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Xenova Group plc:
Addiction Treatment Vaccines
Xenova Buyout of Residual ImmuLogic Interests
Slough, UK, January 15, 2003 –
Xenova Group plc (NASDAQ NM: XNVA; London Stock Exchange: XEN) today
announces that it has reached an agreement with ImmuLogic
Pharmaceutical Corporation Liquidating Trust (“ImmuLogic”) under
which Xenova will buy out all remaining ImmuLogic rights to future
milestone and royalty payments relating to two of Xenova’s
development stage vaccine programmes, TA-CD and TA-NIC.
Under the terms of the agreement announced today, ImmuLogic will
receive US$1m from Xenova in return for ImmuLogic’s rights to all
future payments relating to the two vaccine programmes. Mutual
releases from claims, proceedings and any other liabilities were
also exchanged.
Under a 1998 Purchase Agreement, Cantab Pharmaceuticals plc
(which merged with Xenova in 2001) undertook to pay ImmuLogic
certain milestone payments relating to the TA-CD and TA-NIC
programmes, payable at the end of each clinical development phase
and valued at up to $11m, plus royalties.
ImmuLogic began voluntary liquidation proceedings in August 1999
and is now expected to complete its liquidation following a final
cash distribution to its former shareholders.
In order to fund the buyout of ImmuLogic’s interests, Xenova has
raised £680,000 before expenses through the placing for cash of
1,766,235 new ordinary shares of 10 pence each. The new shares,
which represent approximately 1.02 per cent of the Company’s issued
share capital prior to the placing, have been placed by Nomura
International plc at a price of 38.5 pence per share. The placing
represents a discount of approximately 9.9 per cent to the closing
middle market price on the London Stock Exchange on 14 January 2003.
Application will be made today for the 1,766,235 new shares to be
admitted to the Official List and to trading on the London Stock
Exchange, with admission expected to become effective on 20 January
2003. When issued, the new shares will rank pari passu in all
respects with the Company’s existing ordinary shares.
Commenting on today’s news, David Oxlade, Chief Executive of
Xenova, said:
“We are delighted with this agreement, which releases Xenova from
large potential payment obligations and consequently increases our
commercial flexibility in relation to both TA-CD and TA-NIC. Both
programmes have a large commercial potential and are designed to
assist the significant number of people worldwide who find it
difficult to overcome their addiction.”
-ends-
CONTACTS
UK:
Xenova Group plc
Tel: +44 (0)1753 706600
David A Oxlade, Chief Executive Officer
Daniel Abrams, Group Finance Director
Hilary Reid Evans, Corporate Communications
Financial Dynamics
Tel: +44 (0)207 831 3113
David Yates/Ben Atwell
US:
Trout Group/BMC Communications
Tel: 001 212 477 9007
Press: Brad Miles (Ext 17) Lauren Tortorete (Ext 20)
Investors: Jonathan Fassberg (Ext 16) Lee Stern (Ext 22)
Notes to Editors
Xenova Group plc's product pipeline focuses principally on the
therapeutic areas of cancer and immune system disorders. Xenova has
a broad pipeline of programmes in clinical development. The Group
has a well-established track record in the identification,
development and partnering of innovative products and technologies
and has partnerships with significant pharmaceutical companies
including Lilly, Pfizer, Celltech, Genentech, QLT and Millennium
Pharmaceuticals.
For
Xenova: Disclaimer to take advantage of the "Safe Harbor" provisions
of the US Private Securities Litigation Reform Act of 1995. This
press release contains "forward-looking statements," including
statements about the discovery, development and commercialisation of
products. Various risks may cause Xenova's actual results to differ
materially from those expressed or implied by the forward looking
statements, including: adverse results in our drug discovery and
clinical development programs; failure to obtain patent protection
for our discoveries; commercial limitations imposed by patents owned
or controlled by third parties; our dependence upon strategic
alliance partners to develop and commercialise products and
services; difficulties or delays in obtaining regulatory approvals
to market products and services resulting from our development
efforts; the requirement for substantial funding to conduct research
and development and to expand commercialisation activities; and
product initiatives by competitors. For a further list and
description of the risks and uncertainties we face, see the reports
we have filed with the Securities and Exchange Commission. We
disclaim any intention or obligation to update or revise any
forward-looking statements, whether as a result of new information,
future events or otherwise.
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