A.P. Pharma Reports 2006 First Quarter Results; Phase 3 Clinical Trial for APF530 Initiated.REDWOOD CITY Redwood City, city (1990 pop. 66,072), seat of San Mateo co., W Calif., on San Francisco Bay; inc. 1868. Manufactures include commmunications, electrical, electronic, and medical equipment. , Calif. -- A.P. Pharma, 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 :APPA), a specialty pharmaceutical company, today reported financial results for the three months ended March 31, 2006. Recent and Financial Highlights --Royalty interests sold for up to $30 million; $25 million cash received at closing. --APF530 Phase 3 clinical trial phase 3 clinical trial Phase 3 study. See Phase study. protocol finalized See finalization. following 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. input. --IRB approval received and initiation of sites begun. --Enrollment expected to be completed by year's end. --Study will enroll approximately 1,350 patients who are being treated with either highly or moderately emetogenic chemotherapy chemotherapy (kē'mōthĕr`əpē), treatment of disease with chemicals or drugs. One chemotherapeutic approach is the development of selectively toxic substances, i.e. . Financial Results During the quarter, the Company completed the sale of its interests in royalties on sales of Retin-A Micro(R) and Carac(R) effective October 1, 2005. The company received $25 million at the closing of the transaction and is entitled en·ti·tle tr.v. en·ti·tled, en·ti·tling, en·ti·tles 1. To give a name or title to. 2. To furnish with a right or claim to something: to receive an additional $5 million on the satisfaction of certain predetermined pre·de·ter·mine v. pre·de·ter·mined, pre·de·ter·min·ing, pre·de·ter·mines v.tr. 1. To determine, decide, or establish in advance: milestones. As a result of the sale, no royalty revenues were recorded for the first quarter of 2006 compared with $1,282,000 in royalty revenues for the first quarter of the prior year. Research and development expense was $3,469,000 for the first quarter of 2006, an increase of 90% compared with $1,822,000 in the prior year first quarter. Higher research and development expense in the 2006 quarter reflects preparations for the Phase 3 clinical trial for APF APF, n the abbreviation for acidulated phosphate fluoride. 530 which has recently been initiated, as announced on April 27, 2006. General and administrative expense was $932,000 for the first quarter of 2006, an increase of 10% compared with $849,000 in the prior year first quarter, due primarily to increased legal and consulting fees. The Company recorded a gain on the sale of its interests in royalties from sales of Retin-A Micro and Carac of $23,421,000 in the first quarter of 2006. Income from continuing operations continuing operations Parts of a business that are expected to be maintained as an ongoing segment of an overall business operation. Income and losses from continuing operations are reported separately if any segments have been discontinued during the was $19,292,000 for the first quarter of 2006, compared with a loss from continuing operations of $1,250,000 in the prior year quarter. Net income for the first quarter of 2006 was $19,299,000, or $0.76 per fully diluted di·lute tr.v. di·lut·ed, di·lut·ing, di·lutes 1. To make thinner or less concentrated by adding a liquid such as water. 2. To lessen the force, strength, purity, or brilliance of, especially by admixture. share, compared with a net loss for the first quarter of 2005 of $1,256,000, or $0.05 per share. Cash, cash equivalents and marketable securities Marketable Securities Very liquid securities that can be converted into cash quickly at a reasonable price. Notes: Marketable securities are very liquid as they tend to have maturities less than one year, and the rate at which these securities can be bought or sold has totaled $26,172,000 as of March 31, 2006. Clinical Update As reported on April 27, 2006, the Company initiated a Phase 3 clinical trial using APF530, its product candidate for the prevention of chemotherapy-induced nausea and vomiting Nausea and Vomiting Definition Nausea is the sensation of being about to vomit. Vomiting, or emesis, is the expelling of undigested food through the mouth. (CINV CINV Chemotherapy Induced Nausea and Vomiting ) in patients undergoing either moderately or highly emetogenic chemotherapy. APF530 contains the 5HT(3) antagonist antagonist /an·tag·o·nist/ (an-tag´o-nist) 1. a substance that tends to nullify the action of another, as a drug that binds to a cell receptor without eliciting a biological response, blocking binding of substances that could anti-nausea drug granisetron formulated for·mu·late tr.v. for·mu·lat·ed, for·mu·lat·ing, for·mu·lates 1. a. To state as or reduce to a formula. b. To express in systematic terms or concepts. c. with the Company's proprietary Biochronomer(TM) drug delivery system. The APF530 Phase 3 pivotal trial protocol includes a total of approximately 1,350 patients with approximately half receiving moderately emetogenic chemotherapy agents in one group and approximately half receiving highly emetogenic chemotherapeutic agents This is a list of specific pharmacologic agents that are known to be of use in the treatment of cancer, otherwise known as chemotherapeutic agents. This list is organized by "type" of agent, though the subsections are not necessarily definitive and are subject to revision. in another group. In each group there will initially be three arms of approximately 225 patients each; two arms will be treated with APF530, high and low dose form and a third arm will be treated with the currently approved dose of palonosetron (brand name ALOXI(R)). The study's primary endpoint is to establish the efficacy of APF530 for the prevention of acute onset (first 24 hours) and delayed onset (4-5 days) CINV in patients receiving either moderately or highly emetogenic chemotherapy. No other 5HT(3) antagonist is currently approved for the prevention of both acute and delayed CINV for both moderately and highly emetogenic chemotherapy. Conference Call As noted during the conference call on March 15, 2006 for year-end results, the Company will not hold a conference call to discuss first quarter 2006 results. The Company expects to hold conference calls in the future to provide updates on the progress of the APF530 Phase 3 clinical trial. About A.P. Pharma A.P. Pharma is a specialty pharmaceutical company focused on the development of ethical (prescription) pharmaceuticals utilizing its proprietary polymer-based drug delivery systems. The Company's primary focus is the development and commercialization of its bioerodible injectable in·ject·a·ble adj. Capable of being injected. Used of a drug. n. A drug or medicine that can be injected. and implantable systems under the trade name Biochronomer. Initial target areas of application for the Company's drug delivery technology include anti-nausea, pain management, anti-inflammation and DNA/RNAI applications. For further information visit the Company's web site at www.appharma.com. 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. Except for historical information, this news release contains certain forward-looking statements that involve risks and uncertainties including, among others, uncertainty associated with timely development, approval, launch and acceptance of new products, satisfactory completion of clinical studies, establishment of new corporate alliances and progress in research and development programs. Other risks and uncertainties associated with the Company's business and prospects are identified in the Company's filings with the Securities and Exchange Commission. The Company does not undertake to revise these forward-looking statements to reflect events or circumstances CIRCUMSTANCES, evidence. The particulars which accompany a fact. 2. The facts proved are either possible or impossible, ordinary and probable, or extraordinary and improbable, recent or ancient; they may have happened near us, or afar off; they are public or occurring in the future.
A.P. PHARMA, INC.
Income Statement Highlights
(in thousands, except per share data)
(Unaudited)
Three Months Ended
March 31, March 31,
2006 2005
Royalties $ 0 $ 1,282
Contract Revenues 0 78
Total Revenues 0 1,360
Operating Expenses:
Research & Development 3,469 1,822
General & Administrative 932 849
Total Operating Expenses 4,401 2,671
Operating Loss (4,401) (1,311)
Interest Income, Net 262 72
Gain on Sale of Interest in Royalties 23,421 0
Other Income (Expense) 10 (11)
Income (Loss) from Continuing
Operations 19,292 (1,250)
Loss from Discontinued Operations 0 (18)
Gain on Disposition of Discontinued
Operations 7 12
Net Income (Loss) $ 19,299 $ (1,256)
Basic Earnings (Loss) Per Share:
Income (Loss) from Continuing
Operations $ 0.77 $ (0.05)
Net Income (Loss) $ 0.77 $ (0.05)
Diluted Earnings (Loss) Per Share:
Income (Loss) from Continuing
Operations $ 0.76 $ (0.05)
Net Income (Loss) $ 0.76 $ (0.05)
Shares used in Calculating Earnings
(Loss)
Per Share:
Basic 25,207 25,046
Diluted 25,483 25,046
A.P. PHARMA, INC.
Balance Sheet Highlights
(in thousands)
March 31, December 31,
2006 2005(1)
(Unaudited)
Assets
Cash, Cash Equivalents and Marketable
Securities $ 26,172 $ 5,809
Accounts Receivable, Net 75 1,519
Other Current Assets 365 320
Total Current Assets 26,612 7,648
Property and Equipment, Net 1,095 1,164
Other Non-Current Assets 139 157
Total Assets $ 27,846 $ 8,969
Liabilities and Stockholders' Equity
Current Liabilities $ 2,218 $ 2,766
Stockholders' Equity 25,628 6,203
Total Liabilities and Stockholders'
Equity $ 27,846 $ 8,969
(1) Derived from our audited financial statements for the year ended
December 31, 2005 included in the Company's 2005 Annual Report on
Form 10-K filed with the Securities and Exchange Commission.
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