“Officials promise rapid rollout of COVID-19 vaccine in December - BetaBoston” plus 1 more

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Officials promise rapid rollout of COVID-19 vaccine in December - BetaBoston Posted: 29 Nov 2020 10:04 AM PST "We, from a federal perspective, have promised and set everything up so we can quickly review those EUAs and hopefully start sending out vaccines within 24 to 48 hours," Adams said on "Fox News Sunday." Advertisement Adams said he expects 40 million vaccine doses to be produced by the end of the year and for most Americans to have access to a vaccine by early in the second quarter of 2021. On NBC's "Meet the Press," top U.S. infectious-diseases specialist Anthony Fauci said the government "almost certainly" will be vaccinating portions in the first priority of the population by the end of December. "If we can hang together as a country and do these kinds of things to blunt these surges until we get a substantial proportion of the population vaccinated, we can get through this," he said. "There really is light at the end of the tunnel." United Airlines Holdings Inc. began operating charter flights on Friday to position doses of Pfizer's vaccine for quick distribution once approved, Dow Jones reported. A week ago, the chief executive officer of CVS Health Corp. said the pharmacy chain is ready to quickly vaccinate residents at thousands of long-term care facilities. In a separate interview on ABC's "This Week," Fauci said Covid jabs won't be "centrally mandated" in U.S., but that some local officials or employers might apply pressure to get people vaccinated. Advertisement "Any individual group can mandate vaccines in certain ways," he said. "Individual units, be they hospitals or other organizations, can do that. It's within their right to say, if you want to work with us, you're going to have to get a vaccine." Fauci said he has some concern about the overall anti-vaccination movement, but said the Covid jab research process has been "scientifically sound." "The process of determining whether it works, whether it's safe and effective has been independent, by independent bodies, and transparent," he said. In his NBC interview, Fauci said he fears the virus' spread will surge in the coming weeks into December. "We might see a surge superimposed upon the surge we're already in," he said. "I don't want to frighten people, except to say it is not too late to do something about this." Adams also implored Americans to help stop the virus' spread in the months remaining before a vaccine is widely available by wearing masks and avoiding gatherings. "It's going to get worse over the next several weeks," Adams said, referring to the rates of infection, hospitalization and deaths resulting from the pandemic. "The actions we take over the next several days will determine how bad it's going to get." Brett Giroir, assistant secretary at the U.S. Department of Health and Human Services, declined to recommend that all Americans who traveled or will travel during holidays quarantine afterward. Advertisement In an interview on CNN, Giroir said those who traveled should decrease unnecessary activities and quarantine only if they had close contact with someone known to have had Covid-19.

Questions loom over covid-therapy access - Arkansas Online Posted: 29 Nov 2020 12:54 AM PST Powerful drugs recently authorized by the U.S. that may prevent those at the earliest stages of covid-19 from suffering severe disease present thorny new challenges, including who will get them and where they'll be administered. Antibody treatments, like one from Regeneron Pharmaceuticals Inc. that was used to treat President Donald Trump, are often administered to patients at their peak contagiousness. Regeneron's drug, along with a therapy from Eli Lilly & Co., were authorized by the Food and Drug Administration for use within 10 days after patients' first symptoms, and doctors will be racing against time to administer them. Though the U.S. has spent hundreds of millions of dollars to snap up the antibody treatments, they will be rationed because of limited supplies. Officials are working to establish sites to infuse the medications to patients with mild to moderate disease who had until recently been advised to stay home during an unprecedented surge in cases. "Having a patient who has a coronavirus infection come to a hospital setting to get an IV injection is a problem, mostly because you have to isolate the patients from the rest of the patient population," Operation Warp Speed leader Moncef Slaoui said. "That's what we are working very hard to solve." The Lilly and Regeneron monoclonal antibodies mimic proteins the body normally makes to block the virus from entering cells; they were cleared by the FDA this month. They're the first drugs authorized specifically for nonhospitalized patients, and are targeted at those at risk of severe symptoms because of older age, obesity and other chronic conditions. [CORONAVIRUS: Click here for our complete coverage » arkansasonline.com/coronavirus] While Trump touted Regeneron's therapy after receiving it in October, infectious-disease doctors note that the evidence supporting the drugs' use in covid-19 is not yet definitive. Yet there's hope they could help the country battle its worst-ever coronavirus surge, as average daily infections soared to almost 170,000 over the past week. About 90,500 Americans were hospitalized with covid-19 as of Thursday, according to the Covid Tracking Project. Coronavirus-beset hospitals are also grappling with more infected staff members, said Allison Suttle, chief medical officer at Sanford Health, a nonprofit health system based in South Dakota. Treatment that keeps patients from being admitted would offer a tantalizing reprieve. "That gives us a lot more breathing room in our hospitals," she said, "that relieves a lot of the issues we're having." Physicians will refer patients for treatment, and in some cases emergency department providers can administer the drugs, U.S. health officials said at a Monday briefing. Yet access issues loom. The U.S. has paid Lilly $375 million to supply 300,000 vials of its antibody, bamlanivimab, over the next two months. It also awarded Regeneron $450 million to make and supply enough doses of its antibody cocktail for another 300,000 patients through the end of January. Both companies intend to scale up supply for the U.S. next year. That still won't be enough for some 300,000 high-risk patients diagnosed each week, according to Lilly Chief Executive Officer David Ricks. The government is distributing the treatments to each state and territory according to the size of their outbreaks, with state and local health departments taking the lead from there. Timely testing, a long-standing challenge in the U.S., is also a key factor. Testing giant Quest Diagnostics Inc., which currently reports average turnaround times of two to three days, prioritizes results for certain patient groups, including those in long-term care facilities, but not based on individual risk factors. "The sooner you have some of the signature symptoms, the sooner you get tested, the sooner you get results, the sooner you'll be a candidate for the medicine," Ricks said. Meanwhile, health officials are determining where and how to infuse the medicine to patients who are still in the early stages of the disease and may be highly infectious. Maryland is setting up four infusion sites around the state, including a covid-19 field hospital at the Baltimore Convention Center, said Howard Haft, an official with the Maryland Department of Health. With about 1,100 doses of Lilly's bamlanivimab, "the challenge is identifying the right patients as early as possible to avoid unnecessary hospitalizations," Haft said. Health officials are looking at ways to prioritize patients for antibody treatment. Northwestern Medicine in Illinois is using a risk score based on factors like age and body mass index, said Tina Stosor, a professor at Northwestern University Feinberg School of Medicine. "People have been calling in from all over to get scheduled," she said.

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