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Emergent Bio’s smallpox vaccine gets US approval for mpox

2024.08.30 10:29

(Reuters) -The U.S. Food and Drug Administration granted expanded approval to Emergent BioSolutions’ smallpox vaccine for use in people at high risk of mpox infection, sending the drugmaker’s shares 5% higher on Friday.

The FDA clearance, announced late on Thursday by the company, makes the vaccine – called ACAM2000 – the second approved shot against mpox in the U.S. after Bavarian Nordic’s Jynneos.

Emergent, which has a market capitalization of about $471 million, in early August forecast sales of up to $490 million from products that are stockpiled by governments, such as the smallpox vaccine and an anthrax shot.

The Emergent vaccine, however, cannot be administered to those with weakened immune systems, including people with HIV. It found limited use during the 2022 mpox outbreak in the U.S, despite being part of the stockpile.

Both Jynneos and ACAM2000 contain vaccinia virus that is closely related to, but less harmful than the viruses that cause smallpox and mpox. ACAM2000 uses a live, infectious form of the vaccinia virus.

Instead of an injection, the Emergent shot is given through a series of small pokes on the skin using a two-pronged needle. The site forms a scab and risks spreading the live virus to other parts of the body or people until it heals.

Still, the approval comes when a new mpox strain, clade Ib, has spread rapidly in Africa. The World Health Organization earlier this month declared mpox a global public health emergency for the second time in two years.

Emergent has said it wants to help address the current outbreak, and last week announced it would donate 50,000 doses of its smallpox vaccine to the Democratic Republic of the Congo and neighboring countries.

The company has expressed an interest to the WHO for ACAM2000 to be given an emergency use listing. The UN agency is expected to grant emergency listing to Jynneos and an mpox vaccine from Japan’s KM Biologics in September.

© Reuters. FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S., August 29, 2020. REUTERS/Andrew Kelly/File Photo

Gaithersburg, Maryland-based Emergent’s shares slumped last year amid weakness in its contract manufacturing business, but have recovered this year on the back of a turnaround plan that includes pivoting away from that segment.

They were last up 4% at $9.24 in early trading. The stock traded at more than $130 at the peak of the pandemic, when the company was a contract manufacturer of Johnson & Johnson (NYSE:)’s COVID-19 vaccines.



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