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Share Name | Share Symbol | Market | Type |
---|---|---|---|
SEB SA | AQEU:SKP | Aquis Europe | Ordinary Share |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.90 | 1.05% | 87.00 | 86.20 | 86.90 | 87.35 | 85.40 | 86.30 | 14,261 | 16:50:22 |
RNS Number:6169L Skyepharma PLC 28 May 2003 For Immediate Release 28 May 2003 ANNUAL GENERAL MEETING STATEMENT LONDON, England, May 28, 2003 -- The Annual General Meeting of SkyePharma Plc (LSE: SKP; Nasdaq: SKYE) was held in London today. All resolutions were passed. Executive Chairman, Ian Gowrie-Smith made the following comments to shareholders: "2002 was SkyePharma's first full year of profitable trading, based on a strong growth in revenues, up by 50%. Over the last five years our revenues have increased at a compound annual growth rate of over 40% - and this year we expect another 40% increase. A year ago, our partner GlaxoSmithKline launched Paxil(R) CR in the USA. Paxil(R) CR now accounts for over one-third of new Paxil(R) prescriptions and nearly 27% of total prescriptions (new and repeat). Successful as Paxil(R) CR is proving to be, I would like to stress the growing strength and breadth of SkyePharma's product portfolio. There are now eight products on the market, validating three of our five delivery technology platforms. We also have a well-filled R&D pipeline. Last year we made significant progress with some of our key projects. In December our partner Novartis filed for approval in both the USA and Europe for a dry powder inhaler formulation of the asthma drug Foradil(R). We expect this product to reach the market in 2004. DepoMorphineTM, a long-acting injectable analgesic for pain relief after surgery, is the most important product we have in development and has the potential to revolutionise pain management after surgery. We have conducted the clinical development of this product. We expect to submit DepoMorphineTM for FDA approval in June, and in Europe in September. On normal review timelines, we anticipate market approvals next year. Propofol IDD-DTM is an improved formulation of the widely-used sedative/anaesthetic propofol. As for DepoMorphineTM, we have taken on the clinical development ourselves. Propofol IDD-DTM has now completed Phase II trials and is expected to enter Phase III clinical trials in the second half of 2003. At the end of last year, we licenced DepoMorphineTM and Propofol IDD-DTM to Endo Pharmaceuticals for North America. The terms validate the high potential we see for these products and justify our decision to undertake development ourselves instead of outlicencing the products at an earlier stage. We expect to appoint European and Japanese licensees for these products later this year. We will be disclosing the first clinical details on DepoMorphineTM and Propofol IDD-DTM at our R&D Day for analysts in the middle of June. In the 2002 Annual Report we provided for the first time guidance on the outlook for the current year and I am happy to reiterate that we expect to report revenues for 2003 in the region of #100 million, up by 40%. Milestone payments are still the major component of our revenues, although part of these relate to prior year agreements. However in 2003, as in past years, most of our revenues are likely to come in the latter part of the year and therefore we may report a loss for the first half. As our pipeline of new products comes to the market, we expect more predictable and regular royalty income and profit sharing progressively to replace milestone payments as our primary source of revenues. By 2005 analysts expect royalties to represent about half of our revenues, against 10% last year." SkyePharma PLC develops pharmaceutical products benefiting from world-leading drug delivery technologies that provide easier-to-use and more effective drug formulations. There are now nine approved products incorporating three of SkyePharma's five delivery technologies in the areas of oral, injectable, inhaled and topical delivery, supported by advanced solubilisation capabilities. SkyePharma has two FDA- and EMEA-approved manufacturing plants in San Diego, USA, and Lyon, France. For more information, visit www.skyepharma.com For further information please contact: SkyePharma Plc + 44 (0) 20 7491 1777 Michael Ashton, Chief Executive Officer Peter Laing, Director of Corporate Communications US Investor Relations + 1 (212) 753-5780 Sandra Haughton Buchanan Communications +44 (0) 20 7466 5000 Tim Anderson / Nicola How This information is provided by RNS The company news service from the London Stock Exchange END AGMZGGZKFRKGFZM
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