-----BEGIN PRIVACY-ENHANCED MESSAGE----- Proc-Type: 2001,MIC-CLEAR Originator-Name: webmaster@www.sec.gov Originator-Key-Asymmetric: MFgwCgYEVQgBAQICAf8DSgAwRwJAW2sNKK9AVtBzYZmr6aGjlWyK3XmZv3dTINen TWSM7vrzLADbmYQaionwg5sDW3P6oaM5D3tdezXMm7z1T+B+twIDAQAB MIC-Info: RSA-MD5,RSA, QOBvwET9UoN8nq+Q6rQy0r/tWhtAaZ1phXLYDXZ/x72rzHK8aUIAMqx9r9bsLTLS mRzW5pNMEAM+jHB4UL9/Zw== 0000950005-96-000603.txt : 19960816 0000950005-96-000603.hdr.sgml : 19960816 ACCESSION NUMBER: 0000950005-96-000603 CONFORMED SUBMISSION TYPE: 10-Q PUBLIC DOCUMENT COUNT: 3 CONFORMED PERIOD OF REPORT: 19960630 FILED AS OF DATE: 19960814 SROS: NASD FILER: COMPANY DATA: COMPANY CONFORMED NAME: VIDAMED INC CENTRAL INDEX KEY: 0000929900 STANDARD INDUSTRIAL CLASSIFICATION: SURGICAL & MEDICAL INSTRUMENTS & APPARATUS [3841] IRS NUMBER: 770314454 STATE OF INCORPORATION: DE FISCAL YEAR END: 0630 FILING VALUES: FORM TYPE: 10-Q SEC ACT: 1934 Act SEC FILE NUMBER: 000-26082 FILM NUMBER: 96611851 BUSINESS ADDRESS: STREET 1: 1380 WILLOW ROAD STREET 2: SUITE 101 CITY: MENLO PARK STATE: CA ZIP: 94025 BUSINESS PHONE: 4153288781 MAIL ADDRESS: STREET 1: 1300 WILLOW RD STREET 2: STE 101 CITY: MENLO PARK STATE: CA ZIP: 94025 10-Q 1 FORM 10-Q UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 10-Q [ X ] QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended June 30, 1996 or [ ] TRANSITION REPORTS PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to ------------------ ------------------- Commission File Number: 0-26082 VIDAMED, INC. (exact name of registrant as specified in its charter) Delaware 77-0314454 (State or other jurisdiction of (IRS Employer Identification No.) incorporation or organization) 1380 Willow Road, Suite 101 Menlo Park, CA 94025 (Address of principal executive offices) (415) 328-8781 (Registrant's telephone number, including area code) Indicate by check mark whether the registrant (1) has filed all reports required 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. [ X ] Yes [ ] No The number of outstanding shares of the registrant's Common Stock, $.001 par value, was 10,845,518 as of August 1, 1996. Page 1 of 17 Exhibit Index at Page 16 VIDAMED, INC. INDEX
PART I: FINANCIAL INFORMATION Page Item 1. Condensed consolidated financial statements - unaudited Condensed consolidated balance sheets - June 30, 1996 and December 31, 1995 3 Condensed consolidated statements of operations - three months ended June 30, 1996 and 1995 and six months ended June 30, 1996 and 1995 4 Condensed consolidated statements of cash flows - six months ended June 30, 1996 and 1995 5 Notes to condensed consolidated financial statements 6 Item 2. Management's discussion and analysis of financial condition and results of operations 9 PART II: OTHER INFORMATION Item 1. Legal Proceedings 12 Item 2. Changes in Securities 12 Item 3. Defaults Upon Senior Securities 12 Item 4. Submission of Matters to a Vote of Security Holders 12 Item 5. Other Information 12 Item 6. Exhibits and Reports on Form 8-K 12 Signatures 13
Page 2 of 17 PART I: FINANCIAL INFORMATION ITEM 1. FINANCIAL STATEMENTS VidaMed, Inc. Condensed Consolidated Balance Sheets (In thousands)
June 30, December 31, 1996 1995 --------- --------- (Unaudited) (*) Assets Current Assets: Cash and cash equivalents $ 6,852 $ 5,687 Short-term investments 6,953 8,003 Other current assets 1,811 1,982 -------- -------- Total current assets 15,616 15,672 Property and equipment, net 2,696 2,909 Other assets, net 222 235 -------- -------- Total assets $ 18,534 $ 18,816 ======== ======== Liabilities and stockholders' equity Current liabilities: Notes payable, current portion $ 1,005 $ 3,650 Accounts payable 662 565 Accrued clinical trial costs 773 978 Accrued and other liabilities 3,020 2,636 Current portion of obligations under capital leases 710 696 Deferred revenue 567 779 -------- -------- Total current liabilities 6,737 9,304 Notes payable, noncurrent 1,026 1,543 Other long-term liabilities 822 1,214 Stockholders' equity: Capital stock 55,167 45,088 Accumulated deficit (45,218) (38,333) -------- -------- Total stockholders' equity 9,949 6,755 -------- -------- Total liabilities and stockholders' equity $ 18,534 $ 18,816 ======== ======== * The Balance Sheet at December 31, 1995 has been derived from the audited financial statements at that date but does not include all of the information and footnotes required by generally accepted accounting principles for complete financial statements. See accompanying notes
Page 3 of 17 VidaMed, Inc. Condensed Consolidated Statements of Operations (In thousands except per share amounts) (Unaudited)
Three Months Ended Six Months Ended June 30, June 30, ------------------------------ --------------------------------- 1996 1995 1996 1995 ------------ ---------------- ----------------- --------------- Revenues: Product sales, net $ 496 $ 800 $ 876 $ 1,468 License fees and grant revenue 107 110 215 219 ------------ ---------------- ----------------- --------------- Net revenues 603 910 1,091 1,687 Operating Expenses: Cost of product sales 832 893 1,622 1,830 Research and development 1,339 1,645 2,751 3,088 Selling, general and administrative 1,997 1,882 3,611 3,473 ------------ ---------------- ----------------- --------------- Total operating expenses 4,168 4,420 7,984 8,391 ------------ ---------------- ----------------- --------------- Loss from operations (3,565) (3,510) (6,893) (6,704) Other income(expense), net 11 (182) 8 (321) ------------ ---------------- ----------------- --------------- Net loss $ (3,554) $ (3,692) $ (6,885) $ (7,025) ============ ================ ============== =============== Net loss per share $ (.34) $ (1.54) $ (.70) $ (2.97) ============ ================ ============== =============== Shares used in computing net loss per share 10,420 2,392 9,885 2,362 ============ ================ ============== =============== See accompanying notes.
Page 4 of 17 VidaMed, Inc. Condensed Consolidated Statement of Cash Flows (In thousands) (Unaudited) Six Months Ended June 30, --------------------- 1996 1995 --------------------- Cash flows from operating activities: Net loss $ (6,885) $ (7,025) Adjustments to reconcile net loss to net cash used in operating activities: Depreciation and amortization 712 547 Other 29 1 Changes in assets and liabilities: Other current assets 171 (262) Other assets 13 21 Accounts payable 97 (253) Accrued and other liabilities 179 1,409 Deferred revenue (212) (212) -------- -------- Net cash used in operating activities (5,896) (5,774) -------- -------- Cash flows from investing activities: Expenditures for property and equipment (451) (400) Purchase of short-term investments (7,846) -- Proceeds from maturities of short-term investments 8,834 -- -------- -------- Net cash provided by/(used in) investing activities 537 (400) -------- -------- Cash flows from financing activities: Net cash proceeds from issuance of Common Stock 365 18,071 Principal payments under capital leases (345) (192) Principal payments of long-term debt (10) (8) Principal payments of notes payable (3,162) (71) Net proceeds from issuance of notes payable and convertible notes 9,676 7,169 -------- -------- Net cash provided by financing activities 6,524 24,969 -------- -------- Net increase in cash and cash equivalents 1,165 18,795 Cash and cash equivalents at the beginning of the period 5,687 372 -------- -------- Cash and cash equivalents at the end of the period $ 6,852 $ 19,167 ======== ======== See accompanying notes. Page 5 of 17 VIDAMED, INC. NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS June 30, 1996 (Unaudited) 1. Basis of presentation The accompanying unaudited condensed consolidated financial statements of VidaMed, Inc. (the "Company" or "VidaMed") have been prepared in accordance with generally accepted accounting principles for interim financial information and with the instructions for Form 10-Q and Article 10 of Regulation S-X. The balance sheet as of June 30, 1996 and the statements of operations for the three and six months periods ended June 30, 1996 and 1995, and the statements of cash flows for the six month periods ended June 30, 1996 and 1995, are unaudited but include all adjustments (consisting of normal recurring adjustments) which the Company considers necessary for a fair presentation of the financial position at such dates and the operating results and cash flows for those periods. Although the Company believes that the disclosures in these financial statements are adequate to make the information presented not misleading, certain information normally included in financial statements and related footnotes prepared in accordance with generally accepted accounting principles have been condensed or omitted pursuant to the rules and regulations of the Securities and Exchange Commission. The accompanying financial statements should be read in conjunction with the financial statements and notes thereto included in the Company's annual report on Form 10-K for the year ended December 31, 1995. Results for any interim period are not necessarily indicative of results for any other interim period or for the entire year. 2. Net loss per share Net loss per share is computed using the weighted average number of shares of common stock outstanding during the periods presented. Common equivalent shares are excluded from the computation as their effect is antidilutive, except that, pursuant to the Securities and Exchange Commission Staff Accounting Bulletins, common and common equivalent shares (stock options, warrants, convertible notes and preferred stock) issued during the 12 month period prior to the Company's initial public offering (IPO) have been included in the calculation as if they were outstanding for all periods through March 31, 1995 (using the treasury stock method for stock options and warrants and the if-converted method for convertible notes and preferred stock). Page 6 of 17 The pro forma calculation of net loss per share presented below has been computed as described above but also gives retroactive effect from the date of issuance to the conversion of the convertible preferred stock which automatically converted to common shares upon closing of the Company's initial public offering. Three months ended Six months ended June 30, 1995 June 30, 1995 ----------------- ---------------- Pro forma net loss per share $ ( .63) $ (1.21) ================= ================ Shares used in computation 5,860,000 5,830,000 ================= ================ 3. Initial public offering In June 1995, the Company completed an initial public offering ("IPO") of 3,565,000 shares of Common Stock at a price to the public of $6.50 per share. The net proceeds of the offering to the Company, after deducting underwriting discounts and expenses, were $20.8 million. Upon completion of the IPO all then outstanding shares of convertible preferred stock were automatically converted into shares of Common Stock. Upon completion of the IPO $1,518,805 of convertible notes issued during March and April 1995 were automatically converted into 333,800 shares of common stock. The conversion price equaled 70% of the IPO price. 4. Inventories Inventories are stated at the lower of cost (determined using the first-in, first-out method) or market value. Inventories at June 30, 1996 and December 31, 1995 consist of the following: June 30, December 31, 1996 1995 ----------------- ---------------- Raw Materials $ 356,000 $ 507,000 Work in process 235,000 154,000 Finished Goods 475,000 684,000 ----------------- ---------------- $ 1,066,000 $ 1,345,000 ================== ================ 5. Intellectual Property Litigation Risks The Company is aware that EP Technologies, Inc. ("EPT") and the University of California ("UC") have filed a United States patent application in the field of ablation of body tissue. These parties have also requested the United States Patent and Trademark Office to declare an interference with two of VidaMed's United States patent applications on which notices of allowances have been received. The inventors identified on the EPT/UC application are Stuart Edwards, who was previously VidaMed's Chief Executive Officer and was previously the Chief Technical Officer of EPT, and a cardiologist from the University of California, San Francisco, who worked as a consultant to EPT while Mr. Edwards was employed there. Page 7 of 17 Although the Company believes that the interference will not be allowed on the patents, an adverse determination in litigation or interference proceedings to which the Company may become a party could subject the Company to significant liabilities to third parties or require the Company to seek licenses from third parties. There can be no assurance that necessary licenses would be available to the Company on satisfactory terms or at all. Accordingly, an adverse determination in a judicial or administrative proceeding or failure to obtain necessary licenses could prevent the Company from manufacturing and selling its products, which would have a material adverse effect on the Company's business, financial condition and results of operations. 6. Cash, cash equivalents and short-term investments The Company considers all highly liquid investments with an original maturity of 90 days or less to be cash equivalents. The Company invests its excess cash with major banks or investment managers. Short-term investments consist of corporate paper and government securities with remaining maturities at the date of purchase of greater than 90 days and less than one year. Short-term investments are designated as available for sale and carried at fair market value, with unrealized gains and losses reported in stockholders' equity. 7. Convertible notes In March 1996, the Company completed the sale of $10.1 million of 5% convertible subordinated notes (the "Notes"). Interest is payable semiannually in either cash or Common Stock of the Company. The Notes are convertible into Common Stock of VidaMed based upon a percentage (ranging from 80% to 85%) of the average closing bid price over a period of five trading days prior to conversion. As of June 30, 1996 all of the $10.1 million in principal and accrued interest on the Notes had been converted into an aggregate of 1,375,676 shares of Common Stock. Page 8 of 17 ITEM 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS This Management's Discussion and Analysis of Financial Condition and Results of Operations for the three and six months ended June 30, 1996 and 1995, should be read in conjunction with the Management's Discussion and Analysis of Financial Condition and Results of Operations included in the Company's 10K for the year ended December 31, 1995. This Management's Discussion and Analysis of Financial Condition and Results of Operations contains forward-looking statements which involve risks and uncertainties. The Company's actual results may differ significantly from those anticipated by the forward-looking statements. Factors that might cause such a difference include, but are not limited to, those discussed below and in the Company's report on Form 10-K for the year ended December 31, 1995. Overview VidaMed has a limited history of operations and has experienced significant operating losses since inception. As of June 30, 1996, the Company had an accumulated deficit of $45.2 million. The Company commenced sales of its TransUrethral Needle Ablation ("TUNA") system in late 1993. Revenues for the three and six months ended June 30, 1995 also include consulting revenues and electronic component sales by Scionex, a wholly-owned subsidiary acquired in June 1994. Sales by Scionex to third parties have been discontinued as of the end of 1995 as Scionex has directed all of its activities to development and production of the radiofrequency generators for the TUNA System. Revenues for the quarters ended June 30, 1996 and 1995 include license fees for distribution rights in Japan and a United Kingdom government grant. VidaMed anticipates that a substantial amount of its revenues from product sales in the future will be from sales in the United States. The Company filed a premarket 510(k) notification with the Food and Drug Administration ("FDA") for the TUNA System in March 1996. The Company will not be permitted to market the TUNA System for BPH in the United States unless and until approval of such 510(k) notification is received. Currently, VidaMed sells its products primarily internationally to distributors who resell to physicians and hospitals. Sales to distributors are made on open credit terms and may include volume purchase discounts and extended payment terms. Therefore, distributors may purchase several months of inventory at one time to take advantage of discounts and extended payment terms. While revenue from product sales are generally recognized at the time of shipment (net of allowances for discounts and estimated returns), a portion of the Company's initial shipments to distributors have not been recognized as revenues due to extended payment terms or limited sell through experience associated with these distributors. The Company anticipates continuing this revenue recognition policy; however, as its distributor relationships mature, the Company believes that it will recognize a greater portion of revenues upon shipment. The Company expects its operating losses to continue through at least fiscal year 1996 as it continues to expend substantial resources in funding clinical trials in support of regulatory and reimbursement approvals, expansion of marketing and sales activities and research and development. The Company's future profitability will be dependent upon, among other factors, receipt of FDA clearance of the Company's 510(k) notification for the TUNA System, market acceptance of the TUNA System and availability of third- Page 9 of 17 party reimbursement for procedures performed with the TUNA System. There can be no assurance as to when or whether the Company will receive such 510(k) clearance, as to eventual market acceptance or as to the availability of third-party reimbursement, even if 510(k) clearance is received. The Company does not have a backlog of orders for its products in countries where the TUNA System is approved and anticipates that it will continue to manufacture and ship orders after their receipt. Accordingly, the Company does not anticipate that it will develop a significant backlog in the future. Results of Operations Net revenue for the three months ended June 30, 1996 decreased 34% to $603,000 from $910,000 in the three months ended June 30, 1995. Product sales in the second quarter of 1996 decreased 38% to $496,000 from $800,000 in the same period in 1995. The decrease in product sales between the second quarter of 1995 and 1996 is primarily the result of the discontinuance of Scionex sales to third party customers in 1996. Scionex had sales of approximately $550,000 in the first six months of 1995. VidaMed product sales in the second quarter of 1996 increased by 21% from the second quarter of 1995. For the first six months of 1996 net revenue decreased 35% to $1,091,000 from $1,687,000 during the same period in 1995. Product sales for the first six months of 1996 decreased 40% to $876,000 from $1,468,000 during the same period in 1995. The decrease in product sales is primarily due to the discontinuance of Scionex sales to third party customers. Cost of product sales decreased 7% to $832,000 in the three months ended June 30, 1996 from $893,000 in the three months ended June 30, 1995. For the six months ended June 30, 1996 cost of product sales decreased 11% to $1,622,000 from $1,830,000 in the same period in 1995. The decrease is primarily due to lower product sales in the first six months of 1996, although excess overhead caused by decreased production partially offset the reduction. Research and development expenses decreased 19% to $1,339,000 in the three months ended June 30, 1996 from $1,645,000 in the three months ended June 30, 1995. For the six months ended June 30, 1996 research and development expenses decreased 11% to $2,751,000 from $3,088,000 in the same period in 1995. The decrease was primarily due to lower clinical trial expenses in 1996, but was partially offset by an increase in product development material costs. The decrease in clinical trial costs is due to the completion of the enrollment in the U.S. clinical trials in 1995. Selling, general and administrative expenses increased 6% to $1,997,000 in the three months ended June 30, 1996 from $1,882,000 in the three months ended June 30, 1995. For the six months ended June 30, 1996 selling, general and administrative expenses increased 4% to $3,611,000 from $3,473,000 in the same period in 1995. The increase was primarily due to increased sales and marketing expense in anticipation of the U.S. TUNA product launch. Sales and administrative personnel were hired throughout 1996 in preparation of the TUNA introduction. Total operating expenses in the three months ended June 30, 1996 decreased 6% to $4,168,000 from $4,420,000 in the three months ended June 30, 1995. Total operating expenses for the first six months of 1996 decreased 5% to $7,984,000 from $8,391,000 in the same period in 1995. Page 10 of 17 Other income for the three and six months ended June 30, 1996 was $11,000 and $8,000, respectively, compared to other expense of $182,000 and $321,000 for the comparable periods in 1995. This change is primarily due to interest earned on proceeds from the IPO and Convertible Notes offsetting interest expense. The net loss for the three and six month periods ended June 30, 1996 was $3,554,000 and $6,885,000, respectively, compared to $3,692,000 and $7,025,000 for the comparable periods in 1995. Liquidity and Capital Resources At June 30, 1996 the Company's cash, cash equivalents and short-term investments were $13,805,000, compared to $13,690,000 at December 31, 1995. In June 1995 the Company completed an initial public offering of 3,565,000 shares of Common Stock at a price to the public of $6.50 per share. The net proceeds of the offering to the Company, after deducting underwriting discounts and expenses, were $20.8 million. In March 1996, the Company completed the issuance of $10.1 million in convertible subordinated. As of June 30, 1996 all of the $10.1 million in principal and accrued interest on these notes had been converted into an aggregate of 1,375,676 shares of Common Stock. In April 1995, the Company obtained a $3,000,000 secured credit facility. To date, the Company has borrowed $3,000,000 under this facility. Borrowings bear interest at the prime rate plus 3% per annum plus additional lump-sum interest of 15% of each borrowing, payable at maturity. Repayment is based on a three year amortization schedule. In January and February 1996, the Company repaid $2,700,000 in previously outstanding notes payable issued by the Company in January and February 1995. Interest on these notes accrued at the prime rate. During the six months ended June 30, 1996 and 1995, VidaMed consumed cash in operations of $5,896,000 and $5,774,000, respectively. The changes in cash used in operations were due to increased selling, general and administrative expenses to support increased operations offset by the payment of clinical trial costs. Although VidaMed believes that the proceeds from its initial public offering, the issuance of convertible notes and cash generated from the sale of products will be sufficient to meet the Company's operating and capital requirements through the next twelve months, there can be no assurance that the Company will not require additional financing within this time frame. There can be no assurance that additional financing, if required, will be available on satisfactory terms or at all. In any event, VidaMed may in the future seek to raise additional funds through bank facilities, debt or equity offerings or other sources of capital. VidaMed's future liquidity and capital requirements will depend on numerous other factors, including progress of clinical trials, actions related to regulatory and reimbursement matters, and the extent to which the TUNA system gains market acceptance. Page 11 of 17 VIDAMED, INC. PART II: OTHER INFORMATION Item 1. Legal Proceedings None Item 2. Changes in Securities See page 14 Item 3. Defaults upon Senior Securities None Item 4. Submission of Matters to a Vote of Security Holders See page 14 Item 5. Other Information None Item 6. Exhibits and Reports on Form 8-K a) Exhibits (11.1) Statement Re: Computation of Net Loss Per Share (27.1) Financial Data Schedule b) Reports on Form 8-K. On June 13, 1996, the Company filed a report on Form 8-K presenting certain interim financial information for the purpose of demonstrating compliance with the requirements for continued listing of the Company's Common Stock on the Nasdaq National Market. Page 12 of 17 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. VIDAMED, INC. Date: August 12, 1996 By: /s/ James A. Heisch --------------------------- ------------------------ James A. Heisch President, Chief Executive Officer, Chief Financial Officer (Principal Financial Officer) Date: August 12, 1996 By: /s/ Thomas M. Fahey --------------------------- ------------------------ Thomas M. Fahey Director of Finance (Principal Accounting Officer) Page 13 of 17 PART II. OTHER INFORMATION Item 2. CHANGES IN SECURITIES During the second quarter of 1996 the entire $10.1 million of Convertible Notes issued in the first quarter of 1996 were converted into VidaMed Common Stock. The $10.1 million of Notes and accrued interest were converted into 1,375,676 shares of Common Stock. Item 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS The Company solicited proxies for an annual meeting of stockholders on June 20, 1996 to all of the Company's stockholders. The election of all directors was conducted and the following nominees were elected: David L. Douglass, Stuart D. Edwards, James A. Heisch, Lawrence G. Mohr, Jr., Joseph E. Oesterling, M.D. and Michael H. Spindler. The vote with respect to each nominee was as follows: Votes Votes Name For Withheld -------------------------- ----------- ---------- David L. Douglass 6,796,697 286,410 Stuart D. Edwards 6,796,197 286,910 James A. Heisch 6,796,697 286,410 Lawrence G. Mohr, Jr. 6,796,697 286,410 Joseph E. Oesterling, M.D. 6,798,958 284,149 Michael H. Spindler 6,798,958 284,149 The Company's Stock Plan was amended and the number of shares of Common Stock reserved for issuance under the plan was increased by 1,400,000 to 2,733,334 with 5,360,967 votes in favor, 260,225 votes against and 287,443 abstentions. The Company's Director Stock Plan was amended and the number of shares of Common Stock reserved for issuance under the plan was increased by 100,000 to 200,000 with 5,425,191 votes in favor, 224,904 votes against and 281,734 abstentions. Ernst & Young LLP was ratified as the independent auditors of the Company for the fiscal year ending December 31, 1996 with 6,808,017 votes in favor, 8,576 votes against and 266,514 abstentions. Page 14 of 17 INDEX TO EXHIBITS EXHIBIT NUMBER DESCRIPTION 11.1 Statement regarding computation of net loss per share 27.1 Financial Data Schedule Page 15 of 17 EX-11.1 2 STATEMENT RE: COMPUTATION OF NET LOSS PER SHARE EXHIBIT 11.1 VIDAMED, INC. STATEMENT RE: COMPUTATION OF NET LOSS PER SHARE
Three Months Ended Six Months Ended June 30, June 30, ---------------------------- --------------------------- 1996 1995 1996 1995 ------------- ------------ ------------ ------------- Calculation of shares outstanding for computing net loss per share: Weighted average shares of common stock outstanding 10,420,000 2,392,000 9,885,000 1,827,000 SEC Staff Accounting Bulletin Nos. 55, 64 and 83 "cheap stock" - - - 535,000 ------------- ------------ ------------ ------------- Total shares used in calculation of net loss per share 10,420,000 2,392,000 9,885,000 2,362,000 ============= ============ ============ ============= Net loss $(3,554,000) $(3,692,000) $(6,885,000) $(7,025,000) ============= ============ ============ ============= Net loss per share ($.34) ($1.54) ($.70) ($2.97) ============= ============ ============ ============= Calculation of shares outstanding for computing pro forma net loss per share: Shares used in computing net loss per share: Adjusted to reflect the effect of the assumed conversion of Preferred Stock from the date of issuance - 3,468,000 - 3,468,000 ------------- ------------ ------------ ------------- Shares used in computing pro forma net loss per share - 5,860,000 - 5,830,000 ============= ============ ============ ============= Net loss - $(3,692,000) - $(7,025,000) ============= ============ ============ ============= Pro forma net loss per share - ($.63) - ($1.21) ============= ============ ============ =============
Page 16 of 17 EX-27 3 FINANCIAL DATA SCHEDULE
5 1,000 6-MOS DEC-31-1996 JUN-30-1996 6,852 6,953 480 118 1,066 15,616 4,983 2,287 18,534 6,737 1,653 11 0 0 9,938 18,534 876 1,091 1,622 6,362 (31) 75 (11) (6,851) 34 (6,885) 0 0 0 (6,885) (0.70) (0.70)
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