POZEN Reports Third Quarter 2006 Results.CHAPEL HILL, N.C. -- POZEN Inc. (NASDAQ NASDAQ in full National Association of Securities Dealers Automated Quotations U.S. market for over-the-counter securities. Established in 1971 by the National Association of Securities Dealers (NASD), NASDAQ is an automated quotation system that reports on : POZN), today announced results for the third quarter ended September 30, 2006. Third-Quarter Results POZEN reported a net loss of $4.1 million, or $0.14 per share on a diluted basis, for the third quarter of 2006, compared to a net loss of $4.7 million, or $0.16 per share on a diluted basis, for the third quarter of 2005. For the third quarter of 2006, POZEN reported revenue of $3.4 million as compared to $2.4 million for the third quarter ended September 30, 2005. The increase was primarily due to revenue recognized pursuant to the global collaboration agreement with AstraZeneca. Operating expenses Operating expenses The amount paid for asset maintenance or the cost of doing business, excluding depreciation. Earnings are distributed after operating expenses are deducted. for the third quarter of 2006 totaled $7.9 million as compared to $7.4 million for the same period in 2005. The increase in operating expenses was primarily due to a $1.5 million non-cash stock-based compensation expense as a result of adopting Statement of Financial Accounting Standards 123(R) on January 1, 2006 and an increase in costs associated with the PN program, partially offset by a decrease in costs for the Trexima[TM] program. At September 30, 2006, cash, cash equivalents and short-term investments totaled $66.6 million compared to $45.8 million at December 31, 2005. The increase in cash and cash equivalents resulted from the receipt of a $40 million upfront payment from AstraZeneca in connection with the exclusive global collaboration agreement between the two companies. Nine-Month Results POZEN reported a net loss of $18.9 million, or $0.65 per share on a diluted basis, for the nine-month period ended September 30, 2006, compared with a net loss of $14.2 million, or $0.49 per share on a diluted basis, for the same period in 2005. For the nine months ended September 30, 2006, POZEN reported revenue of $6.5 million compared to $6.4 million for the same period in 2005. Revenue for the 2006 period includes amortization of upfront payments and revenues earned pursuant to our collaboration agreements with AstraZeneca and GlaxoSmithKline. Operating expenses for the nine months ended September 30, 2006 were $26.8 million as compared to $21.4 million for the comparable period in 2005. The increase in operating expenses was primarily due to a $4.7 million non-cash stock-based compensation expense as a result of adopting Statement of Financial Accounting Standards 123(R) on January 1, 2006 and an increase in costs associated with our PN program, partially offset by a decrease in costs for the Trexima program. Corporate Highlights On August 1, 2006, POZEN and AstraZeneca signed a global collaboration agreement for the co-development and commercialization of proprietary fixed dose combinations A fixed dose combination (FDC) is a formulation of two or more active ingredients combined in a single dosage form available in certain fixed doses. Fixed dose combination drug products may improve medication compliance by reducing the pill burden of patients. of the proton pump inhibitor proton pump inhibitor n. A class of drugs that inhibit gastric acid secretion by interfering with the movement of hydrogen ions across cell membranes and are used mainly to treat peptic ulcers, gastroesophageal reflux disease, and esophagitis. esomeprazole magnesium es·o·mep·ra·zole magnesium n. A drug of the proton pump inhibitor class. esomeprazole magnesium Nexium Pharmacologic class: Proton pump inhibitor Therapeutic class: , with the non-steroidal anti-inflammatory drug Non-steroidal anti-inflammatory drugs, usually abbreviated to NSAIDs, are drugs with analgesic, antipyretic and anti-inflammatory effects - they reduce pain, fever and inflammation. naproxen naproxen and naproxen sodium, potent nonsteroidal anti-inflammatory drugs (NSAID) used to alleviate the minor pain of arthritis, menstruation, headaches, and the like, and to reduce fever. in a single tablet. The products will be indicated for the management of pain and inflammation associated with conditions such as osteoarthritis osteoarthritis or osteoarthrosis or degenerative joint disease Most common joint disorder, afflicting over 80% of those who reach age 70. It does not involve excessive inflammation and may have no symptoms, especially at first. and rheumatoid arthritis rheumatoid arthritis Chronic, progressive autoimmune disease causing connective-tissue inflammation, mostly in synovial joints. It can occur at any age, is more common in women, and has an unpredictable course. in patients who are at risk for developing NSAID-associated gastric ulcers gastric ulcer n. An ulcer in the mucous membrane of the stomach. gastric ulcer A hole in gastric mucosa due to gastric secretions, related to H pylori in the mucosa, NSAIDs, cigarette smoking etc; the pain of a GU may . On September 21, 2006, POZEN announced the receipt of the $40 million upfront payment from AstraZeneca. POZEN will receive potential aggregate payments of $160 million for certain development and regulatory milestones; and $175 million of potential sales performance milestones, if certain thresholds are achieved. Royalties will be paid on net sales Net Sales The amount a seller receives from the buyer after costs associated with the sale are deducted. Notes: This amount is calculated by subtracting the following items from gross sales: merchandise returned for credit, allowances for damaged or missing goods, freight . POZEN plans to submit the full response to the approvable letter for Trexima[TM] to the U.S. Food and Drug Administration (FDA FDA abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. ) in November. Subsequent to the submission of the New Drug Application in August 2005, the number of patients treated with Trexima in clinical trials has more than doubled and this data will be incorporated into the full response. The FDA will have up to six months to review the information contained in the full response. Financial Guidance For the fourth quarter of 2006, POZEN expects total revenue to be in the range of $7 to $8 million, including revenue of $3 to $4 million for work performed under the AstraZeneca agreement. Total operating expenses are expected to be in the range of $8.2 to $9.2 million, including $1.5 million of non-cash stock-based compensation expense. For the 2006 year, POZEN expects total revenue to be in the range of $13.5 to $14.5 million, including revenue of $4.7 to $5.7 million for work performed under the AstraZeneca agreement. Total operating expenses for the 2006 year are expected to be in the range of $35 to $36 million. Operating expenses include $6.3 million of estimated non-cash stock-based compensation expense. Third-Quarter Results Webcast POZEN will hold a webcast to present third quarter results and management's outlook on Tuesday, October 31, 2006 at 11:00 a.m. Eastern time. The webcast can be accessed live and will be available for replay at www.pozen.com . About POZEN POZEN is a pharmaceutical company committed to developing therapeutic advancements for diseases with unmet medical needs where it can improve efficacy, safety, and/or patient convenience. POZEN's efforts are focused primarily on the development of pharmaceutical products for the treatment of acute and chronic pain and other pain-related conditions. POZEN has development and commercialization alliances with GlaxoSmithKline for the proposed product candidate Trexima[TM] combining sumatriptan sumatriptan /su·ma·trip·tan/ (soo?mah-trip´tan) a selective serotonin receptor agonist used as the succinate salt in the acute treatment of migraine and cluster headaches. su·ma·trip·tan n. , formulated with RT technology, and naproxen sodium naproxen sodium Aflaxen, Aleve, Anaprox, Anaprox DS, Apo-Napro-Na (CA), Apo-Napro-Na DS (CA), Arthroxen (UK), Napratec (UK), Naprelan, Novo-Naprox Sodium (CA), Novo-Naprox Sodium DS (CA), Synflex (CA), Synflex (UK) Pharmacologic class: in a single tablet for the acute treatment of migraine, which is currently under review by the United States Food and Drug Administration United States Food and Drug Administration (FDA), n.pr a unit of the Public Health Service created to protect the health of the nation against impure and unsafe foods, drugs, and cosmetics. , and with AstraZeneca for proprietary fixed dose combinations of the proton pump inhibitor esomeprazole magnesium with naproxen in a single tablet for conditions such as osteoarthritis and rheumatoid arthritis in patients who are at risk for developing NSAID-associated gastric ulcers. The company's common stock is traded on The Nasdaq Stock Market Nasdaq stock market The first electronic stock market listing over 5000 companies. The Nasdaq stock market comprises two separate markets, namely the Nasdaq National Market, which trades large, active securities and the Nasdaq Smallcap Market that trades emerging growth companies. under the symbol "POZN". For detailed company information, including copies of this and other press releases, see POZEN's website: www.pozen.com . Statements included in this press release that are not historical in nature are "forward-looking statements forward-looking statement A projected financial statement based on management expectations. A forward-looking statement involves risks with regard to the accuracy of assumptions underlying the projections. " within the meaning of the "safe harbor Safe Harbor 1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated. 2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive. " provisions of the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and of 1995. You should be aware that our actual results could differ materially from those contained in the forward-looking statements, which are based on management's current expectations and are subject to a number of risks and uncertainties, including, but not limited to, our failure to successfully commercialize our product candidates; costs and delays in the development and/or FDA approval of our product candidates, including as a result of the need to conduct additional studies, or the failure to obtain such approval of our product candidates, including as a result of changes in regulatory standards or the regulatory environment during the development period of any of our product candidates; uncertainties in clinical trial results or the timing of such trials, resulting in, among other things, an extension in the period over which we recognize deferred revenue or our failure to achieve milestones that would have provided us with revenue; our inability to maintain or enter into, and the risks resulting from our dependence upon, collaboration or contractual arrangements necessary for the development, manufacture, commercialization, marketing, sales and distribution of any products; competitive factors; our inability to protect our patents or proprietary rights and obtain necessary rights to third party patents and intellectual property to operate our business; our inability to operate our business without infringing the patents and proprietary rights of others; general economic conditions; the failure of any products to gain market acceptance; our inability to obtain any additional required financing; technological changes; government regulation; changes in industry practice; and one-time events, including those discussed herein and in our Quarterly Report on Form 10-Q Form 10-Q See 10-Q. for the period ended June 30, 2006. We do not intend to update any of these factors or to publicly announce the results of any revisions to these forward-looking statements. Financial Tables to FollowC* [TABLE OMITTED] [TABLE OMITTED] |
|
||||||||||||||

Printer friendly
Cite/link
Email
Feedback
Reader Opinion