Chinese companies earlier drew attention for giving the vaccine to their top executives and leading researchers before human trials to test their safety and efficacy had even begun.
After the first shot, he had no reaction. But Kan Chai felt woozy following the second dose of a COVID-19 vaccine approved for emergency use in China. ”When I was driving on the road, I suddenly felt a bit dizzy, as if I was driving drunk,” the popular writer and columnist recounted on a webinar earlier this month. ”So I specially found a place to stop the car, rest a bit and then I felt better.”
His is a rare account from the hundreds of thousands of people who have been given Chinese vaccines, before final regulatory approval for general use. It’s an unusual move that raises ethical and safety questions, as companies and governments worldwide race to develop a vaccine that will stop the spread of the new coronavirus.
Chinese companies earlier drew attention for giving the vaccine to their top executives and leading researchers before human trials to test their safety and efficacy had even begun. In recent months, they have injected a far larger number under an emergency use designation approved in June, and that number appears poised to rise.
A Chinese health official said Friday that China, which has largely eradicated the disease, needs to take steps to prevent it from coming back. But one outside expert questioned the need for emergency use when the virus is no longer spreading in the country where it was first detected.
It’s unclear exactly who and how many people have been injected so far, but Chinese vaccine makes have offered some clues. State-owned Sinopharm subsidiary CNBG has given the vaccine to 350,000 people outside its clinical trials, which have about 40,000 people enrolled, a top CNBG executive said recently.
Another company, SinoVac, has injected 90 per cent of its employees and family members, or about 3,000 people, most under the emergency-use provision, CEO Yin Weidong said. It has also provided tens of thousands of rounds of its CoronaVac to the Beijing city government.
Another candidate being jointly developed by the military and Cansino, a biopharmaceutical company, has been approved for emergency use in military personnel. ”The first people to have priority in emergency use are the vaccine researchers and the vaccine manufacturers because when the pandemic comes, if these people are infected then there’s no way to produce the vaccine,” Yin said.
Now, large Chinese firms including telecom giant Huawei and broadcaster Phoenix TV have announced they’re working with Sinopharm to get the vaccine for their employees. Several people who say they work in ‘front-line’ organisations have said on social media that their workplaces have offered vaccinations for about 1,000 yuan (USD 150). They declined to comment, saying they would need permission from their organisation.
In an established but limited practice, experimental medications have been approved historically for use when they are still in the third and last phase of human trials. Chinese companies have four vaccines in phase 3 – two from Sinopharm and one each from SinoVac and Cansino.
The Chinese government referenced the World Health Organisation’s emergency-use principles to create its own through a strict process, National Health Commission official Zheng Zhongwei said at a news conference Friday.
He said there have been no serious side effects in the clinical trials.
”We’ve made it very clear that the COVID-19 vaccine we put into emergency use are safe,” Zheng said. ”Their safety can be ensured but their efficacy is yet to be determined.” Under the emergency rule, high-risk personnel such as medical and customs workers and those who have to work overseas are given priority access, he said. He declined to provide exact numbers.
”In China’s case, the pressure in preventing imported infections and domestic resurgence is still huge,” Zheng said.
But Diego Silva, a lecturer in Bioethics at the University of Sydneym, said that giving vaccines to hundreds of thousands outside of clinical trials doesn’t have ‘scientific merit’ in China, where there are currently very few locally transmitted cases, and incoming arrivals are quarantined centrally.
”If it’s in the US Where the virus is still raging that’s a bit different, but in a country like China it doesn’t seem to make sense to me,” he said. Because there’s not enough of the virus in China locally to deduce anything, you’re introducing a whole host of others factors by injecting people outside of trials.
Zheng said that all those injected under emergency use are being closely tracked for any adverse health effects. Kan Chai, the columnist, wrote in an article posted online in September that despite initial hesitation, he decided to sign up after he heard a state-owned company was looking for volunteers.
He didn’t say whether his was an emergency-use case, but the timing of his vaccination suggests it was. He took the first dose in late July, when the emergency inoculations were getting started and the trials were all but over. ”I’m willing to be a little white mouse, and the biggest reason is because I have trust in our country’s vaccination technology,” he said.
His real name is Li Yong, but his 1.65 million followers on the Twitter-like social platform Weibo know him better by his pen name, which means ’10 years of chopping wood.’ He declined an interview request. He described taking the vaccine in a public webinar hosted by 8am HealthInsight, a popular health media outlet. It’s unclear why he qualified to receive it. Scant information is publicly available about the program’s scope, size, and scientific merit.