Vaxil Provides Update on Research Activities
07 Marzo 2022 - 6:50AM
VAXIL BIO LTD. (“
Vaxil” or the
“
Company”) (TSX VENTURE: VXL), an innovative
immunotherapy biotech company is pleased to provide an update on
its research activities.
Vaxil previously reported therapeutic
success of P-Esbp-DOX, a novel anti-cancer drug, when tested in
vivo in a mouse model of aggressive liver metastasis of colorectal
cancer (CRC). P-Esbp-DOX was developed by Prof. Ayelet David, Head
of the Drug Targeting and Nanomedicine Laboratory, Department of
Clinical Biochemistry and Pharmacology from Ben-Gurion University
of the Negev, for which Vaxil has a worldwide exclusive license.
Following the promising results of the in vivo study, Vaxil is in
the midst of a screening process of contract development and
manufacturing companies for the development of P-Esbp-DOX to be
used in a first in-human clinical trial.
During 2021, Vaxil conducted an initial
in vivo oral vaccine study for a COVID-19 signal peptide-derived
product. Following the identification of an initial signal, Vaxil
decided to try to transition from the ImMucin™ (MUC1 signal
peptide-derived product) injectable platform to an oral delivery
platform. An ImMucin™ oral formulation was developed together with
an oral drug delivery company, and an in vivo study was performed
aimed at testing the ability of the ImMucin™ oral formulation to
induce a systemic immune response in mice. The results, to date,
are inconclusive, and given our limited resources, Vaxil has
decided not to pursue this at this time. Regarding the potential
application of oral delivery to COVID-19, Vaxil is exploring
whether there is value in conducting experiments of the oral
formulation of the potential COVID-19 vaccine candidate in
combination with mRNA vaccines to boost T-cell protection to future
variants.
ABOUT VAXIL
Vaxil is an Israeli immunotherapy biotech
company focused on its novel approach to targeting prominent cancer
markers and infectious diseases. Its lead product ImMucin™
successfully completed a Phase 1/2 clinical trial in multiple
myeloma for which it received orphan drug status from the FDA and
EMA. The Company aims to continue to develop ImMucin™, a potential
COVID-19 vaccine and a tuberculosis vaccine / treatment that has
demonstrated promising preliminary results with further preclinical
evaluation planned. Additional indications and mAb candidates are
under evaluation as immuno-oncology and infectious disease
treatments alone and in combination with other treatments.
Vaxil exploits the unique properties of
signal peptide domains on crucial proteins to develop targeted
therapies against cancer targets and infectious disease pathogens.
These signal peptide domains are identified by VaxHit™, Vaxil’s
proprietary bioinformatic approach. These signal peptides induce a
robust T- and B-cell response across wide and varied HLA subtypes,
while acting as true, universal neoantigens. The peptide platform
targets these cells by “educating” or specifically activating the
immune system to recognize and attack the affected cells. In
addition, Vaxil’s mAb platform directly recognizes the target
protein expressed on malignant cells and recruits other elements of
the immune system to lyse those cells.
Neither TSX Venture Exchange nor its Regulation
Services Provider (as that term is defined in the policies of the
TSX Venture Exchange) accepts responsibility for the adequacy or
accuracy of this release.
Disclaimer: The Company cautions that P-Esbp-DOX, a
novel anti-cancer drug is still under early-stage research and
development and is not making any express or implied claims that it
will become commercial. The TSX Venture Exchange Inc. has in no way
passed upon the merits of the Company and has neither approved nor
disapproved the contents of this press release. This news release
contains forward-looking information, which involves known and
unknown risks, uncertainties and other factors that may cause
actual events to differ materially from current expectation.
Important factors - including the availability of funds, the
results of financing efforts, the results of exploration activities
-- that could cause actual results to differ materially from the
Company's expectations are disclosed in the Company's documents
filed from time to time on SEDAR (see www.sedar.com). Readers
are cautioned not to place undue reliance on these forward-looking
statements, which speak only as of the date of this press release.
The company disclaims any intention or obligation, except to the
extent required by law, to update or revise any forward-looking
statements, whether as a result of new information, future events
or otherwise. This press release does not constitute an offer to
sell or a solicitation of an offer to sell any of the securities
described herein in the United States or elsewhere. These
securities have not been, and will not be, registered in the United
States Securities Act of 1933, as amended, or any state securities
laws, and may not be offered or sold in the United States or to
U.S. persons unless registered or exempt therefrom.
CONTACT INFORMATION
For further information please visit
https://vaxil-bio.com/ or contact:
Gadi Levin, CFO — info@vaxil-bio.com,
647-558-5564
Vaxil Bio (TSXV:VXL)
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