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2003/OB/14
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Oxford
BioMedica Obtains Further Fundamental Patent for LentiViral
Gene Therapy Technology
Oxford
BioMedica plc announced today that it has received allowance
from the US Patent Office
for a further patent covering its proprietary LentiVector
technology. This additional patent compliments the US patent
6,312,682 issued in November 2001 and both include broad
composition of matter claims and methods of production
claims for lentiviral vector gene delivery systems of both
human and non-human origin.
This patent adds
further strength to Oxford BioMedica's
existing patents that cover derivatives of lentiviral vector
systems that, unlike many versions of lentiviral vectors,
have real clinical utility because of their safety. The Oxford
BioMedica team was the first to construct lentiviral vectors
that contain no viral genes at all, and which comprise the
minimum number of viral components in the viral particles.
It is this minimisation of the vectors that is the subject
of these patents. This work was done using vectors based
on HIV and Equine Infectious Anaemia Virus (EIAV), a horse
virus that is not linked to any disease in humans. The EIAV
system is Oxford BioMedica's system of choice because
of its superior safety profile.
Oxford BioMedica's
LentiVector gene delivery technology is arguably the most
potent system currently available for
treating diseases of the central nervous system, particularly
chronic neurodegenerative disorders. Oxford BioMedica has
shown that minimal lentiviral vectors are able to deliver
genes to a wide range of dividing and non-dividing cells,
including neurones in the brain.
This technology
forms the delivery system for several of the Company's products that are approaching the clinical
development stage. ProSavin®, for Parkinsons disease,
is Oxford BioMedica's most advanced programme that
uses the proprietary LentiVector gene delivery system. In
addition to ProSavin, there are three further research/preclinical
stage programmes using the LentiVector system: RetinoStat™,
for retinopathy (vision loss), Innurex™, for nerve
repair in spinal cord injury, and MoNuDin™, for motor
neuron disease.
"Oxford
BioMedica's LentiVector technology is a powerful gene delivery
platform that out-performs other
vector systems in terms of its combination of high gene transfer
efficiencies, duration and regulation of gene expression,
ease of production and safety. This is reflected in the range
of commercial discussions that are underway related to this
technology, and in encouraging results from a number of the
Company's preclinical studies. We are working currently
on taking our first LentiVector-based product into clinical
trials for Parkinson's disease” said Alan Kingsman,
Chief Executive of Oxford BioMedica.
-Ends-
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| Notes
| 1. |
Oxford
BioMedica |
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Established
in 1995 as a spin out from Oxford University, Oxford
BioMedica plc specialises in the development of novel
gene-based therapeutics for the treatment of cancer,
neuro-degenerative disease and other disorders with
major unmet clinical needs. The development pipeline
includes two novel anti-cancer products in clinical
trials and a gene therapy treatment for Parkinson's
disease, which is in late preclinical studies. This
is underpinned by a broad research pipeline and over
70 patent families, about quarter of which are issued.
Oxford BioMedica's products use genes as the
mediators of a therapeutic effect and/or immune response.
The Company's gene therapy products deliver therapeutic
molecules in vivo whilst its gene-based immunotherapy
products deliver genes that recruit the patient's
immune system to mediate a therapeutic effect. The
genes are delivered by the Company's highly engineered
viruses or cells.
BioMedica's lead product TroVax® is an anti-cancer
therapeutic vaccine expected to be useful against a
broad range of tumour types. Two Phase I/II trials
with TroVax have been completed in the UK in late-stage
colorectal cancer patients. Following these successful
Phase I/II trials, TroVax has entered two Phase II
trials in Stage IV colorectal cancer patients receiving
5FU plus either oxaliplatin or irinotecan. The product
is also on target to enter further trials in colorectal,
renal and breast cancer. The renal and breast cancer
trials are to be conducted in the United States under
an Investigational New Drug (IND) application. Data
from the first TroVax Phase II trial is expected to
be available by the end of 2003, in readiness for Phase
III trials in colorectal cancer.
MetXia® is Oxford BioMedica's lead gene-based
cancer therapeutic. The product is based on a highly
engineered retrovirus gene delivery system expressing
a specific human cytochrome P450 gene. MetXia converts
the tumour into a 'drug factory', enabling
increased local production of the anti-tumour, cytotoxic
derivative of the pro-drug cyclophosphamide. MetXia
is potentially useful in the treatment of all solid
tumours and their metastases, particularly those where
cyclophosphamide is commonly used. MetXia is being
investigated in a Phase I/II trial in breast cancer,
and regulatory submissions are under review for trials
in pancreactic cancer.
Oxford BioMedica is headquartered in Oxford, UK and
has a wholly-owned subsidiary in San Diego, USA. BioMedica
has corporate collaborations with Wyeth, IDM, Intervet,
Aliga Pharmaceuticals, Amersham, Arius Research and
Viragen.
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further information please contact: |
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Oxford BioMedica plc
Professor Alan
Kingsman, Chief Executive |
Tel: +44 (0)1865 783 000 |
| City/Financial
Enquiries
Mike
Wort/James Chandler
Beattie Financial |
Tel: +44 (0)20 7398 3300
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Enquiries
Sue
Charles, Katja
Stout,
College Hill - Life Sciences |
Tel:
+44 (0)20 7886 8150 |
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