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News / 28 February 2000
 

 

2000/OB/09

OXFORD BIOMEDICA

Oxford Biomedica Obtains Gene Therapy Patent In The USA

Oxford, England - 28 February 2000. Oxford BioMedica announced today that it had received a Notice of Allowance from the US Patent Office for a patent covering broad aspects of retroviral and lentiviral vector systems. The technology covered by the patent enables BioMedica to create hybrid viruses that can be used in Gene therapy products for a wide range of diseases.

Commenting on the news BioMedica's Chief Executive, Prof. Alan Kingsman said:
"We are, of course, pleased with the granting of this patent in the US although the news came as no surprise. The Company is a leading player in this field and this patent is one of a large family of patents covering many aspects of gene therapy vector design and use. As our patents proceed through the examination process we expect many more similar successes" .


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Notes to Editors

1.

Oxford BioMedica plc
Established in 1995, the Company specialises in the development and application of gene-based therapeutics using advanced gene delivery technologies for the treatment of disease in the areas of Oncology, Viral Infection, Neurobiology and Genetic Deficiency. Oxford BioMedica plc was floated on the UK Alternative Investment Market of the London Stock Exchange in December 1996.

2. Lentivirus vector systems
In gene therapy, the aim is to deliver a gene and its necessary regulatory elements (the gene construct) to the cell surface, using a vector to mediate the transfer across the cell membrane and, in some cases, into the nucleus. A new and potentially very powerful vector system is based on lentiviruses, which have similar features to retroviruses in the ease of manipulation, predictable integration and reliable gene expression and regulation. However, their main advantage over retroviruses is the ability to function in non-dividing cells or cells that are dividing slowly - a feature of many clinically important tissues.

3.

Types of lentiviruses
Lentivirus vectors are constructed from two sources:

  • primate viruses e.g. human or simian immunodeficiency virus (HIV or SIV)
  • non-primate viruses e.g. feline and bovine immunodeficiency viruses (FIV and BIV), and one of the most simple, equine infective anaemia virus (EIAV)

For further information please contact:

 

Oxford BioMedica plc
Professor Alan Kingsman, Chief Executive

Tel: +44 (0)1865 783 000

City/Financial Enquiries
David Simonson, Melanie Toyne Sewell Merlin Financial

Tel: +44 (0)171 606 1244

Scientific/Trade Enquiries
Sue Charles/ Sarah Pattinson, HCC•De Facto Group

Tel: +44 (0)171 496 3300

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