GeoVax Appoints Teresa Lambe, Acclaimed Professor of Vaccinology and Immunology at the Oxford Vaccine Group, to Its Scientific Advisory Board
August 08 2024 - 9:00AM
GeoVax Labs, Inc. (Nasdaq: GOVX), a biotechnology company
developing immunotherapies and vaccines against cancers and
infectious diseases, today announced the appointment of Teresa
Lambe, PhD, OBE, FMedSci to its Scientific Advisory Board.
Professor Lambe is the Calleva Head of Vaccine Immunology at the
Oxford Vaccine Group within the University of Oxford and a
Principal Investigator at the Pandemic Sciences Institute (PSI).
She served as one of the Principal Investigators who oversaw the
Oxford/AstraZeneca vaccine program; she co-designed the vaccine in
January 2020, led the preclinical studies, and oversaw the delivery
of the immune results needed to support regulatory approval in late
2020. Professor Lambe was appointed as an honorary Officer of the
Order of the British Empire (OBE) for her services to Sciences and
Public Health in the 2021 Queen’s Birthday Honours and received the
Presidential Distinguished Service Award for the Irish Abroad in
2022. In May 2024 she was elected a Fellow of the Academy of
Medical Sciences, one of the most prestigious awards in the
field.
Professor Lambe’s research focuses on delineating the protective
immune response post infection and using these findings to
rationally design vaccination strategies to prevent disease. Her
group is currently developing and testing vaccines against a number
of outbreak pathogens including Crimean-Congo hemorrhagic fever,
Ebola virus, Marburg virus and Coronaviruses. A number of these
vaccines have progressed to clinical trial assessment, including
vaccines against Ebola and Marburg virus.
Dr. Mark Newman, GeoVax’s Chief Scientific Officer, commented,
“We are thrilled to welcome Professor Lambe to our Scientific
Advisory Board. Her extensive experience and groundbreaking work in
vaccine development, particularly her pivotal role in the
development of the Oxford/AstraZeneca COVID-19 vaccine, will be
invaluable as we continue to advance our own vaccine and
immunotherapy programs. Her expertise dovetails perfectly with our
product portfolio, including the recent BARDA Project NextGen Award
for the development of next-generation COVID-19 vaccines. Her
insights will be crucial in accelerating our efforts to bring
innovative solutions to high-risk and immunocompromised
populations.”
David Dodd, GeoVax’s Chairman and CEO, added, “Professor Lambe’s
expertise in immunology and her innovative approach to vaccine
development align perfectly with GeoVax’s mission to address some
of the world’s most challenging infectious diseases. Her insights
and guidance will be critical as we move forward with our clinical
trials and seek to bring new, life-saving therapies to market.”
Professor Lambe expressed her enthusiasm about joining GeoVax,
stating, “I am honored to join the Scientific Advisory Board of
GeoVax. The Company’s dedication to developing innovative vaccines
and immunotherapies is truly inspiring. I look forward to working
with the team and contributing to the advancement of their
promising pipeline of candidates.”
About GeoVax
GeoVax Labs, Inc. is a clinical-stage biotechnology company
developing novel vaccines for many of the world’s most threatening
infectious diseases and therapies for solid tumor cancers. The
company’s lead clinical program is GEO-CM04S1, a next-generation
COVID-19 vaccine for which GeoVax was recently awarded a
BARDA-funded contract to sponsor a 10,000-participant Phase 2b
clinical trial to evaluate the efficacy of GEO-CM04S1 versus an
approved COVID-19 vaccine. In addition, GEO-CM04S1 is currently in
three Phase 2 clinical trials, being evaluated as (1) a primary
vaccine for immunocompromised patients such as those suffering from
hematologic cancers and other patient populations for whom the
current authorized COVID-19 vaccines are insufficient, (2) a
booster vaccine in patients with chronic lymphocytic leukemia (CLL)
and (3) a more robust, durable COVID-19 booster among healthy
patients who previously received the mRNA vaccines. In oncology the
lead clinical program is evaluating a novel oncolytic solid tumor
gene-directed therapy, Gedeptin®, in a multicenter Phase 1/2
clinical trial for advanced head and neck cancers. GeoVax has a
strong IP portfolio in support of its technologies and product
candidates, holding worldwide rights for its technologies and
products. The Company has a leadership team who have driven
significant value creation across multiple life science companies
over the past several decades. For more information about the
current status of our clinical trials and other updates, visit our
website: www.geovax.com.
Forward-Looking Statements
This release contains forward-looking statements regarding
GeoVax’s business plans. The words “believe,” “look forward to,”
“may,” “estimate,” “continue,” “anticipate,” “intend,” “should,”
“plan,” “could,” “target,” “potential,” “is likely,” “will,”
“expect” and similar expressions, as they relate to us, are
intended to identify forward-looking statements. We have based
these forward-looking statements largely on our current
expectations and projections about future events and financial
trends that we believe may affect our financial condition, results
of operations, business strategy and financial needs. Actual
results may differ materially from those included in these
statements due to a variety of factors, including whether: GeoVax
is able to obtain acceptable results from ongoing or future
clinical trials of its investigational products, GeoVax’s
immuno-oncology products and preventative vaccines can provoke the
desired responses, and those products or vaccines can be used
effectively, GeoVax’s viral vector technology adequately amplifies
immune responses to cancer antigens, GeoVax can develop and
manufacture its immuno-oncology products and preventative vaccines
with the desired characteristics in a timely manner, GeoVax’s
immuno-oncology products and preventative vaccines will be safe for
human use, GeoVax’s vaccines will effectively prevent targeted
infections in humans, GeoVax’s immuno-oncology products and
preventative vaccines will receive regulatory approvals necessary
to be licensed and marketed, GeoVax raises required capital to
complete development, there is development of competitive products
that may be more effective or easier to use than GeoVax’s products,
GeoVax will be able to enter into favorable manufacturing and
distribution agreements, and other factors, over which GeoVax has
no control.
Further information on our risk factors is contained in our
periodic reports on Form 10-Q and Form 10-K that we have filed and
will file with the SEC. Any forward-looking statement made by us
herein speaks only as of the date on which it is made. Factors or
events that could cause our actual results to differ may emerge
from time to time, and it is not possible for us to predict all of
them. We undertake no obligation to publicly update any
forward-looking statement, whether as a result of new information,
future developments or otherwise, except as may be required by
law.
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