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Thursday, April 15, 2021

Digital health startups want to bring glucose monitors to the masses

 For the 1.6 million people in America living with type 1 diabetes, a continuous glucose monitor can be a lifesaver.

Since the first CGM was approved by the Food and Drug Administration in 1999, the diabetes community has advocated for lower prices and better insurance coverage for the quarter-sized devices, which regularly sample a proxy for blood glucose levels and can sound an alarm when they swing too high or too low. The cost-cutting has had an unexpected side effect: Today, glucose monitors are so cheap they’ve spawned a new crop of digital health startups selling the devices to consumers, many of whom don’t have diabetes.

Glucose monitors are only approved in the U.S. for use in people with diabetes who have a prescription. But through networks of remote physicians assembled by these startups, thousands of people have gained access to the devices with off-label prescriptions. NutriSense has shipped about 20,000 CGM units to users since 2019. A company called January came out of stealth last year after its founding in 2017, and launched its product incorporating glucose and heart rate data this January with the announcement of another $8.8 million in funding. Another startup, Levels, is still in beta, with about 6,000 people having gone through the program — and another 105,000 on the waitlist.

The list goes on. In the U.K., where CGMs are available over the counter, there’s MyLevels. Veri, based in Finland and serving the European market, plans to launch in the United States on May 1. Zoe combines blood glucose with microbiome scans and blood fat for nutritional analysis; another app called Sync is still in development.

Glucose monitors are becoming the backbone of a new movement in consumer tech — one that so far is outpacing the evidence.

“You kind of have this dichotomy with the perceived value of CGM,” said Susan Schembre, a researcher at the University of Arizona who has studied the use of CGMs in healthy people. “We have the consumers really driving the market on one end, and then the science kind of resisting it on the other.”

Eventually, the devices and the evidence will converge. Already, clinical CGMs have expanded from their initial patient population: Doctors regularly prescribe them to people who manage their type 2 diabetes with insulin, and sometimes to help type 2 patients tweak their habits and avoid going on medication. Manufacturers are planning for a future in which patients use the devices to both treat and prevent metabolic issues — dramatically increasing their market share. Consumer tech companies are looking for their slice of the pie.

Prices for CGMs have been dropping steadily over the last two decades. But in the last four years, the devices have become dramatically more affordable for people with diabetes — and helped to kickstart this new industry. While most of the companies selling CGMs to a broader audience claim they can plug in to any device on the market, more than 95% of the sensors they send out are Abbott’s FreeStyle Libre, whose latest version was approved by the FDA in 2018.

The upper-arm sensors, which have a tiny filament that measures glucose in the fluid between your cells, cost $70 and last 14 days; the device to apply them costs $75. The other leading device, Dexcom’s G6, costs about $400. Unlike the G6, which streams glucose values continuously via Bluetooth, the Libre uses near-field communication to pull data from the sensor any time you scan it with a special device or your phone. (Technically, that makes it a “flash” glucose monitor rather than a CGM.)

That technology, while cheaper than Bluetooth, was a rate-limiting factor for the consumer market. It was only in September 2019 that Apple updated its operating system so its iPhones would allow all apps to use near-field communication; before that, only trusted partners could incorporate the feature into their apps. “iOS 14 release day was really the critical point,” said Dan Zavorotny, co-founder and COO of NutriSense. “We released the day it became possible.”

The flood of startups belies their belief in the opportunity for glucose monitoring to improve health, especially in the U.S., where the burden of metabolic disease is especially high. Each targets a slightly different subset of users while steering clear of any medical claims. January is focusing its product on people with or at risk of developing diabetes. NutriSense, which incorporates advice from a nutritionist, is looking a little further upstream; “a lot of people who come to us are not yet sick, but they’re on the verge,” said Zavorotny. At Levels, meanwhile, “we’re focused on a broader market in terms of lifestyle,” said co-founder and chief medical officer Casey Means.

“As of right now, they’re kind of in a customer discovery phase,” said Schembre. “My perception of going through the process of signing up was that they’re really trying to identify their target market, and how do they need to build their systems to match the desires of that market.”

In the meantime, evidence for each of those user groups is still being generated. In fact, there’s still debate over whether CGMs are even appropriate and effective to use for people with type 2 diabetes who are not on intensive insulin therapy.

That data gap is even more pronounced once you look beyond patients with diabetes and try to understand the role of glucose monitoring in at-risk or healthy populations. That work is happening, albeit slowly, both within the companies and in the academic sphere.

“When you go looking for the data, you find that people are using CGM for different applications, but you don’t really see a paper that says, ‘Here’s how we can use CGM to improve people’s health regardless of their health status,’” said Schembre. “It’s really all quite new.”

That doesn’t seem to bother these companies’ first customers, a self-selecting set of early adopters (Orlando Bloom included) who are willing to shell out for the technology. January’s Season of Me, a 90-day program that includes 28 days of glucose sensors, costs $488, with a $200 promotion to pull in more users. Levels costs $399 for a month, and $350 for NutriSense, with prices dropping if you extend beyond the first month. And there’s little to no chance for reimbursement from insurers.

“The people that will adopt these types of solutions are kind of the same renegades as the first Fitbit users,” said Marissa Schlueter, a telehealth analyst at CB Insights.

Those prices will necessarily limit the scale of the consumer CGM market for now. But the promise of getting in on the ground floor could be well worth the sacrifice — and explain why so many companies have tried to establish themselves early.

“It’s a very nascent market, and I think there’s definitely room for more than a dozen companies,” said Noosheen Hashemi, CEO and co-founder of January. The falling cost of FreeStyle Libre and other CGMs also provides a natural on-ramp for diabetes device manufacturers eyeing an expansion into broader metabolic management.

In a February investor presentation, Dexcom put its core user base — people with type 1 diabetes, and people with type 2 who are reliant on intensive insulin therapy — at about 4 million people in the U.S. But if it expanded to make its devices accessible to Americans with type 2 diabetes who don’t already use insulin and those with prediabetes, it could reach another 30 million and 88 million potential users, respectively. “We’ve made significant progress in our work to bring Dexcom’s CGM to people with type 2 diabetes, including both those on intensive insulin therapy and those who are not,” said Dexcom CEO Kevin Sayer in the company’s latest earnings call.

Abbott’s ambition is clear when you look across the ocean, where the company has launched the Libre Sense, a version of its glucose sensor modified for sports, in Europe.

In 2020, the company received a CE mark for the Bluetooth-enabled device, with a limited glucose reporting range that prevents its use in diabetes management. Through a partnership with Atlanta-based company Supersapiens, Abbott is targeting the device to athletes, who can use the continuous data to fuel up to just the right level. In its latest earnings call, CEO Robert Ford called it “the first product in our strategy to expand use of our wearable biosensors technology into mass market opportunities beyond diabetes.”

While the pandemic has delayed the device’s path to FDA approval, said Phil Southerland, CEO and founder of Supersapiens, “we’re getting a lot of data so when we finally do come to the U.S. we’ll come with the perfect mousetrap to drive value to the consumer.”

You can see that glimmer in Dexcom’s eye, too, in the accelerometer rumored to be included in the company’s next CGM rollout, the G7. “For CGM to be widely adopted by other consumer groups, it will take CGM systems and user experiences designed specifically for those populations,” the company said in a statement.

Abbott and Dexcom don’t promote the use of their FDA-approved devices for off-label use; in a statement, Abbott emphasized that it is not affiliated nor partnering with companies using the FreeStyle Libre in this way.

“The other companies are taking the Uber approach of, ‘We don’t care about the rules, we don’t care about the FDA, and we’re going to come to market now using off-label usage,’” said Southerland.

But these consumer-focused companies, by introducing a wider audience to the concept of continuous glucose monitoring, are laying the groundwork for a strategy that device manufacturers — Abbott, Dexcom, Medtronic, and a slew of new entrants expected in the next several years — are likely to appreciate.

Some of these consumer companies’ users will be at risk of developing diabetes, with emerging signs of insulin resistance. So as clinical evidence accumulates, CGMs could be adopted and approved as a preventive tool for people with prediabetes, or even pre-prediabetes. Critically, that use case would also likely lead to insurance reimbursement pathways.

“There’s a baseline case for wellness, but it also can be a really good way to monitor situations before it gets out of hand and someone develops prediabetes and then eventually diabetes,” said Schlueter. “That’s the goal here with all these.”

https://www.statnews.com/2021/04/15/continuous-glucose-monitoring-nutrisense-january/

Merck’s Covid-19 push narrows further

 Merck & Co had already bowed out of the Covid-19 vaccine arena. Now its efforts at developing a therapy for the virus have taken a step back too.

The company said today that it was discontinuing development of MK-7110, which it gained through its $425m buyout of Oncoimmune, in hospitalised Covid-19 patients. As for its second big hope, the oral antiviral molnupiravir, Merck has scrapped a trial in hospitalised patients; all expectations for the project now rest on a pivotal study in outpatients.

The antiviral pipeline for treating Covid-19 thus now looks even sparser. And the developments are yet another example of how several big names in the vaccine and antiviral space have stumbled, while newcomers have capitalised on opportunities arising from the pandemic.

Oncoimmune move

The discontinuation of MK-7110, a recombinant fusion protein previously known as CD24Fc, also raises questions about Merck’s decision to shell out for Oncoimmune in November.

The move had been based on encouraging data from an interim analysis of a phase 3 trial in hospitalised Covid-19 patients; Merck had clearly hoped that this study would be enough for emergency use authorisation. But in February it said the FDA wanted more data.

Given the new clinical trials that would be needed, plus work on manufacturing, Merck noted today that even if things went well MK-7110 would not be available until the first half of 2022. Among other reasons for scrapping MK-7110, the company cited “the availability of a number of medicines for patients hospitalised with Covid-19” by this time. And perhaps the pandemic will be all but over by then.

MK-7110 is also in development for other indications, the most advanced being graft-versus-host disease, so maybe Merck can still recoup some of the cash it has spent.

Molnupiravir hopes

In any case, Merck’s only Covid-19 hope is now molnupiravir, which is being developed in collaboration with Ridgeback Biotherapeutics.

And this project’s only shot is in outpatients. Merck today said it had decided to discontinue the phase 2/3 Move-In study in hospitalised patients, after the phase 2 portion had shown that molnupiravir was unlikely to show a benefit.

Maybe this is not surprising: many other agents have struggled to make an impact in this population, and it seems that most therapies need to be given early in the course of disease to have a chance of having an effect.

If antivirals are broadly ineffective in hospitalised Covid-19 patients this could be bad news for the likes of Roche and Pfizer, which both have inpatient trials of their agents ongoing.

Results released by Merck today from the phase 2 portion of the Move-Out outpatient study do appear to suggest that earlier is better. Merck revealed no data, but claimed that molnupiravir’s effects were most pronounced in patients who had had symptoms for five days or less.

The company is therefore amending the phase 3 part of Move-Out to focus on this population, and plans to start enrolling into it by late April or early May, with final data due in September/October.

Mizuho analysts still believe that an oral drug that could meaningfully alter the course of mild disease could be a game changer but, with an EUA slated for the second half of this year at the earliest, the group could be running out of time to make an impact in Covid-19.

Antivirals in development for Covid-19 
Project Company Setting Note
Veklury  (IV)Gilead FDA-approved in Covid-19 patients requiring hospitalisation; Gilead discontinued ph3 study in high-risk outpatients (NCT04501952) on 12 AprRepurposed Ebola research project 
Molnupiravir (oral) Merck & Co/Ridgeback Ph3 in outpatients (Move-Out, NCT04575597); Merck discontinued ph2/3 trial in hospitalised pts (Move-In; NCT04575584) on 15 Apr Repurposed flu antiviral 
AT-527 (oral) Roche/AteaPh2 in hospitalised pts (NCT04396106); ph2 in outpatients (NCT04709835); ph3 planned in outpatients Repurposed hep C antiviral 
Ensovibep (IV)Novartis/Molecular Partners Ph2 in symptomatic pts (NCT04834856); ph2/3 in ambulatory pts (Empathy, NCT04828161) starting imminently; ph3 in hospitalised pts (Activ-3, NIH-sponsored) plannedDesigned for Sars-Cov-2
PF-07304814 (IV) Pfizer Ph1 in hospitalised pts (NCT04535167, excludes severely ill or with certain pre-existing conditions) Repurposed Sars research project 
MP0423 (IV)Novartis/Molecular Partners Preclinical Designed for Sars-Cov-2; could be better against variants than ensovibep thanks to different targeting mechanisms 
Source: Evaluate Pharma & clinicaltrials.gov.

https://www.evaluate.com/vantage/articles/news/trial-results/mercks-covid-19-push-narrows-further

Cancer biotech Tango to go public through $350M SPAC deal

 

  • Tango Therapeutics plans to become a publicly traded company through a merger with a "blank check" acquisition company that will infuse Tango with about $353 million to develop its pipeline of experimental cancer drugs.
  • BCTG Acquisition Corp., the special purpose acquisition company, or SPAC, will enter the deal with $167 million in its trust account. Institutional investors pledged another $186 million through a private investment in public equity, or PIPE, the companies said Wednesday.
  • Current Tango investors will see their equity converted to common stock. Investors who participated in the PIPE are paying $10 per share to hold part of the new company, which will trade under the symbol TNGX. The companies expect the deal to close in the third quarter.

Tango needs the cash to advance a promising cancer drug pipeline from preclinical testing into human trials. The company said its goal is to file applications for clinical studies every 12 to 18 months, including three in the period through 2023.

First up will be Tango’s lead product, dubbed TNG908, that's designed to attack tumor cells while sparing normal cells. The company plans to file an investigational new drug, or IND, application for TNG908 in the fourth quarter. Tango expects to file an IND for its USP1 inhibitor for breast, ovarian and prostate cancer in 2022 and another one for an undisclosed target in 2023 for a form of lung cancer.

Investors in the PIPE for the new combined company include Gilead, which already holds a stake in Tango and has been working with the biotech since 2018 on cancer drug development. Last year, Gilead expanded an earlier deal for five potential oncology targets to add 10 more.

BCTG, which is sponsored by Boxer Capital, said its acquisition search focused on finding a company with a unique approach to treating cancer. The new combined company will be led by Tango’s current CEO, Barbara Weber.

The biotech industry is likely to see many more SPAC deals after a what Deloitte calls a record-breaking year for SPAC initial public offerings in 2020. Just in the last couple of months, the DNA-testing giant 23andMe, proteomics company SomaLogic and the health intelligence company Sema4 have all agreed to SPAC acquisitions.

SPACs allow companies and investors to side-step the traditional IPO process, moving quickly to get a hefty return on their investment if everything goes right. The sponsor of a SPAC puts some upfront money at risk in case a deal doesn’t happen, but then gets to claim a large chunk of the new company.

Even as SPACs have drawn interest in biotech and other sectors, IPOs among drug companies are booming. But with SPACs increasingly entering the mix, there may be more competition for deals. SPACs generally have two years to find a target, and there are a lot of blank check companies currently active.

The Securities and Exchange Commission, meanwhile, is taking a close look at the surge of SPACs, according to John Coates, acting director of the division of corporate finance. In a speech last week, Coates noted that shareholder advocates have raised concerns about fees, conflicts and sponsor compensation.

https://www.biopharmadive.com/news/cancer-biotech-tango-to-go-public-through-350m-spac-deal/598392/

India’s biggest cities shut down as new virus cases hit 200K

 India’s two largest cities imposed stringent restrictions on movement and one planned to use hotels and banquet halls to treat coronavirus patients as new infections in the country shot past 200,000 Thursday amid a devastating surge that is straining a fragile health system.

The soaring cases and deaths come just months after India thought it had seen the worst of the pandemic — and have forced the country to delay exports of vaccines abroad. India is a major producer of COVID-19 shots, and its pivot to focus on domestic demand has weighed heavily on global efforts to end the pandemic.

New Delhi announced stay-at-home orders for the weekend, though essential workers will be able to move about if they have a pass from local authorities. Restaurants, malls, gyms and spas will be shut down. Movie theaters will close on weekends, but can operate on weekdays at a third of their capacity.

Arvind Kejriwal, Delhi’s top elected official, said that despite rise in infections, 5,000 hospital beds are still available in the capital and more capacity is being added. But still, more than a dozen hotels and wedding banquet halls were ordered to be converted into COVID-19 centers where doctors from nearby hospitals will treat the moderately ill.

“The surge is alarming,” said S.K. Sarin, a government health expert in New Delhi.

The moves in the capital came after similar measures were imposed in the worst-hit state of Maharashtra, home to financial capital, Mumbai. The bustle of India’s biggest city ebbed after authorities closed most industries, businesses and public places Wednesday night and put limits on the movement of people for 15 days. Train and plane travel was still allowed, however.

In recent days, the city has seen an exodus of panic-stricken day laborers, hauling backpacks and flocking to overcrowded trains.

Dozens of other towns and cities have also imposed nighttime curfews.

The surge in cases was weighing on hospitals in Maharashtra, Madhya Pradesh, Gujarat and several other states, where many reported a shortage of oxygen tanks. Imran Sheikh, a resident of the city of Pune in Maharashtra, said he was asked to supply his own oxygen tank for a relative undergoing COVID-19 treatment.

Cremation and burial grounds in the worst-hit areas were finding it difficult to cope with the increasing number of bodies arriving for last rites, according to Indian media reports.

Shahid Jamil, a virologist, said the recent local and state elections with massive political rallies and a major Hindu festival during which hundreds of thousands of devotees bathed in the Ganges river were super-spreader events.

The 200,739 new infections recorded Thursday are about twice the number of daily cases that were recorded during the last peak, in September. The Health Ministry also reported 1,038 deaths from COVID-19 in the past 24 hours, pushing the toll over 173,000.

India’s toll of 14 million cases puts it second behind the United States. It ranks fourth in deaths after the U.S., Brazil and Mexico — though, with nearly 1.4 billion people, it has a much larger population than any of those countries. Experts say even these figures are likely an undercount.

As it struggles with the caseload, India is ramping up its vaccination drive. The Health Ministry said the total vaccinations crossed 114 million with more than 3 million doses administered on Wednesday.

When infections began plummeting in India in September, many concluded the worst had passed. Masks and social distancing were abandoned. When cases began rising again in February, authorities were left scrambling.

https://apnews.com/article/migrant-workers-mumbai-weddings-india-coronavirus-pandemic-766287564341fc7b4281b208bfdad630

GLAXOSMITHKLINE: Goldman Sachs gives a Buy rating

 Goldman Sachs is positive on the stock with a Buy rating. The target price is unchanged at GBX 1810

https://www.marketscreener.com/quote/stock/GLAXOSMITHKLINE-PLC-9590199/news/GLAXOSMITHKLINE-nbsp-Goldman-Sachs-gives-a-Buy-rating-32976007/

Japanese partner initiated pivotal late-stage studies of Ardelyx's lead candidate

 Shares of Ardelyx (NASDAQ:ARDX) were soaring 8.9% as of 2:57 p.m. EDT on Wednesday. The big jump came after the company announced that its Japanese partner, Kyowa Kirin, has begun four late-stage clinical studies evaluating Ardelyx's lead candidate tenapanor in treating hyperphosphatemia, a disorder where there's an abnormally high level of phosphate in the blood.


Kyowa Kirin's initiation of multiple phase 3 studies is good news for Ardelyx in a couple of ways. For one thing, it triggered a $5 million milestone payment. More importantly, it gets the two collaboration partners even closer to potential regulatory approval for tenapanor in Japan.

Ardelyx received a $30 million up-front payment from Kyowa Kirin in 2017 when the Japanese drugmaker licensed tenapanor, and it stands to receive a total of up to $55 million in development milestone payments plus up to 8.5 billion yen (around $78 million based on current exchange rates) in commercialization milestones. Ardelyx will also receive royalties in the high teens if tenapanor wins approval in Japan.


While the start of Japanese clinical studies is good news for Ardelyx, a more important milestone for the biotech stock is only a couple of weeks away. By April 29, the Food and Drug Administration should announce its approval decision for tenapanor in controlling phosphorus levels in adult patients with chronic kidney disease.

https://www.fool.com/investing/2021/04/14/why-ardelyx-stock-soared-today/

More COVID state shutdowns unlikely, despite CDC suggestion

 When one of the nation’s top health officials this week suggested states dealing with a spring spike of coronavirus cases should “shut things down,” the remark landed with a thud.

Even Democratic governors and lawmakers who supported tough stay-at-home orders and business closures to stem previous COVID-19 outbreaks say they’re done with that approach. It’s a remarkable turnaround for governors who have said from the beginning of the pandemic that they will follow the science in their decision-making, but it’s also a nod to reality: Another round of lockdown orders would likely just be ignored by a pandemic-weary public.

The political dynamics have changed markedly in recent weeks as vaccination rates have grown, warmer weather has returned, and the public and business owners have become increasingly vocal about reopening schools and loosening restrictions around social gatherings.

“I think we have a real compliance issue if we try to go back to the sort of restrictions that were in place in March and April of last year,” said Pennsylvania state Rep. Mike Zabel, a Democrat who had supported previous shutdown orders by Gov. Tom Wolf, a fellow Democrat. “I don’t think there’s any appetite for that in Pennsylvania at all.”

COVID-19 cases have been increasing in Pennsylvania, and Centers for Disease Control and Prevention data shows it has one of the highest per capita case counts in the nation over the past week. Even so, Wolf’s administration said it “has no plans at this time to reinstitute any shutdown orders.” It instead noted that mask-wearing, gathering limits and social distancing remain required as the state gradually reopens.

Other governors also are staying on course to reopen society as they simultaneously expand vaccine eligibility, potentially complicating President Joe Biden’s efforts to conquer the pandemic.

Michigan Gov. Gretchen Whitmer, a Democrat, has pleaded unsuccessfully with the Biden administration to redirect more vaccine doses to her state as it struggles with the nation’s highest COVID-19 case rate. But the CDC director, Dr. Rochelle Walensky, said Monday that vaccines wouldn’t immediately quell a surge because they take up to six weeks to take full effect.

“The answer to that is to really close things down, to go back to our basics, to go back to where we were last spring, last summer and to shut things down, to flatten the curve, to decrease contact with one another, to test,” Walensky said.

That didn’t seem to sway Whitmer, who kept tough restrictions in place for months when COVID-19 cases surged last spring and fall but has been reluctant this time to go beyond the mask mandate and capacity limits. She has instead urged a voluntary two-week suspension of indoor restaurant dining, in-person high school classes and youth sports.

“When we can’t take action to protect ourselves, the government must step in. That’s where we were a year ago. That’s where we were four months ago,” Whitmer said. “We’re in a different moment. Every one of us has the ability and knowledge to do what it takes.”

She primarily blamed lack of compliance and the new coronavirus variants for the recent spike in cases. Adopting language used by Republican governors earlier in the pandemic, Whitmer and some other Democratic governors are urging people to take personal responsibility for behaviors that will help limit the spread of the virus.

Since the start of this year, the number of people going to restaurants and bars has noticeably increased while public support has declined for shutting down businesses and limiting travel, according to the COVID States Project, which has surveyed public attitudes and behaviors since the pandemic began.

That means governors must weigh what the public would be willing to do as they consider how to respond to a resurgence of cases fueled by the new variants, said James Druckman, a political science professor at Northwestern University in Illinois who is part of the survey consortium.

“It’s unrealistic to engage in complete shutdowns or closing of public spaces at this point,” he said. “I think you’d see a lot of people, including business owners, not following those types of things.”

New York Gov. Andrew Cuomo and other top Democratic and Republican leaders have not expressed any support for putting restrictions back in place, even though Cuomo has acknowledged the state is facing increased detection of potentially more contagious variants.

The Democratic governor has said people want their children in classrooms and that the struggling hospitality and restaurant industries need help. He blamed any uptick in COVID-19 cases on “human behavior.”

“It is a matter of personal responsibility,” Cuomo said at a Tuesday event that he barred reporters from attending. “You tell me how you act, I’ll tell you your likelihood of getting COVID.”

New York Assembly Minority Leader Will Barclay, a Republican, said he would be against re-imposing a lockdown: “Taking any steps backward would have serious social and economic consequences,” he said.

In Colorado, a statewide mask mandate remains in effect until May 6. But Democratic Gov. Jared Polis plans to transfer decisions about other public health orders to county governments on Friday. That will put Colorado in line with some Republican-led states such as Missouri, which has left decisions about business shutdowns in the hands of local officials since last summer.

Although Colorado has seen COVID-19 cases and deaths rise over the past two weeks, Polis said the lack of hospitalizations among older adults shows vaccines are working. The governor said he doesn’t think closures are necessary, but “people should honor that at the local level” if imposed.

A spokesperson said Illinois Gov. J.B. Pritzker, a Democrat, is concerned about a recent increase in COVID-19 cases but noted that hospitals have capacity and added that there is no need to repeat the earlier shutdowns. In Delaware, where cases have been high, Democratic Gov. John Carney said he hopes to avoid tightening restrictions that he has gradually eased over recent months.

Reinstituting shutdowns not only would lead to political backlash but also would be psychologically difficult for some people, who just recently have begun to experience renewed freedoms after a year of restrictions.

“From a social science perspective, the decision from the governor to not go towards a lockdown I think is a sensible one,” said Dominique Brossard, chair of the Department of Life Sciences Communication at the University of Wisconsin. “You need to work with what you have as far as people’s psychological state.”

https://apnews.com/article/pandemics-health-coronavirus-pandemic-1443e391cd99a96d377dda34ac3cd19c