping to beat the odds, President TrumpDonald John TrumpMore than a dozen people wounded in shooting near Chicago funeral home Cleveland Indians players meet with team leadership to discuss potential name change Pelosi calls coronavirus the 'Trump virus' MORE launchedOperation Warp Speedlast May. The operation creates apartnershipbetween private drug developers and several federal agencies to develop and distribute avaccineby January.

Having considered14 different drugdevelopers, Operation Warp Speed recentlyselected five finalistsfor its partnership. Sparing no expense, it has distributed over$2 billionin R&D funds to these producers.

But why only five?

Even the most promising potentialvaccinesarejust beginningthe large-sample human-testingvaccineapproval process, the most time-consuming and difficult component. With over100vaccinesunder development, there are a variety of options to diversify the risk for finalists that do not receive approval.

Evidence indicates that including more drug developers would provide us with the highest chance to get avaccine. A model created byAccelerated Health Technologiespredicts that a candidate pool of15-20vaccineswould have an 80-to-90 percent chance for one to succeed.

Perhaps more important, providing a few producers with extensive financial support is no substitute for the collaboration among a diverse set of researchers that is often required to make a medicinal breakthrough. In his book "TheOrganization of Inquiry,"economist Gordon Tullock stressed that the scientific field closely resembles thedivision of labor, where a large network of scientists collaborates directly or indirectly by working on narrow aspects of a larger puzzle.

Similar collaboration has brought us pathbreakingvaccinedevelopment before.

From 2014 to 2016 the Ebola virus rapidly spread through western Africa, where it caused over11,000 deaths. Similar to COVID-19, Ebola was difficult to contain and exceptionallydifficultto develop avaccinefor.

Despite the odds, scientists, public-health experts, and drug producers indirectly collaborated across the globe to create a "miracle"vaccinewithin a year. As one "STAT"articlenotes:

While thevaccinehas come to be known as Mercks Ebolavaccine, in reality, scores of researchers and Ebola outbreak response workers in Canada, the U.S., Europe, and Africa played a role in paving Ervebos path to licensure, whether that was in designing it, conducting pivotal pre-clinical studies in animals, or the clinical trials Merck used to support its application.

Our best hope to develop a COVID-19vaccinequickly is to allow drug developers to employ a diverse set of approaches and let the scientific method dictate solutions. Unfortunately, I fear Operation Warp Speed undermines this approach with government-selected winners and losers, which decreases the chances of success. Heres hoping Im wrong.

Raymond J.Marchis a research fellow and director of FDAReview.org at theIndependent Instituteand an assistant professor of agribusiness and applied economics and faculty fellow in the Center for the Study of Public Choice and Private Enterprise at North Dakota State University.

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How to get a COVID-19 vaccine faster | TheHill - The Hill

Mandatory COVID-19 vaccinations? Here’s what states and employers can legally require – The Conversation US

July 22, 2020

A safe and effective vaccine could end the coronavirus pandemic, but for it to succeed, enough people will have to get inoculated.

Recent polls suggest that the U.S. is far from ready. Most surveys have found that only about two-thirds of adults say they would get the vaccine. While that might protect most people who get vaccinated, it may be insufficient to reach herd immunity and stop the viruss spread.

As a law professor who has written about the legal questions around vaccination laws, employment discrimination and religious exemptions, I see four possible approaches that governments and employers can take to ensure enough Americans are immunized against COVID-19.

Which ones are legal might surprise you.

The most intrusive policy would involve government mandating vaccination for all Americans, with the exception of those with a medical exemption.

People are often surprised to learn that states would likely have the legal right to enforce such a rule.

In the 1905 landmark case Jacobson v. Massachusetts, the United States Supreme Court upheld the constitutionality of a state criminal law that required all adult inhabitants of Cambridge to get a smallpox vaccine or be fined. The Supreme Court explained that an individuals liberty rights under the U.S. Constitution are not absolute and the mandatory vaccination law was necessary to promote public health and safety.

While Jacobson v. Massachusetts is over 100 years old, courts continue to rely on the reasoning of the case. State governments still occasionally enact broad compulsory vaccination policies. In 2019, in the midst of a measles outbreak, New York City mandated that anyone over six months of age who lived, went to school or worked in several ZIP codes within the city had to be vaccinated against measles or be subject to a fine.

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Requiring people to be vaccinated against the SARS-CoV-2 coronavirus could similarly be justified by governments need to promote public health and safety. In late May, the New York State Bar Associations Health Law Section even recommended mandatory COVID-19 vaccination for all Americans.

Yet in the United States today, where even mask mandates are controversial, it is unlikely that many states will enact a compulsory vaccination policy for everyone. Additionally, there is a risk that heavy-handed public health tactics can backfire and escalate tensions, increase mistrust of government and unintentionally increase the influence of the anti-vaccination movement.

A less intrusive tactic would be for state governments to require COVID-19 vaccinations for only certain segments of the population.

All 50 states currently have some type of compulsory vaccination laws covering K-12 schoolchildren, and many states have compulsory vaccination laws covering college students. These laws typically allow for some type of medical exemption. States may also have mandatory vaccination laws covering employees in nursing homes and health care facilities.

If states required this type of targeted mandatory COVID-19 vaccination, they could cover those most at risk and those most likely to be in contact with others in ways that could stem the viruss spread.

Another approach would be legislation that requires proof of vaccination to obtain a passport, use public transportation or go to a gym.

One of the most controversial issues surrounding compulsory vaccination laws is the religious or philosophical exemption, which some states have eliminated in recent years. In the aftermath of the recent measles outbreaks, both New York and California eliminated these exemptions from vaccination laws covering schoolchildren. Courts have explained that while compulsory vaccination laws may burden religious practices, religious exemptions are not constitutionally required under the First Amendments free exercise clause since mandatory vaccination does not single out religion and is not motivated by a desire to interfere with religion.

Private employers have significant flexibility for requiring vaccination. Yet few businesses outside of health care facilities have done so, partly out of fear that employees would consider these policies to be unacceptable invasions of their personal lives.

There is a risk in a unionized workplace that a mandatory vaccination policy could be struck down if it violates a collective bargaining agreement. However, unlike government-mandated policies, these would not be subject to constitutional restrictions.

Employers may also be concerned that if policies do not include significant religious exemptions, workers could sue, claiming religious discrimination. However, it is unlikely that federal law would require employers to accommodate employees requesting a religious exemption to a COVID-19 vaccine. Under Title VII of the 1964 Civil Rights Act, the federal law prohibiting religious discrimination in the workplace, employers are not required to accommodate religious employees if doing so involves more than a de minimis, or minimal cost.

Certainly, in the midst of one of the worst public health and financial crises in recent history, there is a significant cost to having an unimmunized workforce.

Beyond mandates and laws, employers, politicians and government agencies have other ways to encourage people to get vaccinated. In particular, the messages they send matter. That was evident in the public controversy over mask-wearing after President Donald Trump and other prominent Republicans ridiculed the precaution.

In New York, Gov. Andrew Cuomo mandated wearing face masks in public, but he also successfully convinced New Yorkers to wear them by emphasizing that doing so showed respect for others, particularly essential workers, health care providers and high-risk individuals.

Government can similarly encourage Americans to get vaccinated through education campaigns led by trusted community members, such as religious leaders or celebrities. During the New York measles outbreak, the Orthodox Jewish Nurses Association was at the forefront of educating the Orthodox Jewish community on the safety and efficacy of vaccination.

Government and employers also could make vaccines free and available at convenient locations.

As the U.S. government fast-tracks the development of potential vaccines, its important to remember that a COVID-19 vaccine will stop the virus only if enough people get vaccinated. Now is the time for governments and employers to develop policies to ensure it succeeds.

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Mandatory COVID-19 vaccinations? Here's what states and employers can legally require - The Conversation US

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