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 September
30, 2015
or
| ¨ | Transition
report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 |
For the transaction period from _____________
to _____________
Commission file number 333-62216
HEALTH DISCOVERY CORPORATION
(Exact name of registrant as specified in
its charter)
Georgia |
|
74-3002154 |
(State or other jurisdiction of incorporation or organization) |
|
(IRS Employer Identification No.) |
4243
Dunwoody Club Drive
Suite
202
Atlanta,
Georgia 30350
(Address of principal executive offices)
(678)
336-5300
(Registrant's
telephone number, including area code)
(Former name, former address and former fiscal
year,
if
changed since the last report)
Indicate
by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the 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 the filing requirements for at least the past 90 days. Yes x 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 (§232.405 of this chapter) during the preceding 12 months
(or for such shorter period that the registrant was required to submit and post such files). Yes x 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 definition of “large accelerated filer,” “accelerated filer” and “smaller
reporting company” in Rule 12b-2 of the Exchange Act. (check one):
|
Large Accelerated Filer ¨ |
Non-Accelerated Filer ¨ |
|
|
|
|
|
(do not check if a smaller reporting company) |
|
|
|
|
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 ¨ No x
APPLICABLE ONLY TO CORPORATE ISSUERS
Indicate the number of shares outstanding
of each of the issuer's classes of common stock, as of the latest practicable date:
Class: |
Outstanding as of November 16, 2015 |
|
|
Common Stock, no par value |
268,718,989 |
|
|
Series A Preferred Stock |
0 |
|
|
Series B Preferred Stock |
0 |
|
|
Series C Preferred Stock |
30,000,000 |
TABLE OF CONTENTS
PART I — FINANCIAL INFORMATION
Item 1. Financial Statements
HEALTH DISCOVERY CORPORATION
Balance Sheets
(unaudited)
| |
September 30, | | |
December 31, | |
| |
2015 | | |
2014 | |
Assets | |
| | | |
| | |
Current Assets | |
| | | |
| | |
Cash | |
$ | 506,551 | | |
$ | 7,642 | |
Accounts Receivable | |
| - | | |
| 1,969 | |
Investment in Available For Sale Securities (Note G) | |
| 104,434 | | |
| 362,373 | |
| |
| | | |
| | |
Total Current Assets | |
| 610,985 | | |
| 371,984 | |
| |
| | | |
| | |
Equipment, Less Accumulated Depreciation of $60,496 and $59,765 as of September 30, 2015 and December 31, 2014, respectively | |
| 389 | | |
| 1,120 | |
| |
| | | |
| | |
Other Assets | |
| | | |
| | |
Patents, Less Accumulated Amortization of $2,979,048 and $2,782,009 as of September 30, 2015 and December 31, 2014, respectively | |
| 1,006,746 | | |
| 1,203,785 | |
| |
| | | |
| | |
Total Assets | |
$ | 1,618,120 | | |
$ | 1,576,889 | |
| |
| | | |
| | |
Liabilities and Stockholders' Equity | |
| | | |
| | |
| |
| | | |
| | |
Current Liabilities | |
| | | |
| | |
Accounts Payable - Trade | |
$ | 19,768 | | |
$ | 239,910 | |
Dividends Payable | |
| 206,637 | | |
| 373,346 | |
Deferred Revenue | |
| 43,388 | | |
| 43,388 | |
| |
| | | |
| | |
Total Current Liabilities | |
| 269,793 | | |
| 656,644 | |
| |
| | | |
| | |
Long Term Liabilities | |
| | | |
| | |
Deferred Revenue | |
| 115,699 | | |
| 148,240 | |
| |
| | | |
| | |
Total Liabilities | |
| 385,492 | | |
| 804,884 | |
| |
| | | |
| | |
Stockholders' Equity | |
| | | |
| | |
Series C Preferred Stock, Convertible, 30,000,000
Shares Authorized, 30,000,000 Issued and Outstanding at September 30, 2015 6,640,000 Issued and Outstanding at December 31,
2014 | |
| 900,000 | | |
| 332,000 | |
Common Stock, No Par Value, 300,000,000 Shares Authorized 268,718,989 Shares Issued and Outstanding at September 30, 2015 261,384,810 Shares Issued and Outstanding at December 31, 2014 | |
| 27,393,858 | | |
| 27,055,938 | |
Accumulated Deficit | |
| (27,061,230 | ) | |
| (26,615,933 | ) |
| |
| | | |
| | |
Total Stockholders' Equity | |
| 1,232,628 | | |
| 772,005 | |
| |
| | | |
| | |
Total Liabilities and Stockholders' Equity | |
$ | 1,618,120 | | |
$ | 1,576,889 | |
See accompanying notes to financial statements.
HEALTH DISCOVERY CORPORATION
Statements of Operations
(unaudited)
For the Three and Nine Months Ended September
30, 2015 and 2014
| |
Three Months | | |
Three Months | | |
Nine Months | | |
Nine Months | |
| |
Ended | | |
Ended | | |
Ended | | |
Ended | |
| |
September 30, | | |
September 30, | | |
September 30, | | |
September 30, | |
| |
2015 | | |
2014 | | |
2015 | | |
2014 | |
| |
| | |
| | |
| | |
| |
Revenues: | |
| | | |
| | | |
| | | |
| | |
Licensing & Development | |
$ | 12,050 | | |
$ | 256,247 | | |
$ | 33,754 | | |
$ | 773,901 | |
| |
| | | |
| | | |
| | | |
| | |
Operating Expenses: | |
| | | |
| | | |
| | | |
| | |
Amortization | |
| 65,680 | | |
| 65,679 | | |
| 197,039 | | |
| 197,039 | |
Professional and Consulting Fees | |
| 30,965 | | |
| 26,985 | | |
| 129,377 | | |
| 144,700 | |
Legal Fees | |
| 9,000 | | |
| 14,792 | | |
| 37,357 | | |
| 49,171 | |
Research & Development Fees | |
| 9,000 | | |
| 23,438 | | |
| 31,813 | | |
| 70,763 | |
Compensation | |
| 48,328 | | |
| 62,955 | | |
| 142,665 | | |
| 202,311 | |
Other General and Administrative Expenses | |
| 33,633 | | |
| 35,562 | | |
| 116,843 | | |
| 129,803 | |
Total Operating Expenses | |
| 196,606 | | |
| 229,411 | | |
| 655,094 | | |
| 793,787 | |
| |
| | | |
| | | |
| | | |
| | |
(Loss) Income From Operations | |
| (184,556 | ) | |
| 26,836 | | |
| (621,340 | ) | |
| (19,886 | ) |
| |
| | | |
| | | |
| | | |
| | |
Other Income (Expense) | |
| | | |
| | | |
| | | |
| | |
Unrealized Gain (Loss) on Available for Sale Securities (Note G) | |
| (17,917 | ) | |
| 87,431 | | |
| (160,706 | ) | |
| (57,619 | ) |
Realized Gain on Available for Sale Securities (Note G) | |
| 27,192 | | |
| 192,783 | | |
| 232,937 | | |
| 295,349 | |
Forgiveness on Payables (Note H) | |
| 121,503 | | |
| - | | |
| 121,503 | | |
| - | |
Settlement Expense | |
| - | | |
| - | | |
| (17,693 | ) | |
| - | |
Total Other Income | |
| 130,778 | | |
| 280,214 | | |
| 176,041 | | |
| 237,730 | |
| |
| | | |
| | | |
| | | |
| | |
Net (Loss) Income | |
| (53,778 | ) | |
| 307,050 | | |
| (445,299 | ) | |
$ | 217,844 | |
| |
| | | |
| | | |
| | | |
| | |
Preferred Stock Dividends | |
| - | | |
| 17,800 | | |
| - | | |
| 52,820 | |
| |
| | | |
| | | |
| | | |
| | |
Net (Loss) Earnings Attributable to Common Stockholders | |
$ | (53,778 | ) | |
$ | 289,250 | | |
$ | (445,299 | ) | |
$ | 165,024 | |
| |
| | | |
| | | |
| | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Weighted Average Outstanding Shares – basic and diluted | |
| 266,052,322 | | |
| 252,557,310 | | |
| 265,163,433 | | |
| 252,557,310 | |
| |
| | | |
| | | |
| | | |
| | |
(Loss) Earnings Per Share – basic and diluted | |
$ | (0.0001 | ) | |
$ | 0.0011 | | |
$ | (0.0017 | ) | |
$ | 0.0007 | |
See accompanying notes to financial statements.
HEALTH DISCOVERY CORPORATION
Statements of Cash Flows
(unaudited)
For the
Nine Months Ended September 30, 2015 and 2014
| |
2015 | | |
2014 | |
Cash Flows From Operating Activities | |
| | | |
| | |
Net (Loss) Income | |
$ | (445,299 | ) | |
$ | 217,844 | |
Adjustments to Reconcile Net (Loss) Income to Net Cash
Used in Operating Activities: | |
| | | |
| | |
Stock-based Compensation for Employees | |
| 11,512 | | |
| 11,511 | |
Stock-based Compensation for Directors and Consultants | |
| 39,700 | | |
| 44,634 | |
Realized Gain on Investments
in Available for Sale Securities
Measured in Accordance with the Fair Value Option | |
| (232,937 | ) | |
| (295,349 | ) |
Unrealized Loss on
Investments in Available for Sale Securities
Measured in Accordance with the Fair Value Option | |
| 160,706 | | |
| 57,619 | |
Depreciation and Amortization | |
| 197,770 | | |
| 200,766 | |
Decrease in Accounts Receivable | |
| 1,969 | | |
| 80 | |
Decrease in Deferred Revenue | |
| (32,541 | ) | |
| (768,741 | ) |
Decrease in Accounts Payable – Trade | |
| (98,639 | ) | |
| (3,449 | ) |
Forgiveness
on Accounts Payable – Trade | |
| (121,503 | ) | |
| - | |
Increase in Available for Sale Securities | |
| (1,294 | ) | |
| - | |
Decrease in Accrued Liabilities | |
| - | | |
| (2,500 | ) |
Net Cash Used in Operating Activities | |
| (520,556 | ) | |
| (537,585 | ) |
| |
| | | |
| | |
Cash Flows From Investing Activities: | |
| | | |
| | |
Proceeds from Sale of Available for Sale Securities | |
| 331,465 | | |
| 437,448 | |
Net Cash Provided by Investing Activity | |
| 331,465 | | |
| 437,448 | |
| |
| | | |
| | |
Cash Flows From Financing Activities: | |
| | | |
| | |
Proceeds from Common Stock Issuance | |
| 120,000 | | |
| - | |
Proceeds from Series C Preferred Stock Issuance | |
| 568,000 | | |
| 147,000 | |
Net Cash Provided by Financing Activity | |
| 688,000 | | |
| 147,000 | |
| |
| | | |
| | |
Net Increase in Cash | |
| 498,909 | | |
| 46,863 | |
| |
| | | |
| | |
Cash, at Beginning of Period | |
| 7,642 | | |
| 71,991 | |
| |
| | | |
| | |
Cash, at End of Period | |
$ | 506,551 | | |
$ | 118,854 | |
See accompanying notes to financial statements.
HEALTH DISCOVERY CORPORATION
Notes to Financial Statements (unaudited)
Note A - BASIS OF PRESENTATION
Health Discovery Corporation
(the “Company”) is a biotechnology-oriented company that has acquired patents and has patent pending applications for
certain machine learning tools, primarily pattern recognition techniques using advanced mathematical algorithms to analyze large
amounts of data thereby uncovering patterns that might otherwise be undetectable. Such machine learning tools are currently
in use for diagnostics and drug discovery, but are also marketed for other applications. The Company licenses the use
of its patent protected technology and may provide services to develop specific learning tools under development agreements or
to sell to third parties.
The accounting principles
followed by the Company and the methods of applying these principles conform to accounting principles generally accepted in the
United States of America (GAAP). In preparing financial statements in conformity with GAAP, management is required to make estimates
and assumptions that affect the reported amounts in the financial statements. Actual results could differ significantly from those
estimates.
The interim financial
statements included in this report are unaudited but reflect all adjustments which, in the opinion of management, are necessary
for a fair presentation of the financial position and results of operations for the interim periods presented. All such adjustments
are of a normal recurring nature. The results of operations for the three and nine months ended September 30, 2015 are not necessarily
indicative of the results of a full year’s operations and should be read in conjunction with the financial statements and
footnotes included in the Company’s annual report on Form 10-K for the year ended December 31, 2014.
Note B – REVENUE RECOGNITION
Revenue is generated
through the sale or license of patented technology and processes and from services provided through development agreements. These
arrangements are generally governed by contracts that dictate responsibilities and payment terms. The Company recognizes
revenues as they are earned over the duration of a license agreement or upon the sale of any owned patent once all contractual
obligations have been fulfilled. If a license agreement has an undetermined or unlimited life, the revenue is recognized
over the remaining expected life of the patents. Revenue is recognized under development agreements in the period the services
are performed.
The Company treats
the incremental direct cost of revenue arrangements, which consists principally of employee bonuses, as deferred charges and these
incremental direct costs are amortized to expense using the straight-line method over the same term as the related deferred revenue
recognition.
Deferred revenue represents
the unearned portion of payments received in advance for licensing and development agreements. The Company had total unearned revenue
of $159,087 as of September 30, 2015. Unearned revenue of $43,388 is recorded as current and $115,699 is classified as long-term.
Note C - NET (LOSS) INCOME PER SHARE
Basic Earnings Per
Share (“EPS”) includes no dilution and is computed by dividing income or loss attributable to common shareholders by
the weighted average number of common shares outstanding for the period. Diluted EPS reflects the potential dilution of securities
that could share in the earnings or losses of the entity.
Due to the net loss
for the three and nine month periods ended September 30, 2015, the calculation of diluted per share amounts would create
an anti-dilutive result and therefore are not presented in the following table.
HEALTH DISCOVERY CORPORATION
Notes to Financial Statements (unaudited),
continued
Note C - NET (LOSS) INCOME PER SHARE,
continued
The following is an
analysis of the basic and diluted earnings per common share computations for the three and nine months ended September 30, 2014:
| |
Three months ended
September 30, 2014 | | |
Nine months ended
September
30, 2014 | |
Basic: | |
| | | |
| | |
Net income attributable to common shareholders | |
$ | 289,250 | | |
$ | 165,024 | |
Basic weighted average common shares outstanding | |
| 252,557,310 | | |
| 252,557,310 | |
Basic earnings per common share | |
$ | 0.0001 | | |
$ | 0.0001 | |
| |
| | | |
| | |
Diluted: | |
| | | |
| | |
Net income attributable to common shareholders | |
$ | 289,250 | | |
$ | 165,024 | |
Basic weighted average common shares outstanding | |
| 252,557,310 | | |
| 252,557,310 | |
| |
| | | |
| | |
Effect of dilutive securities: | |
| | | |
| | |
Conversion of options and warrants | |
| - | | |
| - | |
Conversion of preferred shares to common shares | |
| - | | |
| - | |
Diluted weighted average common shares outstanding | |
| 252,557,310 | | |
| 252,557,310 | |
Diluted earnings per common share | |
$ | 0.0001 | | |
$ | 0.0001 | |
During the three and
nine month periods ended September 30, 2014, 18,890,000 outstanding stock options and warrants were not included in the computation
of diluted earnings per common share because to do so would have an antidilutive effect due to the fact that the strike prices
were higher than the market price for the Company’s common stock. In addition, for the three and nine month periods ended
September 30, 2014, 14,967,500 in convertible preferred stock was not included in the diluted earnings per common share calculation
because to do so would have had an antidilutive effect due to the fact that the strike prices were higher than the market price
for the Company’s common stock.
Note D - STOCK-BASED COMPENSATION and
other EQUITY BASED PAYMENTS
Stock-based expense
included in our net loss for the three months and nine months ended September 30, 2015 consisted of $17,071 and $51,212,
respectively, for stock options granted to officers and directors. Stock-based expense included in our net income for the
three months and nine months ended September 30, 2014 consisted of $18,714 and $56,145, respectively, for stock
options granted to officers and directors.
As of September 30,
2015, there was $68,962 of unrecognized cost related to stock option grants. The cost is to be recognized over the remaining
vesting periods that average approximately 1.0 year.
There were no grants,
exercises, forfeitures or expirations of stock options for the three and nine month periods ended September 30, 2015. There were
grants of warrants relating to the issuance of Series C Preferred Stock and Common Stock during the three month period ended September
30, 2015. As of September 30, 2015, there were 46,750,000 option and warrant shares outstanding with a weighted average exercise
price of $0.032.
HEALTH DISCOVERY CORPORATION
Notes to Financial Statements (unaudited),
continued
Note D – STOCK-BASED COMPENSATION
AND OTHER EQUITY BASED PAYMENTS, continued
The following schedule
summarizes combined stock option and warrant information for the nine months ended September 30, 2015.
|
|
Option and Warrant Shares |
|
Weighted Average Exercise Price |
Outstanding, December 31, 2014 |
|
19,390,000 |
|
|
|
|
$0.034 |
|
|
|
|
|
|
|
|
|
|
|
|
Granted |
|
27,360,000 |
|
|
|
|
0.030 |
|
|
Exercised |
|
- |
|
|
|
|
- |
|
|
Forfeited |
|
- |
|
|
|
|
- |
|
|
Expired un-exercised |
|
- |
|
|
|
|
- |
|
|
Outstanding, September 30, 2015 |
|
46,750,000 |
|
|
|
|
$0.032 |
|
|
The following schedule
summarizes combined stock option and warrant information as of September 30, 2015:
Exercise Prices |
|
|
Number Outstanding |
|
Weighted-
Average
Remaining
Contractual
Life (years) |
|
|
Number Exercisable |
|
Weighted
Average
Remaining
Contractual Life
(years) of
Exercisable
Warrants |
|
$ 0.027 |
|
|
3,000,000 |
|
|
|
|
7.75 |
|
|
2,000,000 |
|
|
|
|
7.75 |
|
$ 0.030 |
|
|
34,000,000 |
|
|
|
|
8.75 |
|
|
34,000,000 |
|
|
|
|
8.75 |
|
$ 0.036 |
|
|
7,750,000 |
|
|
|
|
8.00 |
|
|
5,000,000 |
|
|
|
|
8.00 |
|
$ 0.040 |
|
|
1,000,000 |
|
|
|
|
2.25 |
|
|
1,000,000 |
|
|
|
|
2.25 |
|
$ 0.050 |
|
|
1,000,000 |
|
|
|
|
2.25 |
|
|
1,000,000 |
|
|
|
|
2.25 |
|
Total |
|
|
46,750,000 |
|
|
|
|
|
|
|
43,000,000 |
|
|
|
|
|
|
The weighted average
remaining life of all outstanding warrants and options at September 30, 2015 is 7.75 years. The aggregate intrinsic value of all
options and warrants outstanding and exercisable as of September 30, 2015 was zero, based on the market closing price of $0.026
on September 30, 2015, less exercise prices.
Note E - PATENTS
The Company has acquired
and developed a group of patents related to biotechnology and certain machine learning tools used for diagnostic and drug discovery.
Legal costs associated with patent acquisitions and the application processes for new patents are capitalized as patent
assets. The Company has recorded as other assets $1,006,746 in patents and patent related costs, net of $2,979,048 in accumulated
amortization, at September 30, 2015.
Amortization charged
to operations for the three months and nine months ended September 30, 2015 was $65,680 and $197,039, respectively. For
the three months and nine months ended September 30, 2014, amortization charged to operations was $65,679 and $197,039, respectively.
Estimated amortization expense for the next four years is $262,720 per year.
HEALTH DISCOVERY CORPORATION
Notes to Financial Statements (unaudited),
continued
Note F – STOCKHOLDERS’ EQUITY
Series B Preferred Stock
The Company sold to
individual investors a total of 19,402,675 shares of Series B Preferred Stock for $1,490,015, net of associated expenses,
in 2009.
The Series B Preferred
Stock was converted into Common Stock of the Company in the fourth quarter of 2014, which was the fifth anniversary of the date
of issuance as outlined in the original purchase agreement.
Dividends have been
accrued for the Series B Preferred Stock in the amount of $373,346 as of December 31, 2014. The Company gave the Series B holders
the choice of either (1) Common Stock for the amount of the dividend accrued based upon the price of $0.05 per share or (2) to
defer payment of the dividend in cash until the Company is able to pay, at the sole discretion of the Company. During the first
quarter of 2015, $166,709 in dividends were paid with the issuance of 3,334,179 shares of Common Stock. The remaining accrued dividend
is recorded as a current liability in the amount of $206,637 as of September 30, 2015.
Series C Preferred Stock
In the fourth quarter
of 2013, the Board of Directors authorized the issuance of Series C Preferred Shares in private placement transactions. As of
December 31, 2014 and September 30, 2015, the Company had issued a total of 6,640,000 and 30,000,000 preferred shares, respectively.
The Series C Preferred Shares were fully subscribed in the third quarter 2015. The Company received total net proceeds
of $900,000, of which $568,000 was received in the period ended September 30, 2015. The Series C Preferred Shares are accompanied
by $0.03 warrants and $0.03 contingency warrants. The contingency warrants will be issued only if the Company has not attained
profitability by the end of the first quarter 2016. The holders must exercise fifty percent of the warrants if the market price
for the Company’s common stock is $0.20 for a period of thirty consecutive calendar days. The holders must also
exercise fifty percent of the warrants if the market price for the Company’s common stock is $0.30 for a period
of thirty consecutive calendar days. The warrants were valued at $0.025 each using the Black Scholes Method.
The Series C Preferred
Stock has not been registered under either federal or state securities laws and must be held until a registration statement covering
such securities is declared effective by the Securities and Exchange Commission or an applicable exemption applies.
The Series C Preferred
Stock may be converted into Common Stock of the Company at the option of the holder, without the payment of additional consideration
by the holder, so long as the Company has a sufficient number of authorized shares to allow for the exercise of all of its outstanding
warrants and options. The Shares of Series C Preferred Stock must be converted into Common Stock of the Company either by the demand
by the shareholder or at the fifth anniversary of the date of issuance. If the Company were to be dissolved, the Series C Preferred
Stock receives preferential treatment over Common Stock.
Note G – INVESTMENT IN AVAILABLE FOR SALE SECURITIES
The Company has elected
the fair value option in accordance with ASC 825, Financial Instruments, as it relates to its shares held in NeoGenomics’
common stock that were acquired resulting from the NeoGenomics Master License Agreement executed on January 6, 2012. Management
made the election for the fair value option related to this investment because it believes the fair value option for the NeoGenomics
common stock provides a better measurement from which to compare financial statements from reporting period to reporting period.
No other financial assets or liabilities are measured at fair value using the fair value option.
HEALTH DISCOVERY CORPORATION
Notes to Financial Statements (unaudited),
continued
Note G – INVESTMENT IN AVAILABLE FOR SALE SECURITIES,
continued
The Company’s
investment in NeoGenomics’ common stock is recorded on the accompanying balance sheets under the caption Investment in Available
for Sale Securities. The carrying value of this investment on the date of acquisition approximated $1,945,000. The change in fair
value from December 31, 2014 to September 30, 2015 was a net gain of $72,231 for the remaining 18,000 shares held and is classified
as other income (expense) under the captions Realized and Unrealized (Loss) Gain on Available for Sale Securities in the accompanying
statements of operations. The change in fair value from December 31, 2013 to September 30, 2014 was a net gain of $237,730 and
is classified as other income (expense) under the captions Realized and Unrealized (Loss) Gain on Available for Sale Securities
for the nine months ended September 30, 2014 in the accompanying statements of operations. The Company classifies its investment
as an available for sale security and the fair value is considered a Level 1 investment in the fair value hierarchy. The September
30, 2015 fair value of the investment of $104,434 is for the remaining shares held and is calculated using the closing stock price
of the NeoGenomics common stock at the end of the reporting period. As of September 30, 2015, the Company held 18,000 shares of
NeoGenomics stock as compared to 86,900 shares as of December 31, 2014.
Note H – COMMITMENTS AND CONTINGENCIES
On July 17, 2013, the
Company received a Civil Investigative Demand (the "Demand") from the Federal Trade Commission of the United States of
America (the "FTC") relating to the Company's MelApp software application. In the Demand, the FTC has requested information
relating to potentially unfair or deceptive acts or practices related to (i) false advertising and (ii) consumer privacy and data
security, in violation of Trade Commission Act, 15 U.S.C. Sections 45 and 42.
On February 23, 2015,
the FTC notified the Company of its approval, by a vote of 4-1, to accept an Agreement Containing Consent Order (“Agreement”).
This Agreement is for settlement purposes only. The Company neither admits nor denies any of the allegations, except as specifically
stated in the Agreement. The Company believes the effort to contest this matter with the FTC would require funds greater than the
Company has at its disposal.
The
Agreement does, among other things, bar the Company from claiming that any device detects or diagnoses melanoma or its risk factors,
or increases users’ chances of early detection, unless the representation is not misleading and supported by competent and
reliable scientific evidence in the form of human clinical testing of the device. The Agreement also prohibits the Company from
making any other misleading or unsubstantiated claims about a device’s health benefits or efficacy, unless the representation
is not misleading and supported by competent and reliable scientific evidence in the form of human clinical testing of the device.
Finally, the Company was required to pay $17,693 to the FTC, which was accrued during the three month period ended March
31, 2015. This amount is included as Settlement Expense in the accompanying statements of operations.
The Company’s
balance sheet for the year ended December 31, 2014 reflected an accrued liability of approximately $239,910 for professional services.
In an effort to conserve cash, the Company worked with several of the vendors regarding a portion of this amount by negotiating
with the service providers regarding potential reduction of the amount billed. During the quarter ended September 30,
2015, the Company and the service providers negotiated the amounts owed and as a result, the Company recorded a decrease in accounts
payables of $121,503.
The Company is subject
to various claims primarily arising in the normal course of business. Although the outcome of these matters cannot be
determined, the Company does not believe it is probable that any such claims will result in material costs and expenses.
HEALTH DISCOVERY CORPORATION
Notes to Financial Statements (unaudited),
continued
Note I – FINANCIAL CONDITION
We have prepared our
financial statements on a “going concern” basis, which presumes that we will be able to realize our assets and discharge
our liabilities in the normal course of business for the foreseeable future.
Our ability to continue
as a going concern is dependent upon our licensing arrangements with third parties, achieving profitable operations, obtaining
additional financing and successfully bringing our technologies to the market. The successful outcome of these matters cannot
be predicted at this time. Our financial statements have been prepared on a going concern basis and do not include any adjustments
to the amounts and classifications of the assets and liabilities that might be necessary should we be unable to continue in business.
At September 30, 2015,
we had $506,551 cash on hand along with stock available for sale worth $104,434. The Company’s plan to have sufficient cash
to support operations is comprised of generating revenue through its relationship with NeoGenomics, providing services related
to those patents, selling its NeoGenomics stock, and obtaining additional equity or debt financing.
As a result, the Company
focused its efforts to secure funds via licensing activity or other forms of fund raising either in the debt or equity markets. In
addition, prior to the beginning of this year, the Company began raising capital through the Series C Preferred Stock offering.
The Series C Preferred Stock offering was fully subscribed and completed in August 2015. As a result, the Company received $568,000
in 2015 in addition to the $332,000 received in prior years for a total of $900,000.
The Company believes
the funds received from the Series C Preferred Stock offering, along with disciplined expense management, will allow the Company
to maintain operations through 2016. While the Company believes these efforts will create a profitable future, there is no guarantee
the Company will be successful in these efforts.
Item
2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
Corporate Overview
Our Company is a pattern
recognition company that uses advanced mathematical techniques to analyze large amounts of data to uncover patterns that might
otherwise be undetectable. The Company operates primarily in the field of molecular diagnostics where such tools are critical to
scientific discovery. The terms artificial intelligence and machine learning are sometimes used to describe pattern recognition
tools.
HDC’s mission
is to use its patents, intellectual prowess, and clinical partnerships principally to identify patterns that can advance the science
of medicine, as well as to advance the effective use of our technology in other diverse business disciplines, including the high-tech,
financial, and healthcare technology markets.
Our historical foundation
lies in the molecular diagnostics field where we have made a number of discoveries that play a role in developing more personalized
approaches to the diagnosis and treatment of certain diseases. However, our Support Vector Machine (“SVM”) assets in
particular have broad applicability in many other fields. Intelligently applied, HDC’s pattern recognition technology can
be a portal between enormous amounts of otherwise undecipherable data and truly meaningful discovery.
Our Company’s
principal asset is its intellectual property which includes advanced mathematical algorithms called SVM and Fractal Genomic
Modeling (“FGM”), as well as biomarkers that we discovered by applying our SVM and FGM techniques to
complex genetic and proteomic data. Biomarkers are biological indicators or genetic expression signatures of certain disease states.
Our intellectual property is protected by over 60 patents that have been issued or are currently pending around the world.
HEALTH DISCOVERY CORPORATION
Management’s Discussion and Analysis,
continued
Our business model
has evolved over time to respond to business trends that intersect with our technological expertise and our capacity to professionally
manage these opportunities. In the beginning, we sought only to use our SVMs internally in order to discover and license our biomarker
signatures to various diagnostic and pharmaceutical companies. Today, our commercialization efforts include: utilization of our
discoveries and knowledge to help develop diagnostic and prognostic predictive tests; licensing of the SVM and FGM technologies
directly to diagnostic companies; and, the potential formation of new ventures with domain experts in other fields where our pattern
recognition technology holds commercial promise.
Operational Activities
The Company markets
its technology and related developmental expertise to prospects in the healthcare, biotech, and life sciences industries. Given
the scope of some of these prospects, the sales cycle can be quite long, but management believes that these marketing efforts may
produce favorable results in the future.
NeoGenomics License
On January 6, 2012,
we entered into a Master License Agreement (the “NeoGenomics License”) with NeoGenomics Laboratories, Inc. (“NeoGenomics
Laboratories”), a wholly owned subsidiary of NeoGenomics, Inc. (“NeoGenomics”). Pursuant to the terms of the
NeoGenomics License, we granted to NeoGenomics Laboratories and its affiliates an exclusive worldwide license to certain of our
patents and know-how to use, develop and sell products in the fields of laboratory testing, molecular diagnostics, clinical pathology,
anatomic pathology and digital image analysis (excluding non-pathology-related radiologic and photographic image analysis) relating
to the development, marketing production or sale of any “Laboratory Developed Tests” or LDTs or other products used
for diagnosing, ruling out, predicting a response to treatment, and/or monitoring treatment of any or all hematopoietic and solid
tumor cancers excluding cancers affecting the retina and breast cancer. We retain all rights to in-vitro diagnostic (IVD) test
kit development.
Upon execution of the
NeoGenomics License, NeoGenomics paid us $1,000,000 in cash and issued to us 1,360,000 shares of NeoGenomic’s common stock,
par value $0.001 per share, which had a market value of $1,945,000 using the closing price of $1.43 per share for NeoGenomic’s
common stock on the OTC Bulletin Board on January 6, 2012. In addition, the NeoGenomics License provides for milestone payments
in cash or stock, based on sublicensing revenue and revenue generated from products and services developed as a result of the NeoGenomics
License. Milestone payments will be in increments of $500,000 for every $2,000,000 in GAAP revenue recognized by NeoGenomics up
to a total of $5,000,000 in potential milestone payments. After $20,000,000 in cumulative GAAP revenue has been recognized by NeoGenomics,
we will receive a royalty of (i) 6.5% (subject to adjustment under certain circumstances) on net revenue generated from all Licensed
Uses except for the Cytogenetic Interpretation System and the Flow Cytometry Interpretation System and (ii) a royalty of 50% of
net revenue (after the recoupment of certain development and commercialization costs) that NeoGenomics derives from any sublicensing
arrangements it may put in place for the Cytogenetic Interpretation System and the Flow Cytometry Interpretation System.
NeoGenomics agreed
to use its best efforts to commercialize certain products within one year of the date of the license, subject to two one-year extensions
per product if needed, including a “Plasma Prostate Cancer Test”, a “Pancreatic Cancer Test”, a “Colon
Cancer Test”, a “Cytogenetic Interpretation System”, and a “Flow Cytometry Interpretation System.”
NeoGenomics has completed both of its one-year extension terms of the license. While those one-year extension terms are complete,
the Company and NeoGenomics continue to collaborate on efforts to commercialize the licensed technologies.
If NeoGenomics
has not generated $5.0 million of revenue for Health Discovery Corporation from products, services and
sublicensing arrangements by January 2017, we may, at our option, revoke the exclusivity with respect to any one or more of
the initial licensed products, subject to certain conditions.
The Company believes
our relationship with NeoGenomics is instrumental in our medical and diagnostic testing development. We further believe the majority,
if not all, of our applications in the medical field will be done in conjunction with NeoGenomics.
HEALTH DISCOVERY CORPORATION
Management’s Discussion and Analysis,
continued
Plasma Test for Prostate Cancer
NeoGenomics is developing
a Blood Test for Prostate Cancer under the direction of Dr. Maher Albitar using the genes patented by HDC. The test is performed
on blood plasma and urine rather than only prostate tissue biopsies. NeoGenomics completed Phase I of their research and published
the results in 2014. Additionally, NeoGenomics completed Phase II of their prostate test validation in 2014. The results were largely
the same as those published regarding Phase I. NeoGenomics is currently conducting a clinical trial for this test. NeoGenomics
has announced their expectation is to launch this test in 2016.
Cytogenetic Analysis
Cytogenetic analysis
is the science of studying chromosomes. Microscopic evaluation of individual chromosomes remains the first step in the evaluation
of the human genome. Cytogenetic analysis is performed on almost all patients with hematopoietic diseases (blood cancers such as
leukemia and lymphoma) and on a significant number of patients with solid tumors. The collected data is useful for diagnosis, prognosis
and monitoring of diseases. Currently, specially trained technicians perform most of the analysis manually. The work is labor-intensive
and subjective. Computer automation of this work could significantly reduce cost and improve the quality of the test.
NeoGenomics is currently
working on development, validation and commercialization of this new image analysis tool for cytogenetic analysis under the direction
of Dr. Maher Albitar. The Company and NeoGenomics have spent a considerable amount of time using SVM Technology to create significant
improvement in cytogenetic analysis. NeoGenomics is currently beta testing this co-developed technology within their facilities.
One of the goals with this technology is for NeoGenomics to sub-license this technology after successful internal testing and validation.
Per the license agreement, HDC will receive a portion of the sub-license revenue generated by NeoGenomics.
Flow Cytometry
Management believes
that our efforts to develop an SVM-based diagnostic test to help interpret flow cell cytometry data for myelodysplastic syndrome
(pre-leukemia) has resulted in a successful proof of concept. The Company, along with NeoGenomics, is now capable of completing
development, final validation and commercialization of the new diagnostic test for the interpretation of flow cytometry data. This
test has been licensed to NeoGenomics for final development and work has begun on the further development of this technology.
SVM Capital, LLC
In January 2007, SVM
Capital, LLC (“SVM Capital”) was formed as a joint venture between HDC and Atlantic Alpha Strategies, LLC (“Atlantic
Alpha”) to explore and exploit the potential applicability of our SVM technology to quantitative investment management techniques. Atlantic
Alpha’s management has over thirty years of experience in commodity and futures trading.
In November 2012, Atlantic
Alpha began auditable formal live trading by applying SVM technology to quarterly fundamental corporate data such as
sales, earnings and projected earnings. The SVM algorithm is utilized to select U.S. stocks which are expected to outperform or
underperform in the next quarter based on current data while at the same time rendering superior portfolio risk metrics. This application
of SVM technology allows the creation of a variety of equity portfolios. SVM Capital has been pleased with the results of
the application of the SVM technology.
On June 16, 2015, SVM
Capital joined Manifold Partners, LLC (“Manifold Partners”) as a partner. Manifold Partners
is a San Francisco-based multi-strategy portfolio management firm specializing in quantitative investment methodologies. This new
collaboration will be known as Manifold Vector. SVM Capital specializes in the application of an artificial intelligence technique
to investment strategies. SVM Capital has developed mathematical algorithms to rank-order S&P 500 stocks to determine investment
desirability, including long and short equity positions. Importantly, only fundamental corporate data is analyzed, which Manifold
Partners believes to be unique in the quantitative investment field. This technology is an outgrowth of the machine learning techniques
created the Company. A thorough exposition of SVM Capital may be found on the appropriate link in HDC's web page.
HEALTH DISCOVERY CORPORATION
Management’s Discussion and Analysis,
continued
Intellectual Property Developments
The Company now holds
the exclusive rights to 53 issued U.S. and foreign patents covering uses of SVM and FGM technology for discovery of knowledge from
large data sets. The Company also has 10 pending U.S. and foreign patent applications covering uses of the SVM technology as well
as diagnostic methods that have been discovered using the SVM technology. The reduction in the total number of issued and pending
patents during 2014 resulted from the Company’s decision to allow certain foreign patents issued and/or filed in countries
that were deemed to have lower strategic value to lapse. In addition, a few U.S. patents that were either near the ends of their
terms and/or had parallel applications with broader claims in force were allowed to expire. In addition, significant changes in
the U.S. Patent Laws relating to the eligibility of certain subject matter for patent protection influenced the Company’s
decision to abandon a few of its pending U.S. applications. This in turn reduced the Company’s total expenses for patent
maintenance.
Intel Update
The Company’s
patent application that was submitted to provoke an interference with Intel’s Patent No. 7,685,077 remains pending. The application
file was transferred to the U.S. Patent Office’s Interference Division in December 2014 and is awaiting further action.
Three Months Ended September 30, 2015
Compared with Three Months Ended September 30, 2014
Revenue
For the three months
ended September 30, 2015, revenue was $12,050 compared with $256,247 for the three months ended September 30, 2014. The revenue
earned during the third quarter of 2015 is related to the revenue recognition of the Vermillion settlement and the revenue earned
during the third quarter of 2014 is primarily related to the licensing revenue recognition for the NeoGenomics License.
Operating and Other Expenses
Amortization expense
was $65,680 for the three months ended September 30, 2015 and $65,679 for the three months ended September 30,
2014. Amortization expense relates primarily to the costs associated with filing patent applications and acquiring rights to the
patents.
Professional and consulting
fees totaled $30,965 for the three months ended September 30, 2015, compared with $26,985 for the same 2014 period. These fees
consist primarily of patent filing and maintenance costs, professional fees, and accounting fees. The increase was due
to higher patent filing fees.
Legal fees decreased
over the three-month period with fees totaling $9,000 during the three months ended September 30, 2015 and $14,792 during the same
period in 2014. The decrease was related to elimination of legal costs incurred in the second quarter 2014 related to the Company’s
resolution of the FTC matter.
Research and development
expense was $9,000 for the three months ended September 30, 2015, and $23,438 for the same period in 2014. This expense for research
and development relates primarily to work completed under the NeoGenomics License.
Compensation expense
of $48,328 for the three months ended September 30, 2015 was lower than the $62,955 reported for the comparable 2014 period. The
decrease is attributed to the sacrifices made by current management through reduction, or elimination of, compensation in order
to preserve cash.
Other general and administrative
expense decreased to $33,633 for the three months ended September 30, 2015, compared to $35,562, for the same period in 2014. This
expense remains lower than earlier periods principally due to a reduction in all non-essential costs by the new leadership beginning
in August 2013.
Loss / Income from Operations
The loss from operations
for the three months ended September 30, 2015 was $184,556, compared to income from operations of $26,836 for the three months
ended September 30, 2014. The loss was due to the reduction in revenue recognized, specifically the revenue from the NeoGenomics
license.
HEALTH DISCOVERY CORPORATION
Management’s Discussion and Analysis,
continued
Other Income and Expense
The Company received
a portion of the NeoGenomics license fee in NeoGenomics stock. The Company has chosen to measure the gain or loss on the value
of this asset using the fair value option method. During the three month period ended September 30, 2015, the change in the NeoGenomics
stock fair value increased by $9,275, which is recorded as other income (expense) in the statements of operations. During the same
three month period in 2014, the change in the NeoGenomics stock fair value increased by $280,214.
As previously discussed
in Note H to the financial statements, the Company negotiated a reduction of amounts owed with certain service providers. As a
result, the Company realized an increase in other income and expense (forgiveness on payables) of $121,503.
Net Loss / Income
The net loss for the
three months ended September 30, 2015 was $53,778, compared to net income of $307,050 for the three months ended September 30,
2014. The change was due primarily to the expiration of the revenue recognition related to the NeoGenomics license and the gain
on available for sale securities.
The loss attributable
to common shareholders was $53,778 for the three months ended September 30, 2015 compared to income of $289,250 in the three months
ended September 30, 2014. This significant change is related to the expiration of the NeoGenomics license revenue recognition,
which occurred in the three-month period ended September 30, 2014, and the gain on available for sale securities.
Basic and diluted loss
per share was $0.0001 for the three-month period ended September 30, 2015 compared to earnings per share of $0.0011 for the quarterly
period ended September 30, 2014.
Nine Months Ended September 30, 2015
Compared with Nine Months Ended September 30, 2014
Revenue
For the nine months
ended September 30, 2015, revenue was $33,754 compared with $773,901 for the nine months ended September 30, 2014. Revenue is recognized
for licensing and development fees over the period earned. The revenue earned is almost entirely related to the licensing revenue
recognition for the NeoGenomics License, which expired in 2014.
Operating and Other Expenses
Amortization expense
was $197,039 for both the nine months ended September 30, 2015 and 2014. Amortization expense relates primarily to the costs associated
with filing patent application and acquiring rights to the patents.
Professional and consulting
fees were $129,377 for the nine months ended September 30, 2015 compared with $144,700 for the same 2014 period. The decrease was
due to the elimination or reduction of professional services provided to the Company.
Legal fees totaled
$37,357 during the nine months ended September 30, 2015 compared to $49,171 during the same period in 2014. The reduction was related
to legal costs in 2014 pertaining to the Company’s matter with the FTC.
Research and Development
fees were $31,813 for the nine months ended September 30, 2015 and $70,763 for the same period in 2014. This expense for research
and development relates primarily to work completed under the NeoGenomics License.
Compensation expense
of $142,665 for the nine months ended September 30, 2015 was less than the $202,311 reported for the comparable 2014 period. The
decrease is attributed to the sacrifices made by current management through reduction, or elimination of, compensation in order
to preserve cash.
Other general and
administrative expenses decreased to $116,843 for the nine months ended September 30, 2015 compared to $129,803 in 2014.
This decrease was due to the reduction in all non-essential costs by the new leadership beginning in August 2013.
HEALTH DISCOVERY CORPORATION
Management’s Discussion and Analysis,
continued
Loss from Operations
The loss from
operations for the nine months ended September 30, 2015 was $621,340 compared to $19,886 for the comparable period
ended September 30, 2014. The increased loss was due to the reduction in revenue recognized, specifically the revenue from
the NeoGenomics license.
Other Income and Expense
The Company received
a portion of the NeoGenomics license fee in NeoGenomics stock. The Company has chosen to measure the gain or loss on the value
of this asset using the fair value option method. During the nine month period ended September 30, 2015, the NeoGenomics stock
fair value increased by $72,231, which is recorded as other income in the statements of operations. During the same period in 2014,
the NeoGenomics stock increased by $237,730.
As previously discussed
in Note H to the financial statements, the Company negotiated a reduction of amounts owed with certain service providers. As a
result, the Company realized an increase in other income and expense (forgiveness of payables) of $121,503.
As a result of the
settlement with the FTC over actions by previous management, the Company recognized a settlement expense of $17,693 during the
first quarter 2015.
Net Loss / Income
The net loss for the
nine months ended September 30, 2015 was $445,299 compared to net income of $217,844 for the nine months ended September 30, 2014.
This reversal from a net income to a net loss was due to the reduction in revenue recognized, specifically the revenue from the
NeoGenomics license.
The net income attributable
to common shareholders was $445,299 for the nine months ended September 30, 2015 compared to a net income of $165,024 in the nine
months ended September 30, 2014.
Basic and diluted
loss per share was $0.0017 for the nine-month period ended September 30, 2015 compared to earnings per share of $0.0007
for the nine month period ended September 30, 2014.
Liquidity and Capital Resources
We have prepared our
financial statements on a “going concern” basis, which presumes that we will be able to realize our assets and discharge
our liabilities in the normal course of business for the foreseeable future.
Our ability to continue
as a going concern is dependent upon our licensing arrangements with third parties, achieving profitable operations, obtaining
additional financing and successfully bringing our technologies to the market. The successful outcome of these matters cannot
be predicted at this time. Our financial statements have been prepared on a going concern basis and do not include any adjustments
to the amounts and classifications of the assets and liabilities that might be necessary should we be unable to continue in business.
At September 30,
2015, we had $506,551 of cash on hand along with stock available for sale worth $104,434. The Company’s plan to
have sufficient cash to support operations is comprised of generating revenue through its relationship with NeoGenomics,
providing services related to those patents, selling its NeoGenomics Stock, and obtaining additional equity or debt
financing.
As a result, the Company
is focusing its efforts to secure funds via licensing activity or other forms of fund raising either in the debt or equity markets. In
addition, prior to the beginning of this year, the Company began raising capital through the Series C Preferred Stock offering.
The Series C Preferred offering was subsequently completed in August 2015. In addition, the Company believes the NeoGenomics relationship
will provide revenue to the Company in 2016, though no assurances to this effect can be made at this time. Therefore, the
Company believes the Series C Preferred Stock offering, along with disciplined expense management, will allow the Company to maintain
operations through 2016.
HEALTH DISCOVERY CORPORATION
Management’s Discussion and Analysis,
continued
Off-Balance Sheet Arrangements
The Company has no
off-balance sheet arrangements that provide financing, liquidity, market or credit risk support or involve leasing, hedging or
research and development services for our business or other similar arrangements that may expose us to liability that is not expressly
reflected in the financial statements.
Forward-Looking Statements
This Report contains
certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 12E of the Securities
Exchange Act of 1934, including or related to our future results, certain projections and business trends. Assumptions relating
to forward-looking statements involve judgments with respect to, among other things, future economic, competitive and market conditions
and future business decisions, all of which are difficult or impossible to predict accurately and many of which are beyond our
control. When used in this Report, the words “estimate,” “project,” “intend,” “believe,”
“expect” and similar expressions are intended to identify forward-looking statements. Although we believe that assumptions
underlying the forward-looking statements are reasonable, any of the assumptions could prove inaccurate, and we may not realize
the results contemplated by the forward-looking statement. Management decisions are subjective in many respects and susceptible
to interpretations and periodic revisions based on actual experience and business developments, the impact of which may cause
us to alter our business strategy or capital expenditure plans that may, in turn, affect our results of operations. In light of
the significant uncertainties inherent in the forward-looking information included in this Report, you should not regard the inclusion
of such information as our representation that we will achieve any strategy, objective or other plans. The forward-looking statements
contained in this Report speak only as of the date of this Report as stated on the front cover, and we have no obligation to update
publicly or revise any of these forward-looking statements. These and other statements which are not historical facts are based
largely on management’s current expectations and assumptions and are subject to a number of risks and uncertainties that
could cause actual results to differ materially from those contemplated by such forward-looking statements. These risks and uncertainties
include, among others, the failure to successfully develop a profitable business, delays in identifying customers, and the inability
to retain a significant number of customers, as well as the risks and uncertainties described in the “Risk Factors”
section to our Annual Report for the fiscal year ended December 31, 2014.
Item
3. Quantitative and Qualitative Disclosures about Market Risk
Not Applicable.
Item 4. Controls and Procedures
As of the end of the
period covered by this report (the “Evaluation Date”), we carried out an evaluation regarding the fiscal quarter ended
September 30, 2015, under the supervision and with the participation of our management, including our Interim Chief Executive Officer,
who is also serving as our Principal Financial Officer, of the effectiveness of the design and operation of our disclosure controls
and procedures pursuant to Rule 13a-15 under the Securities Exchange Act of 1934, as amended (the “Exchange Act”). Based
upon this evaluation, our management concluded that, as of the Evaluation Date, our disclosure controls and procedures were effective
to provide reasonable assurance that information required to be disclosed in the reports that are filed or submitted under the
Exchange Act is recorded, processed, summarized, and reported within the time periods specified by the Securities and Exchange
Commission’s rules and forms and that our disclosure controls and procedures are designed to ensure that information required
to be disclosed in the reports that we file or submit under the Exchange Act is accumulated and communicated to our management
including our Chief Executive Officer, as appropriate, to allow timely decisions regarding required disclosure.
Because of the inherent
limitations in all control systems, no evaluation of controls can provide absolute assurance that the Company’s disclosure
controls and procedures will detect or uncover every situation involving the failure of persons within the Company to disclose
material information otherwise required to be set forth in the Company’s periodic reports.
HEALTH DISCOVERY CORPORATION
The Company’s
management is also responsible for establishing and maintaining adequate internal control over financial reporting to provide reasonable
assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in
accordance with generally accepted accounting principles. As of the Evaluation Date, no changes in the Company’s
internal control over financial reporting occurred that have materially affected or are reasonably likely to materially affect,
the Company’s internal control over financial reporting.
Our Annual Report on
Form 10-K contains information regarding a material weakness in our internal control over financial reporting as of December 31,
2014 due to an inadequate segregation of duties resulting from our small number of employees.
PART II — OTHER INFORMATION
Item 1. Legal Proceedings
None.
Item 1A. Risk Factors
In addition to the
other information set forth in this report, you should carefully consider the risk factors discussed in Part I, “Item 1A.
Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2014, which could materially affect our business,
financial condition or future results. The risks described in our Annual Report on Form 10-K are not the only risks facing our
Company. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial also may materially
adversely affect our business, financial condition and/or operating results.
Item 2. Unregistered Sales of Equity
Securities and Use of Proceeds
In the fourth quarter
of 2013, the Board of Directors authorized the issuance of Series C Preferred Shares in private placement transactions. As of
December 31, 2014 and September 30, 2015, the Company had issued a total of 6,640,000 and 30,000,000 preferred shares, respectively.
The Series C Preferred Shares were fully subscribed in the third quarter 2015. The Company received total net proceeds of $900,000,
of which $568,000 was received in the period ended September 30, 2015. The Series C Preferred Shares are accompanied by $0.03
warrants and $0.03 contingency warrants. The contingency warrants will be issued only if the Company has not attained profitability
by the end of the first quarter 2016. The holders must exercise fifty percent of the warrants if the market price for the Company’s
common stock is $0.20 for a period of thirty consecutive calendar days. The holders must also exercise fifty percent
of the warrants if the market price for the Company’s common stock is $0.30 for a period of thirty consecutive calendar
days. The warrants were valued at $0.025 each using the Black Scholes Method.
The Series C Preferred
Stock has not been registered under either federal or state securities laws and must be held until a registration statement covering
such securities is declared effective by the Securities and Exchange Commission or an applicable exemption applies.
The Series C Preferred Stock may be converted into Common Stock of the Company at the option of the
holder, without the payment of additional consideration by the holder, so long as the Company has a sufficient number of authorized
shares to allow for the exercise of all of its outstanding warrants and options. The Shares of Series C Preferred Stock must be
converted into Common Stock of the Company either by the demand by the shareholder or at the fifth anniversary of the date of
issuance. If the Company were to be dissolved, the Series C Preferred Stock receives preferential treatment over Common Stock.
Item 3. Defaults upon Senior Securities
Not applicable.
Item 4. Mine Safety Disclosures
Not applicable.
Item 5. Other Information
None.
Item 6. Exhibits
The following exhibits
are attached hereto or incorporated by reference herein (numbered to correspond to Item 601(a) of Regulation S-K, as promulgated
by the Securities and Exchange Commission) and are filed as part of this Form 10-Q:
31.1 |
Rule 13a-14(a)/15(d)-14(a) Certifications of Chief Executive Officer and Principal Financial Officer. Filed herewith. |
|
|
32.1 |
Section 1350 Certifications of Chief Executive Officer and Principal Financial Officer. Filed herewith. |
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.
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Health Discovery Corporation |
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Registrant |
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Date: November 16, 2015 |
By: |
/s/ Kevin Kowbel |
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Printed Name: Kevin Kowbel |
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Title: Interim Chief Executive Officer, Principal Financial Officer, and Principal Accounting Officer |
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EXHIBIT 31.1
CERTIFICATIONS PURSUANT TO SECTION 302 OF
THE SARBANES-OXLEY ACT OF 2002
I, Kevin Kowbel, certify that:
1. I have reviewed this quarterly report on Form 10-Q of Health Discovery Corporation (the “Registrant”);
2. Based on my knowledge, this quarterly report does not contain any untrue statement of a material fact or omit to
state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made,
not misleading with respect to the period covered by this report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly
present in all material respects the financial condition, results of operations and cash flows of the Registrant as of, and for,
the periods presented in this report;
4. As the Registrant’s sole certifying officer. I am responsible for establishing and maintaining disclosure controls
and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal controls over financial reporting (as defined
in Exchange Act Rules 13a-15(f)) for the Registrant and have:
a) designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under
my supervision, to ensure that material information relating to the Registrant, including its consolidated subsidiaries, is made
known to me by others within those entities, particularly during the period in which this report is being prepared;
b) designed such internal controls over financial reporting, or caused such internal controls over financial reporting to be
designed under my supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation
of financial statements for external purposes in accordance with generally accepted accounting principles;
c) evaluated the effectiveness of the Registrant’s disclosure controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report
based on such evaluation; and
d) disclosed in this report any change in the Registrant’s internal control over financial reporting that occurred during
the Registrant’s most recent fiscal quarter (the Registrant’s fourth fiscal quarter in the case of an annual report)
that has materially affected, or is reasonably likely to materially affect, the Registrant’s internal control over financial
reporting;
5. The Registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal
control over financial reporting, to the Registrant’s auditors and the audit committee of Registrant’s board of directors
(or persons performing the equivalent functions):
e) all significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting
which are reasonably likely to adversely affect the Registrant’s ability to record, process, summarize and report financial
information; and
f) any fraud, whether or not material, that involves management or other employees who have a significant role in the Registrant’s
internal control over financial reporting.
Date: November 16, 2015 |
/s/ Kevin Kowbel |
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Kevin Kowbel |
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Interim Chief Executive Officer, Principal Financial Officer and Principal Accounting Officer |
EXHIBIT 32.1
CERTIFICATIONS PURSUANT TO 18 U.S.C. SECTION
1350 AS ADOPTED PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
The undersigned hereby certifies, pursuant
to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that this Quarterly Report on
Form 10-Q for the period ended September 30, 2015 fully complies with the requirements of Section 13(a) or 15(d) of the Securities
Exchange Act of 1934, as amended, and the information contained in such report fairly presents, in all material respects, the financial
condition and results of operations of the Company.
Date: November 16, 2015
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/s/ Kevin Kowbel |
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Kevin Kowbel |
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Interim Chief Executive Officer, Principal Financial Officer, and Principal Accounting Officer |
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