UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 10-QSB [X] QUARTERLY REPORTS UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE QUARTERLY PERIOD ENDED MARCH 31, 1999. OR [ ] QUARTERLY REPORTS UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE TRANSITION PERIOD FROM _______ TO_______ Commission File No. 0-19844 PARACELSIAN, INC. ----------------- (Exact name of small business issuer as specified in its charter) Delaware 16-1399565 -------- ---------- (State or other jurisdiction of (I.R.S. Employer incorporation or organization) Identification No.) 222 Langmuir Laboratories, Cornell Technology Park, Ithaca, New York 14850 - -------------------------------------------------------------------- ----- (address of principal executive offices) Zip Code Issuer's telephone number: (607) 257-4224 -------------- Check whether the issuer (1) filed all reports to be filed by Section 13 or 15(d) of the Securities Exchange Act during the past 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 [ ] There were 19,324,661 shares of Common Stock outstanding at May 12, 1999. PARACELSIAN, INC. AND SUBSIDIARY Index Page ---- PART I. - FINANCIAL INFORMATION Item 1. Financial Statements Consolidated Balance Sheet as of March 31, 1999 (Unaudited) 3 Consolidated Statements of Operations for the three and six months ended March 31, 1999 and 1998 and the cumulative period from inception to March 31, 1999 (Unaudited) 4 Consolidated Statements of Cash Flows for the six months ended March 31, 1999 and 1998 and the cumulative period from inception to March 31, 1999 (Unaudited) 5 Notes to Consolidated Financial Statements (Unaudited) 7 Item 2 - Management's Discussion and Analysis of Financial Condition and Results of Operations. 9 PART II - OTHER INFORMATION Item 1 - Legal Proceedings 11 Item 6 - Exhibits and Reports on Form 8-K 11 Signatures 11 Paracelsian, Inc. and Subsidiary (A Development Stage Company) Consolidated Balance Sheet March 31, 1999 (Unaudited) ASSETS Current Assets: Cash and cash equivalents $ 109,038 Inventory 171,689 Prepaid expenses and other current assets 22,452 ------------ Total current assets 303,179 ------------ Equipment, net 238,286 Other Assets: TCM extracts on-hand 233,469 Licensing agreement, net 79,258 Patents and trademarks, net 208,461 Note receivable 148,750 ------------ 669,938 ------------ $ 1,211,403 ============ LIABILITIES AND STOCKHOLDERS' EQUITY Current Liabilities: Accounts payable $ 193,598 Accrued expenses 34,388 Current portion of capital lease obligations 11,015 Current portion of notes payab1e 8,277 ------------ Total current liabilities 257,278 Long-term Liabilities Long-term portion of capital lease obligation 14,837 Long-term portion of notes payab1e 7,279 ------------ Total current and long-term liabilities 289,394 ------------ Commitments and Contingency Stockholders' Equity: Common stock, $.01 par value; 35,000,000 shares authorized; 19,176,513 shares outstanding March 1999 191,765 Additional paid-in capital 23,681,304 Deficit accumulated during the development stage (21,608,545) Treasury stock, at cost; 265,478 shares (1,342,515) ------------ Total stockholders' equity 922,009 ------------ $ 1,211,403 ============ See accompanying notes to consolidated financial statements. 3 Paracelsian, Inc. and Subsidiary (A Development Stage Company) Consolidated Statements of Operations For the three and six months ended March 31, 1999 and 1998, And the cumulative period from inception to March 31, 1999 (Unaudited) Cumulative Three Months Ended Six Months Ended Period from March 31, March 31, Inception to ---------------------------- ---------------------------- March 31, Revenues: 1999 1998 1999 1998 1999 ------------ ------------ ------------ ------------ ------------ Marketing rights -- -- -- -- 254,995 Products 5,948 1,675 7,653 1,675 184,678 Product testing 5,229 12,050 15,489 33,970 56,907 Development fees 98,000 -- 98,000 -- 98,000 Product royalties -- -- -- -- 1,246 Subscription revenue -- -- -- -- 31,625 ------------ ------------ ------------ ------------ ------------ 109,177 13,725 121,142 35,645 627,451 Operating expenses: Research and product engineering 202,938 194,675 376,515 377,157 8,052,730 General and administrative 382,478 297,161 723,961 555,401 12,195,650 Product launch costs -- -- -- -- 300,544 Cost of products sold -- -- -- -- 95,023 ------------ ------------ ------------ ------------ ------------ 585,416 491,836 1,100,476 932,558 20,643,947 ------------ ------------ ------------ ------------ ------------ Loss from operations during the development stage (476,239) (478,111) (979,334) (896,913) (20,016,496) Interest income, net -- 12,889 -- 26,702 497,463 Gain on sale of assets -- 1,700 -- 6,968 38,488 ------------ ------------ ------------ ------------ ------------ Net loss during the development stage (476,239) (463,522) (979,334) (863,243) (19,480,545) ============ ============ ============ ============ ============ Basic and diluted net loss per share (0.03) (0.03) (0.05) (0.06) ============ ============ ============ ============ Weighted average number of shares outstanding 18,953,365 15,576,296 18,602,128 15,576,296 ============ ============ ============ ============ See accompanying notes to consolidated financial statements. 4 Paracelsian, Inc. and Subsidiary (A Development Stage Company) Consolidated Statements of Cash Flows For the six months ended March 31, 1999 and 1998, And the cumulative period from inception to March 31, 1999 (Unaudited) Cumulative Six Months Ended Period from March 31, Inception to ---------------------------- March 31, 1999 1998 1999 ------------ ------------ ------------ Cash flows from operating activities: Net loss $ (979,334) $ (863,243) $(19,480,545) Adjustments to reconcile net loss to net cash used in operating activities: Gain on the sale of assets -- (1,700) (6,968) Non-cash compensation expense 119,828 -- 1,362,103 Other non-cash expenses -- -- 1,742,754 Depreciation and amortization 214,650 214,650 1,901,495 Changes in assets and liabilities: (Increase) decrease in inventory -- (15,366) (171,689) (Increase) decrease in prepaid expenses and other current assets 61,725 21,050 6,968 (Decrease) increase in accounts payable 123,963 (142,226) 548,120 (Decrease) increase in due to related party -- (11,555) -- (Decrease) increase in accrued expenses (90,450) (43,609) 71,888 ------------ ------------ ------------ Net cash used in operating activities (549,618) (841,999) (14,025,874) ------------ ------------ ------------ Cash flows from investing activities: Purchase of equipment (1,636) (31,212) (735,037) Proceeds from sale of equipment -- 1,700 26,968 Acquisition of licensed technology -- -- (53,656) Acquisition of patents and trademarks (33,758) -- (464,337) Acquisition of New Century Nutrition newsletter -- -- (350,000) Acquisition of option for East West Herbs, Ltd. and related acquisition costs -- -- (92,866) Loan to from East West Herbs, Ltd. -- -- (340,000) Proceeds from East West Herbs, Ltd. -- 42,500 42,500 ------------ ------------ ------------ Net cash used in investing activities (35,394) 12,988 (1,966,428) ------------ ------------ ------------ Cash flows from financing activities: Sale of common stock, initial public offering, net of costs -- -- 5,124,014 Sale of common and preferred stock, net of costs 445,980 500,000 11,276,089 Proceeds from the exercise (redemption) of warrants -- -- 1,186,295 Proceeds from the exercise of options 31,400 -- 68,900 Purchase of treasury stock -- -- (1,342,515) Cost of warrant dividend -- -- (63,102) Payment on equipment contract -- -- (90,950) Payment on capital lease obligations (3,993) -- (9,148) Payment on notes payable (29,879) -- (48,243) ------------ ------------ ------------ Net cash (used in) provided by financing activities 443,508 500,000 16,101,340 ------------ ------------ ------------ Net increase (decrease) in cash and cash equivalents (141,504) (329,011) 109,038 Cash and cash equivalents, beginning of period 250,542 886,249 -- ------------ ------------ ------------ Cash and cash equivalents, end of period $ 109,038 $ 557,238 $ 109,038 ============ ============ ============ See accompanying notes to consolidated financial statements. 5 Paracelsian, Inc. and Subsidiary (A Development Stage Company) Consolidated Statements of Cash Flows For the six months ended March 31, 1999 and 1998, And the cumulative period from inception to March 31, 1999 (Unaudited) Cumulative Six Months Ended Period from March 31, Inception to ---------------------------- March 31, 1999 1998 1999 ------------ ------------ ------------ Supplemental disclosures: Cash paid during the period for interest $ 2,835 $ 2,485 $ 29,897 ============ ============ ============ Supplemental disclosure of non-cash investing and financing activities: Fair value of assets acquired, net of cash acquired $ -- $ -- $ 1,733,212 Less - liabilities assumed -- -- 83,212 Less - issuance of common stock -- -- 1,644,000 ------------ ------------ ------------ Net cash paid $ -- $ -- $ 6,000 ============ ============ ============ Warrant dividend $ -- $ -- $ 500,000 Issuance of common stock/warrants for services and to reduce short-term liabilities $ 150,914 $ -- $ 716,145 Purchase of equipment $ -- $ -- $ 90,950 Repayment of officer stock subscription receivable $ -- $ -- $ 89,850 Issuance of common stock for licensing and technology rights $ -- $ -- $ 3,338 See accompanying notes to consolidated financial statements. 6 PARACELSIAN, INC. AND SUBSIDIARY (A Development Stage Company) NOTES TO CONSOLIDATED FINANCIAL STATEMENTS MARCH 31, 1999 (Unaudited) 1. BASIS OF PRESENTATION The consolidated financial statements included herein have been prepared in accordance with generally accepted accounting principles without audit, pursuant to the rules and regulations of the Securities and Exchange Commission applicable to quarterly reporting on Form 10-QSB and reflect, in the opinion of the Company, all adjustments necessary to present fairly the financial position and results of operations for Paracelsian, Inc. and its consolidated subsidiary. All such adjustments are of a normal and recurring nature. Certain information and footnote disclosures normally included in financial statements, prepared in accordance with generally accepted accounting principles, have been condensed or omitted as permitted by such regulations. These consolidated financial statements and related notes should be read in conjunction with the consolidated financial statements and related notes included in the Company's Annual Report on Form 10-KSB for the fiscal year ended September 30, 1998. 2. ORGANIZATION, BUSINESS, AND RISK FACTORS: ORGANIZATION AND BUSINESS Paracelsian, Inc., (the "Company") is a bio-science and technology company that utilizes its proprietary screening technology to identify novel therapeutic compounds from herbal and other botanical sources and to define and/or confirm the biological mechanisms through which traditional herbs and other botanicals provide the therapeutic or functional benefits suggested by their traditional use. This technology has been developed by the Company to identify potential products that inhibit the biological signals generated by targeted cells that result in controlled or uncontrolled growth and division. The Company's screening technology evaluates the effects of herbal and other botanical products on intracellular signals referred to as "Signal Transduction Technology." Cell division is one of the basic steps in biology necessary for normal growth of tissues to support life. The Company's technology enables researchers to observe signal transduction and measure the effects of chemicals contained in synthetic or natural compounds, and chemicals occurring in nature such as herbs and combinations of herbal extracts, on cell division. In the course of these observations, the Company can distinguish the effects of such chemicals on targeted cells, thereby screening compounds to identify those with promising favorable therapeutic effects. (This proprietary technology, including the components, methods, procedures and know-how employed in this screening process, is referred to herein as the "Screening Technology") In October 1994, Pacific Liaisons (Pacific), a partnership engaged in identifying and acquiring biologically active drugs, natural products and foods from Eastern Asia, merged with a wholly-owned subsidiary of the Company and the Company now maintains a large library of natural medicinal extracts. These extracts are being processed with the Company's screening technology to identify potential candidates for drug or dietary supplement development. The Company also has access to the informational database related to the medicinal extracts, which contains, among other things, a history of the usage of each extract. DEVELOPMENT STAGE COMPANY AND RISK FACTORS The Company is considered to be a development stage company as defined in Statement of Financial Accounting Standards No. 7, "Accounting and Reporting by Development Stage Enterprises." Since inception, the Company has been primarily engaged in research, product engineering and raising capital. The Company, as a development stage enterprise, has yet to generate significant revenues and has no assurance of substantial future revenues. The Company is subject to a number of risks that may affect its ability to become an operating enterprise or impact its ability to remain in existence, including risks related to successful development and marketing of its products, patent protection of proprietary technology, government regulation, competition from substitute products (including technologies that may not yet have been developed), dependence on key employees and the need to obtain additional funds that may not be available to it. 7 As shown in the accompanying financial statements, the Company incurred a net loss of approximately $979,000 for the six months ended March 31, 1999 and had working capital of approximately $46,000 at March 31, 1999. The Company continues to expend funds on product research and development and general and administrative expenses, however, under the direction of a new management team and Board since January, 1998, the business plan has been revised, and efforts have been focused on developing a recurring revenue stream. Revenues from the BioFIT(TM) quality assurance program and from development of the AhIMMUNOASSAY dioxin screen commenced during the second quarter of fiscal 1999. The Company raised $217,500 in March 1999 and $100,000 in May 1999 through private placements of its common stock. Management believes that it can raise additional capital through similar private placements, if needed, and that the combination of such capital and the anticipated revenue stream will enable the Company to continue its operations and emerge from the development stage in 1999. 3. SIGNIFICANT ACCOUNTING POLICIES: CONSOLIDATION The consolidated financial statements of the Company include the accounts of Paracelsian, Inc. and its wholly owned subsidiary ParaComm, Inc. formerly known as Para Acquisition Corp. All intercompany balances and transactions have been eliminated. CASH AND CASH EQUIVALENTS Cash equivalents consist of highly liquid investments with an original maturity of three months or less. The Company had no cash equivalents as of March 31, 1999. RESEARCH AND PRODUCT ENGINEERING Company-sponsored research and product engineering expenditures have been charged to expense as incurred. These costs consist primarily of employee salaries and direct laboratory costs. The cost of extracts used in research and development activities is expensed as consumed. NET LOSS PER SHARE Basic loss per share is computed by dividing the net loss by the weighted-average number of common shares outstanding during the period. The Company's basic and diluted per share amounts are the same since the assumed exercise of stock options and warrants are anti-dilutive. PATENTS AND TRADEMARKS The Company has acquired or applied for certain patent and trademark rights. Costs associated with the acquisition and application for these rights have been capitalized and are being amortized on the straight-line method over the estimated legal life of the assets which range from 15 to 17 years. EQUIPMENT AND DEPRECIATION Equipment is stated at cost and is depreciated over the estimated useful lives of the assets using the straight-line method. USE OF ESTIMATES The preparation of the consolidated financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosure of contingent assets and liabilities at the date of the financial statements. Estimates also affect the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates. 8 ITEM 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS Six months Ended March 31, 1999 as compared to the Six months Ended March 31, 1998 As a development stage enterprise, the Company, since inception, has been primarily engaged in research, product engineering, and capital formation. As such, the Company has not generated significant revenue to date on a recurring basis. Since January 1998, a significant portion of the new management team's strategy has been focused on the development of its BioFIT (TM) (Bio Functional Integrity Tested) quality assurance program. This unique testing program is able to certify consistent bio-functionality of herbal and other dietary supplements. This new "functional" approach to quality assurance will assist consumers in selecting herbs and other botanical products based on their demonstrated biological activity, rather than relying solely on analytical techniques which measure only the presence or absence of certain marker compounds. The Company has entered into an agreement with R.P. Scherer North America that establishes them as the exclusive marketing and distribution agent for the BioFIT (TM) certification program in the dietary supplement and OTC market segments in North America. The agreement also provides for collaboration between the two companies on the development of new dietary supplements and OTC products. The agreement, among other things, provides for payments to the Company for the development of each bioassay, payment for each certification, and payment of royalties on all sales of BioFIT (TM) certified products. In March 1999, Paracelsian entered into a letter agreement (to be followed by a definitive agreement) with R.P. Scherer Limited of Swindon, England whereby Paracelsian will grant exclusive distribution rights to Scherer for the BioFIT(TM) program in Europe, Scandinavia, the Middle East and Africa. The agreement will provide for the payment of development fees, certification fees, and royalties subject to certain regulatory approvals and other milestones. Paracelsian has begun the initial phase of a collaboration with Kubota Corporation of Osaka, Japan to further develop and implement the use of Paracelsian's patented dioxin testing system know as the Ah Immunoassay(TM). Under this collaboration, Paracelsian will develop an advanced sample preparation system which will facilitate the widespread use of the assay to monitor the levels of dioxin in the smoke and ash of municipal waste incinerators operated by Kubota and others. Paracelsian and Kubota have begun negotiations for a more comprehensive agreement under which Kubota would pay Paracelsian a license fee for the use and distribution of the Ah Immunoassay(TM). Under this agreement, Paracelsian would receive both an initial license fee and an ongoing payment for each use or sale of the assay, with a minimum annual payment required under the agreement to maintain exclusivity. The commencement of revenues from the BioFIT (TM) program began in January 1999,and management anticipates a gradual ramp-up and expansion of the program throughout the year. Consequently, the Company is expected to emerge from the development stage during 1999. RESULTS OF OPERATIONS The Company's net loss for the second quarter of fiscal 1999 was approximately $476,000 compared to $478,000 in the second quarter of fiscal1998. For the six months ended March 31, 1999, the net loss was $979,000, compared to $897,000 for the comparable period of the preceding year. Revenues for the three and six month periods were $109,000 and $121,000 in 1999 as compared to $14,000 and $36,000 in 1998. The increase in revenues is primarily attributable to initial development fees under the BioFit (TM) program with R.P. Scherer ($50,000) and fees from the Kubota Copration ($48,000) for development work on the Ah Immunoassay(TM). Operating expenses for the fiscal 1999 periods are modestly higher than the comparable periods in fiscal 1998, reflecting the gradual build up of personnel and related costs associated with the development of the BioFit (TM) certification program. Additionally, the 1999 periods include $78,000 of non-cash compensation associated with the vesting of stock options previously granted to the Chief Executive Officer. 9 LIQUIDITY & CAPITAL RESOURCES As of March 31, 1999, the Company had cash of $109,000 and net working capital of $46,000. Subsequent to quarter end, the Company received $50,000 from R.P. Scherer representing the initial payment under the European portion of the BioFit (TM) development program. Additionally, in early May 1999, the Company completed a private placement of its common stock for $100,000 at 67.5 cents per share, bringing the total private placements completed since fiscal year end to $567,500. Current monthly cash requirements in order to sustain meaningful operations are approximately $100,000. Management believes, based on its recent experience, that it can continue to raise incremental capital through private placements, if needed, to support its operations until such time as the revenue stream is sufficient to provide for continuing operations. Such private placements, if any, will likely require discounts from then current market prices, reflecting the risk associated with trading restrictions, trading volume and volatility, and stock price support levels. Management will continue to evaluate the most cost effective means of raising any additional needed capital, including the feasibility of adjusting exercise prices on outstanding options or warrants as appropriate. There can be no assurance that additional financing will be available on acceptable terms or at all. YEAR 2000 COMPLIANCE The Company continues to monitor its exposure to the year 2000 computer problem. Management believes that all of the Company's date sensitive computer equipment and software is Y2K compliant, and is not aware of any vendor or customer Y2K problems that could have a significant impact on the financial position or results of operations of the Company. To date, the Company has not incurred any significant expense with respect to this issue and does not anticipate any significant related expense in the future. 10 PART II OTHER INFORMATION Item 1. LEGAL PROCEEDINGS HADYK, ET AL. V. JOHN G. BABISH, ET AL. This case was commenced in New York State Supreme Court (Onondaga County) in June 1993 by certain persons, individually and doing business as In Vitro Bioanalytic Systems, against the Company, Dr. John G. Babish, a former officer and director of the Company, and Edward Heslop, a founding shareholder of the Company, primarily as an action for money damages and injunctive relief against the Company for alleged misappropriation of proprietary information and unfair competition. The plaintiffs allege, among other things, that in 1990, prior to the Company's incorporation, a partnership had been formed with Messrs. Babish and Heslop to commercialize products that the Company was developing. Damages, an accounting and an injunction are being sought against the Company. By decision dated September 14, 1994, the Court dismissed certain of the plaintiffs' claims against the Company while permitting a claim alleging unfair competition to proceed. Discovery has been temporarily stayed pending resolution of a motion for summary judgment brought by certain of the Company's co-defendants. That motion, if successful, will fully resolve the case in favor of the Company. The Company believes that the suit against it is without merit and intends to defend the case vigorously. Item 6(a) EXHIBITS None Item 6(b) REPORTS ON FORM 8-K. None SIGNATURES In accordance with Section 13 or 15(d) of the Securities and Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized. Date May 21, 1999 PARACELSIAN, INC. By: /s/ BERNARD M. LANDES --------------------------------------- Bernard M. Landes President and Chief Executive Officer 11