Month: November 2020

Recordings Reveal WHO’s Analysis of Pandemic in Private

As the coronavirus explodes again, the World Health Organization finds itself both under intense pressure to reform and holding out hope that U.S. President-elect Joe Biden will reverse a decision by Washington to leave the health agency.
With its annual meeting underway this week, WHO has been sharply criticized for not taking a stronger and more vocal role in handling the pandemic. For example, in private internal meetings in the early days of the virus, top scientists described some countries’ approaches as “an unfortunate laboratory to study the virus” and a “macabre” opportunity to see what worked, recordings obtained by The Associated Press show. Yet in public, the U.N. health agency lauded governments for their responses.
Biden has promised to overturn President Donald Trump’s decision in June to cut off funds to WHO and withdraw the U.S. WHO has also bowed to demands from member countries for an independent panel to review its management of the pandemic response, and WHO Director-General Tedros Adhanom Ghebreyesus said Monday that the agency welcomed “any and all attempts” to strengthen it “for the sake of the people we serve.”
One of the central dilemmas facing the WHO is that it has no enforcement powers or authority to independently investigate within countries. Instead, the health agency relies on behind-the-scenes talks and the cooperation of member states.
Critics say WHO’s traditional aversion to confronting its member countries has come at a high price. As COVID-19 spread, WHO often shied away from calling out countries, as big donors such as Japan, France and Britain made repeated mistakes, according to dozens of leaked recordings of internal WHO meetings and documents from January to April obtained by The Associated Press.
Some public health experts say WHO’s failure to exert its influence lent credence to countries adopting risky outbreak policies, possibly compromising efforts to stop the virus.
“We need WHO to be bold and to use their political power to name and shame because the consequences are so devastating,” said Sophie Harman, a professor of international politics at Queen Mary University in London. “This is their Spanish flu moment … By not speaking up when countries are doing questionable things, WHO is undermining its own authority while the planet burns.”
Others said it would be politically unwise for WHO to be too outspoken unless countries give the agency more power and the ability to censure countries — an option that Germany and France have recently proposed.
“If Tedros was to take a very aggressive stance toward member countries, there would be repercussions,” said Suerie Moon, co-director of the Global Health Centre at the Graduate Institute of Geneva, referring to WHO’s director-general.
WHO spokeswoman Farah Dakhlallah said that since the beginning of the coronavirus outbreak, “WHO officials have had and continue to have, frank and open discussions with government counterparts … We are proud of an organizational culture that fosters candid discussion with the aim of reaching life-saving solutions.”
One of the scientists in the meetings, emergencies chief Dr. Michael Ryan, also laid out WHO’s approach in answer to a media question March 11 on whether the agency was willing to say which countries weren’t doing enough.
“The answer to that question is, you know who you are,” Ryan said. “The WHO doesn’t interact in public debate or criticize our member states in public. What we try to do is work with our member states constructively.”
It’s not unprecedented, however, for WHO to publicly question its member states. It threatened to close its China office when the country was hiding cases during the SARS outbreak, loudly called for Nigeria to reverse its boycott of the polio vaccine in 2003 and accused Tanzania of not sharing enough information about an Ebola epidemic last year.
The review of WHO’s role in the pandemic comes at a critical time because the agency is now tasked with helping to buy and distribute coronavirus vaccines around the world once any prove effective, especially to poorer nations. Some countries, including the U.S. and Russia, have refused to join the effort, but on Sunday, WHO chief scientist Dr. Soumya Swaminathan said she hoped Biden’s election would “open the door” to U.S. inclusion.
WHO’s reticence to call out countries started with China, as the AP earlier reported. Despite a January meeting between Tedros and Chinese President Xi Jinping, information on the outbreak was still sparse throughout February. Maria Van Kerkhove, WHO’s technical lead for COVID-19, noted that the agency lacked “enough detail to say what has worked and what hasn’t.”
Yet at a media briefing shortly afterwards, Tedros said, “China is doing many good things that are slowing the virus and the facts speak for themselves.”
Also in February, WHO scientists were concerned about Japan. On Feb. 1, a passenger who disembarked the Diamond Princess cruise ship in Hong Kong tested positive for the coronavirus. At the ship’s next stop in Yokohama, 10 more cases were found and authorities put all 3,711 people on board under lockdown.
Ryan told reporters at the time: “Let’s be careful here not to overreact.” But on Feb. 10, the case count nearly doubled overnight.
“(That’s) not surprising given the nature of the response of the investigation,” Ryan said at an internal meeting, saying only a small number of epidemiologists had been assigned to the outbreak. “If you double the number of cases in a ship in a day, something is not right.”
Dr. Thomas Grein, WHO’s chief of acute events management team, reported to his colleagues that WHO had discussed the outbreak with their Japanese counterparts, but failed to glean much useful information.
“It’s a very, very sensitive issue and we need to tread carefully,” he warned.
Although WHO was keenly aware the situation was deteriorating, scientists said the outbreak could help in understanding COVID-19 transmission patterns.
“(It’s) unfortunate, but a useful opportunity to study the natural history of the virus,” Ryan said.
Several days later, Japanese outbreak specialist Dr. Kentaro Iwata went aboard the Diamond Princess and called the response “completely chaotic.” Soon afterward, WHO announced more than half of the world’s known COVID-19 cases outside China were aboard the Diamond Princess.
“It was very obvious on that cruise ship that things were going badly wrong and WHO should have said something,” said Lawrence Gostin, director of the WHO Collaborating Center on Public Health Law and Human Rights at Georgetown University. “When what countries are doing is flat-out wrong, we need WHO to say so.”
While WHO wasn’t specific, Tedros said on Feb. 26: “One of the biggest challenges we face is that too many affected countries are still not sharing data with WHO.”
Throughout February and March, COVID-19 triggered outbreaks in South Korea, Singapore, Iran and elsewhere. The virus also gained a foothold in Italy, turning Europe into the epicenter of the pandemic.
At WHO, officials worried in internal meetings about the lack of information from European member states. Grein said WHO’s efforts to get more detail about the spiraling outbreaks had “spectacularly failed.”
Yet on March 8, Tedros tweeted that “the government & the people of Italy are taking bold, courageous steps aimed at slowing the spread of the #coronavirus & protecting their country & world.” Three days later, Tedros declared COVID-19 to be a pandemic, saying the announcement was made partly due to “alarming levels of inaction” by countries, which he didn’t name.
Georgetown University’s Gostin said WHO should be obligated to publicly report when countries aren’t sharing enough data.
“If a country is not providing vital epidemiological or biological information, then WHO and the world are flying blind in an outbreak and we can’t have that,” he said.
WHO also complained in private about Western countries hoarding scarce pandemic supplies.
“We had the terrible situation yesterday with (protective personal equipment) where all the supplies were requisitioned in France and we lost access,” Ryan told his colleagues. He said WHO needed to pressure countries and companies to avoid similar situations.
As countries across Europe moved to adopt social distancing measures and cancel mass gatherings in early March, Ryan noticed one country didn’t: Britain.
“There isn’t a single sports event in Europe and yet all of the Premier League matches in the U.K. are to go ahead as normal,” he said. Ryan described Britain’s pandemic strategy as “problematic” after hearing the U.K.’s chief scientific officer publicly say the country was aiming for herd immunity.
“For that to happen, hundreds of thousands and millions of older people are going to become infected and there is just going to be so much death,” Ryan said. Still, he said, the different approaches to tackling COVID-19 globally could prove to be “a massive ecological study” that would allow WHO to document what worked best.
“It’s macabre in some ways, but it’s reality,” he said.
Going forward, WHO’s role in the continued unfolding of the pandemic will depend in part on the panel review. Harman, the expert from Queen Mary University, sympathized that WHO had enormous responsibility in the early months of COVID-19, but said even greater challenges loom now.
“This is not an experiment for WHO to learn lessons for the future, the stakes are too high for that,” she said. “With the next wave of the pandemic, I think the time for quiet diplomacy has passed.”

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Developing Nations Could Lose Out in Race for Coronavirus Vaccine

A vaccine for the coronavirus has proved 90% effective after early trials, according to its joint developers Pfizer and BioNTech. It’s raised hopes that the global coronavirus pandemic can be brought under control in the coming months – but as Henry Ridgwell reports, the nature of the vaccine means less developed health systems face major challenges in rolling out any inoculation programs.Camera: Henry Ridgwell    
Producer:  Henry Ridgwell, Mary Cieslak 

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Iconic Australian Telescope Celebrates Indigenous Astronomy 

Australia’s most famous radio telescope that played a key role in televising the Apollo 11 moon landing in 1969 has been given a new Aboriginal name. Known as “The Dish,” the telescope near Parkes in New South Wales, 380 kilometers west of Sydney, will also be called “Murriyang,” meaning “Skyworld” in the local indigenous language.   The Parkes Observatory has three telescopes. All have been given new Aboriginal names in respect of the astronomical knowledge of Australia’s original inhabitants, whose stories of creation, known as the Dreaming, are told by the stars.   The largest telescope, which has discovered hundreds of new galaxies and rapidly spinning neutron stars called pulsars, is also to be known as “Murriyang” or “Skyworld.” The others have Aboriginal names meaning “Smart Eye” and “Smart Dish.”   Dr. John Reynolds is the director of the Australia Telescope National Facility, which is run by the national science agency, the CSIRO.   “I think the bestowing of traditional names is very significant because not only does it recognize the traditional custodians of the land where the telescopes sit, but it highlights the link between the oldest science, astronomy, and the longest continuous civilization in the world that has been practicing astronomy for generations. The new name for the familiar Parkes dish — the big 64-meter [dish] — is Murriyang, which represents the sky world in the Wiradjuri dreaming,” said Reynolds.  The names were chosen by Wiradjuri elders, who say it is one of their proudest moments.   While it is operated mainly for astronomy research, the Parkes telescope has a long history of being contracted by international space agencies to track and receive data from spacecraft. In 2012, it helped to monitor NASA’s Curiosity rover during its descent onto the surface of Mars.   But perhaps its most famous mission was its part in receiving television signals on a momentous day in July 1969 during the Apollo 11 moon landing.   The story was made into a popular movie “The Dish” in 2000, which helped to cement the facility’s legendary status in Australian science.   The telescope weighs 1,000 tons and only receives signals from space, but never sends them. It was officially opened in October 1961.  

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New US Army Museum Opens On Veterans Day

For the first time, the United States Army has its own museum.  The National Museum of the United States Army opens on Veterans Day Wednesday in Fort Belvoir, Virginia. The Army is the only U.S. military service that did not have a national museum. Located 32 kilometers from Washington, D.C., the museum traces the history of the country’s oldest military service, which began 245 years ago in 1775.The exterior of the National Museum of the United States Army at twilight. The simplicity and sharpness of the exterior allows reflections to be cast on the façade transforming the character of the building through every season and time of day.The large five-story complex features interactive and dramatic historical exhibits, along with thousands of documents, images, artwork and artifacts, big and small. They include an iconic Sherman tank used in World War II, a helicopter from the Vietnam War, an armored personnel carrier from the Iraq War in 2003, and a saddle for horseback riding by Army special forces in the mountains of Afghanistan in 2001.     A life-size exhibit illustrates American forces storming the beaches of Normandy on D-Day during World War II.   Helmets, swords and medals are also featured, and even a watch that was found in a damaged section of the Pentagon after the 9/11 attacks.Cast figures, lighting effects, imagery, and sounds of distant battle recreate a setting based on a famous photograph of the Meuse-Argonne Allied Offensive during World War I.Although many exhibits focus on wartime activities, the museum also highlights peacekeeping operations and humanitarian missions around the world, Tammy Call, director of the museum, told VOA.  A major exhibit called Soldier Stories tells “the individual soldier story” as part of the comprehensive history, explained Call, a civilian who is an Army veteran, “and so it allows us to get very personal and reflective,” she added.   Jack Querfeld, director of internal affairs at the American Legion headquarters in Indianapolis, Indiana, was impressed that the various battles shown in the exhibits “put a human face on it, instead of just saying we fought here.” “The National Army Museum will be a place for members of the total Army family to gather and share their stories,” said Ryan D. McCarthy, secretary of the Army. That means a lot to B.J. Lawrence, executive director for the Washington, D.C., office of the Veterans of Foreign Wars. Lawrence was an Army sergeant in South Korea in the early 1980s.The “Huey” was the iconic helicopter of the Vietnam War. The helicopters arrived in Vietnam in 1962 as aerial ambulances.He said the museum is “phenomenal,” and as he toured the complex, he found “the exhibits that pertain to the Korean War had an especially touching effect on me.”   “I continue to advocate to bring the soldiers home that were missing in action,” Lawrence said. Querfeld said, “I think the museum will help children now and those from generations to come understand what their military forefathers experienced.”  The museum “tells us how important military service is to our nation,” Lawrence said. “And it helps to explain and put into perspective why the American people enjoy the freedoms they do today.” 

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US Records 1 Million COVID-19 Cases in First 10 Days of November

The United States on Monday reported more than 1 million new cases of COVID-19 in just the first 10 days of November.The U.S. has recorded over 10 million cases of COVID-19 — the highest of any country in the world — according to the Johns Hopkins Coronavirus Resource Center.Midwestern states are being hit the hardest, with hospitalization rates in the region reaching record highs. The COVID-19 Tracking Project said more than 59,000 people were hospitalized nationwide on Monday.On the same day that the U.S. recorded this spike, two U.S. drug companies announced developments in the fight against the virus.Pfizer announced that its experimental vaccine was 90% effective in preventing the virus in participants without evidence of prior infection.U.S.-based drugmaker Eli Lilly and Canadian-based biotech firm AbCellera announced a new antibody drug known as bamlanivimab. It is part of a class of treatments known as monoclonal antibodies, which are made to act as immune cells that scientists hope can fight off the virus. The antibody therapy is similar to one given to U.S. President Donald Trump after he tested positive for COVID-19 early last month.The FDA has approved the antibody drug for people 12 and older who are at risk of developing a serious form of COVID-19.FILE – A man holds a mock syringe as demonstrators protest against Sao Paulo state governor Joao Doria and China’s Sinovac COVID-19 vaccine, in Sao Paulo, Brazil, Nov. 1, 2020.Just hours after news of a breakthrough in the effort to develop a safe and effective COVID-19 vaccine, Brazil halted late-stage clinical trials of another potential vaccine.The country’s health regulator, Anvisa, announced Monday that it was pausing tests of CoronaVac, developed by Chinese pharmaceutical company Sinovac, after an “adverse, serious event” with a volunteer participant. The event occurred on October 29, but the statement did not go into any other details.The clinical trials in Brazil are being conducted by Sao Paulo-based research institute Butantan. Dimas Covas, the head of the state-run institute, told a local television station that a volunteer had died but that the death was not due to the vaccine.The Sinovac vaccine is the third to be put on hold after a volunteer became ill after being inoculated. U.S. pharmaceutical giant Johnson & Johnson put a hold on its late-stage clinical trials of its COVID-19 vaccine last month, while another U.S.-based drugmaker, AstraZeneca, halted its late-stage trial of a vaccine developed with the University of Oxford in September after a volunteer in Britain was diagnosed with transverse myelitis, an inflammatory syndrome that affects the spinal cord and is often sparked by viral infections.It is not uncommon for clinical trials to be suspended if a volunteer falls ill so that organizers can determine whether the illness is due to the vaccine. But Brazilian President Jair Bolsonaro, who has often expressed mistrust of China, has openly doubted the effectiveness of the Sinovac vaccine and has insisted that his government will not purchase the drug.People wait next to their cars outside the Cotugno hospital as the battle with the coronavirus disease (COVID-19) intensifies, in Naples, Italy, Nov. 9, 2020.Cases spike in EuropeCOVID-19 infections have spiked in other parts of the world, including in Europe, where some governments have instituted lockdown measures to slow the spread of the virus. Globally the number of confirmed cases is more than 50 million, with 1.2 million deaths and 33 million people recovered.According to The Associated Press, intensive care units in France, Italy and Spain are low on hospital beds and staff as case numbers continue to increase.The situation is worsening in Italy, where five more regions have been placed in the government’s so-called “orange” zone of its new three-tiered system that imposes various degrees of restrictions.The system splits Italy’s 20 regions into three zones — red, orange and yellow — with red indicating the most restricted areas and yellow the least restricted.Abruzzo, Umbria, Tuscany, Liguria and Basilicata will join the southern regions of Puglia and Sicily in the orange, or medium, zone; under this zone, residents can move freely within their towns or cities, but cannot leave them, while bars and restaurants are limited to delivery and takeout service.The northern province of Bolzano has been placed in the red zone, joining its sister regions of Lombardy, Piedmont, Valle d’Aosta and the southern region of Calabria. Residents in these zones will not be allowed to leave their homes except for work or medical reasons.All of Italy is under a curfew from 10 p.m. to 5 a.m., while museums and shopping centers are closed on the weekends and high school classes switch from in-person to online.Italy has 960,373 confirmed novel coronavirus cases, including 41,750 deaths, according to the Johns Hopkins Coronavirus Resource Center.

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ByteDance Challenges Trump’s TikTok Divestiture Order

ByteDance, the Chinese parent company of video-sharing app TikTok, filed a petition late Tuesday with a U.S. Appeals Court challenging a Trump administration order set to take effect Thursday requiring it to divest TikTok. President Donald Trump in an Aug. 14 order directed ByteDance to divest the app within 90 days, which falls on Thursday. “Facing continual new requests and no clarity on whether our proposed solutions would be accepted, we requested the 30-day extension that is expressly permitted in the August 14 order,” TikTok said in a statement. “Without an extension in hand, we have no choice but to file a petition in court to defend our rights,” the company said. FILE – Women wearing masks to prevent the spread of the coronavirus chat as they pass by the headquarters of ByteDance, owners of TikTok, in Beijing, China, Aug. 7, 2020.The White House and Treasury declined to comment. The Justice Department did not immediately comment. The Trump administration contends TikTok poses national security concerns as the personal data of U.S. users could be obtained by China’s government. TikTok, which has over 100 million U.S. users, denies the allegations. The petition names Trump, Attorney General William Barr, Treasury Secretary Steven Mnuchin and the Committee on Foreign Investment in the United States (CFIUS), the inter-agency panel that reviews certain transactions involving foreign investment on national security concerns. It says the CFIUS action and Trump order “seek to compel the wholesale divestment of TikTok, a multibillion-dollar business built on technology developed by” ByteDance “based on the government’s purported national security review of a three-year-old transaction that involved a different business.” That order was based on a government review of ByteDance’s 2017 acquisition of U.S. social media app Musical.ly, which ByteDance merged into TikTok. Separate restrictions on TikTok from the U.S. Commerce Department have been blocked by federal courts, including restrictions on transactions that were scheduled to take effect Thursday that TikTok warned could effectively ban the app’s use in the United States. Talks have been ongoing to finalize a preliminary deal for Walmart Inc and Oracle Corp to take stakes in a new company to oversee U.S. operations. Trump has said the deal had his “blessing.” 

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Slam Poets Convene in Mali for Festival

Mali this year struggled with an Islamist insurgency, a worldwide pandemic, and an August military coup, all of which left most cultural events in the West African nation in shambles.But Mali’s annual International Festival of Slam and Humor, FISH, was merely delayed until November, after a post-coup curfew was lifted.Twenty-three-year-old Malian Aïcha Diarra first learned of competitive, performance poetry – Slam Poetry - when her high school held a contest.She has been a slam poet ever since and competes at FISH every year.  She performed on stage for the first time in nearly a year at this year’s festival, which she said brought her great joy.Diarra sees her art as a form of activism to highlight the struggles of Malian women and girls. Sitting on a graffiti-covered rooftop in Bamako, she says many of the topics in her poems are considered too bold in conservative Mali.But, she says, some people congratulate her for daring to talk about taboo subjects such as circumcision of young girls.Cultural crossroadsSlam Poetry is a relatively new music scene in Mali, a country with deep musical traditions that is seen as a cultural crossroads in Africa. Slam Poetry first appeared in Mali in 2006, years after it gained popularity in the United States, and FISH started in 2014.The annual festival is run by Malian group Agoratoire, founded by one of Mali’s first slam poets, Aziz Koné. The theme for this year’s festival is Peace and Social Cohesion.Just days before the festival, France, the region’s former colonial power, launched airstrikes in central Mali that killed more than 50 jihadists.Mali has been struggling against an Islamist insurgency spreading in the Sahel region along with thousands of U.N. and French troops.Anger over the ongoing conflict fueled mass protests that led the military in August to oust President Ibrahim Boubacar Keita.Despite the unrest, the festival – and Mali’s slam poets – have seen their support base grow, including among musicians.Poets as musiciansDjelimady Cissoko is an executive member of the Malian Federation of Artists.  He teaches the kora – a West African stringed instrument – to students at the National Arts Institute.Cissoko says the slam poets are considered full-fledged musicians.Undeterred by the region’s ongoing conflict and unrest at home, Mali’s slam poets are passionate about their art and a better future for their country. 

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Slam Poets Convene in Mali for Festival

Mali – known for its music and cultural events – attracted artists from around West Africa to this year’s annual slam poetry festival. Reporter Annie Risemberg followed one young Malian poet who is bucking stereotypes in the conservative nation in this report from Bamako.

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New 3-D Weather-Mapping Program Could Revolutionize Forecasting

As severe weather events increase in frequency and intensity across the U.S. and around the world, scientists and forecasters are seeking more effective weather-mapping programs. VOA’s Julie Taboh has more.
Camera: Adam Greenbaum   Produced by: JulieTaboh/Adam Greenbaum
 

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’Lockdown’ Named 2020 Word of the Year

The Collins English Dictionary has named “lockdown” its Word of the Year for 2020.
 
The word, which the dictionary said surged in usage from 4,000 logged uses last year to more than a quarter million this year, refers to “the containment measure implemented by governments around the world to mitigate the spread of COVID-19.”
 
Several other pandemic-related words were also in the running such as “social distancing” and “coronavirus,” but lockdown won out in the end.  
 
Not all the contenders were pandemic-related, with “BLM” (Black Lives Matter) and “Megxit” also vying for word of the year.
 
Megxit refers to Britain’s Prince Harry and his American wife Meghan Markle’s decision to step down as senior royals  and spend more time abroad.
 
Lockdown, the dictionary said in a news release, “with its heavy, clunking syllables and heavier associations, is the condition we’ve most dreaded in 2020 – a state of national stasis, where almost everything that constitutes normal public life is suspended.” 

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EU Files Antitrust Charges Against Amazon Over Use of Data

European Union regulators have filed antitrust charges against Amazon, accusing the e-commerce giant of using data to gain an unfair advantage over merchants using its platform.
The EU’s executive commission, the bloc’s top antitrust enforcer, said Tuesday that the charges have been sent to the company.
The commission said it takes issue with Amazon’s systematic use of non-public business data to avoid “the normal risks of competition and to leverage its dominance” for e-commerce services in France and Germany, the company’s two biggest markets in the EU.
The EU started looking into Amazon in 2018 and has been focusing on its dual role as a marketplace and retailer.
In addition to selling its own products, the U.S. company allows third-party retailers to sell their own goods through its site. Last year, more than half of the items sold on Amazon worldwide were from these outside merchants.
Executive Vice President Margrethe Vestager, the EU commissioner in charge of competition, said it’s not a problem that Amazon is a successful business but “our concern is very specific business conduct which appears to distort genuine competition.”
Amazon faces a possible fine of up to 10% of its annual worldwide revenue, which could amount to billions of dollars. The company rejected the accusations.
“We disagree with the preliminary assertions of the European Commission and will continue to make every effort to ensure it has an accurate understanding of the facts,” the company said in a statement.
The company can, under EU rules, reply to the charges in writing and present its case in an oral hearing.
Vestager also opened a second investigation into Amazon over whether it favors its own products and those from third-party merchants that use its logistics and delivery services.
It’s the EU’s latest effort to curb the power of big technology companies, following a series of multi-billion-dollar antitrust fines against Google in previous years.

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Pakistan Says Pfizer Vaccine Not Suited for Developing Nations 

A top Pakistani government scientist says Pfizer’s coronavirus vaccine is not suited for Pakistan, or other developing countries because of the -80°C temperatures it needs to be kept at, and the need for a second shot.The American pharmaceutical company announced Monday that late-stage testing on its potential two-dose vaccine indicates it is more than 90% effective in preventing the virus in participants without evidence of prior infection.The revelation is being hailed as a rare piece of positive news in the fight against the pandemic that has globally infected more than 50 million people, with 1.2 million deaths and 33 million people recovered.But Professor Atta Ur Rahman, who heads Pakistan’s Task Force on Science and Technology, said Tuesday it is “premature at least” for his country or others in the developing world to celebrate the Pfizer vaccine.“This is a messenger RNA vaccine and it has to be transported at -80°C, so this vaccine is not suited for developing countries,” Rahman told VOA. “The cold storage infrastructure and chains to take this from the airport across the cities and across the countries are missing in the developing world,” the professor explained.He went on to note that COVID-19 patients would require two doses of the Pfizer vaccine three weeks apart and “a low-temperature carriage” requirement makes it all the more difficult in Pakistan, where average summer temperatures in southern and southwestern regions soar to between 40°C and 50°C.COVID-19 is the disease caused by the coronavirus.FILE – Students wear protective face masks, maintaining a safe distance as they attend a class amid COVID-19 pandemic in Peshawar, Pakistan, Sept. 30, 2020.Own clinical trials on Chinese vaccinesRahman said Pakistan is also conducting its own final-phase clinical trials on two Chinese-made single-dose vaccines in partnership with China. He says that the vaccines can be transported in normal temperatures, unlike the Pfizer vaccine.“Our trials are going on very well. The results are very positive as far as I am aware… Both these vaccines do not have this -80°C transportation problem. I expect the vaccines to be better suited for Pakistan than the Pfizer vaccine.” One of the vaccines under trial in Pakistan has been developed by Chinese biotech firm CanSinoBio and is already undergoing Phase 3, or large-scale, testing on humans in several countries, including China, Russia, Chile and Argentina.Rahman said the clinical trials in Pakistan, which began in September, will take at least three months and that the results will then be sent back to China to be evaluated.Pakistan has documented nearly 347,000 infections, with 7,000 deaths and almost 320,000 people recovered since the pandemic hit the country of about 220 million in February.The number of cases in Pakistan has steadily declined to a few hundred a day since mid-June, when the daily rate of infection spiked at more than 6,000.But officials in recent days have warned the South Asian nation is experiencing a second wave of infections, reporting 1,637 new cases and 23 deaths Tuesday. The resurgence has prompted the government to revive some restrictions on public movement to stem the spread of the ailment. 

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US Supreme Court to Hear Obamacare Case

The U.S. Supreme Court heard oral arguments Tuesday in a Republican effort to strike down the Affordable Care Act health care law.The hearing comes weeks after Justice Amy Coney Barrett joined the court, giving conservatives a 6-3 majority.At the center of the case is a requirement in the 2010 law for most people to have a minimum level of health insurance or face a financial penalty.In a 2012 case, the Supreme Court ruled that provision was allowed on the basis that it represented a tax that Congress is allowed to levy. In 2017, the Republican-controlled Congress and set the penalty to zero.A group of states, led by Texas, is leading the current charge to dismantle the health care law, commonly known as Obamacare.  They argue that the mandate for individuals to purchase health coverage is unconstitutional, and that without that provision, the entire Affordable Care Act must be struck down.Part of the original congressional intent in requiring people to have coverage was that it would bring more healthy people into the system who would pay premiums without using many services, helping to offset costs of individuals who needed more care, including those with pre-existing conditions who had previously been denied coverage.Texas and its partners argue that eliminating the individual mandate would create an imbalance and push health costs unfairly higher.The opposition is led by California, and points to the 2017 action by Congress as evidence that lawmakers had no problem with removing only the penalty for the individual mandate while allowing the rest of the Affordable Care Act to remain in place. They further argue that as the law stands, with no penalty in place, it merely encourages people to have health insurance, and thus cannot be seen as an unconstitutional imposition by the government.The court is expected to issue its ruling in the case by late June or early July.Of the justices who were members of the court during the 2012 case, Justices Samuel Alito and Clarence Thomas voted to strike down the entire law.  Chief Justice John Roberts and Justices Stephen Breyer, Elena Kagan and Sonia Sotomayor voted to uphold it.Justices Barrett, Brett Kavanaugh and Neil Gorsuch have since joined the court. If the court strikes down the law, up to 20 million people could lose their health coverage and insurance companies could be allowed to deny coverage to people with pre-existing conditions. 

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Brazil Suspends Trials of COVID-19 Vaccine in its Final Trials Before Possible Approval

Brazil’s health regulator Anvisa suspended clinical trials of a Chinese firm’s coronavirus vaccine after an unspecified “adverse incident” involving a volunteer recipient late last month. Anvisa would only say such incidents could involve a death or serious disability resulting in hospitalization.  Anvisa’s action with the CoronaVac vaccine occurred the same day a rival, U.S. pharmaceutical company, Pfizer, announced its vaccine has shown 90 percent effectiveness. Word of Pfizer’s vaccine success sent global financial markets soaring. Both the Pfizer and the Chinese Sinovac vaccine are in Phase III trials, the last stage of testing before regulators give it clearance for public use. Brazil has the highest coronavirus tally in Latin America, with more than 5,664,000 confirmed cases and 162,397 deaths, according to the Johns Hopkins University and Medicine Coronavirus Resource Center. 

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US Allows Emergency Use of COVID-19 Antibody Drug

U.S. health officials have allowed emergency use of the first antibody drug to help the immune system fight COVID-19, an experimental approach against the virus that has killed more than 238,000 Americans.  The Food and Drug Administration on Monday cleared the experimental drug from Eli Lilly for people 12 and older with mild or moderate COVID-19 not requiring hospitalization. It’s a one-time treatment given through an IV.  The therapy is still undergoing additional testing to establish its safety and effectiveness. It is similar to a treatment President Donald Trump received after contracting the virus last month. Lilly’s studies of the antibody drug are continuing. Early results suggest it may help clear the coronavirus sooner and possibly cut hospitalizations in people with mild to moderate COVID-19. A study of it in hospitalized patients was stopped when independent monitors saw the drug did not seem to be helping in that situation. The government previously reached an agreement to buy and supply much of the early production of Lilly’s drug. FILE – Lab technicians load vials of investigational coronavirus disease (COVID-19) treatment drug remdesivir at a Gilead Sciences facility in La Verne, California, March 18, 2020. (Gilead Sciences Inc/Handout)Only one drug, Gilead Sciences’ remdesivir, has full FDA approval for treating COVID-19. Government treatment guidelines also back using dexamethasone and other steroids for certain severely ill, hospitalized patients. One other treatment has an emergency use designation now: convalescent plasma, made from the blood of COVID-19 survivors. No large studies have shown it to be more effective than usual care alone, however.  The new drug is part of an emerging family of biologic therapies that offer a promising new approach to preventing serious disease and death from COVID-19. Experts say the infused drugs could serve as a therapeutic bridge to help manage the virus until vaccines are widely available. The drugs are laboratory-made versions of antibodies, blood proteins the body creates to help target and eliminate foreign infections. The new therapies are concentrated versions of the antibodies that proved most effective against the virus in patient studies. Regeneron Pharmaceuticals Inc. also has asked for emergency authorization for an antibody drug it is testing, the one Trump received. FILE – Medical technicians work at a drive-thru coronavirus testing facility at the Regeneron Pharmaceuticals company’s Westchester campus in Tarrytown, New York, September 17, 2020.FDA regulators authorized the Lilly drug using their emergency powers to quickly speed the availability of experimental drugs and other medical products during public health crises. Potential benefits must outweigh risksIn normal times the FDA requires “substantial evidence” to show that a drug is safe and effective, usually through one or more large, rigorously controlled patient studies. But during public health emergencies the agency can lower those standards and require only that an experimental treatment’s potential benefits outweigh its risks. The emergency authorization functions like a temporary approval for the duration of the COVID-19 pandemic. To win full approval, Lilly will have to submit additional research to fully define the drug’s safety and benefit for patients.  The government has signed an agreement with Lilly to spend $375 million to buy 300,000 vials of the drug. How many doses that would provide is unclear. Each vial contains 70 milligrams and that dose proved ineffective in the early results. It took four times that amount — 2,800 milligrams — to show any effect. The Lilly drug is authorized for people 12 and older who weigh at least 40 kilograms (about 88 pounds), and who are at high risk for progressing to severe COVID-19 and/or hospitalization. This includes those who are 65 years of age or older, or who have certain chronic medical conditions. 

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British Prime Minister Johnson Welcomes Pfizer/BioNTech Vaccine News

British Prime Minister Boris Johnson welcomed the news from pharmaceutical company Pfizer that one of its potential vaccines showed better than 90% efficacy in Phase 3 tests. But he cautioned that a vaccine is still a long way off and that one vaccine is not a solution.Speaking to reporters in London, Johnson said the data released Monday by Pfizer and its German partner, BioNTech, indicated the vaccine is safe, but the findings must be peer reviewed.Johnson stressed these are the “very, very early days” of this vaccine search, and he compared this news to “the distant bugle of the scientific calvary coming over the brow of the hill.” The prime minister said the bugle is louder, but the calvary is still a long way off.Johnson said the British government earlier this year ordered 40 million doses of the Pfizer/BioNTech vaccine, enough for one-third of the British population. He said they had ordered 300 million more doses from five other potential vaccines as well.But the prime minister said if the Pfizer vaccine proves effective and passes all appropriate safety checks, then the government will begin a nationwide vaccine distribution program administered by the National Health Service.Johnson was also asked about the results of the U.S. election being called for Joe Biden, with Kamala Harris as his vice president-elect. He congratulated the two Democrats and said while his government has had a good relationship with the Trump administration, he has no doubt that will continue under Biden.Johnson said he was particularly excited to work with the incoming administration in their efforts to fight climate change.

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Emmy-Winning Visual Effects Artist Draws From Her Cambodian Roots

From a child of immigrants drawing on the walls of the family’s house to an Emmy-winning visual effects artist drawing for Hollywood, a Cambodian American talent represents a classic success story of the American dream. Now, she hopes to bring the dream to her motherland. VOA’s Chetra Chap reports.Camera: Sisovann Pin 

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HUD Secretary Ben Carson Tests Positive for Coronavirus

The secretary of Housing and Urban Development, Ben Carson, has tested positive for the coronavirus, according to a department spokesperson. The HUD secretary “is in good spirits and feels fortunate to have access to effective therapeutics which aid and markedly speed his recovery,” the agency’s deputy chief of staff, Coalter Baker, said in a statement. After experiencing symptoms, Carson, 69, went to Walter Reed National Military Medical Center where he was tested, reports say. The noted pediatric neurosurgeon is expected to fully recover. A memo sent to HUD staff said Carson was “resting at his house and is already beginning to feel better.” Anyone who came into contact with Carson will be notified, the memo said. Carson was one of several people who attended an election night party at the White House on Tuesday, where few attendees wore masks or practiced social distancing, several news organizations have reported. Also, the White House recently announced that chief of staff Mark Meadows and other staffers had tested positive for the virus that causes the COVID-19 disease. Meadows’ diagnosis was announced November 6. A few weeks ago, President Donald Trump was hospitalized at Walter Reed after he was diagnosed with the coronavirus.President-elect Joe Biden has called on Americans to wear a mask. He said at a news conference Monday that wearing a mask is “not a political statement.” Carson joined the Trump administration in 2017. Carson ran unsuccessfully as a Republican presidential candidate in 2016. 
 
 

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Twitter Could Strip Trump of Certain Privileges Post-Presidency

Twitter says it could strip President Donald Trump’s account of certain privileges when projected election winner Joe Biden takes office on January 20.
 
Trump’s recent tweets alleging voter fraud in the November 3 election have been tagged by Twitter, with notices that say for example, “This claim about voter fraud is disputed.”
 
Ordinarily, Twitter would remove such tweets, but affords world leaders some further latitude.
 
“A critical function of our service is providing a place where people can openly and publicly respond to their leaders and hold them accountable,” a Twitter spokesman told the Bloomberg news agency. “With this in mind, there are certain cases where it may be in the public’s interest to have access to certain tweets, even if they would otherwise be in violation of our rules.”
 
This policy, however, does not apparently extend to former leaders, Twitter told the Reuters news organization.
 
“This policy framework applies to current world leaders and candidates for office, and not private citizens when they no longer hold these positions,” a Twitter spokesman told Reuters in a statement.
 
Trump is refusing to concede the election, alleging voter fraud. He is suing various states over what he says are irregularities.  
 
Media organizations, including VOA, have projected Biden as the winner of the election, with 279 electoral votes.

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Pfizer Says COVID-19 Vaccine 90% Effective in Trials

Pharmaceutical company Pfizer says late-stage testing on its potential COVID-19 vaccine indicates it is more than 90 percent effective.
Pfizer’s chairman and chief executive, Albert Bourla, along with its partner,  BioNTech, made the announcement Monday regarding the Phase 3, late-stage study of their potential vaccine. The statement said the study showed the vaccine to be more than 90 percent effective in preventing the virus in participants without evidence of prior infection in the first interim efficacy analysis.
The analysis was conducted by an independent data monitoring board, which examined 94 infections recorded so far in a study that has enrolled nearly 44,000 people in the United States and five other countries.
In his statement, Bourla said the results demonstrate the potential vaccine can help prevent COVID-19 in the majority of people who receive it. He cautioned, however, that while this is a critical first step, these efficacy results alone will not allow the companies to apply for U.S. Food and Drug Administration ((FDA)) Emergency Use Authorization.  
He said more data on safety is also needed, adding, “We are continuing to accumulate that safety data as part of our ongoing clinical study.
“We estimate that a median of two months of safety data following the second and final dose of the vaccine candidate – required by FDA’s guidance for potential Emergency Use Authorization – will be available by the third week of November,” he said.
The top infectious disease expert in the U.S., Dr. Anthony Fauci, has said he was looking for a vaccine with 70- to 75 percent efficacy and that even 50 percent was acceptable.
From his Twitter account, U.S. President Donald Trump noted the reported 90 percent efficiency, calling it “SUCH GREAT NEWS,” and that the stock market was “UP BIG” as a result.STOCK MARKET UP BIG, VACCINE COMING SOON. REPORT 90% EFFECTIVE. SUCH GREAT NEWS!— Donald J. Trump (@realDonaldTrump) November 9, 2020President-elect Joe Biden praised the development announced by Pfizer in a statement Monday but warned that the “end of the battle against COVID-19 is still months away.”Statement by President-elect Biden on Pfizer’s vaccine progress: pic.twitter.com/eOiLZnqO8N— Biden-Harris Presidential Transition (@Transition46) November 9, 2020The news comes as drug makers and research centers around the world scramble to deliver a safe and effective vaccine in an attempt to bring an end to the coronavirus pandemic that has claimed more than 1.25 million lives worldwide, according to the Johns Hopkins University.

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Virgin Hyperloop Hosts First Human Ride on New Transport System

Richard Branson’s Virgin Hyperloop has completed the world’s first passenger ride on a super high-speed levitating pod system, the company said on Sunday, a key safety test for technology it hopes will transform human and cargo transportation. Virgin Hyperloop executives Josh Giegel, its Chief Technology Officer, and Sara Luchian, Director of Passenger Experience, reached speeds of up to 107 miles per hour (172 km per hour) at the company’s DevLoop test site in Las Vegas, Nevada, the company said. “I had the true pleasure of seeing history made before my very eyes,” said Sultan Ahmed Bin Sulayem, Chairman of Virgin Hyperloop and Group Chairman and Chief Executive of DP World. Los Angeles-based Hyperloop envisions a future where floating pods packed with passengers and cargo hurtle through vacuum tubes at 600 miles an hour (966 kph) or faster.Virgin Hyperloop test in Las Vegas, Nevada, Nov. 9, 2020.In a hyperloop system, which uses magnetic levitation to allow near-silent travel, a trip between New York and Washington would take just 30 minutes. That would be twice as fast as a commercial jet flight and four times faster than a high-speed train. The company has previously run over 400 tests without human passengers at the Nevada site. The test comes a month after Reuters first reported that Virgin Hyperloop picked the U.S. state of West Virginia to host a $500 million certification center and test track that will serve as a proving ground for its technology. The company is working toward safety certification by 2025 and commercial operations by 2030, it has said.  Canada’s Transpod and Spain’s Zeleros also aim to upend traditional passenger and freight networks with similar technology they say will slash travel times, congestion and environmental harm linked with petroleum-fueled machines. 

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Tropical Storm Eta Hits Florida Keys

Tropical Storm Eta made landfall late Sunday in the Florida Keys on its way into the eastern Gulf of Mexico before taking another aim at the southeastern U.S. state later this week. The U.S. National Hurricane Center said the storm had maximum sustained winds of 100 kilometers per hour as it brought heavy rainfall and life-threatening flash floods to parts of southern Florida. Forecasters expect the storm to strengthen slightly into a hurricane later Monday or Tuesday but weaken again into a tropical storm before making a mainland Florida landfall. Officials have closed beaches, ports and coronavirus testing sites in the state and urged people to stay home. Florida’s governor has also declared a state of emergency in several counties to speed the government’s response. Forecasters expect Eta to drop 15 to 30 centimeters of rain on central and southern Florida through Friday. Parts of the Bahamas, Jamaica and Cuba will also see some heavy rains. Eta was a strong hurricane when it hit Nicaragua last week, bringing flooding rains to communities from Panama to Mexico. Rescuers in Guatemala continued searching Sunday for people caught in a landslide and authorities raised the official death toll to 27 with more than 100 people still missing. The storm has been blamed for at least 20 deaths in southern Mexico and at least 20 more in Honduras. 

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