SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 10-Q Quarterly Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 For the quarter ended September 30, 2000 Commission file number 0-11550 Pharmos Corporation ------------------- (Exact name of registrant as specified in its charter) Nevada 36-3207413 ------ ---------- (State or other jurisdiction of (IRS Employer Id. No.) incorporation or organization) 99 Wood Avenue South, Suite 301 Iselin, NJ 08830 (Address of principal executive offices) Registrant's telephone number, including area code: (732) 452-9556 Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes X No . ----- ----- As of November 2, 2000, the Registrant had outstanding 53,879,343 shares of its $.03 par value Common Stock. Part I. Financial Information Item 1 Financial Statements Pharmos Corporation (Unaudited) Condensed Consolidated Balance Sheets - -------------------------------------------------------------------------------- September 30, December 31, 2000 1999 ------------- -------------- Assets Cash and cash equivalents ............................................................. $ 23,737,327 $ 2,918,554 Inventories ........................................................................... 1,114,423 1,837,751 Receivables ........................................................................... 1,254,237 961,769 Prepaid royalties ..................................................................... 104,974 284,193 Prepaid expenses and other current assets ............................................. 310,759 222,391 ------------- ------------- Total current assets ............................................................. 26,521,720 6,224,658 Fixed assets, net ..................................................................... 1,435,944 1,183,859 Prepaid royalties, net of current portion ............................................. 143,333 166,477 Restricted cash ....................................................................... 4,006,294 -- Other assets .......................................................................... 922,436 216,300 ------------- ------------- Total assets ..................................................................... $ 33,029,727 $ 7,791,294 ------------- ------------- Liabilities and Shareholders' Equity Note payable .......................................................................... $ -- $ 338,128 Accounts payable ...................................................................... 299,499 680,054 Accrued expenses ...................................................................... 871,988 711,189 Accrued wages and other compensation .................................................. 722,896 549,542 Advances against future sales ......................................................... 758,366 2,010,000 ------------- ------------- Total current liabilities ........................................................ 2,652,749 4,288,913 Advances against future sales, net of current portion ................................. 1,000,000 1,177,565 Convertible debentures, net ........................................................... 6,533,415 -- Other liabilities ..................................................................... 100,000 100,000 ------------- ------------- Total liabilities ................................................................ 10,286,164 5,566,478 ------------- ------------- Shareholders' equity Common stock, $.03 par value; 80,000,000 shares authorized, 53,879,343 and 45,424,401 shares issued and outstanding (excluding $551 in 2000 and 1999, held in Treasury) in 2000 and 1999, respectively .................................................... 1,616,016 1,362,181 Paid in capital ..................................................................... 107,913,889 83,372,742 Accumulated deficit ................................................................. (86,786,342) (82,510,107) ------------- ------------- Total shareholders' equity ....................................................... 22,743,563 2,224,816 ------------- ------------- Commitments and contingencies Total liabilities and shareholders' equity ....................................... $ 33,029,727 $ 7,791,294 ------------- ------------- The accompanying notes are an integral part of these condensed consolidated financial statements. 2 Pharmos Corporation (Unaudited) Condensed Consolidated Statements of Operations - -------------------------------------------------------------------------------- Three Months Ended September 30, 2000 1999 ------------ ------------ Revenues Product sales .......................................................... $ 1,661,735 $ 833,118 License fee ............................................................ 100,000 -- ------------ ------------ 1,761,735 833,118 Cost of Goods Sold ......................................................... 580,202 265,649 ------------ ------------ Gross Margin ........................................................... 1,181,533 567,469 ------------ ------------ Expenses Research and development, net .......................................... 1,362,475 839,390 Selling, general and administrative .................................... 999,987 599,174 Patents ................................................................ 46,536 61,781 Depreciation and amortization .......................................... 167,620 85,353 ------------ ------------ Total operating expenses ............................................ 2,576,618 1,585,698 ------------ ------------ Loss from operations ....................................................... (1,395,085) (1,018,229) ------------ ------------ Other income (expense): Interest income ........................................................ 314,905 34,378 Other income (expense), net ............................................ (9,192) 20,805 Interest expense ....................................................... (441,787) (9,239) ------------ ------------ Other income(expense), net ............................................. (136,074) 45,944 ------------ ------------ Net loss ................................................................... (1,531,159) (972,285) ------------ ------------ Less: Preferred stock dividends ........................................ -- (246) ------------ ------------ Net loss applicable to common shareholders ................................. ($ 1,531,159) ($ 972,531) ============ ============ Net loss per share applicable to common stockholders - basic and diluted ............................. ($ .03) ($ .02) ============ ============ Weighted average shares outstanding ........................................ 52,986,170 43,664,398 ============ ============ The accompanying notes are an integral part of these condensed consolidated financial statements. 3 Pharmos Corporation (Unaudited) Condensed Consolidated Statements of Operations - -------------------------------------------------------------------------------- Nine Months Ended September 30, 2000 1999 ------------ ------------ Revenues Product sales ................................................................ $ 3,740,152 $ 2,024,329 License fee .................................................................. 100,000 -- ------------ ------------ 3,840,152 2,024,329 Cost of Goods Sold ............................................................... 1,337,893 564,444 ------------ ------------ Gross Margin ................................................................. 2,502,259 1,459,885 ------------ ------------ Expenses Research and development, net ................................................ 3,733,144 2,591,722 Selling, general and administrative .......................................... 2,838,476 1,844,477 Patents ...................................................................... 128,433 153,174 Depreciation and amortization ................................................ 376,838 253,464 ------------ ------------ Total operating expenses .................................................. 7,076,891 4,842,837 ------------ ------------ Loss from operations ............................................................. (4,574,632) (3,382,952) ------------ ------------ Other income (expense): Interest income .............................................................. 739,345 97,523 Other income (expense), net .................................................. (2,370) (1,881) Interest expense ............................................................. (438,578) (21,151) ------------ ------------ Other income, net ............................................................ 298,397 74,491 ------------ ------------ Net loss ......................................................................... (4,276,235) (3,308,461) Less: Dividend embedded in convertible preferred stock Preferred stock dividends .................................................... -- (22,253) ------------ ------------ Net loss applicable to common shareholders ....................................... ($ 4,276,235) ($ 3,330,714) ============ ============ Net loss per share applicable to common stockholders - basic and diluted ................................... ($ .08) ($ .08) ============ ============ Weighted average shares outstanding .............................................. 51,506,739 42,104,485 ============ ============ The accompanying notes are an integral part of these condensed consolidated financial statements. 4 Pharmos Corporation (Unaudited) Condensed Consolidated Statements of Cash Flows - -------------------------------------------------------------------------------- Nine Months Ended September 30, 2000 1999 ------------ ------------ Cash flows from operating activities Net loss ..................................................................... ($ 4,276,235) ($ 3,308,461) ------------ ------------ Adjustments to reconcile net loss to net cash flow used in operating activities Depreciation and amortization ........................................... 376,838 253,464 Changes in operating assets and liabilities Inventory ............................................................... 723,328 (352,539) Receivables ............................................................. (292,468) 114,597 Prepaid expenses and other current assets ............................... (88,368) (157,295) Advanced royalties ...................................................... 202,363 115,499 Other assets ............................................................ -- 2,203 Accounts payable ........................................................ (380,555) (237,626) Accrued expenses ........................................................ 160,799 (253,312) Accrued wages ........................................................... 173,354 51,910 ------------ ------------ Total adjustments ....................................................... 875,291 (463,099) ------------ ------------ Net cash flows used in operating activities .................................. (3,400,944) (3,771,560) ------------ ------------ Cash flows from investing activities Purchases of fixed assets, net ............................................ (550,440) (189,351) ------------ ------------ Net cash flows used in investing activities .................................. (550,440) (189,351) ------------ ------------ Cash flows from financing activities Advances against future sales, net ........................................ (1,429,199) (741,915) Proceeds from issuances of common stock, exercise of warrants and value ascribed to the beneficial conversion feature, net .................................... 22,219,549 -- Proceeds from exercise of equity credit line .............................. 2,145,905 3,903,014 Increase in debt payable,net .............................................. (338,128) 438,781 Increase convertible debentures, net ...................................... 6,178,324 -- Increase in restricted cash ............................................... (4,006,294) -- ------------ ------------ Net cash flows provided by financing activities .............................. 24,770,157 3,599,880 ------------ ------------ Net increase (decrease) in cash and cash equivalents ........................... 20,818,773 (361,031) Cash and cash equivalents at beginning of year ................................. 2,918,554 3,452,916 ------------ ------------ Cash and cash equivalents at end of period ..................................... $ 23,737,327 $ 3,091,885 ============ ============ The accompanying notes are an integral part of these condensed consolidated financial statements. 5 Pharmos Corporation Notes to Condensed Consolidated Financial Statements Basis of Presentation The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with generally accepted accounting principles for interim financial information pursuant to the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by generally accepted accounting principles for complete financial statements. In the opinion of management, all adjustments, consisting of normal recurring accrual adjustments, considered necessary for a fair presentation have been included. Operating results for the three-month and nine-month periods ended September 30, 2000, are not necessarily indicative of the results that may be expected for the year ended December 31, 2000. 1. The Company Pharmos Corporation (the "Company") is a bio-pharmaceutical company that develops and commercializes products for the ophthalmic, central nervous system, neurological and other key healthcare markets. The Company has a diverse product pipeline that includes marketed products with superior therapeutic indices, and drug candidates with enhanced molecular structures that display improved safety and/or efficacy properties compared to the parent molecules or to competing products. The Company has executive offices in Iselin, New Jersey and also conducts operations through its wholly owned subsidiary, Pharmos, Ltd., in Rehovot, Israel. In March 1998, the Company received approval for three separate New Drug Applications ("NDA") from the U.S. Food and Drug Administration ("FDA"). These approvals were for Lotemax(R) and Alrex(R). Lotemax has been approved for the treatment of several ocular inflammatory indications, including uveitis, and for post-operative inflammation. Alrex has been approved for the treatment of seasonal allergic conjunctivitis. 2. Liquidity and Business Risks While the Company has generated revenue through the sale of its approved products in the market, it has incurred operating losses since its inception. At September 30, 2000, the Company has an accumulated deficit of $86,786,342. Such losses have resulted principally from costs incurred in research and development and from general and administrative expenses. The Company has funded its operations through the use of cash obtained principally from third party debt and equity financing. Management believes that cash and cash equivalents of $23.7 million as of September 30, 2000, combined with restricted cash and anticipated cash inflows from revenues derived from sales of Lotemax and Alrex, can support the Company's continuing operations. In order to finance the development of its drug pipeline, the Company is continuing to actively pursue various funding options, including strategic corporate alliances, equity offerings, business combinations, and the establishment of research and development partnerships. There can be no assurance that the Company will be successful in commercializing its new product candidates. 6 Pharmos Corporation Notes to Condensed Consolidated Financial Statements 3. Significant Accounting Policies Revenue recognition Sales revenue is recognized upon shipment of products to customers, less allowances for estimated returns and discounts. License fees and royalties are recognized when earned in accordance with the underlying agreements. Revenue for contracted research and development services is recognized as performed. Revenue from these contracts is recognized as costs are incurred (as defined in the contract), generally direct labor and supplies plus agreed overhead rates. Any advance payments on contracts are deferred until the related services are performed. All of the Company's revenues from product sales are principally derived from one customer. Inventories Inventories consist of loteprednol etabonate, the compound used in the Company's products, Lotemax and Alrex, and is stated at the lower of cost or market with cost determined on a weighted average basis. Reclassifications Certain amounts for 1999 have been reclassified to conform to the fiscal 2000 presentation. Such reclassifications did not have an impact on the Company's financial position or results of operations. 4. Collaborative Agreements In June 1995, the Company entered into a marketing agreement (the "Marketing Agreement") with Bausch & Lomb Pharmaceuticals, Inc. ("Bausch & Lomb") to market Lotemax and Alrex, on an exclusive basis in the United States following receipt of FDA approval. The Marketing Agreement also covers the Company's third loteprednol etabonate based product, LE-T. Under the Marketing Agreement, Bausch & Lomb purchases the active drug substance (loteprednol etabonate) from the Company. A second agreement, covering Europe, Canada and other selected countries, was signed in December 1996 ("the New Territories Agreement"). Through September 30, 2000, Bausch and Lomb has provided the Company with $5 million in cash advances against future sales, of which approximately $1.8 million was outstanding at September 30, 2000. An additional $1 million is due from Bausch & Lomb upon the receipt of regulatory approval for LE-T in the United States. Bausch & Lomb is entitled to recoup the advances by withholding certain amounts against payments for future purchases of the active drug substance, based on the advances made, until all the advances have been repaid. The Company may be obligated to repay such advances if it is unable to supply Bausch & Lomb with certain specified quantities of the active drug substance. The portion of advances expected to be recouped by Bausch and Lomb during the following twelve months, based on management's estimate of product sales to Bausch & Lomb, has been presented as a current liability in the accompanying balance sheet at September 30, 2000 and December 31, 1999. Bausch & Lomb also collaborates in the development of products by making available amounts up to 50% of the Phase III clinical trial costs. The Company has retained certain conditional co-marketing rights to all of the products covered by the Marketing Agreement and the New Territories Agreement. 5. Private Placement In September 2000, the Company completed a private placement of Convertible Debentures, common stock and warrants to purchase shares of common stock with institutional investors, generating gross proceeds of $11 million. The Convertible Debentures, which generated gross proceeds of $8 million, are due in February 2002 and carry a 6% interest payable in cash or common stock. The Convertible Debentures are convertible into common shares of the Company at the conversion price of $3.83 per share and are convertible beginning October 31, 2000. Under 7 Pharmos Corporation Notes to Condensed Consolidated Financial Statements certain anti-dilutive conditions, the conversion price may change. Until converted into common stock, the terms of the Convertible Debentures require the Company to deposit $4 million in an escrow account. The escrowed capital is shown as Restricted Cash on the Company's Balance Sheet and will be released to the Company in proportion to the amount of Convertible Debentures converted into common shares or upon the repayment of the debt. Current accounting standards, including Emerging Issues Task Force Issue No. 98-5, Accounting for Convertible Securities with Beneficial Conversion Features or Contingently Adjustable Conversion Ratios, require the company to compute the Beneficial Conversion Feature ("BCF") of the convertible debt. The BCF must be capitalized and amortized from the closing date until the earliest date that the investors have the right to convert the debt into common shares. The BCF was computed at approximately $1.1 million, $355,091 of which has been amortized and included as interest expense for the three and nine month periods ending September 30, 2000. Additionally, the discount on the Convertible Debenture will be amortized to interest expense over the life of the debt. This amount was computed at approximately $ .8 million, $44,494 of which has been amortized and included as interest expense for the three and nine month periods ending September 30, 2000. The Company issued 821,515 common shares in the private placement that generated gross proceeds of $3 million. Under the terms of the transaction, the number of shares is subject to a possible one-time adjustment which, if effected, would not change the proceeds to the Company. The investors have an option, in the form of a warrant, to purchase an additional $2 million of common shares for a period of one year provided that the future purchase price is greater than the initial closing price of $3.65 per share. The maximum number of shares that can be issued from this warrant is 547,945 and is part of the maximum number of warrants issued for the total private placement of 1,115,730, including placement agent warrants. Issuance costs related to the Convertible Debentures of approximately $.8 million, including the value of 187,929 warrants to purchase common shares at prices ranging from $4.34 to $4.56, have been capitalized. The issuance costs are included in the Company's Other Assets and will be amortized over the life of the debt. For the three and nine month periods ending September 30, 2000, $43,590 has been expensed. 6. Common and Preferred Stock Transactions During the third quarter of 2000, the Company issued warrants to purchase up to 1,115,730 shares of common stock at prices ranging from $3.65 to $6.08 per share and expiring in 2001 and 2005 in connection with the $11 million private placement described in Note 5. During the third quarter of 2000, the Company issued 374,525 shares of its common stock upon the exercise of stock options and warrants, and received consideration of $687,391. During the second quarter of 2000, the Company issued 55,750 shares of its common stock upon the exercise of stock options and warrants, and received consideration of $334,061. During the first quarter of 2000, the Company issued 4,500,000 shares of its common stock in various private equity sales, and received consideration, net of offering costs and expenses, of $12,648,383. During the first quarter of 2000, the Company issued 2,184,728 shares of its common stock upon the exercise of stock options and warrants, and received consideration of $4,035,855. The Company entered into a Private Equity Line of Credit Agreement (the "Credit Agreement") as of December 10, 1998, and as amended on December 18, 1998, with Dominion Capital Fund, Ltd., which subsequently assigned its rights to Centennial Parkway LLC (the "Investor"). Pursuant to the terms of the Credit Agreement, the Company may, from time to time during a specified term, cause the Investor to purchase up to an aggregate of $10,000,000 of the Company's common stock, par value $.03 per share (the "Common Stock"). The price per share of Common Stock to be paid by the Investor is to be determined at the time of each purchase according to a specified formula which is based upon the average closing bid price of the Common Stock on the principal trading exchange or market for the Common Stock (the "Principal Market") over a prescribed, five-day period. With each purchase of Common Stock, the Investor is also to receive warrants exercisable for a number of shares of Common Stock equal to ten percent of the number of shares of Common Stock purchased at an exercise price per share equal to 125% 8 Pharmos Corporation Notes to Condensed Consolidated Financial Statements of the closing bid price of the Common Stock on the Principal Market on a specified date. As of September 30, 2000, $1.7 million remained available under the equity line of credit. During the second quarter of 2000, under terms of the Credit Agreement, the Company issued 150,000 shares of its Common Stock and warrants to purchase 12,574 shares of its Common Stock to the Investor for consideration of $553,655, net of fees. The warrants have an exercise price of $5.00 per share and expire in the second quarter of 2003. During the first quarter of 2000, under terms of the Credit Agreement, the Company issued 368,424 shares of its Common Stock and warrants to purchase 38,588 shares of its Common Stock to the Investor for consideration of $1,592,250, net of fees. The warrants have exercise prices ranging from $2.19 to $16.80 per share and expire in the first quarter of 2003. During the third quarter of 2000, the Company issued warrants to purchase 8,000 shares of its common stock as compensation to a consultant. The warrants were immediately exercisable, have an exercise price of $1.19 per share and expire by August 2005. During the second quarter of 2000, the Company issued warrants to purchase 16,000 shares of its common stock as compensation to a consultant. The warrants were immediately exercisable, have an exercise price of $1.19 per share and expire by June 2005. During the first quarter of 2000, the Company issued warrants to purchase 8,000 shares of its common stock as compensation to a consultant. The warrants were immediately exercisable, have an exercise price of $1.19 per share and expire by February 2005. 7. Segment and Geographic Information The Company is active in one business segment: designing, developing, selling and marketing pharmaceutical products. The Company maintains development operations in the United States and Israel. The Company's selling operations are maintained in the United States. Geographic information for the three and nine months ending September 30, 2000 and 1999 are as follows: Three months ended September 30, Nine months ended September 30, ---------------------------------- ---------------------------------- 2000 1999 2000 1999 ---- ---- ---- ---- Net revenues United States ........................ $ 1,761,735 $ 833,118 $ 3,840,152 $ 2,024,329 Israel ............................... -- -- -- -- ----------- ----------- ----------- ----------- $ 1,761,735 $ 833,118 $ 3,840,152 $ 2,024,329 =========== =========== =========== =========== Net loss United States ........................ ($1,432,454) ($ 960,662) ($4,000,498) ($3,255,628) Israel ............................... (98,705) (11,623) (275,737) (52,833) ----------- ----------- ----------- ----------- ($1,531,159) ($ 972,285) ($4,276,235) ($3,308,461) =========== =========== =========== =========== 9 Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations Results of Operations Quarters ended September 30, 2000 and 1999 Product sales revenue totaled $1,661,735 for the quarter ended September 30, 2000 compared to $833,118 for the quarter ended September 30, 1999. Increased sales volumes resulted from market share growth and price increases for the Company's ophthalmic products, Lotemax and Alrex. Additionally, the Company recorded License revenue of $100,000 for the quarter ended September 30, 2000. Cost of goods sold for the quarter ended September 30, 2000 totaled $580,202 compared to $265,649 for the quarter ended September 30, 1999. The increase reflects the higher sales volumes. Cost of goods sold includes the cost of the active drug substance and licensing costs. Total operating expenses increased $990,920 or 62%, from $1,585,698 in 1999 to $2,576,618 in 2000. The increase is primarily due to higher research and development expenses, increased general and administrative expenses and higher amortization and depreciation expenses. Net research and development expenses increased by $523,085 or 62%, from $839,390 in 1999 to $1,362,475 in 2000. The increase in R&D expense is primarily due a higher level of activity in the Company's dexanabinol analog program and increased expenses relating to its development of dexanabinol for traumatic brain injury. Dexanabinol is a neuroprotective agent for the treatment of central nervous system ("CNS") disorders. Additionally, spending on the Company's discovery and early stage programs increased. General and administrative expenses increased by $400,813 or 67%, from $599,174 in 1999 to $999,987 in 2000. The increase is primarily due to higher staffing costs and increased investor relations activity. Depreciation and amortization expenses increased by $82,267, or 96%, from $85,353 in 1999 to $167,620 in 2000. The increase reflects increased depreciation expense relating to laboratory equipment purchases. Other income, net, decreased by $182,018, from net income of $45,944 in 1999 to a net charge of $136,074 in 2000. While interest income increased significantly as a result of higher average cash balances, the increases were more than offset by the non-cash charges of $399,585 for the amortization of the Beneficial Conversion Feature and the debt discount from the private placement of convertible debentures in September 2000. Nine months ended September 30, 2000 and 1999 Product sales revenue totaled $3,740,152 for the nine months ended September 30, 2000 compared to $2,024,329 for the nine months ended September 30, 1999. Increased sales volumes resulted from market share growth and higher prices for the Company's ophthalmic products, Lotemax and Alrex. Additionally, the Company recorded license income of $100,000 for the nine months ended September 30, 2000. Cost of goods sold for the nine months ended September 30, 2000 totaled $1,337,893 compared to $564,444 for the nine months ended September 30, 1999. The increase reflects the volume difference between the two periods. Cost of goods sold includes the cost of the active drug substance and licensing costs. Total operating expenses increased $2,234,054 or 46%, from $4,842,837 in 1999 to $7,076,891 in 2000. The increase is primarily due to higher research and development expenses and increased general and administrative expenses. 10 Net research and development expenses increased by $1,141,422, or 44%, from $2,591,722 in 1999 to $3,733,144 in 2000. The increase in R&D expense is primarily due to a higher level of activity in the Company's dexanabinol analog program and increased expenses relating to its development of dexanabinol for traumatic brain injury, as well as additional spending on the Company's discovery and early stage programs. General and administrative expenses increased by $993,999 or 54%, from $1,844,477 in 1999 to $2,838,476 in 2000. The increase is primarily due to higher staffing costs and increased investor relations activity. Depreciation and amortization expenses increased by $123,374, or 49%, from $253,464 in 1999 to $376,838 in 2000, reflecting increased depreciation expense relating to laboratory equipment purchases. The increase reflects increased depreciation expense relating to laboratory equipment purchases. Other income, net, increased by $223,906, from $74,491 in 1999 to $298,397 in 2000. Interest income increased by $641,823 as a result of higher average cash balances. However, the increased interest income was partially offset by the non-cash charges of $399,585 for the amortization of the Beneficial Conversion Feature and the debt discount from the private placement of convertible debentures in September 2000. Liquidity and Capital Resources The Company had no sources of recurring revenues until the commencement of product sales in April 1998, and has incurred operating losses since its inception. At September 30, 2000, the Company has an accumulated deficit of $86,786,342. The Company has financed its operations with public and private offerings of securities, advances and other funding pursuant to a marketing agreement with BLP, research contracts, license fees, royalties and sales, and interest income. The Company had working capital of $23.9 million, including cash and cash equivalents of $23.7 million, as of September 30, 2000. The Company also had $4 million of restricted cash held in escrow until the Company's convertible debentures are converted into common shares of the Company by the investor or are repaid by the Company. On December 10, 1998, the Company obtained a $10 million equity line of credit with a single institutional investor. As of September 30, 2000, $1.7 million remained available under the equity line of credit. On September 1, 2000, the Company completed a private placement of convertible debentures, common stock and warrants to purchase shares of common stock with institutional investors, generating total gross proceeds of $11 million. The convertible debentures, which generated gross proceeds of $8 million, are due in February 2002 and carry a 6% interest payable in cash or common stock. The convertible debentures are convertible into common shares of the Company at the conversion price of $3.83 per share and are convertible beginning October 31, 2000. Under certain anti-dilutive conditions, the conversion price may change. The issuance of common shares in the private placement generated gross proceeds of $3 million. The investors have an option, in the form of a warrant, to purchase an additional $2 million of common shares for a period of one year provided that the future purchase price is greater than the initial closing price of $3.65 per share. Management believes that the equity line of credit, existing cash and cash equivalents combined with anticipated cash inflows from investment income, R&D grants and proceeds from sales of the drug substance for Lotemax and Alrex to BLP will be sufficient to support the Company's regular operations. The Company expects to commence the final phase of clinical development on the Company's dexanabinol (HU-211) drug candidate in the near future. The total cost of this phase of development is expected to range between $15 million and $25 million over the next 3 years. The Company continues to actively pursue various funding options, including strategic corporate alliances, additional equity offerings, business combinations and the establishment of product related research and development limited partnerships, to obtain the additional financing that is required to continue the development of its products and bring them to commercial markets. 11 Statements made in this document related to the development, commercialization and market expectations of its drug products, to the establishment of corporate collaborations, and to the Company's operational projections are forward-looking and are made pursuant to the safe harbor provisions of the Securities Litigation Reform Act of 1995. Such statements involve risks and uncertainties, which may cause results to differ materially from those, set forth in these statements. Among the factors that could result in a materially different outcome are the inherent uncertainties accompanying new product development, action of regulatory authorities and the results of further trials. Additional economic, competitive, governmental, technological, marketing and other factors identified in Pharmos' filings with the Securities and Exchange Commission could affect such results. Part II Other Information Item 1 Legal Proceedings NONE Item 2 Changes in Securities NONE Item 3 Defaults upon Senior Securities NONE Item 4 Submission of Matters to Vote of Security Holders NONE Item 5 Other Information NONE Item 6 Exhibits and Reports on Form 8-K (a) Exhibits: None. (b) Reports on Form 8-K: 1. Form 8-K dated September 8, 2000 (earliest event reported September 1, 2000); Item 5 was reported. 12 SIGNATURE PAGE Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized. PHARMOS CORPORATION Dated: November 14, 2000 by: /s/ Robert W. Cook ------------------ Robert W. Cook Vice President Finance and Chief Financial Officer (Principal Accounting and Financial Officer) 13