The U.S. Military has awarded an $855 million contract to pharmaceutical firm AstraZeneca for the "manufacture, distribution and storage" of the monoclonal antibody mixture therapy often called Evusheld.

The drug, designed to assist these with allergy symptoms or immune methods that reply poorly to vaccines, was granted emergency authorization by the Meals and Drug Administration (FDA) in December and has been in brief provide since.

The brand new settlement is for 1 million doses of Evusheld in complete, together with the five hundred,000 introduced final month, bringing the overall variety of doses ordered by the U.S. authorities to 1.7 million, AstraZeneca mentioned in an announcement issued to Newsweek. The contract shall be accomplished via work in "numerous places," with an estimated completion date of March 31, 2023, in response to the Division of Protection (DOD).

As Newsweek beforehand reported, Evusheld was accepted in December to deal with sufferers with circumstances that forestall their immune system from offering an sufficient response to COVID vaccines, or those that cannot be vaccinated due to an allergic response to an preliminary dose of the COVID vaccine or particular person elements of the shot.

"With continued circumstances of COVID-19 throughout the U.S. and within the wake of the Omicron variant, there stays a crucial want to offer further safety to immunocompromised sufferers who're most susceptible to the virus," Government Vice President and President of AstraZeneca's BioPharmaceuticals Enterprise Unit Ruud Dobber mentioned within the assertion. "We're proud to proceed enjoying a number one position within the combat in opposition to COVID-19 with Evusheld."

AstraZeneca Army Evusheld Monoclonal Antibody COVID Treatment
The U.S. Military has awarded an $855 million contract to AstraZeneca for the manufacturing of Evusheld. Above, a photograph taken Tuesday reveals a field of Evusheld on the AstraZeneca facility for organic medicines in Södertälje, south of Stockholm, Sweden.Jonathan Nackstrand/AFP through Getty Photographs

Scientific trials have proven the drug to be about 77 p.c efficient—and 83 p.c efficient within the high-risk class it was initially accepted for—in stopping a COVID an infection, and supplied safety for about six months.

Evusheld is given in two injections administered in succession and delivers antibodies immediately into one's immune system, reasonably than a standard vaccine that causes an immune system to develop its personal antibodies to combat off future COVID an infection.

Folks with a weakened immune system as a result of a genetic situation or illnesses like most cancers are examples of people that might obtain a COVID vaccine however not produce the immune system response essential to create antibodies, Newsweek beforehand reported.

As of final month, the federal authorities, which controls the distribution of the doses of the therapy already bought, distributed about 400,000 doses and ordered 1.2 million in complete, in response to NPR.

A Division of Well being and Human Providers (DHHS) spokesperson beforehand advised Newsweek that there are an estimated 7 million folks throughout the U.S. who might qualify to be used of the drug as a result of they're immunocompromised.

Well being officers have mentioned that Evusheld shouldn't be handled as an alternative choice to a vaccine for everybody and its supposed use was solely to offer it to these with compromised immune methods or different medical the explanation why a vaccine was not an sufficient choice.

The low provide has led some well being care amenities to place the names of certified sufferers right into a "lottery" to determine who would obtain the scarce doses, NPR reported.

Newsweek additionally reached out to the Division of Protection for remark.

Replace 02/11/22, 7:25 p.m. ET: This text has been up to date with an announcement from AstraZeneca.

Replace 02/11/22, 6:40 p.m. ET: This text has been up to date with further context and data on Evusheld.