Celyad Oncology provides an update on its strategic business model, continuing to focus on opportunities to fully harness the true potential of its proprietary technology platforms and intellectual property
21 December 2022 - 5:00PM
Celyad Oncology (Euronext & Nasdaq: CYAD) (the “Company”), a
biotechnology company focused on the discovery and development of
innovative technologies for chimeric antigen receptor (CAR) T-cell
therapies, today provides an update on its Celyad 2.0 business
strategy which has been adopted and implemented over the last few
months.
In keeping with this strategy, the Company
intends to focus on maximizing its valuable intellectual property
(IP) estate, and strengthening its research focus.
- The Company has
compiled a foundational and broad IP estate that controls key
aspects of developing therapies in the allogeneic cell therapy
space. The patents around allogeneic CAR T-cell therapies and
NKG2D-based therapies provide an avenue to develop intellectual
property programs and to partner with outside parties around the
licensing of these patents.
- In addition to
IP partnering transactions, Celyad 2.0 will prioritize discovery
research in areas of expertise where it can leverage the
differentiated nature of its platforms. The Company is implementing
a differentiated and innovative strategy, tackling the major
current limitations of CAR T-cell therapies. This strategy
includes:
-
Multiplexing approach of the short hairpin RNA
(shRNA) platform, allowing multiple genes, including essential and
functional genes, to be modulated simultaneously;
- Dual CAR
development of a next-generation NKG2D-based CAR which may
help to overcome resistance and immune escape often observed with
traditional single targeting approaches; and
-
Development of B7-H6-targeting immunotherapies as
the Company believes that B7-H6 is an underappreciated target that
could change the paradigm of cell therapy due to its broad
expression in a large variety of cancers.
Celyad Oncology is of the opinion that it will
potentially create more shareholder value by licensing its patent
estate and further strengthening its research efforts to improve
the differentiated nature of its platforms.
Based on a strategic and financial review, the
Company has decided to discontinue the development of its remaining
clinical program CYAD-211 (the allogeneic shRNA-based, anti-BCMA
CAR T candidate for relapsed or refractory multiple myeloma (r/r
MM)). There were no safety concerns leading to this decision and
all patients previously treated with CYAD-211 will continue to
receive their protocol-defined follow-up.
The key data points of the program are as
follows:
- 19 r/r MM patients have been
treated with CYAD-211 in the IMMUNICY-1 trial which was developed
to validate shRNA technology in the clinic;
- The observed safety profile,
including the lack of observed Graft-versus-Host disease, provides
proof-of-concept for the use of shRNA technology for allogeneic CAR
Ts;
- Out of 17 evaluable patients, a
partial response was achieved in five patients. One patient was
recently re-treated with a second dose of CYAD-211 after having
reached stable disease post first infusion; and
- Enhanced lymphodepletion did not
seem to improve clinical activity nor persistence of the cells
post-infusion.
Anticipated milestones for
2023
-
The Company will take part in several conferences including The
World Oncology Cell Therapy Congress in April and the Society for
Immunotherapy of Cancer’s (SITC) 38th Annual Meeting in November;
and
- The Company will
provide updates on the potential proof-of-concept of the dual CAR
and multiplexing research programs and on business development in
the second quarter of
2023.
About Celyad OncologyCelyad
Oncology is a biotechnology company focused on the discovery and
development of innovative technologies chimeric antigen receptor
(CAR) T-cell therapies. The Company is focusing on opportunities to
fully harness the true potential of its proprietary technology
platforms and intellectual property and support the development of
next-generation CAR T candidates in solid tumors and hematological
malignancies. Celyad Oncology is based in Mont-Saint-Guibert,
Belgium and New York, NY. For more information, please visit
www.celyad.com.
Celyad Oncology Forward-Looking
StatementThis release may contain forward-looking
statements, within the meaning of applicable securities laws,
including the Private Securities Litigation Reform Act of 1995, as
amended, including, without limitation, statements regarding
beliefs about and expectations for the Company’s updated strategic
business model, including associated potential benefits,
transactions and partnerships, and statements regarding the
potential value of the Company’s IP. The words “will,” “believe,”
“potential,” “continue,” “target,” “could” and similar expressions
are intended to identify forward-looking statements, although not
all forward-looking statements contain these identifying words. Any
forward-looking statements in this release are based on
management’s current expectations and beliefs and are subject to a
number of known and unknown risks, uncertainties and important
factors which might cause actual events, results, financial
condition, performance or achievements of Celyad Oncology to differ
materially from those expressed or implied by such forward-looking
statements. Such risks and uncertainties include, without
limitation, risks related to the material uncertainty about the
Company’s ability to continue as a going concern; the Company’s
ability to realize the expected benefits of its updated strategic
business model; the Company’s ability to develop its IP assets and
enter into partnerships with outside parties; the Company’s ability
to enforce its patents and other IP rights; the possibility that
the Company may infringe on the patents or IP rights of others and
be required to defend against patent or other IP rights suits; the
possibility that the Company may not successfully defend itself
against claims of patent infringement or other IP rights suits,
which could result in substantial claims for damages against the
Company; the possibility that the Company may become involved in
lawsuits to protect or enforce its patents, which could be
expensive, time-consuming, and unsuccessful; the Company’s ability
to protect its IP rights throughout the world; the potential for
patents held by the Company to be found invalid or unenforceable;
and other risks identified in Celyad Oncology’s U.S. Securities and
Exchange Commission (SEC) filings and reports, including in the
latest Annual Report on Form 20-F filed with the SEC and subsequent
filings and reports by Celyad Oncology. These forward-looking
statements speak only as of the date of publication of this
document and Celyad Oncology’s actual results may differ materially
from those expressed or implied by these forward-looking
statements. Celyad Oncology expressly disclaims any obligation to
update any such forward-looking statements in this document to
reflect any change in its expectations with regard thereto or any
change in events, conditions or circumstances on which any such
statement is based, unless required by law or regulation.
Celyad Oncology Investor and Media
Contact:Celyad Oncology investors@celyad.com
Source: Celyad Oncology SA
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