Vaxil Provides Strategy Update From Conclusion of COVID-19 Challenge Study
17 Fevereiro 2021 - 3:25PM
VAXIL BIO LTD. (“
Vaxil” or the
“
Company”) (TSX VENTURE: VXL), an innovative
immunotherapy biotech company specializing in cancer and infectious
diseases, today reports results of the previously disclosed
COVID-19 vaccine candidate challenge experiment and the strategy
going forward.
Vaxil established the USAMRIID collaboration
(CRADA) based on the global need for a viable COVID-19 vaccine
utilizing an alternative technology that demonstrates cellular and
humoral responses, both of which are necessary. In this rapidly
moving pandemic, variants have become the established infection
model, which can be better addressed with Vaxil’s SP approach.
Neutralizing antibody technologies may require frequent
modifications while Vaxil’s signal peptide (“SP”)
technology may provide long-term efficacy as the virus mutates.
The USAMRIID COVID-19 mouse model challenge
experiment demonstrated that Vaxil’s SP-based vaccine candidate
generated a specific immune response. This was not, however,
accompanied by vaccine protection of the animals.
The Company plans to conduct additional analyses
and on the basis of the understanding obtained, refine aspects of
experiment design, including dosing levels and regimens, and
alternate animal models that may allow future investigation of the
unique and specific aspects of SP’s as immunogens. In addition, the
Company will evaluate alternate peptide delivery approaches,
including oral administration. This strategy focuses future efforts
on the unique benefits of SP’s to sustain Vaxil’s competitive
advantage over the longer term, beyond the current crisis
environment, when it can realistically achieve approval for human
use.
The Company’s strategy to deliver value over the
long-term is based on potentially unique benefits of SPs including
their broad and strong immune response, both cellular and humoral,
their reduced propensity to genetic mutation and the advantage of
efficient manufacturing.
“We were pleased to see the encouraging immune
response and are excited to pursue further testing to highlight the
unique advantages of SPs as a technology, though we had hoped to be
able to demonstrate higher levels of protection in our first
challenge experiment. It’s not uncommon to see such results at this
early stage. We will work diligently with our international team of
experts to further understand the data as COVID-19 is unfortunately
going to be around for a long time. Whilst we had hoped to get into
the clinic sooner, we believe that our technology could still be
very relevant in the fight against COVID-19 and other infectious
diseases,” said David Goren, Vaxil’s Chairman and Chief Executive
Officer, and continued, “thanks to our relatively strong balance
sheet, we have sufficient funds to continue the pre-clinical
development of our potential vaccine and our other research
programs.”
Dr. Michael Berelowitz, Vaxil’s newly appointed
senior advisor the board of directors added: “Vaxil’s innovative
approach in targeting the SP domain of clinically meaningful cancer
and infectious disease molecules provided the stimulus for joining
the company. The demonstration in this study of COVID-19 SP
immunogenicity provides support and impetus for the concept. These
results, together with those previously seen in multiple myeloma
and tuberculosis, provide support for the Vaxil strategy moving
forward and their investigative approach toward developing critical
new therapeutics.”
The Company is not making any express or implied
claims that it has completed developing or will be successful in
developing a COVID-19 (or SARS-CoV-2) vaccine at this time.
ABOUT VAXIL
The company posts periodic updates through
videos from the official company’s youtube channel
https://www.youtube.com/channel/UC0M029aN8g6beW09Drgt0dQ
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 COVID-19
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 COVID-19
Vaccine Development is still under early stage research and
development and is not making any express or implied claims that it
has the ability to eliminate the COVID-19 virus at this time. 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.
About the U.S. Army Medical Research
Institute of Infectious Diseases
For over 50 years, USAMRIID has provided leading
edge medical capabilities to deter and defend against current and
emerging biological threat agents. The Institute is the only
laboratory in the Department of Defense equipped to safely study
highly hazardous viruses requiring maximum containment at Biosafety
Level 4. Research conducted at USAMRIID leads to medical solutions
- vaccines, drugs, diagnostics, information, and training programs
- that benefit both military personnel and civilians. Established
in 1969, the Institute plays a key role as the lead military
medical research laboratory for the Defense Threat Reduction
Agency's Joint Science and Technology Office for Chemical and
Biological Defense. USAMRIID is a subordinate laboratory of the
U.S. Army Medical Research and Development Command. For more
information, visit http://www.usamriid.army.mil.
[The information contained in this press release
does not necessarily reflect the position or the policy of the
Government and no official endorsement should be inferred.]
CONTACT INFORMATIONFor further information please
visit http://vaxil-bio.com/ or contact:North Equities,
info@northequities.com David Goren, CEO -- info@vaxil-bio.com,
+972 (52) 720-6000Company Youtube channel
Vaxil Bio (TSXV:VXL)
Gráfico Histórico do Ativo
De Dez 2024 até Jan 2025
Vaxil Bio (TSXV:VXL)
Gráfico Histórico do Ativo
De Jan 2024 até Jan 2025