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Oxford BioMedica and VIB-K.U.Leuven Announce Collaborative Research Project Funded by The Motor Neurone Disease Association to Develop MoNuDin for Treatment of Amyotrophic Lateral Sclerosis - 01/07/20102010/OB/15
Oxford (UK) and Leuven (Belgium) – 1 July 2010: Oxford BioMedica (LSE: OXB), the leading UK gene therapy company, VIB, a life sciences research institute in Flanders, Belgium and the UK Motor Neurone Disease Association (MND Association) are pleased to announce the award by MND Association of a research grant to support the further preclinical evaluation of MoNuDin® for the treatment of amyotrophic lateral sclerosis (ALS, or Lou Gehrig’s disease). The grant is for £255,000 and will fund a collaborative project between Oxford BioMedica and the research group of Professor Peter Carmeliet, Director of the VIB Vesalius Research Center and Professor of Medicine at K.U. Leuven. ALS is the most common form of motor neurone disease and is characterised by the loss of motor neurones in the brain and spinal cord resulting in progressive paralysis. Life expectancy ranges from two to five years from the onset of symptoms. There are currently no curative treatments available. Gene therapy offers potential as a novel therapeutic approach for the treatment of this devastating disease.
The collaboration will utilise Oxford BioMedica’s advanced LentiVector® gene delivery technology to compare the therapeutic potential of two forms of vascular endothelial growth factor (VEGF). Previous preclinical studies carried out by Oxford BioMedica and VIB, also funded by the MND Association, have shown that one form of VEGF delayed disease onset, slowed disease progression and extended life expectancy in ALS research models. This project will also evaluate the optimal delivery protocol for these gene therapy approaches.
Professor Peter Carmeliet, Director of the VIB Vesalius Research Center, commented: "Thanks to this important funding by the MND Association, we are able to continue the excellent collaboration with Oxford Biomedica which brings all parties involved to the frontline of biotechnology. I am especially pleased by this type of collaboration between innovative biotech companies and academia because they offer an important leverage for successful development of pharmaceuticals."
MoNuDin® is based on Oxford BioMedica’s advanced LentiVector® gene delivery technology and is designed to protect motor neurones susceptible to degeneration as a result of ALS through the delivery of a neuroprotective VEGF gene. Oxford BioMedica is also conducting further preclinical studies of MoNuDin® in the area of ALS in collaboration with the ALS Therapy Development Institute.
Oxford BioMedica’s Chief Scientific Officer, Dr Stuart Naylor, commented: “We are delighted to have received funding from the MND Association for this exciting collaborative project on the further development of MoNuDin®. We are also very pleased to be working again with the excellent research team of Professor Carmeliet at VIB. Together we aim to further the preclinical development of MoNuDin® and accelerate its progression to clinical studies.”
Dr Brian Dickie, Director of Research Development at the MND Association, said: “One of the major hurdles to treating motor neurone disease is ensuring that therapeutic agents are delivered to their site of action in the brain and spinal cord. We are delighted to support a research initiative which combines innovative approaches to drug delivery with the development of a promising therapeutic compound.” - Ends -
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