World

WHO panel approves emergency use of China's Sinopharm vaccine

The World Health Organization gave emergency use authorization Friday to a COVID-19 vaccine manufactured by China's Sinopharm, potentially paving the way for millions of the doses to reach needy countries through a UN-backed program rolling out coronavirus vaccines.

Move paves way for shot to be included in COVAX global vaccine-sharing program

A nurse gives a shot of the Sinopharm COVID-19 vaccine developed by Beijing Institute of Biological Products to a man at a community health station in Nantong in east China's Jiangsu province on Feb. 8. The World Health Organization has given emergency use authorization to the vaccine. (Chinatopix/The Associated Press)

The World Health Organization gave emergency use authorization Friday to a COVID-19 vaccine manufactured by China's Sinopharm, potentially paving the way for millions of the doses to reach needy countries through a UN-backed program rolling out coronavirus vaccines.

The decision by a WHO technical advisory group, a first for a Chinese vaccine, opens the possibility that Sinopharm's offering could be included in the UN-backed COVAX program in coming weeks or months and distributed through UN children's agency UNICEF and WHO's Americas regional office.

Aside from efficacy numbers, the Chinese manufacturer has released very little public data about its two vaccines — one developed by its Beijing Institute of Biological Products and the other by the Wuhan Institute of Biological Products.

The Beijing shot, which has already been exported to some countries, is one the WHO advisory group considered for the emergency use listing.

"This afternoon, WHO gave emergency use listing to sign off on Beijing's COVID-19 vaccine, making it the sixth vaccine to receive WHO validation for safety, efficacy and quality," WHO director general Tedros Adhahom Ghebreysus said.

The Sinopharm vaccine will join ones made by Pfizer-BioNTech, Johnson & Johnson, Moderna, AstraZeneca and a version of the AstraZeneca vaccine made by the Serum Institute of India, in receiving the coveted authorization from the UN health agency.

"This expands the list of vaccines that COVAX can buy and gives countries confidence to expedite their own regulatory approval and to import and administer a vaccine," Tedros said at a Geneva news conference.

Up to 79% effectiveness 

Previously, a separate group advising WHO on vaccines said it was "very confident" the Sinopharm vaccine protects people ages 18 to 59. The group said it had a "low level of confidence" in the vaccine's efficacy for people 60 and over. Its members said they had "very low confidence" in the available data about serious side-effects in that age group.

Sinopharm hasn't published its late-stage test results in scientific journals, so the WHO requested a breakdown of its data, which come mostly from the United Arab Emirates.

"[We] came to the conclusion that there is enough evidence of safety and the capacity of the vaccine to prevent severe disease or symptomatic and hospitalized cases up to 79 per cent," said Dr. Alejandro Cravioto, who heads the WHO advisory group on immunizations. "The information we have for people over 60 is still very scarce."

"There is no reason to think that the vaccine would behave differently in this older age group," he added.

Workers transport boxes of Sinopharm's COVID-19 vaccine from a truck to a cold storage facility of Guangdong Center for Disease Control and Prevention in Guangzhou, in the southeastern Chinese province of Guangdong, on April 8. (cnsphoto/Reuters)

Arnaud Didierlaurent, a professor at the University of Geneva's medical school who chairs the advisory group, said it had requested additional studies from Sinopharm, and that there would be "continuous evaluation" of the vaccine.

"In fact, the work does not stop after the listing," he said.

'Another safe and effective tool'

Gavi, the Vaccine Alliance, which co-runs COVAX, welcomed WHO's emergency approval.

"This means the world has yet another safe and effective tool in the fight against this pandemic," the alliance said. The public-private partnership said it was in discussions with several manufacturers, including Sinopharm, "to expand and diversify the portfolio further and secure access to additional doses" for countries in the COVAX program.

COVAX aims to send vaccines for free to 92 lower-income countries and to help another 99 countries and territories procure them. It was not immediately clear when the Sinopharm vaccine might be made available to the COVAX portfolio.

The program, which has already distributed over 54 million doses of COVID-19 vaccines but faces limited supplies from Western countries and India, has been working hard to strike deals as part of its goal to procure two billion doses by the end of the year.

WATCH | WHO urges global COVID-19 vaccine equity:

WHO comments on need for global COVID-19 vaccine equity

The National

1 month ago
2:04
People in wealthier countries are getting vaccinated at a much faster rate than those in poorer countries despite efforts by the World Health Organization and the international community to make COVID-19 vaccine accessibility equitable around the world. 2:04

Limited public data

Suerie Moon, co-director of the Global Health Program at Geneva's Graduate Institute, said WHO's decision on the Sinopharm COVID-19 vaccine and other Chinese vaccines will "carry a lot of weight" because of limited information publicly available about them.

"The decision is also sure to be scrutinized all around for any whiff of political bias, and no doubt the committee members were very well aware of this," she said, noting that the decision could also be a boon for developing countries.

"If there is a greenlight, these vaccines could boost the thin stream of supplies that has been channelled through COVAX to date," she said, as the program has been hit hard by export bans limiting vaccine supply from India. India has kept those doses amid a surge of cases at home.

Moon also said if Chinese suppliers start channeling large volumes, "this would signal a step-change in their participation in global vaccine markets." Before the pandemic, India was a well-integrated player in the global health vaccine supply system, but China was not, she said.

WHO's decision on Sinopharm, months in the making, was particularly complex because the vaccine has not faced the high-level scrutiny of a rigorous medicines regulator like those in Europe and the U.S.

The WHO panel relied frequently on those Western agencies' findings when it came to vaccines that it has already approved emergency use.

Many officials in countries without such regulatory structures rely on WHO's emergency use listings to authorize vaccine rollouts for their populations.

'Inactivated' vaccines

Hundreds of millions of Chinese vaccines have already been delivered to dozens of countries around the world through bilateral deals as many scrambled to secure supplies after rich countries had reserved the vast majority of supplies from Western pharmaceutical makers.

While China has five shots in use, the majority of its exports abroad come from two companies: Sinopharm and Sinovac. A decision on Sinovac is expected next week, WHO said.

Boxes of the Chinese Sinopharm COVID-19 vaccine are unloaded from a Pakistan Air Force plane on arrival at Nur Khan Airbase in Rawalpindi, Pakistan, on Feb. 1. (Pakistan Ministry of Health/The Associated Press)

The Chinese vaccines are "inactivated" vaccines, made with killed coronavirus. Most other COVID-19 vaccines being used around the world, particularly in the West, are made with newer technologies that instead target the "spike" protein that coats the surface of the coronavirus.

The WHO, in what it called a first, said the vaccine would come a small sticker on the vaccine vials that changes colour as it is exposed to heat, which will inform health workers about whether the vaccine can be safely used.

Sinopharm said last month that over 100 million doses of its two vaccines have been used across the world.

Sinovac, by comparison, has shared more data. Last month, a study published by a team of scientists in Brazil confirmed a previously reported efficacy rate of over 50 per cent. A real-world study in Chile last month found an efficacy rate of 67 per cent.

Add some “good” to your morning and evening.

A variety of newsletters you'll love, delivered straight to you.

Sign up now

now