OXFORD BIOMEDICA AWARDED £0.5 MILLION FROM THE UK DEPARTMENT OF HEALTHGENE THERAPY RESEARCH PROGRAMME.
Oxford, UK: 29 March 2004 - Oxford BioMedica announced today that the Department of Health has awarded the Company £0.5 million to develop its proprietary LentiVector(R) technology for use in the treatment of single gene inherited disorders. The focus of the work is to be haemophilia A, a condition caused by a defective gene for Factor VIII, a key component of the mechanism for forming blood clots.
The LentiVector technology, developed primarily for theCompany's neurotherapy pipeline, can be used in many areas outside the field of neurobiology. It is ideally suited to the treatment of single gene disorders where therapy is based on functional correction of a defective gene in patients. In this situation, there is a need for long-term, stable and predictable gene activity and this can be achieved with the LentiVector technology.
Three years ago the Company initiated a programme to develop a product known as RequinateTM. Requinate comprises a LentiVector gene delivery system carrying a modified version of the human Factor VIII gene. During this exploratory programme the Company solved several problems that had been encountered by others attempting gene therapy for haemophilia. However, since haemophilia falls outside of the Company's therapeutic focus of cancer and neurotherapy, the programme has received minimal internal resources. The new money from the Department of Health will enable the Company to progress the Requinate haemophilia programme without compromising progress of its cancer and neurotherapy products. The current market for Factor VIII treatment is in excess of $1.0 billion.
Commenting on the award, Oxford BioMedica's Chief Executive, Prof. Alan Kingsman said "We are pleased to see the Department of Health implementing the government's decision to place gene-based medicine in the mainstream of healthcare in the UK. We are also delighted to be the only company selected to contribute to this initiative and to aid in the process of bringing products to the market that will directly benefit patients with genetic diseases. Oxford BioMedica is currently evaluating how it can expand the application of the LentiVector technology for other inherited disorders, in addition to haemophilia, while retaining its essential focus on bringing its current product pipeline in cancer and neurotherapy to the market as quickly as possible".
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Notes to editors
1. Oxford BioMedica
Oxford BioMedica(LSE: OXB) is a biopharmaceutical company specialising in the development of novel gene-based therapeutics with a focus on the areas of oncology and neurotherapy. The Company was established in 1995 as a spin out from Oxford University, and is listed on the London Stock Exchange.
In addition to its technical expertise in gene delivery, Oxford BioMedica has in-house clinical, regulatory and manufacturing know-how. The development pipeline includes two novel anti-cancer products in clinical trials; and two neurotherapy products in advanced preclinical development for Parkinson's disease and retinopathy. The Company is underpinned by an extensive preclinical and research portfolio and about 70 patent families, which represents one of the broadest patent estates in the field.
The Company has a staff of circa 65 split between its main facilities in Oxford and its wholly owned subsidiary, BioMedica Inc, in San Diego, California. Oxford BioMedica has corporate collaborations with Wyeth,Intervet, Merck & Co, Amersham and Kiadis. |