North Korea COVID-19 Vaccination Plan Facing Challenges

As North Korea faces a rising number of COVID-19 cases, simply having vaccines may be insufficient to roll out a countrywide immunization process that experts say needs to be accompanied by adequate cold storage units and trained medical and technical staff that the nation lacks.

Pyongyang announced on Tuesday that “more than 32,810 fevered cases” were detected in the country from June 12 to 13, through its state media Korea Central News Agency (KCNA). The total, “since late April,” surged past 4.5 million as of June 14, added the KCNA.

Outbreak first reported in May

North Korea first reported the outbreak of the virus on May 12. Until Pyongyang acknowledged the outbreak, it claimed zero cases since the global pandemic in early 2020.

The regime is battling the spread with “vigorous” anti-epidemic work by conducting tests to “confirm coronavirus infected cases” in Pyongyang, border areas and high-risk regions. It is also implementing quarantine measures such as installing “more than 11,300 temporary quarantine wards,” said the KCNA on a separate report on Tuesday.

Gavi, a global vaccine distribution network, told VOA’s Korean Service that North Korea “has accepted an offer of vaccines from China and has started to administer doses.”

Gavi, attributing comments to a spokesperson, did not say when the immunization began and what kind of WHO-approved Chinese vaccines such as Sinopharm, Sinovac or CanSino were sent.

North Korea, however, did not indicate it has begun a countrywide vaccination program that experts say is the only viable way to try to prevent severe illnesses and deaths.

Arthur Reingold, division head of epidemiology at University of California who served as a member of the WHO’s Strategic Advisory Group of Experts on Immunization (SAGE) from 2005 to 2012, said, “Vaccination with an effective SARS-Cov-2 vaccine is really the only approach that can limit morbidity, hospitalization, (and) death at this point.”

SARS-CoV-2 is the severe acute respiratory syndrome coronavirus 2 that causes coronavirus disease 2019, which came to be called COVID-19.

Gavi ‘ready to support’

Pyongyang has not accepted vaccine offers from the U.S., South Korea or international vaccine sharing programs such as Gavi. The Gavi spokesperson said it “has always been ready to support Pyongyang should it request our assistance, but so far,” did not receive “formal request for COVID-19 vaccine support.”

Heeje Lee is a researcher with the Korea Health Policy Project at Harvard Medical School who has traveled to North Korea multiple times since 2016 to teach at Pyongyang University of Science and Technology, North Korea. He told VOA’s Korean Service that the regime might have opted out of conducting a massive vaccination program due to medical challenges.

“Considering and weighing benefits and risks, they might have selected the zero-COVID strategy instead of nationwide vaccination,” Lee said. “They are very good at mobilization. It might have been easier for them to control behavior of the population such as lockdown and border closure than handling medical accidents from the vaccination.”

Experts said North Korea needs to overcome several medical and technical hurdles if it wants to begin a COVID-19 immunization program as it would need to import cold storage units and medical and technical experts. This is especially true if Pyongyang wants to use the mRNA vaccines, which need careful handling.

David Salisbury, associate fellow of Global Health Program at Chatham House, a policy institute in London, and director of immunization at the U.K.’s Department of Health until 2013, said, “Given the very demanding cold chain requirements for mRNA vaccines, this is likely to be very difficult for North Korea.”

The most effective vaccines, such as Pfizer and Moderna, use mRNA technology that instructs cells in the body to produce protein, which triggers immunity against the virus.

Pfizer vaccines are shipped at temperatures between minus 90-60 degrees Celsius and can be stored in the freezer between minus 25-15 degrees Celsius for up to two weeks.

Moderna vaccines are shipped at temperatures between minus 50-15 degrees Celsius and can be stored in the freezer at the same temperature.

After thawing, both vaccines can be kept in the refrigerator between 2-8 degrees Celsius for up to one month.

“Those [mRNA] vaccines need to be shipped and stored in very cold freezers and then thawed and delivered, by needle injection within several hours, perhaps a day,” said John Moore, a professor of microbiology and immunology at Weill Cornell Medical College in New York City.

“There are real logistical challenges to providing and using these freezers,” he said. “The mRNA (vaccines) may just be more than what the North Koreans can actually handle.”

Chinese vaccines and Novavax must also be kept in refrigerator temperature of approximately 4 degrees Celsius, said Moore.

Nagi Shafik, former project manager for WHO and UNICEF in North Korea, said, “If we are going to use the mRNA vaccines (such as) Pfizer or Moderna, (North Korea) will need ultra-cold refrigerators, which UNICEF can provide as they did with other countries.”

In 2021, UNICEF delivered 800 ultra-cold storage units to about 70 countries to store COVID-19 mRNA vaccines.

The Gavi spokesperson told VOA’s Korean Service on Friday that “regarding challenges of mRNA vaccines … that’s something we’d only be able to comment on if/when (North Korea) submits an updated national vaccine deployment plan as part of a request for support.”

VOA’s Korean Service contacted North Korea’s mission to the U.N., asking whether it is willing to accept mRNA vaccines if they are offered but did not receive a reply.

Turning to other vaccines

Due to the challenges of using mRNA vaccines, Moore said North Korea could resort to other vaccines.

“Chinese vaccines … are easier to use,” Moore said. “Those vaccines are mediocre by our standards but would be able to reduce the incidence of severe and fatal infections.” Sinopharm vaccines have an efficacy rate of 79%, and Sinovac vaccines are 51% effective, according to the WHO.

“There’s also another highly effective Western vaccine called Novavax,” which is “more potent” than Chinese vaccines, said Moore. Novavax vaccines have a 90% efficacy rate. In comparison, Pfizer and Moderna mRNA vaccines both have a 95% efficacy rate.

However, to be used properly, all these vaccines — particularly the mRNA vaccines — would require North Korea to accept outside medical experts who can administer immunizations, according to experts.

Country ‘will need help’

“North Korea will need help from global partners to acquire all the necessary knowledge for the vaccination” as well as “technical experts to make sure the cold chain works properly,” said Lee.

North Korea “would need few medical experts to administer the process of vaccination and storing vaccine,” said Shafik.

Experts said Pyongyang would also need to obtain power sufficient to run cold storage units – for both mRNA and non-mRNA vaccines – throughout the nation of nearly 26 million people.

North Korea lacks a reliable power supply, often struggling to keep lights on. According to the CIA World Factbook, only 26% of its total population had access to electricity in 2019.

Lee said North Korea has “solar refrigeration and solar panels” that are available in case of interruption on the electricity supply. However, Shafik said, solar-powered cold units may need to be supplemented for mass immunization.

“UNICEF had provided some solar energy (powered) refrigerators and (they are) working well for a ‘regular’ vaccination program,” Shafik said. “But for mass vaccination, there could be some modifications and other arrangement(s) to be considered before the campaign.”

Source: Voice of America

FDA Advisers Move COVID-19 Shots Closer for Kids Under 5

COVID-19 shots for U.S. infants, toddlers and preschoolers moved a step closer Wednesday.

The Food and Drug Administration’s outside vaccine advisers gave a thumbs-up to Moderna’s two shots for the littlest kids. The panel is set to vote later Wednesday on whether to also recommend Pfizer’s three-shot series for those youngsters.

The outside experts voted unanimously that the benefits of Moderna’s shots outweigh any risks for children under 5 — that’s roughly 18 million youngsters.

They are the last remaining group in the U.S. to get vaccinated, and many parents have been anxious to protect their little children. If all the regulatory steps are cleared, shots should be available next week.

“This is a long-awaited vaccine,” said panel member Dr. Jay Portnoy of Children’s Hospital in Kansas City, Missouri. “There are so many parents who are absolutely desperate to get this vaccine, and I think we owe it to them to give them a choice to have the vaccine if they want to.”

Dr. Peter Marks, FDA’s vaccine chief, opened the meeting with data showing a “quite troubling surge” in young children’s hospitalizations during the omicron wave, and noted that 442 children under 4 have died during the pandemic. That’s far fewer than adult deaths but should not be dismissed in considering the need for vaccinating the youngest kids, he said.

“Each child that’s lost essentially fractures a family,” Marks said.

FDA reviewers said both brands appear to be safe and effective for children as young as 6 months old in analyses posted ahead of the all-day meeting. Side effects, including fever and fatigue, were generally minor in both, and less common than seen in adults.

The two vaccines use the same technology, but there are differences. In a call with reporters earlier this week, vaccine experts noted that the shots haven’t been tested against each other, so there’s no way to tell parents if one is superior.

“That is a really important point,”‘ said Dr. Jesse Goodman of Georgetown University, a former FDA vaccine chief. “You can’t compare the vaccines directly.”

If the FDA agrees with its advisers and authorizes the shots, there’s one more step. The Centers for Disease Control and Prevention will decide on a formal recommendation after its own advisers meet Saturday. If the CDC signs off, shots could be available as soon as Monday or Tuesday at doctor’s offices, hospitals and pharmacies.

Pfizer’s vaccine is for children 6 months through 4 years. Moderna’s vaccine is for 6 months through 5 years.

Moderna’s shots are one-quarter the dose of the company’s adult shots. Two doses appeared strong enough to prevent severe illness but only about 40% to 50% effective at preventing milder infections. Moderna has added a booster to its study and expects to eventually offer one.

Pfizer’s shots are just one-tenth its adult dose. Pfizer and partner BioNTech found that two shots didn’t provide enough protection in testing, so a third was added during the omicron wave.

Pfizer’s submitted data found no safety concerns and suggested that three shots were 80% effective in preventing symptomatic coronavirus infections. But that was based on just 10 COVID-19 cases. The calculation could change as more cases occur in the company’s ongoing studies.

The same FDA panel on Tuesday backed Moderna’s half-sized shots for ages 6 to 11 and full-sized doses for teens. If authorized by the FDA, it would be the second option for those age groups. Currently, the Pfizer vaccine is their only choice.

The nation’s vaccination campaign started in December 2020 with the rollout of adult vaccines from Pfizer and Moderna, with health care workers and nursing home residents first in line. Teens and school-age children were added last year.

Moderna said in April that it is also seeking regulatory approval outside the U.S. for its little kid shots. According to the World Health Organization, 12 other countries already vaccinate kids under 5, with other brands.

In the U.S., it remains uncertain how many parents want their youngest children vaccinated. While COVID-19 is generally less dangerous for young children than older kids and adults, there have been serious cases and some deaths. Many parents trying to keep unvaccinated tots safe have put off family trips or enrolling children in day care or preschool.

Still, by some estimates, three-quarters of all children have already been infected. Only about 29% of children ages 5 to 11 have been vaccinated since Pfizer’s shots opened to them last November — a rate far lower than public health authorities consider ideal.

Dr. Nimmi Rajagopal, a family medicine physician at Cook County Health in Chicago, said she’s been preparing parents for months.

“We have some that are hesitant, and some that are just raring to go,” she said.

Source: Voice of America

TAAG opens China/Brazil route for cargo transport

Luanda – Angola’s Airlines TAAG starts operating this week on the Changsha/Luanda/São Paulo route (China, Angola and Brazil), for the exclusive transport of cargo, with an annual turnover of US$200 million.

The completion of this operation results from a commercial agreement signed between TAAG and the Chinese aviation business group Lucky Aviation on Wednesday in Luanda.

Speaking at the signing ceremony, TAAG CEO, Eduardo Fairen, explained that the route will be operated, initially, by a Boeing 777-200 ER type aircraft.

The aircraft, with a capacity of 56 tons of various goods, with stress to raw material, agricultural products, electronic material, clothing, among other goods, will make two flights a week (about 80 hours of flights).

As for the agreement, the CEO said that, later, TAAG plans to scale to other Chinese cities, focusing on Hong Kong, Chengdu Tianfu, Guangzhou, Chengdu Shuangliu, Shanghai Hongqiao and Beijing, capital of China.

The general representative of China Lucky Aviation (CLCA) in Angola, Tongxi Li, said that the agreement signed will generate 200 direct jobs at Angola’s airports.

He said the partnership between Lucky Aviation and TAAG is an example of successful economic cooperation and bringing the commercial aviation sector closer between the two countries.

Tongxi Li assured that CLCA is working, with the support of the two governments to build two international air logistics hubs for passengers and cargo, selecting Angola as a key country, in the context of supporting the improvement of the international image of Angolan airports.

Source: Angola Press News Agency

Elections2022: CASA-CE coalition formalizes candidacy

Luanda – The political coalition CASA-CE submitted Wednesday to the Constitutional Court (TC) the process for the formalization of its candidacy, to run for the general elections to take place in August 24, in Angola.

The process was delivered by the Coalition’s delegate for candidacies, Carlos Jacinto, to the director of the Office of Political Parties of the TC, Mauro Alexandre.

With this step, the Broad Convergence for the Salvation of Angola – Electoral Coalition (CASA-CE) becomes the second political organization to formalize the candidacy at the TC, after the ruling MPLA.

There are now 10 days left to the end of the candidacies delivery process for analysis by the Constitutional Court, which started on June 6.

After all processes are assessed by the said court, the political groups will have 10 more days to correct any flaws or insufficiency detected in their respewctive processes, according to the electoral law.

Founded by politician Abel Chivukuvuku, on April 03, 2012, almost four months before the general elections of that year, CASA-CE is currently the third political force in the country, after MPLA and UNITA, with 16 MPs represented in the Parliament as a result of the general elections held in 2017.

Since February 2021, the coalition is being led by Manuel Fernandes, who replaced André Gaspar Mendes de Carvalho, that replaced the founder of the coalition Abel Chivuvukuvu.

CASA-CE is composed of the Party of Free Alliance of Angolan Majority (PALMA), the Party of Support for Democracy and Development of Angola – Patriotic Alliance (PADDA-AP), the Angolan Pacific Party (PPA), the National Party for the Salvation of Angola (PNSA) and the Democratic Party for the Progress of Angola National Alliance (PDP-ANA).

Of the four elections already held in the country, CASA-CE’s first participation in a general election was in 2012, when it obtained eight representatives in Parliament with almost six percent of the vote.

In 2017, CASA-CE won 643,961 votes (9.4 percent), corresponding to the current 16 MPs, surpassing the Social Renewal Party (PRS), until then the second largest opposition party.

These will be the first democratic elections to include the vote of Angolans living abroad, following a constitutional revision approved in 2021.

The August’s general elections will be the fifth in the country’s history, since the abandonment of the one-party system (1991), with an inaugural vote followed by a violent post-election crisis in 1992.

The September 1992 crisis degenerated into a prolonged armed conflict that interrupted the regularity of the democratic process until 2008, the year the second election took place in Angola.

With the end of the war in February 2002, the country returned to the polls successively in 2008, 2012, and 2017.

Source: Angola Press News Agency

Sonangol reassures normal gas production and supply in Angola

Luanda – The Gas and Renewable Energy Business Unit (UNGER) of the state-owned oil company Sonangol, said Wednesday it has available enough butane to supply the domestic market.

In a press release, UNGER reacts to a fake news circulating on social networks, which “advises” families to have full reserve butane-gas as some constraints in the supply of the product are supposedly foreseen in the last week of July and early August, due to alleged maintenance at the Luanda Refinery.

According to UNGER, its production and distribution system are in full operation all over the country without any indicator or prospect of change in the near future.

The company reiterates its appeal to citizens to purchase butane in the usual manner, at official retailers and not to mind those rumours circulating in social networks, most likely with the aim to generate price hike of the product in the market.

Source: Angola Press News Agency