Evaxion announces positive preclinical data for cytomegalovirus (CMV) vaccine program EVX-V1
November 12 2024 - 7:00AM
- New preclinical data
demonstrates that CMV antigens identified with Evaxion’s
AI-Immunology™ platform trigger targeted immune
responses
- Results also showcase the
successful design of a proprietary prefusion glycoprotein B (gB)
antigen with ability to neutralize the virus
- Evaxion is advancing these
new findings to develop a multi-component CMV vaccine
candidate
- About 1 in 200 babies is
born with congenital CMV infection and the virus infects
approximately 60% to 70% of adults in developed countries. No
approved CMV vaccine exists today
COPENHAGEN, Denmark, November 12, 2024 - Evaxion
Biotech A/S (NASDAQ: EVAX) (“Evaxion”), a clinical-stage TechBio
company specializing in developing AI-Immunology™ powered vaccines,
announces new positive preclinical data from its ongoing
cytomegalovirus (CMV) vaccine program named EVX-V1. The data will
be presented today at the 9th International Conference on Vaccines
Research & Development, taking place in Boston, USA.
The data demonstrates that the antigens
identified with Evaxion’s AI-Immunology™ platform effectively
trigger targeted immune responses, including induction of both CMV
reactive B and T cells. To further enhance vaccine effectiveness,
Evaxion has additionally designed a proprietary prefusion gB
antigen, a well-established CMV vaccine component known to offer
partial virus neutralization. New preclinical data confirms that
Evaxion’s proprietary gB antigen successfully induced a specific
immune response comparable to that of the conventional gB
antigen.
Based on these findings, we expect to combine
AI-Immunology™ identified CMV vaccine antigens with our proprietary
prefusion gB antigen in a future vaccine candidate. This novel
multi-target approach stands out from traditional methods focusing
on a limited set of glycoproteins involved in viral entry.
Combatting the virus from numerous angles is expected to enhance
the efficacy of our future vaccine.
The new data has been generated in collaboration
with Expres2ion Biotechnologies as part of the research
collaboration initiated in December 2022. The antigens identified
through Evaxion’s AI-Immunology™ platform have been produced using
ExpreS2ion’s ExpreS2™ technology.
“We are pleased with these positive outcomes of
the initial preclinical studies in our CMV vaccine program,
demonstrating our AI-Immunology™ platform’s ability to identify
novel antigens to combat viral diseases. These encouraging data
bring us one step closer to developing an effective CMV vaccine.
Our AI-Immunology™ platform enables a novel and broader approach to
tackling CMV, and we look forward to presenting the findings at the
conference and engaging in discussions with virology experts,” says
Birgitte Rønø, CSO of Evaxion.
Conference presentation
details:Abstract Title:
Revolutionizing Cytomegalovirus Vaccine Development with
AISession: Novel
Approaches, Technology & Delivery PlatformsDate/Time:
November 12, 2024, at 09.40 EST/15.40
CET
Presenter: Gry
Persson, Senior Project Manager at Evaxion
About cytomegalovirus
(CMV)About 1 in 200 babies is born with congenital CMV
infection. About 1 in 5 babies with the infection will have
congenital disabilities or other long-term health problems. CMV
infects approximately 60% to 70% of adults in developed countries
and nearly 100% in developing economies, driving demand for CMV
treatment. Despite decades of research, no CMV vaccine has been
approved to date.
CMV treatment market size was valued at $474.6
million in 2023 and is anticipated to register an annual growth
(CAGR) of 6.6% between 2024 and 2032. This growth is propelled by
increasing awareness and prevalence of CMV infection and the
development of new and effective treatments.
CMV is the most complex of all herpes viruses
and is a widespread infection transmitted in body fluids. Once
infected, the virus stays for life. People with weakened immune
systems, including organ transplant patients, can develop severe
symptoms affecting, for example, eyes, lungs, and liver, and
congenitally infected babies may suffer from intellectual
disability and loss of vision and hearing.
Contact
information Evaxion Biotech A/SMads KronborgVice
President, Investor Relations & Communication+45 53 54 82
96mak@evaxion-biotech.com
About EVAXION Evaxion Biotech
A/S is a pioneering TechBio company based upon its AI platform,
AI-Immunology™. Evaxion’s proprietary and scalable AI prediction
models harness the power of artificial intelligence to decode the
human immune system and develop novel immunotherapies for cancer,
bacterial diseases, and viral infections. Based upon
AI-Immunology™, Evaxion has developed a clinical-stage oncology
pipeline of novel personalized vaccines and a preclinical
infectious disease pipeline in bacterial and viral diseases with
high unmet medical needs. Evaxion is committed to transforming
patients’ lives by providing innovative and targeted treatment
options. For more information about Evaxion and its groundbreaking
AI-Immunology™ platform and vaccine pipeline, please visit our
website.
Forward-looking
statement This announcement contains
forward-looking statements within the meaning of Section 27A
of the Securities Act of 1933, as amended, and Section 21E of the
Securities Exchange Act of 1934, as amended. The
words “target,” “believe,” “expect,” “hope,” “aim,” “intend,”
“may,” “might,” “anticipate,” “contemplate,” “continue,”
“estimate,” “plan,” “potential,” “predict,” “project,” “will,” “can
have,” “likely,” “should,” “would,” “could,” and other words and
terms of similar meaning identify forward-looking
statements. Actual results may differ materially from those
indicated by such forward-looking statements as a result of various
factors, including, but not limited to, risks related to: our
financial condition and need for additional capital; our
development work; cost and success of our product development
activities and preclinical and clinical trials; commercializing any
approved pharmaceutical product developed using our AI platform
technology, including the rate and degree of market acceptance of
our product candidates; our dependence on third parties including
for conduct of clinical testing and product manufacture; our
inability to enter into partnerships; government regulation;
protection of our intellectual property rights; employee matters
and managing growth; our ADSs and ordinary shares, the impact
of international economic, political, legal, compliance, social and
business factors, including inflation, and the effects on
our business from the worldwide ongoing COVID-19 pandemic and
the ongoing conflict in the region
surrounding Ukraine and Russia and the Middle
East; and other uncertainties affecting our business
operations and financial condition. For a further discussion
of these risks, please refer to the risk factors included in our
most recent Annual Report on Form 20-F and other
filings with the U.S. Securities and Exchange Commission
(SEC), which are available
at www.sec.gov. We do not assume any
obligation to update any forward-looking statements except as
required by law.
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