BioNTech Completes Acquisition of Biotheus
03 Février 2025 - 12:45PM
- Acquisition to
strengthen key pillar of BioNTech’s oncology strategy aimed at
establishing BNT327 as a pan-tumor technology platform for the
treatment of advanced cancers
-
With the closing of the transaction, BioNTech will expand its
capabilities to develop, manufacture and commercialize novel BNT327
combinations and next-generation bispecific antibodies
-
Biotheus will become a new indirect Chinese subsidiary of BioNTech,
adding a local research and development hub and an advanced
biologics manufacturing facility to the Company’s network
MAINZ, Germany, February 3, 2025 (GLOBE
NEWSWIRE) -- BioNTech SE (Nasdaq: BNTX,
“BioNTech” or “the Company”) announced today the completion of the
acquisition of Biotheus (“Biotheus”), a clinical-stage
biotechnology company dedicated to the discovery and development of
novel antibodies to address unmet medical needs of patients with
oncological or inflammatory diseases. The acquisition was announced
on November 2024 and builds on the successful collaboration on the
late-stage clinical asset BNT327, an investigational bispecific
antibody targeting PD-L1 and VEGF-A, and other bispecific antibody
candidates.
The transaction is part of BioNTech’s oncology
strategy, aimed at expanding the Company’s capabilities to
research, develop and commercialize BNT327 as a pan-tumor
technology platform for combination therapies. With this completion
of the acquisition, BioNTech obtains full global rights to BNT327
and rights to all other candidates of Biotheus’ pipeline as well as
to its in-house antibody generation platform and bispecific
antibody drug conjugate capability. Biotheus will operate as a new
indirect Chinese subsidiary of BioNTech, adding a local research
and development hub and an advanced biologics manufacturing
facility to the Company’s network.
The total consideration to acquire 100 percent
of the issued share capital by Biotheus amounts to $800 million,
predominantly in cash, with a small portion in BioNTech American
Depositary Shares, plus additional performance-based payments of up
to $150 million if certain milestones are met.
About BNT327BNT327 is a novel
investigational bispecific antibody combining two complementary,
validated mechanisms in oncology into one single molecule. BNT327
combines PD-L1 checkpoint inhibition aimed at restoring T cells’
ability to recognize and destroy tumor cells with the
neutralization of VEGF-A. The blocking of VEGF-A is aimed at
reversing the tumor’s immuno-suppressive effect in its
microenvironment and cutting off the blood and oxygen supply that
feeds tumor cells (anti-angiogenesis effect), with the intention of
preventing the tumor from growing and proliferating. BNT327 may be
differentiated via its mechanism of action of targeting PD-L1 on
the tumor cells aimed at enriching BNT327 in the tumor
microenvironment and promoting localized anti-cancer activity. The
co-localized blockade of the PD-(L)1 pathway and the VEGF-A driven
formation of an immuno-suppressive microenvironment has been shown
to deliver synergistically enhanced anti-tumor immune responses in
several solid tumor types.1,2
More than 750 patients have been treated with
BNT327 in clinical trials to date. Multiple clinical trials are
currently ongoing evaluating BNT327 either as a monotherapy or in
combination with other treatment modalities targeting different
oncogenic pathways in various solid tumor indications. Multiple
global trials are ongoing or planned to start in 2025, including
three global clinical trials with registrational potential in
first-line small cell lung cancer (“SCLC”), non-small cell lung
cancer (“NSCLC”) and triple-negative breast cancer (“TNBC”).
Additional trials will explore combining BNT327 and BioNTech’s
proprietary antibody-drug conjugate candidates (“ADCs”). If
successfully developed and approved, BioNTech aims to use this
bispecific antibody candidate as a next-generation immuno-oncology
(“IO”) backbone in combination with other treatment modalities
targeting a broad range of cancer indications.
About BioNTechBiopharmaceutical New
Technologies (BioNTech) is a global next generation immunotherapy
company pioneering novel investigative therapies for cancer and
other serious diseases. BioNTech exploits a wide array of
computational discovery and therapeutic drug platforms with the
intent of rapid development of novel biopharmaceuticals. Its broad
portfolio of oncology product candidates includes individualized
and off-the-shelf mRNA-based therapies, innovative chimeric antigen
receptor (CAR) T cells, several protein-based therapeutics,
including bispecific immune checkpoint modulators, targeted cancer
antibodies and antibody-drug conjugate (ADC) therapeutics, as well
as small molecules. Based on its deep expertise in mRNA vaccine
development and in-house manufacturing capabilities, BioNTech and
its collaborators are researching and developing multiple mRNA
vaccine candidates for a range of infectious diseases alongside its
diverse oncology pipeline. BioNTech has established a broad set of
relationships with multiple global and specialized pharmaceutical
collaborators, including DualityBio, Fosun Pharma, Genentech, a
member of the Roche Group, Genevant, Genmab, MediLink, OncoC4,
Pfizer and Regeneron.
For more information, please
visit www.BioNTech.com.
BioNTech Forward-Looking StatementsThis
press release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995, as
amended, including, but not limited to, statements concerning
expectations regarding the impact of this acquisition on BioNTech’s
business; the creation of long-term value for BioNTech and Biotheus
shareholders; potential synergies between BioNTech and Biotheus and
their businesses; BioNTech’s ability to research, develop and
potentially commercialize BNT327 and potentially other assets in
Biotheus’ pipeline; the expansion of BioNTech’s operations in
China; the initiation, timing, progress, results, and cost of
BioNTech’s research and development programs, including BioNTech’s
current and future preclinical studies and clinical trials,
including statements regarding the expected timing of initiation,
enrollment, and completion of studies or trials and related
preparatory work and the availability of results, and the timing
and outcome of applications for regulatory approvals and marketing
authorizations; BioNTech’s expectations regarding potential future
commercialization in oncology, including goals regarding timing and
indications; the targeted timing and number of additional
potentially registrational trials, and the registrational potential
of any trial BioNTech may initiate; discussions with regulatory
agencies; BioNTech’s expectations with respect to intellectual
property; and the impact of BioNTech’s collaboration and licensing
agreements. In some cases, forward-looking statements can be
identified by terminology such as “will,” “may,” “should,”
“expects,” “intends,” “plans,” “aims,” “anticipates,” “believes,”
“estimates,” “predicts,” “potential,” “continue,” or the negative
of these terms or other comparable terminology, although not all
forward-looking statements contain these words. The forward-looking
statements in this press release are based on BioNTech’s current
expectations and beliefs of future events, and are neither promises
nor guarantees. You should not place undue reliance on these
forward-looking statements because they involve known and unknown
risks, uncertainties, and other factors, many of which are beyond
BioNTech’s control, and which could cause actual results to differ
materially and adversely from those expressed or implied by these
forward-looking statements. These risks and uncertainties include,
but are not limited to: the reaction of BioNTech and Biotheus’
competitors and business partners to the proposed transaction; the
retention of Biotheus employees; BioNTech’s plans for Biotheus; the
future development of BioNTech’s business and the possibility that
integration following the transaction may be more difficult than
expected; the risk that Biotheus’ collaborations will not continue
or will not be successful; risks related to Biotheus’ ability to
protect and maintain its intellectual property position; risks
related to Biotheus’ capital requirements, use of capital and
unexpected expenditures, including Biotheus’ ability to manage
operating expenses or obtain funding to support planned business
activities or to explore and establish strategic alternative
transactions; risks related to Biotheus’ ability to attract and
retain personnel; the uncertainties inherent in research and
development; competition from other product candidates Biotheus’
and its counterparties’ ability to manage and source necessary
energy resources; BioNTech’s ability to identify research
opportunities and discover and develop investigational medicines;
the ability and willingness of BioNTech’s third-party collaborators
to continue research and development activities relating to
BioNTech's development candidates and investigational medicines;
BioNTech’s ability to manage its development; regulatory
developments in the United States and other countries; BioNTech’s
ability to effectively scale its production capabilities and
manufacture its products and product candidates; risks relating to
the global financial system and markets; and other factors not
known to BioNTech at this time.
You should review the risks and uncertainties
described under the heading “Risk Factors” in BioNTech’s Report on
Form 6-K for the period ended September 30, 2024 and in
subsequent filings made by BioNTech with the SEC, which are
available on the SEC’s website at www.sec.gov. These
forward-looking statements speak only as of the date hereof. Except
as required by law, BioNTech disclaims any intention or
responsibility for updating or revising any forward-looking
statements contained in this press release in the event of new
information, future developments or otherwise.
CONTACTS
Investor Relations Michael Horowicz
Investors@biontech.de
Media Relations Jasmina Alatovic Media@biontech.de
-----1 Tzuri N, et al. Sci Rep. 2023;13(1):11923. 2 Kim HJ, et
al. Arch Pharm Res. 2022;45(6):401-416.
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