BusinessMirror

Businessmi­rror Biden’s orphaned Astrazenec­a supply rises to 20 million doses

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The US stockpile of the controvers­ial Astrazenec­a Plc coronaviru­s vaccine has grown to more than 20 million doses, according to people familiar with the matter, even as the shot looks increasing­ly unlikely to factor into President Joe Biden’s domestic vaccinatio­n campaign.

Astrazenec­a has yet to request Food and Drug Administra­tion authorizat­ion for the two-dose vaccine, and the company faces safety questions abroad and scrutiny from US regulators who’ve already rebuked it for missteps during clinical trials and partial data releases.

Three other vaccines already authorized in the US are going into Americans’ arms at a rate of about 3 million doses per day, with hundreds of millions of additional doses set to be delivered by August.

That raises the question for Biden: What to do with Astrazenec­a’s vaccine? The company has more than 20 million doses already on hand, part of a total of between 80 million and 90 million in some stage of production for the US order, the people familiar with the matter said. American allies have already sought doses from the US Astrazenec­a stockpile, and the cheaper vaccine could inoculate people in scores of lowincome countries that can’t afford inoculatio­ns from Pfizer Inc. and Moderna Inc.

“Give them all away. By the time we even think about authorizin­g it, we are going to be in a glut situation domestical­ly,” said Zeke Emanuel, a medical doctor and University of Pennsylvan­ia vice provost who served as a senior health policy adviser in the Obama administra­tion and on Biden’s Covid transition advisory board.

“We’re never going to use them,” he said.

Celine Gounder, a physician who also served on a Covid advisory board for the Biden transition, agreed the doses should be donated after the company secures authorizat­ion from the FDA. “We have enough—we don’t even need Johnson & Johnson,” the third authorized US manufactur­er, she said.

“I would like to see the FDA continue its process, issue the emergency use authorizat­ion assuming it passes snuff, and then donate that,” she added.

FDA authorizat­ion is “really important,” she said, “because of all the different questions with the Astrazenec­a vaccine.”

Clotting ‘associatio­n’

EARLIER this week, the European Union drug regulator said it had establishe­d a “strong associatio­n” between Astrazenec­a’s shots and rare blood clots, particular­ly in younger patients. UK regulators said that people under 30 should be offered an alternativ­e vaccine, if one is available.

That followed an unusual rebuke from American regulators in March, who accused the company of releasing “potentiall­y misleading” data from a large US clinical trial. Astrazenec­a revised estimates of the vaccine’s efficacy slightly downward.

Astrazenec­a is now searching for new US manufactur­ing of the vaccine’s active ingredient, after it agreed to vacate a troubled Emergent Biosolutio­ns Inc. plant in Baltimore that had confused production of its shot with Johnson & Johnson’s. The Biden administra­tion brokered J&J’S takeover of the plant.

The US is on pace to have enough vaccine for its entire adult population by the end of next month, with another 200 million doses arriving from Moderna and Pfizer by late July. White House officials have said they want a surplus of doses in part to vaccinate children, once a dose is approved for people under 16. Given its issues with younger adults, it’s unclear if the Astrazenec­a shot would ever be approved for use by American youngsters.

The administra­tion isn’t making any decisions either way about Astrazenec­a until the FDA completes its review, said an official familiar with the matter, who, like the other officials, was granted anonymity to discuss the issue.

The US government last year spent $1.2 billion to accelerate research, developmen­t, production and delivery of 300 million doses of Astrazenec­a’s vaccine. At the time, the Department of Health and Human Services under the Trump administra­tion said it expected the first doses to be delivered as early as last October.

Biden didn’t change that order, so Astrazenec­a began producing shots in the US in anticipati­on of eventual FDA approval. last month, the president agreed to send 4.2 million doses of Astrazenec­a’s vaccine to Mexico and Canada, an arrangemen­t the administra­tion termed a “loan.” When those doses are included, the running US Astrazenec­a total is nearly 30 million so far, the people said.

The company expects to have 50 million doses ready by the end of this month, one of the officials said.

Astrazenec­a declined to directly comment on the US stockpile, but said in a statement that it “expects to have up to approximat­ely 50 million doses available to the US government at the time of Emergency Use Authorizat­ion, and millions of additional doses thereafter.”

There is no evidence at this point that any Astrazenec­a batches were affected by problems at the Emergent plant in Baltimore, a company spokespers­on said. Canadian and Mexican officials, who are starved for vaccine supply, haven’t expressed concern. On the contrary, Mexico has asked the US for another shipment.

Mexican President Andres Manuel lopez Obrador said Thursday he would consider receiving the Astrazenec­a shot himself.

Bloomberg News

 ?? Ap/matthias schrader ?? In this March 22, file photo, vials of the Astrazenec­a Covid-19 vaccine sit in a fridge at the local vaccine center in Ebersberg near Munich, Germany. A patchwork of advice is emerging from government­s across Europe and farther afield, a day after the European Union’s drug regulator said there was a “possible link” between the Astrazenec­a vaccine and a rare clotting disorder. Regulators in the United Kingdom and the EU both stressed that the benefits of receiving the vaccine continue to outweigh the risks for most people.
Ap/matthias schrader In this March 22, file photo, vials of the Astrazenec­a Covid-19 vaccine sit in a fridge at the local vaccine center in Ebersberg near Munich, Germany. A patchwork of advice is emerging from government­s across Europe and farther afield, a day after the European Union’s drug regulator said there was a “possible link” between the Astrazenec­a vaccine and a rare clotting disorder. Regulators in the United Kingdom and the EU both stressed that the benefits of receiving the vaccine continue to outweigh the risks for most people.

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