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China’s COVID spike not due to lifting of restrictions, WHO director says

  • WHO says China’s control measures were not stopping COVID-19
  • Countries should ask are the right people sufficiently vaccinated
  • Open channels between China and WHO – Ryan

GENEVA, Dec 14 (Reuters) – COVID-19 infections were exploding in China well before the government’s decision to abandon its strict “zero-COVID” policy, a World Health Organization director said on Wednesday, quashing suggestions that the sudden reversal caused a spike in cases.

The comments by the WHO’s emergencies director Mike Ryan came as he warned of the need to ramp up vaccinations in the world’s No. 2 economy.

Speaking at a briefing with media, he said the virus was spreading “intensively” in the nation long before the lifting of restrictions.

“There’s a narrative at the moment that China lifted the restrictions and all of a sudden the disease is out of control,” he said.

“The disease was spreading intensively because I believe the control measures in themselves were not stopping the disease. And I believe China decided strategically that was not the best option anymore.”

Beijing started pivoting away from its signature “zero-COVID” policy this month after protests against the economically damaging curbs championed by President Xi Jinping.

The sudden loosening of restrictions has sparked long queues outside fever clinics in a worrying sign that a wave of infections is building, even though official tallies of new cases have trended lower recently as authorities eased back on testing.

In its most recent COVID report for the week to Nov. 27, the WHO said China had reported increasing hospitalisations for four consecutive weeks.

“So the challenge that China and other countries still have is: are the people that need to be vaccinated, adequately vaccinated, with the right vaccines and the right number of doses and when was the last time those people had the vaccines,” said Ryan.

WESTERN VACCINE

The elation in China that met the changes in policy allowing people to live with the virus has quickly faded amid mounting concerns about surging infections because the population lacks “herd immunity” and has low vaccination rates among the elderly.

WHO’s senior epidemiologist Maria Van Kerkhove said the UN agency was providing technical advice to China and Ryan said there were open channels.

Among the first major announced deals in which a Western drugmaker will supply China with COVID therapies, China Meheco Group Co Ltd (600056.SS) said on Wednesday it would import and distribute Pfizer’s (PFE.N) oral COVID-19 treatment Paxlovid.

Earlier in the briefing, WHO chief Tedros Adhanom Ghebreyesus said he was “hopeful” that the pandemic, which has killed more than 6.6 million people since it emerged in Wuhan, China three years ago, will no longer be considered a global emergency some time next year.

Reporting by Emma Farge in Geneva;
Writing by Josephine Mason in London; Editing by Alison Williams, Raissa Kasolowsky, Alexandra Hudson

Our Standards: The Thomson Reuters Trust Principles.

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Biden takes aim at Big Pharma, Republicans in California

IRVINE, Calif., Oct 14 (Reuters) – U.S. President Joe Biden criticized Republicans and drug companies during a stop at a California community college on Friday as he campaigned for fellow Democrats in November’s midterm elections.

Biden’s trip includes stops in California on Friday and Oregon on Saturday as the president looks to position his party, the Democrats, as a champion of consumers and lower healthcare costs at a time that inflation ranks among voters’ top concerns. The midterm elections are on Nov. 8.

“We took on Big Pharma and we beat them, finally,” Biden said, referring to the recently passed Inflation Reduction Act’s provisions allowing Medicare to negotiate lower drug prices, caps the cost senior citizens are charged for prescriptions and lowers insulin prescriptions to $35 for Medicare beneficiaries.

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Biden promised to cap the insulin price at $35 for all Americans if Democrats keep the House and Senate. Most forecasts show Democrats with a slight advantage in the Senate and Republicans with a larger advantage in the House.

He claimed that Republicans will repeal the prescription drug price caps and take away Medicare’s ability to negotiate drug prices if they take control.

Biden’s motorcade was greeted in Irvine by more than 1,000 raucous protesters calling for Democracy in Iran, where anti-government demonstrations have raged for several weeks.

The president made reference to the protests in his remarks, saying that the United States stood with the Iranian people.

“He was moved by the protests that he saw from … Iranian Americans who were there,” White House spokeswoman Karine Jean-Pierre said later. “It struck him and he wanted to comment about that at the top.”

The president was introduced by Democratic Representative Katie Porter, who has grilled bank and drug company executives on their profits in widely viewed Congressional hearings.

“Here’s the stone cold truth. Corporate greed worsens health outcomes, rips off taxpayers and threatens our capitalist economy,” Porter said, accusing the pharmaceutical industry of crushing competition and price transparency.

Biden signed an order Friday requiring the U.S. Department of Health & Human Services (HHS) to outline within 90 days how it will use new models of care and payment to cut drug costs.

Data on Thursday showed U.S. consumer prices jumped 8.2% in the 12 months through September, after peaking above 9% in the summer and growing at their fastest pace since 1981. Healthcare costs were partly to blame in the most recent month, along with food and rent.

HHS was given the power to promote new approaches to lowering costs and widening care through an Innovation Center, created by a 2010 healthcare reform law known as Obamacare and housed at the Centers for Medicare and Medicaid Services.

Some 65 million Americans are enrolled in Medicare programs, which have repeatedly come under fire for its cost to taxpayers.

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Reporting by Trevor Hunnicutt and Jeff Mason; Additional reporting by Dan Whitcomb; Editing by Heather Timmons, David Gregorio & Shri Navaratnam

Our Standards: The Thomson Reuters Trust Principles.

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End of COVID pandemic is ‘in sight’ -WHO chief

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Sept 14 (Reuters) – The world has never been in a better position to end the COVID-19 pandemic, the head of the World Health Organization said on Wednesday, his most optimistic outlook yet on the years-long health crisis which has killed over six million people.

“We are not there yet. But the end is in sight,” WHO Director-General Tedros Adhanom Ghebreyesus told reporters at a virtual press conference.

That was the most upbeat assessment from the UN agency since it declared an international emergency in January 2020 and started describing COVID-19 as a pandemic three months later.

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The virus, which emerged in China in late 2019, has killed nearly 6.5 million people and infected 606 million, roiling global economies and overwhelming healthcare systems.

The rollout of vaccines and therapies have helped to stem deaths and hospitalisations, and the Omicron variant which emerged late last year causes less severe disease. Deaths from COVID-19 last week were the lowest since March 2020, the U.N. agency reported.

Still on Wednesday, he again urged nations to maintain their vigilance and likened the pandemic to a marathon race.

“Now is the time to run harder and make sure we cross the line and reap the rewards of all our hard work.”

Countries need to take a hard look at their policies and strengthen them for COVID-19 and future viruses, Tedros said. He also urged nations to vaccinate 100% of their high-risk groups and keep testing for the virus.

The WHO said countries need to maintain adequate supplies of medical equipment and healthcare workers.

“We expect there to be future waves of infections, potentially at different time points throughout the world caused by different subvariants of Omicron or even different variants of concern,” said WHO’s senior epidemiologist Maria Van Kerkhove.

With over 1 million deaths this year alone, the pandemic remains an emergency globally and within most countries.

“The COVID-19 summer wave, driven by Omicron BA.4 and BA.5, showed that the pandemic is not yet over as the virus continues to circulate in Europe and beyond,” a European Commission spokesperson said.

WHO’s next meeting of experts to decide whether the pandemic still represents a public health emergency of international concern is due in October, a WHO spokesperson said.

GLOBAL EMERGENCY

“It’s probably fair to say most of the world is moving beyond the emergency phase of the pandemic response,” said Dr Michael Head, senior research fellow in global health at Southampton University.

Governments are now looking at how best to manage COVID as part of their routine healthcare and surveillance, he said.

Europe, the United Kingdom and the United States have approved vaccines that target the Omicron variant as well as the original virus as countries prepare to launch winter booster campaigns.

In the United States, COVID-19 was initially declared a public health emergency in January 2020, and that status has been renewed quarterly ever since.

The U.S. health department is set to renew it again in mid-October for what policy experts expect is the last time before it expires in January 2023.

U.S. health officials have said that the pandemic is not over, but that new bivalent vaccines mark an important shift in the fight against the virus. They predict that a single annual vaccine akin to the flu shot should provide a high degree of protection and return the country closer to normalcy.

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Reporting by Manas Mishra, Khushi Mandowara in Bengaluru, Ahmed Aboulenein in Washington and Jennifer Rigby in London; Editing by Shounak Dasgupta, William Maclean, Josephine Mason, Elaine Hardcastle

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U.S. judge blocks Idaho abortion ban in emergencies; Texas restrictions allowed

FILE PHOTO – Abortion rights protesters participate in nationwide demonstrations following the leaked Supreme Court opinion suggesting the possibility of overturning the Roe v. Wade abortion rights decision, in Houston, Texas, U.S., May 14, 2022. REUTERS/Callaghan O’Hare

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Aug 24 (Reuters) – A federal judge on Wednesday blocked Idaho from enforcing a ban on abortions when pregnant women require emergency care, a day after a judge in Texas ruled against President Joe Biden’s administration on the same issue.

The conflicting rulings came in two of the first lawsuits over Biden’s attempts to keep abortion legal after the conservative majority U.S. Supreme Court in June overturned the 1973 Roe v. Wade decision that legalized the procedure nationwide.

Legal experts said the dueling rulings in Idaho and Texas could, if upheld on appeal, force the Supreme Court to wade back into the debate.

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About half of U.S. states have or are expected to seek to ban or curtail abortions following Roe’s reversal. Those states include Idaho and Texas, which like 11 others adopted “trigger” laws banning abortion upon such a decision.

Abortion is already illegal in Texas under a separate, nearly century-old abortion ban that took effect after the U.S. Supreme Court’s decision. Idaho’s trigger ban takes effect on Thursday, the same day as in Texas and Tennessee.

In Idaho, U.S. District Judge B. Lynn Winmill agreed with the U.S. Department of Justice that the abortion ban taking effect Thursday conflicts with a federal law that ensures patients can receive emergency “stabilizing care.”

Winmill, who was appointed to the court by former Democratic President Bill Clinton, issued a preliminary injunction blocking Idaho from enforcing its ban to the extent it conflicts with federal law, citing the threat to patients.

“One cannot imagine the anxiety and fear (a pregnant woman) will experience if her doctors feel hobbled by an Idaho law that does not allow them to provide the medical care necessary to preserve her health and life,” Winmill wrote.

The Justice Department has said the federal Emergency Medical Treatment and Labor Act requires abortion care in emergency situations.

“Today’s decision by the District Court for the District of Idaho ensures that women in the State of Idaho can obtain the emergency medical treatment to which they are entitled under federal law,” U.S. Attorney General Merrick Garland said in a written statement.

“The Department of Justice will continue to use every tool at its disposal to defend the reproductive rights protected by federal law,” Garland said. The DOJ has said that it disagrees with the Texas ruling and is considering next legal steps.

U.S. District Judge James Wesley Hendrix ruled in the Texas case that the U.S. Department of Health and Human Services went too far by issuing guidance that the same federal law guaranteed abortion care.

Hendrix agreed with Texas Attorney General Ken Paxton, a Republican, that the guidance issued in July “discards the requirement to consider the welfare of unborn children when determining how to stabilize a pregnant woman.”

Hendrix, an appointee of former President Donald Trump, said the federal statute was silent as to what a doctor should do when there is a conflict between the health of the mother and the unborn child and that the Texas law “fills that void.”

Hendrix issued an injunction barring enforcement of the HHS guidance in Texas and against two groups of anti-abortion doctors who also challenged it, saying the Idaho case showed a risk the Biden administration might try to enforce it.

Hendrix declined to issue a nationwide injunction as Paxton wanted.

Appeals are expected in both cases and would be heard by separate appeals courts, one based in San Francisco with a reputation for leaning liberal and another in New Orleans known for conservative rulings.

Greer Donley, an assistant professor at the University of Pittsburgh Law School and expert on abortion law, said that if the conflicting rulings were upheld the U.S. Supreme Court may feel pressured to intervene.

“Without a federal right abortion, this is the type of legal chaos that most people were predicting would be happening,” she said.

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Reporting by Nate Raymond in Boston; Additional reporting by Dan Whitcomb in Los Angeles; Editing by Grant McCool and Christopher Cushing

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Nate Raymond

Thomson Reuters

Nate Raymond reports on the federal judiciary and litigation. He can be reached at nate.raymond@thomsonreuters.com.

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Fauci, face of U.S. COVID response, to step down from government posts

  • Immunologist served as adviser to seven presidents
  • Fauci was vilified by Trump and Republican lawmakers
  • He faced death threats over pandemic policies

Aug 22 (Reuters) – Dr. Anthony Fauci, the top U.S. infectious disease official who became the face of America’s COVID-19 pandemic response under Presidents Donald Trump and Joe Biden, announced on Monday he is stepping down in December after 54 years of public service.

Fauci, whose efforts to fight the pandemic were applauded by many public health experts even as he was vilified by Trump and many Republicans, will leave his posts as chief medical adviser to Biden and director of the U.S. National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH). Fauci, 81, has headed NIAID since 1984.

The veteran immunologist has served as an adviser to seven U.S. presidents beginning with Republican Ronald Reagan, focusing on newly emerging and re-emerging infectious disease dangers including HIV/AIDS, Ebola, Zika, monkeypox and COVID-19.

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Fauci endured criticism from Trump and various conservatives and even death threats against him and his family from people who objected to safeguards such as vaccination, social distancing and masking that he advocated to try to limit the lethality of the COVID-19 pandemic. After defeating Trump in the 2020 election, Biden made Fauci his chief medical adviser.

“I definitely feel it was worth staying as long as I have. It is unfortunate, but it is a fact of life that we are living in a very, very divisive society right now,” Fauci told Reuters on Monday.

Fauci said he never considered resigning due to the threats against him.

“I don’t like the idea that I have to have armed federal agents with me. That’s not a happy feeling. It’s reality. And you’ve got to deal with reality,” Fauci said.

Republican lawmakers including fierce critic Rand Paul, with whom Fauci tangled during Senate hearings, vowed on Monday to investigate him if they gain control of either the House of Representatives or Senate in November’s congressional elections.

“As he leaves his position in the U.S. Government, I know the American people and the entire world will continue to benefit from Dr. Fauci’s expertise in whatever he does next,” Biden said in a statement. “The United States of America is stronger, more resilient and healthier because of him.”

Fauci signaled his impending departure last month, telling Reuters he would retire by the end of Biden’s first term, which runs to January 2025, and possibly earlier. read more

The United States leads the world in recorded COVID-19 deaths with more than one million. In the first months of the pandemic in 2020, Fauci helped lead scientific efforts to develop and test COVID-19 vaccines in record time and took part in regular televised White House briefings alongside Trump.

Fauci became a popular and trusted figure among many Americans as the United States faced lockdowns and rising numbers of COVID-19 deaths, even inspiring the sale of cookies and bobblehead dolls featuring his likeness.

However, Fauci drew the ire of Trump and many Republicans for cautioning against reopening the U.S. economy too quickly and risking increased infections and for opposing the use of unproven treatments such as the malaria drug hydroxychloroquine.

‘A DISASTER’

Democrats accused Trump of presiding over a disjointed response to the pandemic and of disregarding advice from public health experts including Fauci. Trump in October 2020, weeks before his re-election loss, called Fauci “a disaster” and complained that Americans were tired of hearing about the pandemic. Trump even made fun of Fauci’s off-target ceremonial first pitch at a Washington Nationals baseball game.

Fauci sometimes publicly contradicted Trump’s statements about the pandemic. Fauci said on Monday that while he respects the office of the presidency, he felt he had to speak out “when things were said that were outright untrue and quite misleading.”

“I didn’t take any great pleasure in that,” Fauci said.

Paul frequently attacked Fauci during Senate hearings on the pandemic. read more

Fauci has accused Paul of spreading misinformation. Paul on his website has accused Fauci of “lying about everything from masks to the contagiousness of the virus.” Fauci during one hearing noted that Paul placed fundraising appeals on his website next to a call to have him fired.

Fauci said staying on until December allows for a search for a new director of NIAID, an institute with an annual budget exceeding $6 billion, and the appointment of an acting chief. Fauci also said he wanted to remain to help address an expected autumn upswing in COVID-19 infections.

Fauci made clear that while he will be leaving government service, he will not be retiring. He said in the future he hopes to use his expertise to help inspire a new generation of doctors to pursue careers in public health, medicine and science.

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Reporting by Leroy Leo in Bengaluru and Julie Steenhuysen in Chicago; Additional reporting by Kanishka Singh in Washington; Editing by Will Dunham and Sriraj Kalluvila

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‘Living with COVID’: Where the pandemic could go next

LONDON/CHICAGO, Aug 1 (Reuters) – As the third winter of the coronavirus pandemic looms in the northern hemisphere, scientists are warning weary governments and populations alike to brace for more waves of COVID-19.

In the United States alone, there could be up to a million infections a day this winter, Chris Murray, head of the Institute of Health Metrics and Evaluation (IHME), an independent modeling group at the University of Washington that has been tracking the pandemic, told Reuters. That would be around double the current daily tally.

Across the United Kingdom and Europe, scientists predict a series of COVID waves, as people spend more time indoors during the colder months, this time with nearly no masking or social distancing restrictions in place.

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However, while cases may surge again in the coming months, deaths and hospitalizations are unlikely to rise with the same intensity, the experts said, helped by vaccination and booster drives, previous infection, milder variants and the availability of highly effective COVID treatments.

“The people who are at greatest risk are those who have never seen the virus, and there’s almost nobody left,” said Murray.

These forecasts raise new questions about when countries will move out of the COVID emergency phase and into a state of endemic disease, where communities with high vaccination rates see smaller outbreaks, possibly on a seasonal basis.

Many experts had predicted that transition would begin in early 2022, but the arrival of the highly mutated Omicron variant of coronavirus disrupted those expectations.

“We need to set aside the idea of ‘is the pandemic over?'” said Adam Kucharski, an epidemiologist at the London School of Hygiene and Tropical Medicine. He and others see COVID morphing into an endemic threat that still causes a high burden of disease.

“Someone once told me the definition of endemicity is that life just gets a bit worse,” he added.

The potential wild card remains whether a new variant will emerge that out-competes currently dominant Omicron subvariants.

If that variant also causes more severe disease and is better able to evade prior immunity, that would be the “worst-case scenario,” according to a recent World Health Organization (WHO) Europe report.

“All scenarios (with new variants) indicate the potential for a large future wave at a level that is as bad or worse than the 2020/2021 epidemic waves,” said the report, based on a model from Imperial College of London.

CONFOUNDING FACTORS

Many of the disease experts interviewed by Reuters said that making forecasts for COVID has become much harder, as many people rely on rapid at-home tests that are not reported to government health officials, obscuring infection rates.

BA.5, the Omicron subvariant that is currently causing infections to peak in many regions, is extremely transmissible, meaning that many patients hospitalized for other illnesses may test positive for it and be counted among severe cases, even if COVID-19 is not the source of their distress.

Scientists said other unknowns complicating their forecasts include whether a combination of vaccination and COVID infection – so-called hybrid immunity – is providing greater protection for people, as well as how effective booster campaigns may be.

“Anyone who says they can predict the future of this pandemic is either overconfident or lying,” said David Dowdy, an infectious disease epidemiologist at Johns Hopkins Bloomberg School of Public Health.

Experts also are closely watching developments in Australia, where a resurgent flu season combined with COVID is overwhelming hospitals. They say it is possible that Western nations could see a similar pattern after several quiet flu seasons.

“If it happens there, it can happen here. Let’s prepare for a proper flu season,” said John McCauley, director of the Worldwide Influenza Centre at the Francis Crick Institute in London.

The WHO has said each country still needs to approach new waves with all the tools in the pandemic armory – from vaccinations to interventions, such as testing and social distancing or masking.

Israel’s government recently halted routine COVID testing of travelers at its international airport, but is ready to resume the practice “within days” if faced with a major surge, said Sharon Alroy-Preis, head of the country’s public health service.

“When there is a wave of infections, we need to put masks on, we need to test ourselves,” she said. “That’s living with COVID.”

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Reporting by Jennifer Rigby and Julie Steenhuysen; Additional reporting by Maayan Lubell; Editing by Michele Gershberg and Bill Berkrot

Our Standards: The Thomson Reuters Trust Principles.

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‘Living with COVID’: Where the pandemic could go next

LONDON/CHICAGO, Aug 1 (Reuters) – As the third winter of the coronavirus pandemic looms in the northern hemisphere, scientists are warning weary governments and populations alike to brace for more waves of COVID-19.

In the United States alone, there could be up to a million infections a day this winter, Chris Murray, head of the Institute of Health Metrics and Evaluation (IHME), an independent modeling group at the University of Washington that has been tracking the pandemic, told Reuters. That would be around double the current daily tally.

Across the United Kingdom and Europe, scientists predict a series of COVID waves, as people spend more time indoors during the colder months, this time with nearly no masking or social distancing restrictions in place.

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However, while cases may surge again in the coming months, deaths and hospitalizations are unlikely to rise with the same intensity, the experts said, helped by vaccination and booster drives, previous infection, milder variants and the availability of highly effective COVID treatments.

“The people who are at greatest risk are those who have never seen the virus, and there’s almost nobody left,” said Murray.

These forecasts raise new questions about when countries will move out of the COVID emergency phase and into a state of endemic disease, where communities with high vaccination rates see smaller outbreaks, possibly on a seasonal basis.

Many experts had predicted that transition would begin in early 2022, but the arrival of the highly mutated Omicron variant of coronavirus disrupted those expectations.

“We need to set aside the idea of ‘is the pandemic over?'” said Adam Kucharski, an epidemiologist at the London School of Hygiene and Tropical Medicine. He and others see COVID morphing into an endemic threat that still causes a high burden of disease.

“Someone once told me the definition of endemicity is that life just gets a bit worse,” he added.

The potential wild card remains whether a new variant will emerge that out-competes currently dominant Omicron subvariants.

If that variant also causes more severe disease and is better able to evade prior immunity, that would be the “worst-case scenario,” according to a recent World Health Organization (WHO) Europe report.

“All scenarios (with new variants) indicate the potential for a large future wave at a level that is as bad or worse than the 2020/2021 epidemic waves,” said the report, based on a model from Imperial College of London.

CONFOUNDING FACTORS

Many of the disease experts interviewed by Reuters said that making forecasts for COVID has become much harder, as many people rely on rapid at-home tests that are not reported to government health officials, obscuring infection rates.

BA.5, the Omicron subvariant that is currently causing infections to peak in many regions, is extremely transmissible, meaning that many patients hospitalized for other illnesses may test positive for it and be counted among severe cases, even if COVID-19 is not the source of their distress.

Scientists said other unknowns complicating their forecasts include whether a combination of vaccination and COVID infection – so-called hybrid immunity – is providing greater protection for people, as well as how effective booster campaigns may be.

“Anyone who says they can predict the future of this pandemic is either overconfident or lying,” said David Dowdy, an infectious disease epidemiologist at Johns Hopkins Bloomberg School of Public Health.

Experts also are closely watching developments in Australia, where a resurgent flu season combined with COVID is overwhelming hospitals. They say it is possible that Western nations could see a similar pattern after several quiet flu seasons.

“If it happens there, it can happen here. Let’s prepare for a proper flu season,” said John McCauley, director of the Worldwide Influenza Centre at the Francis Crick Institute in London.

The WHO has said each country still needs to approach new waves with all the tools in the pandemic armory – from vaccinations to interventions, such as testing and social distancing or masking.

Israel’s government recently halted routine COVID testing of travelers at its international airport, but is ready to resume the practice “within days” if faced with a major surge, said Sharon Alroy-Preis, head of the country’s public health service.

“When there is a wave of infections, we need to put masks on, we need to test ourselves,” she said. “That’s living with COVID.”

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Reporting by Jennifer Rigby and Julie Steenhuysen; Additional reporting by Maayan Lubell; Editing by Michele Gershberg and Bill Berkrot

Our Standards: The Thomson Reuters Trust Principles.

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If you are high risk, do not wait for updated COVID vaccines, experts say

CHICAGO, July 29 (Reuters) – People at high risk of severe disease who have yet to get a second COVID-19 booster should not wait for next-generation, Omicron-targeted vaccines expected in the fall, five vaccine experts told Reuters.

In many countries, including the United States, the BA.5 Omicron subvariant of the virus is surging, but current vaccines continue to offer protection against hospitalization for severe disease and death.

And, as the virus evolves, it is not known what version will be widely circulating in the fall or whether new vaccines – expected to target BA.4/5 in the United States and BA.1 in Europe – will be a good match.

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“If you need a booster, get it now,” said Dr. John Moore, a professor of microbiology and immunology at Weill Cornell Medical College, who co-wrote an editorial on the subject published on Friday.

In the United States, regulators have asked Pfizer Inc (PFE.N) with partner BioNTech SE (22UAy.DE) and Moderna Inc (MRNA.O) to develop vaccine boosters that target both the BA.4 and BA.5 Omicron cousins, as well as the original virus.

The government on Friday said it had ordered 66 million doses of Moderna’s shot in a $1.74 billion deal. Combined with the 105 million doses already on order of Pfizer/BioNTech, the full tally is 171 million shots, which are expected in early fall. read more

Regulators in Europe, meanwhile, have signaled that they would be willing to use whichever Omicron-based booster is available to Europe soonest, which may well be the one aimed at the BA.1 variant that drove last winter’s record surge in infections.

U.S. regulators are hoping an updated vaccine that targets the original strain and an Omicron variant will offer broader protection against future variants, and believe a booster that is closest to the circulating version is valuable.

Given the current surge and people’s waning immunity, experts told Reuters the best booster for those at risk is the one at hand.

Only about 30% of people 50 and older who are eligible for a fourth vaccine dose have received one, and fewer than 10% of those aged 50-64, according to the U.S. Centers for Disease Control and Prevention. For those under age 50 or with no major risk factors, a fourth dose has not been approved and there is little support for it among scientific experts.

Moore said the evidence he has seen, including at a June U.S. Food and Drug Administration meeting and since, suggests that the benefit of a BA.4/5 booster compared to the original vaccine is “negligible” in terms of preventing infection.

“The public should not regard these Omicron-based boosters as some kind of magic bullet that’s going to change the face of the pandemic and solve all their problems. It will have a marginal impact compared to the booster we currently have,” he said.

‘TOO MANY PEOPLE ARE WAITING’

Dr Eric Topol, a genomics expert and director of the Scripps Research Translational Institute in La Jolla, California, said getting a second booster offers a survival benefit over just one booster that has been documented in five different studies.

“Too many people are waiting when we have really good proof,” he said.

Dr. Bob Wachter, chief of medicine at the University of California, San Francisco, said the evidence is increasingly clear that the longer a person has gone since their last booster, the less protection they have against infection and severe disease.

“There’s a ton of COVID around, and it’s a very infectious agent,” he said.

BA.5 has driven a wave of new cases globally, and now makes up nearly 82% of all U.S. coronavirus infections. read more

Wachter is not convinced retooled BA.4/5 vaccines will be ready to roll out in two months. “It seems a bit ambitious to me, and even if they hit the timeline, it will probably go to the highest-risk groups first,” he said. “I think it’s probably three or four months away for the average person.”

Pfizer told Reuters it has a few million shots of a BA.4/5 vaccine manufactured.

As for the newly authorized Novavax Inc (NVAX.O) vaccine, the company has yet to seek approval for its use as a booster.

Moore, who participated in the Novavax clinical trial, said while it is an excellent vaccine, the company’s boosters are unlikely to be available soon. Novavax has said it is developing a BA.4/5 booster and is aiming to have it ready by the fourth quarter.

“Whatever is in the pipeline is months away,” Topol said. “This is a more virulent, more pathogenic version of the virus and being protected as best you can is smart.”

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Reporting by Julie Steenhuysen, additional reporting by Mike Erman in Maplewood, N.J.; Editing by Caroline Humer, Bill Berkrot and Cynthia Osterman

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Europe must act now or risk tougher COVID measures later, WHO official says

LONDON, July 19 (Reuters) – European nations must accelerate vaccine uptake and bring back mask wearing to tackle a surge in COVID-19 cases driven by an Omicron offshoot and avoid stricter measures later in the year, a senior World Health Organization official said on Tuesday.

In an interview with Reuters, WHO Regional Director for Europe Hans Kluge urged countries to take action now to avoid overwhelming health systems in the autumn and winter as the Omicron subvariant, BA.5, continues to spread rapidly.

Close to three million new COVID-19 cases were reported in Europe last week, which accounted for nearly half of all new cases globally. Hospitalisation rates have doubled over the same period, and close to 3,000 people die of the disease every week, Kluge said in an accompanying statement.

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“There is a rise in cases … amidst a society which is functioning almost as before,” he said, stressing the need for “pandemic stabilisers” such as a second booster dose ahead of the expected variant-specific vaccines in the autumn, as well as the promotion of mask wearing and better ventilation.

These stabilisers must be implemented to avoid much stricter measures, he said, adding: “I don’t think society is ready for ordered lockdowns.”

When the pandemic began in 2020, governments boosted spending to help cushion the impact of lockdowns on their economies and struggling health systems but piled up large debts and are reluctant to repeat those policies.

“People sometimes ask, is the virus back?,” said Kluge. “It has never gone away. It’s still there. It’s spreading. It is mutating. And unfortunately, it’s still taking a lot of lives.”

After two and a half years of the pandemic and related lockdowns and disruptions, countries are now also having to deal with surging inflation and increased food insecurity caused partly by Russia’s invasion of Ukraine, but governments still need to invest further in healthcare, Kluge said.

“And if governments won’t do it, well, then society will not be better prepared for the future,” he added.

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Reporting by Natalie Grover in London; Editing by Jacqueline Wong and Gareth Jones

Our Standards: The Thomson Reuters Trust Principles.

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Why world’s first malaria shot won’t reach millions of children who need it

LONDON/KISUMU, Kenya, July 13 (Reuters) – After decades of work, the World Health Organization endorsed the first-ever malaria vaccine last year – a historic milestone that promised to drive back a disease that kills a child every minute.

In reality, efforts are falling well short of that, with a lack of funding and commercial potential thwarting GSK Plc’s capacity to produce as many doses of its shot as needed, according to Reuters interviews with about a dozen WHO officials, GSK staff, scientists and non-profit groups.

The British drugmaker committed to produce up to 15 million doses every year through 2028, following 2019 pilot programs – considerably less than the WHO says is needed. It is currently unlikely to make more than a few million annually before 2026, according to a source close to the vaccine rollout.

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A GSK spokesperson told Reuters that it could not make enough of its vaccine Mosquirix to meet the vast demand without more funds from international donors, without giving details on the numbers of doses it expected to produce annually in the first years of the roll-out.

“Demand over the next five to 10 years will probably outstrip the current forecasts on supply,” said Thomas Breuer, GSK’s chief global health officer.

The vaccine’s effectiveness at preventing severe cases of malaria in children is relatively low, at around 30% in a large-scale clinical trial. Some officials and donors are hoping that a second shot being tested by Oxford University may prove better, cheaper and easier to produce in bulk.

Yet the world’s inability to fund more Mosquirix shots dismays many in Africa. Children on the continent account for the vast majority of the roughly 600,000 global malaria deaths every year.

“Mosquirix has the potential to save a lot of precious lives before another new vaccine arrives,” said Kwame Amponsa-Achiano, a public health specialist leading a pilot vaccination program in Ghana. “The more we wait, the more children die needlessly.”

Rebecca Adhiambo Kwanya in the Kenyan city of Kisumu needs no convincing: her four-year-old child Betrun has suffered numerous malaria bouts since birth, yet her 18-month-old Bradley – vaccinated in the pilot program – hasn’t caught it.

“My elder one was not vaccinated and he was sick on and off,” she said. “But the smaller one, he got the vaccine and he was not even sick.”

The limited international appetite to produce and distribute more Mosquirix stands in stark contrast to the record speed and funds with which wealthy countries secured vaccines for COVID-19, a disease that poses relatively little risk to children.

Unlike many pharmaceutical products, there is no major market for a malaria vaccine in the developed world, where drug companies typically make the large profits that they say allows them to make their products available at far lower prices in poorer countries.

“This is a disease of the poor, so it’s not been that appealing in terms of the market,” said Corine Karema, chief executive of the nonprofit RBM Partnership to End Malaria, which is working with governments in Africa to eliminate the disease.

“But one kid dies of malaria every minute – that’s unacceptable.”

EXTRA DATA, ADDED YEARS

In the coming weeks, global health organizations will announce the next steps to make Mosquirix widely available, including the first procurement deal and the WHO’s recommended allocation to prioritize roughly 10 million children at highest risk, the source familiar with the rollout plans said.

Long-term, WHO officials say roughly 100 million doses a year of the four-dose vaccine will be needed, which would cover around 25 million children. When the U.N. agency backed Mosquirix last October, it said that even a smaller supply could save 40,000 to 80,000 lives each year, without specifying the number of doses required. read more

GSK’s maximum target of 15 million doses could prevent up to about 20,000 deaths each year, according to a Reuters review of the malaria vaccine models used by WHO.

Yet even hitting 15 million could take years, according to several officials at the WHO and elsewhere in the malaria effort who said wider distribution beyond the pilot countries was unlikely before early 2024, and even then it would start slowly.

GSK also has to upgrade its manufacturing capacity to reach its target. It said it had set up a funding deal with international vaccine alliance Gavi to help stockpile a key ingredient of the shot to ensure there was no gap in supply during that process.

“We are on course to complete the agreed stockpiling volume,” said a spokesperson.

The drugmaker has invested 700 million pounds ($840 million)in the vaccine’s development and says it won’t charge more than 5% above the cost to produce it.

“No company wants to be in a situation where you build manufacturing which oversupplies the market and vaccines will not be used,” said Breuer said, referring to a future split in demand between Mosquirix and the Oxford vaccine, if approved.

After 2028, India’s Bharat Biotech will take over production of Mosquirix’s key ingredient.

GSK’s Breuer expects the deal with Bharat to accelerate production. The British drugmaker will continue to produce the adjuvant – immune-boosting portion – of the vaccine, and recently committed to doubling production to 30 million doses annually, without offering a timeline.

Bharat Biotech, which has yet to outline its manufacturing plans, did not respond to requests for comment.

LOSING SOMEONE TO MALARIA

GSK has donated 10 million doses to pilot programs in Ghana, Kenya and Malawi, and less than half have been shipped so far. The countries plan to expand campaigns this year and next using a mix of the remaining donations and purchased shots.

GSK said a WHO decision to collect additional data on safety and effectiveness from the pilot programs had added years to the launch process, during which it had to idle a dedicated production facility.

The WHO said safety questions had to be addressed before approval, and that it was working urgently to boost supply.

Mary Hamel, the agency’s malaria vaccine implementation head, told Reuters that COVID vaccines had shown how quickly things could move with the political will and funding – which she said malaria had never had.

Mosquirix has been in development since the 1980s, in part because of the complexity of targeting the malaria parasite.

Its regulatory pathway has also been slow. In 2015, GSK published results from a large-scale clinical trial showing vaccine reduced the risk of severe malaria by about 30%. The WHO sought more data on the shot’s safety and effectiveness, gathering information from 2019 during the pilot vaccination programs, before endorsing Mosquirix.

In the past, such real-world data on a vaccine has often been tracked after it has been authorized for use.

“Would we have done it in the West? I don’t know,” said WHO’s Hamel, who was not involved in the decision, referring to holding up the deployment of shots to collect extra data.

BIG DONOR: NO SILVER BULLET

Now recommended for use, it is not clear how the shot’s distribution will be financed long-term. Funding for malaria totaled $3.3 billion in 2020, less than half of the estimated need, the WHO said, for tools such as treatments, bed nets and insecticides.

Adding malaria vaccines could cost between $325 million and more than $600 million annually, depending on how widely they are used, according to a study by global health researchers published in the Lancet journal in 2019. The WHO estimates that the GSK vaccine will cost around $5 per dose.

Two of the biggest funders behind the development and pilot programs for Mosquirix, the Bill and Melinda Gates Foundation and the Global Fund to Fight AIDS, Tuberculosis and Malaria, told Reuters they were committing almost no additional financing to deploy the vaccine.

“It’s not a silver bullet, and it’s relatively expensive compared to other interventions used for malaria,” said Peter Sands, head of the Global Fund. “The fundamental issue with malaria isn’t actually about tools. It’s about the fact that we spend far too little money on it.”

The Gates Foundation said it would continue to back research into how to best use the “historic” vaccine, but “concerns about the relatively low efficacy, short duration, and constrained supply challenges” meant it would not fund deployment.

Gavi is currently the only significant source of funding for a wider Mosquirix rollout. It has approved about $155 million for 2022 through 2025, alongside some funding from the countries themselves. Internal documents seen by Reuters suggest Gavi’s investment in the first year is only expected to be $20 million.

A source familiar with the plans said the group hoped that getting the vaccine rolled out, and countries showing demand, would make the case for more investment.

OXFORD SHOT IN THE WORKS

Several global health officials said future funding from donors might be better committed to a new shot from the scientists at Oxford University who developed AstraZeneca’s COVID vaccine.

Data from small trials showed 77% efficacy over a 12-month period, if given to babies shortly before the peak malaria season. Results from a much larger clinical trial are expected in the coming weeks. Some researchers suggest the GSK vaccine, too, may show higher effectiveness if given seasonally.

Oxford scientist Adrian Hill told Reuters his team aims to secure a WHO recommendation for their malaria shot within a year of submitting data to the agency.

The Serum Institute of India, which will manufacture the vaccine, told Reuters it expects to be able to make up to 200 million doses annually by the end of 2024.

In the years ahead, there are also hopes for a shot being developed by BioNTech (22UAy.DE), using the same mRNA technology as their successful COVID vaccine made with Pfizer . BioNTech aims to begin human trials by the end of 2022.

But in the years before either of those shots might be used, there will not be enough vaccines even for those 10 million children the WHO says are most at risk.

“We should have had this vaccine a long time ago,” said Alassane Dicko, professor of public health at the University of Science, Techniques and Technologies of Bamako in Mali, who has led some of the Mosquirix trials.

“We have to do more.”

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Reporting by Jennifer Rigby and Natalie Grover in London, and Maggie Fick in Nairobi; Additional reporting by Baz Ratner in Kisumu, Kenya; Editing by Michele Gershberg and Pravin Char

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