Antisoma strategy update - joint statement from the Chairman and CEO
LONDON, UK -- (MARKET WIRE) -- April 19, 2007 --
Future opportunities
Today's AS1404 licensing deal with Novartis is a great achievement.
It is also an important step along the way to making Antisoma a
significant and self-sustaining bio-pharmaceutical company. Our
recent successes have provided us with an unprecedented opportunity
to take our business forward. This will involve further expansion and
diversification of our product pipeline. It will also entail a
transition towards a business with a substantial role in
commercialising its own products.
Expanding and diversifying the pipeline
The Board believes that the Company's risk-reward profile could be
significantly enhanced by further expansion of its pipeline. To this
end, the Board plans an active programme of in-licensing and to
examine opportunities to acquire other oncology companies.
Building a sales and marketing operation
An attractive feature of the deal announced today is the opportunity
for Antisoma to participate in selling its own products in the USA.
Should AS1404 reach the market, the agreement includes the potential
for Novartis to fund certain of Antisoma's commercialisation costs.
This could make it easier for Antisoma to bring other products to
market, allowing the Company to retain more of their value. The Board
intends to continue to develop AS1411 independently with this
possibility in mind. It will also consider potential sales synergies
when seeking new assets for the pipeline.
Maximising the support of capital markets
Antisoma appreciates the strong support it has received from its
investors through its listing on the London Stock Exchange. As stated
previously, the Board also sees attractions in taking an additional
listing in the United States. This would broaden the capital base
supporting the Company's development. Many of the products Antisoma
would like to acquire are owned by US companies. Dollar-denominated
stock would be a valuable currency for licensing and acquisitions.
The Board will continue to evaluate the potential for a US listing
and when this would best be timed.
Dialogue with shareholders
Antisoma's Board intends to discuss the above plans with
shareholders. Resolutions supporting the plans will be put to an EGM.
They will include a renewal of the Company's authority to issue new
shares up to around a third of the issued number. This will provide
the Board with flexibility to conclude small and medium-sized
acquisitions for equity. Any larger M&A opportunities would be
subject to shareholder approval in a further EGM.
The Board is also minded to seek a renewal of its authority to issue
shares for cash in a non-pre-emptive issue. This would provide
flexibility, for example to offer new shares as American Depositary
Receipts (ADRs) should the Board decide to list the Company in the
US. In assessing the need for any issue of new ADRs, the Board would
consider the demand for conversion of existing ordinary shares to
ADRs. The principal aim of any new issue would be to ensure that the
resulting total number of ADRs represented enough of the Company's
equity and traded with sufficient liquidity to make them a valuable
acquisition currency.
Positive outlook
The period ahead will be an exciting one. We have formed a great
partnership with Novartis to develop and commercialise AS1404.
Further important phase II data on AS1404 are expected this year.
Other drugs in our pipeline, notably AS1411, are showing real
promise. We are now very well equipped to acquire and develop new
products and to continue to grow the business.
Barry Price, Chairman
Glyn Edwards, CEO
Enquiries:
Glyn Edwards, CEO
Daniel Elger, Director of Communications +44 (0)20 8799 8200
Antisoma plc
Mark Court/Lisa Baderoon/Rebecca Skye Dietrich +44 (0)20 7466 5000
Buchanan Communications
Brian Korb
The Trout Group +1 646 378 2923
Except for the historical information presented, certain matters
discussed in this statement are forward looking statements that are
subject to a number of risks and uncertainties that could cause
actual results to differ materially from results, performance or
achievements expressed or implied by such statements. These risks and
uncertainties may be associated with product discovery and
development, including statements regarding the company's clinical
development programmes, the expected timing of clinical trials and
regulatory filings. Such statements are based on management's current
expectations, but actual results may differ materially.
Background on Antisoma
Based in London, UK, Antisoma is a biopharmaceutical company that
develops novel products for the treatment of cancer. Antisoma fills
its development pipeline by acquiring promising new product
candidates from internationally recognised academic or cancer
research institutions. Its core activity is the preclinical and
clinical development of these drug candidates. Please visit
www.antisoma.co.uk for further information about Antisoma.
Enquiries:
Glyn Edwards, CEO
Daniel Elger, Director of Communications +44 (0)20 8799 8200
Antisoma plc
Mark Court/Lisa Baderoon/Rebecca Skye Dietrich +44 (0)20 7466 5000
Buchanan Communications
Brian Korb
The Trout Group +1 646 378 2923
SOURCE: Antisoma