CytoMed Therapeutics Limited (NASDAQ: GDTC) (“CytoMed” or the
“Company”) today released a letter to shareholders from the
Chairman of the Company’s Board of Directors (the “Board”) as it
welcomes the new year ahead of its full-year audited results
announcement due by end-April, the full text of which is provided
below. All shareholders of CytoMed are encouraged to read.
Dear Shareholders,
The Board of CytoMed wishes you a healthy and
prosperous Year of the Snake.
The snake’s ability to shed its skin is often
compared to rebirth and renewal, representing adaptability and
growth in Chinese mythology. The snake’s calm and quiet nature also
embodies deep thought and strategic planning to embrace change and
explore new possibilities. Its connection to transformation makes
the Snake Year a relevant time for pursuing ambitious goals and
doing things differently from others in the same bio-eco
system.
But first a quick recap.
Based in Singapore and Malaysia, we are not in
cancer targets discovery, a disease diagnostic company, a research
biotech nor medical device company or a CDMO or CRO. Capitalizing
on Asia’s low-cost infrastructure and talents, we make affordable
GMP-grade immune cells to be infused into no-option patients to
alleviate their cancers or autoimmune diseases. This operation
continued to grow in 2024 especially with rising interest from
doctors and researchers in donor-derived off-the-shelf allogeneic
gamma delta T cells, a rare subset of cancer-killing T cells. We
are proud of our accomplishments in 2024 driven by our dedicated
employees and management team along with the effectiveness of our
strategy. We achieved decent growth in our topline (based on the
unaudited financials), product development, strategic partnership
and internationalization. Details will be announced when
available.
Here is a quick recap of our accomplishments in
2024 and an outline of our direction for 2025:
Clinical stage biopharma
Late last year, CytoMed became a clinical stage
biopharma with the first patient safely dosed in November 2024
under a clinical trial approved in Singapore. Termed ANGELICA
trial, this is a first-in-human CAR T trial in the world involving
CytoMed’s patented donor-derived allogeneic gamma delta T cells
which express a chimeric antigen receptor (“CAR”) which can
recognize many types of cancers, both hematological and solid
cancers. As a phase 1 trial, the number of patients to be recruited
is typically small, not more than 20 late stage cancers. The
National Medical Research Council of Singapore has awarded a
significant grant to implement this trial in Singapore.
Successful acquisition of a licenced
cord blood bank
This cord blood bank will provide rare and
precious cord blood as cost-free raw materials for our strategic
expansion into a new class of cord blood-derived therapeutics for
auto-immunes and cancers due to its naïve cord properties. We
purchased this bank for approximately US$ 450,000 and intend to
spinoff this subsidiary in future as a separate cord blood-based
biopharma for example manufacturing cord blood-derived Natural
Killer cells, widely researched for its safe and potentially
effective remedy for autoimmune diseases. There are few providers
of cord blood-derived therapeutics due to the unavailability of low
cost cord blood units.
International strategic
partnership
We initiated strategic collaboration to bring
our technology to China and India, two nearby large Asian economies
with abundant cancer cases. We can also tap on these low cost
regional countries to make affordable therapies. China scientists
reportedly now publish the most research papers in the world. India
is well-known to make very affordable medicines.
One step closer to the clinic for our
novel hybrid immune cell made from induced pluripotent stem cells
(“iPSC”)
CytoMed has generated the critical cell banks
for the iPSC-derived hybrid of gamma delta T and Natural Killer
cell technology and is currently undergoing process development
into a potentially very potent cancer-killing immunotherapy product
to treat a range of cancers.
Artificial Intelligence (“AI”)
project
We are participating in a proposed international
project involving the use of AI and our gamma delta T cells in the
treatment of infectious diseases in developing countries.
Tapping on fast growing medical tourism
in Asia
Looking ahead to 2025, an important milestone is
our initial clinical readout of our ANGELICA trial anticipated by
mid of this year. We are also working on submitting a US FDA IND
for our donor-derived allogeneic gamma delta T cells. We continue
to seek out like-minded partners especially to deploy our
allogeneic gamma delta T cells in combinational therapies such as
with antibodies. To enhance our profile in the US, we are
establishing a presence in New York so we can be in the same time
zone, be closer to our US investors and look out for opportunities
including M&A, strategic alliances and learn of new
technologies. As Chairman and substantial shareholder of CytoMed,
to show commitment and resolve to our shareholders, the US presence
will be motivated and funded in my private capacity using personal
donated shares and will not risk the Company’s resources.
In summary, be like the snake and transform,
renew. International medical tourism in Asia is fast growing so
there are lots of opportunities to develop this new science of cell
therapy which is very expensive in the West or inaccessible despite
passing of the Right-to-Try bill in the US due to fear of
litigation in the US. In 2025, we intend to implement radical
revenue-generating methods to address no-option late stage diseased
patients on a compassionate, or named patient basis (alternatively
known as special access or accelerated access programme depending
on which regulator) including investing in clinics and partnering
hospitals and medical cancer centres in the region. Although our
IPO on NASDAQ in 2023 was very modest raising only US$ 10 million
gross (net US$ 8 million after expenses), due to our cost-efficient
operations in Asia and exercising financial prudence, we have
sufficient cash runway of more than a year. We should prepare to
strengthen our financials at the right time in 2025 and plan well
ahead for funds to pounce on new opportunities including M&A.
The team is very busy with many projects.
DeepSeek is AI’s disruptor for its low R&D
investment cost and accessibility. Low cost allogeneic
off-the-shelf cell therapies for various types of cancers, both
hematological and solid cancers, may be biotech’s DeepSeek
moment.
Happy new year of the Snake!
About CytoMed Therapeutics Limited
(CytoMed)
Incorporated in 2018, CytoMed was spun off from
the Agency for Science, Technology and Research (A*STAR),
Singapore’s leading research and development agency in the public
sector. CytoMed is a biopharmaceutical company focused on
harnessing its licensed proprietary technologies, namely gamma
delta T cell and iPSC-derived gamma delta Natural Killer T cell, to
create novel cell-based allogeneic immunotherapies for the
treatment of various human cancers. The development of novel
technologies has been inspired by the clinical success of existing
CAR-T therapies in treating haematological malignancies, as well as
the current clinical limitations and commercial challenges in
extrapolating the CAR-T principle into the treatment of solid
tumours. For more information, please visit www.cytomed.sg and
follow us on Twitter (“X”) @CytomedSG, on LinkedIn, and
Facebook.
Forward-Looking Statements
This press release contains forward-looking
statements as defined by the Private Securities Litigation Reform
Act of 1995. Forward-looking statements include statements
concerning plans, objectives, goals, strategies, future events or
performance, and underlying assumptions and other statements that
are other than statements of historical facts. When the Company
uses words such as “may, “will, “intend,” “should,” “believe,”
“expect,” “anticipate,” “project,” “estimate” or similar
expressions that do not relate solely to historical matters, it is
making forward-looking statements. Forward-looking statements are
not guarantees of future performance and involve risks and
uncertainties that may cause the actual results to differ
materially from the Company’s expectations discussed in the
forward-looking statements. These statements are subject to
uncertainties and risks including, but not limited to, the
following: the Company’s plans to develop and commercialize its
product candidates; the initiation, timing, progress and results of
the Company’s current and future pre-clinical studies and clinical
trials and the Company’s R&D programs; the Company’s
expectations regarding the impact of future COVID-19 outbreak on
its business, the Company’s industry and the economy; the Company’s
estimates regarding expenses, future revenue, capital requirements
and needs for additional financing; the Company’s ability to
successfully acquire or obtain licenses for additional product
candidates on reasonable terms; the Company’s ability to establish
and maintain collaborations and/or obtain additional funding and
assumptions underlying or related to any of the foregoing and other
risks contained in reports filed by the Company with the SEC. For
these reasons, among others, investors are cautioned not to place
undue reliance upon any forward-looking statements in this press
release. Additional factors are discussed in the Company’s filings
with the SEC, which are available for review at www.sec.gov. The
Company undertakes no obligation to publicly revise these
forward–looking statements to reflect events or circumstances that
arise after the date hereof.
Contact :
CytoMed Therapeutics
Limitedenquiry@cytomed.sgAttention : Evelyn Tan, Chief
Corporate Officer
CytoMed Therapeutics (NASDAQ:GDTC)
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