UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549 

 


 

FORM 10-Q

 


 

(Mark One)

 

 

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

 

For the quarterly period ended June 30, 2021

 

 

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

 

For the transition period from                            to                          

 

Commission file number: 001-38659

 

BIOSIG TECHNOLOGIES, INC.

(Exact name of registrant as specified in its charter)

     

Delaware

 

26-4333375

(State or other jurisdiction of incorporation

or organization)

 

(IRS Employer Identification No.)

     

54 Wilton Road, 2nd Floor

Westport, CT

 

06880

(Address of principal executive office)

 

(Zip Code)

     

(203) 409-5444

(Registrant’s telephone number, including area code)

 

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading Symbol(s)

Name of each exchange on which registered

Common Stock, par value $0.001 per share

BSGM

The NASDAQ Capital Market  

 

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.  Yes ☒   No ☐

 

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§ 229.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).  Yes ☒   No ☐

 

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

 

Large accelerated filer

 

Accelerated filer

Non-accelerated filer

 

Smaller reporting company

Emerging growth company

     

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).  Yes ☐   No ☒

 

As of August 11, 2021, there were 34,923,860 shares of registrant’s common stock outstanding. 

 

 

 

 

TABLE OF CONTENTS

 

PART I.          FINANCIAL INFORMATION

   
         
 

ITEM 1.

Financial Statements

   
         
   

Condensed consolidated balance sheets as of June 30, 2021 (unaudited) and December 31, 2020

 

3

         
   

Condensed consolidated statements of operations for the three and six months ended June 30, 2021 and 2020 (unaudited)

 

4

         
   

Condensed consolidated statement of changes in equity for the three and six months ended June 30, 2021 (unaudited)

 

5

         
   

Condensed consolidated statement of changes in equity for the three and six months ended June 30, 2020 (unaudited)

 

6

         
   

Condensed consolidated statements of cash flows for the six months ended June 30, 2021 and 2020 (unaudited)

 

7

         
   

Notes to condensed consolidated financial statements (unaudited)

 

8-32

         
 

ITEM 2.

Management’s Discussion and Analysis of Financial Condition and Results of Operations

 

33-41

 

ITEM 3.

Quantitative and Qualitative Disclosures about Market Risk

 

42

 

ITEM 4.

Controls and Procedures

 

42

         

PART II.          OTHER INFORMATION

   
         
 

ITEM 1.

Legal Proceedings

 

43

 

ITEM 1A.

Risk Factors

 

43

 

ITEM 2.

Unregistered Sales of Equity Securities and Use of Proceeds

 

43

 

ITEM 3.

Defaults Upon Senior Securities

 

43

 

ITEM 4.

Mine Safety Disclosures

 

43

 

ITEM 5.

Other Information

 

43

 

ITEM 6.

Exhibits

 

43

         
 

SIGNATURES

 

45

 

 

 

 

PART I FINANCIAL INFORMATION

 

ITEM 1. FINANCIAL STATEMENTS

 

BIOSIG TECHNOLOGIES, INC.

 

CONDENSED CONSOLIDATED BALANCE SHEETS

 

(In Thousands, Except Par Value and Share Amounts)

 

 

                 
   

June 30,

   

December 31,

 
   

2021

   

2020

 
   

(unaudited)

         

ASSETS

               

Current assets:

               

Cash

  $ 15,504     $ 28,268  

Accounts receivable, net

    199       -  

Inventory

    731       768  

Prepaid expenses and vendor deposits

    515       301  

  Total current assets

    16,949       29,337  
                 

Property and equipment, net

    388       289  
                 

Right-to-use assets, net

    252       306  
                 

Other assets:

               

Patents, net

    336       346  

Trademarks

    1       1  

Prepaid expenses, long term

    -       5  

Deposits

    101       102  
                 

  Total assets

  $ 18,027     $ 30,386  
                 

LIABILITIES AND EQUITY

               

Current liabilities:

               

Accounts payable and accrued expenses, including $80 and $317 to related parties as of June 30, 2021 and December 31, 2020, respectively

  $ 3,027     $ 4,722  

Deferred revenue, short term

    32       -  

Dividends payable

    77       73  

Lease liability, short term

    247       313  

  Total current liabilities

    3,383       5,108  
                 

Deferred revenue, long term

    21       -  

Lease liability, long term

    1       1  

  Total long term debt

    22       1  
                 

Total liabilities

    3,405       5,109  
                 

Commitments and contingencies (Note 11)

               
                 

Series C 9% Convertible Preferred Stock, $0.001 par value, $1,000 stated value, authorized 4,200 shares, 105 shares issued and outstanding; liquidation preference of $105 as of June 30, 2021 and December 31, 2020

    105       105  
                 

Equity:

               

Preferred stock, $0.001 par value, authorized 1,000,000 shares, designated 200 shares of Series A, 600 shares of Series B, 4,200 shares of Series C, 1,400 shares of Series D, 1,000 shares of Series E, 200,000 shares of Series F Preferred Stock, none issued of Series F Preferred Stock

    -       -  

Common stock, $0.001 par value, authorized 200,000,000 shares, 32,205,479 and 30,764,792 issued and outstanding as of June 30, 2021 and December 31, 2020, respectively

    32       31  

Additional paid in capital

    187,136       181,344  

Accumulated deficit

    (173,025 )     (157,005 )

Total stockholders' equity attributable to BioSig Technologies, Inc.

    14,143       24,370  

Non-controlling interest

    374       802  

  Total equity

    14,517       25,172  
                 

Total liabilities and equity

  $ 18,027     $ 30,386  

 

See the accompanying notes to the unaudited condensed consolidated financial statements

 

3

 

BIOSIG TECHNOLOGIES, INC.

 

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

 

(In Thousands, Except Par Value and Share Amounts)

 

(unaudited)

 
                                 
   

Three months ended June 30,

    Six months ended June 30,  
   

2021

   

2020

   

2021

   

2020

 

Revenue:

                               

Product sales

  $ 199     $ -     $ 314     $ -  

Service

    8       -       11       -  

  Total Revenue

    207       -       325       -  
                                 

Cost of goods sold

    62       -       161       -  
                                 

Gross profit

    145       -       164       -  
                                 

Operating expenses:

                               

Research and development

    1,667       5,718       2,933       10,645  

General and administrative

    6,480       16,608       13,751       24,464  

Depreciation and amortization

    49       22       91       43  

  Total operating expenses

    8,196       22,348       16,775       35,152  
                                 

Loss from operations

    (8,051 )     (22,348 )     (16,611 )     (35,152 )
                                 

Other income (expense):

                               

Interest income, net

    -       3       1       43  

Loss on foreign currency translation

    -       (1 )     -       (1 )
                                 

Loss before income taxes

    (8,051 )     (22,346 )     (16,610 )     (35,110 )
                                 

Income taxes (benefit)

    -       -       -       -  
                                 

Net loss

    (8,051 )     (22,346 )     (16,610 )     (35,110 )
                                 

Non-controlling interest

    350       3,158       590       4,586  
                                 

Net loss attributable to BioSig Technologies, Inc.

    (7,701 )     (19,188 )     (16,020 )     (30,524 )
                                 

Preferred stock dividend

    (3 )     (5 )     (5 )     (9 )
                                 

NET LOSS ATTRIBUTABLE TO COMMON SHAREHOLDERS

  $ (7,704 )   $ (19,193 )   $ (16,025 )   $ (30,533 )
                                 

Net loss per common share, basic and diluted

  $ (0.24 )   $ (0.72 )   $ (0.50 )   $ (1.20 )
                                 

Weighted average number of common shares outstanding, basic and diluted

    32,169,191       26,537,058       31,878,283       25,463,154  

 

See the accompanying notes to the unaudited condensed consolidated financial statements

 

4

 

BIOSIG TECHNOLOGIES, INC.

 

 CONDENSED CONSOLIDATED STATEMENT OF CHANGES IN EQUITY

 

THREE AND SIX MONTHS ENDED JUNE 30, 2021

 

(In Thousands, Except Par Value and Share Amounts)

 

 

                   

Additional

            Non-          
   

Common stock

   

Paid in

   

Accumulated

   

controlling

         
   

Shares

   

Amount

   

Capital

   

Deficit

   

Interest

   

Total

 

Balance, December 31, 2020

    30,764,792     $ 31     $ 181,344     $ (157,005 )   $ 802     $ 25,172  

Common stock issued for services

    406,692       -       1,777       -       -       1,777  

Common stock issued upon exercise of options at $2.96 per share

    9,375       -       28       -       -       28  

Sale of common stock under At-the-market offering, net of transaction expenses of $40

    251,720       -       1,300       -       -       1,300  

Stock based compensation

    682,202       1       721       -       20       742  

Preferred stock dividend

    -       -       (2 )     -       -       (2 )

Net loss

    -       -       -       (8,319 )     (240 )     (8,559 )

Balance, March 31, 2021 (unaudited)

    32,114,781       32       185,168       (165,324 )     582       20,458  

Common stock for services

    36,948       -       140       -       -       140  

Change in fair value of modified options

    -       -       313       -       8       321  

Stock based compensation

    53,750       -       1,518       -       134       1,652  

Preferred stock dividend

    -       -       (3 )     -       -       (3 )

Net loss

    -       -       -       (7,701 )     (350 )     (8,051 )

Balance, June 30, 2021 (unaudited)

    32,205,479     $ 32     $ 187,136     $ (173,025 )   $ 374     $ 14,517  

 

See the accompanying notes to the unaudited condensed consolidated financial statements

 

5

 

BIOSIG TECHNOLOGIES, INC.

 CONDENSED CONSOLIDATED STATEMENT OF CHANGES IN EQUITY

THREE AND SIX MONTHS ENDED JUNE 30, 2020

(In Thousands, Except Par Value and Share Amounts)

 

                   

Additional

            Non-          
   

Common stock

   

Paid in

   

Accumulated

   

controlling

         
   

Shares

   

Amount

   

Capital

   

Deficit

   

Interest

   

Total

 

Balance, December 31, 2019

    23,323,087     $ 23     $ 115,910     $ (104,787 )   $ 515     $ 11,661  

Sale of common stock

    2,500,000       2       9,050       -       -       9,052  

Common stock issued upon conversion of Series C Preferred Stock at $3.75 per share

    2,667       -       10       -       -       10  

Common stock issued settlement of Series C Preferred Stock accrued dividends at $5.39 per share

    1,083       -       6       -       -       6  

Common stock issued upon cashless exercise of warrants

    10,574       -       -       -       -       -  

Common stock issued upon cashless exercise of options

    11,141       -       -       -       -       -  

Common stock issued upon exercise of warrants at an average of $3.75 per share

    80,432       1       301       -       -       302  

Fair value of subsidiary shares issued to acquire research and development from Trek Therapeutics, PBC

    -       -       2,440       -       735       3,175  

Stock based compensation

    81,334       -       3,628       -       785       4,413  

Preferred stock dividend

    -       -       (5 )     -       -       (5 )

Net loss

    -       -       -       (11,335 )     (1,428 )     (12,763 )

  Balance, March 31, 2020 (unaudited)

    26,010,318       26       131,340       (116,122 )     607       15,851  

Sale of common stock

    2,187,500       2       16,160       -       -       16,162  

Sale of subsidiary shares to non-controlling interest

    -       -       7,124       -       3,468       10,592  

Common stock issued for services

    15,038       -       108       -       -       108  

Fair value of subsidiary shares issued to acquire research and development

    -       -       1,051       -       249       1,300  

Common stock issued upon conversion of Series C Preferred Stock at $3.75 per share

    26,667       -       100       -       -       100  

Common stock issued for settlement of Series C Preferred Stock accrued dividends at $4.47 per share

    14,433       -       65       -       -       65  

Common stock issued upon cashless exercise of warrants

    2,266       -       -       -       -       -  

Common stock issued upon cashless exercise of options

    149,602       -       -       -       -       -  

Common stock issued upon exercise of options at an average of $4.66 per share

    478,451       1       2,228       -       -       2,229  

Common stock issued upon exercise of warrants at an average of $3.87 per share

    189,388       -       733       -       -       733  

Stock based compensation

    53,000       -       9,595       -       1,628       11,223  

Preferred stock dividend

    -       -       (5 )     -       -       (5 )

Net loss

    -       -       -       (19,188 )     (3,158 )     (22,346 )

  Balance, June 30, 2020 (unaudited)

    29,126,663       29       168,499       (135,310 )     2,794       36,012  

 

See the accompanying notes to the unaudited condensed consolidated financial statements

 

6

 

BIOSIG TECHNOLOGIES, INC.

 

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

 

(In Thousands, Except Par Value and Share Amounts)

 

(unaudited)

 
                 
   

Six months ended June 30,

 
   

2021

   

2020

 

CASH FLOWS FROM OPERATING ACTIVITIES:

               

Net loss

  $ (16,610 )   $ (35,110 )

Adjustments to reconcile net loss to cash used in operating activities:

               

Depreciation and amortization

    91       43  

Amortization of right to use assets

    230       227  

Equity based compensation

    4,311       15,745  

Change in fair value of modified options

    321       -  

Fair value of subsidiary stock issued to acquire research and development from Trek Therapeutics, PBC

    -       3,175  

Fair value of subsidiary stock issued to acquire research an development

    -       1,300  

Changes in operating assets and liabilities:

               

Accounts receivable

    (199 )     -  

Inventory

    37       (222 )

Prepaid expenses and other

    (209 )     (770 )

Deferred revenue

    53       -  

Accounts payable and accrued expenses

    (1,693 )     1,615  

Operating lease liabilities

    (242 )     (226 )

  Net cash used in operating activities

    (13,910 )     (14,223 )
                 

CASH FLOWS FROM INVESTING ACTIVITIES:

               

Purchase of property and equipment

    (182 )     (28 )

  Net cash used in investing activity

    (182 )     (28 )
                 

CASH FLOWS FROM FINANCING ACTIVITIES:

               

Proceeds from sale of common stock, net of issuance costs

    -       25,214  

Proceeds from sale subsidiary stock to non-controlling interest, net of issuance costs

    -       10,592  

Proceeds from sale of common stock under a At-the-market offering, net of issuance costs

    1,300       -  

Proceeds from exercise of options

    28       2,229  

Proceeds from exercise of warrants

    -       1,035  

  Net cash provided by financing activities

    1,328       39,070  
                 

Net (decrease) increase in cash and cash equivalents

    (12,764 )     24,819  
                 

Cash and cash equivalents, beginning of the period

    28,268       12,108  

Cash and cash equivalents, end of the period

  $ 15,504     $ 36,927  
                 

Supplemental disclosures of cash flow information:

               

Cash paid during the period for interest

  $ -     $ -  

Cash paid during the period for income taxes

  $ -     $ -  
                 

Non cash investing and financing activities:

               

Common stock issued upon conversion of Series C Preferred Stock and accrued dividends

  $ -     $ 180  

Dividend payable on preferred stock charged to additional paid in capital

  $ 5     $ 9  

Record right-to-use assets and related lease liability

  $ 218     $ -  

 

See the accompanying notes to the unaudited condensed consolidated financial statements

 

7

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

NOTE 1 – NATURE OF OPERATIONS AND BASIS OF PRESENTATION

 

BioSig Technologies, Inc. was initially incorporated on February 24, 2009 under the laws of the State of Nevada and subsequently re-incorporated in the state of Delaware in 2011. The Company is principally devoted to improving the standard of care in electrophysiology with its initial product offering, the PURE EP™ System, designed for enhanced cardiac signal acquisition, digital signal processing, and analysis during ablation of cardiac arrhythmias. The Company has generated minimal revenue to date and consequently its operations are subject to all risks inherent in business enterprises in early commercialization stage.

 

On November 7, 2018, the Company formed a subsidiary under the laws of the State of Delaware originally under the name of NeuroClear Technologies, Inc. which was renamed to ViralClear Pharmaceuticals, Inc. (“ViralClear”) in March 2020. The subsidiary was established to pursue additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology, and subsequently in 2020, was repurposed to develop merimepodib, a broad-spectrum anti-viral agent that showed potential for the treatment of COVID-19. Since late 2020, ViralClear has been realigned with its original objective of pursuing additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology.

 

In 2019 and 2020, ViralClear sold an aggregate of 1,965,240 shares of its common stock to investors for net proceeds of $15.6 million and issued an aggregate of 894,869 shares of its common stock in connection with acquiring assets and with know-how agreements. As of June 30, 2021, the Company had a majority interest in ViralClear of 69.95%.  

 

On July 2, 2020, the Company formed an additional subsidiary, NeuroClear Technologies, Inc., a Delaware corporation.  

 

The unaudited condensed consolidated financial statements include the accounts of BioSig Technologies, Inc., its wholly owned subsidiary, NeuroClear Technologies, Inc. and its majority owned subsidiary, ViralClear Pharmaceuticals, Inc. as the “Company” or “BioSig”.

 

The unaudited condensed consolidated financial statements of the Company have been prepared in accordance with accounting principles generally accepted in the United States (“GAAP”) for interim financial information and the instructions to Form 10-Q and Rule 8-03 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included.

 

The condensed consolidated balance sheet as of December 31, 2020 has been derived from audited financial statements.

 

Operating results for the three and six months ended June 30, 2021 are not necessarily indicative of results that may be expected for the year ending December 31, 2021. These unaudited condensed consolidated financial statements should be read in conjunction with the audited financial statements for the year ended December 31, 2020 filed with the Company’s Form 10-K with the Securities and Exchange Commission on March 15, 2021.

 

COVID-19

 

On March 11, 2020, the World Health Organization declared a pandemic related to the rapidly spreading coronavirus (COVID-19) outbreak, which has led to a global health emergency.  The full public-health impact of the ongoing pandemic is currently indeterminable and rapidly evolving, and the related health crisis has adversely affected and may continue to adversely affect the global economy, resulting in delaying to our commercialization objectives of the PURE EP Systems into 2022.

 

8

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

NOTE 2 MANAGEMENTS LIQUIDITY PLANS

 

BioSig Technologies, Inc.’s primary efforts are principally devoted to improving the standard care of electrophysiology with its PURE EP System’s enhanced signal acquisition, digital signal processing, and analysis during ablation of cardiac arrhythmias; NeuroClear’s and ViralClear’s efforts are in developing additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology. The Company has experienced net losses and negative cash flows from operations since inception and expects these conditions to continue for the foreseeable future. Further, the Company has generated minimal revenues and there is no assurance that the Company will be able to generate cash flow to fund operations. In addition, there can be no assurance that the Company's ongoing research and development will be successfully completed or that any product will be commercially viable.

 

We expect to incur losses from operations for the near future. Additionally, we expect to incur increasing marketing and commercialization expenses related to our PURE EP system in addition to research and development costs relating to the PURE EP and other product candidates, including expenses related to clinical trials. We expect that our general and administrative expenses will increase in the future as we expand our business development, add infrastructure and incur additional costs related to being a public company, including incremental audit fees, investor relations programs and increased professional services.

 

If additional financing is not available or is not available on acceptable terms, we may be required to delay, reduce the scope of or eliminate our research and development programs, reduce our commercialization efforts or obtain funds through arrangements with collaborative partners or others that may require us to relinquish rights to certain product candidates that we might otherwise seek to develop or commercialize independently.

 

At June 30, 2021, the Company had working capital of approximately $13.6 million. During the six months ended June 30, 2021, the Company raised approximately $1.3 million, net of expenses, through an At-the-market offering. In addition, subsequent to June 30, 2021, the Company raised approximately $9.1 million from the sale of its common stock, net of expenses. Also, the Company began its commercial operations with the sale of the PURE EP device. At June 30, 2021 the Company has effective Forms S-3, shelf registration statements for an aggregate of $116.0 million.

 

At June 30, 2021, the Company had cash of approximately $15.5 million, which together with approximately $9.1 million raised subsequent to June 30, 2021 through the date of the filing of this report and the expected commercial growth, constitutes sufficient funds for the Company to meet its commercialization efforts, research and development and other funding requirements for at least the next 12 months from the date of issuance of these unaudited financial statements.

 

NOTE 3 SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

Use of Estimates

 

The preparation of these unaudited condensed consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date of the unaudited condensed consolidated financial statements and the reported amounts of revenues and expenses during the reporting period. Significant estimates include the recoverability and useful lives of long-lived assets, the fair value of long-term operating leases, patent capitalization, fair value of acquired assets, the fair value of the Company’s stock, stock-based compensation, fair values relating to warrant and other derivative liabilities and the valuation allowance related to deferred tax assets. Actual results may differ from these estimates.

 

Revenue Recognition

 

The Company derives its revenue primarily from the sale of its medical device, the PURE EP™ System, and well as related support and maintenance services and software upgrades in connection with the system.

 

9

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

The Company recognizes revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

 

The Company determines revenue recognition through the following five steps:

 

 

Identify the contract with the customer;

 

 

Identify the performance obligations in the contract;

 

 

Determine the transaction price;

 

 

Allocate the transaction price to the performance obligation in the contract; and

 

 

Recognize revenue when, or as, the performance obligations are satisfied.

 

Performance obligations are the unit of accounting for revenue recognition and generally represent the distinct goods or services that are promised to the customer. If the Company determines that it has not satisfied a performance obligation, it will defer recognition of the revenue until the performance obligation is deemed to be satisfied. Support, maintenance, and software upgrades are performance obligations over a defined period and are recognized ratably over the contractual service period. Customers typically purchase these services with the initial sale of the PURE EP System and do not have the right to terminate their contracts unless we fail to perform material obligations.

 

The Company may execute more than one contract with a single customer. If so, it is evaluated whether the agreements were negotiated as a package with a single objective, whether the amount of consideration to be paid in one agreement depends on the price and/or performance of another agreement, or whether the goods or services promised in the agreements represent a single performance obligation. The conclusions reached can impact the allocation of the transaction price to each performance obligation and the timing of revenue recognition related to those arrangements.

 

The Company records accounts receivable for amounts invoiced to customers for which the Company has an unconditional right to consideration as provided under the contractual arrangement. Unbilled receivables, if any, include amounts related to the Company’s contractual right to consideration for completed performance obligations not yet invoiced. Deferred revenue includes payments received in advance of performance under the contract. Our unbilled receivables and deferred revenue are reported on an individual contract basis at the end of each reporting period. Unbilled receivables are classified as current or noncurrent based on the timing of when we expect to bill the customer. Deferred revenue is classified as current or noncurrent based on the timing of when we expect to recognize revenue.

 

The Company’s unconditional right to consideration for goods and services transferred to the customer is included in accounts receivable, net (if any) in the Company’s unaudited condensed consolidated balance sheet.

 

A reconciliation of contract liabilities with customers is presented below:

 

   

Balance at

December 31, 2020

(000’s)

   

Consideration Received

(000’s)

   

Recognized in Revenue

(000’s)

   

Balance at

June 30, 2021

(000’s)

 

Product revenue

  $ -     $ 314     $ (314

)

  $ -  

Service revenue

    -       64       (11

)

    53  

Total

  $ -     $ 378     $ (325

)

  $ 53  

 

10

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

The table below summarizes our deferred revenue as of June 30, 2021 and December 31, 2020:

 

   

June 30,

2021

(000’s)

   

December 31,

2020

(000’s)

 

Deferred revenue-current

  $ 32     $ -  

Deferred revenue-noncurrent

    21       -  

Total deferred revenue

  $ 53     $ -  

 

We had one customer which accounted for approximately 96% of our revenue in the three months ended June 30, 2021 and two customers which accounted for approximately 61% and 39% of our revenue in the six months ended June 30, 2021.

 

At June 30, 2021, the Company had one customer representing 100% of the outstanding accounts receivable.

 

Cost of Goods Sold

 

Cost of goods sold consists primarily of the delivered cost of our medical device(s) sold.

 

Allowance for Doubtful Accounts

 

The Company adjusts accounts receivable down to net realizable value with its allowance methodology. In determining the allowance for doubtful accounts for estimated losses, aged receivables are analyzed periodically by management. Each identified receivable is reviewed based upon historical collection experience, financial condition of the client and the status of any open or unresolved issues with the client preventing the payment thereof. Corrective action, if necessary, is taken by the Company to resolve open issues related to unpaid receivables. The allowance for doubtful accounts was $0 at June 30, 2021. The Company believes that its reserve is adequate, however results may differ in future periods. For the six months ended June 30, 2021 and 2020, bad debt expense totaled $0.

 

Fair Value of Financial Instruments

 

Accounting Standards Codification subtopic 825-10, Financial Instruments (“ASC 825-10”) requires disclosure of the fair value of certain financial instruments. The carrying value of cash and cash equivalents, accounts payable and accrued liabilities as reflected in the balance sheets, approximate fair value because of the short-term maturity of these instruments. All other significant financial assets, financial liabilities and equity instruments of the Company are either recognized or disclosed in the financial statements together with other information relevant for making a reasonable assessment of future cash flows, interest rate risk and credit risk. Where practicable the fair values of financial assets and financial liabilities have been determined and disclosed; otherwise only available information pertinent to fair value has been disclosed.

 

The Company follows Accounting Standards Codification subtopic 820-10, Fair Value Measurements and Disclosures (“ASC 820-10”) and ASC 825-10, which permits entities to choose to measure many financial instruments and certain other items at fair value.

 

Concentrations of Credit Risk

 

Financial instruments and related items, which potentially subject the Company to concentrations of credit risk, consist primarily of cash and cash equivalents. The Company places its cash and temporary cash investments with credit quality institutions. At times, such amounts may be in excess of the FDIC insurance limit.  At June 30, 2021 and December 31, 2020, deposits in excess of FDIC limits were $15.0 million and $27.8 million, respectively.

 

Inventory

 

The inventory is comprised of work in process and finished goods available for sale and are stated at the lower of cost or net realizable value using specific identification method for serial numbered inventory and first-in, first-out method for all other inventory for valuation. The inventory at June 30, 2021 and December 31, 2020 were $731,054 and $768,319, respectively.

 

11

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Prepaid Expenses and Vendor Deposits

 

Prepaid expenses and vendor deposits are comprised of prepaid insurance, operating expenses and other prepayments.

 

Leases

 

The Company determines if a contractual arrangement is a lease at inception. Operating leases are included in operating lease right-of-use (“ROU”) assets, current operating lease liabilities, and noncurrent operating lease liabilities on the Company’s condensed consolidated balance sheet. The Company evaluates and classifies leases as operating or finance leases for financial reporting purposes. The classification evaluation begins at the commencement date and the lease term used in the evaluation includes the non-cancellable period for which the Company has the right to use the underlying asset, together with renewal option periods when the exercise of the renewal option is reasonably certain and failure to exercise such option which result in an economic penalty. All the Company’s real estate leases are classified as operating leases. ROU assets represent the Company’s right to use an underlying asset for the lease term and lease liabilities represent the Company’s obligation to make lease payments arising from the lease. Operating lease ROU assets and liabilities are recognized at the commencement date of the lease based on the present value of lease payments over the lease term.

 

The lease payments included in the present value are fixed lease payments. As most of the Company’s leases do not provide an implicit rate, the Company estimates its collateralized incremental borrowing rate, based on information available at the commencement date, in determining the present value of lease payments. The Company applies the portfolio approach in applying discount rates to its classes of leases. The operating lease ROU assets include any payments made before the commencement date. Lease expense for lease payments is recognized on a straight-line basis over the lease term. The Company does not currently have subleases. The Company does not currently have residual value guarantees or restrictive covenants in its leases.

 

Property and Equipment

 

Property and equipment are stated at cost and depreciated using the straight-line method over their estimated useful lives of 3 to 5 years. When retired or otherwise disposed, the related carrying value and accumulated depreciation are removed from the respective accounts and the net difference less any amount realized from disposition, is reflected in earnings.

 

Impairment of Long-lived Assets

 

The Company recognizes an impairment of long-lived assets used in operations, other than goodwill, when events or circumstances indicate that the asset might be impaired and the estimated undiscounted cash flows to be generated by those assets over their remaining lives are less than the carrying amount of those items. The net carrying value of assets not recoverable is reduced to fair value, which is typically calculated using the discounted cash flow method. The Company did not recognize and record any impairments of long-lived assets used in operations during the three and six months ended June 30, 2021 and 2020.

 

Research and Development Costs

 

The Company accounts for research and development costs in accordance with the Accounting Standards Codification subtopic 730-10, Research and Development (“ASC 730-10”). Under ASC 730-10, all research and development costs must be charged to expense as incurred. Accordingly, internal research and development costs are expensed as incurred. Third-party research and developments costs are expensed when the contracted work has been performed or as milestone results have been achieved. Company-sponsored research and development costs related to both present and future products are expensed in the period incurred. The Company incurred research and development expenses of $1.7 million and $2.9 million for the three and six months ended June 30, 2021 and $5.7 million and $10.6 million for the three and six months ended June 30,2020, respectively.

 

Net Income (loss) Per Common Share

 

The Company computes earnings (loss) per share under Accounting Standards Codification subtopic 260-10, Earnings Per Share (“ASC 260-10”). Net loss per common share is computed by dividing net loss by the weighted average number of shares of common stock outstanding during the period.  Diluted earnings per share, if presented, would include the dilution that would occur upon the exercise or conversion of all potentially dilutive securities into common stock using the “treasury stock” and/or “if converted” methods as applicable.

 

12

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

The computation of basic and diluted loss per share as of June 30, 2021 and 2020 excludes potentially dilutive securities when their inclusion would be anti-dilutive, or if their exercise prices were greater than the average market price of the common stock during the period.

 

Potentially dilutive securities excluded from the computation of basic and diluted net income (loss) per share are as follows: 

 

   

June 30,

2021

   

June 30,

2020

 

Series C convertible preferred stock

    52,028       38,084  

Options to purchase common stock

    4,004,622       3,732,705  

Warrants to purchase common stock

    887,262       1,764,827  

Restricted stock units to acquire common stock

    292,250       128,334  

Totals

    5,236,162       5,663,950  

 

Stock Based Compensation

 

The Company measures the cost of services received in exchange for an award of equity instruments based on the fair value of the award as measured on the grant date. The fair value amount is then recognized over the period during which services are required to be provided in exchange for the award, usually the vesting period.

 

Income Taxes

 

The Company follows Accounting Standards Codification subtopic 740-10, Income Taxes (“ASC 740-10”) for recording the provision for income taxes. Deferred tax assets and liabilities are computed based upon the difference between the financial statement and income tax basis of assets and liabilities using the enacted marginal tax rate applicable when the related asset or liability is expected to be realized or settled. Deferred income tax expenses or benefits are based on the changes in the asset or liability during each period. If available evidence suggests that it is more likely than not that some portion or all of the deferred tax assets will not be realized, a valuation allowance is required to reduce the deferred tax assets to the amount that is more likely than not to be realized. Future changes in such valuation allowance are included in the provision for deferred income taxes in the period of change. Deferred income taxes may arise from temporary differences resulting from income and expense items reported for financial accounting and tax purposes in different periods.

 

Patents, Net

 

The Company capitalizes certain initial asset costs in connection with patent applications including registration, documentation and other professional fees associated with the application. Patent costs incurred prior to the Company’s U.S. Food and Drug Administration (“FDA”) 510(k) application on March 28, 2018 were charged to research and development expense as incurred. Commencing upon first in-man trials on February 18 and 19, 2019, capitalized costs are amortized to expense using the straight-line method over the lesser of the legal patent term or the estimated life of the product of 20 years. During the three and six months ended June 30, 2021, the Company recorded amortization of $4,752 and $9,503; and $4,751 and $9,502 for the three and six months ended June 30, 2020 to current period operations, respectively.

 

Warranty

 

The Company generally warrants its products to be free from material defects and to conform to material specifications for a period of up to two (2) years. Warranty expense is estimated based primarily on historical experience and is reflected in the financial statements.

 

13

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Non-controlling Interest

 

The Company’s non-controlling interest represents the non-controlling shareholders ownership interests related to the Company’s subsidiary, ViralClear Pharmaceuticals, Inc. The Company reports its non-controlling interest in subsidiaries as a separate component of equity in the consolidated balance sheets and reports both net loss attributable to the non-controlling interest and net loss attributable to the Company’s common shareholders on the face of the consolidated statements of operations. The Company’s equity interest in ViralClear is 69.95% and the non-controlling stockholders’ interest is 30.05% as of June 30, 2021. This is reflected in the unaudited condensed consolidated statements of changes in equity.

 

Segment Information

 

Operating segments are identified as components of an enterprise about which separate discrete financial information is available for evaluation by the chief operating decision maker, or decision-making group, in making decisions how to allocate resources and assess performance. The information disclosed herein represents all of the material financial information related to the Company’s principal operating segments. (See Note 12 – Segment Reporting).

 

Reclassifications

 

Certain reclassifications have been made to prior periods’ data to conform with the current year’s presentation. These reclassifications had no effect on reported income or losses.

 

Recent Accounting Pronouncements

 

There were various updates recently issued, most of which represented technical corrections to the accounting literature or application to specific industries and are not expected to a have a material impact on the Company’s financial position, results of operations or cash flows.

 

NOTE 4 PROPERTY AND EQUIPMENT

 

Property and equipment as of June 30, 2021 and December 31, 2020 is summarized as follows:

 

   

June 30,

2021

(000’s)

   

December 31,

2020

(000’s)

 

Computer equipment

  $ 358     $ 234  

Furniture and fixtures

    83       75  

Manufacturing equipment

    34       34  

Testing/Demo equipment

    145       96  

Total

    620       439  

Less accumulated depreciation

    (232

)

    (150

)

Property and equipment, net

  $ 388     $ 289  

 

Property and equipment are stated at cost and depreciated using the straight-line method over their estimated useful lives of 3 to 5 years. When retired or otherwise disposed, the related carrying value and accumulated depreciation are removed from the respective accounts and the net difference less any amount realized from disposition, is reflected in earnings.

 

Depreciation expense was $45,113 and $81,947 for three and six months ended June 30, 2021 and $17,457 and $33,721 for the three and six months ended June 30, 2020, respectively.

 

14

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

NOTE 5 – RIGHT TO USE ASSETS AND LEASE LIABILITY

 

Operating leases:

 

On February 10, 2021 the Company entered into a Sixth Amendment to the Office Lease at 12424 Wilshire Blvd in Los Angeles dated August 9, 2011 – it is the Fourth Extended Term with respect to Suite 745 and the Expansion Term with respect to Suite 740 which is from July 1, 2021 until June 30, 2022 with a fixed monthly rent equal to $13,702 (down from $16,289); and the security deposit will be reduced by $5,448 so that the balance remaining shall be $27,404.

 

The Company determined that the Sixth Amendment was a lease modification and accordingly reassessed the lease classification, remeasured the lease liability and adjusted the right-to-use asset. At February 10, 2021 the Company removed the remaining right-to-use net assets of $60,881 and related lease liability of $63,076 and recorded right-to-use assets and related lease liability of $217,903.

 

On October 1, 2019, the Company entered into a lease agreement whereby the Company leased approximately 1,400 square feet of office space in Rochester, Minnesota commencing November 1, 2019 and expiring on October 31, 2021 at an initial rate of $3,411 per month with escalating payments. The lease agreement includes an option to extend the lease for two additional periods of two years each past its initial term. At lease modification date, the Company estimated the lease liability and the right of use assets at present value using the Company’s estimated incremental borrowing rate of 8%.

 

As of June 30, 2021, the Company had outstanding five leases with aggregate payments of $38,897 per month, expiring through December 31, 2022.

 

Right to use assets is summarized below:

 

   

June 30,

2021

(000’s)

   

December 31,

2020

(000’s)

 

Right to use assets, net

  $ 808     $ 1,087  

Less accumulated depreciation

    (556

)

    (781

)

Right to use assets, net

  $ 252     $ 306  

 

During the three and six months ended June 30, 2021, the Company recorded $126,638 and $245,239 and $126,811 and $246,218 for the three and six months ended June 30, 2020 as lease expense to current period operations, respectively.

 

Lease liability is summarized below:

 

   

June 30,

2021

(000’s)

   

December 31,

2020

(000’s)

 

Total lease liability

  $ 248     $ 314  

Less: short term portion

    (247

)

    (313

)

Long term portion

  $ 1     $ 1  

 

Maturity analysis under these lease agreements are as follows (000’s):

 

Remainder of 2021

  $ 173  

Year ended December 31, 2022

    83  

Total

    256  

Less: Present value discount

    (8

)

Lease liability

  $ 248  

 

15

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Lease expense for the three months ended June 30, 2021 and 2020 was comprised of the following:

 

   

June 30,

2021

(000’s)

   

June 30,

2020

(000’s)

 

Operating lease expense

  $ 119     $ 114  

Short-term lease expense

    8       13  

Total

  $ 127     $ 127  

 

Lease expense for the six months ended June 30, 2021 and 2020 was comprised of the following:

 

   

June 30,

2021

(000’s)

   

June 30,

2020

(000’s)

 

Operating lease expense

  $ 230     $ 227  

Short-term lease expense

    15       18  

Variable lease expense

    -       1  

Total

  $ 245     $ 246  

 

NOTE 6 – ACCOUNTS PAYABLE AND ACCRUED EXPENSES

 

Accounts payable and accrued expenses at June 30, 2021 and December 31, 2020 consist of the following:

 

   

June 30,

2021

(000’s)

   

December 31,

2020

(000’s)

 

Accrued accounting and legal

  $ 170     $ 177  

Accrued reimbursements and travel

    45       56  

Accrued consulting

    97       256  

Accrued research and development expenses

    1,920       3,127  

Accrued product purchases

    154       30  

Accrued marketing

    8       -  

Accrued office and other

    105       127  

Accrued payroll

    515       936  

Accrued settlement related to arbitration

    13       13  
    $ 3,027     $ 4,722  

 

NOTE 7 – SERIES C 9% CONVERTIBLE PREFERRED STOCK

 

Series C 9% Convertible Preferred Stock

 

On January 9, 2013, the Board of Directors authorized the issuance of up to 4,200 shares of 9% Series C Convertible Preferred Stock (the “Series C Preferred Stock”).

 

16

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

The Series C Preferred Stock is entitled to preference over holders of junior stock upon liquidation in the amount of $1,000 plus any accrued and unpaid dividends; entitled to dividends as a preference to holders of junior stock at a rate of 9% per annum of the stated value of $1,000 per share, payable quarterly beginning on September 30, 2013 and are cumulative.  The holders of the Series C Preferred Stock vote together with the holders of our common stock on an as-converted basis but may not vote the Series C Preferred Stock in excess of the beneficial ownership limitation of the Series C Preferred Stock.  The beneficial ownership limitation is 4.99% of our then outstanding shares of common stock following such conversion or exercise, which may be increased to up to 9.99% of our then outstanding shares of common stock following such conversion or exercise upon the request of an individual holder.  The beneficial ownership limitation is determined on an individual holder basis, such that the as-converted number of shares of one holder is not included in the shares outstanding when calculating the limitation for a different holder.

 

As a result of an amendment to the conversion price of our Series C Preferred Stock, the conversion price effective as of December 31, 2020 was $3.75 per share, subject to certain reset provisions. On April 30, 2021, the conversion price was reset to $3.68 per share. The effect was de minimis.

 

The Series C Preferred Stock contains triggering events which would, among other things, require redemption (i) in cash, at the greater of (a) 120% of the stated value of $1,000 or (b) the product of (I) the variable weighted average price of our common stock on the trading day immediately preceding the date of the triggering event and (II) the stated value divided by the then conversion price or (ii) in shares of our common stock, equal to a number of shares equal to the amount set forth in (i) above divided by 75%. As of June 30, 2021, the aggregate stated value of our Series C Preferred Stock was $105,000. The triggering events include our being subject to a judgment of greater than $100,000 or our initiation of bankruptcy proceedings. If any of the triggering events contained in our Series C Preferred Stock occur, the holders of our Series C Preferred Stock may demand redemption, an obligation the Company may not have the ability to meet at the time of such demand.  The Company will be required to pay interest on any amounts remaining unpaid after the required redemption of our Series C Preferred Stock, at a rate equal to the lesser of 18% per annum or the maximum rate permitted by applicable law. Accordingly, the Company has classified the Series C Preferred Stock as a mezzanine obligation in the accompanying consolidated balance sheets.

 

Series C Preferred Stock issued and outstanding totaled 105 as of June 30, 2021 and December 31, 2020.  As of June 30, 2021 and December 31, 2020, the Company has accrued $76,903 and $72,217 dividends payable on the Series C Preferred Stock.

 

NOTE 8 – STOCKHOLDER EQUITY

 

Shareholder rights plan

 

On July 14, 2020, our board of directors adopted a stockholder rights plan (the “Rights Plan”) and declared a dividend of one preferred share purchase right for each outstanding share of BioSig’s common stock to stockholders of record on July 27, 2020, and one right will be issued for each new share of common stock issued thereafter. Each right will initially trade with common stock, and will allow its holder to purchase from BioSig one one-thousandth of a share of Series F Junior Participating Preferred stock, par value $0.001 per share, for an exercise price of $50.00, once the rights become exercisable. In the event that a person or group acquires beneficial ownership of 12% or more of BioSig’s then outstanding common stock, subject to certain exceptions, each right would entitle its holder (other than such person or members of such group) to purchase additional shares of BioSig’s common stock having a market value of two times the exercise price of the right. In addition, at any time after a person or group acquires 12% or more of BioSig’s outstanding common stock (unless such person or group acquires 50% or more), the Board may exchange one share of BioSig’s common stock for each outstanding right (other than rights owned by such person or group, which would have become void). The Rights Plan could make it more difficult for a third party to acquire control of BioSig or a large block of our common stock without the approval of our board of directors. The rights will expire on July 13, 2021, unless terminated earlier by our board of directors

 

Preferred stock

 

The Company is authorized to issue 1,000,000 shares of $0.001 par value preferred stock. As of June 30, 2021, and December 31, 2020, the Company has designated 200 shares of Series A preferred stock, 600 shares of Series B preferred stock, 4,200 shares of Series C Preferred Stock, 1,400 shares of Series D Preferred Stock, 1,000 shares of Series E Preferred Stock and 200,000 shares of Series F Preferred Stock. As of June 30, 2021, and December 31, 2020, there were no outstanding shares of Series A, Series B, Series D, Series E and Series F preferred stock.

 

17

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Common stock

 

BioSig Technologies, Inc.

 

The Company is authorized to issue 200,000,000 shares of $0.001 par value common stock. As of June 30, 2021 and December 31, 2020, the Company had 32,205,479 and 30,764,792 shares issued and outstanding, respectively.

 

In January 2021, the Company issued an aggregate of 658,868 shares of its common stock for services at a fair value previously recorded in 2020 of $2,658,224

 

During the six months ended June 30, 2021, the Company issued 443,640 shares of common stock for services at a fair value of $1,917,465.

 

During the six months ended June 30, 2021, the Company issued 9,375 shares of common stock in exchange for proceeds of $27,750 from the exercise of options.

 

During the six months ended June 30, 2021, the Company issued an aggregate of 77,084 shares of its common stock for vested restricted stock units as stock-based compensation.

 

Open Market Sale Agreement

 

On August 28, 2020, the Company entered into an Open Market Sale Agreement (the “Sales Agreement”) with Jefferies LLC to act as the Company’s sales agent and/or principal (“Jefferies” or the “Agent”), with respect to the issuance and sale of up to $45.0 million of the Company’s shares of common stock from time to time in an at-the-market offering.

 

Upon delivery of a placement notice and subject to the terms and conditions of the Sales Agreement, Jefferies may sell the Shares by any method permitted by law deemed to be an “at the market offering” as defined in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended. The Company may sell the common stock in amounts and at times to be determined by the Company from time to time subject to the terms and conditions of the Sales Agreement, but it has no obligation to sell any of the Shares under the Sales Agreement. The Company or Jefferies may suspend or terminate the offering of Shares upon notice to the other party and subject to other conditions. Jefferies will act as sales agent on a commercially reasonable efforts basis consistent with its normal trading and sales practices and applicable state and federal law, rules and regulations and the rules of Nasdaq.

 

The Company paid Agent a commission equal to 3.0% of the gross proceeds from the sale of the Shares pursuant to the Sales Agreement. The Company has also agreed to provide Jefferies with customary indemnification and contribution rights.

 

The offering of Shares pursuant to the Sales Agreement will terminate upon the earlier of (i) the sale of all common stock subject to the Sales Agreement or (ii) termination of the Sales Agreement in accordance with its terms.

 

The common stock was sold and issued pursuant the Company’s shelf registration statement on Form S-3 (File No. 333-230448), which was previously declared effective by the Securities and Exchange Commission, and a related prospectus.

 

From January 15, 2021 through February 16, 2021, the Company sold 251,720 shares of its common stock through the Open Market Sales Agreement for net proceeds of $1,300,135, after transactional costs of $40,365.

 

On March 25, 2021, the Company delivered written notice to Jefferies to terminate the Sales Agreement effective as of April 8, 2021, pursuant to Section 7(b)(i) thereof. The Company was not subject to any termination penalties related to the termination of the Sales Agreement.

 

18

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

NOTE 9 – OPTIONS, RESTRICTED STOCK UNITS AND WARRANTS

 

BioSig Technologies, Inc.

 

2012 Equity Incentive Plan

 

On October 19, 2012, the Board of Directors of BioSig Technologies, Inc. approved the 2012 Equity Incentive Plan (the “Plan”) and terminated the Long-Term Incentive Plan (the “2011 Plan”). The Plan (as amended) provides for the issuance of options, stock appreciation rights, restricted stock and restricted stock units to purchase up to 14,474,450 shares of the Company’s common stock to officers, directors, employees and consultants of the Company. Under the terms of the Plan the Company may issue Incentive Stock Options as defined by the Internal Revenue Code to employees of the Company only and nonstatutory options. The Board of Directors of the Company or a committee thereof administers the Plan and determines the exercise price, vesting and expiration period of the grants under the Plan.

 

However, the exercise price of an Incentive Stock Option should not be less than 110% of fair value of the common stock at the date of the grant for a 10% or more stockholder and 100% of fair value for a grantee who is not 10% stockholder. The fair value of the common stock is determined based on the quoted market price or in absence of such quoted market price, by the administrator in good faith.

 

Additionally, the vesting period of the grants under the Plan will be determined by the administrator, in its sole discretion, with an expiration period of not more than ten years. There are 3,804,032 shares remaining available for future issuance of awards under the terms of the Plan as of June 30, 2021.

 

Options

 

Option valuation models require the input of highly subjective assumptions. The fair value of stock-based payment awards was estimated using the Black-Scholes option model with a volatility figure derived from an index of historical stock prices of comparable entities until sufficient data exists to estimate the volatility using the Company’s own historical stock prices. Management determined this assumption to be a more accurate indicator of value. The Company accounts for the expected life of options based on the contractual life of options for non-employees.

 

For employees, the Company accounts for the expected life of options in accordance with the “simplified” method, which is used for “plain-vanilla” options, as defined in the accounting standards codification. The risk-free interest rate was determined from the implied yields of U.S. Treasury zero-coupon bonds with a remaining life consistent with the expected term of the options.  The fair value of stock-based payment awards during the three and six months ended June 30, 2021 was estimated using the Black-Scholes pricing model.

 

During the six months ended June 30, 2021, the Company granted an aggregate of 754,500 options to officers, directors and key consultants.

 

The following table presents information related to stock options at June 30, 2021:

 

Options Outstanding

   

Options Exercisable

 
               

Weighted

         
               

Average

   

Exercisable

 

Exercise

   

Number of

   

Remaining Life

   

Number of

 

Price

   

Options

   

In Years

   

Options

 

$

2.51-5.00

     

2,447,257

     

7.2

     

1,545,675

 
 

5.01-7.50

     

1,289,032

     

5.9

     

1,013,760

 
 

7.51-10.00

     

203,333

     

8.2

     

115,133

 
 

10.01-12.50

     

65,000

     

8.9

     

48,332

 
         

4,004,622

     

6.9

     

2,722,900

 

 

19

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

A summary of the stock option activity and related information for the Plan for the six months ended June 30, 2021 is as follows:

 

                   

Weighted-Average

         
           

Weighted-Average

   

Remaining

   

Aggregate

 
   

Shares

   

Exercise Price

   

Contractual Term

   

Intrinsic Value

 

Outstanding at December 31, 2020

   

3,568,497

   

$

5.59

     

7.0

   

$

110,961

 

Grants

   

754,500

     

4.14

     

10.0

   

$

-

 

Exercised

   

(9,375

)

 

$

2.96

             

-

 

Forfeited/expired

   

(309,000

)

 

$

7.23

             

-

 

Outstanding at June 30, 2021

   

4,004,622

   

$

5.20

     

6.9

   

$

190,635

 

Exercisable at June 30, 2021

   

2,722,900

   

$

5.35

     

5.8

   

$

66,322

 

 

The aggregate intrinsic value in the preceding tables represents the total pretax intrinsic value, based on options with an exercise price less than the stock price of BioSig Technologies, Inc. of $3.86 as of June 30, 2021, which would have been received by the option holders had those option holders exercised their options as of that date.

 

On January 12, 2021, BioSig Technologies, Inc. granted 387,500 options to purchase the company stock in connection with the services rendered at the exercise price of $4.23 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning January 12, 2022 for two years.

 

On February 16, 2021, BioSig Technologies, Inc. granted 102,000 options to purchase the company stock in connection with the services rendered at the exercise price of $4.97 per share for a term of ten years with one-third vesting on the one year anniversary and two-thirds vesting quarterly thereafter beginning February 16, 2022 for two years.

 

On April 9, 2021, BioSig Technologies, Inc. granted 90,000 options to purchase the company stock in connection with the services rendered at the exercise price of $4.38 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning April 9, 2022 for two years.

 

On April 13, 2021, BioSig Technologies, Inc. granted 25,000 options to purchase the company stock in connection with the services rendered at the exercise price of $4.42 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning April 13, 2022 for two years.

 

On May 18, 2021, BioSig Technologies, Inc. granted 150,000 options to purchase the company stock in connection with the services rendered at the exercise price of $3.20 per share for a term of ten years with one-third vesting on the one year anniversary and two-thirds vesting quarterly thereafter beginning May 18, 2022 for two years.

 

The following assumptions were used in determining the fair value of options during the six months ended June 30, 2021:

 

Risk-free interest rate

   

0.83% - 1.30

%

Dividend yield

   

0

%

Stock price volatility

   

89.23% to 95.98

%

Expected life

 

6 years

 

Weighted average grant date fair value

 

$

3.63

 

 

On June 28, 2021, in connection with the exit of two members of the Company’s board of directors, the Company extended the life of 145,000 previously issued director options from the contractual 90 days from termination of service to the earlier of the initial life or June 28, 2023. The change in estimated fair value of the modified options of $182,514 was charged to current period operations.

 

20

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

The following assumptions were used in determining the change in fair value of the modified options at June 28, 2021:

 

Risk-free interest rate

   

0.05% - 0.25

%

Dividend yield

   

0

%

Stock price volatility

   

88.57

%

Expected life

 

0.25– 2 years

 

 

On June 30, 2021, in connection with the resignation of a member of the Company’s board of directors, the Company entered into a one year consulting contract and extended the life of 221,240 previously issued director options from the contractual 90 days from termination of service to the earlier of the initial life or two years after service contract completion. The change in estimated fair value of the modified options of $111,402 was charged to current period operations

 

The following assumptions were used in determining the change in fair value of the modified options at June 30, 2021:

 

Risk-free interest rate

   

0.06% - 0.46

%

Dividend yield

   

0

%

Stock price volatility

   

88.59

%

Expected life

 

0.59– 3 years

 

 

The fair value of all options vesting during the three and six months ended June 30, 2021 of $613,806 and $1,190,692 and $3,628,181 and $4,251,874 for the three and six months ended June 30, 2020, respectively, was charged to current period operations.  Unrecognized compensation expense of $4,336,644 at June 30, 2021 will be expensed in future periods.

 

Warrants

 

The following table summarizes information with respect to outstanding warrants to purchase common stock of BioSig Technologies, Inc. at June 30, 2021: 

 

Exercise

   

Number

 

Expiration

Price

   

Outstanding

 

Date

$

4.80

     

125,000

 

February 2025

$

6.16

     

568,910

 

November 2027

$

6.85

     

193,352

 

July 2021 to August 2021

         

887,262

   

 

A summary of the warrant activity for the six months ended June 30, 2021 is as follows:

 

                   

Weighted-Average

         
           

Weighted-Average

   

Remaining

Contractual

   

Aggregate

 
   

Shares

   

Exercise Price

   

Term

   

Intrinsic Value

 

Outstanding at December 31, 2020

    1,446,200     $ 5.44       3.3     $ 1,500  

Grants

    -                          

Exercised

    -                          

Expired

    (558,938

)

  $ 4.36       -       -  

Outstanding at June 30, 2021

    887,262     $ 6.12       4.6     $ -  
                                 

Vested and expected to vest at June 30, 2021

    887,262     $ 6.12       4.6     $ -  

Exercisable at June 30, 2021

    887,262     $ 6.12       4.6     $ -  

 

21

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

The aggregate intrinsic value in the preceding tables represents the total pretax intrinsic value, based on options with an exercise price less than the company’s stock price of $3.86 of June 30, 2021, which would have been received by the option holders had those option holders exercised their options as of that date.

 

Restricted Stock Units

 

The following table summarizes the restricted stock activity for the six months ended June 30, 2021:

 

Restricted shares issued as of December 31, 2020

    218,334  

Granted

    251,000  

Vested and issued

    (77,084

)

Forfeited

    (100,000

)

Total

    292,250  

Comprised of:

       

Vested restricted shares as of June 30, 2021

    50,000  

Unvested restricted shares as of June 30, 2021

    242,250  

Total

    292,250  

 

On January 4, 2021, the Company granted 220,000 restricted stock units for services with 105,000 vesting one-third on the one-year anniversary and two-thirds vesting quarterly thereafter beginning January 4, 2022 for two years and with 115,000 vesting quarterly for one year.

 

On March 8, 2021 the Company granted 31,000 restricted stock units for services vesting on August 31, 2021.

 

On June 1, 2021, in connection with the termination of an employee, the Company accelerated vesting of 30,000 previously granted restricted stock units from a three-year period to fully vested. The change in vesting of the modified restricted stock unit resulted in a $109,725 charge to current period operations.

 

On June 30, 2021, in connection with the resignation of a member of the Company’s board of directors, the Company accelerated vesting of 50,000 previously granted restricted stock units from a three-year period to fully vested. The change in vesting of the modified restricted stock unit resulted in a $232,375 charge to current period operations.

 

Stock based compensation expense related to restricted stock grants was $610,995 and $710,115 for the three and six months ended June 30, 2021 and $428,820 and $830,298 for the three and six months ended June 30, 2020, respectively. As of June 30, 2021, the stock-based compensation relating to restricted stock of $538,983 remains unamortized. 

 

ViralClear Pharmaceuticals, Inc.

 

2019 Long-Term Incentive Plan

 

On September 24, 2019, ViralClear’s Board of Directors approved the 2019 Long-Term Incentive Plan (as subsequently amended, the “ViralClear Plan”). The ViralClear Plan was approved by BioSig as ViralClear’s majority stockholder. The ViralClear Plan provides for the issuance of options, stock appreciation rights, restricted stock and restricted stock units to purchase up to 4,000,000 shares of ViralClear’s common stock to officers, directors, employees and consultants of the ViralClear. Under the terms of the ViralClear Plan, ViralClear may issue Incentive Stock Options as defined by the Internal Revenue Code to employees of ViralClear only and nonstatutory options. The Board of Directors of ViralClear or a committee thereof administers the ViralClear Plan and determines the exercise price, vesting and expiration period of the grants under the ViralClear Plan.

 

However, the exercise price of an Incentive Stock Option should not be less than 110% of fair market value of the common stock at the date of the grant for a 10% or more stockholder and 100% of fair market value for a grantee who is not 10% stockholder. The fair market value of the common stock is determined based on the quoted market price or in absence of such quoted market price, by the administrator in good faith.

 

22

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Additionally, the vesting period of the grants under the ViralClear Plan will be determined by the administrator, in its sole discretion, with an expiration period of not more than ten years. There are 1,987,000 shares remaining available for future issuance of awards under the terms of the ViralClear Plan.

 

ViralClear Options

 

A summary of the stock option activity and related information for the ViralClear Plan for the six months ended June 30, 2021 is as follows:

 

                   

Weighted-Average

 
           

Weighted-Average

   

Remaining

Contractual

 
   

Shares

   

Exercise Price

   

Term

 

Outstanding at December 31, 2020

    1,527,666     $ 5.00       3.96  

Grants

    -                  

Exercised

    -                  

Forfeited/expired

    (852,666

)

  $ 5.00          

Outstanding at June 30, 2021

    675,000     $ 5.00       8.17  

Exercisable at June 30, 2021

    616,665     $ 5.00       8.11  

 

The following table presents information related to stock options at June 30, 2021:

 

Options Outstanding

   

Options Exercisable

 
               

Weighted

         
               

Average

   

Exercisable

 

Exercise

   

Number of

   

Remaining Life

   

Number of

 

Price

   

Options

   

In Years

   

Options

 

$

5.00

     

675,000

     

8.17

     

616,665

 

 

The fair value of the stock-based payment awards was estimated using the Black-Scholes option model with a volatility figure derived from an index of historical stock prices of comparable entities with the market value of stock price based on recent sales. The Company accounts for the expected life of options in accordance with the “simplified” method, which is used for “plain-vanilla” options, as defined in the accounting standards codification. The risk-free interest rate was determined from the implied yields of U.S. Treasury zero-coupon bonds with a remaining life consistent with the expected term of the options. 

 

On June 30, 2021, in connection with the resignation of a member of the Company’s board of directors, the Company entered into a one year consulting contract and extended the life of 25,000 previously issued director options from the contractual 90 days from termination of service to the earlier of the initial life or two years after service contract completion. The change in estimated fair value of the modified options of $26,577 was charged to current period operations.

 

The following assumptions were used in determining the change in fair value of the modified options at June 30, 2021:

 

Risk-free interest rate

   

0.07% - 0.46

%

Dividend yield

   

0

%

Stock price volatility

   

88.59

%

Expected life

 

1.253 years

 

 

The fair value of all options vesting during the three and six months ended June 30, 2021 of $36,521 and $73,041 and $5,594,152 for the three and six months ended June 30, 2020, respectively, was charged to current period operations.  Unrecognized compensation expense of $255,645 at June 30, 2021 will be expensed in future periods.

 

23

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Warrants (ViralClear)

 

The following table presents information related to warrants (ViralClear) at June 30, 2021:

 

Exercise

   

Number

 

Expiration

Price

   

Outstanding

 

Date

$

5.00

     

473,772

 

November 2027

 

10.00

     

6,575

 

May 2025

         

480,347

   

 

Restricted stock units (ViralClear)

 

The following table summarizes the restricted stock activity for the six months ended June 30, 2021:

 

Restricted shares issued as of December 31, 2020

    1,420,716  

Granted

    -  

Issued

    (40,000

)

Forfeited

    (82,716

)

Total

    1,298,000  

Comprised of:

       

Vested restricted shares as of June 30, 2021

    818,000  

Unvested restricted shares as of June 30, 2021

    480,000  

Total

    1,298,000  

 

On June 30, 2021, in connection with the resignation of a member of the Company’s board of directors, the Company removed contingency requirements and accelerated vesting of 160,000 previously granted ViralClear restricted stock units. The change in the modified restricted stock unit resulted in a $212,959 charge to current period operations.

 

Stock based compensation expense related to restricted stock unit grants of ViralClear was $391,881 and $421,032 for the three and six months ended June 30, 2021 and $1,572,581 and $4,959,996 for the three and six months ended June 30, 2020, respectively. As of June 30, 2021, the stock-based compensation relating to restricted stock of $459,958 remains unamortized. 

 

NOTE 10 NON-CONTROLLING INTEREST

 

On November 7, 2018, the Company formed ViralClear for the purpose to pursue additional applications of the PURE EP™ signal processing technology outside of electrophysiology and subsequently in 2020 was repurposed to develop a broad-spectrum anti-viral agent that had potential against the COVID-19 virus. In late 2020, ViralClear again was repurposed back to pursuing additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology.

 

As of June 30, 2021 and December 31, 2020, the Company had a majority interest in ViralClear of 69.95% and 70.21%, respectively.  

 

A reconciliation of the ViralClear Pharmaceuticals, Inc. non-controlling loss attributable to the Company:

 

Net loss attributable to the non-controlling interest for the three months ended June 30, 2021 (000’s):

 

Net loss

  $ (1,167

)

Average Non-controlling interest percentage of profit/losses

    30.0

%

Net loss attributable to the non-controlling interest

  $ (350

)

 

24

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Net loss attributable to the non-controlling interest for the three months ended June 30, 2020 (000’s):

 

Net loss

  $ (13,111

)

Average Non-controlling interest percentage of profit/losses

    24.1

%

Net loss attributable to the non-controlling interest

  $ (3,158

)

 

Net loss attributable to the non-controlling interest for the six months ended June 30, 2021 (000’s):

 

Net loss

  $ (1,971

)

Average Non-controlling interest percentage of profit/losses

    29.9

%

Net loss attributable to the non-controlling interest

  $ (590

)

 

Net loss attributable to the non-controlling interest for the six months ended June 30, 2020 (000’s):

 

Net loss

  $ (20,732

)

Average Non-controlling interest percentage of profit/losses

    22.1

%

Net loss attributable to the non-controlling interest

  $ (4,586

)

 

The following table summarizes the changes in non-controlling interest for the six months ended June 30, 2021 (000’s):

 

Balance, December 31, 2020

  $ 802  

Allocation of equity to non-controlling interest due to equity-based compensation issued

    162  

Net loss attributable to non-controlling interest

    (590

)

Balance, June 30, 2021

  $ 374  

 

NOTE 11 COMMITMENTS AND CONTINGENCIES

 

Licensing agreements

 

2017 Know-How License Agreement

 

On March 15, 2017, the Company entered into a know-how license agreement with Mayo Foundation for Medical Education and Research whereby the Company was granted an exclusive license, with the right to sublicense, certain know how and patent applications in the field of signal processing, physiologic recording, electrophysiology recording, electrophysiology software and autonomics to develop, make and offer for sale.  The agreement expires in ten years from the effective date.

 

The Company is obligated to pay to Mayo Foundation a 1% or 2% royalty payment on net sales of licensed products, as defined.

 

Patent and Know-How License Agreement EP Software Agreement

 

On November 20, 2019, the Company entered into a patent and know-how license agreement (the “EP Software Agreement”) with Mayo Foundation for Medical Education and Research (“Mayo”).  The EP Software Agreement grants to the Company an exclusive worldwide license, with the right to sublicense, within the field of electrophysiology software and under certain patent rights as described in the EP Software Agreement  (the “Patent Rights”), to make, have made, use, offer for sale, sell and import licensed products and a non-exclusive license to the Company to use the research and development information, materials, technical data, unpatented inventions, trade secrets, know-how and supportive information of Mayo to develop, make, have made, use, offer for sale, sell, and import licensed products. The EP Software Agreement will expire upon the later of either (a) the expiration of the Patent Rights or (b) the 10th anniversary of the date of the first commercial sale of a licensed product, unless earlier terminated by Mayo for the Company’s failure to cure a material breach of the EP Software Agreement, the Company’s or a sublicensee’s commencement of any action or proceedings against Mayo or its affiliates other than for an uncured material breach of the EP Software Agreement by Mayo, or insolvency of the Company.

 

25

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

In connection with the EP Software Agreement, the Company issued to Mayo an 8-year warrant (the “EP Software Warrant”) to purchase 284,455 shares of the Company’s common stock at an exercise price of $6.16.  The EP Software Warrant is immediately exercisable and may be exercised on a cashless basis if there is no effective registration statement registering or a current prospectus available for the resale of the shares underlying the EP Software Warrant. The Company agreed to pay Mayo an upfront consideration of $25,000.  The Company also agreed to make earned royalty payments to Mayo in connection with the Company’s sales of the licensed products to third parties and sublicense income received by the Company and to make milestone payments of up to $625,000 in aggregate.

 

Amended and Restated Patent and Know-How License Agreement Tools Agreement

 

On November 20, 2019, the Company entered into an amended and restated patent and know-how license agreement (the “Tools Agreement”) with Mayo. The Tools Agreement contains terms of license grant substantially identical to the EP Software Agreement, although it is for different patent rights and covers the field of electrophysiology systems.

 

In connection with the Tools Agreement, the Company issued to Mayo an 8-year warrant (the “Tools Warrant”) to purchase 284,455 shares of the Company’s common stock at an exercise price of $6.16.  The Tools Warrant is immediately exercisable and may be exercised on a cashless basis if there is no effective registration statement registering or a current prospectus available for the resale of the shares underlying the Tools Warrant. The Company agreed to pay Mayo an upfront consideration of $100,000.  The Company also agreed to make earned royalty payments to Mayo in connection with the Company’s sales of the licensed products to third parties and sublicense income received by the Company and to make milestone payments of up to $550,000 in aggregate. In June 2021, patent rights were issued (“Valid Claim) as defined whereby the Company paid Milestone one of $75,000.

 

ViralClear Patent and Know-How License Agreement

 

On November 20, 2019, the Company’s majority-owned subsidiary, ViralClear, entered into a patent and know-how license agreement (the “ViralClear Agreement”) with Mayo.  The ViralClear Agreement contains terms of license grant substantially identical to the EP Software Agreement and the Tools Agreement, although it is for different patent rights and covers the field of stimulation and electroporation for hypotension/syncope management, renal and non-renal denervation for hypertension treatment, and for use in treatment of arrhythmias in the autonomic nervous system.

 

In connection with the ViralClear Agreement, NeuroClear issued to Mayo an 8-year warrant (the “ViralClear Warrant”) to purchase 473,772 shares of ViralClear’s common stock at an exercise price of $5.00 per share.  The ViralClear Warrant is immediately exercisable and may be exercised on a cashless basis if there is no effective registration statement registering or a current prospectus available for the resale of the shares underlying the ViralClear Warrant. ViralClear agreed to pay Mayo an upfront consideration of $50,000.  ViralClear also agreed to make earned royalty payments to Mayo in connection with ViralClear’s sales of the licensed products to third parties and sublicense income received by the Company and to make milestone payments of up to $700,000 in aggregate. . In June 2021, patent rights were issued (“Valid Claim) as defined whereby the Company paid Milestone one of $75,000.

 

Trek Therapeutics, PBC

 

In the event of sublicensing, sale, transfer, assignment or similar transaction, ViralClear agreed to pay Trek 10% of the consideration received.

 

As part of the acquired assets, ViralClear received an assignment and licensing rights agreement from Trek with a third-party vendor regarding certain formulas and compounds usage. The agreement calls for milestone payments upon marketing authorization (as amended and defined with respect of product in a particular jurisdiction in the territory, the receipt of all approvals from the relevant regulatory authority necessary to market and sell such product in any such jurisdiction, excluding any pricing approval or reimbursement authorization) in any first and second country of $10 million and $5 million, respectively, in addition to 6% royalty payments.

 

26

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

3LP Advisors LLC (d/b/a Sherpa Technology Group)

 

On November 1, 2017, in connection with Mr. Filler joining the Company’s Board of Directors, the Company entered into a Master Services Agreement with 3LP Advisors LLC (d/b/a Sherpa Technology Group) (“Sherpa”) and an initial statement of work (the “SOW”), pursuant to which Sherpa will develop, execute and expand the Company’s intellectual property strategy over the course of the next approximately 18 months by evaluating the business and technology landscape in which the Company operates, and charting and executing a strategy of patent filing and licensing. In connection with the SOW, the Company paid Sherpa fee of (i) $200,000 in cash, of which $25,000 will be paid on January 1, 2018, with the remainder paid upon completion of certain objectives, and (ii) a ten-year option to purchase up to 120,000 of the Company’s common stock at an exercise of $3.75 per share of common stock, of which 60,000 options vest immediately and 60,000 options were performance conditioned and subsequently vested. The SOW has been extended through 2021 at a monthly rate of $15,000 per month. Mr. Filler is the general counsel and partner of Sherpa. 

 

During the three and six months ended June 30, 2021, the Company paid $45,000 and $90,000 and $72,500 and $147,500 for the three and six months ended June 30, 2020, respectively, as patent costs, consulting fees and expense reimbursements. As of June 30, 2021 and December 31, 2020, there was an unpaid balance of $15,000 and $15,000, respectively. As of June 28, 2021, Mr. Filler is no longer a member of the Company’s board of directors.

 

Defined Contribution Plan

 

Effective January 1, 2019, the Company established a qualified defined contribution plan (the “401(k) Plan”) pursuant to Section 401(k) of the Code, whereby all eligible employees may participate. Participants may elect to defer a percentage of their annual pretax compensation to the 401(k) plan, subject to defined limitations. The Company is required to make contributions to the 401(k) Plan equal to 3 percent of each participant’s eligible compensation, subject to limitations under the Code. For the three and six months ended June 30, 2021, the Company charged operations $56,962 and $128,427 and $43,482 and $81,683 for the three and six months ended June 30, 2020, respectively, for contributions under the 401(k) Plan.

 

Purchase commitments

 

As of June 30, 2021, the Company had aggregate purchase commitments of approximately $2,357,529 for future services or products, some of which are subject to modification or cancellations.

 

Litigation

 

Aurigene Pharmaceutical Services LTD vs. ViralClear Pharmaceuticals Inc. and BioSig Technologies, Inc.

 

On January 8, 2021, Aurigene Pharmaceutical Services, LTD (“Aurigene”) filed a complaint with the United States District Court for the District of Connecticut claiming the Company is in default of certain milestone payments for manufacturing and services under contracts dated June 23, 2020 and July 16, 2020 in aggregate amount of $1,530,000. The Company contends that it is not a proper party to the lawsuit since the agreements at issue were signed by a subsidiary. The Company also contends that Aurigene is not entitled to the relief it seeks, because it did not meet its own obligations under the contracts, including several manufacturing milestones. The Company intends to defend itself vigorously.

 

The Company is subject at times to other legal proceedings and claims, which arise in the ordinary course of its business.  Although occasional adverse decisions or settlements may occur, the Company believes that the final disposition of such matters should not have a material adverse effect on its financial position, results of operations or liquidity.  

 

NOTE 12 SEGMENT REPORTING

 

In accordance with ASC 280-10, the Company reports segment information based on the “management” approach. The management approach designates the internal reporting used by management for making decisions and assessing performance as the source of the Company’s reportable segments. The Company has three reportable segments: BioSig Technologies, Inc. (parent), NeuroClear Technologies, Inc. and ViralClear Pharmaceuticals, Inc.

 

27

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Information concerning the operations of the Company’s reportable segments is as follows:

 

Summary Unaudited condensed consolidated Statement of Operations for the three months ended June 30, 2021 (000’s):

 

   

BioSig

Technologies, Inc.

   

ViralClear

Pharmaceuticals, Inc.

   

NeuroClear

Technologies,

Inc.

   

Total

 

Revenue:

                               

Product sales

  $ 199     $ -     $ -     $ 199  

Service

    8       -       -       8  

Total Revenue

    207       -       -       207  
                                 

Cost of goods sold

    62       -       -       62  
                                 

Gross profit

    145       -       -       145  
                                 

Operating expenses:

                               

Research and development

    1,455       212       -       1,667  

General and administrative

    5,523       953       4       6,480  

Depreciation and amortization

    48       1       -       49  

Total operating expenses

    7,026       1,166       4       8,196  
                                 

Loss from operations

    (6,881

)

    (1,166

)

    (4

)

    (8,051

)

                                 

Other income:

                               

Interest income and other income, net

    -       -       -       -  
                                 

Net loss

  $ (6,881

)

  $ (1,166

)

  $ (4

)

  $ (8,051

)

 

Summary Unaudited condensed consolidated Statement of Operations for the three months ended June 30, 2020 (000’s):

 

   

BioSig

Technologies, Inc

   

ViralClear

Pharmaceuticals, Inc.

   

Total

 

Operating expenses:

                       

Research and development

  $ 1,087     $ 4,631     $ 5,718  

General and administrative

    8,128       8,480       16,608  

Depreciation and amortization

    22       -       22  

Total operating expenses

    9,237       13,111       22,348  
                         

Loss from Operations

    (9,237

)

    (13,111

)

    (22,348

)

                         

Other income:

                       

Interest income and other income, net

    2       -       2  
                         

Net loss

  $ (9,235

)

  $ (13,111

)

  $ (22,346

)

 

28

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Summary Unaudited condensed consolidated Statement of Operations for the six months ended June 30, 2021 (000’s):

 

   

BioSig

Technologies, Inc.

   

ViralClear

Pharmaceuticals, Inc.

   

NeuroClear

Technologies,

Inc.

   

Total

 

Revenue:

                               

Product sales

  $ 314     $ -     $ -     $ 314  

Service

    11       -       -       11  

Total Revenue

    325       -       -       325  
                                 

Cost of goods sold

    161       -       -       161  
                                 

Gross profit

    164       -       -       164  
                                 

Operating expenses:

                               

Research and development

    2,731       202       -       2,933  

General and administrative

    11,980       1,767       4       13,751  

Depreciation and amortization

    89       2       -       91  

Total operating expenses

    14,800       1,971       4       16,775  
                                 

Loss from operations

    (14,636

)

    (1,971

)

    (4

)

    (16,611

)

                                 

Other income:

                               

Interest income and other income, net

    1       -       -       1  
                                 

Net loss

  $ (14,635

)

  $ (1,971

)

  $ (4

)

  $ (16,610

)

 

Summary Unaudited condensed consolidated Statement of Operations for the six months ended June 30, 2020 (000’s):

 

   

BioSig

Technologies, Inc

   

ViralClear

Pharmaceuticals, Inc.

   

Total

 

Operating expenses:

                       

Research and development

  $ 2,414     $ 8,231     $ 10,645  

General and administrative

    11,949       12,515       24,464  

Depreciation and amortization

    43       -       43  

Total operating expenses

    14,406       20,746       35,152  
                         

Loss from Operations

    (14,406

)

    (20,746

)

    (35,152

)

                         

Other income:

                       

Interest and other income, net

    28       14       42  
                         

Net loss

  $ (14,378

)

  $ (20,732

)

  $ (35,110

)

 

29

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Summary of assets at June 30, 2021 (000’s):

 

 

   

BioSig

Technologies, Inc.

   

ViralClear

Pharmaceuticals, Inc.

   

NeuroClear

Technologies,

Inc.

   

Total

 

Cash

  $ 12,445     $ 3,059     $ -     $ 15,504  

Accounts receivable

    199       -       -       199  

Inventory

    731       -       -       731  

Other current assets

    513       2       -       515  

Total operating assets

    13,888       3,061       -       16,949  
                                 

Property and equipment, net

    382       6       -       388  

Right-to-use assets, net 

    252       -       -       252  

Other assets

    438       -       -       438  
                                 

Total assets

  $ 14,960     $ 3,067     $ -     $ 18,027  

 

NOTE 13 RELATED PARTY TRANSACTIONS

 

At June 30, 2021 and December 31, 2020, the Company had reimbursable travel, compensation and other related expenses due related parties of $80,000 and $317,000, respectively.

 

On November 1, 2017, in connection with Mr. Filler joining the Company’s Board of Directors, the Company entered into a Master Services Agreement with 3LP Advisors LLC (d/b/a Sherpa Technology Group) (“Sherpa”) and an initial statement of work (the “SOW”), pursuant to which Sherpa will develop, execute and expand the Company’s intellectual property strategy over the course of the next approximately 18 months by evaluating the business and technology landscape in which the Company operates, and charting and executing a strategy of patent filing and licensing. In connection with the SOW, the Company paid Sherpa fee of (i) $200,000 in cash, of which $25,000 was paid on January 1, 2018, with the remainder to be paid upon completion of certain objectives, and (ii) a ten-year option to purchase up to 120,000 of the Company’s common stock at an exercise of $3.75 per share of common stock, of which 60,000 options vest immediately and 60,000 options were performance conditioned and subsequently vested.  Mr. Filler is the general counsel and partner of Sherpa. 

 

During the three and six months ended June 30, 2021, the Company paid $45,000 and $90,000 and $72,500 and $147,500 for the three and six months ended June 30, 2020, respectively, as patent costs, consulting fees and expense reimbursements. As of June 30, 2021 and December 31, 2020, there was an unpaid balance of $15,000 and $15,000, respectively. As of June 28, 2021, Mr. Filler is no longer a member of the Company’s board of directors.

 

On January 5, 2021, the Company issued an aggregate of 450,000 shares of common stock to officers of the Company as part of annual compensation.

 

NOTE 14 – FAIR VALUE MEASUREMENT

 

The Company adopted the provisions of Accounting Standards Codification subtopic 825-10, Financial Instruments (“ASC 825-10”). ASC 825-10 defines fair value as the price that would be received from selling an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. When determining the fair value measurements for assets and liabilities required or permitted to be recorded at fair value, the Company considers the principal or most advantageous market in which it would transact and considers assumptions that market participants would use when pricing the asset or liability, such as inherent risk, transfer restrictions, and risk of nonperformance. ASC 825-10 establishes a fair value hierarchy that requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value. ASC 825-10 establishes three levels of inputs that may be used to measure fair value:

 

Level 3 – Unobservable inputs to the valuation methodology that are significant to the measurement of fair value of assets or liabilities.

 

All items required to be recorded or measured on a recurring basis are based upon level 3 inputs.

 

30

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

To the extent that valuation is based on models or inputs that are less observable or unobservable in the market, the determination of fair value requires more judgment. In certain cases, the inputs used to measure fair value may fall into different levels of the fair value hierarchy. In such cases, for disclosure purposes, the level in the fair value hierarchy within which the fair value measurement is disclosed and is determined based on the lowest level input that is significant to the fair value measurement.

 

The carrying value of the Company’s cash and cash equivalents, accounts payable and other current assets and liabilities approximate fair value because of their short-term maturity.

 

As of June 30, 2021, and December 31, 2020, the Company did not have any items that would be classified as level 1, 2 or 3 disclosures.

 

As of June 30, 2021, and December 31, 2020, the Company did not have any derivative instruments that were designated as hedges.

 

There were no derivative and warrant liability as of June 30, 2021 and December 31, 2020.

 

NOTE 15 SUBSEQUENT EVENTS

 

Equity issuances:

 

On July 1, 2021, the Company issued 80,000 shares of its common stock to a consultant for services rendered valued at $348,000.

 

On July 1, 2021, ViralClear issued 206,250 shares of its common stock in exchange for the cashless exercise of 550,000 options previously granted on October 16, 2019.

 

On July 6, 2021, the Company issued 28,750 shares of its common stock for vested restricted stock units.

 

On July 12, 2021, the Company issued 16,310 shares of its common stock in connection with the resignation of a member of the Company’s board of directors on June 30, 2021 for services rendered valued at $62,957.

 

On July 12, 2021, the Company issued 50,000 shares of its common stock for fully vested restricted stock units.

 

On July 30, 2021, the Company issued an aggregate of 13,321 shares of its common stock for services.

 

On August 2, 2021, the Company issued 30,000 shares of its common stock for accelerated vested restricted stock units dated January 4, 2021.

 

On August 3, 2021, the Company granted an aggregated of 75,000 options to purchase shares of its common stock to three employees. The options are exercisable at $3.61 per share for ten years with one-third vesting on the first anniversary of the date of grant, and the remaining two-thirds vesting in substantially equal quarterly installments over the following two years.

 

Equity financing

 

On July 2, 2021, the Company entered into an underwriting agreement (the “Underwriting Agreement”) with Laidlaw & Company (UK) Ltd. (the “Underwriter”), relating to an underwritten public offering of 2,500,000 shares (the “Shares”) of the Company’s common stock, $0.001 par value per share (the “Common Stock”). All of the Shares were sold by the Company. The public offering price of the Shares was $4.00 per share, and the Underwriter agreed to purchase the Shares from the Company pursuant to the Underwriting Agreement at a price of $3.68 per share. After the underwriting discount and offering expenses, the Company received net proceeds from the offering of approximately $9.1 million. Pursuant to the Underwriting Agreement, the Company has also granted the Underwriter an option to purchase up to 375,000 additional shares of Common Stock, or 15% of the number of Shares sold in the offering, at a price of $3.68 per share, for a period of 30 days from the date of the Underwriting Agreement, of which none were exercised.

 

31

 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2021

(unaudited)

 

Pursuant to the Underwriting Agreement, the Company issued to the Underwriter or its designees warrants to purchase up to an aggregate 125,000 shares of Common Stock, or 5% of the number of Shares sold in the offering (the “Underwriter Warrants”). The Underwriter Warrants are exercisable following the date of issuance, July 7, 2021 and ending five years from the date of the execution of the Underwriting Agreement, July 2, 2026, at a price per share equal to $4.80 per share (120% of the public offering price per Share) and are exercisable on a “cashless” basis. The Company also agreed to reimburse the Underwriter for certain of their out-of-pocket expenses incurred in connection with the offering, including, among other things, the reasonable fees and expenses of counsel, which fees and expenses may not exceed $100,000.

 

Operating leases:

 

On August 2, 2021, the Company executed the extension of its Rochester, Minnesota office lease for an additional 24 months beginning November 1, 2021 through October 31, 2023. During the extended period, the Company’s base rent will remain the same for the first year and increase 3% in the second year.

 

On August 3, 2021, the Company entered into a lease agreement whereby the Company leased approximately 6,600 square feet of office space in Westport, Connecticut commencing September 1, 2021 and expiring on December 31, 2024 at an initial rate of $14,828 per month with escalating payments. The lease agreement includes rent abatement for the first 4 months with rental payments commencing on January 1, 2022. At the lease execution date, the Company estimated the lease liability and the right of use assets at present value using the Company’s estimated incremental borrowing rate of 6.5%. In conjunction with the lease, the Company terminated, without penalty, the lease at 54 Wilton Road, Westport, CT effective September 4, 2021.

 

 

 

32

 

ITEM 2.  MANAGEMENTS DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

 

This Managements Discussion and Analysis of Financial Condition and Results of Operations includes a number of forward-looking statements that reflect Managements current views with respect to future events and financial performance. You can identify these statements by forward-looking words such as may, will, expect, anticipate, believe, estimate and continue, or similar words. Those statements include statements regarding the intent, belief or current expectations of us and members of our management team as well as the assumptions on which such statements are based. Prospective investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risk and uncertainties, and that actual results may differ materially from those contemplated by such forward-looking statements.

 

Readers are urged to carefully review and consider the various disclosures made by us in this report and in our other reports filed with the Securities and Exchange Commission. Important factors currently known to Management could cause actual results to differ materially from those in forward-looking statements. We undertake no obligation to update or revise forward-looking statements to reflect changed assumptions, the occurrence of unanticipated events or changes in the future operating results over time. We believe that our assumptions are based upon reasonable data derived from and known about our business and operations. No assurances are made that actual results of operations or the results of our future activities will not differ materially from our assumptions. Factors that could cause differences include, but are not limited to, expected market demand for our products, fluctuations in pricing for materials, and competition.

 

Business Overview

 

BioSig Technologies, Inc.

 

We are a medical technology company that is commercializing our PURE EP™ System which is an advanced signal acquisition and processing platform designed to provide essential diagnostic signals with high clinical value in all types of cardiac catheter ablations.

 

PURE EP™ is designed to address long-standing limitations that slow and disrupt cardiac catheter ablation procedures, such as environmental lab noise, signal saturation, slow signal recovery, and inaccurate display of fractionated potentials.

 

Cardiac catheter ablation is a procedure that involves delivery of energy through the tip of a catheter that scars or destroys heart tissue to correct heart rhythm disturbances. In August 2018, we received 510(k) clearance from the U.S. Food and Drug Administration (the “FDA”) to market our PURE (Precise Uninterrupted Real-time evaluation of Electrograms) EP™ System.

 

PURE EP™ is a signal processing platform that combines advanced hardware and software to address known challenges associated to signal acquisition, to enable electrophysiologists to see more signals and analyze them in real-time. The device aims to minimize noise and artifacts from cardiac recordings and acquire high-fidelity cardiac signals. Improving fidelity of acquired cardiac signals may potentially increase the diagnostic value of these signals, thereby possibly improving accuracy and efficiency of the EP studies and ablation procedures.

 

Our initial focus is on improving intracardiac signal acquisition and enhancing diagnostic information for catheter ablation procedures for complex arrhythmias like ventricular tachycardia (“VT”), a potentially life-threatening arrhythmia, and atrial fibrillation (“AF”), the most common cardiac arrhythmia associated with a fivefold risk of stroke.

 

During 2019, we began conducting our first clinical observational patient cases using the PURE EP™ System at Texas Cardiac Arrhythmia Institute at St. David’s Medical Center in Austin, Texas; Prisma Health at Greenville Health System in South Carolina; Indiana University; and Santa Barbara Cottage Hospital in California.

 

The initial experience across these early evaluation centers showed that the PURE EP™ System functions as designed: we received positive feedback from the EP users about the improved signal detection and fidelity during ablation procedures on patients with various arrhythmias, such as ischemic ventricular tachycardia, AF, atypical flutter, atrioventricular nodal reentry tachycardia (AVNRT), supraventricular tachycardia, premature ventricular contractions (PVC), and a rare case of dual septal pathway.

 

In November 2019, we commenced our first clinical study for the PURE EP™ System titled, “Novel Cardiac Signal Processing System for Electrophysiology Procedures (PURE EP 2.0 Study).” Texas Cardiac Arrhythmia Research Foundation (TCARF) in Austin, Texas, was the first institution to conduct patient cases under the clinical study; Mayo Clinic in Jacksonville, Florida was the second institution; and Massachusetts General Hospital (MGH) was the third to conduct patient cases under the same clinical study.

 

33

 

On April 13, 2021, we announced the completion of the enrollment in the PURE EP 2.0 Study. A total of 51 cardiac ablation procedures have been evaluated (>400 cardiac signal samples) across the three medical centers of excellence with unblinded clinical data initially released during a conference call on July 26, 2021, and at the Heart Rhythm 2021 convention with a physician presentation titled, “PURE EP: Clinical Data to Clinical Applications” delivered by Christopher McLeod, M.D., Ch.B. of Mayo Clinic in Jacksonville, Florida.

 

The PURE EP 2.0 Study showed 93.6% of the PURE EP signals were rated as superior or equivalent for the cumulative dataset with a superior rating seen 4x more often than equivalent. The study manuscript is currently in review for publication.

 

The PURE EP 2.0 Study objective was to validate the superiority quality of the PURE EP signals and determine the clinical value of the PURE EP signal when compared to conventional sources.

 

We continue to install PURE EP™ Systems at centers of excellence for clinical evaluation under our market development plan. The PURE EP™ System has been utilized at several institutions, including the University of Pennsylvania Hospital; Overland Park Regional Medical System in Overland Park, Kansas; Deborah Heart and Lung Center in Browns Mills, New Jersey; Houston Methodist in Texas; and Medical City North Hills in North Richland Hills, Texas.

 

To date, more than 1,100 patient procedures have been conducted with the PURE EP System by more than 50 electrophysiologists across eleven different clinical sites in the United States.

 

In addition to clinical evaluation, we have conducted pre-clinical evaluation under several study protocols with the PURE EP™ System. At Mayo Clinic in Rochester, Minnesota, we have performed twenty-five experiments in various animal models; we also conducted a pre-clinical study at the Mount Sinai Hospital in New York, New York, with an emphasis on the VT model; and six experiments to date during a study at the University of Pennsylvania. We intend to continue additional research and development studies with our technology at Mayo Clinic and the University of Pennsylvania. We also intend to continue additional clinical external evaluation at a select number of other centers.

 

We have made progress towards obtaining a European CE marking certificate for medical devices. We have commenced audit preparation for the International Organization for Standardization (“ISO”) 13485 with the expectation to proceed with the audit to obtain the ISO 13485 Certification in the second half of 2021 and CE Marking in the first half of 2022, subject to the guidance from the European notified body.

 

In December 2020, we announced that three PURE EP™ Systems were contracted for purchase by St David’s Healthcare of Austin, Texas and were subsequently sold in February 2021. These units were our first commercial sale. We also sold two PURE EP™ Systems to Mayo Foundation for Medical Education and Research in 2021 and we are in active discussions with several accounts about the acquisition of the PURE EP™ System. We anticipate our initial customers will be medical centers of excellence and other healthcare facilities that operate EP labs.

 

ViralClear Pharmaceuticals, Inc.

 

ViralClear Pharmaceuticals, Inc. (“ViralClear”) is a majority-owned subsidiary of the Company originally known as NeuroClear Technologies, Inc. The subsidiary was established November 2018 to pursue additional applications of the PURE EP™ signal processing technology outside of EP. In March 2020, it was renamed ViralClear to develop merimepodib, a broad-spectrum anti-viral agent that showed potential to treat COVID-19. We currently do not intend to further develop merimepodib. As of June 30, 2021, the Company retains 69.95% ownership of ViralClear.

 

Results of Operations (000s)

 

We anticipate that our results of operations will fluctuate for the foreseeable future due to several factors, such as the progress of our research and development and commercialization efforts, the timing and outcome of future regulatory submissions and uncertainty around the current pandemic. Due to these uncertainties, accurate predictions of future operations are difficult or impossible to make.

 

Three Months Ended June 30, 2021 Compared to Three Months Ended June 30, 2020 (000s)

 

Revenues and Cost of Goods Sold. Revenue for the three months ended June 30, 2021 totaled $207 comprised of product sales of $199 and recognized service revenue of $8 as compared to nil for the three months ended June 30, 2020.

 

We derive our revenue primarily from the sale of our medical device, PURE EP system, as well as related support and maintenance services and software upgrades in connection with the system.

 

34

 

We recognize revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

 

Cost of sales for the three months ended June 30, 2021 was $62 comprised of the delivered product as compared to nil for the three months ended June 30, 2020.

 

Gross profit from the three months ended June 30, 2021 was $145 or 70.05% as compared to nil for the three months ended June 30, 2020.

 

Research and Development Expenses. Research and development expenses for the three months ended June 30, 2021 were $1,667, a decrease of $4,051, or 70.85%, from $5,718 for the three months ended June 30, 2020. This decrease is primarily due to acquired research and development cost incurred during the three months ended June 30, 2020 of $2,355 in the ViralClear segment as compared to $150 for the current period and the ceasing of Merimepodib development in 2020. Research and development expenses were comprised of the following:

 

Three months ended:

 

   

June 30,

2021

(000’s)

   

June 30,

2020

(000’s)

 

Salaries and equity compensation

  $ 776     $ 757  

Consulting expenses

    165       1,145  

Research and clinical studies and design work

    396       319  

Acquired Research and Development

    150       2,355  

Data/AI development

    84       126  

Regulatory

    9       5  

Product development

    -       833  

Formulation

    -       115  

Travel, supplies, other

    87       63  

Total

  $ 1,667     $ 5,718  

 

Stock based compensation for research and development personnel was $16 and $274 for the three months ended June 30, 2021 and 2020, respectively.

 

General and Administrative Expenses. General and administrative expenses for the three months ended June 30, 2021 were $6,480, a decrease of $10,128, or 61.0%, from $16,608 incurred in the three months ended June 30, 2020. This decrease is primarily due to reduction in the activities of our ViralClear segment, net with an increase in employee performance pay and staff in the current period as compared to the same period in the prior year and additional service provider fees paid.

 

Payroll related expenses decreased to $2,124 in the current period from $2,185 for the three months ended June 30, 2020, a decrease of $61, or 2.8%.  The decrease was due to reduction in 2021 of the ViralClear pharma operations, net with performance pay and added staff in the later part of 2020 and 2021 for commercialization and support personnel.  We incurred $1,965 in stock-based compensation in connection with the vesting of stock and stock options issued to board members, officers, employees and consultants for the three months ended June 30, 2021 as compared to $11,058 in stock-based compensation for the same period in 2020.

 

Professional services for the three months ended June 30, 2021 totaled $384, a decrease of $289, or 42.9%, over the $673 recognized for the three months ended June 30, 2020. Of professional services, legal fees totaled $248 for the three months ended June 30, 2021; a decrease of $320, or 56.3%, from $568 incurred for the three months ended June 30, 2020. The decrease is primarily due to costs incurred in 2020 for financing, contract work and patent filings for the ViralClear segment not incurred in current period. Accounting fees incurred in the three months ended June 30, 2021 amounted to $39, a decrease of $66, or 62.9%, from $105 incurred in same period last year. In 2020, we incurred additional audit costs associated with internal control and ViralClear audits in addition to our yearend requirements. 

 

35

 

Consulting, public and investor relations fees for the three months ended June 30, 2021 were $758 as compared to $1,528 incurred for the three months ended June 30, 2020, a decrease of $770, or 50.4%. The decrease in consulting, marketing and investor relations fees during the three months ended June 30, 2021 related to our ceasing pharma operations in 2020 in the ViralClear segment, net with our continued efforts to develop our recognition throughout the medical industry in an effective manner.

 

Travel, meals and entertainment costs for the three months ended June 30, 2021 were $309, an increase of $260, or 530.6%, from $49 incurred in the three months ended June 30, 2020. Travel, meals and entertainment costs include travel related to business development and financing. The increase in 2021 was due to the lifting of various restrictions imposed by the COVID-19 outbreak leading to increased commercialization effort in 2021 as compared to 2020.

 

Rent for the three months ended June 30, 2021 totaled $117, an increase of $2, or 1.7%, from $119 incurred in three months ended June 30, 2020. The increase in rent for 2021 as compared to 2020 is due primarily increase in warehousing costs in 2021.  

 

Depreciation and Amortization Expense. Depreciation and amortization expense for the three months ended June 30, 2021 totaled $49, an increase of $27, or 122.7%, over the expense of $22 incurred in the three months ended June 30, 2020, as a result of the adding additional office computers and other equipment.

 

Preferred Stock Dividend. Preferred stock dividend for the three months ended June 30, 2021 totaled $3, a decrease of $2, or 40.0%, from $5 incurred during the three months ended June 30, 2020. Preferred stock dividends are related to the dividends accrued on our Series C Preferred Stock issued during the period from 2013 through 2015. The decrease in 2021 as compared to 2020 is the result of conversions in 2020.  

 

Net Loss available to BioSig Technologies, Inc. Common Shareholders. As a result of the foregoing, net loss available to common shareholders for the three months ended June 30, 2021 was $7,704 compared to a net loss of $19,193 for the three months ended June 30, 2020.

 

Six Months Ended June 30, 2021 Compared to Six Months Ended June 30, 2020 (000s)

 

Revenues and Cost of Goods Sold. Revenue for the six months ended June 30, 2021 totaled $325 comprised of product sales of $314 and recognized service revenue of $11 as compared to nil for the six months ended June 30, 2020.

 

We derive our revenue primarily from the sale of our medical device, PURE EP system, as well as related support and maintenance services and software upgrades in connection with the system.

 

We recognize revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

 

Cost of sales for the six months ended June 30, 2021 was $161 comprised of the delivered product as compared to nil for the six months ended June 30, 2020.

 

Gross profit for the six months ended June 30, 2021 was $164 or 50.5% as compared to nil for the six months ended June 30, 2020.

 

Research and Development Expenses. Research and development expenses for the six months ended June 30, 2021 were $2,933, a decrease of $7,712, or 72.4%, from $10,645 for the six months ended June 30, 2020. This decrease is primarily due to acquired research and development cost incurred during the six months ended June 30, 2020 of $5,880 in the ViralClear segment as compared to $150 for the current period and the ceasing of pharma development in 2020. Research and development expenses were comprised of the following:

 

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Six months ended:

 

   

June 30,

2021

(000’s)

   

June 30,

2020

(000’s)

 

Salaries and equity compensation

  $ 1,275     $ 1,649  

Consulting expenses

    354       1,264  

Research and clinical studies and design work

    691       485  

Acquired Research and Development

    150       5,880  

Data/AI development

    211       252  

Regulatory

    68       31  

Product development

    15       833  

Formulation

    -       115  

Travel, supplies, other

    169       136  

Total

  $ 2,933     $ 10,645  

 

Stock based compensation for research and development personnel was $83 and $588 for the six months ended June 30, 2021 and 2020, respectively.

 

General and Administrative Expenses. General and administrative expenses for the six months ended June 30, 2021 were $13,751, a decrease of $10,713, or 43.8%, from $24,464 incurred in the six months ended June 30, 2020. This decrease is primarily due to reduction in the activities of our ViralClear segment, net with an increase in employee performance pay and staff in the current period as compared to the same period in the prior year and additional service provider fees paid.

 

Payroll related expenses increased to $3,973 in the current period from $3,488 for the six months ended June 30, 2020, an increase of $485, or 13.9%.  The increase was due to performance pay and added staff in the later part of 2020 and 2021 for commercialization and support personnel.  We incurred $4,551 in stock-based compensation in connection with the vesting of stock and stock options issued to board members, officers, employees and consultants for the six months ended June 30, 2021 as compared to $15,157 in stock-based compensation for the same period in 2020.

 

Professional services for the six months ended June 30, 2021 totaled $764, a decrease of $400, or 34.4%, over the $1,164 recognized for the six months ended June 30, 2020. Of professional services, legal fees totaled $556 for the six months ended June 30, 2021; a decrease of $398, or 41.7%, from $954 incurred for the six months ended June 30, 2020. The decrease is primarily due to costs incurred in 2020 for financing. Accounting fees incurred in the six months ended June 30, 2021 amounted to $111, a decrease of $100 or 47.4%, from $211 incurred in same period last year. In 2020, we incurred additional audit costs associated with internal control and ViralClear audits in addition to our yearend requirements. 

 

Consulting, public and investor relations fees for the six months ended June 30, 2021 were $2,132 as compared to $2,814 incurred for the six months ended June 30, 2020, a decrease of $682, or 24.2%. The decrease in consulting, marketing and investor relations fees during the six months ended June 30, 2021 related to our continued efforts to develop our recognition throughout the medical industry in an effective manner.

 

Travel, meals and entertainment costs for the six months ended June 30, 2021 were $418, an increase of $165, or 65.2%, from $253 incurred in the six months ended June 30, 2020. Travel, meals and entertainment costs include travel related to business development and financing. The increase in 2021 was due to lifting of various restrictions imposed by the COVID-19 outbreak as compared to 2020.

 

Rent for the six months ended June 30, 2021 totaled $234, an increase of $4, or 1.7%, from $238 incurred in six months ended June 30, 2020. The increase in rent for 2021 as compared to 2020 is due primarily to temporary rentals in 2021 as compared to 2020.  

 

Depreciation and Amortization Expense. Depreciation and amortization expense for the six months ended June 30, 2021 totaled $91, an increase of $48, or 111.6%, over the expense of $43 incurred in the six months ended June 30, 2020, as a result of the adding additional office computers and other equipment.

 

Preferred Stock Dividend. Preferred stock dividend for the six months ended June 30, 2021 totaled $5, a decrease of $4, or 44.4% from $9 incurred during the six months ended June 30, 2020. Preferred stock dividends are related to the dividends accrued on our Series C Preferred Stock issued during the period from 2013 through 2015. The decrease in 2021 as compared to 2020 is the result of conversions in 2020.  

 

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Net Loss available to BioSig Technologies, Inc. Common Shareholders. As a result of the foregoing, net loss available to common shareholders for the six months ended June 30, 2021 was $16,025 compared to a net loss of $30,533 for the six months ended June 30, 2020.

 

Segment Results

 

The Company reports segment information based on the “management” approach. The management approach designates the internal reporting used by management for making decisions and assessing performance as the source of the Company’s reportable segments.

 

Summary Statement of Operations for the three and six months ended June 30, 2021 as compared to the three and six months ended June 30, 2020 are detailed in Note 12 of the accompanying unaudited condensed consolidated financial statements.

 

COVID-19

 

On March 11, 2020, the World Health Organization (the “WHO”) declared a pandemic related to the rapidly spreading coronavirus (COVID-19) outbreak, which has led to a global health emergency. The full public-health impact of the ongoing pandemic is currently indeterminable and rapidly evolving, and the related health crisis has adversely affected and may continue to adversely affect the global economy, resulting in delaying to our commercialization objectives of the PURE EP Systems into 2022.

 

Liquidity and Capital Resources ($000s)

 

As of June 30, 2021, we had a working capital of $13,566, comprised of cash of $15,504, accounts receivable of $199, inventory of $731 and prepaid expenses and vendor deposits of $515, which was offset by $3,027 of accounts payable and accrued expenses, accrued dividends on preferred stock issuances of $77 and current portions of deferred revenue of $32 and of lease liability of $247.  For the six months ended June 30, 2021, we used $13,910 of cash in operating activities and $182 of cash in investing activities.

 

Six Months Ended June 30, 2021 Compared to Six Months Ended June 30, 2020 (000s)

 

Cash provided by financing activities totaled $1,328, comprised of proceeds from the sale of our common stock under our at-the-marketing offering of $1,300 and proceeds from exercise of options of $28.

 

In the comparable period in 2020, our aggregate cash provided by financing activities totaled $39,070, comprised of proceeds from the sale of our common stock of $25,214, proceeds from the sale of our subsidiary common stock of $10,592 and proceeds from exercise of options and warrants of $3,264. At June 30, 2021, we had cash of $15,504 compared to $36,927 at June 30, 2020. Our cash is held in bank deposit accounts. At June 30, 2021 and June 30, 2020, we had no convertible debentures outstanding.

 

Cash used in operations for the six months ended June 30, 2021 and 2020 was $13,910 and $14,223, respectively, which represent cash outlays for research and development and general and administrative expenses in such periods. The decreases in cash outlays principally resulted from ceasing our ViralClear segment’s pharma operations in 2020, net with additional operating costs, general and administrative expenses in 2021 and with an increase in our operating assets of $371 and a decrease in our operating liabilities of $1,884.

 

We used $182 cash for investing activities for the six months ended June 30, 2021, compared to $28 for the six months ended June 30, 2020.  For the current period and comparable period, we purchased computer and other equipment.

 

We had an accumulated deficit as of June 30, 2021 of $173.0, as well as a net loss attributable to BioSig Technologies, Inc. of $16.0 and negative operating cash flows. We expect to continue incurring losses and negative cash flows from operations until our products (primarily PURE EP System) reach full commercial profitability. We believe that our existing cash on hand will be sufficient to enable us to fund our projected operating requirements for approximately one year and a day from the date of filing of this report. However, we may need to raise additional funds more quickly if one or more of our assumptions prove to be incorrect or if we choose to expand our product development efforts more rapidly than we presently anticipate. We also may decide to raise additional funds before we require them if we are presented with favorable terms for raising capital.

 

Our plans include the continued commercialization of the PURE EP System and other applications of our core technology and raising capital through the sale of additional equity securities, debt or capital inflows from strategic partnerships. There are no assurances, however, that we will be successful in obtaining the level of financing needed for our operations. The ongoing COVID-19 pandemic has resulted and continues to result in significant financial market volatility and uncertainty in recent months.

 

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A continuation or worsening of the levels of market disruption and volatility seen in the recent past could have an adverse effect on our ability to access capital and on the market price of our common stock, and we may not be able to successfully raise capital through the sale of our securities.

 

Our Series C Preferred Stock contains triggering events which would, among other things, require redemption (i) in cash, at the greater of (a) 120% of the stated value of $1 or (b) the product of (I) the variable weighted average price of our common stock on the trading day immediately preceding the date of the triggering event and (II) the stated value divided by the then conversion price or (ii) in shares of our common stock, equal to a number of shares equal to the amount set forth in (i) above divided by 75%. As of June 30, 2021, the aggregate stated value of our Series C Preferred Stock was $105. The triggering events include our being subject to a judgment of greater than $100 or our initiation of bankruptcy proceedings. If any of the triggering events contained in our Series C Preferred Stock occur, the holders of our Series C Preferred Stock may demand redemption, an obligation we may not have the ability to meet at the time of such demand.  We will be required to pay interest on any amounts remaining unpaid after the required redemption of our Series C Preferred Stock, at a rate equal to the lesser of 18% per annum or the maximum rate permitted by applicable law.

 

We expect to incur losses from operations for the near future. We expect to incur increasing marketing and commercialization expenses related to our PURE EP system in addition to additional research and development costs relating to the PURE EP and other product candidates, including expenses related to clinical trials. We expect that our general and administrative expenses will increase in the future as we expand our business development, add infrastructure and incur additional costs related to being a public company, including incremental audit fees, investor relations programs and increased professional services.

 

Our future capital requirements will depend on a number of factors, including the progress of our research and development of product candidates, the timing and outcome of regulatory approvals, the costs involved in preparing, filing, prosecuting, maintaining, defending and enforcing patent claims and other intellectual property rights, the status of competitive products, the availability of financing and our success in developing markets for our product candidates.

 

Future financing may include the issuance of equity or debt securities, obtaining credit facilities, or other financing mechanisms. Even if we are able to raise the funds required, it is possible that we could incur unexpected costs and expenses or experience unexpected cash requirements that would force us to seek alternative financing. Furthermore, if we issue additional equity or debt securities, existing holders of our securities may experience additional dilution or the new equity securities may have rights, preferences or privileges senior to those of existing holders of our securities.

 

If additional financing is not available or is not available on acceptable terms, we may be required to delay, reduce the scope of or eliminate our research and development programs, reduce our commercialization efforts or obtain funds through arrangements with collaborative partners or others that may require us to relinquish rights to certain product candidates that we might otherwise seek to develop or commercialize independently.

 

Equity Financing

 

On July 2, 2021, we entered into an underwriting agreement (the “Underwriting Agreement”) with Laidlaw & Company (UK) Ltd. (the “Underwriter”), relating to an underwritten public offering of 2,500,000 shares (the “Shares”) of the Company’s common stock. All the Shares were sold by the Company. The public offering price of the Shares was $4.00 per share, and the Underwriter agreed to purchase the Shares from us pursuant to the Underwriting Agreement at a price of $3.68 per share. After the underwriting discount and offering expenses, we received net proceeds from the offering of approximately $9,100.

 

Pursuant to the Underwriting Agreement, we also granted the Underwriter an option to purchase up to 375,000 additional shares of Common Stock, or 15% of the number of Shares sold in the offering, at a price of $3.68 per share, for a period of 30 days from the date of the Underwriting Agreement. None were exercised.

 

Pursuant to the Underwriting Agreement, we issued to the Underwriter or its designees warrants to purchase up to an aggregate 125,000 shares of common stock, or 5% of the number of Shares sold in the offering (the “Underwriter Warrants”). The Underwriter Warrants are exercisable as of the date of issuance and ending July 2, 2026, at a price per share equal to $4.80 per share (120% of the public offering price per Share) and are exercisable on a “cashless” basis. We also agreed to reimburse the Underwriter for certain of their out-of-pocket expenses incurred in connection with the offering, including, among other things, the reasonable fees and expenses of counsel, which fees and expenses may not exceed $100.

 

The Shares were sold and issued pursuant to the Company’s shelf registration statement on Form S-3 (Registration Statement No. 333-251859) previously filed with the Securities and Exchange Commission and declared effective by the Securities and Exchange Commission on January 12, 2021. A preliminary prospectus supplement and prospectus supplement and the accompanying prospectus relating to the offering have been filed with the Securities and Exchange Commission. The offering closed on July 7, 2021.

 

39

 

Off-Balance Sheet Arrangements

 

We do not have any off-balance sheet arrangements.

 

Critical Accounting Policies and Estimates

 

Our discussion and analysis of our financial condition and results of operations are based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities and expenses. We evaluate our estimates and judgments on an ongoing basis. We base our estimates on historical experience and on assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates.

 

We believe the following critical accounting policies affect our more significant judgments and estimates used in the preparation of our financial statements.

 

Revenue Recognition

 

We derive its revenue primarily from the sale of its medical device, the PURE EP™ System, and well as related support and maintenance services and software upgrades in connection with the system.

 

We recognize revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

 

We determine revenue recognition through the following five steps:

 

 

Identify the contract with the customer;

 

 

Identify the performance obligations in the contract;

 

 

Determine the transaction price;

     
 

Allocate the transaction price to the performance obligation in the contract; and

 

 

Recognize revenue when, or as, the performance obligations are satisfied.

 

Performance obligations are the unit of accounting for revenue recognition and generally represent the distinct goods or services that are promised to the customer. If we determine that it has not satisfied a performance obligation, it will defer recognition of the revenue until the performance obligation is deemed to be satisfied. Support, maintenance, and software upgrades are performance obligations over a defined period and are recognized ratably over the contractual service period. Customers typically purchase these services with the initial sale of the PURE EP System and do not have the right to terminate their contracts unless we fail to perform material obligations.

 

We may execute more than one contract with a single customer. If so, it is evaluated whether the agreements were negotiated as a package with a single objective, whether the amount of consideration to be paid in one agreement depends on the price and/or performance of another agreement, or whether the goods or services promised in the agreements represent a single performance obligation. The conclusions reached can impact the allocation of the transaction price to each performance obligation and the timing of revenue recognition related to those arrangements.

 

We record accounts receivable for amounts invoiced to customers for which the Company has an unconditional right to consideration as provided under the contractual arrangement. Unbilled receivables, if any, include amounts related to our contractual right to consideration for completed performance obligations not yet invoiced. Deferred revenue includes payments received in advance of performance under the contract. Our unbilled receivables and deferred revenue are reported on an individual contract basis at the end of each reporting period. Unbilled receivables are classified as current or noncurrent based on the timing of when we expect to bill the customer. Deferred revenue is classified as current or noncurrent based on the timing of when we expect to recognize revenue.

 

40

 

Allowance for Doubtful Accounts

 

The Company adjusts accounts receivable down to net realizable value with its allowance methodology. In determining the allowance for doubtful accounts for estimated losses, aged receivables are analyzed periodically by management. Each identified receivable is reviewed based upon historical collection experience, financial condition of the client and the status of any open or unresolved issues with the client preventing the payment thereof. Corrective action, if necessary, is taken by the Company to resolve open issues related to unpaid receivables. The allowance for doubtful accounts was Nil at June 30, 2021. The Company believes that its reserve is adequate, however results may differ in future periods. For the six months ended June 30, 2021 and 2020, bad debt expense totaled $0.

 

Research and Development

 

We account for research and development costs in accordance with the Accounting Standards Codification subtopic 730-10, Research and Development (“ASC 730-10”). Under ASC 730-10, all research and development costs must be charged to expense as incurred. Accordingly, internal research and development costs are expensed as incurred. Third-party research and development costs are expensed when the contracted work has been performed or as milestone results have been achieved. Company-sponsored research and development costs related to both present and future products are expensed in the period incurred.

 

Stock Based Compensation

 

All stock-based payments to employees and to nonemployee directors for their services as directors consisted of grants of restricted stock and stock options, which are measured at fair value on the grant date and recognized in the statements of operations as compensation expense over the relevant vesting period. Restricted stock payments and stock-based payments to nonemployees are recognized as an expense over the period of performance. 

 

Such payments are measured at fair value at the earlier of the date a performance commitment is reached, or the date performance is completed. In addition, for awards that vest immediately and are non-forfeitable, the measurement date is the date the award is issued.

 

On October 29, 2014, our common stock commenced trading on OTCQB and on September 21, 2018 on the NASDAQ Capital Market under the symbol “BSGM.”  Fair value of options are typically determined by the sales prices of our common stock for the 10 trading days immediately preceding the date of the award.

 

Use of Estimates

 

The preparation of these unaudited condensed consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date of the unaudited condensed consolidated financial statements and the reported amounts of revenues and expenses during the reporting period. Significant estimates include the recoverability and useful lives of long-lived assets, the fair value of long-term operating leases, patent capitalization, fair value of acquired assets, the fair value of the Company’s stock, stock-based compensation, fair values relating to warrant and other derivative liabilities and the valuation allowance related to deferred tax assets. Actual results may differ from these estimates.

 

Acquisition of Intellectual Property

 

Intellectual property acquired are accounted for under the acquisition method of accounting. This method requires the recording of acquired assets, including separately identifiable intangible assets, and assumed liabilities at their acquisition date fair values. The method records any excess purchase price over the fair value of acquired net assets as goodwill.

 

The acquired intellectual property from the Trek acquisition was considered unproven compounds, the success of which was uncertain at the time of the acquisition. Accordingly, the fair value of the consideration paid was charged as acquired research and development to current period operations.

 

Income Taxes

 

Deferred income tax assets and liabilities are determined based on the estimated future tax effects of net operating loss and credit carryforwards and temporary differences between the tax basis of assets and liabilities and their respective financial reporting amounts measured at the current enacted tax rates. We record an estimated valuation allowance on our deferred income tax assets if it is not more likely than not that these deferred income tax assets will be realized. We recognize a tax benefit from an uncertain tax position only if it is more likely than not that the tax position will be sustained on examination by taxing authorities, based on the technical merits of the position. The tax benefits recognized in the financial statements from such a position are measured based on the largest benefit that has a greater than 50% likelihood of being realized upon ultimate settlement.

 

41

 

ITEM 3.  QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

 

Not required under Regulation S-K for “smaller reporting companies.”

 

ITEM 4.  CONTROLS AND PROCEDURES

 

Evaluation of Disclosure Controls and Procedures

 

As required under Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended (the “Exchange Act”), we carried out an evaluation, with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, of the effectiveness of our disclosure controls and procedures (as defined under Rule 13a-15(e) under the Exchange Act) as of the end of the period covered by this report. Based upon that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures were effective to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act, is recorded, processed, summarized and reported, within the time periods specified in the Securities and Exchange Commission’s rules and forms, and that such information is accumulated and communicated to our management, including our Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure.

 

Changes in Internal Controls over Financial Reporting

 

There have been no changes in our internal controls over financial reporting (as defined in Rule 13a-15(f) and 15d-(f) of the Exchange Act) that occurred during the last fiscal quarter to which this report relates that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

42

 

PART II.          OTHER INFORMATION

 

ITEM 1.  LEGAL PROCEEDINGS

 

Aurigene Pharmaceutical Services LTD vs. ViralClear Pharmaceuticals Inc. and BioSig Technologies, Inc.

 

On January 8, 2021, Aurigene Pharmaceutical Services, LTD (“Aurigene”) filed a complaint with the United States District Court for the District of Connecticut claiming the Company is in default of certain milestone payments for manufacturing and services under contracts dated June 23, 2020 and July 16, 2020 in aggregate amount of $1,530,000. The Company contends that it is not a proper party to the lawsuit since the agreements at issue were signed by a subsidiary. The Company also contends that Aurigene is not entitled to the relief it seeks, because it did not meet its own obligations under the contracts, including several manufacturing milestones. The Company intends to defend itself vigorously.

 

From time to time, we may become involved in other various lawsuits and legal proceedings which arise in the ordinary course of business. However, litigation is subject to inherent uncertainties, and an adverse result in these or other matters may arise from time to time that may harm our business. We are currently not aware of any such legal proceedings or claims that we believe will have, individually or in the aggregate, a material adverse effect on our business, financial condition or operating results.

 

There are no material proceedings in which any of our directors, officers or affiliates or any registered or beneficial shareholder of more than 5% of our common stock is an adverse party or has a material interest adverse to our interest.

 

ITEM 1A.  RISK FACTORS

 

Not required under Regulation S-K for “smaller reporting companies” 

 

ITEM 2.  UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

 

On April 30, 2021, BioSig Technologies, Inc. issued 30,000 shares of common stock to Lyons Capital, LLC in exchange for consulting services rendered with a fair value of $110,400, pursuant to engagement letter, dated April 15, 2021.

 

The issuance of the shares of common stock to Lyons Capital LLC was not registered under the Securities Act of 1933, as amended (the “Securities Act”), or the securities laws of any state, and the shares of the common stock were issued in reliance on the exemption from registration under the Securities Act pursuant to Section 4(a)(2) of the Securities Act.

 

ITEM 3.  DEFAULTS UPON SENIOR SECURITIES

 

None.

 

ITEM 4.  MINE SAFETY DISCLOSURES

 

None.

 

ITEM 5.  OTHER INFORMATION

 

None

 

ITEM 6.  EXHIBITS

 

1.1

Underwriting Agreement, dated July 2, 2021, by and between BioSig Technologies, Inc. and Laidlaw & Company (UK) Ltd. (incorporated by reference to Exhibit 1.1 to the Form 8-K filed on July 6, 2021)

3.1

Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form S-1 filed on July 22, 2013)

3.2

Certificate of Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.2 to the Form S-1 filed on July 22, 2013)

 

43

 

3.3

Certificate of Second Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.3 to the Form S-1 filed on July 22, 2013)

3.4

Certificate of Third Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.5 to the Form S-1/A filed on January 21, 2014)

3.5

Certificate of Fourth Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.6 to the Form S-1/A filed on March 28, 2014)

3.6

Certificate of Fifth Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on August 21, 2014)

3.7

Certificate of Sixth Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on November 25, 2016)

3.8

Certificate of Designation of Preferences, Rights and Limitations of Series D Convertible Preferred Stock (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on November 9, 2017)

3.9

Certificate of Designation of Preferences, Rights and Limitations of Series E Convertible Preferred Stock (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on February 16, 2018)

3.10

Certificate of Seventh Amendment to the Amended and Restated Certificate of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on September 10, 2018)

3.11

Bylaws of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.4 to the Form S-1 filed on July 22, 2013)

3.12

Amended and Restated Bylaws of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on September 27, 2019)

3.13

Amendment No. 1 to Amended and Restated Bylaws of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on October 22, 2019)

3.14

Certificate of Designations of Series F Junior Participating Preferred Stock of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on July 17, 2020)

4.1

Form of Underwriter Warrant (incorporated by reference to Exhibit 4.1 to the Form 8-K filed on July 6, 2021)

10.1**

Ninth Amendment to the BioSig Technologies, Inc. 2012 Equity Incentive Plan (incorporated by reference to Exhibit 10.1 to the Form 8-K filed on June 29, 2021)

10.2

Availability Retainer Agreement, dated June 30, 2021, by and between BioSig Technologies, Inc. and Jeffrey O’Donnell (incorporated by reference to Exhibit 10.1 to the Form 8-K filed on July 1, 2021)

31.01*

Certification of Chief Executive Officer pursuant to Exchange Act Rules 13a-14(a) and 15d-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

31.02*

Certification of Chief Financial Officer pursuant to Exchange Act Rules 13a-14(a) and 15d-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

32.01*

Certifications of Chief Executive Officer and Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

101 INS*

Inline XBRL Instance Document

101 SCH*

Inline XBRL Taxonomy Extension Schema Document

101 CAL*

Inline XBRL Taxonomy Calculation Linkbase Document

101 DEF*

Inline XBRL Taxonomy Extension Definition Linkbase Document

101 LAB*

Inline XBRL Taxonomy Labels Linkbase Document

101 PRE*

Inline XBRL Taxonomy Presentation Linkbase Document

104*

Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)

 

* Filed herewith.

** Indicates a management contract or compensatory plan.

 

44

 

SIGNATURES

 

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

 

 

BIOSIG TECHNOLOGIES, INC.

     

Date: August 11, 2021

By:

/s/ Kenneth L. Londoner

 
   

Kenneth L. Londoner

   

Chairman & Chief Executive Officer (Principal Executive Officer)

     
     

Date: August 11, 2021

By:

/s/ Steven Chaussy

 
   

Steven Chaussy

   

Chief Financial Officer (Principal Accounting Officer)

 

 

 

 

 

45
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