[December 14, 2017] |
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Aura Biosciences Announces Publication of Preclinical Data Supporting AU-011's Potent and Selective Anti-cancer Activity in Ocular Melanoma Tumors
Aura Biosciences, a biotechnology company developing a new class of
therapies to target and selectively destroy cancer cells using viral
nanoparticle conjugates, today announced that researchers at
Massachusetts Eye and Ear (MEE), Emory University and the National
Cancer Institute (NCI) have generated preclinical data that demonstrate
the ability of light-activated AU-011 to target and selectively destroy
ocular melanoma tumors, both in vitro and in vivo, in an
orthotopic animal model that highly mimics the location and progression
of the disease in humans. These results have been published
in the peer-reviewed journal, Molecular Cancer Therapeutics.
Aura's lead program, light-activated AU-011, is being developed for the
treatment of primary ocular melanoma, a rare and life-threatening
disease with no approved FDA therapies, and is currently in Phase 1b/2
clinical testing. Researchers believe AU-011's high tumor specificity
and targeting capability, due to its ability to selectively bind to
heparan sulfate proteoglycans (HSPG) on the surface membrane of tumor
cells, may be key to avoiding damage to the main ocular structures and
preserving patients' vision
"These data offer strong support for the basis of our clinical program,
which we are currently investigating in patients with primary ocular
melanoma," said Elisabet de los Pinos, Ph.D., founder and CEO of Aura.
"Our ultimate goal is to offer a first-line treatment option that can
achieve local tumor control, while enabling patients to maintain their
vision."
Currently available treatment options to control local tumor growth,
such as plaque radiotherapy, are highly invasiveand not tumor-specific,
often resulting in severe and vision-threatening complications. The data
published today suggest that AU-011 may be further investigated as a
novel first-line treatment option that can enable early intervention and
potentially become the standard of care for patients with early-stage
ocular melanoma.
About ocular melanoma Ocular melanoma, also known as uveal
or choroidal melanoma, is a rare and aggressive eye cancer. Ocular
melanoma is the most common primary ocular tumor and develops in the
uveal tract of the eye. No targeted therapies are available at present,
and current radiotherapy treatments can be associated with severe visual
loss and other long-term sequelae such as dry eye, glaucoma, cataracts
and radiation retinopathy. The most common current treatment is plaque
radiotherapy, which involves surgical placement of a radiation device
against the exterior of the eye over the tumor. This technique can
control the melanoma but can also lead to radiation-related cataract,
retinopathy, optic nerve damage and loss of vision. The alternative is
enucleation, or removal of the eye. Ocular melanoma metastasizes to the
liver in about 40 percent of cases in the long-term (source: OMF),
and only 10 to 15 percent of patients whose melanoma has metastasized
survive beyond five years after diagnosis (source: ACS).
About light-activated AU-011 AU-011 is a first-in-class
targeted therapy in development for the primary treatment of ocular
melanoma. The therapy consists of viral nanoparticle conjugates that
bind selectively to unique receptors on cancer cells in the eye and is
derived from technology originally pioneered by Dr. John Schiller of the
Center for Cancer Research at the National Cancer Institute (NCI),
recipient of the 2017 Lasker-DeBakey Award. Upon activation with an
ophthalmic laser, the drug rapidly and specifically disrupts the
membranes of tumor cells while sparing key eye structures, which may
allow for the potential of preserving patients' vision and reducing
other long-term complications of treatment. This therapy can be
delivered using equipment commonly found in the ophthalmologist's office
and does not require a surgical procedure, pointing to a potentially
less invasive, more convenient therapy for patients and physicians.
AU-011 for ocular melanoma has been granted orphan drug and fast track
designations by the U.S. Food and Drug Administration and is currently
in clinical development.
About Aura Biosciences Aura Biosciences is developing a new
class of therapies to selectively target and destroy cancer cells. Its
lead program, AU-011 in ocular melanoma, is being developed under a
CRADA with the National Cancer Institute (NCI), part of the National
Institutes of Health. For more information, visit www.aurabiosciences.com.
View source version on businesswire.com: http://www.businesswire.com/news/home/20171214005990/en/
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