GeoVax Announces First Patients Vaccinated in Phase 2 Clinical Trial of COVID-19 Vaccine Booster in Patients with Chronic Lymphocytic Leukemia
August 10 2023 - 09:00AM
Seeking Improved Immune Response vs mRNA
Vaccine
Full Patient Enrollment Expected Within Six
Months
via NewMediaWire — GeoVax Labs, Inc. (Nasdaq:
GOVX), a biotechnology company developing immunotherapies and
vaccines against cancers and infectious
diseases, today announced that vaccinations have begun in
an investigator-initiated clinical trial (ClinicalTrials.gov
Identifier: NCT05672355) of GEO-CM04S1 in patients with
chronic lymphocytic leukemia (CLL), being conducted at City of Hope
National Medical Center.
Despite a high vaccination rate, CLL patients may be at high
risk for lethal COVID-19 infection due to poor immune response to
currently available vaccines. The GEO-CM04S1 vaccine uses a
modified vaccinia virus (MVA) backbone to carry SARS-CoV-2 virus
antigens that may be more effective at inducing COVID-19 immunity
in patients with poor humoral immune responses since MVA strongly
induces T cell expansion even in the background of
immunosuppression. By targeting both the spike (S) and nucleocapsid
(N) protein antigens, GEO-CM04S1 broadens the specificity of the
immune responses and protects against the loss of efficacy
associated with current vaccines due to the significant sequence
variation observed with the spike antigen.
The study is examining the use of two injections
of GEO-CM04S1, three months apart, to assess immune responses in
these vulnerable patients, with an mRNA vaccine (currently, the
Pfizer-BioNTech Bivalent vaccine) as the control arm. Participants
will be randomized 1:1 to receive two boosters with either the
GEO-CM04S1 or the control vaccine. The primary immune response
outcome will be assessed at 56 days following the first booster
injection. Up to 40 participants in each arm will be vaccinated,
with immune responses evaluated and compared at the interim and
final analyses.
David Dodd, GeoVax President and CEO, stated, “We
are very pleased with the rapid start for this third important
study for GEO-CM04S1, which we expect will achieve full patient
enrollment within six months. We believe the GEO-CM04S1 vaccine,
containing the two antigens, S and N, along with the recognized
antibody and cellular immune responses resulting from the MVA
approach, has the potential to offer greater booster protection
than that from the current vaccines in use, as well as provide a
greater degree of protection within immunocompromised patients. We
expect the CLL trial will add to the data coming from our other
ongoing trials, confirming the potential benefit of GEO-CM04S1 in
another population of immunocompromised individuals. We look
forward to sharing progress reports as we advance.”
About GEO-CM04S1GEO-CM04S1 is a
next-generation COVID-19 vaccine based on GeoVax’s MVA viral vector
platform, which supports the presentation of multiple vaccine
antigens to the immune system in a single dose. GEO-CM04S1 presents
both the spike and nucleocapsid antigens of SARS-CoV-2 and is
specifically designed to induce both antibody and T cell responses
to non-variable parts of the virus. The more broadly specific and
functional engagement of the immune system is designed to protect
against the new and continually emerging variants of COVID-19.
Based on data from animal models and a completed Phase 1 clinical
study, vaccine-induced immune responses were shown to recognize
both early and later variants of SARS-CoV-2, including the Omicron
variant. Vaccines of this format should not require repeated
modification and updating.
A recent presentation of unpublished data from the
open-label portion of the Phase 2 trial of GEO-CM04S1
(ClinicalTrials.gov Identifier: NCT04977024) in patients
undergoing hematological cancer treatment (i.e., patients who
have reduced immune system function as a result of treatment)
indicates that GEO-CM04S1 is highly immunogenic in these patients,
inducing both antibody responses, including neutralizing
antibodies, and T cell responses. These data support the planned
progression of the Phase 2 clinical study, which will include a
direct comparison to currently approved mRNA vaccines. GEO-CM04S1
also continues to advance in another Phase 2 clinical trial as a
booster for healthy patients who have previously received the
Pfizer or Moderna mRNA vaccine (ClinicalTrials.gov
Identifier: NCT04639466). Data from these studies will form
the basis for comparing vaccine potential in unique patient groups
as well as the general population.
About GeoVaxGeoVax Labs, Inc. is a
clinical-stage biotechnology company developing novel therapies and
vaccines for solid tumor cancers and many of the world’s most
threatening infectious diseases. The company’s lead program in
oncology is a novel oncolytic solid tumor gene-directed therapy,
Gedeptin®, presently in a multicenter Phase 1/2 clinical trial for
advanced head and neck cancers. GeoVax’s lead infectious disease
candidate is GEO-CM04S1, a next-generation COVID-19 vaccine
targeting high-risk immunocompromised patient populations.
Currently in three Phase 2 clinical trials, GEO-CM04S1 is being
evaluated as 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, and as a booster vaccine in patients with chronic
lymphocytic leukemia (CLL). In addition, GEO-CM04S1 is in a Phase 2
clinical trial evaluating the vaccine as a more robust, durable
COVID-19 booster among healthy patients who previously received the
mRNA vaccines. GeoVax has a leadership team who have driven
significant value creation across multiple life science companies
over the past several decades. For more information, visit our
website: www.geovax.com.
Forward-Looking StatementsThis 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.
Investor Relations Contact:Rich CockrellCG
Capital404-736-3838govx@cg.capital
Media Contact:Susan
Robertssr@roberts-communications.com202-779-0929
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