MaxCyte, Inc., (Nasdaq: MXCT; LSE: MXCT), a leading,
cell-engineering focused company providing enabling platform
technologies to advance the discovery, development, and
commercialization of next-generation cell-based therapeutics and
innovative bioprocessing applications, today announced it has
entered into a strategic platform license (SPL) agreement with
Legend Biotech, a global leader in cell therapy.
Under the terms of the SPL, Legend Biotech
obtains a non-exclusive worldwide license to use MaxCyte’s Flow
Electroporation® technology and ExPERT™ platform in connection with
the research, clinical development and commercialization of
cell-based therapeutical products (Licensed Products). In return,
MaxCyte will be eligible to receive annual licensing fees and
milestones from Legend Biotech during clinical development and,
upon successful commercialization, is eligible to receive licensing
fees and royalties on net sales of licensed products.
“We are looking forward to supporting Legend
Biotech’s non-viral engineered cell therapy program as they expand
their portfolio with new delivery modalities. As a leading provider
of cell-engineered platform technologies for drug developers, our
global infrastructure allows us to provide Legend Biotech with
technical, scientific, and regulatory support to advance its
non-viral engineered therapeutic pipeline across all major
regions,” said Maher Masoud, President and CEO of
MaxCyte. “We are thrilled to enable Legend Biotech in
scaling and optimizing its manufacturing process to meet their
expanding clinical and commercial needs.”
“MaxCyte’s clinical manufacturing platform,
non-viral cell engineering technology, and regulatory expertise
will support the development of our product pipeline across a wide
variety of cell types and modalities,” said Ying Huang PhD,
Chief Executive Officer of Legend Biotech. “Our goal is to
transform the treatment landscape by creating a broad portfolio of
cell therapies to help strengthen patients’ immune systems and
fight disease.”
MaxCyte’s ExPERT™ instrument portfolio is the
next generation of leading, clinically-validated electroporation
technology for complex and scalable cell engineering. By delivering
high transfection efficiency, seamless scalability and enhanced
functionality, the ExPERT™ platform delivers the high-end
performance essential to enabling the next wave of biological and
cellular therapeutics. Legend Biotech is MaxCyte’s 28th clinical /
commercial partnership overall, each partnership generates
pre-commercial milestone revenue, the vast majority of which
includes program-related revenue.
About MaxCyte
At MaxCyte, we pursue cell engineering
excellence to maximize the potential of cells to improve patients’
lives. We have spent more than 20 years honing our expertise by
building best-in-class platforms, perfecting the art of the
transfection workflow, and venturing beyond today’s processes to
innovate tomorrow’s solutions. Our ExPERT™ platform, which is based
on our Flow Electroporation® technology, has been designed to
support the rapidly expanding cell therapy market and can be
utilized across the continuum of the high-growth cell therapy
sector, from discovery and development through commercialization of
next-generation, cell-based medicines. The ExPERT family of
products includes: four instruments, the ATx™, STx™, GTx™ and VLx
™; a portfolio of proprietary related processing assemblies or
disposables; and software protocols, all supported by a robust
worldwide intellectual property portfolio. By providing our
partners with the right technology platform, as well as scientific,
technical and regulatory support, we aim to guide them on their
journey to transform human health. Learn more at maxcyte.com and
follow us on X (formerly Twitter) and LinkedIn.
Forward-Looking Statements
This press release contains "forward-looking
statements" within the meaning of the "safe harbor" provisions of
the Private Securities Litigation Reform Act of 1995. These
statements about us and our industry involve substantial known and
unknown risks, uncertainties, and assumptions, including those
described in Item 1A under the heading “Risk Factors” and elsewhere
in our report on Form 10-K, that may cause our actual results,
performance or achievements to be materially different from any
future results, performance or achievements expressed or implied by
the forward-looking statements. All statements other than
statements of historical facts contained in this press release,
including statements regarding our future results of operations or
financial condition, business strategy and plans and objectives of
management for future operations, are forward-looking statements.
Forward-looking statements include, but are not limited to,
statements about the Company’s expectations regarding annual
licensing revenue, pre-commercial milestone revenue, including
program related revenue and royalties on sales of products. In some
cases, you can identify forward-looking statements because they
contain words such as "may," “might,” "will," "could," "would,"
"should," "expect," "plan," "anticipate," "intend," "believe,"
“expect,” "estimate," “seek,” "predict," “future,” "project,"
"potential," "continue," “contemplate,” "target,” the negative of
these words and similar words or expressions. These statements are
inherently uncertain, and investors are cautioned not to unduly
rely on these statements. The forward-looking statements contained
in this press release, include, without limitation, statements
concerning the following: our expected future growth and success of
our business model; the size and growth potential of the markets
for our products, and our ability to serve those markets, increase
our market share, and achieve and maintain industry leadership; our
ability to expand our customer base and enter into additional SPL
partnerships; our expectation that our partners will have access to
capital markets to develop and commercialize their cell therapy
programs; our financial performance and capital requirements; the
adequacy of our cash resources and availability of financing on
commercially reasonable terms; our expectations regarding our
ability to obtain and maintain intellectual property protection for
our products, as well as our ability to operate our business
without infringing the intellectual property rights of others; our
expectations regarding general market and economic conditions that
may impact investor confidence in the biopharmaceutical industry
and affect the amount of capital such investors provide to our
current and potential partners; and our use of available capital
resources.
These and other risks and uncertainties are
described in greater detail in Item 1A , entitled "Risk Factors,”
in our Annual Report on Form 10-K for the year ended December 31,
2023, filed with the Securities and Exchange Commission (“SEC”) on
March 12, 2024, as well as in discussions of potential risks,
uncertainties, and other important factors in the other filings
that we make with the Securities and Exchange Commission from time
to time, including in our Form 10-Q for the quarter ended March 31,
2024, filed with the SEC on May 7, 2024. These documents are
available through the Investor Menu, Financials section, under “SEC
Filings” on the Investors page of our website
at http://investors.maxcyte.com. Any forward-looking
statements in this press release are based on our current beliefs
and opinions on the relevant subject based on information available
to us as of the date of such press release, and you should not rely
on forward-looking statements as predictions of future events. We
undertake no obligation to update any forward-looking statements
made in this press release to reflect events or circumstances after
the date of this press release or to reflect new information or the
occurrence of unanticipated events, except as required by law.
MaxCyte Contacts:
US IR AdviserGilmartin
GroupDavid Deuchler, CFA+1 415-937-5400ir@maxcyte.com
US Media
RelationsSpectrum Seismic
CollaborativeAnya Bolshemabolshem@spectrumscience.com
Nominated Adviser and Joint Corporate
BrokerPanmure GordonEmma Earl / Freddy CrossleyCorporate
BrokingRupert Dearden+44 (0)20 7886 2500
UK IR AdviserICR
ConsiliumMary-Jane ElliottChris Welsh+44 (0)203 709
5700maxcyte@consilium-comms.com
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