Pfizer Will Seek Emergency Approval For Covid-19 Vaccine In November, After Election

Pfizer will apply to the U.S. Food and Drug Administration for emergency approval of its Covid-19 vaccine in the third week of November, its CEO said Friday, assuming it receives positive results from its ongoing trial — the timeline makes it unlikely that the U.S. will have a vaccine before the election but leaves open the possibility of one being authorized this year.

Pfizer’s CEO Albert Bourla said the company would file for emergency approval as soon as safety data is available, assuming those results are positive.

The FDA requires at least two months of safety data on half of trial participants to grant emergency approval, he said, as well as information on effectiveness and proof it can be manufactured safely.

The safety data is likely to take the longest to collect — Bourla said Pfizer expects to have manufacturing data before that and should know whether or not the vaccine is effective by the end of October. 

The company will continue to monitor and report safety data for all trial participants for two years, Bourla said.

Bourla said the November timeline reflects the company’s “best estimates,” noting that this could change.

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Key Background

Bourla’s statement cements Pfizer’s status as a frontrunner — alongside Germany’s BioNTech, who it is developing the vaccine with — in the global race to develop a safe and effective Covid-19 vaccine. Excluding Russia and China, which have licensed vaccines for domestic use, no manufacturer has been granted regulatory approval for a vaccine anywhere in the world. If Pfizer manages to stick to this timeline, it could be the first. 

Crucial Quote

Pfizer and other vaccine-makers have grown increasingly frustrated with the persistent politicization of potential Covid-19 vaccines by high-ranking officials, most notably President Trump, who has claimed one will be ready before the November 3 election. Bourla’s letter does little to hide this annoyance,stating: “To ensure public trust and clear up a great deal of confusion, I believe it is essential for the public to understand our estimated timelines for each of these three areas.”

Further Reading

Pfizer to seek FDA approval for Covid -19 vaccine in November (Financial Times)

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Robert Hart

 Robert Hart

I am a London-based reporter for Forbes covering breaking news. Previously, I have worked as a reporter for a specialist legal publication covering big data and as a freelance journalist and policy analyst covering science, tech and health. I have a master’s degree in Biological Natural Sciences and a master’s degree in the History and Philosophy of Science from the University of Cambridge. Follow me on Twitter @theroberthart or email me at rhart@forbes.com 

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