A sign featuring the AstraZeneca Plc logo stands at the company's DaVinci building at the Melbourn Science Park in Cambridge, U.K., on Monday, June 8, 2020 | Jason Alden/Bloomberg
A sign featuring the AstraZeneca Plc logo stands at the company's DaVinci building at the Melbourn Science Park in Cambridge, UK | Jason Alden | Bloomberg File photo
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Bloomberg: One of the most promising coronavirus vaccines has stumbled, delivering a reality check about the odds of clinical development and the safety risks involved.

The news that AstraZeneca Plc paused tests of its experimental shot after one patient became ill is a routine event for the pharma industry. It could be a harbinger of something worrisome or entirely unrelated to the vaccine.

But in a world crippled by the pandemic, the setback comes as a reminder that vaccines can fail, or worse, that they can sometimes deliver more harm than good — a disclaimer for politicians and governments promising that a Covid-19 fix is around the corner. Drugmakers just this week pledged to make safety a priority and take the time necessary to let science prevail.

The halt “shows the perils of rushing to market,” said Sam Fazeli, an analyst for Bloomberg Intelligence, adding that no vaccine candidate is immune to such misfortunes, especially now that the experimental products are being injected in tens of thousands of people in the last crucial phase of clinical tests.

Astra’s situation reinforces the need for discipline that comes with following the traditional testing process. Yet that’s no easy message for people waiting for progress after months of lockdowns and economic uncertainty.

Independent researchers are poring over the one patient’s unexplained illness, which took place in the U.K. arm of the test, to determine whether it happened by chance or as a result of the treatment, according to Astra.

The halt “shows that the system works,” said Ugur Sahin, the chief executive officer of rival vaccine maker BioNTech SE. Physicians running the trial and other experts will now assess the case, and if no strong connection to the vaccine is found, the study will probably continue with special measures in place to detect other such cases, he said in a telephone interview.

Drugmakers have condensed the development timeline for their vaccines — normally a matter of years — down to months, with early results from some of the frontrunners expected in coming weeks. Some of the data could deliver more surprises: Typically only 6% of experimental vaccines are successful. A vaccine against HIV has eluded scientists for decades.

Also read: Oxford Covid vaccine trial paused after unexplained illness, AstraZeneca says it’s ‘routine’

The Astra suspension will likely delay the study results that were due in November, Adam Barker, an analyst at Shore Capital, wrote in a note to clients. The company is developing the shot with the University of Oxford. It could also impact others relying on a similar technology, such as Johnson & Johnson and China’s CanSino Biologics Inc., if the issue is related to the adenoviral vector used, according to Bloomberg Intelligence’s Fazeli.

The news shouldn’t affect other rival products such as Pfizer Inc.’s and partner BioNTech’s, which could have crucial test readings by October. Other drugmakers working on shots include Moderna Inc., Sanofi and China’s SinoVac Biotech Ltd.

“Any vaccine trial has to go through rigid ethical approval,” said Liu Peicheng, a spokesman for SinoVac, adding that the Astra setback wouldn’t affect the company’s plans or timeline.

Politicians have helped stoke expectations about a vaccine. Health officials in the U.S. and President Donald Trump have said an immunization is possible before the end of the year, and potentially as early as next month.

But guaranteeing a product that is safe may take longer — especially since the shot could end up being administered to millions of people who are healthy and would only get a mild illness with Covid-19.

Need to pause

“The vaccine would be given to many, many people to prevent an illness that would likely do no harm to them, in order to prevent spread in the community to more vulnerable people,” Shore’s Barker said. “In that scenario, safety becomes absolutely everything. Any major safety issue would ultimately be terminal to any vaccine candidate.”

Russia has tried to leapfrog the process in the race to be first with a Covid-19 shot, approving its Sputnik V product before it’s undergone full testing and drawing widespread skepticism. A group of international scientists have questioned results from a study of the vaccine, saying some of the findings appeared improbable.

“The world is entirely focused on having a vaccine,” said Kristine Macartney, director of Australia’s National Centre for Immunisation Research and Surveillance. “But we just need to pause and see what the next few days bring.”

Also read: Oxford’s new Covid vaccine begins human trials in partnership with Serum Institute of India


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  1. The common man is the worst sufferer of this entire pandemic.The lockdown measures are not going to affect either the scientist’s families or the politicians.It’ s easy to keep on delaying trials and the stuff but the ground reality is way more horrifying. All what is now is a big covid market that has great potential for people to profit.

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