Pfizer to seek regulatory approval within days as vaccine proves 95% effective
US drugmaker and partner BioNTech say vaccine protected people of all ages and ethnicities, with no significant safety problems in trials
Pfizer said on Wednesday a final analysis of clinical-trial data showed its Covid-19 vaccine was 95% effective, paving the way for the company to apply for the first US regulatory authorisation for a coronavirus shot within days.
The US drugmaker and partner BioNTech said their vaccine protected people of all ages and ethnicities, with no significant safety problems so far in a trial that includes almost 44,000 participants.
Pfizer shares rose 2.7% in premarket trading, with BioNTech American depositary receipts up 7.3%. European stocks extended their gains after the news, with the Stoxx Europe 600 up 0.4%
The update is the latest in a string of promising developments on the vaccine front in recent days. Moderna’s rival shot appears equally effective, judging from data published earlier this week, and a third contender, from AstraZeneca and the University of Oxford, is expected to release trial results in coming days.
The Pfizer-BioNTech data shows 170 trial participants contracted Covid-19 overall. Eight participants who got the vaccine fell ill, while 162 cases were seen among those who got the placebo. The shot helped to prevent severe disease, according to the analysis, with nine of 10 severe cases in the trial occurring in the placebo group.
The vaccine’s efficacy in people older than 65 was more than 94%, the companies said.
Most people who received the shot tolerated it well. Severe fatigue was seen in 3.8% of volunteers after the second dose in the two-shot regimen, but that was the only severe side effect that occurred in more than 2% of people, according to the analysis.
Pfizer and BioNTech said last week that an initial readout showed the vaccine was more than 90% effective. The news helped spark a broad stock-market rally on hopes that the shot could help control a pandemic that has killed more than 1.3-million people worldwide.
On Monday, Moderna released its own promising results and said it expected to be able to apply for emergency authorisation in the US within weeks.
Pfizer and BioNTech plan to seek US emergency authorisation “within days”, according to the release.
On Tuesday, Pfizer CEO Albert Bourla said at a conference that the companies had gathered the two-month safety follow-up data required by the US Food and Drug Administration.
Both the Moderna and the Pfizer-BioNTech vaccines are based on messenger RNA, a new type of vaccine technology that is able to be deployed quickly. It essentially transforms the body’s cells into tiny vaccine making machines. The vaccines instruct cells to make copies of the coronavirus spike protein, stimulating the production of protective antibodies.
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