AstraZeneca to Seek U.S. Approval of COVID Vaccine

The company will ask the FDA for full regulatory approval rather than fast-track emergency use authorization.

A health worker prepares a shot of the AstraZeneca COVID-19 vaccine at the Central Vaccination Center in Bangkok, July 22, 2021.
A health worker prepares a shot of the AstraZeneca COVID-19 vaccine at the Central Vaccination Center in Bangkok, July 22, 2021.
AP Photo/Sakchai Lalit

LONDON (AP) — AstraZeneca said Thursday that it intends to seek U.S. approval for its COVID-19 vaccine in the second half of this year, further delaying the long-awaited application.

The Anglo-Swedish drugmaker announced the new timetable as it said the company and its partners have delivered more than 1 billion doses of the vaccine to over 170 countries where it is already authorized for use.

AstraZeneca said it has decided to ask the U.S. Food and Drug Administration for full regulatory approval of the vaccine, rather than the fast-track emergency use authorization originally anticipated. As part of this Biologics License Application, the FDA has requested extensive data from clinical trials around the world, as well as data on real world use of the vaccine.

“We have an enormous amount of data, clinical data and all of the data coming from the work we’ve done around the world,″ CEO Pascal Soriot said on a conference call with reporters. “A BLA is a much bigger submission than the emergency use approval.”

The news on the U.S. filing is being closely watched because the timetable has slipped in recent months. When AstraZeneca released data from its U.S. trial of the vaccine on March 22, company officials said they expected to seek FDA authorization in the first half of April.

Among the concerns AstraZeneca will have to address are reports that the vaccine may be linked to rare blood clots, which have caused some countries to limit its use in younger people.

The AstraZeneca vaccine is already in widespread use around the world following approval by regulators in the European Union, World Health Organization, U.K. and other countries.

While the U.S. is currently “well supplied" with vaccines, AstraZeneca believes its shot could “play a role in the future," Soriot said.

“It’s a good vaccine, and we just want to make sure it’s ready to be used if needed," he said.

AstraZeneca said Thursday that it delivered 319 million doses of the vaccine in the first half of this year, $1.17 billion in revenue. AstraZeneca has pledged to deliver the vaccine on a non-profit basis as long as the pandemic lasts.

Despite complaints from the EU about its vaccine supply, the 27-nation bloc received more doses directly from AstraZeneca than any other single entity in the six months through June. The company shipped 97 million doses to the EU, while Brazil got 65 million and the U.K. 52 million, AstraZeneca said. Gavi, an alliance that secures vaccines for low-income countries, received 49 million doses, and another 57 million doses went to other countries.

Sub-licensees, including the Serum Institute of India, supplied millions more doses.

The vaccine was developed by Oxford University researchers, who licensed the technology to AstraZeneca in an effort to tap into the company’s global manufacturing and distribution capacity. AstraZeneca, in turn, authorizes other companies to produce the shots around the world.

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