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U.K. regulator to assess AstraZeneca’s vaccine candidate amid trial questions

Britain asked its regulator on Friday to assess AstraZeneca’s COVID-19 vaccine for a possible rollout, while the Philippines and Thailand secured millions of doses, giving the shot a vote of confidence after experts raised questions about trial data.

The U.K. government, which has secured 100 million doses of the vaccine developed by AstraZeneca and Oxford University, has targeted a rollout to begin before Christmas.

“We have formally asked the regulator to assess the Oxford/AstraZeneca vaccine, to understand the data and determine whether it meets rigorous safety standards,” British Health Secretary Matt Hancock said.

“This letter is an important step towards deploying a vaccine as quickly as safely possible.”

In the global race to develop vaccines against COVID-19, AstraZeneca’s candidate is viewed as offering one of the best hopes for many developing countries because of its cheaper price and ability to be transported at normal fridge temperatures.

The Thai government signed a deal on Friday to procure 26 million doses of the vaccine to fight the pandemic, which has killed more than 1.4 million people globally. Officials in the Philippines said they would secure 2.6 million shots and were negotiating a possible purchase of a further 1 million doses.

The announcements came after some scientists raised doubts about the robustness of results showing the shot was 90 per cent effective in a sub-group of trial participants who, by error initially, received a half dose followed by a full dose.

President of AstraZeneca in Thailand James Teague attends an agreement signing ceremony in Bangkok on Thursday for the country to purchase AstraZeneca’s potential COVID-19 vaccine. (Chalinee Thirasupa/Reuters/Pool)

AstraZeneca CEO Pascal Soriot said on Thursday that the drugmaker was likely to run an additional global trial to assess the efficacy of its vaccine using the lower dosage.

The company had released trial data on Monday that showed its experimental vaccine prevented on average 70 per cent of COVID-19 cases in late-stage trials in Britain and Brazil.

While the success rate was 90 per cent in the sub-group, some experts said the relatively small number of participants made it harder to be confident in the findings.

AstraZeneca said the administering of the half dose had been reviewed and approved by independent data safety monitors and the U.K. regulator, adding the regulator publicly confirmed there was “no concern.”

Confusion ‘problematic’ for public confidence

When the full dose was given twice, as it was for most trial participants, the success rate was 62 per cent — still above the 50 per cent required by U.S. regulators. Europe’s drug regulator has said it will not set a minimum level of efficacy.

If a vaccine has an efficacy of 50 per cent, it means that if 100 people who have not been exposed to the virus are immunized with the shot, 50 of them would not get infected, on average.

AstraZeneca’s CEO says the drugmaker will likely to run an additional global trial to assess the efficacy of its coronavirus vaccine using the lower dosage. (Dado Ruvic/Reuters)

A spokesperson for Oxford University said additional data from international trials would help researchers assess the vaccine’s efficacy among a more diverse population.

But Pauline Londeix, co-founder of French drug transparency group OT-Med, said apparent confusion over the trial results was “very problematic for public confidence in vaccines.”

“It has largely to do with the race drugmakers are engaged in currently, which leads them to present vaccine candidates in the best possible way and not release full protocols and results. It is the opposite of what is needed in our view.”

Trial redo helpful for confidence

Dr. Michael Gardam, an infectious disease specialist at Women’s College Hospital in Toronto, said AstraZeneca almost needs to start the clinical trial over again.

“Whenever you’ve got a trial that the company wasn’t entirely truthful with what happened in the beginning, that sets people’s confidence back,” Gardam said on CBC News Network on Thursday.

“I think doing the big trial redo that they are talking about is going to be very helpful for that confidence, but that’s also going to set them back six months. The real problem here is people are really on edge and any little tweak that happens, people worry about it and rightly so.”

Nonetheless, Britain’s top science adviser said the interim results showed the AstraZeneca vaccine was successful.

“The headline result is the vaccine works and that’s very exciting,” Patrick Vallance said on Thursday during a news conference with Prime Minister Boris Johnson.

AstraZeneca expects 4 million doses to be available in Britain by the end of December. Britain’s Medicines and Healthcare products Regulatory Agency (MHRA) started an accelerated “rolling review” of the vaccine at the start of this month as data comes in on safety and efficacy.

Dr. Howard Njoo, Canada’s deputy chief public health officer, said Wednesday that the vaccine trial questions reinforces the need for regulators to do their due diligence in reviewing vaccine candidates.

Federal officials say Canada has agreements with these vaccine manufacturers: AstraZeneca, GlaxoSmithKline/Sanofi, Johnson & Johnson, Medicago, Moderna, Novavax and Pfizer. 

A peer-reviewed analysis of data from the AstraZeneca-Oxford trial will be published in The Lancet in the coming weeks.

The U.S. Food and Drug Administration (FDA), has not commented on the trial results. The European Medicines Agency said on Thursday it would “assess data on the efficacy and safety of the vaccine in the coming weeks.”

Moncef Slaoui, scientific adviser for the U.S. government’s vaccine program Operation Warp Speed, has noted that no-one in the sub-group that got the initial half dose was older than 55 — suggesting that regimen’s efficacy in older people was unproven.

“There are a number of variables that we need to understand, and what has been the role of each one of them in achieving the difference in efficacy,” Slaoui told a briefing on Tuesday.

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