Filed Pursuant to Rule 424(b)(3)
File Number 333-142130
PROSPECTUS SUPPLEMENT NO. 21
Prospectus Supplement No. 21
to Prospectus dated June 22, 2007
as supplemented by
Prospectus Supplement No. 1 dated July 13, 2007
and
Prospectus Supplement No. 2 dated August 20, 2007
and
Prospectus Supplement No. 3 dated October 25, 2007
and
Prospectus Supplement No. 4 dated November 19, 2007
and
Prospectus Supplement No. 5 dated January 30, 2008
and
Prospectus Supplement No. 6 dated March 5, 2008
and
Prospectus Supplement No. 7 dated April 4, 2008
and
Prospectus Supplement No. 8 dated May 21, 2008
and
Prospectus Supplement No. 9 dated August 8, 2008
and
Prospectus Supplement No. 10 dated August 15, 2008
and
Prospectus Supplement No. 11 dated August 22, 2008
and
Prospectus Supplement No. 12 dated August 29, 2008
and
Prospectus Supplement No. 13 dated November 17, 2008
and
Prospectus Supplement No. 14 dated April 16, 2009
and
Prospectus Supplement No. 15 dated May 21, 2009
and
Prospectus Supplement No. 16 dated August 17, 2009
and
Prospectus Supplement No. 17 dated November 20, 2009
and
Prospectus Supplement No. 18 dated February 4, 2010
and
Prospectus Supplement No. 19 dated April 7, 2010
and
Prospectus Supplement No. 20 dated May 17, 2010
QUANTRX BIOMEDICAL CORPORATION
This Prospectus Supplement No. 21 supplements our prospectus dated June 22, 2007, as supplemented by Prospectus Supplement No. 1 dated July 13, 2007, Prospectus Supplement No. 2 dated August 20, 2007, Prospectus Supplement No. 3 dated October 25, 2007, Prospectus Supplement No. 4 dated November 19, 2007, Prospectus Supplement No. 5 dated January 30, 2008, Prospectus Supplement No. 6 dated March 5, 2008, Prospectus Supplement No. 7 dated April 4, 2008, Prospectus Supplement No. 8 dated May 21, 2008, Prospectus Supplement No. 9 dated August 8, 2008, Prospectus Supplement No. 10 dated August 15, 2008, Prospectus Supplement No. 11 dated August 22, 2008, Prospectus Supplement No. 12 dated August 29, 2008, Prospectus No. 13 dated November 17, 2008, Prospectus Supplement No. 14 dated April 16, 2009, Prospectus Supplement No. 15 dated May 21, 2009, Prospectus Supplement No. 16 dated August 17, 2009, Prospectus Supplement No. 17 dated November 20, 2009, Prospectus No. 18 dated February 4, 2010, Prospectus Supplement No. 19 dated April 7, 2010, and Prospectus Supplement No. 20 dated May 17, 2010. The shares of our common stock that are the subject of the prospectus have been registered to permit their resale to the public by the selling stockholders named in the prospectus. We are not selling any shares of common stock in this offering and therefore will not receive any proceeds from such offering, except upon the exercise of warrants.
Our common stock is quoted on the Over-The-Counter Bulletin Board under the symbol QTXB.OB. The high and low prices for shares of our common stock on August 6, 2010, were $0.17 and $0.17 per share, respectively, based upon bids that represent prices quoted by broker-dealers on the OTC Bulletin Board.
This Prospectus Supplement includes the Quarterly Report on Form 10-Q filed by us with the U.S. Securities and Exchange Commission on August 6, 2010 and the Current Reports on Form 8-K filed by us with the U.S. Securities and Exchange Commission on July 22, 2010 and June 9, 2010.
YOU SHOULD READ THE PROSPECTUS AND THIS PROSPECTUS SUPPLEMENT NO. 21 CAREFULLY BEFORE YOU INVEST, INCLUDING THE RISK FACTORS THAT BEGIN ON PAGE 4 OF THE PROSPECTUS.
NEITHER THE U.S. SECURITIES AND EXCHANGE COMMISSION NOR ANY STATE SECURITIES COMMISSION HAS APPROVED OR DISAPPROVED OF THESE SECURITIES OR DETERMINED IF THIS PROSPECTUS SUPPLEMENT IS TRUTHFUL OR COMPLETE. ANY REPRESENTATION TO THE CONTRARY IS A CRIMINAL OFFENSE.
The date of this Prospectus Supplement is August 9, 2010.
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 10-Q
x | QUARTERLY REPORT UNDER SECTION 13 OR 15 (d) OF THE SECURITIES |
EXCHANGE ACT OF 1934
For the quarterly period ended June 30, 2010
OR
¨ | TRANSITION REPORT PURSUANT TO SECTION 13 OR 15 (d) OF THE SECURITIES |
EXCHANGE ACT OF 1934
For the transition period from _________to_________
Commission File No. 0-17119
QUANTRX BIOMEDICAL CORPORATION
(Exact Name of Registrant as Specified in Its Charter)
Nevada | 33-0202574 | |
(State or Other Jurisdiction of | (I.R.S. Employer | |
Incorporation or Organization) | Identification Number) |
100 S. Main Street, Suite 300, Doylestown, PA 18901
(Address of Principal Executive Offices) (Zip Code)
(267) 880-1595
(Registrant’s Telephone Number, Including Area Code)
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 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
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). ¨ Yes ¨ No
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act.:
Large accelerated filer ¨ | Accelerated filer ¨ |
Non-accelerated filer ¨ | Smaller reporting company x |
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). ¨ Yes x No
The number of shares outstanding of the issuer’s common stock as of August 6, 2010 was 44,427,630.
PART I - FINANCIAL INFORMATION | ||
ITEM 1. | Financial Statements | |
Consolidated Balance Sheets as of June 30, 2010 (Unaudited) and December 31, 2009 | 4 | |
Consolidated Statements of Operations (Unaudited) for the three and six months ended June 30, 2010 and 2009 | 5 | |
Consolidated Statements of Cash Flows (Unaudited) for the six months ended June 30, 2010 and 2009 | 6 | |
Condensed Notes to (Unaudited) Consolidated Financial Statements | 7 | |
ITEM 2. | Management’s Discussion and Analysis of Financial Condition and Results of Operations | 18 |
ITEM 4. | Controls and Procedures | 25 |
PART II - OTHER INFORMATION | ||
ITEM 1. | Legal Proceedings | 25 |
ITEM 2. | Unregistered Sales of Equity Securities; and Use of Proceeds | 26 |
ITEM 3. | Defaults Upon Senior Securities | 26 |
ITEM 4. | Reserved | 26 |
ITEM 5. | Other Information | 26 |
ITEM 6. | Exhibits | 26 |
Signatures | 27 |
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PART I – FINANCIAL INFORMATION
CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING INFORMATION
THIS QUARTERLY REPORT ON FORM 10-Q, INCLUDING EXHIBITS HERETO, CONTAINS FORWARD-LOOKING STATEMENTS WITHIN THE MEANING OF SECTION 27A OF THE SECURITIES ACT OF 1933, AS AMENDED, AND SECTION 21E OF THE SECURITIES EXCHANGE ACT OF 1934, AS AMENDED. THESE FORWARD-LOOKING STATEMENTS ARE TYPICALLY IDENTIFIED BY THE WORDS “ANTICIPATES,” “BELIEVES,” “EXPECTS,” “INTENDS,” “FORECASTS,” “PLANS,” “ESTIMATES,” “MAY,” “FUTURE,” “STRATEGY,” OR WORDS OF SIMILAR MEANING. VARIOUS FACTORS COULD CAUSE ACTUAL RESULTS TO DIFFER MATERIALLY FROM THOSE EXPRESSED IN THE FORWARD-LOOKING STATEMENTS; INCLUDING THOSE DESCRIBED IN “RISK FACTORS” IN OUR ANNUAL REPORT ON FORM 10-K FOR THE YEAR ENDED DECEMBER 31, 2009. WE ASSUME NO OBLIGATIONS TO UPDATE THESE FORWARD-LOOKING STATEMENTS TO REFLECT NEW INFORMATION, ACTUAL RESULTS, CHANGES IN ASSUMPTIONS, OR CHANGES IN OTHER FACTORS, EXCEPT AS REQUIRED BY LAW.
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ITEM 1. | Financial Statements |
QUANTRX BIOMEDICAL CORPORATION |
CONSOLIDATED BALANCE SHEETS |
June 30, 2010 | December 31, 2009 | |||||||
(unaudited) | ||||||||
ASSETS | ||||||||
Current Assets: | ||||||||
Cash and cash equivalents | $ | 128,101 | $ | 376,211 | ||||
Accounts receivable | 160,315 | 41,128 | ||||||
Accounts receivable – related party | 380,652 | 31,500 | ||||||
Interest receivable – related party | 55,689 | 47,689 | ||||||
Other receivable | 63,000 | - | ||||||
Inventories | 4,578 | 4,681 | ||||||
Prepaid expenses | 31,328 | 128,228 | ||||||
Note receivable – related party | 200,000 | 200,000 | ||||||
Total Current Assets | 1,023,663 | 829,437 | ||||||
Investments | 200,000 | 200,000 | ||||||
Investment in joint venture | - | 63,601 | ||||||
Property and equipment, net | 144,346 | 179,590 | ||||||
Intangible assets, net | 50,936 | 59,780 | ||||||
Security deposits | 11,093 | 11,093 | ||||||
Total Assets | $ | 1,430,038 | $ | 1,343,501 | ||||
LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT) | ||||||||
Current Liabilities: | ||||||||
Accounts payable | $ | 1,001,613 | $ | 749,225 | ||||
Accounts payable – related party | 143,987 | - | ||||||
Accrued expenses | 385,000 | 233,000 | ||||||
Deferred revenue | 8,172 | - | ||||||
Deferred revenue – related party | - | 337,160 | ||||||
Security deposits | 2,000 | 2,000 | ||||||
Total Current Liabilities | 1,540,772 | 1,321,385 | ||||||
Notes payable, long-term | 44,000 | 44,000 | ||||||
Total Liabilities | 1,584,772 | 1,365,385 | ||||||
Commitments and Contingencies | - | - | ||||||
Stockholders’ Equity (Deficit): | ||||||||
Preferred stock; $0.01 par value, 25,000,000 authorized shares; Series A-1 convertible preferred shares: 4,060,397 shares issued and outstanding | 40,604 | 40,604 | ||||||
Common stock; $0.01 par value; 150,000,000 authorized; 44,427,630 shares issued and outstanding | 444,276 | 444,276 | ||||||
Additional paid-in capital | 47,787,597 | 47,756,355 | ||||||
Accumulated deficit | (48,427,211 | ) | (48,263,119 | ) | ||||
Total Stockholders’ Equity (Deficit) | (154,734 | ) | (21,884 | ) | ||||
Total Liabilities and Stockholders’ Equity (Deficit) | $ | 1,430,038 | $ | 1,343,501 |
The accompanying condensed notes are an integral part of these interim financial statements.
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QUANTRX BIOMEDICAL CORPORATION |
CONSOLIDATED STATEMENTS OF OPERATIONS |
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||||||
(unaudited) | (unaudited) | (unaudited) | (unaudited) | |||||||||||||
Revenues: | ||||||||||||||||
Revenues | $ | 19,428 | $ | 172,415 | $ | 29,438 | $ | 331,902 | ||||||||
Revenues – related party | 621,612 | - | 1,270,893 | - | ||||||||||||
Total Revenues | 641,040 | 172,415 | 1,300,331 | 331,902 | ||||||||||||
Costs and Operating Expenses: | ||||||||||||||||
Cost of goods sold (excluding depreciation and amortization) | 97 | 112 | 129 | 1,463 | ||||||||||||
Sales, general and administrative | 279,526 | 326,745 | 583,103 | 861,635 | ||||||||||||
Professional fees | 178,879 | 40,141 | 428,430 | 89,168 | ||||||||||||
Research and development | 529,087 | 126,465 | 1,133,433 | 284,277 | ||||||||||||
Amortization | 4,540 | 5,852 | 8,844 | 11,704 | ||||||||||||
Depreciation | 15,909 | 17,318 | 32,815 | 35,144 | ||||||||||||
Total Costs and Operating Expenses | 1,008,038 | 516,633 | 2,186,754 | 1,283,391 | ||||||||||||
Loss from Operations | (366,998 | ) | (344,218 | ) | (886,423 | ) | (951,489 | ) | ||||||||
Other Income (Expense): | ||||||||||||||||
Interest and dividend income | 5,127 | 6,086 | 11,387 | 29,219 | ||||||||||||
Interest expense | (1,599 | ) | (205,517 | ) | (2,777 | ) | (383,593 | ) | ||||||||
Rental income | 4,125 | 5,665 | 8,250 | 11,535 | ||||||||||||
Amortization of debt discount to interest expense | - | (128,102 | ) | - | (272,146 | ) | ||||||||||
Amortization of deferred finance costs to interest expense | - | - | - | (8,693 | ) | |||||||||||
Loss from deconsolidation of subsidiary | - | (43,286 | ) | - | (43,286 | ) | ||||||||||
Loss from deconsolidated subsidiary | - | (41,533 | ) | - | (272,579 | ) | ||||||||||
Loss from joint venture | - | - | (63,601 | ) | - | |||||||||||
Gain on sale of investments | 501,250 | 751,250 | ||||||||||||||
Net gain on disposition of assets | 20,251 | - | 17,822 | - | ||||||||||||
Total Other Income (Expense), net | 529,154 | (406,687 | ) | 722,331 | (939,543 | ) | ||||||||||
Income (Loss) Before Taxes | 162,156 | (750,905 | ) | (164,092 | ) | (1,891,032 | ) | |||||||||
Provision for Income Taxes | - | - | - | - | ||||||||||||
Net Income (Loss) | $ | 162,156 | $ | (750,905 | ) | $ | (164,092 | ) | $ | (1,891,032 | ) | |||||
Basic and Diluted Net Loss per Common Share | $ | nil | $ | (0.02 | ) | $ | nil | $ | (0.04 | ) | ||||||
Basic and Diluted Weighted Average Shares Used in per Share Calculation | 44,427,630 | 43,221,312 | 44,427,630 | 43,109,536 |
The accompanying condensed notes are an integral part of these interim financial statements.
5
QUANTRX BIOMEDICAL CORPORATION |
CONSOLIDATED STATEMENTS OF CASH FLOWS |
Six Months Ended June 30, | ||||||||
2010 | 2009 | |||||||
(unaudited) | (unaudited) | |||||||
CASH FLOWS FROM OPERATING ACTIVITIES: | ||||||||
Net loss | $ | (164,092 | ) | $ | (1,891,032 | ) | ||
Adjustments to reconcile net loss to net cash used by operating activities: | ||||||||
Depreciation and amortization | 41,659 | 46,848 | ||||||
Interest expense related to amortization of non-cash discount, non-cash beneficial conversion feature and deferred financing costs | - | 280,839 | ||||||
Expenses related to employee stock based compensation | 30,992 | 241,604 | ||||||
Expenses (remeasurement adjustment) related to options issued to non-employees | - | (1,667 | ) | |||||
Expenses (remeasurement adjustment) related to common stock warrants issued for consulting | 250 | 7,333 | ||||||
Non-cash incremental fair value of modified warrants issued for interest | - | 6,250 | ||||||
Non-cash fair value of warrants issued for interest | - | 72,075 | ||||||
Non-cash fair value of common stock issued for interest | - | 78,000 | ||||||
Loss from deconsolidation of subsidiary | - | 43,286 | ||||||
Loss from deconsolidated subsidiary | - | 272,579 | ||||||
Loss from joint venture | 63,601 | - | ||||||
Net gain on disposition of assets and investments | (769,072 | ) | - | |||||
Issuance of convertible notes for accrued interest | - | 175,895 | ||||||
Interest income settled in common stock of former subsidiary | - | (18,000 | ) | |||||
(Increase) decrease in: | ||||||||
Accounts receivable | (468,339 | ) | (61,048 | ) | ||||
Interest receivable | (8,000 | ) | (8,000 | ) | ||||
Other receivable | (63,000 | ) | - | |||||
Inventories | 103 | 1,594 | ||||||
Prepaid expenses | 96,900 | 18,711 | ||||||
Deposits | - | 581 | ||||||
Security deposits | - | (426 | ) | |||||
Increase (decrease) in: | ||||||||
Accounts payable | 396,375 | 122,226 | ||||||
Accrued expenses | 152,000 | 44,221 | ||||||
Deferred revenue | (328,988 | ) | (27,777 | ) | ||||
Net Cash Used by Operating Activities | (1,019,611 | ) | (595,908 | ) | ||||
CASH FLOWS FROM INVESTING ACTIVITIES: | ||||||||
Cash proceeds from sale of investment securities | 751,250 | - | ||||||
Cash paid for asset acquisition deposit | - | (125,000 | ) | |||||
Cash proceeds from sale of equipment | 20,251 | - | ||||||
Cash advances to subsidiary prior to deconsolidation | - | (13,800 | ) | |||||
Net Cash Provided (Used) by Investing Activities | 771,501 | (138,800 | ) | |||||
CASH FLOWS FROM FINANCING ACTIVITIES: | ||||||||
Proceeds from issuance of promissory notes | - | 350,000 | ||||||
Proceeds from issuance of senior secured convertible notes | - | 425,000 | ||||||
Proceeds from issuance of senior secured promissory notes | - | 250,000 | ||||||
Repayment of short-term debt | - | (65,000 | ) | |||||
Payments on loan payable used to finance equipment purchase | - | (5,731 | ) | |||||
Net Cash Provided by Financing Activities | - | 954,269 | ||||||
Net Increase (Decrease) in Cash and Cash Equivalents | (248,110 | ) | 219,561 | |||||
Net Cash of Deconsolidated Subsidiary | (413 | ) | ||||||
Cash and Cash Equivalents, Beginning of Period | 376,211 | 66,226 | ||||||
Cash and Cash Equivalents, End of Period | $ | 128,101 | $ | 285,374 | ||||
Supplemental Cash Flow Disclosures: | ||||||||
Interest expense paid in cash | $ | 2,777 | $ | 16,510 | ||||
Income tax paid | $ | - | $ | - | ||||
Supplemental Disclosure of Non-Cash Activities: | ||||||||
Fair value of common stock issued with convertible notes | $ | - | $ | 85,803 | ||||
Fair value of warrants issued with convertible notes | $ | - | $ | 33,487 | ||||
Fair value of beneficial conversion feature embedded in convertible notes | $ | - | $ | 6,325 | ||||
Fair value of common stock issued with promissory notes | $ | - | $ | 28,488 | ||||
Fair value of warrants issued with promissory notes | $ | - | $ | 39,666 | ||||
Increase in payables related to purchase of fixed assets | $ | - | $ | 3,000 | ||||
Exchange of promissory notes for senior secured convertible note | $ | - | $ | 707,890 | ||||
Elimination of deconsolidated subsidiary accounts: | ||||||||
Prepaid expenses | $ | - | $ | 104,506 | ||||
Property and equipment, net | $ | - | $ | 274,404 | ||||
Intangible assets, net | $ | - | $ | 1,907,193 | ||||
Deposits | $ | - | $ | 3,565 | ||||
Accounts payable | $ | - | $ | 1,311,839 | ||||
Accrued expenses | $ | - | $ | 215,050 | ||||
Additional paid-in-capital | $ | - | $ | 479,129 |
The accompanying condensed notes are an integral part of these interim financial statements.
6
QUANTRX BIOMEDICAL CORPORATION |
CONDENSED NOTES TO CONSOLIDATED FINANCIAL STATEMENTS |
June 30, 2010 |
Description of Business and Basis of Presentation
QuantRx Biomedical Corporation was incorporated on December 5, 1986, in the State of Nevada. The Company’s principal business office is located at 100 South Main Street, Suite 300, Doylestown, Pennsylvania. QuantRx also has a research and development facility in Portland, Oregon.
QuantRx is a diagnostics company focused on the development and commercialization of innovative diagnostic products for the Point-of-Care (POC) markets based on its patented technology platforms for the worldwide healthcare industry. These platforms include: RapidSense® and Q-Reader™ point-of-care testing products based on QuantRx’s core intellectual property related to lateral flow techniques for the consumer and healthcare professional markets and PAD technology for the consumer markets for the treatment of hemorrhoids, minor vaginal infection, urinary incontinence, and other medical needs. Additionally, the Company has made significant investments in a company developing Single Nucleotide Polymorphism (SNP) chips, genome-based diagnostic chips for the next generation of genomic and proteomic diagnostic markets and in its formerly majority-owned subsidiary, FluoroPharma, Inc. (FluoroPharma), a company developing molecular imaging agents for Positron Emission Tomography (PET) and fluorescence imaging with initial application in cardiovascular disease, to provide clinical support for the Company’s POC cardiac diagnostics.
The Company’s overall growth strategy is to: (i) leverage its broad-based intellectual property (IP) and patent portfolio to develop new and innovative diagnostic products; (ii) commercialize products through corporate partners and distributors; and (iii) contract manufacturing to third parties while maintaining control over the manufacturing process.
The interim consolidated financial statements are unaudited; however, in the opinion of management, they include all adjustments (consisting only of normal recurring adjustments) necessary for a fair statement of financial position and results of operations for the periods reported. The interim financial statements have been prepared pursuant to the rules and regulations of the Securities and Exchange Commission. Certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States of America have been condensed or omitted pursuant to such rules and regulations, although QuantRx believes that the disclosures included herein are adequate to make the information presented not misleading. Operating results for the periods presented are not necessarily indicative of future results. These interim financial statements should be read in conjunction with the financial statements and notes to financial statements included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2009, which was filed with the SEC on March 31, 2010.
On July 30, 2009, QuantRx and NuRx Pharmaceuticals, Inc. jointly formed QN Diagnostics, LLC, a Delaware limited liability company, with each company owning 50% of the joint venture. The purpose of the joint venture is to develop and commercialize products incorporating our lateral flow strip technology and related lateral flow strip readers. See Note 3 and 14.
7
These consolidated financial statements include the accounts of the Company and its formerly majority-owned subsidiary, FluoroPharma. Effective May 5, 2009, QuantRx and FluoroPharma executed transactions that resulted in QuantRx no longer having a controlling ownership interest, resulting in the deconsolidation of FluoroPharma. QuantRx has restated its financial statements as of January 1, 2009, to reflect the results of its former subsidiary as a one-line item, and beginning May 5, 2009, our financial statements reflect our investment in FluoroPharma under the equity method of accounting. See Note 5 for additional information. When used in these notes, the terms “Company,” “we,” “our,” “ours,” or “us” mean QuantRx Biomedical Corporation, a Nevada corporation.
1. | Management Statement Regarding Going Concern |
The Company has not generated sufficient revenues from operations to meet its operating expenses. For this reason, the Company has historically financed its operations primarily through issuances of equity securities and the proceeds of debt instruments. In the past, the Company has also provided for its cash needs by issuing common stock, options and warrants for certain operating costs, including consulting and professional fees.
The Company formed a strategic joint venture (See Note 3) to fund the development and commercialization of its lateral flow based products; however, management believes that given the cash position of the joint venture and the current economic environment, there is still doubt about our ability to continue as a going concern. The Company has disposed of certain assets and investments to fund current operations. See Note 5. Additionally, the Company is pursuing other funding options, including equity offerings and debt financings; however, there can be no assurance that we will be successful in our efforts to raise additional capital or to raise funds through additional divestures.
Management believes that the successful growth and operation of the Company’s business is dependent upon our ability to do any or all of the following:
· | finalize development and commercialization of our products; |
· | achieve synergy and financial stability within our joint venture to allow for commercialization of products and continued development of products in its pipeline; |
· | obtain adequate sources of debt or equity financing to pay unfunded operating expenses and fund certain long-term business operations until commercialization becomes profitable; |
· | manage or reduce operating expenses, including potential consolidation of operations in Portland, Oregon; and |
· | develop new relationships with product distributors and other points of distribution for the Company’s products; |
There can be no assurance that the Company will be successful in achieving its long-term plans as set forth above, or that such plans, if consummated, will enable the Company to obtain profitable operations or continue in the long-term as a going concern.
8
2. | Summary of Significant Accounting Policies |
Accounting for Share-Based Payments
QuantRx follows the provisions of ASC Topic 718, which establishes the accounting for transactions in which an entity exchanges equity securities for services and requires companies to expense the estimated fair value of these awards over the requisite service period. QuantRx uses the Black-Scholes option pricing model in determining fair value. Accordingly, compensation cost has been recognized using the fair value method and expected term accrual requirements as prescribed, which resulted in employee stock-based compensation expense for three and six months ended June 30, 2010 of $7,950 and $30,992, respectively and $14,125 and $241,604 for the three and six months ended June 30, 2009, respectively.
Black Scholes Option Pricing Model
The following assumptions were determined at the beginning of each year and have been utilized in all Black Scholes calculations for each year:
2010 | 2009 | |||||||
Risk-free interest rate | 2.43 | % | 3.24 | % | ||||
Expected volatility | 72 | % | 70 | % | ||||
Dividend yield | 0 | % | 0 | % |
Earnings per Share
The Company computes net income (loss) per common share in accordance with ASC Topic 260. Net income (loss) per share is based upon the weighted average number of outstanding common shares and the dilutive effect of common share equivalents, such as options and warrants to purchase common stock, convertible preferred stock and convertible notes, if applicable, that are outstanding each year. Basic and diluted earnings per share were the same at the reporting dates of the accompanying financial statements, as all common stock equivalents outstanding for the three months ended June 30, 2010 were deemed to be antidilutive; moreover, including common stock equivalents in the calculation of diluted earnings per share would have been antidilutive for the six months ended June 30, 2010 and the three and six months ended June 30, 2009.
As of June 30, 2010, the Company had outstanding options exercisable for 2,795,500 shares of its common stock, warrants exercisable for 12,911,466 shares of its common stock, and preferred shares convertible into 8,120,794 shares of its common stock. The above options, warrants, and preferred shares were deemed to be antidilutive for the three and six months ended June 30, 2010.
As of June 30, 2009, the Company had outstanding options exercisable for 2,280,500 shares of its common stock, warrants exercisable for 9,643,434 shares of its common stock, and debt securities convertible into 7,833,531 shares of its common stock. The above options, warrants, and convertible debt securities were deemed to be antidilutive for the three and six months ended June 30, 2009.
9
Fair Value
The Company has adopted ASC Topic 820, “Fair Value Measurements and Disclosures” for both financial and nonfinancial assets and liabilities. We have not elected the fair value option for any of our assets or liabilities.
Noncontrolling Interest
In January 2009, we adopted an amendment to ASC Topic 810 “Consolidation”, which required us to make certain changes to the presentation of our financial statements. This amendment requires noncontrolling interests to be treated as a separate component of equity, not as a liability or other item outside of permanent equity. Upon a loss of control, the interest sold, as well as any interest retained, is required to be measured at fair value, with any gain or loss recognized in earnings. The statement requires that the noncontrolling interest continue to be attributed its share of losses even if that attribution results in a deficit noncontrolling interest balance; if this would result in a material change to consolidated net income, pro forma financial information is required. As of January 1, 2009, the Company presented its financial statements in accordance with this statement. However, on May 5, 2009, QuantRx and FluoroPharma reorganized their relationship by terminating their investment agreement and related agreements. The termination of these investment agreements, which were originally executed on March 10, 2006, allowed FluoroPharma to close an equity financing with third party investors. In conjunction with the termination of these agreements and the additional investment in FluoroPharma by third parties, QuantRx agreed to convert all outstanding receivables from FluoroPharma into common stock of FluoroPharma. As a result of these transactions and the third party investment, QuantRx’s ownership interest in FluoroPharma’s issued and outstanding capital stock was reduced to a noncontrolling interest, which resulted in deconsolidation and a loss at deconsolidation in accordance with ASC 810. See Note 5 for additional details.
Recent Accounting Pronouncements
In April 2010, the FASB issued ASU No. 2010-17, “Revenue Recognition – Milestone Method (Topic 605).” This ASU provides guidance on defining a milestone and determining when it may be appropriate to apply the milestone method of revenue recognition for research and development transactions. This update will be effective in the second quarter of 2010. Adoption of this update is not anticipated to have a material impact on the Company’s consolidated results of operation or financial position.
In January 2010, the FASB issued ASU No. 2010-06, “Fair Value Measurements and Disclosures (Topic 820): Improving Disclosures about Fair Value Measurements.” This ASU requires additional disclosures about significant unobservable inputs and transfers within Level 1 and 2 measurements. Adoption of this update did not have any impact on the Company’s consolidated results of operation or financial position.
In October 2009, the FASB issued ASU No. 2009-13, “Revenue Recognition (ASC 605): Multiple-Deliverable Revenue Arrangements.” The guidance modifies the fair value requirements of ASC 605-25 by providing principles for allocation of consideration among its multiple elements, allowing more flexibility in identifying and accounting for separate deliverables under an arrangement. This guidance will be effective for revenue arrangements entered into or materially modified during 2010. Adoption of this update did not have any impact on the Company’s consolidated results of operation or financial position.
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Reclassifications
Certain reclassifications have been made in the presentation of the financial statements for the three and six months ended June 30, 2009 to conform to the presentation of the financial statements for the three and six months ended June 30, 2010.
Use of Estimates
The accompanying financial statements are prepared in conformity with accounting principles generally accepted in the United States of America, and include certain estimates and assumptions which affect the reported amounts of assets and liabilities at the date of the financial statements, and the reported amounts of revenues and expenses during the reporting period. Accordingly, actual results may differ from those estimates.
3. | Investment in Joint Venture – QN Diagnostics, LLC |
On July 30, 2009, QuantRx and NuRx Pharmaceuticals, Inc. (NuRx) jointly formed QN Diagnostics, LLC (QND), a Delaware limited liability company. QuantRx contributed certain intellectual property and other assets related to its lateral flow strip technology and related lateral flow strip reader technology with a fair value of $5,450,000, and NuRx contributed $5,000,000 in cash to QND. NuRx and QuantRx each own a 50% interest in QND. The purpose of the joint venture is to develop and commercialize products incorporating the lateral flow strip technology and related lateral flow strip readers.
The joint venture is currently managed by a board consisting of two QuantRx designees and two NuRx designees. Subject to certain exceptions, board decisions are made by majority vote, provided that QuantRx and NuRx have veto rights with respect to certain matters. Since QuantRx does not have control of the joint venture, QuantRx accounts for the investment in QND utilizing the equity method of accounting.
Under the terms of the agreements, QND made a $2,000,000 cash distribution to QuantRx. QuantRx is committed to further capital contributions aggregating $1.55 million, comprised of: milestone payments to PRIA Diagnostics (see Note 4) in QuantRx common stock (fair value of $750,000); transfer of fixed assets with a fair value of $100,000 at QND’s discretion; and a $700,000 sustaining capital contribution as required by QND. Subsequent sustaining capital contributions will be made by QuantRx and NuRx on an equal basis.
QuantRx and QND also entered into a one year Development and Services Agreement on July 30, 2009, pursuant to which QND pays a monthly fee to QuantRx in exchange for QuantRx providing all services related to the development, regulatory approval and commercialization of lateral flow products. The revenues recognized by QuantRx associated with the QND Development and Services Agreement in the three and six months ended June 30, 2010 were $621,612 and $1,270,893, and the expenses related to this agreement for the same periods were $621,612 and $1,270,893. Expenses are included in each appropriate expense category in the statement of operations. As of June 30, 2010 and December 31, 2009, deferred revenues related to the Development and Services Agreement with QND were $0 and $337,160, respectively. As of June 30, 2010 and December 31, 2009, accounts receivable from QND related to the Development and Services Agreement were $380,652 and $31,500, respectively. See Note 14, Subsequent Events.
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Summarized financial information of QND for the three and six months ended June 30, 2010, is estimated as follows: current assets: $280,000; noncurrent assets: $5,001,000; total assets: $5,281,000; current liabilities: $446,000; revenues and gross profit: $75,000 and $150,000; net loss: $671,000 and $1,383,000. For the three and six months ended June 30, 2010, QuantRx recorded losses from QND under the equity method of $0 and $63,601, representing the Company’s 50% portion of QND’s net loss, limited to the remaining asset value on QuantRx’s balance sheet. QuantRx is acting as an agent on behalf of QND in servicing a development agreement; QuantRx’s balance sheet reflects the outstanding receivable and offsetting payable to QND of $144,000 and $25,000 at June 30, 2010 and December 31, 2009, respectively. There were no other intercompany profits to eliminate.
4. | PRIA Asset Purchase Agreement |
On July 30, 2009, the Company executed an asset purchase agreement with PRIA Diagnostics, LLC, pursuant to which PRIA agreed to sell to QuantRx certain of PRIA’s patents, trademarks, other intellectual property assets and certain fixed assets. The aggregate purchase price for such assets was $725,000, comprised of cash and shares of QuantRx common stock.
Under the asset purchase agreement, QuantRx is required to make additional contingent payments, in the form of cash and common stock, upon the occurrence of certain milestone events. Such cash milestone payments will be made by QN Diagnostics (see Note 3). In addition, QND is required to pay royalties to PRIA on a quarterly basis upon the commercialization of a product utilizing the acquired technologies for five years from the initial sale date of the first such product sold. QuantRx also agreed under the asset purchase agreement to offer to PRIA the first opportunity to manufacture certain products utilizing the acquired technologies before entering into any agreement or arrangement with a third party to manufacture such products.
5. | Investments |
FluoroPharma, Inc.
On May 5, 2009, QuantRx and FluoroPharma reorganized their relationship by terminating their investment agreement and related agreements. The termination of these agreements, which were originally executed on March 10, 2006, allowed FluoroPharma to close an equity financing with third party investors. Contemporaneously, QuantRx agreed to convert all outstanding receivables from FluoroPharma, consisting of previously issued notes and related accrued interest and advances in the aggregate amount of $1,568,567, into 1,148,275 shares of common stock of FluoroPharma. As a result of these transactions and the third party investment, QuantRx’s ownership interest in FluoroPharma’s issued and outstanding capital stock was reduced to a noncontrolling interest, which resulted in deconsolidation. QuantRx has no continuing obligations or commitments to FluoroPharma.
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At May 5, 2009, QuantRx’s remaining net basis of the investment in FluoroPharma, inclusive of receivables from FluoroPharma, was $43,286, after taking into account previously recorded losses of $5,056,304 ($231,046 in the first quarter of 2009) related to the consolidated results of FluoroPharma. These losses have been included in our consolidated financial statements commencing April 1, 2007, the original date of consolidation, through May 4, 2009, and are net of losses allocated to the then noncontrolling interests as applicable. On May 5, subsequent to the execution of the aforementioned transactions which led to the deconsolidation of FluoroPharma, QuantRx’s ownership of the outstanding capital stock of FluoroPharma was reduced to a noncontrolling interest. At deconsolidation the fair market value of QuantRx’s remaining noncontrolling interest in FluoroPharma was $842,876, based on the third party investment; however, FluoroPharma had a deficit equity balance, which resulted in QuantRx writing off the remaining basis in the investment of $43,286 and recording a loss from deconsolidation of $43,286 in accordance with ASC Topic 810.
In the three and six months ended June 30, 2010, QuantRx entered into Security Purchase Agreements with certain qualified institutional buyers and accredited investors in which QuantRx sold 668,333 and 1,001,666 shares of FluoroPharma, Inc. class A common stock at a price of $0.75 per share for aggregate proceeds of $501,250 and $751,250, resulting in gains on disposition of $501,250 and $751,250, respectively. As of June 30, 2010, $63,000 related to the agreements is reflected as an other receivable. See Note 14, Subsequent Events.
Effective May 5, 2009, our financial statements reflect our investment in FluoroPharma under the equity method of accounting. As of June 30, 2010 and December 31, 2009, QuantRx owned approximately 27.98% and 39.81%, respectively, of the issued and outstanding capital stock of FluoroPharma. However, at June 30, 2010, due to FluoroPharma’s issuance of a separate class of common stock in 2009, QuantRx held 12.32% of the voting rights of FluoroPharma.
At June 30, 2010, FluoroPharma’s condensed financial information was estimated as follows: expenses and net losses for the three and six months ended June 30, 2010 were estimated at $150,000 and $305,000, respectively. QuantRx’s estimated allocation of the net loss of $48,000 and $107,000 for these periods was not recorded, in accordance with the equity method of accounting, since the remaining investment in FluoroPharma has a carrying value of $0.
6. | Intangible Assets |
Intangible assets as of the balance sheet dates consisted of the following:
June 30, 2010 | December 31, 2009 | |||||||
Licensed patents and patent rights | $ | 50,000 | $ | 50,000 | ||||
Patents | 41,004 | 41,004 | ||||||
Website development | 40,750 | 40,750 | ||||||
Less: accumulated amortization | (80,818 | ) | (71,974 | ) | ||||
Intangibles, net | $ | 50,936 | $ | 59,780 |
The Company’s intangible assets are carried at the legal cost to obtain them. Intangible assets are amortized using the straight line method over the estimated useful life. Useful lives are as follows: licensed patents and patent rights, eight to 15 years; patents, 17 years; technology license, five years; and website development costs, three years. Amortization expense totaled $4,540 and $8,844 for the three and six months ended June 30, 2010 and $5,852 and $11,704 for the three and six months ended June 30, 2009, respectively. Impairment will be considered in accordance with the Company’s impairment policy which requires at least an annual analysis. No impairment was recognized as of June 30, 2010.
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7. | Other Balance Sheet Information |
Components of selected captions in the accompanying balance sheets consist of:
June 30, 2010 | December 31, 2009 | |||||||
Prepaid expenses: | ||||||||
Prepaid consulting – related party | $ | - | $ | 83,375 | ||||
Prepaid insurance | 22,008 | 22,960 | ||||||
Prepaid rent | 5,309 | 16,533 | ||||||
Other | 4,011 | 5,360 | ||||||
Prepaid expenses | $ | 31,328 | $ | 128,228 | ||||
Property and equipment: | ||||||||
Computers and office furniture, fixtures and equipment | $ | 122,007 | $ | 124,877 | ||||
Machinery and equipment | 181,347 | 181,347 | ||||||
Leasehold improvements | 92,233 | 92,233 | ||||||
Less: accumulated depreciation | (251,241 | ) | (218,867 | ) | ||||
Property and equipment, net | $ | 144,346 | $ | 179,590 | ||||
Accrued expenses: | ||||||||
Payroll and related | $ | 327,000 | $ | 175,000 | ||||
Professional fees | 25,000 | 41,500 | ||||||
Other | 33,000 | 16,500 | ||||||
Accrued expenses | $ | 385,000 | $ | 233,000 |
8. | Deferred Revenue |
On May 19, 2008, QuantRx and CytoCore, Inc. entered into a worldwide distribution and supply agreement for specified PAD technology of QuantRx. The agreement specified monthly license fees during CytoCore’s expected development period and additional milestone payments based upon CytoCore’s achievement of certain development and sales milestones. QuantRx received an up-front, non-refundable payment of $100,000 upon execution of this agreement, which was recorded as deferred revenue and was amortized into revenue over the expected development period of the agreement, estimated as 18 months. QuantRx recognized revenue related to this agreement of $33,335 and $66,670 in the three and six months ended June 30, 2009. In the second quarter of 2010, CytoCore advanced an additional $20,000 toward an extension of this agreement in accordance with the original agreement. QuantRx recognized revenue of $11,828 in the second quarter of 2010 from this extension, with the remaining $8,172 recorded as deferred revenue at June 30, 2010.
9. | Short-term Notes Payable |
In July 2009, QuantRx made full settlement with all holders of QuantRx convertible and promissory notes, and obtained the release of all security interests in QuantRx assets granted to those note holders. In connection with the full settlement of these notes and the release of all liens in favor of such note holders, each note holder received either cash in an amount equal to the outstanding principal and accrued interest, shares of the newly created Series A-1 convertible preferred stock (see Note 10), or a combination of both. In the aggregate, $1,335,156 was paid and 4,060,397 shares of Series A-1 convertible preferred stock with a fair value of $4,060,397 were issued to the note holders to settle the outstanding $5,281,765 in convertible and promissory notes and $113,778 in related accrued interest. In the three and six months ended June 30, 2009, $203,698 and $380,384 in interest expense, $128,102 and $272,146 in amortization of debt discount and $0 and $8,693 in amortization of deferred finance costs was recorded, respectively.
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10. | Preferred Stock |
The Company has authorized 25,000,000 shares of preferred stock, of which 9,750,000 are designated Series A convertible preferred stock, $0.01 par value, and 10,000,000 are designated Series A-1 convertible preferred stock, $0.01 par value. The remaining 5,250,000 authorized preferred shares have not been designated by the Company. At June 30, 2010 and December 31, 2009, 4,060,397 shares of Series A-1 preferred stock were outstanding.
In the third quarter of 2009, the Company issued 4,060,397 shares of Series A-1 preferred stock to certain holders of the Company’s promissory notes in exchange for the cancellation of their respective notes and the releases of any security interests.
11. | Common Stock, Options and Warrants |
The Company has authorized 150,000,000 shares of its common stock, $0.01 par value. In December 2009, the shareholders of the Company approved an increase to authorized common stock from 75,000,000 to 150,000,000 shares. The increase took effect in January 2010.
In the first six months of 2010, no common stock, or options or warrants to purchase common stock were issued or granted.
2007 Incentive and Non-Qualified Stock Option Plan
The fair value of options granted under the Company’s 2007 Incentive and Non-Qualified Stock Option Plan is recorded as compensation expense over the vesting period, or, for performance based awards, the expected service term. Total compensation cost related to QuantRx’s employee options was $7,950 and $30,992 for the three and six months ended June 30, 2010 and $14,125 and $87,704 for the three and six months ended June 30, 2009, respectively. Compensation cost related to QuantRx’s non-employee options was a reduction of $1,667 based on a remeasurement adjustment in the six months ended June 30, 2009.
12. | Related Party Transactions |
In the fourth quarter of 2009, warrants to purchase 1,750,000 shares of common stock were granted in settlement of $195,000 in outstanding accounts payable and a financial advisory services contract with Burnham Hill Partners, of which a beneficial owner of more than 5% of QuantRx common stock is a managing member. The warrants have an exercise price of $0.55 and a term of five years. Of the $100,050 allocated to the financial advisory services contract, $33,350 and $83,375 was expensed as consulting expense in the three and six months ended June 30, 2010 and $0 and $83,375 was recorded as prepaid consulting as of June 30, 2010 and December 31, 2009, respectively.
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13. | Commitments and Contingencies |
QN Diagnostics and PRIA Diagnostics
QuantRx is committed to further capital contributions to QN Diagnostics aggregating $1.55 million, comprised of: payment of milestone payments with PRIA Diagnostics in QuantRx common stock (fair value of $750,000); transfer of fixed assets with a fair value of $100,000 at QND’s discretion; and a $700,000 sustaining capital contribution as required by QND. Subsequent sustaining capital contributions will be made by QuantRx and NuRx on an equal basis. Should either party fail to make sustaining contributions as required, such party would be subject to a reduction in ownership interest and loss of a board seat. See Notes 3, 4 and 14.
Operating Leases
QuantRx leases office space and research and development lab space under operating leases that expire at various times through 2011. Some of these leases include allocations for common expenses subject to future adjustment. Rent expense related to operating leases was approximately $32,795 and $66,467 for the three and six months ended June 30, 2010 and $31,857 and $65,501 for the three and six months ended June 30, 2009, respectively. In connection with facility leases, the Company has made security deposits totaling $10,310, which are included in long-term assets in the balance sheet. Future minimum lease obligations for operating leases as of June 30, 2010 are estimated as follows:
Remainder of year ending December 31, 2010 | $ | 67,600 | ||
Year ending December 31, 2011 | 89,107 | |||
Total minimum payments | $ | 156,707 |
In February 2007, the Company began subleasing research and development lab space under the noncancellable operating leases. The sublease can be terminated upon ninety days notice by either party, and a $2,000 security deposit is being held by QuantRx pursuant to the terms of the lease. Sublease income was $4,125 and $8,250 for the three and six months ended June 30, 2010, and $5,665 and $11,535 for the three and six months ended June 30, 2009, respectively, and is recorded in other income.
Executive Employment Contracts
We have entered into employment contracts with key executives that provide for the continuation of salary to the executives if terminated for reasons other than cause or in connection with a change in control of QuantRx, as defined in those agreements. At June 30, 2010, the future employment contract commitment for such key executives based on these termination clauses was approximately $636,000, or in the case of a change of control, $1,272,000. In addition, the agreement states that if QuantRx were to sell all of its shares of capital stock or assets, or perform a material acquisition of another entity, QuantRx will pay a completion bonus.
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Legal Contingencies
We may occasionally become subject to legal proceedings and claims that arise in the ordinary course of our business. It is impossible for us to predict with any certainty the outcome of any disputes that may arise, and we cannot predict whether any liability arising from claims and litigation will be material in relation to our financial position or results of operations.
14. | Subsequent Events |
Limited Liability Company Agreement with NuRx Pharmaceuticals, Inc.
On July 20, 2010, QuantRx notified NuRx Pharmaceuticals, Inc., QuantRx’s partner in the QND joint venture, that NuRx was in material breach of the QND operating agreement, and had 60 days from the date of the notification to cure such breach. The notification is related to nonpayment of fees in accordance with the Development and Services Agreement between QuantRx and QND. Should the breach remain uncured, QuantRx reserved the right to terminate the QND operating agreement.
Merger Agreement
On January 29, 2010, QuantRx entered into an Agreement and Plan of Merger with NuRx and NP Acquisition Corporation, a wholly-owned subsidiary of QuantRx. The Merger Agreement provided that at closing, NP Acquisition Corp. would be merged with and into NuRx, with NuRx continuing as the surviving corporation and a wholly-owned subsidiary of QuantRx.
On July 20, 2010, QuantRx terminated the Merger Agreement pursuant to Section 7.02(b) thereof, which permits any party to the Merger Agreement to terminate the Merger Agreement if the merger contemplated thereby was not consummated on or before June 30, 2010. QuantRx did not incur any termination penalties as a result of such termination.
Sale of FluoroPharma Stock
In the third quarter of 2010, QuantRx entered into Security Purchase Agreement with a qualified institutional buyer in which QuantRx sold 100,000 shares of FluoroPharma, Inc. class A common stock at a price of $0.75 per share for an aggregate amount of $75,000 resulting in a gain on disposition of $75,000. Subsequent to this sale, QuantRx held 26.8% (11.8% of the voting rights) of FluoroPharma’s issued and outstanding common stock.
Preferred Stock Dividend
On July 30, 2010, the Board of Directors of QuantRx declared a stock dividend on the Series A-1 convertible preferred stock. The certificate of designation provides for preferential dividends of 8% per annum, therefore the Company will issue 324,831 shares of Series A-1 convertible preferred stock.
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ITEM 2. Management's Discussion and Analysis of Financial Condition and Results of Operations
The following discussion of our financial condition should be read in conjunction with the financial statements and notes to financial statements included elsewhere in this filing. The following discussion (as well as statements in Item 1 above and elsewhere) contains forward-looking statements within the meaning of the Private Securities Litigation Act of 1995 that involve risks and uncertainties. Some or all of the results anticipated by these forward-looking statements may not occur. Forward-looking statements involve known and unknown risks and uncertainties including, but not limited to, trends in the biotechnology, healthcare, and pharmaceutical sectors of the economy; competitive pressures and technological developments from domestic and foreign genetic research and development organizations which may affect the nature and potential viability of our business strategy; and private or public sector demand for products and services similar to what we plan to commercialize. We disclaim any intention or obligation to publicly announce the results of any revisions to any of the forward-looking statements contained herein to reflect future events or developments.
Unless otherwise indicated or the context otherwise requires, all references in this report to “we,” “our,” “ours,” “us,” the “Company” or similar terms refer to QuantRx Biomedical Corporation, a Nevada corporation.
Overview
QuantRx Biomedical Corporation was incorporated on December 5, 1986 in the State of Nevada. The Company’s principal business office is located at 100 South Main Street, Suite 300, Doylestown, Pennsylvania. QuantRx also has a research and development facility in Portland, Oregon.
QuantRx is a broad-based diagnostics company focused on the development and commercialization of innovative point-of-care diagnostic products based on its patented technology platforms for the worldwide healthcare industry. The Company’s overall growth strategy is to: (i) leverage its broad-based intellectual property (IP) and patent portfolio to develop new and innovative diagnostic products; (ii) commercialize products through corporate partners and distributors; and (iii) contract manufacturing to third parties while maintaining control over the manufacturing process.
QN Diagnostics
On July 30, 2009, QuantRx and NuRx Pharmaceuticals, Inc. (NuRx) entered into agreements to form QN Diagnostics, LLC (QND), a Delaware limited liability company. Pursuant to the agreements, QuantRx contributed certain intellectual property and other assets related to its lateral flow strip technology and related lateral flow strip reader technology with a fair value of $5,450,000, and NuRx contributed $5,000,000 in cash to QND. Following the respective contributions by NuRx and QuantRx to the joint venture, NuRx and QuantRx each own a 50% interest in QND. The purpose of the joint venture is to develop and commercialize products incorporating the lateral flow strip technology and related lateral flow strip readers.
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The joint venture is currently managed by a board consisting of two QuantRx designees and two NuRx designees. Subject to certain exceptions, board decisions are made by majority vote, provided that QuantRx and NuRx have veto rights with respect to certain matters. Since QuantRx does not have control of the joint venture, QuantRx accounts for the investment in QND utilizing the equity method of accounting.
Under the terms of the agreements, QND made a $2,000,000 cash distribution to QuantRx. QuantRx is committed to further capital contributions aggregating $1.55 million, comprised of: payment of milestone payments with PRIA Diagnostics (see Note 5 of the financial statements) in QuantRx common stock (fair value of $750,000); transfer of fixed assets with a fair value of $100,000 at QND’s discretion; and a $700,000 sustaining capital contribution as required by QND. Subsequent sustaining capital contributions will be made by QuantRx and NuRx on an equal basis.
QuantRx and QND also entered into a one year Development and Services Agreement on July 30, 2009, pursuant to which QND pays a monthly fee to QuantRx in exchange for QuantRx providing all services related to the development, regulatory approval and commercialization of lateral flow products. The revenues recognized by QuantRx associated with the QND Development and Services Agreement in the three and six months ended June 30, 2010 were $621,612 and $1,270,893, and the expenses related to this agreement for the same periods were $621,612 and $1,270,893. Expenses are included in each appropriate expense category in the statement of operations. As of June 30, 2010 and December 31, 2009, deferred revenues related to the Development and Services Agreement with QND were $0 and $337,160, respectively. As of June 30, 2010 and December 31, 2009, accounts receivable from QND related to the Development and Services Agreement were $380,652 and $31,500, respectively.
In the second quarter of 2010, QuantRx submitted an application for 510(k) clearance to the FDA for the Q-Reader™ thyroid testing system following the completion of clinical testing. This regulatory stage follows the completion of studies showing that the innovative Q-Reader thyroid testing system is capable of providing healthcare practitioners with laboratory level quantitative results within minutes, rather than waiting for results to be returned from a commercial laboratory. The 510(k) submission, together with the completion of a pre-production sample of the Q-Reader, satisfied the final two milestones contained in QND’s operating agreements.
On July 20, 2010, QuantRx notified NuRx Pharmaceuticals, Inc., QuantRx’s partner in the QND joint venture, that NuRx was in material breach of the QND operating agreement, and had 60 days from the date of the notification to cure such breach. The notification is related to nonpayment of fees in accordance with the Development and Services Agreement between QuantRx and QND. Should the breach remain uncured, QuantRx reserved the right to terminate the QND operating agreement.
FluoroPharma
On May 5, 2009, QuantRx and FluoroPharma reorganized their relationship by terminating their investment agreement and related agreements. The termination of these agreements, which were originally executed on March 10, 2006, allowed FluoroPharma to close an equity financing with third party investors. In conjunction with the termination of these agreements and the additional investment in FluoroPharma, QuantRx agreed to convert all outstanding receivables from FluoroPharma, consisting of previously issued notes and related accrued interest and advances in the aggregate amount of $1,568,567, into 1,148,275 shares of common stock of FluoroPharma. As a result of these transactions and the third party investment, QuantRx’s ownership interest in FluoroPharma’s issued and outstanding capital stock was reduced to a noncontrolling interest, which resulted in the deconsolidation of FluoroPharma as a subsidiary of the Company. Subsequent to the termination of the agreements between QuantRx and FluoroPharma, QuantRx has no continuing obligations or commitments to FluoroPharma.
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At May 5, 2009, QuantRx’s remaining net basis of the investment in FluoroPharma, inclusive of receivables from FluoroPharma, was $43,286, after taking into account previously recorded losses of $5,056,304 ($231,046 in the first quarter of 2009; $272,579 through deconsolidation) related to the consolidated results of FluoroPharma. These losses have been included in our consolidated financial statements commencing April 1, 2007, the original date of consolidation, through May 4, 2009, and are net of losses allocated to the then noncontrolling (formerly minority) interests as applicable. On May 5, subsequent to the execution of the aforementioned transactions which led to the deconsolidation of FluoroPharma, QuantRx’s ownership of the outstanding capital stock of FluoroPharma was reduced to a noncontrolling interest of 45.55%. At deconsolidation the fair market value of QuantRx’s remaining noncontrolling interest in FluoroPharma was $842,876, based on the third party investment; however, FluoroPharma had a deficit equity balance, which resulted in QuantRx writing off the remaining basis in the investment of $43,286 and recording a loss from deconsolidation of $43,286. QuantRx has reflected the results of its former subsidiary as a one-line item as of January 1, 2009. QuantRx’s allocation of FluoroPharma’s net loss for the period commencing May 5, 2009 through June 30, 2010, was not recorded ($420,000), since the remaining investment in FluoroPharma had a carrying value of $0 as of the deconsolidation of FluoroPharma at May 5, 2009.
In the three and six months ended June 30, 2010, QuantRx entered into Security Purchase Agreements with certain qualified institutional buyers and accredited investors in which QuantRx sold 668,333 and 1,001,666 shares of FluoroPharma, Inc. class A common stock at a price of $0.75 per share for aggregate proceeds of $501,250 and $751,250, resulting in gains on disposition of $501,250 and $751,250, respectively. As of June 30, 2010, $63,000 related to the agreements is reflected as an other receivable.
Effective May 5, 2009, our financial statements reflect our investment in FluoroPharma under the equity method of accounting. As of June 30, 2010 and December 31, 2009, QuantRx owned approximately 27.98% and 39.81%, respectively, of the issued and outstanding capital stock of FluoroPharma. However, at June 30, 2010, due to FluoroPharma’s issuance of a separate class of common stock in 2009, QuantRx held 12.32% of the voting rights of FluoroPharma.
FluoroPharma is currently seeking financing which could result in a disposition of all or a portion of QuantRx’s investment in FluoroPharma as part of a strategic transaction.
Consolidated Results of Operations
Total revenues for the three months ended June 30, 2010 and 2009 were $641,040 and $172,415, respectively. Total revenues for the six months ended June 30, 2010 and 2009 were $1,300,331 and $331,902, respectively. The increase in revenues of $468,625 and $968,429 is primarily due to $621,612 and $1,270,893 in related party revenues from the Development and Services Agreement with QND.
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Sales, general and administrative expense for the three months ended June 30, 2010 and 2009 was $279,526 and $326,745, respectively, and for the six months ended June 30, 2010 and 2009, was $583,103 and $861,635, respectively. The decrease of $47,219 and $278,532 is due primarily to decreased personnel expenses.
Professional fees for the three months ended June 30, 2010 and 2009, were $178,879 and $40,141, respectively, and for the six months ended June 30, 2010 and 2009, were $428,430 and $89,168, respectively. Professional fees include the costs of legal, consulting and auditing services provided to us. The increase of $138,738 and $339,262 is primarily due to increased legal and financial advisory consulting fees.
Research and development expense for the three months ended June 30, 2010 and 2009, were $529,087 and $126,465, respectively, and for the six months ended June 30, 2010 and 2009, were $1,133,433 and $284,277, respectively. The increase of $402,622 and $849,156 is primarily due to increased consulting, personnel and supply and material expenses related to the Development and Services Agreement with QND.
The Company’s net income for the three months ended June 30, 2010 was $162,156 and net loss for the three months ended June 30, 2009 was $750,905. Net loss for the six months ended June 30, 2010 and 2009, was $164,092 and $1,891,032, respectively. The income for the quarter is primarily due to the contract development agreement with QND and a $501,250 gain on disposition of common stock of our former subsidiary. The decreased loss for the six months is due to these factors along with the absence of interest expense and amortization of debt discount following the July 2009 settlement of QuantRx’s short-term notes.
Liquidity and Capital Resources
As of June 30, 2010, QuantRx had cash and cash equivalents of $128,101, as compared to cash and cash equivalents of $376,211 as of December 31, 2009. The net decrease in cash of $248,110 for the six months ended June 30, 2010, is primarily attributable to net cash used for operating activities of $1,019,611 offset by $688,250 in cash proceeds received in the six months ended June 30, 2010 related to the sale of stock in our former subsidiary. QuantRx has used its proceeds from dispositions as well as its revenues to fund current operating expenses and investments intended to strategically expand our platforms and technologies.
QuantRx has not generated sufficient revenues from operations to meet its operating expenses. For this reason, QuantRx has historically financed its operations primarily through issuances of equity and the proceeds of debt instruments. In the past, QuantRx has also provided for its cash needs by issuing common stock, options and warrants for certain operating costs, including consulting and professional fees.
QuantRx formed a strategic joint venture (See Note 3 to the consolidated financial statements for more information) to fund the development and commercialization of its lateral flow based products; however, management believes that given the cash position of the joint venture and the current economic environment, there is still doubt about our ability to continue as a going concern. QuantRx has disposed of certain assets and investments to fund current operations. See Note 5 to the consolidated financial statements for more information. Additionally, QuantRx is pursuing other funding options, including equity offerings and debt financings; however, there can be no assurance that we will be successful in our efforts to raise additional capital or to raise funds through additional divestures.
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Management believes that the successful growth and operation of QuantRx’s business is dependent upon our ability to do any or all of the following:
· | finalize development and commercialization of our products; |
· | achieve synergy and financial stability within our joint venture to allow for commercialization of products and continued development of products in its pipeline |
· | obtain adequate sources of debt or equity financing to pay unfunded operating expenses and fund certain long-term business operations until commercialization becomes profitable; |
· | manage or reduce operating expenses, including potential consolidation of operations in Portland, Oregon; and |
· | develop new relationships with product distributors and other points of distribution for the Company’s products; |
There can be no assurance that we will be successful in achieving our long-term plans as set forth above, or that such plans, if consummated, will enable us to obtain profitable operations or continue in the long-term as a going concern.
Off-Balance Sheet Arrangements
As described above, on July 30, 2009, QuantRx formed a joint venture with NuRx Pharmaceuticals, Inc., whereby, pursuant to the terms of the operating agreements, each member will be required to make sustaining capital contributions from time to time as the Board of the joint venture determines is necessary. Should the Board of the joint venture determine that additional capital contributions are required, such sustaining capital contributions will be made by QuantRx and NuRx on an equal basis provided that QuantRx solely will be responsible for making a sustaining capital contribution with respect to the first $700,000 determined to be required by the Board of the joint venture.
We have not entered into any other transactions with unconsolidated entities in which we have financial guarantees, subordinated retained interests, derivative instruments or other contingent arrangements that expose us to material continuing risks, contingent liabilities or any other obligations under a variable interest in an unconsolidated entity that provides us with financing, liquidity, market risk or credit risk support.
Critical Accounting Policies
Revenue Recognition
The Company recognizes revenue in accordance with SEC Staff Accounting Bulletin Topic 13 when persuasive evidence of an arrangement exists and delivery has occurred, provided the fee is fixed or determinable and collection is probable. The Company assesses whether the fee is fixed and determinable based on the payment terms associated with the transaction. If a fee is based upon a variable such as acceptance by the customer, the Company accounts for the fee as not being fixed and determinable. In these cases, the Company defers revenue and recognizes it when it becomes due and payable. Up-front engagement fees are recorded as deferred revenue and amortized to income on a straight-line basis over the term of the agreement, although the fee is due and payable at the time the agreement is signed or upon annual renewal. Payments related to substantive, performance-based milestones in an agreement are recognized as revenue upon the achievement of the milestones as specified in the underlying agreement when they represent the culmination of the earnings process.
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The Company assesses the probability of collection based on a number of factors, including past transaction history with the customer and the current financial condition of the customer. If the Company determines that collection of a fee is not reasonably assured, revenue is deferred until the time collection becomes reasonably assured. Significant management judgment and estimates must be made and used in connection with the revenue recognized in any accounting period. Material differences may result in the amount and timing of our revenue for any period if our management made different judgments or utilized different estimates.
The Company recognizes revenue from nonrefundable minimum royalty agreements from distributors or resellers upon delivery of product to the distributor or reseller, provided no significant obligations remain outstanding, the fee is fixed and determinable, and collection is probable. Once minimum royalties have been received, additional royalties are recognized as revenue when earned based on the distributor’s contractual reporting obligations. QuantRx is able to recognize minimum royalty payments on an accrual basis, as they are specified in the contract. However, since the Company cannot forecast product sales by licensees, royalty payments that are based on product sales by the licensees are not determinable until the licensee has completed their computation of the royalties due and/or remitted their cash payment to us. Should information on licensee product sales become available so as to enable QuantRx to recognize royalty revenue on an accrual basis, materially different revenues and results of operations could occur.
Our strategy includes entering into collaborative agreements with strategic partners for the development, commercialization and distribution of our product candidates. Such collaboration agreements may have multiple deliverables. In arrangements with multiple deliverables where we have continuing performance obligations, contract, milestone and license fees are recognized as revenue together with any up-front payments over the term of the arrangement as performance obligations are completed, unless the deliverable has stand-alone value and there is objective, reliable evidence of fair value of the undelivered element in the arrangement. In the case of an arrangement where it is determined there is a single unit of accounting, all cash flows from the arrangement are considered in the determination of all revenue to be recognized. Cash received in advance of revenue recognition is recorded as deferred revenue.
Use of Estimates
The preparation of financial statements and related disclosures in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, revenues and expenses and related disclosures of contingent assets and liabilities in the financial statements and accompanying notes. The accounting policies discussed below are considered by management to be the most important to the Company’s financial condition and results of operations, and require management to make its most difficult and subjective judgments due to the inherent uncertainty associated with these matters. All significant estimates and assumptions are developed based on the best information available to us at the time made and are regularly reviewed and adjusted when necessary. We believe that our estimates and assumptions are reasonable under the circumstances; however, actual results may vary from these estimates and assumptions. Additional information on significant accounting principles is provided in Note 1 of the attached financial statements.
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Impairment of Assets
We assess the impairment of long-lived assets, including our other intangible assets, whenever events or changes in circumstances indicate that their carrying value may not be recoverable. The determination of related estimated useful lives and whether or not these assets are impaired involves significant judgments, related primarily to the future profitability and/or future value of the assets. Changes in our strategic plan and/or market conditions could significantly impact these judgments and could require adjustments to recorded asset balances. We hold investments in companies having operations or technologies in areas which are within or adjacent to our strategic focus when acquired, all of which are privately held and whose values are difficult to determine. We record an investment impairment charge if we believe an investment has experienced a decline in value that is other than temporary. Future changes in our strategic direction, adverse changes in market conditions or poor operating results of underlying investments could result in losses or an inability to recover the carrying value of the investments that may not be reflected in an investment’s current carrying value, thereby possibly requiring an impairment charge in the future.
In determining fair value of assets, QuantRx bases estimates on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about carrying values of assets that are not readily apparent from other sources. Actual fair value may differ from management estimates resulting in potential impairments causing material changes to certain assets and results of operations.
Share-based Payments
We grant options to purchase our common stock to our employees and directors under our stock option plan. We estimate the value of stock option awards on the date of grant using a Black-Scholes pricing model (Black-Scholes model). The determination of the fair value of share-based payment awards on the date of grant using the Black-Scholes model is affected by our stock price as well as assumptions regarding a number of complex and subjective variables. These variables include, but are not limited to, our expected stock price volatility over the term of the awards, actual and projected employee stock option exercise behaviors, and risk-free interest rate. If factors change and we employ different assumptions in future periods, the compensation expense that we record may differ significantly from what we have recorded in the current period.
We determine the fair value of the share-based compensation awards granted to non-employees as either the fair value of the consideration received or the fair value of the equity instruments issued, whichever is more reliably measurable. If the fair value of the equity instruments issued is used, it is measured using the stock price and other measurement assumptions as of the earlier of either of (1) the date at which a commitment for performance by the counterparty to earn the equity instruments is reached or (2) the date at which the counterparty’s performance is complete.
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Estimates of share-based compensation expenses are significant to our financial statements, but these expenses are based on option valuation models and will never result in the payment of cash by us.
The above listing is not intended to be a comprehensive list of all of our accounting policies. In most cases, the accounting treatment of a particular transaction is specifically dictated by accounting principles generally accepted in the United States.
ITEM 4. | Controls and Procedures |
(a) | Evaluation of Disclosure Controls and Procedures |
The Company maintains disclosure controls and procedures that are designed to ensure that information required to be disclosed in our SEC reports is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and that such information is communicated to our management including our Chief Executive Officer and Chief Financial Officer as appropriate. With the supervision and with the participation of our management, including the Chief Executive Officer and Chief Financial Officer, we have evaluated the effectiveness of our disclosure controls and procedures (as defined under Exchange Act Rules 13a-15(e) and 15(d)-15(e)), as of the end of the period covered by this report. Based on that evaluation, our Chief Executive Officer and Chief Financial Officer have concluded that these disclosure controls and procedures were effective as of June 30, 2010.
(b) | Changes in Internal Control over Financial Reporting |
During the period covered by this quarterly report on Form 10-Q, there were no changes in our internal control over financial reporting that have materially affected, or are reasonably likely to affect, our internal control over financial reporting.
Given the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that misstatements due to error or fraud will not occur or that all control issues and instances of fraud, if any, will have been detected. These inherent limitations include the realities that judgments in decision-making can be faulty, and that breakdowns can occur because of simple error or mistake. Further, the design of a control system must reflect the fact that there are resource constraints, and that the benefits of a control system must be considered relative to its cost. The design of any system of controls is also based in part on certain assumptions regarding the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under all potential future conditions.
PART II - OTHER INFORMATION
ITEM 1. | Legal Proceedings. |
As of the date hereof, there are no material pending legal proceedings to which we are a party to or of which any of our property is the subject.
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ITEM 2. | Unregistered Sales of Equity Securities, and Use of Proceeds |
As of the date hereof, there were no additional sales of unregistered securities other than as reported in prior reports on Forms 10-K, 10-Q or 8-K.
ITEM 3. | Defaults Upon Senior Securities |
None.
ITEM 4. | Reserved |
ITEM 5. | Other Information |
None.
ITEM 6. | Exhibits |
Exhibit | Description | |
31.1 | Certification of Chief Executive Officer required under Rule 13a-14(a) or Rule 15d-14(a) of the Securities and Exchange Act of 1934, as amended. | |
31.2 | Certification of Chief Financial Officer required under Rule 13a-14(a) or Rule 15d-14(a) of the Securities and Exchange Act of 1934, as amended. | |
32.1* | Certification of Chief Executive Officer required under Rule 13a-14(a) or Rule 15d-14(a) of the Securities and Exchange Act of 1934, as amended, and 18 U.S.C. Section 1350. | |
32.2* | Certification of Chief Financial Officer required under Rule 13a-14(a) or Rule 15d-14(a) of the Securities and Exchange Act of 1934, as amended, and 18 U.S.C. Section 1350. |
*The certifications attached as Exhibits 32.1 and 32.2 accompany this Quarterly Report on Form 10-Q pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 and shall not be deemed “filed” by QuantRx Biomedical Corporation for purposes of Section 18 of the Exchange Act, or otherwise subject to the liability of that section.
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SIGNATURES
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.
QuantRx Biomedical Corporation | ||||
Date: August 6, 2010 | By: | /s/ Walter Witoshkin | ||
Walter Witoshkin | ||||
Chairman & CEO | ||||
Date: August 6, 2010 | By: | /s/ Sasha Afanassiev | ||
Sasha Afanassiev | ||||
CFO, Treasurer & VP of Finance |
27
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): July 20, 2010
QUANTRX BIOMEDICAL CORPORATION
(Exact name of registrant as specified in its charter)
Nevada | 0-17119 | 33-0202574 |
(State or other jurisdiction of incorporation) | (Commission File Number) | (IRS Employer Identification No.) |
100 S. Main Street, Suite 300
Doylestown, Pennsylvania 18901
(Address of principal executive offices) (Zip Code)
Registrant’s telephone number, including area code: (267) 880-1595
Not applicable
(Former name or former address if changed since last report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
þ | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
¨ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
¨ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
¨ | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 1.02 Termination of a Material Definitive Agreement.
On July 20, 2010, QuantRx Biomedical Corporation, a Nevada corporation, delivered notice to NuRx Pharmaceuticals, Inc., a Nevada corporation, terminating, effective immediately, the Agreement and Plan of Merger (the “Merger Agreement”), dated as of January 29, 2010, by and among QuantRx Biomedical Corporation, NP Acquisition Corporation, a Nevada corporation and a wholly-owned subsidiary of QuantRx, and NuRx Pharmaceuticals, Inc.
QuantRx terminated the Merger Agreement pursuant to Section 7.02(b) thereof, which permits any party to the Merger Agreement to terminate the Merger Agreement if the merger contemplated thereby was not consummated on or before June 30, 2010. QuantRx did not incur any termination penalties as a result of such termination.
QuantRx and NuRx are currently parties to a joint venture, the purpose of which is to research, develop and commercialize products incorporating the lateral flow strip technology and related lateral flow strip readers.
QuantRx filed a Current Report on Form 8-K regarding the execution of the Merger Agreement with the Securities and Exchange Commission on January 29, 2010. QuantRx filed a Current Report on Form 8-K regarding its joint venture with NuRx with the SEC on August 5, 2009.
SIGNATURES
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 hereunto duly authorized.
QUANTRX BIOMEDICAL CORPORATION | |
Dated: July 22, 2010 | By: /s/ Walter Witoshkin |
Name: Walter Witoshkin | |
Title: Chairman and Chief Executive Officer |
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): June 9, 2010
QUANTRX BIOMEDICAL CORPORATION
(Exact name of registrant as specified in its charter)
Nevada | 0-17119 | 33-0202574 |
(State or other jurisdiction of incorporation) | (Commission File Number) | (IRS Employer Identification No.) |
100 S. Main Street, Suite 300
Doylestown, Pennsylvania 18901
(Address of principal executive offices) (Zip Code)
Registrant’s telephone number, including area code: (267) 880-1595
Not applicable
(Former name or former address if changed since last report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
¨ | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
¨ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
¨ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
¨ | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 7.01 Regulation FD Disclosure
On June 9, 2010, QuantRx Biomedical Corporation issued a press release, a copy of which is attached as Exhibit 99.1 and incorporated herein by reference.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
Exhibit No. | Description | |
99.1 | Press Release, dated June 9, 2010 |
SIGNATURES
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 hereunto duly authorized.
QUANTRX BIOMEDICAL CORPORATION | |||
Dated: June 9, 2010 | By: | /s/ Walter Witoshkin | |
Name: Walter Witoshkin | |||
Title: Chairman and Chief Executive Officer |