Emergent BioSolutions (NYSE: EBS) today announced it is proactively
working with the World Health Organization (WHO) and the U.S.
government to partner and help address the current mpox outbreak
across Central Africa, and has pledged to donate 50,000 doses of
its ACAM2000®, (Smallpox (Vaccinia) Vaccine, Live), through Direct
Relief, a humanitarian relief organization with a long history of
providing vital medicines to the Democratic Republic of the Congo
(DRC), as well as the other impacted countries of Burundi, Kenya,
Rwanda, and Uganda. These efforts are in response to the WHO’s
Director-General’s August 14 statement declaring that the upsurge
of mpox in the DRC and a growing number of countries in Africa
constitutes a public health emergency of international concern
(PHEIC) under the International Health Regulations (2005) (IHR).
“Africa CDC estimated they will need 10 million doses to control
the epidemic in the continent,” said Dr. Raina McIntyre, Professor
of Global Biosecurity, NHMRC L3 Research Fellow, Head, Biosecurity
Program, Kirby Institute, University of New South Wales Sydney. “It
is unlikely there will be enough supply of 3rd generation vaccines
to control the epidemic in Africa, given demand in other
countries.”
In October 2023, Emergent filed a supplemental Biologics License
Application (sBLA) to the U.S. Food and Drug Administration (FDA)
seeking an expanded indication for ACAM2000® vaccine to include
immunization against mpox virus. The sBLA, which has an FDA target
for review completion in the third quarter 2024, includes
previously available human safety data and data from a
well-controlled animal study in which ACAM2000® vaccine has been
shown to be effective in protecting against mpox virus exposure.
ACAM2000® is a single-dose vaccine administered via a bifurcated
needle that is dipped into the vaccine solution and the skin is
pricked several times in the upper arm with a droplet of the
vaccine.
Accordingly, Emergent has also responded to the WHO invitation
for manufacturers of mpox vaccines to submit an Expression of
Interest for the WHO’s assessment of ACAM2000® vaccine to be added
as an Emergency Use Listing (EUL), which is a WHO risk-based
procedure for assessing and listing unlicensed medical products in
various countries with the aim of expediting the availability of
these products needed in public health emergency situations like
the current mpox outbreak.
“As the WHO has declared, the mpox outbreak is a public health
emergency of international concern, and Emergent is ready to scale
up response efforts and partner with U.S. and global public health
leaders,” said Joe Papa, president and CEO, Emergent BioSolutions.
“For years, Emergent has supplied ACAM2000® to the U.S. and allied
governments in support of preparedness and stockpiling initiatives.
Currently, we have additional product already in inventory, with
the ability to increase supply by approximately 40 million doses,
if and potentially when needed. In the meantime, 50,000 doses of
ACAM2000® vaccine will be donated to help control the outbreak
across the African continent.”
Mpox is a disease caused by infection with the mpox virus. Mpox
virus is part of the same family of viruses as variola virus,
the virus that causes smallpox. In 2022, the world experienced a
global outbreak of clade II mpox, associated with West Africa,
which led to more than 95,000 cases across 115 non-endemic
countries.
Clade I is endemic to Central Africa and is characterized by
more severe clinical outcomes and a higher case fatality rate. The
recently identified clade Ib variant, exhibiting enhanced
transmissibility through close contact, has led to an increase in
cases, particularly in Central Africa, and a sizable impact on
children and families. According to the WHO, clade I mpox tends to
cause a higher number of severe infections and have a higher
mortality rate than clade II mpox.
Papa continued, “The increasing outbreaks of mpox around the
world should raise concerns and spur ongoing efforts to produce and
stockpile vaccines and treatments to address all orthopox viruses,
including mpox and smallpox.”
In 1980, the WHO officially declared smallpox eradicated;
however, the threat of reemergence by intentional introduction
(e.g., bioterrorism) persists and minimal immunity in populations
today against mpox exists. Vaccines like ACAM2000® formed the basis
of one of the most successfully integrated public health responses
in the eradication of smallpox.
ACAM2000®, (Smallpox (Vaccinia) Vaccine, Live)
ACAM2000® is the primary smallpox vaccine designated for use in a
bioterrorism emergency, with doses having been supplied to the U.S.
Strategic National Stockpile. ACAM2000® is also licensed in Canada,
Australia and Singapore and is currently stockpiled
both in the U.S. and internationally.
ACAM2000® is indicated for active immunization against smallpox
disease for persons determined to be at high risk for smallpox
infection.
The labeling for ACAM2000® contains a contraindication for
individuals with severe immunodeficiency. Severe localized or
systemic infection with vaccinia (progressive vaccinia) may occur
in persons with weakened immune systems. Individuals with severe
immunodeficiency who are not expected to benefit from the vaccine
should not receive ACAM2000®. The risk for experiencing severe
vaccination complications must be weighed against the risk for
experiencing a potentially fatal smallpox infection.
Additionally, there are warnings and precautions for
myocarditis, pericarditis, encephalitis, encephalomyelitis,
encephalopathy, progressive vaccinia, generalized vaccinia, severe
vaccinial skin infections, erythema multiforme major (including
Stevens-Johnson Syndrome), eczema vaccinatum resulting in permanent
sequelae or death, ocular complications, blindness and fetal death.
These have occurred following either primary vaccination or
revaccination with live vaccinia virus smallpox vaccines. These
risks are increased in certain individuals and may result in severe
disability, permanent neurological sequalae and/or death.
Please see full Prescribing Information for full Boxed
Warning and additional safety information.
About Emergent BioSolutionsAt Emergent,
our mission is to protect and enhance life. For 25 years, we’ve
been at work defending people from things we hope will never
happen—so we are prepared just in case they ever do. We provide
solutions for complex and urgent public health threats through a
portfolio of vaccines and therapeutics that we develop and
manufacture for governments and consumers. We also offer a range of
integrated contract development and manufacturing services for
pharmaceutical and biotechnology customers. To learn more about how
we plan to protect or enhance 1 billion lives by 2030, visit
our website and follow us
on LinkedIn, X, Instagram, Apple
Podcasts and Spotify.
Safe Harbor StatementThis communication
includes forward-looking statements within the meaning of the
Private Securities Litigation Reform Act of 1995. All statements,
other than statements of historical fact, including statements
regarding the expected timing for delivery of the ACAM2000® vaccine
and for the completion of the FDA review of the sBLA, and
Emergent’s ability to increase inventories of ACAM2000® vaccine to
meet requested levels within specified time frames, if needed, are
forward-looking statements. We generally identify
forward-looking statements by using words like “anticipate,”
“believe,” “continue,” “could,” “estimate,” “expect,” “forecast,”
“future,” “goal,” “intend,” “may,” “plan,” “position,” “possible,”
“potential,” “predict,” “project,” “should,” “target,” “will,”
“would,” and similar expressions or variations thereof, or the
negative thereof, but these terms are not the exclusive means of
identifying such statements. Forward-looking statements are based
on our current intentions, beliefs and expectations regarding
future events based on information that is currently available. We
cannot guarantee that any forward-looking statement will be
accurate. Readers should realize that if underlying assumptions
prove inaccurate or unknown risks or uncertainties materialize,
actual results could differ materially from our expectations.
Readers are, therefore, cautioned not to place undue reliance on
any forward-looking statements. Any forward-looking statement
speaks only as of the date of this communication and, except as
required by law, we do not undertake any obligation to update any
forward-looking statement to reflect new information, events or
circumstances.
There are a number of important factors that could cause our
actual results to differ materially from those indicated by any
forward-looking statements. Readers should consider this cautionary
statement, as well as the risk factors and other disclosures
included in our periodic reports filed with the Securities and
Exchange Commission, when evaluating our forward-looking
statements.
Investor Contact:Richard S. LindahlExecutive
Vice President, CFOlindahlr@ebsi.com
Media Contact:Assal HellmerVice President,
Communicationsmediarelations@ebsi.com
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