-- Positive interim review of fourth patient cohort by Data Monitoring Committee --
Oxford, UK – 4 August 2011: Oxford BioMedica plc (“Oxford BioMedica” or “the Company”) (LSE: OXB), the leading gene-based biopharmaceutical company, today announces positive interim data from the on-going Phase I/II trial of ProSavin®; for the treatment of Parkinson’s disease (PD). The first three patients in the current six-patient cohort were treated with a 5x dose of ProSavin®, the scaled equivalent to the maximum dose in pre-clinical studies, and have reached their three-month assessment.
Highlights of fourth patient cohort at three months (n=3, 5x dose)
1. Motor function is assessed according to the Unified Parkinson’s Disease Rating Scale (UPDRS) in patients’ “OFF” state (i.e. after withdrawal of PD medication).
John Dawson, Chief Executive Officer of Oxford BioMedica, said: “As expected, the interim data from the 5x dose of ProSavin® already show improvements across several indicators of motor control and the reduction in background L-DOPA support is promising at this stage. Importantly, the DMC has acknowledged that the improvements in motor function with decreased oral dopaminergic therapy observed to date are encouraging and clinically relevant; which further supports our preparations to progress to randomised studies. We look forward to the full cohort 4 three-month results and the six-month primary end-point assessment later this year and are confident that ProSavin® will continue to demonstrate its potential to transform the prospects for Parkinson’s disease patients worldwide.”
The on-going Phase I/II study is designed to assess the safety, efficacy and dose evaluation of ProSavin® in patients with mid-stage PD who are experiencing reduced benefit on L-DOPA “equivalent” therapy. The trial is being conducted at the Henri Mondor Hospital in Paris with Professor Stéphane Palfi as Principal Investigator and Coordinating Investigator, and at Addenbrookes Hospital in Cambridge, UK, with Professor Roger Barker as Principal Investigator.
The primary efficacy end-point of the Phase I/II trial is the six-month UPDRS assessment, results from which are expected to be announced in Q4 2011 following a review of all four cohorts by the study’s independent Data Monitoring Committee (DMC). Planning is well underway for a sham-controlled Phase II study and, subject to the DMC opinion, Oxford BioMedica expects to submit regulatory applications to the EU and US agencies by the end of the year.
2. Cohorts 3 and 4 had more severe mean baseline UPDRS scores than previous cohorts.
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.
For further information please contact
Oxford BioMedica plc
John Dawson, Chief Executive Officer
Stuart Paynter, Chief Financial Officer
Tel: +44 (0)1865 783 000
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