OWC Pharmaceutical Research Corp. - Quarter Report: 2016 June (Form 10-Q)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
___________________
FORM 10-Q
___________________
ý QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended June 30, 2016
Commission file number 0-54856
OWC PHARMACEUTICAL RESEARCH CORP.
(Exact Name of Registrant in its Charter)
Delaware | 98-0573566 |
(State or other Jurisdiction of Incorporation) | (IRS Employer Identification No.) |
22 Shaham Steet, P.O. Box 8324, Petach Tikva, 4918103, Israel
(Address of Registrants Principal Executive Offices and Principal Place of Business)
Registrant's Telephone Number, Including Area Code: Phone: +972 (0) 3-758-2657
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 ¨
Indicate by check mark whether the registrant is a shell company (as
defined in Rule 12b-2 of the Exchange Act). Yes ¨ No x
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer (as defined in Rule 12b-2 of the Exchange Act) or a smaller reporting company .
Large accelerated filer ¨ | Accelerated filer ¨ | Non-Accelerated filer ¨ | Smaller reporting company x |
On August 29, 2016, the Registrant had 81,460,875 shares of common stock outstanding.
Item |
Description |
Page |
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---|---|---|---|---|---|
PART I - FINANCIAL INFORMATION |
|||||
ITEM 1. | FINANCIAL STATEMENTS - UNAUDITED. | 3 | |||
Consolidated Balance Sheets | 3 | ||||
Consolidated Statements of Operations | 4 | ||||
Consolidated Statements of Comprehensive Loss | 5 | ||||
Consolidated Statements of Cash Flows | 6 | ||||
Notes to Unaudited Interim Consolidated Financial Statements | 7 | ||||
ITEM 2. | MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITIONS AND RESULTS OF OPERATIONS. | 13 | |||
ITEM 3. | QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK. | 18 | |||
ITEM 4. | CONTROLS AND PROCEDURES. | 18 | |||
PART II - OTHER INFORMATION |
|||||
ITEM 1. | LEGAL PROCEEDINGS. | 18 | |||
ITEM 1A. | RISK FACTORS. | 18 | |||
ITEM 2. | UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS. | 18 | |||
ITEM 3. | DEFAULT UPON SENIOR SECURITIES. | 18 | |||
ITEM 4. | MINE SAFETY DISCLOSURE. | 18 | |||
ITEM 5. | OTHER INFORMATION. | 19 | |||
ITEM 6. | EXHIBITS. | 19 |
PART I - FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS Back to Table of Contents
OWC Pharmaceutical Research Corp. | ||||
Consolidated Balance Sheets | ||||
At June 30, 2016 (Unaudited) and December 31, 2015 (Audited) | ||||
Back to Table of Contents | ||||
June 30, 2016 | December 31, 2015 | |||
(Unaudited) | (Audited) | |||
ASSETS | ||||
Current assets: | ||||
Cash | $ | 162,283 | $ | 357,161 |
Other receivables | 7,699 | 11,797 | ||
Prepaid expenses | 11,535 | 38,591 | ||
Total current assets | 181,517 | 407,549 | ||
Property and equipment, net | 19,934 | 22,899 | ||
Total Assets | $ | 201,451 | $ | 430,448 |
LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT) | ||||
Current liabilities: | ||||
Accounts payable - trade | $ | 31,713 | $ | 28,125 |
Accrued expenses | 24,418 | 24,607 | ||
Customer deposit | 150,000 | 50,000 | ||
Advances and account payable to related parties | 1,820 | 1,820 | ||
Derivatives | 53,572 | - | ||
Convertible notes payable, net of discount | 51,969 | 3,074 | ||
Convertible note payable, in default | 37,500 | 3,074 | ||
Total current liabilities | 350,992 | 107,626 | ||
Total liabilities | 350,992 | 107,626 | ||
Stockholders' equity (deficit): | ||||
Preferred stock, $0.00001 par value; 20,000,000 shares authorized; no shares issued and outstanding | - | - | ||
Common stock, $0.00001 par value; 500,000,000 shares authorized; and | ||||
81,460,875 issued and outstanding at June 30, 2016 and December 31, 2015 | 815 | 815 | ||
Additional paid in capital | 8,541,599 | 8,533,525 | ||
Common stock subscription receivable | (651,730) | (651,730) | ||
Accumulated deficit | (8,036,984) | (7,548,866) | ||
Accumulated other comprehensive loss | (3,241) | (10,922) | ||
Total stockholders' equity (deficit) | (149,541) | 322,822 | ||
Total Liabilities and Stockholders' equity (deficit) | $ | 201,451 | $ | 430,448 |
See notes to unaudited interim consolidated financial statements. |
OWC Pharmaceutical Research Corp. | ||||||||
Consolidated Statements of Operations | ||||||||
For the Three and Six-Months Ended June 30, 2016 and 2015 (Unaudited) | ||||||||
Back to Table of Contents | ||||||||
For the three |
For the three |
For the six |
For the six |
|||||
months ended |
months ended |
months ended |
months ended |
|||||
June 30, 2016 |
June 30, 2015 |
June 30, 2016 |
June 30, 2015 |
|||||
Revenues |
$ |
- |
$ |
- |
$ |
- |
$ |
- |
Expenses | ||||||||
General and administrative | 84,466 |
532,815 |
306,022 |
824,090 |
||||
Research and development | 34,776 |
76,612 |
71,819 |
189,940 |
||||
(Loss) from operations | (119,242) | (609,427) | (377,841) | (1,014,030) | ||||
Other income (expense): | ||||||||
Interest expense | (40,562) | - | (41,560) | - | ||||
Change in fair value of derivative liabilities | 16,647 | - | (11,598) | - | ||||
Amortization of debt discount | (30,573) | - | (57,119) | - | ||||
Total other (expense) | (54,488) |
- |
(110,277) |
- |
||||
Total costs and expenses | (173,730) | (609,427) | (488,118) | (1,014,030) | ||||
Net income (loss) before income taxes | (173,730) | (609,427) | (488,118) | (1,014,030) | ||||
Income tax | - |
- |
- |
- |
||||
Net income (loss) | $ |
(173,730) |
$ |
(609,427) |
$ |
(488,118) | $ |
(1,014,030) |
Basic and diluted per share amounts: | ||||||||
Basic and diluted net loss | $ |
(0.00) |
$ |
(0.02) |
$ |
(0.01) |
$ | (0.02) |
Weighted average shares outstanding (basic and diluted) | 81,460,875 |
40,129,063 |
$ |
81,460,875 |
$ | 58,799,819 |
||
See notes to unaudited interim financial statements. |
OWC Pharmaceutical Research Corp. | ||||||||
Consolidated Statements Comprehensive Loss | ||||||||
For the Three and Six Months Ended June 30, 2016 and 2015 (Unaudited) | ||||||||
Back to Table of Contents | ||||||||
For the three months | For the three months | For the six months | For the six months | |||||
ended June 30, 2016 | ended June 30, 2015 | ended June 30, 2016 | ended June 30, 2015 | |||||
Net loss | $ | (173,730) | $ | (609,427) | $ | (488,118) | $ | (1,014,030) |
Other comprehensive income, net of tax: | ||||||||
Foreign currency translation adjustments | (3,952) | (650) | 7,681 | (5,608) | ||||
Total other comprehensive income, net of tax | (3,952) | (650) | 7,681 | (5,608) | ||||
Comprehensive loss | $ | (177,682) | $ | (610,077) | $ | (480,437) | $ | (1,019,638) |
See notes to unaudited interim consolidated financial statements. |
OWC Pharmaceutical Research Corp. | ||||
For the Six Months Ended June 30, 2016 and 2015 (Unaudited) |
||||
For the six |
For the six |
|||
months ended |
months ended |
|||
June 30, 2016 |
June 30, 2015 |
|||
Cash flows from operating activities: |
||||
Net loss | $ |
(488,118) |
$ |
(1,014,030) |
Adjustments to reconcile net loss to net cash used in operating activities: | ||||
Derivative valuation adjustments | 11,598 | - | ||
Amortization of debt discount | 57,119 | - | ||
Depreciation expense | 4,825 | 4,524 | ||
Common stock issued for services | - | 241,170 | ||
Warrants issued for services | 8,074 | 10,839 | ||
Changes in net assets and liabilities: | ||||
(Increase) decrease in accounts receivable | 4,098 | 2,612 | ||
(Increase) decrease in accounts receivable - related party | - | 11,188 | ||
(Increase) decrease in prepaid expenses | 27,056 | - | ||
Increase (decrease) in accounts payable - related party | - | 138 | ||
Increase (decrease) in accounts payable | 3,589 | 35,762 | ||
Increase (decrease) in customer deposits | 100,000 | - | ||
Increase (decrease) in accrued expenses | (190) |
(40,697) |
||
Cash used in operating activities | (271,949) |
(751,106) |
||
Cash flow from investing activities: | ||||
Purchase of equipment | (1,860) | (3,179) | ||
Cash used in investing activities | (1,860) |
(3,179) |
||
Cash flow from financing activities: | ||||
Proceeds from issuance of common stock | - | 90,000 | ||
Proceeds of debt borrowings | 78,500 | - | ||
Payment of financing costs | (7,250) | - | ||
Cash provided by financing activities | 71,250 |
90,000 |
||
Foreign currency translation | 7,681 |
(5,608) |
||
Change in cash | (194,878) |
(669,893) |
||
Cash - beginning of period | 357,161 |
1,469,267 |
||
Cash - end of period | $ |
162,283 |
$ |
799,374 |
Supplement cash flow information: | ||||
Non-cash transactions: | ||||
Debt discount arising from derivatives | $ | 41,974 | $ | - |
See notes to unaudited interim financial statements. |
OWC Pharmaceutical Research Corp.
Notes to Unaudited Interim
Consolidated Financial Statements
June 30, 2016
Back to
Table of Contents
1. The Company and Significant Accounting Policies
Organizational Background:
OWC Pharmaceutical Research Corp. ("OWCP" or the "Company") is a Delaware corporation and was incorporated under the laws of the State of Delaware on March 7, 2008. We are a medical cannabis research and development company that applies conventional pharmaceutical research protocols and disciplines to the field of medical cannabis with the objective of establishing a leadership position in the research and development of medical cannabis therapies, products and delivery technologies. We are currently engaged in the research and development of cannabis-based medical products (the "Product Prospects") for the treatment of multiple myeloma, psoriasis and fibromyalgia as well as development of a cannabis soluble tablet delivery system that may have applications for other indications. We also provide consulting services to governmental and private entities to assist them with developing and implementing tailor-made comprehensive medical cannabis programs.The accompanying financial statements of OWCP were prepared from the accounts of the Company under the accrual basis of accounting.
Basis of Presentation:
The accompanying financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America, which contemplate continuation of the Company as a going concern. The Company has not established any source of revenue to cover its operating costs, and as such, has incurred an operating loss since inception. These and other factors raise substantial doubt about the Company's ability to continue as a going concern. The accompanying financial statements do not include any adjustments to reflect the possible future effects on the recoverability and classification of assets or the amounts and classification of liabilities that may result from the possible inability of the Company to continue as a going concern.
Principles of Consolidation:
The financial statements include the accounts of OWC Pharmaceutical Research Corp. and its wholly owned subsidiary One World Cannabis, Inc. (OWC). All significant inter-company balances and transactions have been eliminated.
Significant Accounting Policies
Use of Estimates:
The preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statement and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from the estimates.
Cash and Cash Equivalents:
For financial statement presentation purposes, the Company considers those short-term, highly liquid investments with original maturities of three months or less to be cash or cash equivalents. There were no cash equivalents at June 30, 2016 and December 31, 2015.
Property and Equipment:
New property and equipment are recorded at cost. Property and equipment included in the bankruptcy proceedings and transferred to the Trustee had been valued at liquidation value. Depreciation is computed using the straight-line method over the estimated useful lives of the assets, generally 5 years. Expenditures for renewals and betterments are capitalized. Expenditures for minor items, repairs and maintenance are charged to operations as incurred. Gain or loss upon sale or retirement due to obsolescence is reflected in the operating results in the period the event takes place.
Valuation of Long-Lived Assets:
We review the recoverability of our long-lived assets including equipment, goodwill and other intangible assets, when events or changes in circumstances occur that indicate that the carrying value of the asset may not be recoverable. The assessment of possible impairment is based on our ability to recover the carrying value of the asset from the expected future pre-tax cash flows (undiscounted and without interest charges) of the related operations. If these cash flows are less than the carrying value of such asset, an impairment loss is recognized for the difference between estimated fair value and carrying value. Our primary measure of fair value is based on discounted cash flows. The measurement of impairment requires management to make estimates of these cash flows related to long-lived assets, as well as other fair value determinations.
Foreign Currency:
Non-U.S. entity operations are recorded in the functional currency of each entity. Results of operations for non-U.S. dollar functional currency entities are translated into U.S. dollars using average currency rates. Assets and liabilities are translated using currency rates at period end. Foreign currency translation adjustments are recorded as a component of other comprehensive income (loss) within stockholders' equity.
Stock Based Compensation:
Stock-based awards are accounted for using the fair value method in accordance with ASC 718, Share-Based Payments. Our primary type of share-based compensation consists of stock options. We use the Black-Scholes option pricing model in valuing options. The inputs for the valuation analysis of the options include the market value of the Company's common stock, the estimated volatility of the Company's common stock, the exercise price of the warrants and the risk free interest rate.
Accounting For Obligations And Instruments Potentially To Be Settled In The Company's Own Stock:
We account for obligations and instruments potentially to be settled in the Company's stock in accordance with FASB ASC 815, Accounting for Derivative Financial Instruments. This issue addresses the initial balance sheet classification and measurement of contracts that are indexed to, and potentially settled in, the Company's own stock.
Fair Value of Financial Instruments:
FASB ASC 825, "Financial Instruments," requires entities to disclose the fair value of financial instruments, both assets and liabilities recognized and not recognized on the balance sheet, for which it is practicable to estimate fair value. FASB ASC 825 defines fair value of a financial instrument as the amount at which the instrument could be exchanged in a current transaction between willing parties. At June 30, 2016 and December 31, 2015, the carrying value of certain financial instruments (cash and cash equivalents, accounts payable and accrued expenses.) approximates fair value due to the short-term nature of the instruments or interest rates, which are comparable with current rates.
Fair Value Measurements:
The Company measures fair value under a framework that utilizes a fair value hierarchy that prioritizes the inputs to valuation techniques used to measure fair value. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (level 1 measurements) and the lowest priority to unobservable inputs (level 3 measurements). The three levels of inputs which prioritize the inputs used in measuring fair value are:
Level 1: Inputs to the valuation methodology are unadjusted quoted prices for identical assets or liabilities in active markets that the Company has the ability to access.
Level 2: Inputs to the valuation methodology include:
- Quoted prices
for similar assets or liabilities in active markets;
- Quoted prices for
identical or similar assets or liabilities in inactive markets;
- Inputs
other than quoted prices that are observable for the asset or liability;
- Inputs that are derived principally from or corroborated by observable
market data by correlation or other means.
If the asset or liability has a specified (contractual) term, the level 2 input must be observable for substantially the full term of the asset or liability.
Level 3: Inputs to the valuation methodology are unobservable and significant to the fair value measurement.
The assets or liability's fair value measurement level within the fair value hierarchy is based on the lowest level of any input that is significant to the fair value measurement. Valuation techniques used need to maximize the use of observable inputs and minimize the use of unobservable inputs. The following table presents assets that were measured and recognize at fair value on June 30, 2016 and December 31, 5and the year then ended on a recurring basis:
Fair Value Measurements at June 30, 2016 | ||||||||
Quoted Prices in Active | Significant Other | Significant | ||||||
Markets for Identical Assets | Observable Inputs | Unobservable Inputs | ||||||
Total |
(Level 1) |
(Level 2) |
(Level 3) |
|||||
None | $ |
- | $ |
- |
$ |
- |
$ |
- |
Total assets at fair value | $ |
- |
$ |
- |
$ |
- |
$ |
- |
Fair Value Measurements at December 31, 2015 | ||||||||
Quoted Prices in Active | Significant Other | Significant | ||||||
Markets for Identical Assets | Observable Inputs | Unobservable Inputs | ||||||
Total |
(Level 1) |
(Level 2) |
(Level 3) |
|||||
None | $ |
- | $ |
- |
$ |
- |
$ |
- |
Total assets at fair value | $ |
- |
$ |
- |
$ |
- |
$ |
- |
When the Company changes its valuation inputs for measuring financial assets and liabilities at fair value, either due to changes in current market conditions or other factors, it may need to transfer those assets or liabilities to another level in the hierarchy based on the new inputs used. The Company recognizes these transfers at the end of the reporting period that the transfers occur. For the fiscal periods ended June 30, 2016 and December 31, 2015, there were no significant transfers of financial assets or financial liabilities between the hierarchy levels.
Earnings per Common Share:
We compute net income (loss) per share in accordance with ASC 260, Earning per Share. ASC 260 requires presentation of both basic and diluted earnings per share (EPS) on the face of the income statement. Basic EPS is computed by dividing net income (loss) available to common shareholders (numerator) by the weighted average number of shares outstanding (denominator) during the period. Diluted EPS gives effect to all dilutive potential common shares outstanding during the period using the treasury stock method and convertible preferred stock using the if-converted method. In computing Diluted EPS, the average stock price for the period is used in determining the number of shares assumed to be purchased from the exercise of stock options or warrants. Diluted EPS excludes all dilutive potential shares if their effect is anti-dilutive.
Income Taxes:
We have adopted ASC 740, Accounting for Income Taxes. Pursuant to ASC 740, we are required to compute tax asset benefits for net operating losses carried forward. The potential benefits of net operating losses have not been recognized in these financial statements because the Company cannot be assured it is more likely than not it will utilize the net operating losses carried forward in future years.
We must make certain estimates and judgments in determining income tax expense for financial statement purposes. These estimates and judgments occur in the calculation of certain tax assets and liabilities, which arise from differences in the timing of recognition of revenue and expense for tax and financial statement purposes.
Deferred tax assets and liabilities are determined based on the differences between financial reporting and the tax basis of assets and liabilities using the tax rates and laws in effect when the differences are expected to reverse. ASC 740 provides for the recognition of deferred tax assets if realization of such assets is more likely than not to occur. Realization of our net deferred tax assets is dependent upon our generating sufficient taxable income in future years in appropriate tax jurisdictions to realize benefit from the reversal of temporary differences and from net operating loss, or NOL, carryforwards. We have determined it more likely than not that these timing differences will not materialize and have provided a valuation allowance against substantially all of our net deferred tax asset.
Management will continue to evaluate the realizability of the deferred tax asset and its related valuation allowance. If our assessment of the deferred tax assets or the corresponding valuation allowance were to change, we would record the related adjustment to income during the period in which we make the determination. Our tax rate may also vary based on our results and the mix of income or loss in domestic and foreign tax jurisdictions in which we operate.
In addition, the calculation of our tax liabilities involves dealing with uncertainties in the application of complex tax regulations. We recognize liabilities for anticipated tax audit issues in the U.S. and other tax jurisdictions based on our estimate of whether, and to the extent to which, additional taxes will be due. If we ultimately determine that payment of these amounts is unnecessary, we will reverse the liability and recognize a tax benefit during the period in which we determine that the liability is no longer necessary. We will record an additional charge in our provision for taxes in the period in which we determine that the recorded tax liability is less than we expect the ultimate assessment to be.
ASC 740 which requires recognition of estimated income taxes payable or refundable on income tax returns for the current year and for the estimated future tax effect attributable to temporary differences and carry-forwards. Measurement of deferred income tax is based on enacted tax laws including tax rates, with the measurement of deferred income tax assets being reduced by available tax benefits not expected to be realized.
Uncertain Tax Positions:
When tax returns are filed, it is highly certain that some positions taken would be sustained upon examination by the taxing authorities, while others are subject to uncertainty about the merits of the position taken or the amount of the position that would be ultimately sustained. In accordance with the guidance of FASB ASC 740-10, Accounting for Uncertain Income Tax Positions, the benefit of a tax position is recognized in the financial statements in the period during which, based on all available evidence, management believes it is more likely than not that the position will be sustained upon examination, including the resolution of appeals or litigation processes, if any. Tax positions taken are not offset or aggregated with other positions. Tax positions that meet the more-likely-than-not recognition threshold are measured as the largest amount of tax benefit that is more than 50 percent likely of being realized upon settlement with the applicable taxing authority. The portion of the benefits associated with tax positions taken that exceeds the amount measured as described above should be reflected as a liability for unrecognized tax benefits in the accompanying consolidated balance sheets along with any associated interest and penalties that would be payable to the taxing authorities upon examination.
Our federal and state income tax returns are open for fiscal years ending on or after December 31, 2010. We are not under examination by any jurisdiction for any tax year. At June 30, 2016, we had no material unrecognized tax benefits and no adjustments to liabilities or operations were required under FASB ASC 740-10.
Recent Accounting Pronouncements
Share-Based Payments:
In March 2016, amended guidance was issued for employee share-based payment awards. The amended guidance makes several modifications related to the accounting for forfeitures, employer tax withholding on share-based compensation and excess tax benefits or deficiencies. The amended guidance also clarifies the statement of cash flows presentation for share-based awards. The amended guidance is effective for us prospectively commencing in the first quarter of 2018. Early adoption is permitted.
Deferred Income Taxes:
In November 2015, amended guidance was issued for the balance sheet classification of deferred income taxes. The amended guidance requires the classification of all deferred tax assets and liabilities as noncurrent on the balance sheet instead of separating deferred taxes into current and noncurrent amounts. Early adoption is permitted.
In April 2015, the Financial Accounting Standards Board ("FASB") issued Accounting Standards Update ("ASU") 2015-03, "Interest-Imputation of Interest (Subtopic 835-30): Simplifying the Presentation of Debt Issuance Costs." ASU 2015-03 requires that debt issuance costs related to a recognized debt liability be presented in the balance sheet as a direct deduction from the carrying amount of that debt liability, consistent with debt discounts. Currently, debt issuance costs are recognized as deferred charges and recorded as other assets. The guidance is effective for annual and interim periods beginning after December 15, 2015 with early adoption permitted and is to be implemented retrospectively. Adoption of the new guidance will only affect the presentation of the Company's consolidated balance sheets and will have no impact to our financial statements.
Management does not anticipate that the adoption of these standards will have a material impact on the financial statements.
The preparation of these financial statements in conformity with accounting principles generally accepted in the United States requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. On an on-going basis, we evaluate our estimates, including those related intangible assets, income taxes, insurance obligations and contingencies and litigation. We base our estimates on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other resources. Actual results may differ from these estimates under different assumptions or conditions.
The Financial Statements presented herein have been prepared by us in accordance with the accounting policies described in our December 31, 2015 Annual Report and should be read in conjunction with the Notes to Financial Statements which appear in that report.
In the opinion of management, the information furnished in these interim financial statements reflects all adjustments necessary for a fair statement of the financial position and results of operations and cash flows as of and for the three and six-month periods ended June 30, 2016 and 2015. All such adjustments are of a normal recurring nature. The Financial Statements do not include some information and notes necessary to conform to annual reporting requirements.
2. Stockholders' Equity
During the Year 2016:
Options Issued for Services:
During the three months ended March 31, 2016, we issued 200,000 common stock options. The options valued at $8,074 were granted for services provided by unrelated parties. The fair value of the options was estimated at the date of grant using the Black-Sholes-Merton pricing model. The Black-Sholes-Merton pricing model assumptions used are as follows: expected dividend yield of 0%; risk-free interest rate of 1.11%; expected volatility of 196%, and option term of 2.75 years.
During the Year 2015:
Stock Issued for Cash:
In February of 2015, we sold 800,000 shares to one investor for the offering price of $0.05 per share that resulted in total proceeds of $40,000. We also received $50,000 through a placement of common stock units. Those units were sold at $0.15 per unit. Each unit consisted of one share of common stock and one warrant to purchase common stock. We issued 333,333 shares through March 31st to one investor of this offering. The warrants are exercisable at $0.25 and expired on December 31, 2016.
Stock Issued for Services:
On February 16, 2015, we issued 500,000 shares for consulting services valued at $500 based on the fair market value of the stock on the date of issuance. These shares were subsequently cancelled in April 2015 and the company issued only 100,000 shares instead in July 2015.
Warrants Granted
As part of the 2015 unit offering, the Company issued a total of 333,333 warrants to purchase up to 333,333 shares of common stock at $0.25 per share.
The relative fair value of the warrants attached to the common stock issued was estimated at the date of grant using the Black-Sholes-Merton pricing model. The relative fair value of the attached to the common stock component is $26,416 and the relative fair value of the warrants is $23,584 as of the grant date.
In February, 2015 we issued 64,935 warrants for services. The warrants are exercisable at $0.25 and expire February 23, 2016. We used the Black-Scholes-Merton pricing model and inputs described below to estimate the fair value of $10,839.
The Black-Sholes-Merton pricing model assumptions used are as follows: expected dividend yield of 0%; risk-free interest rate of 0.10%-.0.11%; expected volatility of 242%, and warrant exercise period based upon the stated terms.
3. Related Party Transactions
Due Related Parties:
Amounts due related parties totaled $1,820 and $1,820 at June 30, 2016 and December 31, 2015, respectively. The company paid $0 and $21,943 in rent to a related party during the six-month period ended June 30, 2016 and 2015, respectively.
4. Notes Payable
Unsecured Notes Payable With Conversion Rights:
A convertible note for $78,500 issued on February 2, 2016, bears interest at 8.0% per annum until paid or converted and matures November 2, 2016. Any or all of the outstanding balance of the note may be converted at the option of the holder at any time into common stock of the company at a variable conversion price of 65% of market price. Upon the issuance of the convertible note, the Company bifurcated the embedded conversion feature and recorded an initial derivative liability of $41,974 (the estimated fair market value at the date of grant based on the Binomial option pricing model) all of which was allocated as debt discount.
During 2015 the Company agreed to provide unsecured promissory notes with an unrelated party for $37,500. The note is non-interest bearing and is due on June 16, 2016. The note has not been paid and is in default at June 30, 2016. The note has a future conversion right that allows the holder to convert the principal balance into the Company's common stock at the lender's sole discretion at 50% of the then market price per share. In accordance with ASC 470, the Company has analyzed the beneficial nature of the conversion terms and determined that a beneficial conversion feature (BCF) exists because the effective conversion price was less than the quoted market price at the time of the issuance. The Company calculated the value of the BCF using the intrinsic method as stipulated in ASC 470. The BCF of $37,500 had been recorded as a discount to the notes payable and to Additional Paid-in Capital.
For the six months June 30, 2016, the Company has amortized $57,119 ($0 in 2015) of the discount arising from the embedded derivative and beneficial conversion feature of the two outstanding notes. The aggregate carrying value of the convertible notes is as follows:
June 30, 2016 | December 31, 2015 | |||
Face amount of the notes | $ | (78,500) | $ | 37,500 |
Unamortized discount | (26,531) | (34,426) | ||
Net balance | $ | 51,969 | $ | 3,074 |
5. Derivative Liabilities
Embedded Conversion Feature
To properly account for the convertible notes payable discussed in Note 4, the Company performed a detailed analysis to obtain a thorough understanding of the transaction. The Company reviewed FASB ASC 815, to identify whether any equity-linked features in the notes are freestanding or embedded. The notes were then analyzed in accordance with FASB ASC 815 to determine if the anti-dilution feature should be bifurcated and accounted for at fair value and remeasured at fair value in income. The Company determined that the anti-dilution feature met the requirements for bifurcation pursuant to FASB ASC 815 due to the variable conversion price and therefore accounted for the anti-dilution features of the notes as a derivative liability. Changes in fair value of the derivative financial instruments are recognized in the Company's statement of operations as a derivative valuation gain or loss.
The adjustment to market of $53,572 at June 30, 2016 resulted in a charge of $11,598 for the six months then ended and a gain of $16,647 for the three months then ended.
The Company values its simple conversion option derivatives using the a lattice model. Assumptions used include:
- life through the note maturity date
- expected volatility-152%,
- expected dividends-none
- exercise prices as set forth in the
agreements,
- common stock price of the underlying share on the
valuation date, and
- number of shares to be issued if the instrument is
converted
6. Going Concern
The accompanying financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America, which contemplate continuation of the Company as a going concern. The Company has not established any source of revenue to cover its operating costs, and as such, has incurred an operating loss since inception. Further, as of June 30, 2016, the cash resources of the Company were insufficient to meet its current business plan. These and other factors raise substantial doubt about the Company's ability to continue as a going concern. The accompanying financial statements do not include any adjustments to reflect the possible future effects on the recoverability and classification of asset or the amounts and classification of liabilities that may result from the possible inability of the Company to continue as a going concern.
7. Subsequent Events
There were no subsequent events following the period ended June 30, 2016 and throughout the date of the filing of Form 10-Q.
ITEM 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITIONS AND RESULTS OF OPERATION Back to Table of Contents
The following discussion contains forward-looking statements. Forward-looking statements give our current expectations or forecasts of future events. You can identify these statements by the fact that they do not relate strictly to historical or current facts. They use of words such as "anticipate", "estimate", "expect", "project", "intend", "plan", "believe", and other words and terms of similar meaning in connection with any discussion of future operating or financial performance. From time to time, we also may provide forward-looking statements in other materials we release to the public.
Plan of Operations
We are engaged in research and development of cannabis-based medical products for the treatment of a variety of medical conditions such as multiple myeloma, psoriasis, fibromyalgia, post-traumatic stress disorder (PTSD) and migraine, and (ii) consulting services to companies and governmental agencies with respect to complex international medical cannabis protocols and regulations.
We have not yet commenced any significant activities related to our consulting services.
Our goal is to become a leader in the research and development of cannabis-based medical drugs and treatments. To achieve our goal, we plan to focus our activities on the following areas:
Research and Development
Our research and development is focused primarily on exploring several formulations containing active compounds from the cannabis plant, including (but not exclusive to) the cannabinoids CBD and THC, and identifying potential therapeutic applications of the synergistic effects of these active compounds. The synergistic contributions of our formulations have not yet been scientifically researched and demonstrated. We aim to standardize the formulations across the extracts as a whole, not simply by reference to their key active components (CBD and/or THC).
Although there are existing reports and studies on CBD and THC, our formulations will contain several active compounds from the cannabis plant, that must be fully researched and documented in order to verify its effectiveness to indications, at what doses and which method of administration will be the most appropriate and effective.
One World Cannabis plans to produce pharmaceutical-grade cannabinoid-based products and treatments, that will be standardized in composition, formulation and dose, administered by means of an appropriate and efficient delivery system, and tested in properly controlled pre-clinical and clinical studies. OWC plans to conduct its researche, led by internationally renowned investigators, at the facilities of leading Israeli hospitals and scientific institutions. The Company will adhere to legislation, rules and guidelines regarding the investigations. Dr. Baruch, OWC's Director of Research and Regulatory Affairs, and Alon Sinai, OWC's Chief Operating Officer, will monitor the investigations and researches.
To date, OWC has signed three research collaboration and license agreements with Sheba Academic Medical Center, Tel Hashomer, Israel ("Sheba"). Sheba is a university-affiliated hospital that serves as Israel's national medical center and the most comprehensive medical center in the Middle East. Within the framework of the agreements with Sheba, OWC will initiate three studies at the Sheba facilities to explore the effect of three formulations, all based on active ingredients in the cannabis extracts, on multiple myeloma, psoriasis and fibromyalgia (a specific formulation to each indication).
In addition, OWC signed an R&D service agreement with G.C. Group Ltd., an Israeli pharmaceutical R&D company, in April 2015, to provide formulation development services for OWC's new delivery system in the form of a cannabis soluble tablet. The cannabis soluble tablet could provide physicians with the ability to control and administrate optimal dosage, to replace the most common usage/delivery method of medical cannabis today, which is not acceptable by scientists and physicians, such as smoking, edibles and oil extracts with no adequate means of dosage control. The agreement was terminated on December 31, 2015.
The Company expects to start developing other delivery systems, designed for different indications, during 2016.
The Company has recently signed a Memorandum of Understanding (MoU) with Emilia Cosmetics Ltd., a large Israeli private label manufacturer, for the development, manufacture and marketing of a cannabinoid-based topical cream to treat psoriasis. The Company will initiate the development of the topical cream by the end of the first quarter of 2016, at Emilia Cosmetics labs located in Yerucham, Israel. After the completion of the formulation development, expected to be during the second quarter of 2016, the Company will initiate a phase I study at the Sheba facilities to explore the effect of topical cream on psoriasis. However, we do not know if our expectations will be fulfilled in a timely manner, if at all, or that the costs of development will exceed our anticipation.
To date, One World Cannabis has filed eight provisional patents with the United States Patent and Regulatory Office (USPTO), all related to its line of activity related to cannabis-based medical products. Assuming the successful completion of the clinical trials, of which there can be no assurance, the Company believes that it will be able to retain the intellectual rights and secure patent protections.
While we retain full ownership on our intellectual property rights that we conceived prior to the signing of the research collaboration and license agreements with Sheba Academic Medical Center, the psoriasis and fibromyalgia agreements with Sheba provide that all intellectual property rights that is conceived during the course of the research is to be jointly owned by Sheba and One World Cannabis.
Pursuant to the collaboration agreements, we expect to pay Sheba $330,000 for conducting the multiple myeloma trial between the 3rd quarter of 2015 and the second quarter of 2016. In addition, we expect to commence pre-clinical studies on fibromyalgia and psoriasis during the second quarter of 2016. Pursuant to the collaboration agreements, we are obliged to pay Sheba $300,000 throughout 2016 for conducting the psoriasis research, and $100,000 for the fibromyalgia research during the two years of the study. We currently have the financial resources to fund our obligations under these agreements, but anticipate that we will require additional funding during the next 12 months for our continuing and planned expanded operations.
Research and Development Status
The following table summarizes the stages of development for each of our current Product Prospects.
Target Indication | Collaborator | Status | |||
Multiple Myeloma | Sheba
|
● | Entered into a research agreement for in vitro studies | ||
Academic | ● | Negotiating terms of a research agreement for in vivo studies | |||
Medical Center | ● | Completed one in vitro study | |||
● | Proceeding with further pre-clinical in vitro studies (safety and toxicity, pharmacokinetic, and pharmacodynamic) | ||||
● | Submitted a clinical trial protocol to the Israeli Institutional Review Board and received its approval to commence a clinical study | ||||
● | Intend to commence a clinical study in the first quarter of 2016 | ||||
● | Drafted a clinical trial protocol synopsis, which we believe will assist us in preparing an application for orphan status designation | ||||
● | Entered into a Research Collaboration and License Agreement but have not commenced any studies to date | ||||
Psoriasis | Sheba
Academic Medical Center |
● | Drafted a protocol of a Phase I, double blind, randomized, placebo controlled, multiple escalating dose study to determine the safety, tolerability and pharmacokinetic profile of medical grade cannabis in healthy volunteers | ||
● | Entered into a nonbinding memorandum of understanding for the development, manufacture and marketing of a cannabinoid-based topical cream | ||||
Psoriasis | Emilia Cosmetics Ltd. | ● | Intend to enter into a binding agreement in the second quarter of 2016 | ||
● | Intend to initiate development of the topical cream in the second quarter of 2016 | ||||
● | Entered into a research agreement for in vitro studies \ | ||||
Fibromyalgia | Sheba
Academic Medical Center |
● | Drafted a clinical trial protocol synopsis, which we believe will assist us in preparing an application for orphan status designation | ||
New delivery system - cannabis soluble tablet | G.C.
Group Ltd. |
● | Completed a proof of concept (the R=Research phase) of the desired end product (the soluble tablet) to test the fabric, durability, solidification and other features of the cannabis soluble tablet. |
OWC's Investigation on Multiple Myeloma
Dr. Merav Leiba, Head of Multiple Myeloma Outpatient Clinic and Multiple Myeloma Research Lab at Sheba's Hematology Institute, led the in vitro tests on multiple myeloma. Dr. Leiba, a specialist in Internal Medicine and Hematology, was a postdoctoral fellow at the Jerome Lipper Multiple Myeloma Center at Dana Farber Cancer Institute, Boston, Massachusetts (2006-2008). Dr. Leiba has participated in numerous clinical and investigational studies aimed at developing novel drugs for multiple myeloma.
Our in vitro tests results on multiple myeloma cells studied outside their normal biological context, on which we announced on June 17, 2015, led us to proceed with further pre-clinical study (safety and toxicity, PK, PD) of our formulation, to find out whether it has scientific merit for further development as an investigational new drug. While we are encouraged by the results of the limited in vitro tests, there can be no assurance that any clinical trial will result in commercially viable products or treatments.
Clinical trials are expensive, time consuming and difficult to design and implement. We, as well as the regulatory authorities in Israel and elsewhere, such as an IRB (Helsinki committee), IMCU - Israel Medical Cannabis Unit, or the FDA, may suspend, delay or terminate our clinical trials at any time, may require us, for various reasons, to conduct additional clinical trials, or may require a particular clinical trial to continue for a longer duration than originally planned, including, among others:
● lack of effectiveness of any formulation or delivery system during clinical trials;
● discovery of serious or unexpected toxicities or side effects experienced by trial participants or other safety issues;
● slower than expected rates of subject recruitment and enrollment rates in clinical trials;
● delays or inability in manufacturing or obtaining sufficient quantities of materials for use in clinical trials due to regulatory and manufacturing constraints;
● delays in obtaining regulatory authorization to commence a trial, including IRB approvals, licenses required for obtaining and using cannabis for research, either before or after a trial is commenced;
● unfavorable results from ongoing pre-clinical studies and clinical trials.
● patients or investigators failing to comply with study protocols;
● patients failing to return for post-treatment follow-up at the expected rate;
● sites participating in an ongoing clinical study withdraw, requiring us to engage new sites;
● third-party clinical investigators decline to participate in our clinical studies, do not perform the clinical studies on the anticipated schedule, or act in ways inconsistent with the established investigator agreement, clinical study protocol, good clinical practices, and other Institutional Review Board requirements;
● third-party entities do not perform data collection and analysis in a timely or accurate manner or at all;
● regulatory inspections of our clinical studies require us to undertake corrective action or suspend or terminate our clinical studies;
Any of the foregoing could have a material adverse effect on our business, results of operations and financial condition.
Consulting Services
OWCP believes that the complexity of the medical cannabis programs has created a demand for consulting and advisory services in different aspects of the medical cannabis industry. The Company's services are designed to help government officials, policy-makers and regulatory agencies develop and implement tailor-made comprehensive medical cannabis programs. In addition, One World Cannabis offers medical cannabis regulatory compliance services and patient-care consultancy services.
Our initial activities to secure consulting contracts will be in member states of the European Union and states of the United States that allow for public medical cannabis programs.
OWC management has the expertise in designing training programs for physicians, caregivers, and researches that are essential to the establishment of a successful, patient-focused medical cannabis program. By working with policy-makers, government officials, public agencies, and privately owned businesses, we believe we can also raise the public's awareness of the benefits of cannabis-based treatments and products.
In furtherance of our plans, we may, in the future, consider strategic acquisitions and joint ventures as well as other projects to grow our business activities including but not limited to: product licensing and royalty agreements, consulting, and strategic alliances to support our Product Prospect development. However, there can be no assurance that this strategy will be successful in generating any revenues or growing out business.
Results of Operations during the three months ended June 30, 2016 as compared to the three months ended June 30, 2015
We have not generated any revenue during the three months ended June 30, 2016 and 2015. We have operating expenses related to general and administrative expenses and research and development. During the three months ended June 30, 2016, we incurred a net loss of $173,730 due to general and administrative expenses of $84,466, research and development expenses of $34,776, interest expenses of $40,562, a valuation gain on derivatives of $16,647 and expenses due to amortization of debt discount of $30,573 as compared to a net loss of $609,427 due to general and administrative expenses of $532,815 and research and development expenses of $76,612.
Our general and administrative expenses decreased by $448,349 during the three months ended June 30, 2016 as compared to the same period in the prior year. This decrease of 84% is primarily the result of decreased stock-based compensation. The charge relating to stock-based compensation expense was $0 for the three months ended June 30, 2016, compared to $238,989 for the three months ended June 30, 2015.
Our research and development expenses decreased to $34,776 during the three months ended June 30, 2016, compared to $76,612 during the same period in the prior year. The decrease by $41,836 or 55% was primarily due to decreased payments related to our collaboration agreements.
Results of Operations during the six months ended June 30, 2016 as compared to the six months ended June 30, 2015
We have not generated any revenue during the six months ended June 30, 2016 and 2015. We have operating expenses related to general and administrative expenses and research and development. During the six months ended June 30, 2016, we incurred a net loss of $488,118 due to general and administrative expenses of $306,022, research and development expenses of $71,819, interest expenses of $41,560, a valuation loss on derivatives of $11,598 and expenses due to amortization of debt discount of $57,119 as compared to a net loss of $1,014,030 due to general and administrative expenses of $824,090 and research and development expenses of $189,940.
Our general and administrative expenses decreased by $518,068 during the six months ended June 30, 2016 as compared to the same period in the prior year. This decrease of 63% is primarily the result of decreased stock-based compensation. The charge relating to stock-based compensation expense was $0 for the six months ended June 30, 2016, compared to $241,170 for the six months ended June 30, 2015.
Our research and development expenses decreased to $71,819 during the six months ended June 30, 2016, compared to $189,940 during the same period in the prior year. The decrease by $118,121 or 62% was primarily due to decreased payments related to our collaboration agreements.
Liquidity and Capital Resources
On June 30, 2016, we had current assets of $181,517 consisting of $162,283 in cash, other receivables of $7,699 and prepaid expenses of $11,535. We had property and equipment valued at $19,934, net of $16,688 in accumulated depreciation, as of June 30, 2016. We had total assets of $201,451 as of June 30, 2016.
On December 31, 2015, we had current assets of $407,549 consisting of $357,161 in cash, other receivables of $11,797 and prepaid assets of $38,591. We had property and equipment, net of accumulated depreciation of $11,863, valued at $22,899 as of December 31, 2015. We had total assets of $430,448 as of December 31, 2015.
On June 30, 2016, we had $350,994 in current liabilities consisting of $31,713 in accounts payable, $24,418 in accrued expenses, customer deposits of $150,000, advances and accounts payables to related parties of $1,820, derivative liabilities valued at $53,572, convertible notes payable of $51,969 and a convertible note in default of $37,500.
On December 31, 2015, we had $107,626 in current liabilities consisting of $28,125 in accounts payable, $24,607 in accrued expenses, advances and accounts payables to related parties of $1,820, customer deposits of $50,000 and convertible notes payable of $3,074.
We had negative working capital of $169,475 at June 30, 2016 as compared to positive working capital of $299,923 on December 31, 2015. Our accumulated deficit as of June 30, 2016 and December 31, 2015 were $8,036,984 and $7,548,866, respectively.
We used $271,949 in our operating activities during the six month ended June 30, 2016, which was due to a net loss of $488,118 offset by derivative valuations adjustments of $11,598, amortization of debt discount expense of $57,119, depreciation expense of $4,825, warrant expenses valued at $8,047, a decrease in accounts receivable of $4,098, an increase in accounts payable of $4,098, an increase in customer deposits of $100,000, a decrease in prepaid expenses of $27,056 and a decrease in accrued expenses of $190.
We used $751,106 in our operating activities during the six months ended June 30, 2015, which was due to a net loss of $1,014,030 offset by depreciation expenses of $4,524, shares issued for services valued at $241,170, warrants issued for services valued at $10,839, a decrease in accounts receivable of $11,188, an increase in advances and accounts payable to related parties of $138, an increase in accounts payable of $35,762 and a decrease in accrued expenses of $40,697.
We used $1,860 and $3,179 during the six months ended June 30, 2016 and 2015, respectively, to purchase property and equipment.
Our financing activities during the six months ended June 30, 2016 provided us with $71,250 through proceeds of $78,500 from debt issuance offset buy $7,250 in debt issuance cost. We financed our negative cash flow from operations during the six months ended June 30, 2015 through proceeds from issuance of common stock of $90,000.
Based upon our cash position of $162,283 at June 30, 2016, we believe that we need to raise additional capital, either equity or debt during the second half of fiscal year 2016 in order to fund our plan of operations including our research and development initiatives for the next twelve months. There can be no assurance, however, that additional capital will be sufficient to fund our currently anticipated expenditure requirements for the next twelve-month period nor can there be any assurance that financing will be available at satisfactory terms and conditions or at all, for that matter.
Our auditors have issued an opinion on our financial statements which includes a statement describing our going concern status. This means that there is substantial doubt that we can continue as an on-going business for the next twelve months unless we obtain additional capital to pay our bills and meet our other financial obligations. This is because we have not generated any revenues and no revenues are anticipated until we begin marketing the product. Accordingly, we must raise capital from sources other than the actual sale of the product. We must raise capital to implement our project and stay in business. Even if we raise the maximum amount of money in this offering, we do not know how long the money will last, however, we do believe it will last at least twelve months.
Our lack of operating history may make it difficult to raise capital. Our inability to borrow funds or raise equity capital to facilitate our business plan may have a material adverse effect on our financial condition and future prospects.
Funding of Our Research Programs
On October 22, 2014, we have entered into a collaboration agreement with Sheba Academic Medical Center, a hospital in Tel-Aviv, Israel, relating to the use of cannabis to treat Myeloma. Within the framework of this collaboration agreement, the Company currently conducts pre-clinical studies on multiple myeloma, which have commenced in April 2015 and we commenced pre-clinical studies on fibromyalgia in the second quarter of 2016. Pursuant to the agreement, we are obligated to pay Sheba $330,000 between the third quarter of 2015 and second quarter of 2016.
We are obligated to provide $300,000 in funding in the second quarter of 2016 related to the Psoriasis research conducted at Sheba. We have funding obligations of $100,000 related to the Fibromyalgia research due during two years of the studies.
At present, we use our available working capital to fund these studies. However, we will need to raise additional funding prior to or if clinical studies are to commence.
ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK Back to Table of Contents
None.
ITEM 4. CONTROLS AND PROCEDURES Back to Table of Contents
Evaluation of disclosure controls and procedures. As of June 30, 2016, the Company's chief executive officer and chief financial officer conducted an evaluation regarding the effectiveness of the Company's disclosure controls and procedures (as defined in Rules 13a-15(e) or 15d-15(e) under the Exchange Act).
Management has assessed the effectiveness of our internal control over financial reporting as of June 30, 2016. Management's assessment was based on criteria set forth in Internal Control - Integrated Framework (1992), issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO). Based upon this assessment, management concluded that, as of June 30, 2016, our internal control over financial reporting was not effective, based upon those criteria, as a result of the identification of the material weaknesses described below.
A material weakness is a deficiency or combination of deficiencies in internal control over financial reporting, such that there is a reasonable possibility that a material misstatement of the annual or interim financial statements will not be prevented or detected on a timely basis.
Specifically, management identified the following control weaknesses: (i) the Company has not implemented measures that would prevent one individual from overriding the internal control system. (ii) The Company utilizes accounting software that does not prevent erroneous or unauthorized changes to previous reporting periods and/or can be adjusted so as not to provide an adequate audit trail of entries made in the accounting software.
Accordingly, while the Company has identified certain material weaknesses in its system of internal control over financial reporting, it believes that it has taken reasonable steps to ascertain that the financial information contained in this report is in accordance with generally accepted accounting principles. The Company does not believe that this control weakness has resulted in deficient financial reporting because the Chief Financial Officer and Chief Executive Officers are aware of their responsibilities under the SEC's reporting requirements and personally certify the financial reports.
Management has determined that current resources would be appropriately applied elsewhere and when resources permit, they will alleviate material weaknesses through various steps.
Changes in internal controls. During the quarterly period covered by this report, no changes occurred in our internal control over financial reporting that materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
PART II - OTHER INFORMATION
ITEM 1. LEGAL PROCEEDINGS Back to Table of Contents
We are not currently subject to any material legal proceedings, nor, to our knowledge, is any material legal proceeding threatened against us. However, from time to time, we may become a party to certain legal proceedings in the ordinary course of business.
ITEM 1A. RISK FACTORS Back to Table of Contents
You should carefully consider the Risk Factors in our Annual Report on Form 10-K for the year ended December 31, 2015, which could materially affect our business, financial condition or future results.
ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS Back to Table of Contents
None.
ITEM 3. DEFAULTS UPON SENIOR SECURITIES Back to Table of Contents
None.
ITEM 4. MINE SAFETY DISCLOSURE. Back to Table of Contents
Not applicable.
ITEM 5. OTHER INFORMATION Back to Table of Contents
Not applicable.
ITEM 6. EXHIBITS Back to Table of Contents
(a) The following documents are filed as exhibits to this report on Form 10-Q or incorporated by reference herein. Any document incorporated by reference is identified by a parenthetical reference to the SEC filing that included such document.
Exhibit No. |
Description |
---|---|
31.1 | Section 302 Certification of the Sarbanes-Oxley Act of 2002 of the Company's CEO, Mordechi Bignitz, filed herewith. |
31.2 | Section 302 Certification of the Sarbanes-Oxley Act of 2002 of the Company's CFO, Shmuel De-Saban, filed herewith. |
32.1 | Section 906 of the Sarbanes-Oxley Act of 2002 of Mordechi Bignitz as CEO, filed herewith |
32.2 | Section 906 of the Sarbanes-Oxley Act of 2002 of Shmuel De-Saban as CFO, filed herewith |
SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned.
Signature | Title | Date |
/s/ Mordechai Bignitz | Chief Executive Officer (Principal Executive Officer) | August 29, 2016 |
Mordechai Bignitz | ||
/s/ Shmuel De-Saban | Chief Financial Officer (Principal Financial and Principal Accounting Officer) | August 29, 2016 |
Shmuel De-Saban | ||
Pursuant to the requirements of the Securities Act of 1934, this report has been signed by the following persons on behalf of the registrant and in the capacities and on the dates indicated.
Signature | Title | Date |
/s/ Mordechai Bignitz | Chief Executive Officer | August 29, 2016 |
Mordechai Bignitz | ||
/s/ Mordechai Bignitz | Chairman | August 29, 2016 |
Mordechai Bignitz | ||