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EX-10.1 - EXHIBIT 10.1 - Zander Therapeutics, Incex10_1.htm
EX-32.2 - EXHIBIT 32.2 - Zander Therapeutics, Incex32_2.htm
EX-32.1 - EXHIBIT 32.1 - Zander Therapeutics, Incex32_1.htm
EX-31.2 - EXHIBIT 31.2 - Zander Therapeutics, Incex31_2.htm
EX-31.1 - EXHIBIT 31.1 - Zander Therapeutics, Incex31_1.htm

U.S. SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 FORM 10-Q 

☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended December 31, 2018

☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 

For the transition period from

Commission File No. 333-220790 

ZANDER THERAPEUTICS, INC.
(Exact name of small business issuer as specified in its charter)

 

Nevada 47-4321638
(State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.)

 

  4700 Spring Street, St 304, La Mesa, California 91942  
  (Address of Principal Executive Offices)  
     
  (619)-702-1404  
  (Issuer’s telephone number)  
     
     
  (Former name, address and fiscal year, if changed since last report)  

 

Check whether the issuer (1) has filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the preceding 12 months (or for such shorter period that the issuer was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.

Yes ☒  No ☐

 

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).

Yes ☒  No ☐ 

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company.  See the definitions of “large accelerated filer,” “accelerated filer,” “non-accelerated filer,” and “smaller reporting company” in Rule 12b-2 of the Exchange Act.

 

☐  Large accelerated filer ☐  Accelerated filer
☐  Non-accelerated filer ☒  Smaller reporting company

 

APPLICABLE ONLY TO CORPORATE ISSUERS: 

 

As of December 31, 2018 there were 6,033,001 shares of common stock issued and outstanding.

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act):

Yes ☐  No ☒

 

Transitional Small Business Disclosure Format (Check One)

Yes ☐   No ☒

 

 1 

 

 

PART I - FINANCIAL INFORMATION

 

ITEM 1. FINANCIAL STATEMENTS

 

Zander Therapeutics, Inc      
BALANCE SHEET      
       
       
  

As of

December 31, 2018

(unaudited)

 

As of

June 30,

2018

ASSETS      
CURRENT ASSETS          
Cash   71,345    370,313 
Prepaid Expenses, Related Parties   11,390    66,239 
Prepaid Expenses   6,387    650 
Due From Related Party        35,000 
Accrued Interest Receivable   4,363      
Total Current Assets   93,485    472,202 
OTHER ASSETS          
Convertible Note Receivable, Related Party   350,000      
Investment Securities, Related Party   14,700      
Derivative Asset, Related Party   555,555      
TOTAL OTHER ASSETS   920,255      
Total Assets   1,013,740    472,202 
           
LIABILITIES          
Current Liabilities:          
Accounts Payable   1,363,802    1,087,969 
Accrued Expenses   36,051    11,593 
Total Current Liabilities   1,399,853    1,099,562 
Total Liabilities   1,399,853    1,099,562 
           
STOCKHOLDER'S EQUITY          
Common Stock, Authorized 100,000,000, $0.0001 Par Value 4,758,001 shares and 6,033,001 shares issued and outstanding as of June 30, 2018 and December 31, 2018 respectively   603    475 
Preferred Stock, $0.0001 par value  Authorized  50,000,000 as of December 31, 2018 and June 30, 2018          
Series M Preferred Stock, $0.0001 par,  Authorized 10,000,000 as of December 31, 2018 and June 30,2018 9,000,000 shares outstanding as of June 30, 2018 and December 31, 2018 Respectively   900    900 
Common Stock subscribed for but unissued , 100,000 and 0 shares as of June 30, 2018 and December 31, 2018 respectively        100,000 
Series AA Preferred Stock, $0.0001 par, Authorized 1,000,000; 200 and 200 shares outstanding as of June 30, 2018 and December 31, 2018 , respectfully   0    0 
Additional Paid In Capital   2,534,688    1,620,689 
Contributed Capital, Related Party   413,878    413,878 
Retained Deficit   (3,336,182)   (2,763,302)
Total Stockholder's Equity   (386,113)   (627,359)
TOTAL LIABILITIES AND STOCKHOLDER'S EQUITY   1,013,740    472,202 
           
The Accompanying Notes are an Integral Part of These Financial Statements

 

 2 

 

 

 

Zander Therapeutics, Inc            
STATEMENT OF OPERATIONS            
(unaudited)            
             
             
   Three Months Ended  Six Months Ended
   December 31,
2018
  December 31,
2017
  December 31, 2018  December 31, 2017
 TOTAL REVENUES                    
 COSTS AND EXPENSES                    
 Research and Development:                    
 License Fees Due to Related Party   27,425    27,424    54,849    54,849 
 License Fees   568         568      
 Contract Research Fees             410,000      
 Consulting Costs   14,847         22,594    150 
 Total Research and Development   42,840    27,434    488,011    54,999 
 General and Administrative:                    
 General and Administrative, Paid By Related Party        18,000         36,000 
 General and Administrative   179,349    2,979    360,185    6,135 
 Total General and Administrative   179,349    20,979    360,185    42,135 
 Rent, Paid By Related Party        9,108         18,096 
 Rent   24,000         36,000      
 Consulting:                    
 Consulting Costs, Paid by Related Party        31,141         79,799 
 Consulting Costs   62,100    74,117    235,402    90,136 
 Total Consulting   62,100    105,258    235,402    169,935 
 Total Costs and Expenses   308,289    162,770    1,119,598    285,165 
                     
 OPERATING LOSS   (308,289)   (162,770)   (1,119,598)   (285,165)
 OTHER INCOME AND EXPENSES                    
 Interest Expense, Related Party        (3,867)        (8,699)
 Refunds On Amounts Previously Paid   7,100         7,100      
 Interest Income , Related Party   4,363         4,363      
 Unrealized Gain (Loss), Investment Securities Related Party   (46,550)        (20,300)     
 Gain (Loss) On Derivative   (861,110)        555,556      
 Total Other Income ( Expenses)   (896,197)   (3,867)   546,719    (8,699)
 NET INCOME (LOSS)   (1,204,486)   (166,637)   (572,879)   (293,864)
 Income Taxes                    
 NET INCOME (LOSS)   (1,204,486)   (166,637)   (572,879)   (293,864)
BASIC AND FULLY DILUTED EARNINGS (LOSS) PER SHARE   (0.200)   (0.039)   (0.102)   (0.076)
WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING   6,033,001    4,221,188    5,621,526    3,883,411 
                     
 The Accompanying Notes are an Integral Part of These Financial Statements

 

 3 

 

 

Zander Therapeutics, Inc      
STATEMENT OF CASH FLOWS      
(unaudited)      
       
       
   Six Months Ended
   December 31,
2018
  December 31,
2017
CASH FLOWS FROM OPERATING ACTIVITIES          
Net Income (Loss)   (572,879)   (293,864)
Adjustments to reconcile net Income (loss) to net cash          
Stock Issued for Expenses   7,622    158 
(Increase) Unrealized Gain from Investment Securities   20,300      
(Increase) Decrease in Derivative Income   (555,556)     
Changes in Operating Assets and Liabilities          
Increase (Decrease) in Accounts Payable   275,833      
Increase (Decrease) in Accrued Expenses   24,457    (97,303)
(Increase) Decrease in Due from Related Party   35,000      
(Increase) Decrease in Prepaid Expenses   55,618      
(Increase) Decrease in Accrued Interest Receivable   (4,363)     
Net Cash provided by (used) in Operating Activities   (713,968)   (391,009)
CASH FLOW FROM INVESTING ACTIVITIES          
(Increase) Decrease in Convertible Notes Receivable   (350,000)     
(Increase) Decrease in Investment Securities   (35,000)     
Net Cash Used  by Investing Activities   (385,000)     
CASH FLOWS FROM FINANCING ACTIVITIES          
Common Stock Issued for Cash   800,000    900,000 
Increase (Decrease) in Contributed Capital        133,895 
Increase (Decrease) in Notes Payable        (17,649)
Net Cash provided by (used) in Financing Activities   800,000    1,016,246 
           
Net Increase (Decrease) in Cash   (298,968)   625,237 
           
Cash at Beginning of Period   370,313    96,005 
Cash at End of Period   71,345    721,242 
           
Supplemental Disclosure of Noncash investing and financing activities:          
Common Shares issued, previously subscribed and paid for   100,000    100,000 
 
The Accompanying Notes are an Integral Part of These Financial Statements

 

 4 

 

 

ZANDER THERAPEUTICS, INC.

Notes to Financial Statements

As of December 31, 2018

(unaudited)

 

The accompanying unaudited interim condensed financial statements of Zander Therapeutics, Inc. (“Zander” or “the Company”) have been prepared in accordance with accounting principles generally accepted in the United States of America and the rules of the United States Securities and Exchange Commission (“SEC”), and should be read in conjunction with the audited financial statements and notes thereto contained in the Company’s annual report filed with the SEC on Form 10-K for the year ended June 30, 2018. In general, interim disclosures do not repeat those contained in the annual statements. In the opinion of management, all adjustments consisting of normal recurring adjustments necessary for a fair presentation of financial position and the results of operations for the interim periods presented have been reflected herein. The results of operations for interim periods are not necessarily indicative of the results to be expected for the full year.

 

NOTE 1. ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

Zander Therapeutics , Inc. (“Company”) was organized June 18, 2015 under the laws of the State of Nevada.

  

The Company intends to engage primarily in the development of veterinary medical applications which we intend to license from other entities as well as develop internally.

 

A. BASIS OF ACCOUNTING

 

The financial statements have been prepared using the basis of accounting generally accepted in the United States of America. Under this basis of accounting, revenues are recorded as earned and expenses are recorded at the time liabilities are incurred. The Company has adopted a June 30year-end.

 

B. USE OF ESTIMATES

 

The preparation of financial statements in conformity with generally accepted accounting principles 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.

 

C. CASH EQUIVALENTS

 

The Company considers all highly liquid investments with a maturity of three months or less when purchased to be cash equivalents.

   

D. PROPERTY AND EQUIPMENT

 

Property and equipment are recorded at cost. Maintenance and repairs are expensed in the year in which they are incurred. Expenditures that enhance the value of property and equipment are capitalized.

 

E. FAIR VALUE OF FINANCIAL INSTRUMENTS

 

Fair value is the price that would be received for an asset or the exit price that would be paid to transfer a liability in the principal or most advantageous market in an orderly transaction between market participants on the measurement date.  A fair value hierarchy requires an entity to maximize the use of observable inputs, where available. The following summarizes the three levels of inputs required by the standard that the Company uses to measure fair value:

 

Level 1:  Quoted prices in active markets for identical assets or liabilities

 

Level 2:  Observable inputs other than Level 1 prices such as quoted prices for similar assets or liabilities; quoted prices in markets that are not active or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the related assets or liabilities.

 

Level 3:  Unobservable inputs that are supported by little or no market activity and that are significant to the fair value of the assets or liabilities.

 

 5 

 

 

F. INCOME TAXES

 

The Company accounts for income taxes using the liability method prescribed by ASC 740, “Income Taxes.” Under this method, deferred tax assets and liabilities are determined based on the difference between the financial reporting and tax bases of assets and liabilities using enacted tax rates that will be in effect in the year in which the differences are expected to reverse. The Company records a valuation allowance to offset deferred tax assets if based on the weight of available evidence, it is more-likely-than-not that some portion, or all, of the deferred tax assets will not be realized. The effect on deferred taxes of a change in tax rates is recognized as income or loss in the period that includes the enactment date.

 

The Company applied the provisions of ASC 740-10-50, “Accounting For Uncertainty In Income Taxes”, which provides clarification related to the process associated with accounting for uncertain tax positions recognized in our financial statements. Audit periods remain open for review until the statute of limitations has passed. The completion of review or the expiration of the statute of limitations for a given audit period could result in an adjustment to the Company’s liability for income taxes. Any such adjustment could be material to the Company’s results of operations for any given quarterly or annual period based, in part, upon the results of operations for the given period. As of  December 31, 2018 the Company had no uncertain tax positions, and will continue to evaluate for uncertain positions in the future.

 

The Company generated a deferred tax credit through net operating loss carry forward.  However, a valuation allowance of 100% has been established.

 

Interest and penalties on tax deficiencies recognized in accordance with ACS accounting standards are classified as income taxes in accordance with ASC Topic 740-10-50-19.

 

G.  BASIC EARNINGS (LOSS) PER SHARE

 

The Financial Accounting Standards Board (FASB) issued Accounting Standards Codification (ASC) 260, "Earnings Per Share", which specifies the computation, presentation and disclosure requirements for earnings (loss) per share for entities with publicly held common stock. ASC 260 requires the presentation of basic earnings (loss) per share and diluted earnings (loss) per share. The Company has adopted the provisions of ASC 260 effective from inception.

 

Basic net loss per share amounts is computed by dividing the net income by the weighted average number of common shares outstanding.

 

H. ADVERTISING

 

Costs associated with advertising are charged to expense as incurred. Advertising expenses were $0 for the quarter ended December 31, 2018.

 

I. RESEARCH AND DEVELOPMENT COSTS

 

Research and development expenses relate primarily to the cost of discovery and research programs. Research and development costs are charged to expense as incurred. Research and development expenses consist mainly of License Fees paid to Regen Biopharma, Inc. and others , and fees paid to consultants.

 

License Fees paid to Regen Biopharma, Inc. and others are accrued over the course of the reporting period. The Companies make payments to consultants based on agreed-upon terms and the Company generally accrues expenses based on services performed or over the term of the agreement, as applicable.

 

 6 

 

 

J. STOCK BASED COMPENSATION

 

Stock issued for Non-Employee Services

 

Stock Based compensation to non-employees is accounted for in accordance with ASC 505-50. ASC 505-50 requires entities to account for non-employee equity transactions based on either the fair value of the services received or the fair value of the equity instrument issued utilizing whichever measurement is most reliable

 

Pursuant to ASC 505-50-30-11  an issuer shall measure the fair value of the equity instruments in these transactions using the stock price and other measurement assumptions as of the earlier of the following dates, referred to as the measurement date:

i.The date at which a commitment for performance by the counterparty to earn the equity instruments is reached (a performance commitment); and
ii.The date at which the counterparty’s performance is complete.

 

Stock issued for Employee Compensation 

 

Stock based compensation to employees is accounted for at the award’s fair value at grant, less the amount (if any) paid by the award recipient.

 

K. DERIVATIVE ASSETS AND LIABILITIES.

 

The Company evaluates convertible debt, options, warrants or other contracts, if any, to determine if those contracts or embedded components of those contracts qualify as derivatives to be separately accounted for in accordance with ASC 815 of the FASB Accounting Standards Codification. The result of this accounting treatment is that the fair value of the embedded derivative is marked-to-market each balance sheet date and recorded as either an asset or a liability. In the event that the fair value is recorded as a liability, the change in fair value is recorded in the consolidated statement of operations.

 

The Company analyzes the conversion feature of its Convertible Note Receivable for derivative accounting consideration under ASC 815-15 “Derivatives and Hedging. ASC 815-15 requires that the conversion features are bifurcated and separately accounted for as an embedded derivative contained in the convertible debt. The embedded derivative is carried on the balance sheet at fair value. Any unrealized change in fair value, as determined at each measurement period, is recorded as a component of the income statement and the associated carrying amount on the balance sheet is adjusted by the change. The Company values the embedded derivative using the Black-Scholes pricing model

 

The Black Scoles pricing model used to determine the Derivative Assets on a convertible notes owned by the Company in which an embedded derivative is recognized as of December 31, 2018 utilized the following inputs:

 

Risk Free Interest Rate   2.48%
Expected Term   1.75 Yrs 
Expected Volatility   284.6%
Expected Dividends   0 

 

L. INVESTMENT SECURITIES

 

The Company measures equity investments (except those accounted for under the equity method and those that result in consolidation of the investee) at fair value and recognizes any changes in fair value in net income.

 

 7 

 

 

NOTE 2 .  RECENT ACCOUNTING PRONOUNCEMENTS 

 

June 2014, the Financial Accounting Standards Board issued Accounting Standards Update No. 2014-10, which eliminated certain financial reporting requirements of companies previously identified as "Development Stage Entities" (Topic 915). The amendments in this ASU simplify accounting guidance by removing all incremental financial reporting requirements for development stage entities. The amendments also reduce data maintenance and, for those entities subject to audit, audit costs by eliminating the requirement for development stage entities to present inception-to-date information in the statements of income, cash flows, and shareholder equity. Early application of each of the amendments is permitted for any annual reporting period or interim period for which the entity's financial statements have not yet been issued (public business entities) or made available for issuance (other entities). Upon adoption, entities will no longer present or disclose any information required by Topic 915. The Company has adopted this standard.

 

The following accounting standards updates were recently issued and have not yet been adopted by the Company. These standards are currently under review to determine their impact on the Company’s consolidated financial position, results of operations, or cash flows.

 

In May 2014, FASB issued Accounting Standards Update (ASU) No. 2014-09, Revenue from Contracts with Customers. The revenue recognition standard affects all entities that have contracts with customers, except for certain items. The new revenue recognition standard eliminates the transaction-and industry-specific revenue recognition guidance under current GAAP and replaces it with a principle-based approach for determining revenue recognition. Public entities are required to adopt the revenue recognition standard for reporting periods beginning after December 15, 2016, and interim and annual reporting periods thereafter. Early adoption is not permitted for public entities. The Company has reviewed the applicable ASU and has not, at the current time, quantified the effects of this pronouncement, however it believes that there will be no material effect on the consolidated financial statements.

 

In June 2014, FASB issued Accounting Standards Update (ASU) No. 2014-12 Compensation — Stock Compensation (Topic 718), Accounting for Share-Based Payments When the Terms of an Award Provide That a Performance Target Could Be Achieved after the Requisite Service Period. A performance target in a share-based payment that affects vesting and that could be achieved after the requisite service period should be accounted for as a performance condition under Accounting Standards Codification (ASC) 718, Compensation — Stock Compensation. As a result, the target is not reflected in the estimation of the award's grant date fair value. Compensation cost would be recognized over the required service period, if it is probable that the performance condition will be achieved. The guidance is effective for annual periods beginning after 15 December 2015 and interim periods within those annual periods. Early adoption is permitted. The Company has reviewed the applicable ASU and has not, at the current time, quantified the effects of this pronouncement, however it believes that there will be no material effect on the consolidated financial statements.

 

In August 2014, FASB issued Accounting Standards Update (ASU) No. 2014-15 Preparation of Financial Statements – Going Concern (Subtopic 205-40), Disclosure of Uncertainties about an Entity's Ability to Continue as a Going Concern. Under generally accepted accounting principles (GAAP), continuation of a reporting entity as a going concern is presumed as the basis for preparing financial statements unless and until the entity's liquidation becomes imminent. Preparation of financial statements under this presumption is commonly referred to as the going concern basis of accounting. If and when an entity's liquidation becomes imminent, financial statements should be prepared under the liquidation basis of accounting in accordance with Subtopic 205-30, Presentation of Financial Statements—Liquidation Basis of Accounting. Even when an entity's liquidation is not imminent, there may be conditions or events that raise substantial doubt about the entity's ability to continue as a going concern. In those situations, financial statements should continue to be prepared under the going concern basis of accounting, but the amendments in this Update should be followed to determine whether to disclose information about the relevant conditions and events. The amendments in this Update are effective for the annual period ending after December 15, 2016, and for annual periods and interim periods thereafter. Early application is permitted. The Company will evaluate the going concern considerations in this ASU, however, at the current period, management does not believe that it has met the conditions which would subject these financial statements for additional disclosure.

 

In January 2016, the FASB issued Accounting Standards Update No. 2016-01, Financial Instruments - Overall (Subtopic 825-10): Recognition and Measurement of Financial Assets and Financial Liabilities. ASU 2016-01 requires that equity investments (except those accounted for under the equity method of accounting or those that result in consolidation of the investee) are to be measured at fair value with changes in fair value recognized in net income. The Company has adopted ASU 2016-01 effective the fiscal year ending 2019 .

 

 8 

 

 

NOTE 3. GOING CONCERN

 

The accompanying financial statements have been prepared assuming that the Company will continue as a going concern. The Company generated net losses of $3,336,182 during the period from June 18, 2015 (inception) through December 31, 2018. This condition raises substantial doubt about the Company's ability to continue as a going concern. The Company's continuation as a going concern is dependent on its ability to meet its obligations, to obtain additional financing as may be required and ultimately to attain profitability. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.

 

Management plans to raise additional funds by offering securities for cash. Management has yet to decide what type of offering the Company will use or how much capital the Company will raise. There is no guarantee that the Company will be able to raise any capital through any type of offerings.

 

NOTE 4. INCOME TAXES

 

As of December 31, 2018

 

Deferred tax assets:   
Net operating tax carry forwards  $700,598 
Other   -0- 
Gross deferred tax assets  $700,598 
Valuation allowance  $(700,598)
Net deferred tax assets  $-0- 

 

As of  December 31, 2018 the Company has a  Deferred Tax Asset of  $700,598  completely attributable to net operating loss carry forwards  of approximately $3,336,182 .

 

In addition, if as a result of a stock transfer or a reorganization, a corporation undergoes an “ownership change,” Code Section 382 limits the corporation’s right to use its NOLs each year thereafter to an annual percentage of the fair market value of the corporation at the time of the ownership change (the “Section 382 Limitation”).

 

A corporation is considered to undergo “an ownership change” if, as a result of changes in the stock ownership by “5-percent shareholders” or as a result of certain reorganizations, the percentage of the corporation’s stock owned by those 5-percent shareholders increases by more than 50 percentage points over the lowest percentage of stock owned by those shareholders at any time during the prior three-year testing period. Five-percent shareholders are persons who hold 5% or more of the stock of a corporation at any time during the testing period as well as certain groups of shareholders (based typically on whether they acquired their shares in a single offering or exchange transaction) who are not individually 5-percent shareholders.

 

As the Company will require cash infusions in order to implement its business plan, and as it is probable, although not guaranteed, that such funding needs may be met through the sale of equity securities to “5-percent shareholders”, the Company recognized a valuation allowance equal to the deferred Tax Asset and the Company recorded a valuation allowance reducing all deferred tax assets to 0.

 

Income tax is calculated at the 21% Federal Corporate Rate. (which expire 20 years from the date the loss was incurred)

 

Realization of deferred tax assets is dependent upon sufficient future taxable income during the period that deductible temporary differences and carry forwards are expected to be available to reduce taxable income. The achievement of required future taxable income is uncertain.

 

 9 

 

 

NOTE 5. RELATED PARTY TRANSACTIONS.

 

On June 23, 2015 Regen Biopharma, Inc. ( “Regen”) entered into an agreement (“Agreement”) with The Company whereby Regen granted to The Company an exclusive worldwide right and license for the development and commercialization of certain intellectual property controlled by Regen (“ License IP”) for non-human veterinary therapeutic use for a term of fifteen years.

 

Pursuant to the Agreement, The Company shall pay to Regen one-time, non-refundable, upfront payment of one hundred thousand US dollars ($100,000) as a license initiation fee which must be paid within 90 days of June 23, 2015 and an annual non-refundable payment of one hundred thousand US dollars ($100,000) on July 15th, 2016 and each subsequent anniversary of the effective date of the Agreement

 

The abovementioned payments may be made, at The Company’s discretion, in cash or newly issued common stock of The Company.

 

Pursuant to the Agreement, The Company shall pay to Regen royalties equal to four percent (4%) of the Net Sales , as such term is defined in the Agreement, of any Licensed Products, as such term is defined in the Agreement, in a

 

Pursuant to the Agreement, The Company will pay Regen ten percent (10%) of all consideration (in the case of in-kind consideration, at fair market value as monetary consideration) received by The Company from sublicensees ( excluding royalties from sublicensees based on Net Sales of any Licensed Products for which Regen receives payment pursuant to the terms and conditions of the Agreement).

 

The Company is obligated pay to Regen minimum annual royalties of ten thousand US dollars ($10,000) payable per year on each anniversary of the Effective Date of this Agreement, commencing on the second anniversary of June 23, 2015. This minimum annual royalty is only payable to the extent that royalty payments made during the preceding 12-month period do not exceed ten thousand US dollars ($10,000).

 

The Agreement may be terminated by Regen:

 

If The Company has not sold any Licensed Product by ten years of the effective date of the Agreement or The Company has not sold any Licensed Product for any twelve (12) month period after The Company’s first commercial sale of a Licensed Product.

 

The Agreement may be terminated by The Company with regard to any of the License IP if by five years from the date of execution of the Agreement a patent has not been granted by the United States patent and Trademark Office to Regen with regard to that License IP.

 

The Agreement may be terminated by The Company with regard to any of the License IP if a patent that has been granted by the United States patent and Trademark Office to Regen with regard to that License IP is terminated.

 

The Agreement may be terminated by either party in the event of a material breach by the other party.

 

On December 17, 2018 Regen Biopharma, Inc.(“Licensor”) , KCL Therapeutics, Inc. (“Assignee”) and Zander Therapeutics, Inc. (“Licensee”) entered into a LICENSE ASSIGNMENT AND CONSENT AGREEMENT whereby, with regards to certain intellectual property which was assigned by Regen Biopharma, Inc.(“Assigned Properties”) to its wholly owned subsidiary KCL Therapeutics, Inc., Licensor hereby transfers and assigns to Assignee all rights, duties, and obligations of Licensor under the Agreement with respect to the Assigned Properties , and Assignee agrees to assume such duties and obligations thereunder and be bound to the terms of the Agreement with respect thereto.

 

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Zander and Regen are under common control. David Koos serves as Chairman & CEO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Harry Lander serves as President and Chief Scientific Officer of both Regen BioPharma, Inc. and Zander Therapeutics, Inc. Todd S. Caven serves as CFO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Koos, Lander and Caven also serve as Directors of Zander Therapeutics, Inc. Zander Therapeutics, Inc. is the sole licensee of Regen's NR2F6 intellectual property for veterinary applications.

 

As of December 31, 2018 Zander Therapeutics, Inc. has prepaid $11,390 of fees due to Regen pursuant to the Agreement.

 

On September 30, 2018 Regen Biopharma, Inc. (“Regen”) issued a convertible promissory note in the principal amount of $350,000 (“Note”) to Zander Therapeutics, Inc. (“Zander”). Consideration for the Note consisted of $350,000. A one time interest charge of 10% of the principal amount shall be applied to the principal amount of the Note. The Maturity Date is twenty four months after September 30, 2018 and is the date upon which the Principal Sum of this Note, as well as any unpaid interest and other fees, shall be due and payable.

 

Zander has the right, at any time after the September 30, 2018, at its election, to convert all or part of the outstanding and unpaid Principal Sum and accrued interest (and any other fees) into shares of fully paid and non-assessable shares of Series A Preferred stock of Regen as per this conversion formula: Number of shares receivable upon conversion equals the dollar conversion amount divided by the Conversion Price. The Conversion Price is the greater of $0.0001 or 60% of the lowest trade price in the 25 trading days previous to the conversion. Zander, at any time prior to selling all of the shares from a conversion, may, for any reason, rescind any portion, in whole or in part, of that particular conversion attributable to the unsold shares and have the rescinded conversion amount returned to the Principal Sum with the rescinded conversion shares returned to Regen.

 

On July 3, 2018 Zander Therapeutics , Inc.(“Zander”) entered into a sublease agreement with Entest Biomedical, Inc. (“Entest CA”) whereby Zander would sublet office space located at 4700 Spring Street, Suite 304, La Mesa, California 91942 from Entest CA on a month to month basis for $6,000 per month beginning July 5, 2018.

 

On November 16, 2018 Zander and Entest CA agreed to terminate Zander’s sublease with Entest CA effective the rental period commencing November, 2018.

 

David R. Koos, who serves as Chairman and Chief Executive Officer of Zander also serves as Chairman and Chief Executive Officer of Entest CA.

 

On November 16, 2018 Zander entered into a sublease agreement with BST Partners (“BST”) whereby Zander would sublet office space located at 4700 Spring Street, Suite 304, La Mesa, California 91942 from BST on a month to month basis for $6,000 per month beginning November 5, 2018.

 

BST is controlled by David Koos, Zander’s Chairman and Chief Executive Officer.

 

NOTE 6. INVESTMENT SECURITIES

 

On July 3, 2018 the Company purchased 3,500,000 of the Series A Preferred shares of Regen Biopharma, Inc from Entest Group, Inc. for consideration consisting of $35,000 .

 

The Series A Preferred shares of Regen Biopharma, Inc. described above constitute the Company’s sole investment securities as of December 31, 2018.

 

As of December 31, 2018:

 

  3,500,000 Series A Preferred shares of Regen Biopharma, Inc  
                         
  Basis     Fair Value     Total Unrealized Loss       Net Unrealized Gain or (Loss) during the quarter  ended December 31, 2018  
$ 35,000   $ 14,700   $ (20,300)     $ (46,550)  

 

The Chairman and Chief Executive Officer of Regen is David R. Koos who also serves as the Chairman and Chief Executive Officer of the Company.

 

The President of Regen is Harry Lander who also serves as President of the Company.

 

The Chief Financial Officer of Regen is Todd Caven who also serves as Chief Financial Officer of the Company.

 

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NOTE 7. CONVERTIBLE NOTE RECEIVABLE

 

On September 30, 2018 Regen Biopharma, Inc. (“Regen”) issued a convertible promissory note in the principal amount of $350,000 (“Note”) to Zander Therapeutics, Inc. (“Zander”). Consideration for the Note consisted of $350,000. A one time interest charge of 10% of the principal amount shall be applied to the principal amount of the Note. The Maturity Date is twenty four months after September 30, 2018 and is the date upon which the Principal Sum of this Note, as well as any unpaid interest and other fees, shall be due and payable.

 

Zander has the right, at any time after the September 30, 2018, at its election, to convert all or part of the outstanding and unpaid Principal Sum and accrued interest (and any other fees) into shares of fully paid and non-assessable shares of Series A Preferred stock of Regen as per this conversion formula: Number of shares receivable upon conversion equals the dollar conversion amount divided by the Conversion Price. The Conversion Price is the greater of $0.0001 or 60% of the lowest trade price in the 25 trading days previous to the conversion. Zander, at any time prior to selling all of the shares from a conversion, may, for any reason, rescind any portion, in whole or in part, of that particular conversion attributable to the unsold shares and have the rescinded conversion amount returned to the Principal Sum with the rescinded conversion shares returned to Regen.

 

The Company analyzed the conversion feature of the Note for derivative accounting consideration under ASC 815-15 “Derivatives and Hedging” and determined that the embedded conversion feature should be classified as an asset. ASC 815-15 requires that the conversion features are bifurcated and separately accounted for as an embedded derivative contained in the Company’s convertible debt. The embedded derivative is carried on the balance sheet at fair value. Any unrealized change in fair value, as determined at each measurement period, is recorded as a component of the income statement and the associated carrying amount on the balance sheet is adjusted by the change.

 

The Company values the embedded derivative using the Black-Scholes pricing model and a derivative  asset of $555,555 was recognized by the Company as of December 31,  2018.

 

Zander and Regen are under common control. David Koos serves as Chairman & CEO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Harry Lander serves as President and Chief Scientific Officer of both Regen BioPharma, Inc. and Zander Therapeutics, Inc. Todd S. Caven serves as CFO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Koos, Lander and Caven also serve as Directors of Zander Therapeutics, Inc. Zander Therapeutics, Inc. is the sole licensee of Regen's NR2F6 intellectual property for veterinary applications.

 

NOTE 8. STOCKHOLDERS' EQUITY

 

The stockholders' equity section of the Company contains the following classes of capital stock as December 31, 2018:

 

Common stock, $ 0.0001 par value; 100,000,000 shares authorized: 6,033,001 shares issued and outstanding.

 

With respect to each matter submitted to a vote of stockholders of the Corporation, each holder of Common Stock shall be entitled to cast that number of votes which is equivalent to the number of shares of Common Stock owned by such holder times one (1).

 

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On any voluntary or involuntary liquidation, dissolution or winding up of the Corporation, the holders of the Common Stock shall receive, out of assets legally available for distribution to the Company's stockholders, a ratable share in the assets of the Corporation.

 

Preferred Stock, $0.0001 par value, 50,000,000 shares authorized of which

 

(a) 10,000,000 is designated as Series M Preferred Stock: 9,000,000 shares of Series M Preferred Stock are issued and outstanding as of  December 31, 2018

 

With respect to each matter submitted to a vote of stockholders of the Corporation, each holder of Series M Preferred Stock shall be entitled to cast that number of votes which is equivalent to the number of shares of Series M Preferred Stock owned by such holder times one (1).

 

On any voluntary or involuntary liquidation, dissolution or winding up of the Corporation, the holders of the Series M Preferred Stock shall receive, out of assets legally available for distribution to the Company's stockholders, a ratable share in the assets of the Corporation.

 

(b) 1,000,000 is designated as Series AA Preferred Stock: 200 shares of Series AA Preferred Stock are issued and outstanding as of  December 31, 2018,

 

With respect to each matter submitted to a vote of stockholders of the Corporation, each holder of Series AA Preferred Stock shall be entitled to cast that number of votes which is equivalent to the number of shares of Series AA Preferred Stock owned by such holder times 10,000 (10,000).

 

On any voluntary or involuntary liquidation, dissolution or winding up of the Corporation, the holders of the Series AA Preferred Stock shall receive, out of assets legally available for distribution to the Company's stockholders, a ratable share in the assets of the Corporation.

 

NOTE 9. PRIOR PERIOD ADJUSTMENTS

The Company has adjusted Research and Development Expenses for the Period ended September 30, 2018 in the following manner:

Research and Development Expenses recognized for the period ended September 30, 2018 has been increased by $6,397

The aforementioned adjustments have resulted in an increase in Net Loss for the period ended September 30, 2018 as originally reported of $6,397.

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ITEM 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS.

CERTAIN FORWARD-LOOKING INFORMATION 

Information provided in this Quarterly report on Form 10Q may contain forward-looking statements within the meaning of Section 21E or Securities Exchange Act of 1934 that are not historical facts and information. These statements represent the Company's expectations or beliefs, including, but not limited to, statements concerning future and operating results, statements concerning industry performance, the Company's operations, economic performance, financial conditions, margins and growth in sales of the Company's products, capital expenditures, financing needs, as well assumptions related to the forgoing. For this purpose, any statements contained in this Quarterly Report that are not statement of historical fact may be deemed to be forward-looking statements. These forward-looking statements are based on current expectations and involve various risks and uncertainties that could cause actual results and outcomes for future periods to differ materially from any forward-looking statement or views expressed herein. The Company's financial performance and the forward-looking statements contained herein are further qualified by other risks including those set forth from time to time in the documents filed by the Company with the Securities and Exchange Commission, including the Company's most recent Form 10K for the year ended June 30, 2018. All references to” We”, “Us”, “Company” or the “Company” refer to Zander Therapeutics, Inc.

 

As of June 30, 2018 we had Cash of $370,313 and as of December 31, 2018 we had Cash of $71,345.

 

The decrease in Cash of approximately 80.7% is primarily attributable to the cost of operating the Company’s business partially offset by the sale of $800,000 of common stock by the Company during the quarter ended September 30, 2018 .

 

As of June 30, 2018 we had Prepaid Expenses to Related parties of $66,239 and as of December 31 , 2018 we had prepaid expenses to Related Parties of $11,390.

 

The decrease in Prepaid Expenses to Related parties of 82% is attributable to:

 

(a)The recognition of $24,931 of expenses during the quarter ended September 30, 2018 attributable to an annual anniversary fee of $100,000 due annually to Regen Biopharma, Inc. pursuant to a license granted to Zander by Regen Biopharma, Inc.
(b)The recognition of $2,493 of expenses during the quarter ended September 30, 2018 attributable to minimum royalties of $10,000 due annually to Regen Biopharma, Inc. pursuant to a license granted to Zander by Regen Biopharma, Inc.
(c)The recognition of $24,931 of expenses during the quarter ended December 31, 2018 attributable to an annual anniversary fee of $100,000 due annually originally to Regen Biopharma, Inc. pursuant to a license granted to Zander by Regen Biopharma, Inc.
(d)The recognition of $2,493 of expenses during the quarter ended December 31, 2018 attributable to minimum royalties of $10,000 due annually originally to Regen Biopharma, Inc. pursuant to a license granted to Zander by Regen Biopharma, Inc.

 

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On December 17, 2018 Regen Biopharma, Inc.(“Licensor”) , KCL Therapeutics, Inc. (“Assignee”) and Zander Therapeutics, Inc. (“Licensee”) entered into a LICENSE ASSIGNMENT AND CONSENT AGREEMENT whereby, with regards to certain intellectual property which was assigned by Regen Biopharma, Inc.(“Assigned Properties”) to its wholly owned subsidiary KCL Therapeutics, Inc., Licensor hereby transfers and assigns to Assignee all rights, duties, and obligations of Licensor under the Agreement with respect to the Assigned Properties , and Assignee agrees to assume such duties and obligations thereunder and be bound to the terms of the Agreement with respect thereto.

 

Zander and Regen Biopharma, Inc. are under common control. David Koos serves as Chairman & CEO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Harry Lander serves as President and Chief Scientific Officer of both Regen BioPharma, Inc. and Zander Therapeutics, Inc. Todd S. Caven serves as CFO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Koos, Lander and Caven also serve as Directors of Zander Therapeutics, Inc. KCL Therapeutics, Inc. is a wholly owned subsidiary of Regen BioPharma, Inc. and is also under common control with Zander.

As of June 30, 2018 we had Prepaid Expenses of $650 and as of December 31, 2018 we had Prepaid Expenses of $6,387.

 

The increase in Prepaid Expenses of 89.8%  is primarily attributable to $5745 prepaid of fees prepaid to a member of the Company’s Business Advisory Board during the six months ended December 31, 2018.

 

As of June 30, 2018 we had $35,000 due from related parties and as of December 31,  2018 we had $0 due from related Parties.

 

$35,000 due from related parties as of June 30, 2018 consists of funds advanced to Entest Group, Inc. by the Company in contemplation of the purchase by the Company of 3,500,000 of the Series A preferred Shares of Regen Biopharma, Inc. owned by Entest Group, Inc. from Entest Group, Inc. On July 3, 2018 Zander purchased the aforementioned 3,500,000 of the Series A preferred Shares of Regen Biopharma, Inc. owned by Entest Group, Inc. from Entest Group, Inc. (“Entest”) for the price of $35,000 USD cash. Entest Group, Inc. was a related party under common control until December 2018.

 

As of June 30, 2018 we had Investment Securities of 0 and as of December 31, 2018 we had Investment Securities of $14,700.

 

On July 3, 2018 Zander purchased the aforementioned 3,500,000 of the Series A preferred Shares of Regen Biopharma, Inc. owned by Entest Group, Inc. from Entest Group, Inc. (“Entest”). The 3,500,000 of the Series A preferred Shares of Regen Biopharma, Inc. purchased by Zander are carried at fair value as of the measurement date which is September 30, 2018. Zander and Regen Biopharma, Inc. are under common control. David Koos serves as Chairman & CEO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Harry Lander serves as President and Chief Scientific Officer of both Regen BioPharma, Inc. and Zander Therapeutics, Inc. Todd S. Caven serves as CFO of both Regen BioPharma, Inc. and Zander Therapeutics Inc. Koos, Lander and Caven also serve as Directors of Zander Therapeutics, Inc.

 

As of June 30, 2018 we had Convertible Note Receivable of $0 and as of December 31, 2018 we had Convertible Note Receivable of $350,000.

 

On September 30, 2018 Regen Biopharma, Inc. (“Regen”) issued a convertible promissory note in the principal amount of $350,000 (“Note”) to Zander. Consideration for the Note consisted of $350,000. A one time interest charge of 10% of the principal amount shall be applied to the principal amount of the Note. The Note is due and payable 24 months after the effective date of the Note ( September 30, 2018). Zander may extend any maturity date in three month increments at Zander’s sole discretion.

 

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As of June 30, 2018 we had Accrued Interest Receivable of 0 and as of as of December 31, 2018 we had Accrued Interest Receivable of $4,363.

 

Accrued Interest Receivable of $4,363 earned during the quarter ended December 31, 2018 is attributable to interest earned on a convertible promissory note in the principal amount of $350,000 issued  to the Company by Regen Biopharma, Inc. on September 30, 2018.

 

As of June 30, 2018 we had Derivative Assets of 0 and as of December 31, 2018 we had a Derivative Asset of $555,555.

 

The increase in Derivative Assets is attributable to the recognition by the Company of an embedded conversion feature contained within a $350,000 Convertible Note issued to the Company by Regen Biopharma, Inc.

 

As of June 30, 2018 we had Accounts Payable of $1,087,969 and as of December 31, 2018 we had Accounts Payable of $1,363,802.

 

The increase in Accounts Payable of 25.3 % is primarily attributable to $410,000 of fees payable to Contract Research Organizations incurred during the quarter ended September 30, 2018 offset by payment of trade obligations during the six months ended December 31, 2018.

 

As of June 30, 2018 we had Accrued Expenses of $11,593 and as of December 31, 2018 we had Accrued Expenses of $36,051.

The increase in accrued expenses of 211% is primarily attributable to:

 

(a)Accrual of $33,334 of salaries unpaid to Company officers during the quarter ended December 31,2018
(b)Accrual of $568 of licensing fees payable to Monash University pursuant to an exclusive, royalty bearing, non-transferrable worldwide License granted to the Company to use certain intellectual property owned or controlled by Monash University “(Licensed Intellectual Property”) to research, develop, manufacture, market, use, import, offer for sale and sell drugs and/or therapies for animal health incorporating the Licensed Intellectual Property.

 

Offset by

 

Payment of $9,444 of salary Accrued but unpaid due to the Company’s Chief Executive Officer during the quarter ended September 30, 2018.

 

Material Changes in Results of Operations

 

Revenues from continuing operations were $0 for the quarter ended December 31, 2018 and -0- for the same period ended 2017. Net Loss was $1,204,486 for the quarter ended December 31, 2018 while Net Loss was $166,637 for the same period ended 2017.

 

The largest component contributing to the increase of 622.82% in Net Loss for the quarter ended December 31, 2018 as compared to the same quarter ended 2017 was an $861,110 unrealized loss on derivative assets recognized during the period ended 2018.

 

Operating loss increased approximately 89.4% in the quarter ended December 31, 2018 as compared to the same period ended 2017.

 

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The increase in Operating Losses were primarily attributable to significant increases in Research and Development expenses, Rental expenses and General and Administrative incurred during the quarter ended December 31, 2018 when compared to the same quarter ended 2017. These losses were partially offset by decreases in Consulting Expenses incurred during the quarter ended December 31, 2018 when compared to the same period ended 2017.

 

Revenues from continuing operations were $0 for the six months ended December 31, 2018 and -0- for the same period ended 2017. Net Loss was $572,879 for the six months ended December 31, 2018 while Net Loss was $293,864 for the same period ended 2017.

 

The largest components contributing to the increase of 94.9% in Net Loss for the six months ended December 31, 2018 as compared to the same period ended 2017 were primarily attributable to a significant increase in Research and Development expenses, Rental expenses Consulting Expenses and General and Administrative expenses incurred during the six months ended 2018 when compared to the same period ended 2017. These losses were partially offset by thr recognition by the Company of a $555, 556 unrealized gain on derivative assets recognized during the period ended 2018.

 

Operating loss increased approximately 292.61% in the six months ended December 31, 2018 as compared to the same period ended 2017.

 

The increase in Operating Losses were primarily attributable to significant increases in Research and Development expenses, Consulting Expenses, Rental expenses and General and Administrative incurred during the six months ended December 31, 2018 when compared to the same quarter ended 2017.

 

As of December 31, 2018 we had $71,345 Cash on Hand and Current Liabilities of $1,399,853, such Liabilities consisting of Accounts Payable and Accrued Expenses.

 

We feel we will not be able to satisfy our cash requirements over the next twelve months and shall be required to seek additional financing.

 

We currently plan to raise additional funds primarily by offering securities for cash.

 

On June 12, 2018 Zander Therapeutics, Inc. ( the “Company”) entered into an agreement with Dakoy Capital Markets, LLC whereby the Company retained the services of Dakoy Capital Markets, LLC (“Placement Agent”) to assist the Company in offering of shares of the Company (the “Securities” or “Shares”) for sale on a best efforts basis (“Offering”) . Placement Agent is obligated to use its best efforts to introduce the Company to accredited investors, which may include corporations, partnerships, mutual funds, hedge funds, investment partnerships, securities firms, lending and other institutions and entities, as well as select high net worth individuals (collectively, the “Purchasers”) for the purposes of participating in the Offering. The Company retains the right to employ other agents in connection with the sale of the Securities and the Offering is anticipated to commence within 30 days of the execution of the abovementioned agreement.

 

As compensation for its activities, the Placement Agent shall be paid a commission as follows:

 

A.Cash commission in an amount equal to seven percent (7%) of the total principal amount of gross proceeds of any Securities purchased by investors first introduced to the Company by the Placement Agent (“PA Investors”) and accepted by the Company (such persons being hereinafter referred to as the “PA Investor(s)”), and
B.Options exercisable for five (5) years from the date the Offering closes, to purchase that number of Shares equal to five percent (5%) of the number of Shares of Company sold in the Offering to PA Investors (the “Options Compensation” and together with the Cash Compensation, the “Placement Agent Compensation”). Such options shall be granted at each Closing at an exercise price per share equal to the price of the shares paid by the investors in the Offering. Such Option Compensation shall provide, among other things that the options shall:

 

1. expire five (5) years from the date of issuance; and

 

2. provide for “cashless” exercise; and

 

3. such other terms as are normal and customary for warrants issued to placement agents, including the same registration rights and other rights received by the investors in the Offering.

 

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There is no guarantee that we will be able to raise any capital through any type of offerings. We cannot assure that we will be successful in obtaining additional financing necessary to implement our business plan. We have not received any commitment or expression of interest from any financing source that has given us any assurance that we will obtain the amount of additional financing in the future that we currently anticipate. For these and other reasons, we are not able to assure that we will obtain any additional financing or, if we are successful, that we can obtain any such financing on terms that may be reasonable in light of our current circumstances.

 

During the quarter ended September 30, 2018 Zander raised $800,000 by the sale of securities for cash.

 

As of January 17, 2019 we are not party to any binding agreements which would commit us to any material capital expenditures.

 

Item 3. Quantitative and Qualitative Disclosures About Market Risk

 

As a smaller reporting company, as defined by Rule 229.10(f) (1) of Regulation S-K, we are not required to provide the information required by this Item. We have chosen to disclose, however, that we have not engaged in any transactions, issued or bought any financial instruments or entered into any contracts that are required to be disclosed in response to this item.

 

Item 4. Controls and Procedures.

 

Evaluation of Disclosure Controls and Procedures

 

As of the end of the period covered by this report, the Company carried out an evaluation, under the supervision and with the participation of David Koos, who is the Company’s Principal Executive Officer and Todd S. Caven who is the Company’s Chief Financial Officer and Principal Financial Officer, of the effectiveness of the design and operation of the Company’s disclosure controls and procedures. The Company’s disclosure controls and procedures are designed to provide a reasonable level of assurance of achieving the Company’s disclosure control objectives. The Company’s Principal Executive Officer and Principal Financial Officer have concluded that the Company’s disclosure controls and procedures are, in fact, effective at this reasonable assurance level as of the period covered.

 

Changes in Internal Controls over Financial Reporting

 

In connection with the evaluation of the Company’s internal controls during the period commencing on October 1, 2018 and ending on December 31, 2018, David Koos and Todd S. Caven , who serve as the Company’s Principal Executive Officer and Principal Financial Officer respectively, have determined that there were no changes to the Company’s internal controls over financial reporting that have been materially affected, or is reasonably likely to materially effect, the Company’s internal controls over financial reporting.

 

PART II - OTHER INFORMATION

 

Item 1. Legal Proceedings.

 

There are no material pending legal proceedings to which the Company is a party or of which any of the Company’s property is the subject.

 

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

 

There were no unregistered sales of equity securities of the Company made by the Company during the quarter ended December 31, 2018.

 

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Item 3. DEFAULTS UPON SENIOR SECURITIES

 

None.

 

Item 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS

 

None.

 

Item 5. OTHER INFORMATION

 

None.

 

Item 6. EXHIBITS

 

31.1 Certification of Chief Executive Officer
31.2 Certification of Acting Chief Financial Officer
10.1 License Agreement Monash University
10.2 Sublease BST Partners*

  

*Incorporated by Reference to Exhibit 10.1 of the Company’s Current Report on Form 8-K filed on November 20, 2018

 

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SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities indicated on January 17, 2019.

 

      Zander Therapeutics, Inc.
       
  By:   /s/ David R. Koos
  Name:   David R. Koos
  Title:   Principal Executive Officer
  Date:    January 22,2019

 

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities indicated on January 17,2019.

 

      Zander Therapeutics, Inc.
       
  By:   /s/ David R. Koos
  Name:   David R. Koos
  Title:   Chairman,  Director
  Date:    January 22,2019

 

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities indicated on January 17,2019.

 

      Zander Therapeutics, Inc.
       
  By:   /s/ Todd S. Caven
  Name:   Todd S. Caven
  Title:   Principal Financial Officer
  Date:    January 22,2019

 

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities indicated on January 17,2019.

 

      Zander Therapeutics, Inc.
       
  By:   /s/ Todd S. Caven
  Name:   Todd S. Koos
  Title:   Principal Accounting Officer
  Date:    January 22,2019

 

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities indicated on January 17,2019.

 

      Zander Therapeutics, Inc.
       
  By:   /s/ Todd S. Caven
  Name:   Todd S. Koos
  Title:   Director
  Date:    January 22,2019

 

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