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OXFORD BIOMEDICA AND SANOFI-AVENTIS ENTER GLOBAL
LICENSING AGREEMENT TO DEVELOP AND COMMERCIALISE TROVAX FOR CANCER
Oxford, UK – 28 March 2007: Oxford BioMedica (LSE: OXB) and sanofi-aventis (EURONEXT:
SAN; NYSE: SNY) announced today that they have entered into an exclusive global
licensing agreement to develop and commercialise TroVax® for the treatment and
prevention of cancers.
TroVax® is Oxford BioMedica’s lead cancer immunotherapy. It has been
evaluated in clinical trials involving more than 180 patients with various forms
of cancer. A Phase III trial in renal cancer is ongoing.
Under the terms of this agreement:
Sanofi-aventis will pay Oxford BioMedica up to €518 million (~US$690 million) if
all development and registration targets are met for certain defined
indications. Additional payments will be made if regulatory milestones are
achieved in other cancer types.
Oxford BioMedica will receive an initial payment of €29 million (~US$39 million)
and further near-term payments of €19 million (~US$25 million) as milestones
linked to the ongoing Phase III TRIST study in renal cancer.
Oxford BioMedica is also entitled to escalating royalties on global sales of
TroVax® and to further undisclosed commercial milestones when net sales of
TroVax® reach certain levels.
Oxford BioMedica has an option to develop TroVax® for other cancer types in
exchange for enhanced financial returns, and sanofi-aventis will keep all
commercial rights.
Oxford BioMedica will supply TroVax® to sanofi-aventis on commercial terms.
Oxford BioMedica and sanofi-aventis will co-fund the ongoing Phase III TRIST
study of TroVax® in renal cancer.
Sanofi-aventis will fund all future research, development, regulatory and
commercialisation activities, including the immediate implementation of a
development plan for TroVax® in metastatic colorectal cancer.
Sanofi-aventis will be responsible for the global commercialisation of TroVax®
and will book the sales worldwide. Oxford BioMedica retains an option to
participate in the promotion of TroVax® in the United States and the European
Union.
TroVax® may be developed by sanofi-aventis as a treatment for any cancer
type. Based on the broad distribution of the 5T4 tumour antigen, TroVax® has
potential application in a wide range of solid tumours, including renal,
colorectal, lung, breast and prostate cancer.
Professor Alan Kingsman, Chief Executive of Oxford BioMedica, commented: “We
are delighted to have sanofi-aventis as our partner for TroVax® given their
broad expertise, experience and resources in oncology and their long standing
world-class research and development capabilities in cancer immunology. We look
forward to working with our new partner to advance the development and
commercialisation of TroVax® and, importantly, to provide cancer patients with
new treatment options.”
Analyst meeting:
An analyst briefing will be held at 11.45 am today at the offices of
Buchanan Communications, 45 Moorfields, London EC2Y 9AE.
Web cast:
Simultaneously to the analyst briefing at 11.45 am, there will be a live audio
web cast of the presentation. To connect to the web cast facility, please go to
the Company’s website:
http://www.oxfordbiomedica.co.uk/ approximately 10 minutes (11.35 am)
before the start of the briefing. This will also be available for replay shortly
after the presentation.
-Ends-
For further information, please contact:
Oxford BioMedica plc:
Professor Alan Kingsman, Chief Executive
Tel: +44 (0)1865 783 000
Rothschild
Dr Lynn Drummond
Tel: +44 (0)20 7280 5000
City/Financial Enquiries:
Lisa Baderoon/ Mark Court/ Mary-Jane Johnson
Buchanan Communications
Tel: +44 (0)20 7466 5000
Scientific/Trade Press Enquiries:
Gemma Price/ Holly Griffiths/ Katja Stout
Northbank Communications
Tel: +44 (0)20 7268 3002
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 oncology and
neurotherapy. The Company was established in 1995 as a spin out from Oxford
University, and is listed on the London Stock Exchange.
Oxford BioMedica has core expertise in gene delivery, as well as in-house
clinical, regulatory and manufacturing know-how. In oncology, the pipeline
includes two clinical candidates and a preclinical targeted antibody therapy,
which is being developed in collaboration with Wyeth. The Company has started
Phase III development of its lead cancer immunotherapy product, TroVax, in renal
cancer and has an ongoing Phase II programme in various cancer settings
including renal, colorectal and prostate cancer. In neurotherapy, the Company’s
lead product, ProSavin, is expected to enter clinical trials in Parkinson’s
disease in 2007. The preclinical pipeline includes gene-based products for
vision loss, motor neuron disease and nerve repair.
The Company is underpinned by over 80 patent families, which represent one of
the broadest patent estates in the field. The Company has a staff of 72 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, Sigma-Aldrich, Viragen, MolMed and VIRxSYS; and has
licensed technology to a number of companies including Merck & Co, Biogen Idec,
GlaxoSmithKline and Pfizer.
Further information is available at
www.oxfordbiomedica.co.uk
2. Sanofi-aventis
Sanofi-aventis is one of the world leaders in the pharmaceutical industry,
ranking number one in Europe. Backed by a world-class R&D organisation,
sanofi-aventis is developing leading positions in seven major therapeutic areas:
cardiovascular, thrombosis, oncology, metabolic diseases, central nervous
system, internal medicine and vaccines. Sanofi-aventis is listed in Paris (EURONEXT:
SAN) and in New York (NYSE: SNY).
3. TroVax®
TroVax is Oxford BioMedica’s leading cancer immunotherapy product. It is
designed specifically to stimulate an anti-cancer immune response and has
potential application in most solid tumour types. TroVax targets the tumour
antigen 5T4, which is broadly distributed throughout a wide range of solid
tumours. The presence of 5T4 is correlated with poor prognosis. The product
consists of a poxvirus (MVA) gene transfer system, which delivers the gene for
5T4 and stimulates a patient’s body to produce an anti-5T4 immune response. This
immune response destroys tumour cells carrying the 5T4.
Over 180 patients have been treated with TroVax in clinical trials in renal,
colorectal and prostate cancer. TroVax has been safe and well tolerated in all
trials to date. There have been no serious adverse events related to the
product. The clinical data show that over 95% of patients treated with TroVax
mount an anti-tumour immune response to the 5T4 tumour antigen, and, in a number
of clinical studies, there is a strong correlation between the level of the
immune response elicited by TroVax and the clinical benefit to patients. In
2006, Oxford BioMedica started a Phase III trial of TroVax in renal cancer. The
product has attracted support from Cancer Research UK, the US National Cancer
Institute, and the UK clinical trials network, QUASAR. These organisations are
conducting or plan to conduct clinical trials with TroVax.
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