Heqet will test nanoparticles based on Altamira’s OligoPhore
delivery platform in the regeneration of damaged heart tissue
Altamira Therapeutics Ltd. (“Altamira” or the
“Company”) (Nasdaq:CYTO), a company dedicated to developing and
commercializing RNA delivery technology for targets beyond the
liver, today announced that it has entered into a collaboration and
option agreement with Heqet Therapeutics s.r.l. (“Heqet”) utilizing
the Company’s proprietary OligoPhoreTM delivery platform. Based in
Turin, Italy, Heqet is a biotech spin-out from King’s College
London. It is developing groundbreaking genetic medicines
to reverse the damage of ischemic heart disease.
Under the terms of the agreement, Heqet will
test nanoparticles based on Altamira’s OligoPhore delivery platform
and comprising certain non-coding RNAs (ncRNAs) in the regeneration
of damaged heart tissue following myocardial infarction in animal
models. Upon successful conclusion of the experiments, Heqet will,
under certain conditions, have the option to negotiate with
Altamira for a license to use the Company’s technology and
intellectual property to translate its findings into the
development of therapeutics for cardiac regeneration.
Myocardial infarction (commonly called “heart
attack”) may cause irreversible death (necrosis) of heart muscle
cells (cardiomyocytes) due to prolonged lack of oxygen supply
(ischemia). According to the American Heart Association, in the US
alone there are 605,000 new cases of myocardial infarction and
200,000 recurrent attacks every year.1 The adult human heart has
very limited ability to replace damaged cardiomyocytes, and heart
failure is a common sequela of myocardial infarction. Heart failure
mortality has been estimated at 50 percent of patients at only five
years from diagnosis.2
Heqet was founded by Professor Mauro Giacca, MD,
Ph.D., who serves as Head, School of Cardiovascular Medicine &
Sciences, King's College London. His previous work showed the
feasibility of regeneration of damaged heart tissue by stimulating
the proliferation of cardiomyocytes in animal models of myocardial
infarction through upregulation of certain ncRNAs.3 However,
delivery of the ncRNAs with viral vector technology turned out to
be challenging, not the least since proliferation must be only
temporary.
“We are thrilled to combine Altamira’s
peptide-based delivery technology with our non-coding RNAs, to
further optimize our unique therapeutic approach and improve the
available treatment options for myocardial infarction,” said Anja
Høg, Chief Development Officer at Heqet Therapeutics.
“The promise of regenerating cardiac muscle
continues to intrigue scientists and clinicians worldwide given the
significant complications and high mortality associated with
myocardial infarction,” said Samuel A. Wickline, MD, Altamira’s
Chief Scientific Adviser. “Application of molecular factors that
can stimulate resident myocardial cells to start dividing again
appears to be a very promising novel approach, yet it requires
timely and targeted delivery to cardiomyocytes. We believe that our
peptide-based OligoPhore platform for RNA delivery has the
potential to serve as a safe and effective vehicle for engineering
controlled local cardiac regeneration.”
About OligoPhore
OligoPhore is a versatile platform designed to
enable safe and effective delivery of oligonucleotides such as
siRNA, miRNA or antisense RNA into target cells, using systemic or
local administration. It is based on a proprietary 21 amino acid
peptide that can engage any type of RNA in rapid self-assembly into
a polyplex. The polyplex has a size, charge, and other physical
features that allow it to escape hepatic clearance and thus to
reach target tissues other than the liver. OligoPhore protects the
RNA payload from degradation in the circulation and allows for
rapid cellular uptake, while enabling pH-dependent nucleotide full
endosomal escape and cytoplasmic delivery. Effective delivery and
positive treatment outcomes have been demonstrated in more than 10
diverse murine models of disease so far.
About Altamira Therapeutics
Altamira Therapeutics (Nasdaq:CYTO) is dedicated
to developing and commercializing RNA delivery technology for
extrahepatic targets (OligoPhore™ / SemaPhore™ platforms). The
Company currently has two flagship siRNA programs in preclinical
development beyond in vivo proof of concept: AM-401 for KRAS driven
cancer and AM-411 for rheumatoid arthritis. The versatile delivery
platform is also suited for mRNA and other types of RNA
therapeutics and is planned to be leveraged via out-licensing to
pharma or biotech companies. In addition, Altamira is in the
process of divesting and/or out-licensing its legacy assets in
allergology and viral infection (Bentrio® OTC nasal spray;
commercial) and inner ear therapeutics (AM-125 nasal spray for
vertigo; post Phase 2; Keyzilen® and Sonsuvi® for tinnitus and
hearing loss; Phase 3). Founded in 2003, Altamira is headquartered
in Hamilton, Bermuda, with its main operations in Basel,
Switzerland. For more information, visit:
https://altamiratherapeutics.com/
About Heqet Therapeutics
Heqet Therapeutics, Turin, Italy, is a spin-out
company from King’s College London founded in 2022. It was founded
on ground-breaking research in cardiac regeneration conducted by
Professor Mauro Giacca. The company is currently advancing its
ncRNA-based compounds into preclinical development. At its
inception, Heqet Therapeutics raised GBP 6.6 million (about $8.5
million) in a Series A financing round led by Claris Ventures and
2Invest. https://www.heqettherapeutics.com/
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800-460-0183
Altamira Therapeutics (NASDAQ:CYTO)
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