Judul : AstraZeneca says its COVID-19 vaccine needs 'additional study' - CNA
link : AstraZeneca says its COVID-19 vaccine needs 'additional study' - CNA
AstraZeneca says its COVID-19 vaccine needs 'additional study' - CNA
LONDON: The head of British drug manufacturer AstraZeneca said on Thursday (Nov 26) further research was needed on its COVID-19 vaccine after questions emerged over the protection it offers, but the additional testing is unlikely to affect regulatory approval in Europe.
Instead of adding the trial to an ongoing US process, AstraZeneca might launch a fresh study to evaluate a lower dosage of its vaccine that performed better than a full dosage, AstraZeneca chief executive Pascal Soriot was quoted as saying in a Bloomberg News report.
READ: UK asks regulator to assess AstraZeneca-Oxford vaccine amid questions
AstraZeneca and its partner, the University of Oxford, announced on Monday that it was seeking regulatory approval for the vaccine after it showed an average 70 per cent effectiveness.
That rate jumped to 90 per cent - similar to that in rival vaccines in development by Pfizer/BioNTech and Moderna - when an initial half-dose then a full dose was given to a sub-group of trial participants in error.
US scientists have said the higher rate of effectiveness came during tests in people aged 55 and under and was discovered by accident during the clinical trials.
The head of the Oxford Vaccine Group, Andrew Pollard, said this week that further evidence will be available next month, but the result was still "highly significant".
"Now that we've found what looks like a better efficacy, we have to validate this, so we need to do an additional study," said Soriot.
He said he expected that to be another "international study but this one could be faster because we know the efficacy is high, so we need a smaller number of patients".
READ: AstraZeneca manufacturing error clouds COVID-19 vaccine study results
The additional trial was not likely to delay regulatory approval in Britain and the European Union, Soriot said.
Asked about the Bloomberg report, an AstraZeneca spokesman said there was "strong merit in continuing to further investigate the half-dose/full dose regimen."
"We are further evaluating the data and will work with regulators on the best approach for further evaluation," he said.
"This would add to data from existing trials which are currently being prepared for regulatory submission."
There are high hopes for the AstraZeneca/Oxford vaccine, which Pollard has hailed as a "vaccine for the world" given that it could be cheaper to make, and easier to store and distribute.
It can be stored, transported and handled at normal refrigerated conditions of between two and eight degrees Celsius for at least six months.
Pfizer/BioNTech's offering requires temperatures of -70 degrees Celsius, driving up costs and potentially making it out of reach for lower and middle-income countries.
AstraZeneca/Oxford has also promised to provide its vaccine to the developing world on a non-profit basis.
WAIT AND SEE
The World Health Organization said it looked forward to the full publication of the data from the trial.
"On a review of the detailed data, we will be better positioned to understand the vaccine performance," it said.
READ: 'Infodemic' risks jeopardising COVID-19 vaccines: WHO
The chief medical officer for England, Chris Whitty, also cautioned against drawing premature conclusions, and urged patience until the data were published in peer-reviewed journals.
"It's always a mistake to make too many judgments early and in particular before the independent regulator has had a chance to look at the results," he told a news conference.
Helen Fletcher, professor of immunology at the London School of Hygiene and Tropical Medicine, said the safety data available on the vaccine had been "very robust".
"It's possible that a lower initial vaccine dose could result in higher vaccine efficacy ... More is not necessarily better when it comes to vaccines and immunotherapies," she said.
"It's also possible that a strong immune response to the first vaccine could effectively block an immune response to the second shot of the same virus."
READ: After year-long sprint, COVID-19 vaccines finally at hand
Fletcher's colleague, professor of pharmacoepidemiology Stephen Evans, said speculation about the age distribution in the trials was "not useful to anyone".
"We have good grounds for trusting that the regulation in this high-profile area will be done as carefully or more carefully for these vaccines than for any others in the past," he said.
Gillies O'Bryan-Tear, from the UK Faculty of Pharmaceutical Medicine, said "the eventual efficacy rate may change", but "the validity of the low dose/high dose group results are unlikely to be questioned".
"Even if they (the regulators) decided to ignore the results of the low dose/high dose group, the study of the high dose/high dose patients will still be strongly significant, but I think that it unlikely," he said.
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