4D Molecular Therapeutics (Nasdaq: FDMT, 4DMT or the Company),
a leading clinical-stage genetic medicines company focused on
unlocking the full potential of genetic medicines to treat large
market diseases, today announced the publication of landmark
preclinical data demonstrating the potential of the Company’s
proprietary Therapeutic Vector Evolution (TVE) platform,
intravitreal R100 vector and the R100-based genetic medicine
4D-150. Pioneering efficacy and safety results in a
difficult-to-treat nonhuman primate (NHP) model of wet age-related
macular degeneration (wet AMD) demonstrated the potential of 4D-150
to substantially reduce the treatment burden and improve long-term
vision outcomes for patients with wet AMD, diabetic macular edema
(DME) and diabetic retinopathy (DR). The data were published in
Investigative Ophthalmology & Visual Science (IOVS); December
2024 issue. IOVS is the journal of the Association for Research in
Vision and Ophthalmology (ARVO), a leading basic and translational
research association in ophthalmology.
The publication entitled, “Design and Characterization of a
Novel Intravitreal Dual-Transgene Genetic Medicine for Neovascular
Retinopathies,” reports the results of preclinical discovery,
engineering and characterization studies evaluating the safety,
retinal cell transduction, transgene expression and clinical
activity of proprietary evolved intravitreal vector R100 and
4D-150, an R100-based genetic medicine carrying 2 therapeutic
transgenes: 1) a codon-optimized sequence encoding aflibercept, a
recombinant protein that inhibits VEGF-A, VEGF-B and PlGF, and 2) a
microRNA sequence that inhibits expression of VEGF-C. The data
showed that R100 demonstrated significantly superior human retinal
cell transduction compared to AAV2, and intravitreal administration
of 4D-150 to nonhuman primates was well tolerated and led to robust
panretinal expression of both transgenes, especially within the
macula region; AAV2 was unable to transduce deep retinal cell
layers in the same model. In a difficult-to-treat primate
laser-induced choroidal neovascularization model of wet AMD, 4D-150
completely prevented grade IV angiogenic lesions at all tested
doses.
“We founded 4DMT with the belief that the Nobel Prize-winning
technology of directed evolution could be applied to invent highly
optimized and customized AAV vectors for any tissue in the body.
This proprietary Therapeutic Vector Evolution approach has been
validated through clinical results with three different proprietary
vectors for transgene payload delivery to the retina (R100,
intravitreal), lung airways (A101, aerosol) and heart (C102,
intravenous). R100 was invented to be a potentially best-in-class
intravitreal vector to address and overcome the limitations of
conventional vectors for the retina, and we are now leveraging R100
in our 4D-150 product candidate to potentially bring to market the
first large market genetic medicine to transform vision outcomes
for millions of patients with wet AMD and diabetic eye diseases,”
said David Kirn, M.D., senior author of the paper and Co-founder
and Chief Executive Officer of 4DMT. “This innovative
disease-modifying genetic medicine is designed to continuously
suppress all four major molecular drivers of these diseases for
years, directly at the site of the disease within the macula,
following a single routine clinic-based intravitreal injection.
Standard of care bolus anti-VEGF therapies, which generate billions
in annual sales, cannot achieve this transformative mechanism of
action. The robust results in our primate models reinforce our
confidence in 4D-150's efficacy in patients.”
The publication is available online at
the IOVS website and on the Scientific
Publications page of the 4DMT website.
About 4D-150
4D-150 combines our customized and evolved intravitreal vector,
R100, and a transgene cassette that expresses both aflibercept and
a VEGF-C inhibitory RNAi. This dual-transgene payload inhibits four
members of the VEGF angiogenic family of factors that drive wet AMD
and DME: VEGF A, B, C and PlGF. R100 was invented at 4DMT through
our proprietary Therapeutic Vector Evolution platform; we developed
this platform utilizing principles of directed evolution, a Nobel
Prize-winning technology. 4D-150 is designed for single, low-dose
intravitreal delivery for transgene expression from the retina
without significant inflammation.
About Wet AMD
Wet AMD is a highly prevalent disease with estimated incidence
rate of 200,000 new patients per year in the United States. It is
estimated that the total prevalence of wet AMD in certain major
markets, including the United States and the European Union (major
markets), and Japan, will be greater than 4 million individuals in
the next five years. Wet AMD is a type of macular degeneration
where abnormal blood vessels (choroidal neovascularization or CNV)
grow into the macula, the central area of the retina. As a
consequence, CNV causes swelling and edema of the retina, bleeding
and scarring, and causes visual distortion and reduced visual
acuity. The proliferation and leakage of abnormal blood vessels is
stimulated by VEGF. This process distorts and can potentially
destroy central vision and may progress to blindness without
treatment.
About DME
DME is a highly prevalent disease with significant unmet medical
need. It is estimated that there are approximately one million
individuals with DME in the United States according to published
data. DME is characterized by swelling in the macula due to leakage
from blood vessels, which can lead to blurred vision. DME is
typically treated with intravitreal anti-VEGF agents administered
approximately every 4-12 weeks.
About 4DMT
4DMT is a leading clinical-stage genetic medicines company
focused on unlocking the full potential of genetic medicines to
treat large market diseases in ophthalmology and pulmonology.
4DMT’s proprietary invention platform, Therapeutic Vector
Evolution, combines the power of the Nobel Prize-winning
technology, directed evolution, with approximately one billion
synthetic AAV capsid-derived sequences to invent customized and
evolved vectors for use in our wholly owned and partnered product
candidates. Our product design, development, and manufacturing
engine helps us efficiently create and advance our diverse product
pipeline with the goal of revolutionizing medicine with potential
curative therapies for millions of patients. Currently, 4DMT is
advancing six clinical-stage and one preclinical product candidate,
each tailored to address rare and large market diseases in
ophthalmology, pulmonology and cardiology. In addition, 4DMT is
also advancing programs in CNS through a gene editing partnership.
4D Molecular Therapeutics™, 4DMT™, Therapeutic Vector Evolution™,
and the 4DMT logo are trademarks of 4DMT.
All of our product candidates are in clinical or preclinical
development and have not yet been approved for marketing by the
U.S. Food and Drug Administration (FDA) or any other regulatory
authority. No representation is made as to the safety or
effectiveness of our product candidates for the therapeutic uses
for which they are being studied.
Learn more at www.4DMT.com and follow us on LinkedIn.
Forward Looking Statements:
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995, as amended, including, without limitation, implied and
express statements regarding the therapeutic potential, and
clinical benefits and market potential of 4DMT’s product
candidates, and its R100, A101 and C102 vectors, as well as the
plans, announcements, and related timing for the clinical
development of, regulatory interactions regarding, and potential
commercialization of 4D-150. The words "may," “might,” "will,"
"could," "would," "should," "expect," "plan," "anticipate,"
"intend," "believe," “expect,” "estimate," “seek,” "predict,"
“future,” "project," "potential," "continue," "target" and similar
words or expressions are intended to identify forward-looking
statements, although not all forward-looking statements contain
these identifying words. Any forward looking statements in this
press release are based on management's current expectations and
beliefs and are subject to a number of risks, uncertainties and
important factors that may cause actual events or results to differ
materially from those expressed or implied by any forward-looking
statements contained in this press release, including risks and
uncertainties that are described in greater detail in the section
entitled "Risk Factors" in 4D Molecular Therapeutics’ most recent
Quarterly Report on Form 10-Q as well as any subsequent filings
with the Securities and Exchange Commission. In addition, any
forward-looking statements represent 4D Molecular Therapeutics'
views only as of today and should not be relied upon as
representing its views as of any subsequent date. 4D Molecular
Therapeutics explicitly disclaims any obligation to update any
forward-looking statements. No representations or warranties
(expressed or implied) are made about the accuracy of any such
forward looking statements.
Contacts:
Media:Katherine SmithInizio Evoke
CommsMedia@4DMT.com
Investors:Julian PeiHead of Investor Relations
and Corporate FinanceInvestor.Relations@4DMT.com
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