U.S. SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

   FORM 10-Q/A

Amendment No 2

 

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

 

  For the quarterly period ended March 31, 2016

 

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

 

For the transition period from

 

Commission File No. 333-191725

 

REGEN BIOPHARMA, INC.

(Exact name of small business issuer as specified in its charter)

 

Nevada   45-5192997
(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)

 

None

(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 April 8, 2016 there were 128,253,938 shares of common stock issued and outstanding.

 

As of April 8, 2016 there were 115,881,697 shares of Series A Preferred 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 

 

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EXPLANATORY NOTE:

THIS AMENDMENT NO.2 TO REGEN BIOPHARMA, INC’S (THE “COMPANY”) FORM 10-Q FOR THE PERIOD ENDED MARCH 31, 2016 (“(“ORIGINAL FILING”) IS BEING FILED SOLELY TO AMEND THE FOLLOWING PORTIONS OF AMENDMENT NO.1 OF THE ORIGINAL FILING (“AMENDMENT NO.1”).  

 

PART 1, ITEM 4

 

THE COMPANY HAS NOT MODIFIED OR UPDATED DISCLOSURES PRESENTED IN AMENDMENT NO.1 OR THE ORIGINAL FILING, EXCEPT AS INDICATED ABOVE. ACCORDINGLY, THIS AMENDMENT DOES NOT REFLECT EVENTS OCCURRING AFTER THE DATE OF THE ORIGINAL FILING AND DOES NOT MODIFY OR UPDATE THOSE DISCLOSURES AFFECTED BY SUBSEQUENT EVENTS, EXCEPT AS SPECIFICALLY REFERENCED HEREIN. INFORMATION NOT AFFECTED BY THE ABOVE AMENDMENTS IS UNCHANGED AND REFLECTS THE DISCLOSURES MADE AT THE TIME OF THE ORIGINAL FILING.    

 

 

 

 

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PART I - FINANCIAL INFORMATION

Item 1. - Financial Statements

 

REGEN BIOPHARMA , INC.        
BALANCE SHEET        
         
    As of March 31, 2016 (unaudited) as restated  

As of September 30, 2015

as restated

ASSETS        
CURRENT ASSETS                
Cash     106,024       38,620  
Note Receivable     12,051       12,051  
Prepaid Expenses     1,000       10,000  
Accrued Interest Receivable     1,978       1,381  
Due from Former Employees     15,000          
     Total Current Assets     136,053       62,052  
                 
OTHER ASSETS                
Available for Sale Securities     56,800       158,400  
Total Other Assets     56,800       158,400  
                 
TOTAL ASSETS     192,853       220,452  
                 
LIABILITIES AND STOCKHOLDERS' EQUITY                
Current Liabilities:                
Bank Overdraft     0       0  
Accounts payable     21,283       25,854  
Notes Payable     228,050       222,751  
Accrued payroll taxes     1,946       1,940  
Accrued Interest     31,184       21,093  
Accrued Rent     15,000       10,000  
Accrued Payroll     92,996       36,001  
Due to Shareholder     0          
Total Current Liabilities     390,459       317,639  
Convertible Notes Payable     58,295          
Total Long Term Liabilities     58,295          
Total Liabilities     448,754       317,639  
                 
STOCKHOLDERS' EQUITY (DEFICIT)                
Common Stock ($.0001 par value) 500,000,000 shares authorized;  114,753,938 issued and outstanding as of September 30, 2015 and 128,253,138 shares issued and outstanding March  31, 2016     12,824       11,474  
Preferred Stock, 0.0001 par value, 800,000,000 authorized and 100,000,000 authorized as of December 31,  2015 and September 30, 2015 respectively                
Series A Preferred 90,000,000 Authorized and 300,000,000 authorized, 60,981,697 and 84,881,697 outstanding as of  September  30, 2105 and March 31, 2016 respectively     8,488       6,098  
Series AA Preferred $0.0001 par value 600,000 authorized and 30,000 outstanding as of September 30, 2015 and March  31, 2016     3       3  
Additional Paid in capital     4,038,835       2,679,473  
Contributed Capital     728,658       728,658  
Retained Earnings (Deficit) accumulated during the development stage     (4,909,508 )     (3,489,293 )
Accumulated Other Comprehensive Income     (135,200 )     (33,600 )
Total Stockholders' Equity (Deficit)     (255,900 )     (97,187 )
                 
TOTAL LIABILITIES & STOCKHOLDERS' EQUITY (DEFICIT)     192,853       220,452  
                 
The Accompanying Notes are an Integral Part of These Financial Statements

 

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REGEN BIOPHARMA , INC.                
STATEMENT OF OPERATIONS                
(unaudited)                
                   
     

Quarter Ended March 31, 2016

as restated

     

Quarter Ended March 31, 2015

as restated

     

Six Months Ended March 31, 2016

as restated

     

Six Months Ended March 31, 2015

as restated

   
REVENUES     0       0       0       0    
                                   
COST AND EXPENSES                                  
Research and Development     172,596       22,969       277,919       25,206    
General and Administrative     435,236       303,536       923,831       442,989    
Consulting and Professional Fees     97,547       279,913       178,080       339,761    
Rent     15,000       15,000       30,000       26,871    
Total Costs and Expenses     720,379       621,419       1,409,830       834,828    
                                   
OPERATING LOSS     (720,379 )     (621,419 )     (1,409,830 )     (834,828 )  
                                   
OTHER INCOME & (EXPENSES)                                  
Interest Income     297       291       597       551    
Refunds of amounts previously paid                                  
Interest Expense     (5,089 )     (9,188 )     (10,090 )     (15,230 )  
Interest Expense attributable to                                  
Amortization of Discount     (894 )             (894 )          
Preferred shares issued pursuant to                                  
contractual obligations             (3,154 )             (3,154 )  
TOTAL OTHER INCOME (EXPENSE)     (5,686 )     (12,051 )     (10,387 )     (17,833 )  
                                   
NET INCOME (LOSS)     (726,064 )     (633,470 )     (1,420,217 )     (852,661 )  
BASIC AND FULLY DILUTED                                  
EARNINGS (LOSS) PER SHARE     (0.0058 )     (0.0088 )     (0.0091 )     (0.0092 )  
WEIGHTED AVERAGE NUMBER OF COMMON                                  
SHARES OUTSTANDING     124,875,119       71,986,230       156,418,573       93,139,424    
                                   
The Accompanying Notes are an Integral Part of These Financial Statements  

 

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REGEN BIOPHARMA, INC.        
STATEMENT OF COMPREHENSIVE INCOME        
(unaudited)        
    Quarter  Ended March  31
    as restated
      2016       2015  
Net Income (Loss)     (726,064 )     (633,470 )
Add:                
     Unrealized Gains on Securities     —         —    
Less:                
     Unrealized Losses on Securities     (63,200 )     —    
     Total Other Comprehensive Income (Loss)     (63,200 )     —    
Comprehensive Income     (789,264 )     (633,470 )
                 
                 
      Six Months  Ended March  31  
      as restated  
      2016       2015  
Net Income (Loss)     (1,420,217 )     (852,661 )
Add:                
     Unrealized Gains on Securities     —         —    
Less:                
     Unrealized Losses on Securities     (101,600 )     —    
     Total Other Comprehensive Income (Loss)     (101,600 )     —    
Comprehensive Income     (1,521,817 )     (852,661 )
                 
The Accompanying Notes are an Integral Part of These Financial Statements

 

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REGEN BIOPHARMA , INC.        
STATEMENT OF CASH FLOWS        
(unaudited)        
         
   

Six Months Ended

March 31,

2016

as restated

 

Six Months Ended

March 31,

2015

as restated

CASH FLOWS FROM OPERATING ACTIVITIES                
                 
Net Income (loss)   $ (1,420,217 )     (852,661 )
Adjustments to reconcile net Income to net cash                
                 
Preferred Stock Issued for Expenses             100  
Preferred Stock issued for Interest             891  
Preferred Stock issued pursuant to contractual obligations             3,154  
Common Stock issued to Consultants             226,177  
Preferred Stock issued to Consultants     40       420  
Increase (Decrease) in Interest expense attributable to amortization of Discount     894          
Changes in operating assets and liabilities:                
Increase (Decrease) in Accounts Payable     (4,571 )     12,902  
(Increase) Decrease in Notes Receivable             (1,629 )
(Increase) Decrease in Interest  Receivable     (597 )     (551 )
Increase ( Decrease) in Bank Overdraft             (6,137 )
Increase (Decrease) in accrued Expenses     72,093       19,437  
(Increase) Decrease in Prepaid Expenses     9,000          
(Increase) Decrease in Due from Former Employee     (15,000 )        
Increase in Additional Paid in Capital     495,462       132,603  
Net Cash Provided by (Used in) Operating Activities   $ (862,896 )     (465,294 )
                 
CASH FLOWS FROM FINANCING ACTIVITIES                
Common Stock issued for Cash     475,000          
Preferred Stock issued for Cash     350,001          
Increase in Contributed Capital             85,000  
Increase ( Decrease)  in Notes Payable     5,299       19,582  
Increase in Convertible Notes payable     100,000       882,685  
Increase in Due to Shareholder     0          
                 
Net Cash Provided by (Used in) Financing Activities     930,300       987,267  
                 
Net Increase (Decrease) in Cash   $ 67,404.09       521,974  
                 
Cash at Beginning of Period     38,620       0  
                 
Cash at End of Period   $ 106,024       521,974  
                 
Supplemental Disclosure of Noncash investing and financing activities:                
Common shares Issued for Debt             882,868  
Preferred Shares Issued for Debt             6,000  
                 
The Accompanying Notes are an Integral Part of These Financial Statements

 

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REGEN BIOPHARMA, INC.

Notes to Financial Statements

As of March 31, 2016

 

The accompanying unaudited interim condensed consolidated financial statements of Regen Biopharma , Inc. (“Regen” 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 September 30, 2015. 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

 

The Company was organized April 24, 2012 under the laws of the State of Nevada. The Company is a controlled subsidiary of Bio-Matrix Scientific Group, Inc, (“BMSN”) a Delaware corporation.

 

The Company intends to engage primarily in the development of regenerative medical applications which we intend to license from other entities up to the point of successful completion of Phase I and or Phase II clinical trials after which we would either attempt to sell or license those developed applications or, alternatively, advance the application further to Phase III clinical trials

 

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 September 30 year-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.

 

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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 March 31, 2016 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 three months ended March 31, 2016 and $0 for the three months ended March 31, 2015.

 

NOTE 2.    RECENT ACCOUNTING PRONOUNCEMENTS

 

In 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 us. These standards are currently under review to determine their impact on our 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.

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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 August2014, 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.

 

On January 31, 2013, the FASB issued Accounting Standards Update [ASU] 2013-01, entitled Clarifying the Scope of Disclosures about Offsetting Assets and Liabilities. The guidance in ASU 2013-01 amends the requirements in the FASB Accounting Standards Codification [FASB ASC] Topic 210, entitled Balance Sheet. The ASU 2013-01 amendments to FASB ASC 210 clarify that ordinary trade receivables and receivables in general are not within the scope of ASU 2011-11, entitled Disclosure about Offsetting Assets and Liabilities, where that ASU amended the guidance in FASB ASC 210. As those disclosures now are modified with the ASU 2013-01 amendments, the FASB ASC 210 balance sheet offsetting disclosures now clearly are applicable only where reporting entities are involved with bifurcated embedded derivatives, repurchase agreements, reverse repurchase agreements, and securities borrowing and lending transactions that either are offset using the FASB ASC 210 or 815 requirements, or that are subject to enforceable master netting arrangements or similar agreements. ASU 2013-01 is effective for annual reporting periods beginning on or after January 1, 2013, and interim periods within those annual periods. The adoption of this ASU is not expected to have a material impact on our financial statements.

 

On February 28, 2013, the FASB issued Accounting Standards Update [ASU] 2013-04, entitled Obligations Resulting from Joint and Several Liability Arrangements for Which the Total Amount of the Obligation Is Fixed at the Reporting Date. The ASU 2013-04 amendments add to the guidance in FASB Accounting Standards Codification [FASB ASC] Topic 405, entitled Liabilities and require reporting entities to measure obligations resulting from certain joint and several liability arrangements where the total amount of the obligation is fixed as of the reporting date, as the sum of the following:

 

The amount the reporting entity agreed to pay on the basis of its arrangement among co-obligors.

 

Any additional amounts the reporting entity expects to pay on behalf of its co-obligors.

 

While early adoption of the amended guidance is permitted, for public companies, the guidance is required to be implemented in fiscal years, and interim periods within those years, beginning after December 15, 2013. The amendments need to be implemented retrospectively to all prior periods presented for obligations resulting from joint and several liability arrangements that exist at the beginning of the year of adoption. The adoption of ASU 2013-04 is not expected to have a material effect on the Company’s operating results or financial position.

 

On April 22, 2013, the FASB issued Accounting Standards Update [ASU] 2013-07, entitled Liquidation Basis of Accounting. With ASU 2013-07, the FASB amends the guidance in the FASB Accounting Standards Codification [FASB ASC] Topic 205, entitled Presentation of Financial Statements. The amendments serve to clarify when and how reporting entities should apply the liquidation basis of accounting. The guidance is applicable to all reporting entities, whether they are public or private companies or not-for-profit entities. The guidance also provides principles for the recognition of assets and liabilities and disclosures, as well as related financial statement presentation requirements. The requirements in ASU 2013-07 are effective for annual reporting periods beginning after December 15, 2013, and interim reporting periods within those annual periods. Reporting entities are required to apply the requirements in ASU 2013-07 prospectively from the day that liquidation becomes imminent. Early adoption is permitted. The adoption of ASU 2013-07 is not expected to have a material effect on the Company’s operating results or financial position.

A variety of proposed or otherwise potential accounting standards are currently under study by standard setting organizations and various regulatory agencies.  Due to the tentative and preliminary nature of those proposed standards, the Company’s management has not determined whether implementation of such standards would be material to its financial statements.

 

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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 $ 4,909,508 during the period from April 24, 2012 (inception) through March 31, 2016. 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. During the quarter ended March 31, 2015 the Company raised $265,000 through the issuance of equity securities for cash and $100,000 through the issuance of convertible debentures.

 

During the six months ended March 31, 2016 the Company raised $825,001 through the issuance of equity securities for cash and $100,000 through the issuance of convertible debentures.

 

NOTE 4. NOTES PAYABLE

 

    March 31, 2016
     
David Koos ( Note 8)     50  
Bio Technology Partners Business Trust     36,000  
Bostonia Partners     189,000  
Blackbriar Partners (Note 8)     3,000  
Notes payable   $ 228,050  

 

$50 lent to the Company by David Koos. is due and payable at the demand of the holder and bears simple interest at a rate of 15% per annum.

 

$36,000 lent to the Company by Bio Technology Partners Business Trust. is due and payable at the demand of the holder and bears simple interest at a rate of 10% per annum.

 

$60,000 lent to the Company by Bostonia Partners is due and payable September 16, 2016 and bears simple interest at a rate of 10% per annum

 

$59,000 lent to the Company by Bostonia Partners is due and payable September 22, 2016 and bears simple interest at a rate of 10% per annum.

 

$20,000 lent to the Company by Bostonia Partners is due and payable February 19, 2017 and bears simple interest at a rate of 10% per annum.

 

$30,000 lent to the Company by Bostonia Partners is due and payable February 24, 2017 and bears simple interest at a rate of 10% per annum.

 

$20,000 lent to the Company by Bostonia Partners is due and payable March 8, 2017 and bears simple interest at a rate of 10% per annum.

 

$3,000 lent to the Company by Blackbriar Partners is due and payable February 19, 2017 and bears simple interest at a rate of 10% per annum.

 

NOTE 5. CONVERTIBLE NOTES PAYABLE

 

On March 8, 2016 (“Issue date”) the Company issued a Convertible Note (“Note”) in the face amount of $100,000 for consideration consisting of $100,000 cash. The Note pays simple interest in the amount of 8% per annum . The maturity of the Note is three years from the issue date.

 

The Lender shall have the right from time to time to convert all or a part of the outstanding and unpaid principal amount of this Note into fully paid and non- assessable shares of Common Stock, as such Common Stock exists on the Issue Date, or any shares of capital stock or other securities of the Company into which such Common Stock shall hereafter be changed or reclassified pursuant to the following terms and conditions:

 

(a) For the period beginning on the Issue Date and ending 365 days subsequent to the Issue Date (“Year 1”) a 50% discount to the lowest Trading Price (as defined below) for the Common Stock during the ten (10) Trading Day (as defined below) period ending on the latest complete Trading Day prior to the Conversion Date or ten cents per share (whichever is greater).

 

  10  

 

 

 

(b) For the period beginning one day subsequent to the final day of Year One and ending 365 days subsequent to Year One (“Year 2”) a 35% discount to the lowest Trading Price (as defined below) for the Common Stock during the ten (10) Trading Day (as defined below) period ending on the latest complete Trading Day prior to the Conversion Date or ten cents per share (whichever is greater).

 

(c) For the period beginning one day subsequent to the final day of Year 2 and ending 365 days subsequent to Year 2 (“Year 3”) a 25% discount to the lowest Trading Price (as defined below) for the Common Stock during the ten (10) Trading Day (as defined below) period ending on the latest complete Trading Day prior to the Conversion Date or ten cents per share (whichever is greater).

 

(d) “Trading Price” means the closing bid price on the Over-the-Counter Bulletin Board, or applicable trading market (the “OTCQB”) as reported by a reliable reporting service (“Reporting Service”) designated by the Lender (i.e. Bloomberg) or, if the OTCQB is not the principal trading market for such security, the closing bid price of such security on the principal securities exchange or trading market where such security is listed or traded or, if no closing bid price of such security is available in any of the foregoing manners, the average of the closing bid prices of any market makers for such security that are listed in the “pink sheets” by the National Quotation Bureau, Inc. If the Trading Price cannot be calculated for such security on such date in the manner provided above, the Trading Price shall be the fair market value as mutually determined by the Company and the Lender. “Trading Day” shall mean any day on which the Common Stock is tradable for any period on the OTCQB, or on the principal securities exchange or other securities market on which the Common Stock is then being traded. “Trading Volume” shall mean the number of shares traded on such Trading Day as reported by such Reporting Service. The Conversion Price shall be equitably adjusted for stock splits, stock dividends, rights offerings, combinations, recapitalization, reclassifications, extraordinary distributions and similar events by the Company relating to the Lender’s securities.

 

The Company shall have the right, exercisable on not less than five (5) Trading Days prior written notice to the Lender, to prepay the outstanding Note in part or in full, including outstanding principal and accrued interest.

 

Upon closing of a Transaction Event the Lender shall receive 0 .10% ( one tenth of one percent)of the consideration actually received by the Company from an unaffiliated third party as a result of the closing of a Transaction Event.

 

“Transaction Event” shall mean either of:

 

(a) The sale by the Company of the Company’s proprietary NR2F6 intellectual property to an unaffiliated third party

 

(b) The granting of a license by the Company to an unaffiliated third party granting that unaffiliated third party the right to develop and/or commercialize the Company’s proprietary NR2F6 intellectual property

 

The issuance of the Note amounted in a beneficial conversion feature of $42,600 which is amortized under the Interest Method over the life of the Note. As of March 31, 2016 the unamortized discount on the convertible notes outstanding is $ 41,705. As of March 31, 2016 $100,000 of the principal amount of the Note remains outstanding.

 

The amount by which the Note’s as converted value exceeds the principal amount as of March 31, 2016 is $25,000.

 

NOTE 6. NOTES RECEIVABLE

 

    March 31, 2016
Entest Biomedical, Inc. (Note 8)   $ 12,051  
         
Notes Receivable   $ 12,051  

  

$12,051 lent by the Company to Entest Biomedical, Inc. is due and payable at the demand of the holder and bear simple interest at a rate of 10% per annum.

 

NOTE 7. INCOME TAXES

 

As of March 31, 2016

 

Deferred tax assets:        
Net operating tax carry forwards   $ 1,669,233  
Other     -0-  
Gross deferred tax assets     1,669,233  
Valuation allowance     (1,669,233)  
Net deferred tax assets   $ -0-  

 

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As of March 31, 2016 the Company has a Deferred Tax Asset of $1,669,081 completely attributable to net operating loss carry forwards of approximately $4,909,508 (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. As a result, the Company has recorded a valuation allowance reducing all deferred tax assets to 0.

 

Income tax is calculated at the 34% Federal Corporate Rate. 

 

NOTE 8. RELATED PARTY TRANSACTIONS

 

As of June 30, 2015 the Company has received capital contributions from Bio Matrix Scientific Group, Inc (“BMSN”) , a corporation under common control with the Company and which possesses the majority of the voting power of the shares outstanding of the company, totaling $728,658 and has issued 50,010,000 common shares to BMSN for aggregate consideration of $20,090.

 

The Company utilizes approximately 2,300 square feet of office space at 4700 Spring Street, Suite 304, La Mesa California, 91941 subleased to the Company by Entest BioMedical, Inc. on a month to month basis beginning October 1, 2014. The Chief Executive Officer of Entest Biomedical Inc. is David R. Koos who also serves as the Chief Executive Officer of the Company’s parent and the Company. The sublease is on a month to month basis and rent payable to Entest Biomedical, Inc. by Regen Biopharma Inc is equal to $5,000 per month.

 

As of March 31, 2016 Entest Biomedical Inc. is indebted to the Company in the amount of $12,051. $12,051 lent by the Company to Entest Biomedical, Inc. is due and payable at the demand of the holder and bear simple interest at a rate of 10% per annum.

 

As of September 30, 2015 the Company was indebted to BMSN in the amount of $19,701. $19,701 lent to the Company by Bio Matrix Scientific Group, Inc. was due and payable at the demand of the holder and bear simple interest at a rate of 10% per annum. During the quarter ended December 31, 2015 the Company repaid $19,701 of principal indebtedness due and payable to BMSN. David R. Koos, the Chairman and Chief Executive Officer of the Company, also serves as Chairman and Chief Executive Officer of BMSN. Primarily resulting from BMSN’s ownership of 30,000 shares of the Company’s Series AA Preferred Stock, BMSN possesses the majority of the shareholder voting power .

 

As of March 31, 2016 the Company is indebted to David R. Koos in the amount of $50. $50 lent to the Company by Koos is due and payable at the demand of the holder and bear simple interest at a rate of 10% per annum.

 

As of March 31, 2016 the Company is indebted to Blackbriar Partners in the amount of $3,000. $3,000 lent to the Company by Blackbriar Partners is due and payable February 29, 2017 and bears simple interest at a rate of 10% per annum. David R. Koos, the Chairman and Chief Executive Officer of the Company, also serves as the Chairman and CEO of Blackbriar Partners.

 

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

 

Pursuant to the Agreement, Zander shall pay to The Company 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 the first anniversary of the effective date of the Agreement and each subsequent anniversary.

 

The abovementioned payments may be made, at Zander’s discretion, in cash or newly issued common stock of Zander or in common stock of Entest BioMedical Inc. valued as of the lowest closing price on the principal exchange upon which said common stock trades publicly within the 14 trading days prior to issuance.

 

Pursuant to the Agreement, Zander shall pay to The Company 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 Quarter.

 

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

 

Zander is obligated pay to The Company 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).

 

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The Agreement may be terminated by The Company:

 

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

 

The Agreement may be terminated by Zander 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 The Company with regard to that License IP.

 

The Agreement may be terminated by Zander with regard to any of the License IP if a patent that has been granted by the United States patent and Trademark Office to The Company 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 September 28, 2015 Zander caused to be issued to the Company 8,000,000 of the common shares of Entest Biomedical, Inc in satisfaction of one hundred thousand US dollars ($100,000) to be paid to the Company by Zander as a license initiation fee. Regen Biopharma, Inc. recognized revenue of $192,000 equivalent to the fair value of 8,000,000 of the common shares of Entest Biomedical, Inc as of the date of issuance.

David R. Koos serves as sole officer and director of both Zander and Entest Biomedical, Inc. and also serves as Chairman and Chief Executive Officer of The Company.

 

NOTE 9. COMMITMENTS AND CONTINGENCIES

 

The Company utilizes approximately 2,300 square feet of office space at 4700 Spring Street, Suite 304, La Mesa California, 91941 subleased to the Company by Entest BioMedical, Inc. on a month to month basis beginning October 1, 2014. The Chief Executive Officer of Entest Biomedical Inc. is David R. Koos who also serves as the Chief Executive Officer of the Company’s parent and the Company. The sublease is on a month to month basis and rent payable to Entest Biomedical, Inc. by Regen Biopharma Inc is equal to $5,000 per month.

   

NOTE 10. STOCKHOLDERS’ EQUITY

 

The stockholders’ equity section of the Company contains the following classes of capital stock as March 31, 2016:

 

Common stock, $ 0.0001 par value; 500,000,000 shares authorized: 128,253,138 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).

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, 800,000,000 shares authorized of which 600,000 is designated as Series AA Preferred Stock: 30,000 shares issued and outstanding as of March 31, 2016 and 300,000,000 is designated Series A Preferred Stock of which 84,881,697 shares are outstanding as of March 31, 2016.

The abovementioned shares authorized pursuant to the Company’s certificate of incorporation may be issued from time to time without prior approval of the shareholders. The Board of Directors of the Company shall have the full authority permitted by law to establish one or more series and the number of shares constituting each such series and to fix by resolution full or limited, multiple or fractional, or no voting rights, and such designations, preferences, qualifications, restrictions, options, conversion rights and other special or relative rights of any series of the Stock that may be desired.

 

Series AA Preferred Stock

 

On September 15, 2014 the Company filed a CERTIFICATE OF DESIGNATION (“Certificate of Designations”) with the Nevada Secretary of State setting forth the preferences rights and limitations of a newly authorized series of preferred stock designated and known as “Series AA Preferred Stock” (hereinafter referred to as “Series AA Preferred Stock”).

 

The Board of Directors of the Company have authorized 600,000 shares of the Series AA Preferred Stock, par value $0.0001. 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 ten thousand (10,000). Except as otherwise required by law holders of Common Stock, other series of Preferred issued by the Corporation, and Series AA Preferred Stock shall vote as a single class on all matters submitted to the stockholders.

 

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Series A Preferred Stock

 

On January 15, 2015 the Company filed a CERTIFICATE OF DESIGNATION (“Certificate of Designations”) with the Nevada Secretary of State setting forth the preferences rights and limitations of a newly authorized series of preferred stock designated and known as “Series A Preferred Stock” (hereinafter referred to as “Series A Preferred Stock”).

The Board of Directors of the Company have authorized 300,000,000 shares of the Series A Preferred Stock, par value $0.0001. With respect to each matter submitted to a vote of stockholders of the Corporation, each holder of Series A Preferred Stock shall be entitled to cast that number of votes which is equivalent to the number of shares of Series A Preferred Stock owned by such holder times one . Except as otherwise required by law holders of Common Stock, other series of Preferred issued by the Corporation, and Series A Preferred Stock shall vote as a single class on all matters submitted to the stockholders.

Holders of the Series A Preferred Stock will be entitled to receive, when, as and if declared by the board of directors of the Company (the “Board”) out of funds legally available therefore, non-cumulative cash dividends of $0.01 per quarter. In the event any dividends are declared or paid or any other distribution is made on or with respect to the Common Stock , the holders of Series A Preferred Stock as of the record date established by the Board for such dividend or distribution on the Common Stock shall be entitled to receive, as additional dividends (the “Additional Dividends”) an amount (whether in the form of cash, securities or other property) equal to the amount (and in the form) of the dividends or distribution that such holder would have received had each share of the Series A Preferred Stock been one share of the Common Stock, such Additional Dividends to be payable on the same payment date as the payment date for the Common Stock.

Upon any liquidation, dissolution, or winding up of the Company, whether voluntary or involuntary (collectively, a “Liquidation”), before any distribution or payment shall be made to any of the holders of Common Stock or any other series of preferred stock, the holders of Series A Preferred Stock shall be entitled to receive out of the assets of the Company, whether such assets are capital, surplus or earnings, an amount equal to $0.01 per share of Series A Preferred (the “Liquidation Amount”) plus all declared and unpaid dividends thereon, for each share of Series A Preferred held by them.

If, upon any Liquidation, the assets of the Company shall be insufficient to pay the Liquidation Amount, together with declared and unpaid dividends thereon, in full to all holders of Series A Preferred, then the entire net assets of the Company shall be distributed among the holders of the Series A Preferred, ratably in proportion to the full amounts to which they would otherwise be respectively entitled and such distributions may be made in cash or in property taken at its fair value (as determined in good faith by the Board), or both, at the election of the Board.

11. INVESTMENT SECURITIES

On September 28, 2015 Zander Theraputics, Inc. caused to be issued to Regen Biopharma, Inc. 8,000,000 of the common shares of Entest Biomedical, Inc in satisfaction of one hundred thousand US dollars ($100,000) to be paid to Regen Biopharma, Inc. by Zander Theraputics, Inc as a license initiation fee.

The common shares of Entest Biomedical, Inc described above constitute the Company’s sole investment securities as of March 31, 2016.

  8,000,000     Common Shares of Entest Biomedical, Inc.          
                             
  Basis       Fair Value       Total Unrealized Losses in Other Comprehensive Income       Net Unrealized Gain or (Loss) realized during the quarter  ended March  31, 2016  
$ 192,000     $ 56,800       (135,200 )     (63,200 )

 

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NOTE 12. STOCK TRANSACTIONS

 

Common Stock

 

On January 28, 2016 the Company issued 2,000,000 of its Common Shares for cash consideration of $100,000.

 

On January 29, 2016 the Company issued 30,000 of its Common Shares for cash consideration of $750.

 

On February 2, 2016 the Company issued 270,000 of its Common Shares for cash consideration of $6,750.

 

On February 22, 2016 the Company issued 666,666 of its Common Shares for cash consideration of $33,333.

 

On February 22, 2016 the Company issued 1,000,000 of its Common Shares for cash consideration of $12,500.

 

Series A Preferred Stock

 

On January 28, 2016 the Company issued 1,000,000 shares of its Series A Preferred stock for cash consideration of $50,000.

 

On January 29, 2016 the Company issued 300,000 shares of its Series A Preferred stock for cash consideration of $7,500.

 

On February 22, 2016 the Company issued 333,333 shares of its Series A Preferred stock for cash consideration of $16,666.

 

On March 22, 2016 the Company issued 3,000,000 shares of its Series A Preferred stock for cash consideration of $37,500.

 

NOTE 13. RESTATEMENT OF PREVIOUSLY ISSUED FINANCIAL STATEMENTS

 

Subsequent to the original issuance of Regen’s quarterly financial statements for the period ended March 31, 2016 the Company determined that the recognition of $ 364,822 of expenses recognized during the period resulting from the issuance for less than fair value of equity securities should not have been recognized.

 

  15  

 

 

 

The following tables reflect the corrections:

 

REGEN BIOPHARMA,INC.            
BALANCE SHEET            
               
    As of   Adjustments   As of  
    March 31, 2016       March 31, 2016  
    (unaudited)       Restated  
ASSETS              
CURRENT ASSETS                          
Cash     106,024               106,024    
Note Receivable     12,051               12,051    
Prepaid Expenses     1,000               1,000    
Accrued Interest Receivable     1,978               1,978    
Due from Former Employees     15,000               15,000    
     Total Current Assets     136,053               136,053    
                           
OTHER ASSETS                          
Available for Sale Securities     56,800               56,800    
Total Other Assets     56,800               56,800    
                           
TOTAL ASSETS     192,853               192,853    
                           
LIABILITIES AND STOCKHOLDERS' EQUITY                          
Current Liabilities:                          
Bank Overdraft     0               0    
Accounts payable     21,283               21,283    
Notes Payable     228,050               228,050    
Accrued payroll taxes     1,946               1,946    
Accrued Interest     31,184               31,184    
Accrued Rent     15,000               15,000    
Accrued Payroll     92,996               92,996    
Due to Shareholder     0               0    
Total Current Liabilities     390,459               390,459    
Long Term Liabilities                          
Convertible Notes Payable     58,295               58,295    
Total Long Term Liabilities     58,295               58,295    
Total Liabilities     448,754               448,754    
                           
STOCKHOLDERS' EQUITY (DEFICIT)                          
Common Stock ($.0001 par value) 500,000,000 shares authorized; 114,753,938 issued and outstanding as of September 30, 2015 and 128,253,138 shares issued and outstanding March  31, 2016     12,824               12,824    
Preferred Stock, 0.0001 par value, 800,000,000 authorized and 100,000,000 authorized as of December 31,  2015 and September 30, 2015 respectively                          
Series A Preferred 90,000,000 Authorized and 300,000,000 authorized, 60,981,697 and 84,881,697 outstanding as of  September  30, 2105 and March 31, 2016 respectively     8,488               8,488    
Series AA Preferred $0.0001 par value 600,000 authorized and 30,000 outstanding as of September  30, 2015 and March  31, 2016     3               3    
Additional Paid in capital     14,551,402       (10,512,568 )     4,038,835    
Contributed Capital     728,658               728,658    
Retained Earnings (Deficit) accumulated during the development stage     (15,422,076 )     10,512,568       (4,909,508 )  
Accumulated Other Comprehensive Income     (135,200 )             (135,200 )  
Total Stockholders' Equity (Deficit)     (255,901 )             (255,900 )  
                           
TOTAL LIABILITIES & STOCKHOLDERS' EQUITY (DEFICIT)     192,853               192,853    

 

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REGEN BIOPHARMA , INC.            
STATEMENT OF OPERATIONS            
(unaudited)            
               
      Quarter Ended March 31, 2016       Adjustments       Quarter Ended March 31, 2016 (restated)    
REVENUES     0               0    
                           
COST AND EXPENSES                          
Research and Development     172,596               172,596    
General and Administrative     435,236               435,236    
Consulting and Professional Fees     97,547               97,547    
Rent     15,000               15,000    
Total Costs and Expenses     720,379               720,379    
                           
OPERATING LOSS     (720,379 )             (720,379 )  
                           
OTHER INCOME & (EXPENSES)                          
Interest Income     297               297    
Refunds of amounts previously paid                          
Interest Expense     (5,089 )             (5,089 )  
Interest Expense attributable to                          
Amortization of Discount     (894 )             (894 )  
Loss on issuance of common shares for                          
less than fair value     (364,822 )     364,822       0    
Preferred shares issued pursuant to                          
contractual obligations                          
TOTAL OTHER INCOME (EXPENSE)     (370,508 )             (5,686 )  
                           
NET INCOME (LOSS)     (1,090,886 )             (726,064 )  
BASIC AND FULLY DILUTED EARNINGS (LOSS) PER SHARE     (0.0087 )             (0.0058 )  
WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING     124,875,119               124,875,119    

 

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REGEN BIOPHARMA , INC.            
STATEMENT OF OPERATIONS            
(unaudited)            
               
      Six Months Ended March 31, 2016       adjustments       Six Months Ended March 31, 2016 (restated)    
REVENUES     0               0    
                           
COST AND EXPENSES                          
Research and Development     277,919               277,919    
General and Administrative     923,831               923,831    
Consulting and Professional Fees     178,080               178,080    
Rent     30,000               30,000    
Total Costs and Expenses     1,409,830               1,409,830    
                           
OPERATING LOSS     (1,409,830 )             (1,409,830 )  
                           
OTHER INCOME & (EXPENSES)                          
Interest Income     597               597    
Refunds of amounts previously paid                          
Interest Expense     (10,090 )             (10,090 )  
Interest Expense attributable to                          
Amortization of Discount     (894 )             (894 )  
Loss on issuance of common shares for                          
less than fair value     (1,528,135 )     1,528,135       0    
Preferred shares issued pursuant to                          
contractual obligations                          
TOTAL OTHER INCOME (EXPENSE)     (1,538,522 )             (10,387 )  
                           
NET INCOME (LOSS)     (2,948,352 )             (1,420,217 )  
BASIC AND FULLY DILUTED EARNINGS (LOSS) PER SHARE     (0.0188 )             (0.0091 )  
WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING     156,418,573               156,418,573    

 

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STATEMENT OF COMPREHENSIVE INCOME            
(unaudited)            
    Quarter  Ended March  31
    2016   Adjustments  

2016

(restated)

Net Income (Loss)     (1,090,886 )     364,822       (726,064 )
Add:                        
     Unrealized Gains on Securities     —                 —    
Less:                        
     Unrealized Losses on Securities     (63,200 )             (63,200 )
     Total Other Comprehensive Income (Loss)     (63,200 )             (63,200 )
Comprehensive Income     (1,154,086 )             (789,264 )
                         
                         
       Six Months  Ended March  31   
      2016       Adjustments       2016 (restated)  
Net Income (Loss)     (2,948,352 )     1,528,135       (1,420,217 )
Add:                        
     Unrealized Gains on Securities     —                 —    
Less:                        
     Unrealized Losses on Securities     (101,600 )             (101,600 )
     Total Other Comprehensive Income (Loss)     (101,600 )             (101,600 )
Comprehensive Income     (3,049,952 )             (1,521,817 )

 

 

  19  

 

 

 

REGEN BIOPHARMA , INC.            
STATEMENT OF CASH FLOWS            
(unaudited)            
               
    Six Months Ended   adjustments   Six Months Ended  
    March 31 2016       March 31 2016  
CASH FLOWS FROM OPERATING ACTIVITIES                          
                           
Net Income (loss)     (2,948,352 )   $ 1,528,135       (1,420,217 )  
Adjustments to reconcile net Income to net cash                          
                           
Preferred Stock Issued for Expenses                          
Preferred Stock issued for Interest                          
Preferred Stock issued pursuant to contractual obligations                          
Common Stock issued to Consultants                          
Preferred Stock issued to Consultants     40               40    
Increase (Decrease) in Interest expense attributable to amortization of Discount     894               894    
Changes in operating assets and liabilities:                          
Increase (Decrease) in Accounts Payable     (4,571 )             (4,571 )  
(Increase) Decrease in Notes Receivable                          
(Increase) Decrease in Interest  Receivable     (597 )             (597 )  
Increase ( Decrease) in Bank Overdraft                          
Increase (Decrease) in accrued Expenses     72,093               72,093    
(Increase) Decrease in Prepaid Expenses     9,000               9,000    
(Increase)Decrease in Due from Former Employee     (15,000 )             (15,000 )  
Increase in issuance of stock below fair value     1,528,135     $ (1,528,135 )     0    
Increase in Additional Paid in Capital     495,462               495,462    
Net Cash Provided by (Used in) Operating     (862,896 )             (862,896 )  
                           
CASH FLOWS FROM FINANCING ACTIVITIES                          
Common Stock issued for Cash     475,000               475,000    
Preferred Stock issued for Cash     350,001               350,001    
Increase in Contributed Capital                          
Increase ( Decrease)  in Notes Payable     5,299               5,299    
Increase in Convertible Notes payable     100,000               100,000    
Increase in Due to Shareholder     0               0    
Net Cash Provided by (Used in) Financing     930,300               930,300    
                           
Net Increase (Decrease) in Cash     67,404               67,404    
                           
Cash at Beginning of Period     38,620               38,620    
                           
Cash at End of Period     106,024               106,024    
                           
Supplemental Disclosure of Noncash investing and financing activities:                          
Common shares Issued for Debt                          
Preferred Shares Issued for Debt                          
                           
The Accompanying Notes are an Integral Part of These Financial Statements   

 

  20  

 

 

 

NOTE 13: SUBSEQUENT EVENTS

 

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 10,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) to David Koos, Regen’s Chief Executive Officer, as consideration for efforts expended by Koos with regards to addressing all clinical hold issues identified by the United States Food and Drug Administration (FDA) related to Regen’s Investigational New Drug Application for HemaXellerate..

 

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 10,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) to Harry Lander , Regen’s President and Chief Scientific Officer, as consideration for efforts expended by Lander with regards to addressing all clinical hold issues identified by the United States Food and Drug Administration (FDA) related to Regen’s Investigational New Drug Application for HemaXellerate.

 

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 10,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) to Todd Caven , Regen’s Chief Financial Officer, as consideration for efforts expended by Caven with regards to addressing all clinical hold issues identified by the United States Food and Drug Administration (FDA) related to Regen’s Investigational New Drug Application for HemaXellerate.

 

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 1,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) in settlement of $10,000 of principal indebtedness.

 

  21  

 

 

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. All references to” We”, “Us”, “Company” or the “Company” refer to Regen BioPharma, Inc.

 

Material Changes in Financial Condition

 

As of March 31 2016, we had Cash of $ 106,024 and as of September 30, 2015 we had Cash of $38,620.

 

The increase in Cash of 174 % is primarily attributable to:

The sale of $825,000 of equity securities by the Company

The sale of $100,000 of Convertible Debentures by the Company

Borrowings of $73,000 by the Company

Offset by:

Payment by the Company of $19,701 of principal indebtedness owed by the Company to Bio Matrix Scientific Group, Inc. ( an entity under common control with the Company)

Payment by the Company of $48,000 of principal indebtedness owed by the Company to an unaffiliated third party lender.

Cash expended in the operation of the Company’s business.

As of March 31, 2016 we had Prepaid Expenses of $ 1,000 and as of September 30, 2015 we had Prepaid Expenses of $10,000

 

The decrease in Prepaid Expenses of 90% is attributable to:

 

$10,000 of salary prepaid to the Company’s former Chief Scientific Officer having been reclassified during the quarter ended December 31, 2015 as amounts Due from Former Employee as a result of the resignation of the Company’s former Chief Scientific Officer during the quarter ended December 31, 2015

 

 

  22  

 

 

  

Offset by:

 

$1,000 in salary having been prepaid to an employee during the quarter ended December 31, 2015

 

As of March 31, 2016 we had Amounts Due from Former Employee of $15,000 and as of September 30, 2015 we had Amounts Due from Former Employee of $0.

 

The increase in Amounts Due from Former Employee is attributable to:

 

$10,000 of salary prepaid to the Company’s former Chief Scientific Officer having been reclassified during the quarter ended December 31, 2015 as amounts Due from Former Employee as a result of the resignation of the Company’s former Chief Scientific Officer during the quarter ended December 31, 2015.

 

$5,000 overpayment of salary due to the Company’s former Chief Scientific Officer during the quarter ended December 31, 2015.

As of March 31, 2016 we had Accrued Interest Receivable of $1,978 and as of September 30, 2015 we had Accrued Interest Receivable of $1,381

 

The increase in of Accrued Interest Receivable of approximately 43.2% is attributable to interest accrued but unpaid during the six months ended March 31 , 2016 resulting from amounts due to the Company by Entest Bio-Medical, Inc. David R. Koos serves as Chairman of the Board and Chief Executive Officer of both the Company and Entest Bio-Medical, Inc.

 

As of March 31, 2016 we had Available for Sale Securities of $56,800 and as of September 30, 2015 we had Available for Sale Securities of $158,400

The decrease in Available for Sale Securities of 64.14 % is attributable to unrealized losses recognized on 8,000,000 common shares of Entest Biomedical, Inc. owned by the Company.

As of March 31, 2016 we had Accounts Payable of $21,283 and as of September 30, 2015 we had Accounts payable of $25,854.

The decrease in Accounts Payable of approximately 17.7% is attributable to decreases in outstanding obligations of the Company incurred in the course of business.

As of March 31,2016 we had Convertible Notes Payable of $100,000 and as of September 30, 2015 we had Notes Payable of $0.

The increase in Convertible Notes Payable is attributable to the issuance by the Company of a convertible note in the face amount of $100,000 during the quarter ended March 31, 2016.

As of March 31, 2016, we had Accrued Payroll of $92,996 and as of September 30, 2015 we had Accrued Payroll of $36,001

The increase in Accrued Payroll of approximately 158% is attributable to :

$28,495 in salary expense due to the Company’s President incurred but unpaid during the six months ended March 31, 2016

$15,000 in salary expense due to the Company’s Chief Executive Officer incurred but unpaid during the six months ended March 31, 2016

$13,500 in salary expense due to the Company’s Chief Financial Officer incurred but unpaid during the six months ended March 31, 2016

As of March 31, 2016 we had Accrued Interest of $31,184 and as of September 30, 2015 we had Accrued Interest of $21,093.

The increase in Accrued Interest of approximately 47.8% is attributable to interest expense on Notes Payable and Convertible Notes Payable incurred during the six months ended March 31, 2016 but not yet paid.

As of March 31, 2016 we had Accrued Rent of $15,000 and as of September 30, 2015 we had Accrued Rent of $10,000.

The increase in Accrued Rent of 50% is attributable to:

Rental Expense accrued but unpaid for the months of January 2016, February 2016, and March 2016.

 

  23  

 

  

Material Changes in Results of Operations

Revenues from operations were $0 for the and -0- for the three months ended March 31 , 2015. Net Losses were $726,064 for the three months ended March 31, 2016 and $633,470 for the same period ended 2015. 

The increase in Net Losses of approximately 14.6% is primarily attributable to the recognition during the three months ended March 31, 2016 of higher Research and Development expenses, General and Administrative expenses ,and expense attributable to amortization of discount of beneficial conversion feature recognized on convertible securities when compared to the same period ended 2015 offset by lower consulting and interest expenses incurred during the three months ended March 31, 2016 when compared to the same period ended 2015.

 

Revenues from operations were $0 for the six months ended March 31, 2015 and -0- for the six months ended March 31 , 2016. Net Losses were $ 852,661 for the six months ended March 31, 2015 and $ 1,420,217 for the same period ended 2016.

The increase in Net Losses of approximately 66.5 is primarily attributable to the recognition during the six months ended March 31, 2016 of higher Research and Development expenses, General and Administrative expenses ,and expense attributable to amortization of discount of beneficial conversion feature recognized on convertible securities when compared to the same period ended 2015 offset by lower consulting and interest expenses incurred during the six months ended March 31, 2016 when compared to the same period ended 2015.

 

Liquidity and Capital Resources

 

As of March 31, 2016 we had $106,024in cash and current liabilities of $448,754 such liabilities consisting of Accounts Payable, Notes 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.

 

The Company plans to meet cash needs through applying for governmental and non-governmental grants as well as selling its 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. Management can give no assurance that any governmental or non-governmental grant will be obtained by the Company despite the Company’s best efforts. As of February 19, 2014 The Company has identified the National Heart Lung and Blood Institute Clinical Trial Pilot Studies (R34) grant which provides up to $450,000 in funding over a period of three years as well as the Omnibus Solicitation of the NIH for Small Business Technology Transfer Grant Applications administered by the Small Business Innovation Research (SBIR) program of the National Institute of Health as grants for which the Company intends to apply.

 

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 six months ended March 31, 2016 the Company raised $825,001 through the issuance of equity securities for cash and $100,000 through the issuance of convertible debentures.

 

As of March 31, 2016 the Company was not party to any binding agreements which would commit Regen 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.

 

  24  

 

 

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 not effective at this reasonable assurance level as of the period covered solely because of the material weakness in our internal control over financial reporting described below.

 

The Company’s internal control over financial reporting is a process designed under the supervision of the Company’s management to provide reasonable assurance regarding the reliability of financial reporting and the preparation of the Company’s financial statements for external purposes in accordance with U.S. generally accepted accounting principles.

In designing and evaluating our disclosure controls and procedures, our management recognized that disclosure controls and procedures, no matter how well conceived and operated, can provide only a reasonable, not absolute, assurance that the objectives of the disclosure controls and procedures are met.

The Company’s management assessed the effectiveness of its internal control over financial reporting as of March 31, 2016 based on the framework in 2013 Committee of Sponsoring Organizations of the Treadway Commission, or COSO, framework. Based on its assessment, management believes that, as of March 31, 2016, the Company’s internal control over financial reporting is not effective.

Management identified a material weakness in internal control over financial reporting as of March 31, 2016. 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 Company’s annual or interim financial statements will not be prevented or detected on a timely basis.

We did not design and maintain effective internal control over the accounting for issuances of equity securities of the Company for cash consideration and issuances of equity securities of the Company for conversion of convertible securities. This control deficiency resulted in the improper recognition of $364,822 of expenses recognized during the quarter ended March 31, 2016 resulting from the issuance for less than fair value of equity securities which not have been recognized ( See Note 13 of Notes to Financial Statements.)

Remediation

Plan for Material Weakness in Internal Control over Financial Reporting

The Company’s management has begun to design and implement certain remediation measures to address the above-described material weakness and enhance the Company’s internal control over financial reporting. We will take the following actions to improve the design and operating effectiveness of our internal control in order to remediate this material weakness:

Institute an additional review of any and all issuances of capital stock to ensure the event is recognized in accordance with United States GAAP.

Management's report was not subject to attestation by the Company's registered public accounting firm pursuant to temporary rules of the Securities and Exchange Commission that permit the company to provide only management's report in this annual report. This exemption for smaller reporting companies provided under the temporary rules referenced above has been made permanent under Section 989G of the Dodd-Frank Wall Street Reform and Consumer Protection Act.

 

Changes in Internal Controls over Financial Reporting

 

In connection with the evaluation of the Company's internal controls during the period commencing on January 1, 2016 and ending on March 31, 2016, David Koos and Todd S. Caven , who serve as the Company's Principal Executive Officer and Principal Financial Officer respectively, have determined that, other than as described above, 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.

 

  25  

 

  

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

 

Common Stock

 

On January 28, 2016 the Company issued 2,000,000 of its Common Shares (“Shares”) for cash consideration of $100,000.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes.

 

On January 29, 2016 the Company issued 30,000 of its Common Shares (“Shares”) for cash consideration of $750.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

 

On February 2, 2016 the Company issued 270,000 of its Common Shares(“Shares”) for cash consideration of $6,750.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

On February22, 2016 the Company issued 666,666 of its Common Shares (“Shares”) for cash consideration of $33,333.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes.

 

On February22, 2016 the Company issued 1,000,000 of its Common Shares (“Shares”) for cash consideration of $12,500.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

 

  26  

 

 

  

Series A Preferred Stock

 

On January 28, 2016 the Company issued 1,000,000 shares of its Series A Preferred stock (“Shares”) for cash consideration of $50,000.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

 

On January 29, 2016 the Company issued 300,000 shares of its Series A Preferred stock (“Shares”) for cash consideration of $7,500.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

 

On February 22, 2016 the Company issued 333,333 shares of its Series A Preferred stock (“Shares”) for cash consideration of $16,666.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

 

On March 22, 2016 the Company issued 3,000,000 shares of its Series A Preferred stock (“Shares”) for cash consideration of $37,500.

 

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the Shares stating that the Shares have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of the Shares. Cash proceeds received from sale will be utilized by Regen for general corporate purposes

 

 

  27  

 

  

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 10,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) to David Koos, Regen’s Chief Executive Officer, as consideration for efforts expended by Koos with regards to addressing all clinical hold issues identified by the United States Food and Drug Administration (FDA) related to Regen’s Investigational New Drug Application for HemaXellerate..

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The Shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the Shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the securities comprising the Shares stating that those securities have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of those securities. 

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 10,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) to Harry Lander , Regen’s President and Chief Scientific Officer, as consideration for efforts expended by Lander with regards to addressing all clinical hold issues identified by the United States Food and Drug Administration (FDA) related to Regen’s Investigational New Drug Application for HemaXellerate.

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The Shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the Shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the securities comprising the Shares stating that those securities have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of those securities.

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 10,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) to Todd Caven , Regen’s Chief Financial Officer, as consideration for efforts expended by Caven with regards to addressing all clinical hold issues identified by the United States Food and Drug Administration (FDA) related to Regen’s Investigational New Drug Application for HemaXellerate.

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The Shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the Shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the securities comprising the Shares stating that those securities have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of those securities.

On April 7, 2016 Regen Biopharma, Inc. (“Regen”) issued 1,000,000 shares of Regen’s Series A Preferred Stock (“Shares”) in settlement of $10,000 of principal indebtedness.

The Shares were issued pursuant to Section 4(a) (2) of the Securities Act of 1933, as amended (the “Act”). No underwriters were retained to serve as placement agents for the sale. The Shares were sold directly through our management. No commission or other consideration was paid in connection with the sale of the Shares. There was no advertisement or general solicitation made in connection with this Offer and Sale of Shares. A legend was placed on the certificate that evidences the securities comprising the Shares stating that those securities have not been registered under the Act and setting forth or referring to the restrictions on transferability and sale of those securities

 

Item 3. DEFAULTS UPON SENIOR SECURITIES

 

None.

  

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

 

None.

 

Item 5. OTHER INFORMATION

 

None 

 

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Item 6. EXHIBITS

31.1 Certification of Chief Executive Officer
31.2 Certification of Acting Chief Financial Officer
32.1 Certification of Chief Executive Officer under Section 906 of the Sarbanes-Oxley Act of 2002.
32.2 Certification of Acting Chief Financial Officer under Section 906 of the Sarbanes-Oxley Act of 2002.
10.1 Form of Convertible Note*
10.2 David Koos  Agreement (a)
10.3 Harry Lander Agreement (b)
10.4

Todd Caven Agreement (c)

* filed as exhibit 10.1 with the Company’s form 10-Q for the period March 31, 2016

(a) Incorporated by reference to Exhibit 10.1 of that 8-K dated April 7, 2016
(b) Incorporated by reference to Exhibit 10.2 of that 8-K dated April 7, 2016
(c) Incorporated by reference to Exhibit 10.3 of that 8-K dated April 7, 2016

 

  29  

 

  

SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

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 .

      Regen Biopharma, Inc.
       
  By:   /s/ David R. Koos
  Name:   David R. Koos
  Title:   Principal Executive Officer
  Date:   04/28/2017

 

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 .

      Regen Biopharma, Inc.
       
  By:   /s/ David R. Koos
  Name:   David R. Koos
  Title:   Chairman,  Director
  Date:   04/28/2017

 

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 .

      Regen Biopharma, Inc.
       
  By:   /s/ Todd S. Caven
  Name:   Todd S. Caven
  Title:   Principal Financial Officer
  Date:   04/28/2017

   

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