In the second group, 8,895 participants received a full dose followed by another full dose at least a month later. This group was only 62% protected.
That’s why AstraZeneca says their vaccine is 70% efficace, on average.
But some scientists are questioning why the company would report on a pooled result of two different trials, as it deviates from standard reporting on clinical trials.
And in the days following that announcement, another point of confusion has emerged.
Martedì, Mene Pangalos, AstraZeneca’s Executive Vice President who heads up non-oncology research and development, first explained to Reuters that a lab error was the reason why some volunteers had received a smaller dose — the dose that proved to be 90% efficace. “The reason we had the half dose is serendipity,” Pangalos said, adding that researchers had “underpredicted the dose of the vaccine by half.”
In a statement on Wednesday, Oxford’s communications manager for vaccines told CNN that “dose selection for any new vaccine is a complicated area, and in exploring methods of dose selection, we discovered one gave a lower dose than expected.”
Oxford elaborated further on Thursday, saying in a statement to CNN that a “difference in the manufacturing process” had led to the error.
That manufacturing problem has since been corrected, diceva la dichiarazione, noting that the UK regulator overseeing the trial had agreed to include “both approaches” in Phase 3.
While AstraZeneca and Oxford face criticism about transparency — given that they did not mention the error in their press release announcing the results nor on a press call on Monday — the company believes the world should focus on the trial’s positive results.
Speaking to the Wall Street Journal on Wednesday, Menelas Pangalos AstraZeneca’s Executive Vice-President said, “The mistake is actually irrelevant.
“Whichever way you cut the data — even if you only believe the full-dose, full-dose data… We still have efficacy that meets the thresholds for approval with a vaccine that’s over 60% efficace,” Pangalos said, according to the WSJ.
AstraZeneca and Oxford have yet to put forward a candidate for interview, as requested by CNN.
The US Food and Drug Administration requires a threshold of at least 50% efficacia. It is not clear if the FDA will authorize emergency use however.
AstraZeneca has not yet tested its half-strength dose in the US either.
Di lunedi, Dott. Paul Offit, a member of the FDA’s Vaccines and Related Biological Products Advisory Committee — which will review Covid-19 vaccines before they are put on the market — said the lack of data that led them to their conclusions made it “hard to know the significance of their findings.”
When two other major drugmakers, Pfizer and Moderna, released their efficacy results earlier this month, they did include the data that led to their results.
AstraZeneca presented an analysis of 23,000 participants in its Phase 3 prova.
It said some participants received the Covid-19 vaccine, while others received a different vaccine for an unrelated virus, or placebo injections.