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They Have Alzheimer’s. This Scientific Trial Might Be a Final Hope.

A few years ago, 73-year-old Michael Gross of Mahwah, New Jersey began to realize that something was wrong. “I was confused about words,” he said, “and it just got worse.”

But Mr Gross, the retired head of an advertising agency, was surprised when a doctor suggested a spinal tap to look for proteins that are a sign of Alzheimer’s. He couldn’t have this disease, thought Mr. Gross.

“I said, ‘No way, not me,” he said.

But he did.

He was crying, he was desperate.

Then he asked: What could he do about it?

He switched to the Mediterranean diet. He started exercising. He started doing crossword puzzles and signed up for a challenging brain training session. He found a study on mice that claimed a bright light on their heads helped with Alzheimer’s. He bought the light.

The disease continued. Now he cannot remember the details of a message while reading it.

Mr. Gross, a lifelong Yankees fan, was annoyed the day he forgot the name of the team’s former manager, Casey Stengel, and determined to remember it.

“Every day I wake up and say ‘Casey Stengel, Casey Stengel’,” he says.

Then he forgot the word “sardines”, a staple of his Mediterranean diet. “For a week I said to myself: ‘Sardines, sardines’,” said Mr Gross.

But what he really wanted was treatment strong enough to stop Alzheimer’s disease.

Mr. Gross saw an ad on Facebook for Lilly’s clinical trial. He came for a test that Friday morning to see if he was eligible. It consisted of a brain scan for a protein, tau, found in dead and dying brain neurons. If it had too little dew, it would not be eligible.

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China is beginning scientific trials of a Covid vaccine that may be inhaled

China’s CanSino Biologics will begin clinical trials next week for a Covid-19 vaccine administered by inhalation, the company’s co-founder and chief executive officer Xuefeng Yu told CNBC on Sunday.

The effectiveness rates for China’s Covid vaccines have been found to be lower than those developed by Pfizer-BioNTech and Moderna. Earlier this month, the director of the Chinese Center for Disease Control publicly admitted that Chinese vaccines “don’t have very high protection rates” and that they are considering giving people various Covid shots to make the vaccine more effective.

Yu told CNBC that an inhaled vaccine could be more effective than the injected one because the coronavirus enters the human body through the respiratory tract.

CanSinoBIO is developing the inhalation vaccine together with the Beijing Institute of Biotechnology. The company’s injected adenovirus type 5 vector vaccine – or Ad5-nCoV – has already been approved for use in China and several other countries.

Speaking to CNBC’s Arjun Kharpal at the Boao Forum for Asia in Hainan Province, China, Yu explained that an inhaled vaccine could theoretically provide additional protection by producing antibodies or T cells – white blood cells that are vital to the immune system. activates airways in the EU.

People who received Covid-19 shots at a temporary vaccination site in Kunming, Yunnan Province, China, on April 15, 2021.

Liu Ranyang | China News Service | Getty Images

If that protective layer fails and the virus penetrates deeper into the body, other parts of the immune system could keep fighting the Covid virus, Yu added.

“So you add more layers – makes sense, doesn’t it? That’s why we’re going the mucosal path,” he said.

The CEO said the company used the same concept to develop an inhalation vaccine for tuberculosis, or TB. Studies conducted in Canada showed that the inhaled dose for the TB vaccine needed to protect it “is much, much less than the actual injection,” he said.

Increase the effectiveness of the vaccine

CanSinoBIO’s single-dose injected Covid vaccine has been approved for use in several countries including China, Pakistan, Mexico and Hungary.

The company said preliminary data from third-phase clinical trials overseas showed its vaccine was 68.83% effective at preventing symptomatic Covid-19 disease two weeks after an injection, while the rate after four weeks Fell 65.28%, Reuters reported.

By comparison, updated data showed the Pfizer BioNTech shot was 91% effective at preventing infection, while Moderna said its vaccine was more than 90% effective six months after the second shot.

According to Yu, CanSinoBIO investigated adding a booster shot six months after the first injection, which could improve the immune response to the coronavirus.

“This also suggests that our vaccine could be improved – whether mixed with others or made by ourselves, I think that really requires a scientific study. We actually need data to show which way could be better,” said the CEO.

Reuters reported Monday that Chinese researchers are testing blending Covid vaccines developed by CanSinoBIO and a unit of Chongqing Zhifei Biological Products. The process, which is ongoing in the eastern city of Nanjing, is expected to involve 120 participants, the report said.

China was the first country to report cases of Covid-19 in late 2019 and appears to have largely contained the outbreak. The country has announced that it will vaccinate 40% of its population by June.

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Pfizer begins early stage scientific trial testing oral antiviral drug

Pfizer said Tuesday it had started an early clinical trial of an experimental oral antiviral drug for Covid-19.

The New York-based company announced that the Phase 1 study of the drug PF-07321332 will be conducted in the United States. The drug belongs to a class of drugs called protease inhibitors, and it works by blocking an enzyme that the virus needs to replicate in human cells.

Protease inhibitors are used to treat other viral pathogens such as HIV and hepatitis C.

“Fighting the COVID-19 pandemic requires both preventive vaccination and targeted treatment of those who become infected with the virus,” Pfizer’s chief scientist Mikael Dolsten said in a press release. “Given the way SARS-CoV-2 is mutating and the ongoing global impact of COVID-19, it is likely that access to therapeutic options will be critical both now and after the pandemic.”

The study comes as Pfizer is also working on an intravenously administered protease inhibitor known as PF-07304814. This drug is currently in a Phase 1b clinical trial in patients hospitalized with Covid-19.

A person walks past the Pfizer building in New York City on March 2, 2021.

Carlo Allegri | Reuters

Pfizer already has an approved vaccine in the US with German drug maker BioNTech, but health experts say the world will need a slew of drugs and vaccines to end the pandemic that is infecting more than 29.8 million Americans and is coming soon Has killed at least 542,991 people over a year, according to the Johns Hopkins University.

Preclinical studies have shown that the oral drug, the first orally ingested protease inhibitor for Covid-19 to be studied in clinical trials, has “strong” antiviral activity against the virus.

Because the drug is taken orally, it can be used outside of hospitals for people newly infected with the virus. The researchers hope the drugs will prevent the disease from getting worse and keep people out of the hospital.

Pfizer said it will provide more details on the drug at the Spring American Chemical Society meeting on April 6.

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FDA says photographs for brand spanking new variants will not want giant medical trials

Erick Vazquez receives the Pfizer vaccine during an event to vaccinate approximately 500 healthcare workers and adults over 65 years of age against COVID-19 organized by Labor Community Services, the Los Angeles Federation of Labor, and the St. Johns Well Child and Family Center shaped work of love, in Pico Union, February 13, 2021 in Los Angeles, CA.

Dania Maxwell | Los Angeles Times | Getty Images

The Food and Drug Administration announced Monday that modified Covid-19 vaccines against new, emerging variants can be approved without the need for lengthy clinical trials.

The new guidelines, published in a 24-page document on the FDA’s website, would release the new vaccines as an amendment to a company’s originally approved emergency application, according to the FDA. The company would have to submit new data showing the modified vaccine produces a similar immune response and is safe, similar to annual flu vaccines.

“Preliminary reports from clinical trials evaluating COVID-19 vaccine candidates in several countries, including South Africa, have contributed to concerns that the vaccine may be less effective against variant B.1.351 than against the original virus,” the wrote Agency found in the document with reference to the strain in South Africa. “Therefore, there is an urgent need to initiate the development and evaluation of vaccines against these SARSCoV-2 variants.”

The updated guidelines come because U.S. health officials, including White House Chief Medical Officer Dr. Anthony Fauci, fear the virus could potentially mutate enough to evade the protection of current vaccines and reverse advances in the pandemic.

For the past few weeks, officials have urged Americans to get vaccinated as soon as possible before potentially new and even more dangerous variants of the virus emerge.

As of Sunday, the Centers for Disease Control and Prevention had identified 1,661 cases of variant B.1.1.7, which were first identified in the UK. The agency has identified 22 cases of the B.1.351 strain from South Africa and five cases of P.1, a variant first identified in Brazil.

The FDA approved Pfizer and Moderna’s emergency vaccines in December, and the two drug makers have since announced plans to change their vaccines to target new variants. The guidelines could speed up the regulatory review process for the vaccines.

Public health officials and infectious disease experts said there was a high chance that Covid-19 would become an endemic disease, meaning it will never go away completely, although it will likely spread at lower levels than it is now. Health officials must constantly look for new variants of the virus so scientists can make vaccines against them, medical experts say.

Richard Webby, director of a World Health Organization flu center at St. Jude Children’s Research Hospital, said the clearance process for modified Covid-19 vaccines may be very similar to the procedure for annual flu shots.

The U.S. and other nations need to step up their surveillance of new tribes and then make regular recommendations as to which variants to target, he said in a recent interview. “It’s not there for Covid at the moment.”

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Health

Scientific Trials Are Shifting Out of the Lab and Into Individuals’s Houses

When the pandemic hit last year, clinical trials were affected. Universities closed and hospitals focused on fighting the new disease. Many studies that required repeated personal visits to volunteers have been delayed or canceled.

However, some scientists found creative ways to continue their research even when the personal interaction was inherently risky. They sent medicines Tests conducted via video chat and asked patients to monitor their own vital signs at home.

Many scientists say this shift towards virtual studies is long overdue. If these practices persist, they could make clinical trials cheaper, more efficient and fairer, and provide cutting-edge research opportunities to people who otherwise would not have the time or resources to use them.

“We’ve found that we can do things differently and I don’t think we’ll be going back to the way we used to know,” said Dr. Mustafa Khasraw, a Medical oncologist and clinical trial specialist at Duke University.

According to one analysis, nearly 6,000 studies have been registered on ClinicalTrials.gov stopped between January 1 and May 31, roughly twice as many as in times without a pandemic.

For example, at Johns Hopkins University, researchers delayed their study of how adults ages 65 to 80 metabolized tenofovir, a drug used to prevent and treat HIV

“The idea of ​​recruiting older people who we know are at particular risk – recruiting them to answer a fundamental question that doesn’t immediately change care or affect their health – just didn’t seem like it what we should do, “said Dr. Namandje Bumpus, the pharmacologist leading the study, which is on hold.

In Flint, Michigan, researchers had to stop admitting emergency patients for a hypertension study. Other volunteers dropped out or were difficult to contact.

“Their phone service is down, or they have very different schedules, or they are harder to reach because they care about someone,” said Dr. Lesli Skolarus, a stroke neurologist at the University of Michigan who is leading the study.

Dr. Skolarus and her colleagues have continued the process, albeit with a few changes. Most importantly, they canceled their personal follow-up exams and instead asked participants to take blood pressure cuffs with them and send photos of the readings via SMS.

Other research teams made similar adjustments. Neurologists at Massachusetts General Hospital in Boston revised a pilot study of methylphenidate, the active ingredient in Ritalin, in seniors with mild dementia or cognitive impairment. Instead of going to the hospital every two weeks, study participants now receive their medication in the mail, take cognitive assessments via video conferencing, play brain games on their computers, and conduct daily surveys at home.

“In essence, it is now an entirely virtual study,” said Dr. Steven Arnold, the neurologist who led the study.

Updated

Apr. 18, 2021, 12:04 p.m. ET

Even when scientists can’t eliminate personal visits, they find ways to reduce them. When Lorraine Wilner, a 78-year-old retiree with metastatic breast cancer, first started a clinical trial at Duke University last summer, she had to take a three-hour drive to the Durham, NC campus every four weeks for blood tests and occasionally other tests. She said she always left with a full gas tank. “So I don’t have to stop at a gas station or touch things or go to places where half of the people don’t wear a mask,” she said.

She can now have her blood drawn at a laboratory near her home in Lancaster, SC. The researchers then review the results with her over a video call. She still has to drive to Duke for regular scans, but the reduced travel has been a huge relief. “It makes it a lot more convenient,” she said.

Distance learning is likely to continue in a post-pandemic period, researchers say. Reducing face-to-face visits could make patient recruitment easier and lower dropout rates, which could lead to faster and cheaper clinical trials, said Dr. Ray Dorsey, a neurologist at the University of Rochester who has done remote research for years.

In fact, its inclusion in one of his recent virtual studies tracking people with a genetic predisposition to Parkinson’s actually spike this past spring. “While most clinical trials were suspended or delayed, ours accelerated amid the pandemic,” he said.

Moving to virtual trials could also help diversify clinical research and encourage low-income and rural patients to enroll, said Dr. Hala Borno, oncologist at the University of California at San Francisco. The pandemic, she said, “really allows us to step back and reflect on the burdens we have placed on patients for a long time.”

Virtual trials are not a panacea. Researchers need to ensure that they can thoroughly monitor the volunteer’s health without personal visits and be aware of the fact that not all patients have access to or are familiar with technology.

In some cases, scientists have yet to demonstrate that remote testing is reliable. While Dr. Arnold is optimistic that home cognitive testing could offer a better window into how his patients work on a daily basis, he noted that environments at home are uncontrolled. “Maybe a cat is crawling on you or grandchildren in the next room,” he said.

There is also the unpredictable nature of human behavior. Dr. Brennan Spiegel, gastroenterologist and director of health research at Cedars-Sinai Health System, often uses Fitbits to remotely monitor subjects. But one participant once put the device on a dog. A few others sent their Fitbits through the laundry. “You suddenly get a lot of steps – thousands and thousands of steps,” he said.

And some treatments may not work as well remotely. Last January, Clay Coleman Jr., a 61-year-old Chicago resident, took part in a clinical trial to treat his peripheral artery disease, which caused severe pain with every attempt to walk. “It was very difficult,” said Mr. Coleman, who is not driving. “My legs are very important to me because this is how I get around.”

He hoped the study of taking blood pressure medication and participating in a supervised exercise program could get him back in shape. Three times a week he traveled to a local gym for a structured treadmill workout with an instructor. “I was there maybe six weeks before this virus thing came up,” he said.

Suddenly the gym was out. Instead, Mr. Coleman’s trainer called him regularly and encouraged him to keep moving.

Dr. Mary McDermott, a The general internist at Northwestern University running the study isn’t sure how effective this type of remote coaching will be. “We cannot assume that remote intervention will be the same,” she said. “Or that remote measurements replace everything we have personally done.”

Still, the pandemic has shown that there is room for reform. Dr. Deepak Bhatt, a cardiologist at Brigham and Women’s Hospital in Boston, is part of a team that will start a study of an injectable blood thinner later this year. After the first personal visit to the doctor, the appointments are virtual.

“I’m pretty sure if Covid hadn’t occurred we would have done things the usual way,” he said. Sometimes he added, “It takes a crisis to provoke change.”