Ocean Biomedical, Inc. (NASDAQ: OCEA), a biopharma company working
to accelerate the development and commercialization of
scientifically compelling assets from research universities and
medical centers, announced today that its Scientific Co-founder,
Jack A. Elias, MD, co-authored new findings in the peer-reviewed
journal Immunity that detail the mechanisms behind the role of
chitinase 3-like-1 (CHI3L1) in the growth of triple negative breast
cancer. The groundbreaking discoveries by a team led by Dr. William
Muller at McGill University and in collaboration with Dr. Elias
demonstrates that CHI3L1 stimulates neutrophil elaboration of NETs
which block T cells from contacting and killing the breast cancer
tumor. Additionally, the study provides further evidence of the
potential impact of Ocean’s anti-Chi3L1 antibody in reversing this
process and suppressing breast cancer tumor growth.
This groundbreaking paper deepens the
understanding of how CHI3L1 inhibits the body’s natural ability to
fight breast cancer tumors. It reveals for the first time another
complex pathway by which CHI3L1 inhibits the immune response to
cancer, this time by inducing neutrophil recruitment and NETosis,
which blocks T cell infiltration. The paper also provides yet
another preclinical demonstration of the effectiveness of Ocean’s
Anti-CHI3L1 antibody in reducing the tumor growth by targeting
CHI3L1 and reversing the T cell blockade. This tumor control
pathway, the paper asserts, is likely at work in a range of cancers
beyond breast cancer, and “targeting CHI3L1 may promote anti-tumor
immunity in various tumor types.”
“This complex work by our colleagues at McGill
has provided one of the most exciting discoveries of my lifetime
and adds another layer of understanding about the ways in which
CHI3L1 functions as a ‘master regulator’ that is not only at work
in many cancers, but working in multiple pathways within individual
cancers,” commented Dr. Jack A. Elias, Ocean’s Scientific
Co-founder.
Several publications this year have reinforced
the potential of Ocean’s Anti-CHI3L1 immunotherapy in treating
aggressive cancers. In April, an independent study published in
Cancer Research demonstrated the role of CHI3L1 in modulating
Glioma stem cells and the effectiveness of Ocean’s candidate in
suppressing severe glioblastoma tumor growth.
In October, results published in bioRxiv by
Elias and colleagues at Yale revealed the role of CHI3L1 in the
growth of EGFR-mutant non small cell lung cancer (NSCLC), and the
importance of CHI3L1 in the pathogenesis of therapeutic resistance
in NSCLC. These studies also demonstrated that the anti-CHI3L1
antibody effectively restored therapeutic responsiveness to
tyrosine kinase inhibitors (TKI) in drug resistant NSCLC with the
combination of Ocean’s antibody and a TKI, stopping human tumor
progression by stimulating tumor suppressor genes and inducing
tumor cell death. Although these findings were defined in NSCLC,
they have potential effectiveness in other EGFR-mutation driven
cancers including Glioblastoma and Colon cancer.
“We are excited to see the potential for Ocean’s
cancer immunotherapy candidate demonstrated by a range of studies
in some of the most aggressive cancers,” said Dr. Chirinjeev
Kathuria, Ocean’s Executive Chairman and Founder.
“We are pleased to see additional research about
the potential impact of cancer candidate as we continue to move
towards filing an IND,” said Elizabeth Ng, CEO of Ocean
Biomedical.
Prior research has established that elevated
Chi3L1 levels are associated with many cancers, including
glioblastoma, and may be targeted therapeutically. Recent studies
from Ocean Biomedical have demonstrated that CHI3L1 is a critical
regulator of a number of key cancer-causing pathways, highlighting
its ability to inhibit tumor cell death (apoptosis), its inhibition
of the expression of the tumor suppressors P53, PTEN,
retinoblastoma 1, and Keap1 and its stimulation of the B-RAF
protooncogene. Most recently Dr. Elias’s research team has
discovered that CHI3L1 is a “master regulator” of ICPI, including
key elements of the PD-1 and CTLA4 pathways. In accord with the
importance of these pathways, Ocean has also generated antibodies:
1.) a monoclonal antibody against CHI3L1, 2.)
bispecific antibodies that simultaneously target CHI3L1 and
PD-1, and 3.) a new bispecific antibody that
simultaneously targets CHI3L1 and CTLA4. The impressive
ability of these bispecific antibodies to control primary and
metastatic lung cancer in murine experimental modeling systems have
been discussed in detail in an earlier article in the Journal of
Clinical Investigation, and this expanded approach in Frontiers in
Immunology.
About Ocean Biomedical
Ocean Biomedical, Inc. is a Providence, Rhode
Island-based biopharma company with an innovative business model
that accelerates the development and commercialization of
scientifically compelling assets from research universities and
medical centers. Ocean Biomedical deploys the funding and expertise
to move new therapeutic candidates efficiently from the laboratory
to the clinic, to the world. Ocean Biomedical is currently
developing five promising discoveries that have the potential to
achieve life-changing outcomes in lung cancer, brain cancer,
pulmonary fibrosis, and the prevention and treatment of malaria.
The Ocean Biomedical team is working on solving some of the world’s
toughest problems, for the people who need it most.
To learn more, visit www.oceanbiomedical.com
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The announced discoveries were based solely on
laboratory and animal studies. Ocean Biomedical has not conducted
any studies that show similar efficacy or safety in humans. There
can be no assurances that this treatment will prove safe or
effective in humans, and that any clinical benefits of this
treatment is subject to clinical trials and ultimate approval of
its use in patients by the FDA. Such approval, if granted, could be
years away.
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with rapid technological developments to provide new and innovative
products and services or make substantial investments in
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develop, license or acquire new therapeutics; (ix) the risk that
the Company will need to raise additional capital to execute its
business plan, which may not be available on acceptable terms or at
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The foregoing list of factors is not exhaustive.
You should carefully consider the foregoing factors and the other
risks and uncertainties that are described in the Company’s Annual
Report on Form 10-K for the year ended December 31, 2022 and its
Quarterly Report on Form 10-Q for the quarter ended March 31, 2023,
and which are described in the “Risk Factors” section of the
Company’s definitive proxy statement filed by the Company on
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from time to time with the SEC and which are and will be available
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risks and uncertainties that could cause actual events and results
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any date subsequent to the date of this filing. Accordingly, undue
reliance should not be placed upon the forward-looking
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Ocean Biomedical Media Relationsconnect@oceanbiomedical.com
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