-- First patient treated at Cardiff University, Wales (UK) --
Oxford, UK – 10 July 2012: Oxford BioMedica plc (“Oxford BioMedica” or “the Company”) (LSE: OXB), the leading gene-based biopharmaceutical company, today announces that its partners at Cardiff University, Wales (UK) have initiated a Phase II trial to assess the safety and immunological activity of TroVax®, a therapeutic vaccine developed by Oxford BioMedica, in patients with inoperable metastatic colorectal cancer (CRC). The study will be funded by Cardiff University, with some funding awarded by Cancer Research Wales, and Oxford BioMedica will provide TroVax®. The trial is supported by the Experimental Cancer Medicine Centre (ECMC), Cardiff.
The randomised, open-label Phase II study, entitled “TaCTiCC” (TroVax® and Cyclophosphamide Treatment in Colorectal Cancer), builds on four previous Phase I/II trials conducted by Oxford BioMedica where TroVax® was given to patients with CRC, in addition to research into CRC undertaken by Dr Andrew Godkin and Dr Awen Gallimore at Cardiff University, Wales. Led by Dr Andrew Godkin, the study will enrol up to 54 patients with inoperable metastatic CRC. The study will evaluate whether TroVax®, administered alone or in combination with cyclophosphamide, is effective in the treatment of CRC. The study will assess anti-5T4 immune responses following treatment, in addition to secondary measures of clinical benefit including progression-free survival, objective response rate and overall survival.
Colorectal cancer is the second most common cause of cancer mortality in the UK with an estimated 16,000 deaths per year (source: Cancer Research UK, 2010). TroVax® is a therapeutic vaccine that stimulates the immune system to destroy cancerous cells expressing the 5T4 tumour antigen which is present on most solid tumours. It is well documented that low doses of cyclophosphamide can augment immune responses by decreasing the numbers of a class of blood cell called a “regulatory T cell”. By combining TroVax® with cyclophosphamide, this study will determine whether the combination approach results in stronger immune responses against 5T4 compared to patients treated with TroVax® alone.
Commenting on the collaboration, Stuart Naylor, Chief Scientific Officer at Oxford BioMedica, said: “We believe TroVax® holds great promise in the treatment of colorectal cancer and very much look forward to working with our colleagues at Cardiff University. This important study builds on pioneering work undertaken by Dr Godkin and his team and we are pleased to be able to support the transition into Phase II clinical development.”
Dr Andrew Godkin, Principal Investigator at Cardiff University, commented: “We are very excited in Cardiff to be starting this study. It is a truly translational study in as much as preliminary data have been generated from a series of experiments which started over 10 years ago. There has been a tremendous amount of support from various parties to drive this forward, the logistic hurdles are crossed and we are now ready to go.”
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Notes to editors
About Oxford BioMedica®
Oxford BioMedica (LSE:OXB) is a leading gene and cell therapy company focused on developing life changing treatments for serious diseases. Oxford BioMedica and its subsidiaries (the “Group”) have built a sector leading lentiviral vector delivery platform (LentiVector®) through which the Group develops in vivo and ex-vivo products both in-house and with partners. The Group has created a valuable proprietary portfolio of gene and cell therapy product candidates in the areas of oncology, ophthalmology and CNS disorders. The Group has also entered into a number of partnerships, including with Novartis, Sanofi, GSK, and Immune Design, through which it has long-term economic interests in other potential gene and cell therapy products. Oxford BioMedica is based across several locations in Oxfordshire, UK and employs more than 250 people. Further information is available at www.oxfordbiomedica.co.uk.
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