UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 10-Q
(Mark One)
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QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the quarterly period ended July 31, 2014
or
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TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the transition period from __________ to __________
Commission file number 333-68008
NUVILEX, INC.
(Exact name of registrant as specified in its
charter)
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Nevada |
62-1772151 |
(State or other jurisdiction of incorporation or organization) |
(I.R.S. Employer Identification No.) |
12510 Prosperity Drive, Suite 310, Silver
Spring, Maryland 20904
(Address of principal executive offices)
(917) 595-2850
(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 of
1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2)
has been subject to such filing requirements for the past 90 days. Yes x No o
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) during the preceding 12 months (or for such shorter
period that the registrant was required to submit and post such files). Yes x No o
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.
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Large accelerated filer |
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Accelerated filer |
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Non-accelerated filer |
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Smaller reporting company |
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(Do not check if a smaller reporting company) |
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Indicate by check mark whether the registrant
is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes o No x
As of September 15, 2014, registrant had
710,020,918 outstanding shares of common stock, with a par value of $0.0001.
NUVILEX, INC.
INDEX TO QUARTERLY REPORT ON FORM 10-Q
FOR THE THREE MONTHS ENDED JULY 31, 2014
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PART I. |
FINANCIAL INFORMATION |
3 |
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Item 1. |
Financial Statements |
3 |
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Consolidated Balance Sheets as of July 31, 2014 (Unaudited) and April 30, 2014 |
3 |
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Consolidated Statements of Operations for the Three Months Ended July 31, 2014 and 2013 (Unaudited) |
4 |
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Consolidated Statements of Cash Flows for the Three Months Ended July 31, 2014 and 2013 (Unaudited) |
5 |
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Notes to Condensed Consolidated Financial Statements (Unaudited) |
6 |
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Item 2. |
Management’s Discussion and Analysis of Financial Condition and Results of Operations |
15 |
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Item 3. |
Quantitative and Qualitative Disclosures About Market Risk |
16 |
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Item 4. |
Controls and Procedures |
16 |
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PART II. |
OTHER INFORMATION |
17 |
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Item 1. |
Legal Proceedings |
17 |
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Item 1A. |
Risk Factors |
17 |
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Item 2. |
Unregistered Sales of Equity Securities and Use of Proceeds |
17 |
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Item 3. |
Defaults Upon Senior Securities |
17 |
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Item 4. |
Mine Safety Disclosures |
17 |
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Item 5. |
Other Information |
17 |
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Item 6. |
Exhibits |
18 |
PART I – FINANCIAL INFORMATION
Item 1. Financial Statements.
NUVILEX, INC.
CONSOLIDATED
BALANCE SHEETS
| |
July 31, 2014 | | |
April 30, 2014 | |
ASSETS | |
(unaudited) | | |
(audited) | |
Cash | |
$ | 2,896,939 | | |
$ | 3,616,470 | |
Prepaid and other assets | |
| 172,133 | | |
| 570,106 | |
Total Current Assets | |
| 3,069,072 | | |
| 4,186,576 | |
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| | | |
| | |
Licenses and patents | |
| 3,549,427 | | |
| 3,549,427 | |
Investment in SG Austria | |
| 1,572,193 | | |
| 1,572,193 | |
Other assets | |
| 7,854 | | |
| 7,854 | |
Total Assets | |
$ | 8,198,546 | | |
$ | 9,316,050 | |
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LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT) | |
| | | |
| | |
Current Liabilities | |
| | | |
| | |
Accounts payable | |
| 204,370 | | |
| 188,044 | |
Accrued expenses | |
| 5,262 | | |
| 7,803 | |
Accrued interest, related party | |
| 36,612 | | |
| 33,960 | |
Due to an officer | |
| 125,142 | | |
| 143,859 | |
Total Current Liabilities | |
| 371,386 | | |
| 373,666 | |
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Total Liabilities | |
| 371,386 | | |
| 373,666 | |
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Commitments and Contingencies | |
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Preferred stock, authorized 10,000,000 shares, $0.0001 par value, 0 shares issued and outstanding, respectively | |
| – | | |
| – | |
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Stockholders' Equity (Deficit) | |
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Common stock, authorized 1,490,000,000 shares, $0.0001 par value, 710,356,214 and 690,615,714 shares issued and outstanding, respectively | |
| 71,036 | | |
| 69,063 | |
Additional paid in capital | |
| 78,041,075 | | |
| 75,998,588 | |
Common stock to be issued | |
| – | | |
| 1,574,860 | |
Accumulated deficit | |
| (70,284,951 | ) | |
| (68,700,127 | ) |
Total Stockholders' Equity (Deficit) | |
| 7,827,160 | | |
| 8,942,384 | |
Total Liabilities and Stockholders' Equity (Deficit) | |
$ | 8,198,546 | | |
$ | 9,316,050 | |
The accompanying notes are an integral part
of these consolidated financial statements.
NUVILEX, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
(UNAUDITED)
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For the Three Months Ended July 31, | |
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2014 | | |
2013 | |
Revenues: | |
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Product sales | |
$ | – | | |
$ | – | |
Total revenue | |
| – | | |
| – | |
Cost of revenues | |
| – | | |
| – | |
Gross margin | |
| – | | |
| – | |
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Expenses: | |
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Sales and marketing | |
| 230,500 | | |
| 15,000 | |
Compensation expense | |
| 253,418 | | |
| 1,202,127 | |
Legal & professional fees | |
| 260,864 | | |
| 64,358 | |
General and administrative | |
| 838,378 | | |
| 119,206 | |
Total operating expenses | |
| 1,583,160 | | |
| 1,400,691 | |
Net loss from operations | |
| (1,583,160 | ) | |
| (1,400,691 | ) |
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Other income (expense): | |
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Gain on forgiveness of debt | |
| – | | |
| 1,358,470 | |
Loss on conversion of preferred stock | |
| – | | |
| (640,000 | ) |
Loss on settlement of debt | |
| – | | |
| (3,973,795 | ) |
Interest income | |
| 988 | | |
| – | |
Interest expense | |
| (2,652 | ) | |
| (10,351 | ) |
Total other expense | |
| (1,664 | ) | |
| (3,265,676 | ) |
Net loss | |
$ | (1,584,824 | ) | |
$ | (4,666,367 | ) |
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Basic loss per share | |
$ | (0.00 | ) | |
$ | (0.01 | ) |
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Weighted average shares outstanding | |
| 701,930,165 | | |
| 521,873,196 | |
The accompanying notes are an integral part
of these consolidated financial statements.
NUVILEX, INC.
CONSOLIDATED STATEMENTS OF CASH FLOWS
(UNAUDITED)
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For the Three Months Ended | |
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July 31, | |
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2014 | | |
2013 | |
Cash flows from operating activities: | |
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Net loss | |
$ | (1,584,824 | ) | |
$ | (4,666,367 | ) |
Adjustments to reconcile net loss to net cash used in operating activities: | |
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Stock issued for services | |
| 297,500 | | |
| 1,201,608 | |
Stock issued for compensation | |
| 86,100 | | |
| – | |
Loss on settlement of debt | |
| – | | |
| 3,973,795 | |
Loss on conversion of preferred stock | |
| – | | |
| 640,000 | |
Gain on forgiveness of debt | |
| – | | |
| (1,358,470 | ) |
Change in assets and liabilities: | |
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Decrease in prepaid expenses | |
| 397,973 | | |
| 29,547 | |
Increase in accounts payable | |
| 16,326 | | |
| 965 | |
Increase in accrued interest, related party | |
| 2,652 | | |
| 7,902 | |
Increase (decrease) in accrued expenses | |
| (2,541 | ) | |
| 11,346 | |
Net cash used in operating activities | |
| (786,814 | ) | |
| (159,674 | ) |
Cash flows from investing activities: | |
| | | |
| | |
Payments towards acquisition | |
| – | | |
| (1,568,850 | ) |
Net cash used by investing activities | |
| – | | |
| (1,568,850 | ) |
Cash flows from financing activities: | |
| | | |
| | |
Proceeds from the sale of common stock | |
| 86,000 | | |
| 1,660,000 | |
Proceeds from borrowings, related party | |
| – | | |
| 77,853 | |
Repayment of debt, related party | |
| (18,717 | ) | |
| (2,594 | ) |
Net cash provided by financing activities | |
| 67,283 | | |
| 1,735,259 | |
Net increase /(decrease) in cash | |
| (719,531 | ) | |
| 6,735 | |
Cash at beginning of period | |
| 3,616,470 | | |
| 199,303 | |
Cash at end of period | |
$ | 2,896,939 | | |
$ | 206,038 | |
Supplementary non-cash disclosures: | |
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Cash paid for interest | |
$ | – | | |
$ | – | |
Franchise and income taxes | |
$ | – | | |
$ | – | |
Common stock issued for debt | |
$ | – | | |
$ | 533,598 | |
The accompanying notes are an integral part
of these consolidated financial statements.
NUVILEX, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
JULY 31, 2014
(UNAUDITED)
NOTE 1 – BACKGROUND, ACQUISITION AND LIQUIDITY
Historical Overview of the Company
Past Nutraceutical Company
The Company was founded as DJH International,
Inc. on October 28, 1996. It changed its name to eFoodSafety.com, Inc. following the October 16, 2000 acquisition of Global Procurement
Systems, Inc. The Company acquired Ozone Safe Food, Inc. for common stock on October 29, 2003. The Company's business plan was
to provide methods and products to ensure safety of marketed fruits and vegetables worldwide. On February 4, 2004, the Company
registered shares of common stock with the SEC. It began publicly trading on the OTC Bulletin Board under the trading symbol EFSF.
With unrealized demand for the Company’s
produce sterilization methods and software tracking products, the Company changed its business plan and acquired Knock-Out Technologies,
Ltd. and MedElite, Inc. in May 2004 and August 2005, respectively. Knock-Out Technologies, Ltd. was a developer of natural products
using organic, non-toxic, food grade material. MedElite, Inc. was the exclusive distributor of Talsyn-CI Scar Cream in the United
States, a topical scar- reducing cream. The Company's strategy was to market nutraceutical products. The Company sold its Ozone
Safe Food, Inc. operations in August 2005. In November 2006, the Company formed Cinnergen, Inc. to manufacture and market a non-prescription
liquid nutritional supplement designed to promote healthy glucose metabolism and purEffect, Inc. to manufacture and market purEffect
- a four-step non-prescription acne treatment. On March 10, 2006, the Company licensed the marketing rights for purEffect to Charlston
Kentrist 41 Direct, Inc. (“CK41”). In July 2007, the Company formed, I-Boost to market products to support the immune
system. In March 2008, Cinnechol, Inc. was formed to promote cardiovascular health. In February 2009, the Company sold the rights
to the purEffect product to CK41 for an equity position in CK41 and future royalty compensation. In March 2009, Freedom2 Holdings,
Inc. was acquired to manufacture and market products including Infinitink®, a tattoo ink designed to be easily removed.
On January 20, 2009, the Company changed its
name to Nuvilex, Inc. Its trading symbol on the OTC Bulletin Board® was also changed to NVLX.
Current Biotechnology Company
On May 26, 2011, the Company entered into an
Asset Purchase Agreement (“SG Austria APA”) with SG Austria Private Limited (“SG Austria”) to purchase
100% of the assets and liabilities of SG Austria. As a result, Austrianova Singapore Private Limited ("Austrianova Singapore")
and Bio Blue Bird AG ("Bio Blue Bird"), wholly-owned subsidiaries of SG Austria, were to become wholly owned subsidiaries
of the Company on the condition that the Company pay SG Austria $2.5 million and 100,000,000 shares of the Company’s common
stock and for the Company to receive 100,000 shares of Austrianova Singapore’s common stock and nine Bio Blue Bird bearer
shares.
Through two addenda to the SG Austria APA,
the closing dates were extended. In June 2013, the Company and SG Austria entered into a Third Addendum to the SG Austria APA (“Third
Addendum”). Under the terms of the Third Addendum, the transaction contemplated by the SG Austria APA changed substantially.
The Third Addendum resulted in the Company acquiring 100% of the equity interests in Bio Blue Bird and receiving a 14.5% equity
interest in SG Austria. In addition, the Company received nine bearer shares of Bio Blue Bird. Under the Third Addendum, the Company
paid: (i) $500,000 to retire all outstanding debt of Bio Blue Bird; and (ii) $1.0 million to SG Austria. The Company also paid
SG Austria $1,572,193. The Third Addendum returned the original 100,000,000 shares of common stock to the Company treasury and
the 100,000 Austrianova Singapore shares to SG Austria.
The acquisition of Bio Blue Bird provided the
Company with exclusive, worldwide licenses to use a proprietary cellulose-based live cell encapsulation technology for the development
of treatments for all forms of cancer using certain types of cells. The licenses are pursuant to patents licensed from Bavarian
Nordic A/S and GSF-Forschungszentrum fur Umwelt u. Gesundeit GmbH. These licenses enable the Company to carry out the research
and development of cancer treatments that are based upon the live cell encapsulation technology known as “Cell-in-a-Box
®.”
In July 2013, the Company also acquired from
Austrianova Singapore the exclusive, worldwide license to use the cellulose-based live cell encapsulation technology for the development
of a treatment for diabetes and the use of Austrianova Singapore’s “Cell-in-a-Box ®” trademark
for this technology (“Diabetes Licensing Agreement”). The Company made its first $1,000,000 payment to secure the Diabetes
Licensing Agreement on October 30, 2013. The second and final payment of $1,000,000 was made on February 25, 2014.
NOTE 2 – CAPITALIZATION AND MANAGEMENT PLANS
Capitalization
The Company's financial statements are prepared
using generally accepted accounting principles in the United States (“GAAP”) applicable to a going concern which contemplates
the realization of assets and liquidation of liabilities in the normal course of business. As of July 31, 2014, the Company has
an accumulated deficit of $70,284,951 and incurred a net loss for three months ended July 31, 2014 of $1,584,824.
Funding has been provided by management and
investors to maintain and expand the Company and acquire Bio Blue Bird. New investors enabled the completion of the acquisition
of Bio Blue Bird which provided the Company the ability to begin preparations toward further clinical trials in patients with advanced,
inoperable pancreatic cancer. Additional funding enabled the Company to obtain the diabetes license and to advance the Company’s
preclinical studies and preparations for clinical trials of its product candidates. The remaining challenges, beyond the regulatory
and clinical aspects, include accessing further funding for the Company to cover its future cash flow needs. The Company continues
to acquire additional funds through management's efforts.
The Company requires substantial additional
capital to finance its planned business operations and expects to incur operating losses in future periods due to the expenses
related to the Company’s core businesses. The Company has not realized material revenue since it commenced doing business
in the biotechnology sector, and it is not without doubt that it will be successful in generating revenues in the future in this
sector. The Company believes that cash and cash equivalents as of July 31, 2014 are sufficient to fund its operations through the
end of July 31, 2015.
If the Company is not able to raise substantial
additional capital in a timely manner, the Company may not be able to complete its required preclinical studies and clinical trials
and may be forced to cease operations.
The Company will continue to be dependent on
outside capital to fund its research and operating expenditures for the foreseeable future. If the Company fails to generate positive
cash flows or fails to obtain additional capital when required, the Company may need to modify, delay or abandon some or all of
its business plans.
Management Strategy and Goals
The Company's strategy is to build upon and
advance the success of the previous Phase 1/2 pancreatic cancer clinical trials and develop a treatment for diabetes utilizing
the Cell-in-a-Box® cellulose-based live cell encapsulation technology. Management believes the Company is positioned
to move forward and become a significant biotech company predicated upon this platform technology. Management is committed to becoming
an industry-leading biotechnology company in the treatment of cancer and diabetes.
The Company will seek to raise capital to fund
growth opportunities and provide for its working capital needs as the strategy of the Company is executed. The Company's efforts
to achieve financial stability and to enable it to carry out the strategy of the Company consist of the following:
| · | Completing preparations for the Phase 2b clinical trial in advanced
pancreatic cancer to be carried out by Clinical Network Services in Australia; |
| · | Conducting preclinical studies and clinical trials by Translational
Drug Development in the United States that examine the effectiveness of the Company’s pancreatic cancer treatment in ameliorating
the pain and accumulation of malignant ascites fluid in the abdomen that are characteristic of pancreatic cancer; |
| · | Conducting preclinical studies in connection with the development
of product candidates to treat diabetes; |
| · | Conducting preclinical studies to determine the feasibility of using
constituents (cannabinoids) of marijuana for medical use, including the development of treatments for serious and deadly forms
of cancer; |
| · | Enhancing the Company’s ability to expand into the biotechnology
arena through research and partnering; |
| · | Acquiring new contracts and revenue utilizing both in-house products
and the newly acquired biotechnology licensing rights; |
| · | Developing further uses of the Cell-in-a-Box® technology
through contracts, licensing and joint ventures with other companies; and |
| · | Completing the testing, expansion and marketing of existing products
and newly derived Company product candidates. |
NOTE 3 – SIGNIFICANT ACCOUNTING POLICIES
Unaudited Financial Statements
The accompanying unaudited consolidated financial
statements have been prepared in accordance with GAAP for interim financial information and pursuant to the instructions to Form
10-Q and Article 10 of Regulation S-X. While these statements reflect all normal recurring adjustments which are, in the opinion
of management, necessary for fair presentation of the results of the interim period, they do not include all of the information
and footnotes required by GAAP for complete financial statements. The unaudited interim financial statements should be read in
conjunction with the Company’s annual report on Forms 10-K which contain the audited financial statements and notes thereto,
together with Management’s Discussion and Analysis, for the fiscal year ended April 30, 2014. The interim results for
the three months ended July 31, 2014 are not necessarily indicative of the results for the full fiscal year.
Management further acknowledges it is solely
responsible for adopting sound accounting practices, establishing and maintaining a system of internal accounting controls and
preventing and detecting fraud. The Company's system of internal accounting control is designed to ensure, among other items, that
transactions are recorded and valid and in the proper period in a timely manner to produce financial statements which present fairly
the financial condition, results of operations and cash flows of the Company for the respective periods being presented.
Principles of Consolidation
The accompanying financial statements include
the accounts of the Company and its subsidiaries as of July 31, 2014 Bio Blue Bird and Medical Marijuana Sciences, Inc. (“MMS”).
All significant inter-company balances and transactions have been eliminated in consolidation. See Note 4 for further discussion
on consolidation.
Cash and Cash Equivalents
For purposes of the statement of cash flows,
the Company considers all highly liquid debt instruments purchased with a maturity of three months or less to be cash equivalents
to the extent the funds are not being held for investment purposes. There were no cash equivalents as of July 31, 2014.
Segment Reporting
ASC Topic 280, “Segment
Report,” requires use of the “management approach” model for segment reporting. The management approach model
is based on the way a company’s management organizes segments within the company for making operating decisions and assessing
performance. ASC Topic 280 has no effect on the Company’s consolidated financial statements as the Company consists
of one reportable business segment. All revenue is from biotechnology operations.
Use of Estimates
The preparation of financial statements in
conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities
and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues
and expenses during the reporting period. Actual results could differ from those estimates.
Property and Equipment
Property and equipment are recorded at cost.
Expenditures that increase the useful lives or capacities of the plant and equipment are capitalized. Expenditures for repairs
and maintenance are charged to income as incurred. Depreciation is provided using the straight-line method over the estimated
useful lives as follows:
| · | Computer equipment/software - 3 years |
| · | Furniture and fixtures - 7 years |
| · | Machinery and equipment - 7 years |
| · | Building improvements - 15 years |
Goodwill and other Indefinite-Lived Intangibles
The Company records the excess of purchase
price over the fair value of the identifiable net assets acquired as goodwill and other indefinite-lived intangibles. The Fair
Accounting Standards Board ("FASB") standard on goodwill and other intangible assets prescribes a two-step process for
impairment testing of goodwill and indefinite-lived intangibles, which is performed annually and when an event triggering impairment
may have occurred. The first step tests for impairment, while the second step, if necessary, measures the impairment. The Company
has elected to perform its annual analysis at the end of its reporting year.
Valuation of Long-Lived Assets
The Company accounts for the valuation of long-lived
assets under the FASB standard for accounting for the impairment or disposal of Long-Lived Assets. The FASB standard requires that
long-lived assets and certain identifiable intangible assets be reviewed for impairment whenever events or circumstances indicate
that the carrying amount of an asset may not be recoverable. Recoverability of the long-lived assets is measured by a comparison
of the carrying amount of the asset to future undiscounted net cash flows generated by the asset. If such assets are considered
to be impaired, the impairment to be recognized is measured by the amount by which the carrying amount of the assets exceeds the
estimated fair value of the assets. Assets to be disposed of are reported at the lower of the carrying amount or fair value, less
cost to sell.
Functional Currency
The accounts of Bio Blue Bird are maintained
in Euros. The accounts of this foreign subsidiary were translated into US dollars in accordance with ASC Topic 830 “Foreign
Currency Matters.” According to ASC Topic 830: (i) all assets and liabilities were translated at the exchange rate on the
balance sheet dates; (ii) stockholders’ equity is translated at historical rates; and (iii) statement of operation items
are translated at the weighted average exchange rate for the period. The resulting translation adjustments are reported under other
comprehensive income in accordance with ASC Topic 220, “Comprehensive Income.” Gains and losses resulting from the
translations of foreign currency transactions and balances are reflected in the statements of income.
Foreign Currency Transactions and Comprehensive
Income
GAAP requires that recognized revenue, expenses,
gains and losses be included in net income. Certain statements, however, require entities to report specific changes in assets
and liabilities, such as gain or loss on foreign currency translation, as a separate component of the equity section of the balance
sheet. Such items, along with net income, are components of comprehensive income. Translation gains are classified as an item of
accumulated other comprehensive income in the stockholders’ equity section of the unaudited Consolidated Balance Sheet.
Basic and Diluted Earnings (Loss) per Share
Basic and diluted earnings per share is calculated
using the weighted-average number of common shares outstanding during the period without consideration of the dilutive effect of
stock warrants, convertible notes and convertible preferred shares. All outstanding warrants are convertible into 57,115,600 shares
of common stock.
Fair Value of Financial Instruments
For certain of the Company’s non-derivative
financial instruments, including cash and cash equivalents, receivables, accounts payable and other accrued liabilities, the carrying
amount approximates fair value due to the short-term maturities of these instruments. The estimated fair value of long-term debt
is based primarily on borrowing rates currently available to the Company for similar debt issues. The fair value approximates the
carrying value of long-term debt.
Accounting Standards Codification ("ASC")
Topic 820, “Fair Value Measurements and Disclosures,” requires disclosure of the fair value of financial instruments
held by the Company. ASC Topic 825, “Financial Instruments,” defines fair value, and establishes a three-level valuation
hierarchy for disclosures of fair value measurement that enhances disclosure requirements for fair value measures. The carrying
amounts reported in the consolidated balance sheets for receivables and current liabilities each qualify as financial instruments
and are a reasonable estimate of their fair values because of the short period of time between the origination of such instruments
and their expected realization and their current market rate of interest. The three levels of valuation hierarchy are defined as
follows:
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Level 1. Observable inputs such as quoted prices in active markets; |
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· |
Level 2. Inputs, other than the quoted prices in active markets, that are observable either directly or indirectly; and |
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· |
Level 3. Unobservable inputs in which there is little or no market data, which require the reporting entity to develop its own assumptions. |
The following presents the gross
value of assets and liabilities that were measured and recognized at fair value as of July 31, 2014.
Effective October 1, 2008, the Company
adopted ASC subtopic 820-10, Fair Value Measurements and Disclosures ("ASC 820-10") and Accounting Standards Codification
subtopic 825-10, Financial Instruments ("ASC 825-10"), which permits entities to choose to measure many financial
instruments and certain other items at fair value. Neither of these statements had an impact on the Company's financial position,
results of operations or cash flows. The carrying value of cash, accounts payable and accrued expenses, as reflected in the balance
sheets, approximate fair value because of the short-term maturity of these instruments.
Recent Accounting Pronouncements
In February 2013, the Financial Accounting
Standards Board issued Accounting Standards Update (ASU) No. 2013-02, Comprehensive Income (Topic 220): Reporting of Amounts
Reclassified out of Accumulated Other Comprehensive Income, to improve the transparency of reporting these reclassifications.
Other comprehensive income includes gains and losses that are initially excluded from net income for an accounting period. Those
gains and losses are later reclassified out of accumulated other comprehensive income into net income. The amendments in the ASU
do not change the current requirements for reporting net income or other comprehensive income in financial statements. All of the
information that this ASU requires already is required to be disclosed elsewhere in the financial statements under GAAP. The new
amendments will require an organization to:
| · | Present (either on the face of the statement where net income is presented
or in the notes) the effects on the line items of net income of significant amounts reclassified out of accumulated other comprehensive
income - but only if the item reclassified is required under GAAP to be reclassified to net income in its entirety in the same
reporting period; and |
| · | Cross-reference to other disclosures currently required under GAAP for
other reclassification items (that are not required under GAAP) to be reclassified directly to net income in their entirety in
the same reporting period. This would be the case when a portion of the amount reclassified out of accumulated other comprehensive
income is initially transferred to a balance sheet account (e.g., inventory for pension-related amounts) instead of directly to
income or expense. |
The amendments apply to all public and private
companies that report items of other comprehensive income. Public companies are required to comply with these amendments for all
reporting periods (interim and annual). The amendments are effective for reporting periods beginning after December 15, 2012, for
public companies. Early adoption is permitted. The adoption of ASU No. 2013-02 is not expected to have a material impact on our
financial position or results of operations.
In July 2013, the FASB issued Accounting Standards
Update 2013-11 Income Taxes (Topic 740) Presentation of an Unrecognized Tax Benefit When a Net Operating Loss Carry-forward, a
Similar Tax Loss, or a Tax Credit Carry-forward Exists. An unrecognized tax benefit, or a portion of an unrecognized tax benefit,
should be presented in the financial statements as a reduction to a deferred tax asset for a net operating loss carry-forward,
a similar tax loss or a tax credit carry-forward, except as follows. To the extent that a net operating loss carry-forward, a similar
tax loss or a tax credit carry-forward is not available at the reporting date under the tax law of the applicable jurisdiction
to settle any additional income taxes that would result from the disallowance of a tax position or the tax law of the applicable
jurisdiction does not require the entity to use, and the entity does not intend to use the deferred tax asset for such purpose,
the unrecognized tax benefit should be presented in the financial statements as a liability and should not be combined with deferred
tax assets. The assessment of whether a deferred tax asset is available is based on the unrecognized tax benefit and deferred tax
asset that exist at the reporting date and should be made presuming disallowance of the tax position at the reporting date. This
Update applies to all entities that have unrecognized tax benefits when a net operating loss carry-forward, a similar tax loss,
or a tax credit carry-forward exists at the reporting date. The amendments in this Update are effective for fiscal years, and interim
periods within those years, beginning after December 15, 2013.
The Company has implemented all new accounting
pronouncements that are in effect. These pronouncements did not have any material impact on the financial statements unless
otherwise disclosed, and the Company does not believe that there are any other new accounting pronouncements that have been issued
that might have a material impact on its financial position or results of operations.
Revenue Recognition
Sales of products and related costs of products
sold are recognized when: (i) persuasive evidence of an arrangement exists; (ii) delivery has occurred; (iii) the price is fixed
or determinable; and (iv) collectability is reasonably assured. These terms are typically met upon the prepayment or invoicing
and shipment of products.
Income Taxes
Deferred taxes are calculated using the liability
method whereby deferred tax assets are recognized for deductible temporary differences and operating loss and tax credit carry
forwards and deferred tax liabilities are recognized for taxable temporary differences. Temporary differences are the differences
between the reported amounts of assets and liabilities and their tax bases. Deferred tax assets are reduced by a valuation
allowance when, in the opinion of management, it is more likely than not that some portion or all of the deferred tax assets will
not be realized. Deferred tax assets and liabilities are adjusted for the effects of changes in tax laws and rates on the date
of enactment.
In June 2006, the FASB interpreted
its standard for accounting for uncertainty in income taxes, an interpretation of accounting for income taxes. This
interpretation clarifies the accounting for uncertainty in income taxes recognized in an entity’s financial statements
in accordance the minimum recognition threshold and measurement attributable to a tax position taken on a tax return is
required to be met before being recognized in the financial statements.
The FASB’s interpretation had no material
impact on the Company’s financial statements for the quarter ended July 31, 2014 or the year ended April 30, 2014. Current
tax laws limit the amount of loss available to be offset against future taxable income when a substantial change in ownership occurs.
Therefore, the amount available to offset future taxable income may be limited. No tax benefit has been reported in the financial
statements because the Company believes the carry forwards may expire unused, although acquisition of sufficient operating capital
to complete the acquisition of all of the assets of SG Austria may change this. Accordingly, the potential tax benefits of the
loss carry forwards are offset by a valuation allowance of the same amount.
Research and Development Costs
Expenditures for research and development are
expensed as incurred. Such costs are required to be expensed until the point that technological feasibility is established.
Concentration of Credit Risk
The Company has no significant off-balance-sheet
concentrations of credit risk such as foreign exchange contracts, options contracts or other foreign hedging arrangements. The
Company maintains the majority of its cash balances with one financial institution in the form of demand deposits.
NOTE 4 – BUSINESS ACQUISITION
As of April 30, 2014, the Company had
completed the purchase of Bio Blue Bird. Shares for both Austrianova Singapore and the Company originally held in escrow under
the SG Austria APA have been released from escrow and returned to the respective original owners, with the 100,000,000 shares of
common stock having been returned to the treasury of the Company. Bio Blue Bird is now a wholly owned subsidiary of the Company.
NOTE 5 – DEBT
In February, 2014, the Company settled
its obligation to pay $20,000 plus $6,000 of accrued interest to a note holder with the issuance of 250,000 shares of common
stock. The shares were valued at $45,500 using the closing share price of the common stock on the day of issuance resulting
in a loss on settlement of debt of $19,500.
NOTE
6 – COMMON STOCK TRANSACTIONS
In May 2013, 75,000 shares of common stock
were issued to settle debt of $32,392. The shares were valued using the closing share price of the common stock of the day of issuance,
resulting in a gain on settlement of $21,142.
During the year ended April 30, 2014, a shareholder
converted 8,500 shares of the Company’s Series E Preferred Stock (defined below) into 54,000,000 shares of common stock.
The shares were valued using the closing share price of the common stock on the day of issuance for a total of $6,475,000 resulting
in a loss on conversion of $5,895,000.
During the year ended April 30, 2014, 52,370,000
shares of common stock were issued to officers and directors of the Company for compensation. These shares were valued using the
closing share price of the common stock on the day of issuance for a total non-cash expense of $14,101,788.
During the year ended April 30, 2014, 13,756,666
shares of common stock were issued to consultants for services rendered to the Company. These shares were valued using the closing
share price of the common stock price on the day of issuance for a total non-cash expense of $1,810,348. As of April 30, 2014,
$528,808 of this expense has been deferred to prepaid expenses and will be expensed to future periods as determined by the term
of each agreement.
During the year ended April 30, 2014, the Company
sold 27,000,000 shares of common stock for $4,918,000. As of April 30, 2014, 17,000,000 of these shares had not yet been issued
and are disclosed as common stock to be issued.
During the year ended April 30, 2014, the Company
converted some of its Class A and Class B warrants into 19,649,600 shares of common stock for $1,592,880.
On February 14, 2014, the Company entered into
a stock purchase agreement with Lincoln Park Capital Fund, LLC (“Lincoln Park”). Lincoln Park initially purchased 8
million shares of common stock at $0.25 per share for $2 million and had committed to invest up to an additional $25 million of
equity capital over the term of the stock purchase agreement. As consideration for its commitment to purchase shares of common
stock pursuant to the stock purchase agreement, the Company issued to Lincoln Park 5,062,500 shares of common stock upon execution
of the stock purchase agreement. These shares were valued at $0.169, the closing price of the stock on February 14, 2014, for non-cash
expense of $855,653. On May 28, 2014 the Company and Lincoln Park executed a Mutual Termination and Release Agreement releasing
all parties from certain obligation under the stock purchase agreement. As consideration for terminating the stock purchase agreement,
the Company issued Lincoln Park an additional 1,062,500 shares of common stock. These shares were valued at $0.28 for total non-cash
expense of $297,500.
During the quarter ended July 31, 2014, 300,000
shares of common stock were issued to an officer of the Company for compensation. These shares were valued using the closing share
price of the common stock on the day of issuance for a total non-cash expense of $86,100.
During the quarter ended July 31, 2014, the
Company sold 200,000 shares of common stock for $20,000.
During the quarter ended July 31, 2014, the
Company converted some of its Class B warrants into 550,000 shares of common stock for $66,000.
During the quarter ended July 31, 2014, 17,628,000
shares of common stock were issued to fully satisfy all stock payables due in the amount of $1,574,860.
All shares were issued without registration
under the Securities Act in reliance upon the exemption afforded by Section 4(2) of the Securities Act.
NOTE 7 – PREFERRED STOCK
The Company has one series of preferred stock designated as "Series
E Preferred Stock." The Series E Preferred Stock has the following features:
|
· |
Series E Preferred Stock does not bear any dividends; |
|
· |
Each share of Series E Preferred Stock is entitled to receive its share of assets distributable upon the liquidation, dissolution or winding up of the affairs of the Company. The holders of the Series E Preferred Stock are entitled to receive cash out of the assets of the Company before any amount is paid to the holders of any capital stock of the Company of any class junior in rank to the shares of Series E Preferred Stock; |
|
· |
Each share of Series E Preferred Stock is convertible, at the holder’s option, into shares of common stock, at the average closing bid price of the common stock for five trading days prior to the conversion date; and |
|
· |
At every meeting of stockholders, every holder of shares of Series E Preferred Stock is entitled to 50,000 votes for each share of Series E Preferred Stock, with the same and identical voting rights as a holder of a share of common stock; therefore, the holder of shares of Series E Preferred Stock can effectively increase the Company’s issued common stock shares without a vote of the common stock shareholders, thus enabling any potential shortfall of authorized common stock outstanding from being converted should a holder of Series E Preferred Stock wish to convert. |
During the year ended April 30, 2014, a shareholder
converted 8,500 shares of the Company’s Series E Preferred Stock into 54,000,000 shares of common stock. These shares were
valued using the closing share price of the common stock on the day of issuance for a total of $6,475,000 resulting in a loss on
conversion of $5,895,000.
Holders of Series E Preferred Stock have specific
rights to be paid in cash out of the assets of the Company prior to any junior class of common stock. As a result of the obligations
for Series E Preferred Stock, the Company has determined these redemption features have the potential to be outside the control
of the Company and, therefore, the Company has classified the Series E Preferred Stock outside of shareholder’s equity in
accordance with ASC 480 regarding instruments with debt and equity features. Thus, the full value for the convertible Series E
Preferred Stock was recorded outside of stockholders’ equity in the accompanying unaudited consolidated balance sheet.
NOTE 8 – WARRANTS
A summary of the status of the Company's outstanding
warrants for common stock as of July 31, 2014 and April 30, 2014 and changes during the periods is presented below:
|
|
|
Warrants |
|
|
Weighted
Average
Price |
|
|
Weighted
Average
Fair Value |
|
Outstanding, April 30, 2014 |
|
|
|
57,665,600 |
|
|
$ |
0.18 |
|
|
$ |
0.065 |
|
Exercised |
|
|
|
(550,000) |
|
|
|
– |
|
|
|
– |
|
Issued |
|
|
|
– |
|
|
|
– |
|
|
|
– |
|
Outstanding, July 31, 2014 |
|
|
|
57,115,600 |
|
|
|
0.18 |
|
|
|
0.065 |
|
Exercisable, July 31, 2014 |
|
|
|
57,115,600 |
|
|
$ |
0.18 |
|
|
$ |
0.065 |
|
Range of
Exercise
Prices |
|
Number Outstanding at 7/31/14 |
|
|
Weighted Average Remaining Contractual Life |
|
|
Weighted Average Exercise Price |
|
$0.075, $0.12, and $0.18 |
|
|
57,115,600 |
|
|
|
3.4 |
|
|
$ |
0.18 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
On January 21, 2014, the Company began the
implementation of its “Warrant Conversion Program.” The program consists of having every warrant holder of a Class
A warrant convert his or her Class A warrants (with a conversion price of $0.075 per share) into shares of common stock and receive
an equal number of new Class D warrants (with a conversion price of $0.25 per share). As of July 31, 2014, 18,755,200 Class
A warrants and 2,318,000 Class B warrants were converted for total cash proceeds of $1,658,880.
NOTE 9 – LEGAL PROCEEDINGS
The Company is not currently a party to any
material pending legal proceedings. There are no material legal proceedings to which any property of the Company is subject.
NOTE 10 – RELATED PARTY TRANSACTIONS
As of July 31, 2014 the Company owed $125,142
of principle and $36,612 of accrued interest to an officer. The loan accrues interest at 8% and is due on demand.
NOTE 11 – SIGNIFICANT EVENTS
As discussed above, the Company acquired 100%
of the shares and assets of Bio Blue Bird, including its intellectual property related to the “Cell-in-a-Box®
live cell encapsulation technology. In that same transaction, the Company also received a 14.5% ownership in SG Austria. The Company
also entered into the Diabetes Licensing Agreement with Austrianova Singapore for the treatment of diabetes utilizing the Cell-in-a-Box®
technology. Under the Diabetes Licensing Agreement, the Company was granted an exclusive worldwide license to use the Cell-in-a-Box®
trademark and its associated technology specifically addressing insulin and other critical component production for the treatment
of diabetes. The Company has retained Vantage Point Advisors, Inc. (“VPAI”), to perform a valuation analysis of its
contingent payment liability associated with the future milestone and royalty payments stemming from the Diabetes Licensing Agreement.
The Company has also retained VPAI to perform a valuation analysis of its 14.5% ownership interest in SG Austria. These two valuations
are currently underway and will be completed in the near term. Based upon the results of these valuations, the Company will adjust
the value of its assets as required.
NOTE 12 –
SUBSEQUENT EVENTS
The Company has performed an evaluation of
subsequent events in accordance with ASC Topic 855, noting no additional subsequent events other than those noted below.
Subsequent to July 31, 2014, the Company terminated
a professional service agreement with one of its consultants. In accordance with the terms of that agreement, the service provider
agreed to return 335,296 shares of common stock to the Company.
Item 2. Management’s Discussion and Analysis
of Financial Condition and Results of Operations.
This following information
specifies certain forward-looking statements of our management. Forward-looking statements are statements that estimate
the happening of future events and are not based on historical fact. Forward-looking statements may be identified by
the use of forward-looking terminology, such as “may”, “shall”, “could”, “expect”,
“estimate”, “anticipate”, “predict”, “probable”, “possible”, “should”,
“continue”, or similar terms, variations of those terms or the negative of those terms. Forward-looking
statements should not be read as a guarantee of future performance or results and may not be accurate indications of when such
performance or results will be achieved. Forward-looking statements are based on information we have when those statements are
made or management’s good faith belief as of that time with respect to future events and are subject to risks and uncertainties
that could cause actual performance or results to differ materially from those expressed in or suggested by the forward-looking
statements. The forward-looking statements specified in the following information have been compiled by our management on the basis
of assumptions made by management and considered by management to be reasonable. Our future operating results, however, are impossible
to predict, and no representation, guaranty, or warranty is to be inferred from those forward-looking statements. You are cautioned
not to place undue reliance on these forward-looking statements.
Forward-looking statements include, but are
not limited to, the following:
|
· |
Statements relating to our future business and financial performance; |
|
· |
Statements relating to future preclinical studies, clinical trials and regulatory approvals of our products; |
|
· |
Statements relating to our competitive position; and |
|
· |
Other material future developments that you may take into consideration. |
Results of Operations for the Three Months
Ended July 31, 2014 and 2013
The Company, through its acquisition of Bio
Blue Bird AG (“Bio Blue Bird”), successfully completed its first acquisition as a biotechnology company. Bio Blue Bird
is now a wholly-owned subsidiary of the Company that holds the exclusive worldwide licensing rights to the use of the Cell-in-a-Box®
live cell encapsulation technology for treating pancreatic cancer.
The Company is now actively engaged with Austrianova
Singapore and other entities in preparation for a new Phase 2b clinical trial for the treatment of pancreatic cancer using encapsulated
live cells that are the same as those employed in the previous Phase 1/2 clinical trial. We are currently working together to advance
clinical research and development of new cellular-based therapies in the oncology arena. Due to this significant successful acquisition,
the Company business is that of a biotechnology company with a specialty in the use of the Cell-in-a-Box® live cell
encapsulation technology in developing treatments for serious and deadly diseases. The Company’s focus for the present and
immediate future is in the oncology and diabetes arenas.
Selling, General and Administrative Expenses
For the three months ended July 31, 2014,
sales and marketing expense increased by $215,500 from $15,000 for the same period in the prior year. The increase is a result
of the company’s efforts to promote its new focus on becoming a world-class biotechnology company.
For the three months ended July 31, 2014,
compensation expense decreased by $948,709 to $253,418, as compared to $1,202,127 for the same period in the prior year. The decrease
is a result of fewer shares of common stock being issued for compensation during the period.
For the three months ended July 31, 2014,
legal and professional fees increased by $196,506 to $260,864 from $64,358 for the same period in the prior year. The increase
is attributed to an increase in attorney fees for work being done for the Company.
General and administrative expenses during
the three months ended July 31, 2014 compared to the three months ended July 31, 2013, increased by $719,172 to $838,378 as
compared to $119,206 in the prior period. The increase can be attributed to increased travel expense, investor relations and other
consulting service expense. This expense also includes the $297,500 non-cash expense from the issuance of the common stock to Lincoln
Park in accordance with the provisions of the termination agreement.
During the three months ended July 31, 2014,
net loss decreased by $3,081,543 to $1,584,824, as compared to $4,666,367 in the prior period. The decrease in net loss can mainly
be attributed to the absence of the loss on conversion of preferred stock and conversion of debt that existed in the prior period.
Liquidity and Capital Resources
For the three months ended July 31, 2014, the
Company used cash of $786,814 in operations and obtained cash of $67,283 from financing activities.
On May 28, 2014, the Company entered into a
financial advisory, offering and at the market offering engagement agreement (“Chardan Agreement”), with Chardan Capital
Markets, LLC (“Chardan”) pursuant to which Chardan agreed to use its reasonable best efforts to act as the Company’s
sales agent in connection with the sale of common stock in “at the market” or privately negotiated transactions of
up to $50 million, depending upon market conditions and at the sole discretion of the Company. In connection with such transactions,
the Company agreed to pay Chardan: (i) a cash fee of 3% of the gross proceeds from the sale of any shares of common stock sold
in an “at-the-market” offering and (ii) a cash fee of 7% of the aggregate sales price of any distinct blocks of common
stock sold under the Chardan Agreement, plus five-year warrants representing 5% of the number of shares of common stock sold. In
addition, the Company’s has agreed to reimburse certain expenses of Chardan in an amount not to exceed $15,000.
Item 3. Quantitative and Qualitative
Disclosures about Market Risk.
Not required for smaller reporting companies.
Item 4. Controls and Procedures.
The Company's management, including the Chief
Executive Officer, President and General Counsel of the Company, as its principal executive officer, and the Chief Financial Officer
of the Company, as its principal financial officer (collectively, “Principal Executive Officers”), have evaluated the
effectiveness of the Company's “disclosure controls and procedures,” as such term is defined in Rule 13a-15(e) promulgated
under the Securities Exchange Act of 1934, as amended (“Exchange Act”). Based upon this evaluation, the Principal Executive
Officers have concluded that, as of July 31, 2014, the Company's disclosure controls and procedures were effective for the purpose
of ensuring that the information required to be disclosed in the reports that the Company files or submits to the SEC pursuant
to the Exchange Act is recorded, processed, summarized and reported within the time period specified by the SEC’s rules and
forms and is accumulated and communicated to the Company's management, including its Principal Executive Officer, as appropriate
to allow timely decisions regarding required disclosures.
Although the management of our Company, including
the Principal Executive Officers, believes that our disclosure controls and internal controls currently provide reasonable assurance
that our desired control objectives have been met, management does not expect that our disclosure controls or internal controls
will prevent all error and all fraud. A control system, no matter how well conceived and operated, can provide only reasonable,
not absolute, assurance that the objectives of the control system are met. Further, the design of a control system must reflect
the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because
of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues
and instances of fraud, if any, within our Company 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. Additionally, controls can
be circumvented by the individual acts of some persons, by collusion of two or more people, or by management override of the controls.
The design of any system of controls is also based in part upon certain assumptions about 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.
The Company is not currently a party to any
material pending legal proceedings. There are no material legal proceedings to which any property of the Company is subject.
Item 1A. Risk Factors.
In addition to the other information set forth
in this Report, you should carefully consider the factors discussed in Part I, Item 1A., “Risk Factors” in our Annual
Report on Form 10-K for the fiscal year ended April 30, 2014. The information set forth in these Reports could materially affect
the Company’s business, financial position and results of operations. There are no material changes from the risk factors
set forth in Part I, Item 1A, “Risk Factors,” of our Annual Report on Forms 10-K for the fiscal year ended April 30,
2014.
Item 2. Unregistered Sales of
Equity Securities and Use of Proceeds.
On May 28, 2014, as consideration for terminating
the stock purchase agreement, the Company issued Lincoln Park 1,062,500 shares of common stock. These shares were valued at $0.28
for total non-cash expense of $297,500.
On May 29, 2014, the Company converted outstanding
Class B warrants into 550,000 shares of common stock for total cash proceeds of $66,000. Proceeds are to be used to fund general
operating expenses.
On June 26, 2014, the Company sold 50,000 shares
of common stock to an accredited investor for total cash proceeds of $5,000. Proceeds are to be used to fund general operating
expenses.
On July 16, 2014, the Company sold 100,000
shares of common stock to an accredited investor for total cash proceeds of $10,000. Proceeds are to be used to fund general operating
expenses.
On July 30, 2014, the Company sold 50,000 shares
of common stock to an accredited investor for total cash proceeds of $5,000. Proceeds are to be used to fund general operating
expenses.
The issuance and sale of the restricted shares
of common stock to the aforementioned entities and individuals in each of the transactions described above was made in reliance
on exemptions from registration provided for in Sections 4(2) and 4(5) of the Securities Act of 1933, as amended, including Regulation
D promulgated thereunder.
Item 3. Defaults upon Senior Securities.
None.
Item 4. Mine Safety Disclosure.
Not applicable.
Item 5. Other Information.
(a) None.
(b) Not applicable.
Item 6. Exhibits.
Exhibit No. |
|
Description |
|
Location |
|
|
|
|
|
31.1 |
|
Certification of Chief Executive Officer (Principal Executive Officer) pursuant to Rules 13a-14(a) and 15d-14(a) of the Securities Exchange Act of 1934, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002 |
|
Filed herewith. |
31.2 |
|
Certification of Chief Financial Officer (Principal Financial Officer) pursuant to Rules 13a-14(a) and 15d-14(a) of the Securities Exchange Act of 1934, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002 |
|
Filed herewith. |
|
|
|
|
|
32.1 |
|
Certification of Chief Executive Officer (Principal Executive Officer) pursuant to 18 U.S.C. Section 1350, (Section 906 of the Sarbanes-Oxley Act of 2002). |
|
Filed herewith. |
32.2 |
|
Certification of Chief Financial Officer (Principal Financial Officer) pursuant to 18 U.S.C. Section 1350 (Section 906 of the Sarbanes-Oxley Act of 2002). |
|
Filed herewith. |
101.INS |
|
XBRL Instance Document |
|
Filed or furnished herewith. |
101.SCH |
|
XBRL Taxonomy Extension Schema Document |
|
Filed or furnished herewith. |
101.CAL |
|
XBRL Taxonomy Extension Calculation Linkbase Document |
|
Filed or furnished herewith. |
101.DEF |
|
XBRL Taxonomy Extension Definition Linkbase Document |
|
Filed or furnished herewith. |
101.LAB |
|
XBRL Taxonomy Extension Labels Linkbase Document |
|
Filed or furnished herewith. |
101.PRE |
|
XBRL Taxonomy Extension Presentation Linkbase Document |
|
Filed or furnished herewith. |
SIGNATURE
Pursuant to the requirements of the Securities
Exchange Act of 1934, as amended, the Company has duly caused this Report to be signed by the following persons on behalf of the
Company and in the capacities and on the dates indicated.
NUVILEX, INC.
September 15, 2014 |
By: /s/ Kenneth L. Waggoner |
|
Kenneth L. Waggoner |
|
Principal Executive Officer |
|
|
|
September 15, 2014 |
By: /s/ Patricia Gruden |
|
Patricia Gruden |
|
Principal Financial Officer |
EXHIBIT 31.1
CERTIFICATION PURSUANT TO RULE 13A-14(A)/15D-14(A)
I, Kenneth L. Waggoner, certify that:
1. |
I have reviewed this Quarterly Report on Form 10-Q for the period ended July 31, 2014 of Nuvilex, Inc. (“Report”); |
2. |
Based on my knowledge, the 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 made, not misleading with respect to the period covered by the Report; |
3. |
Based on my knowledge, the financial statements, and other financial information included in the 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 the Report; |
4. |
The Registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-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 our supervision, to ensure that material information relating to the Registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which the Report is being prepared; |
b. |
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our 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 the Report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the periods covered by the Report based on such evaluation; and |
d. |
Disclosed in the 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 the Registrant’s board of directors (or persons performing the equivalent functions): |
a. |
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 |
b. |
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. |
Dated: September 15, 2014 |
By: /s/ Kenneth L. Waggoner |
|
Kenneth L. Waggoner, Chief Executive Officer |
EXHIBIT 31.2
CERTIFICATION PURSUANT TO RULE 13A-14(A)/15D-14(A)
I, Patricia Gruden, certify that:
1. |
I have reviewed this Quarterly Report on Form 10-Q for the period ended July 31, 2014 of Nuvilex, Inc.(“Report”); |
2. |
Based on my knowledge, the 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 made, not misleading with respect to the period covered by the Report; |
3. |
Based on my knowledge, the financial statements, and other financial information included in the 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 the Report; |
4. |
The Registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-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 our supervision, to ensure that material information relating to the Registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which the Report is being prepared; |
b. |
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our 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 the Report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the periods covered by the Report based on such evaluation; and |
d. |
Disclosed in the 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 the Registrant’s board of directors (or persons performing the equivalent functions): |
a. |
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 |
b. |
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. |
Dated: September 15, 2014 |
By: /s/ Patricia Gruden |
|
Patricia Gruden, Chief Financial Officer |
EXHIBIT 32.1
CERTIFICATION PURSUANT TO 18 U.S.C. SECTION
1350, AS ADOPTED PURSUANT
TO SECTION 906 OF THE
SARBANES-OXLEY ACT OF 2002
In connection with the
quarterly report of Nuvilex, Inc. ("Company") on Form 10-Q for the period ended July 31, 2014 (“Report”),
as filed with the United States Securities and Exchange Commission (“SEC”) on the date hereof, I, Kenneth L. Waggoner,
in my capacity as Chief Executive Officer of the Company, hereby certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant
to § 906 of the Sarbanes-Oxley Act of 2002, that:
(i) the Report fully complies
with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and
(ii) the information contained
in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company.
Dated: September 15, 2014 |
By: /s/ Kenneth L. Waggoner |
|
Kenneth L. Waggoner, Chief Executive Officer |
A signed original of
this written statement required by Section 906, or other document authenticating, acknowledging or otherwise adopting the signature
that appears in typed form within the electronic version of this written statement has been provided to the Company and will be
retained by the Company and furnished to the SEC or its staff upon request.
EXHIBIT 32.2
CERTIFICATION PURSUANT TO 18 U.S.C. SECTION
1350, AS ADOPTED PURSUANT
TO SECTION 906 OF THE
SARBANES-OXLEY ACT OF 2002
In connection with the
quarterly report of Nuvilex, Inc. ("Company") on Form 10-Q for the period ended July 31, 2014 (“Report”),
as filed with the United States Securities and Exchange Commission (“SEC”) on the date hereof, I, Patricia Gruden,
in my capacity as Chief Financial Officer of the Company, hereby certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant
to § 906 of the Sarbanes-Oxley Act of 2002, that:
(i) the Report fully complies with the requirements
of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and
(ii) the information contained
in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company.
Dated: September 15, 2014 |
By: /s/ Patricia Gruden |
|
Patricia Gruden, Chief Financial Officer |
A signed original of
this written statement required by Section 906, or other document authenticating, acknowledging or otherwise adopting the signature
that appears in typed form within the electronic version of this written statement has been provided to the Company and will be
retained by the Company and furnished to the SEC or its staff upon request.