Table of Contents



UNITED STATES

 

SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549

 

FORM 10-Q

 

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

 

 

For the Quarterly Period Ended: December 31, 2020 or

 

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

 

 

For the transition period from                                to              

 

 

Commission File No. 001-38247

LOGO_SML.JPG

 

 

 

AYTU BIOSCIENCE, INC.

(www.aytubio.com)

 

Delaware 

47-0883144

(State or other jurisdiction of incorporation or organization)

(IRS Employer Identification No.)

 

373 Inverness Parkway, Suite 206

 

Englewood, Colorado 80112

 

(Address of principal executive offices, including zip code)

 

(720) 437-6580

 

(Registrants telephone number, including area code)

 

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

 

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes ☒ No ☐

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. See the 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 ☒

 

Title of each class

 

Trading Symbol(s)

 

Name of each exchange on which registered

Common Stock, par value $0.0001 per share

 

AYTU

 

The NASDAQ Stock Market LLC

 

As of February 1, 2021, there were 17,882,893 shares of Common Stock outstanding.

 



 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES FOR THE QUARTER ENDED DECEMBER December 31, 2020

 

 

INDEX 

 

PART IFINANCIAL INFORMATION

 

 

Page

Item 1. Consolidated Financial Statements

 

Condensed Consolidated Balance Sheets as of  December 31, 2019 (unaudited) and June 30, 2020 (audited)

4

Condensed Consolidated Statements of Operations for the three and six-months ended December 31, 2020 (unaudited) and December 31, 2019 (unaudited)

6

Condensed Consolidated Statement of Stockholders’ Equity for the year-to-date interim periods ended December 31, 2020 (unaudited) and December 31, 2019 (unaudited)

7

Condensed Consolidated Statements of Cash Flows for the six months ended December 31, 2020 (unaudited) and the six months ended December 31, 2019 (unaudited)

8

Notes to Condensed Consolidated Financial Statements (unaudited)

10

Item 2. Managements Discussion and Analysis of Financial Condition and Results of Operations

27

 

 

Item 3. Quantitative and Qualitative Disclosures About Market Risk

31

 

 

Item 4. Controls and Procedures

31

 

 

PART IIOTHER INFORMATION

 

Item 1. Legal Proceedings

32

 

 

Item 1A. Risk Factors

33

 

 

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

33

 

 

Item 3. Defaults Upon Senior Securities

33

 

 

Item 4. Mine Safety Disclosures

33

 

 

Item 5. Other Information

33

 

 

Item 6. Exhibits

34

 

 

SIGNATURES

 

 

 

 

CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS

 

This Quarterly Report on Form 10-Q includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, or the Exchange Act. All statements other than statements of historical facts contained in this Quarterly Report, including statements regarding our anticipated future clinical and regulatory events, future financial position, business strategy and plans and objectives of management for future operations, are forward-looking statements. Forward looking statements are generally written in the future tense and/or are preceded by words such as “may,” “will,” “should,” “forecast,” “could,” “expect,” “suggest,” “believe,” “estimate,” “continue,” “anticipate,” “intend,” “plan,” or similar words, or the negatives of such terms or other variations on such terms or comparable terminology. Such forward-looking statements include, without limitation: the planned expanded commercialization of our products and the potential future commercialization of our product candidates, our anticipated future cash position; our plan to acquire additional assets; our anticipated future growth rates; anticipated sales increases; anticipated net revenue increases; amounts of certain future expenses and costs of goods sold; anticipated increases to operating expenses, research and development expenses, and selling, general, and administrative expenses; and future events under our current and potential future collaborations.

 

These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including without limitation the risks described in “Risk Factors” in Part II Item 1A of our most recent Annual Report on Form 10- K, and in the reports we file with the Securities and Exchange Commission. These risks are not exhaustive. Moreover, we operate in a very competitive and rapidly changing environment. New risk factors emerge from time to time and it is not possible for our management to predict all risk factors, nor can we assess the impact of all factors on our business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. Forward-looking statements should not be relied upon as predictions of future events. We can provide no assurance that the events and circumstances reflected in the forward-looking statements will be achieved or occur and actual results could differ materially from those projected in the forward-looking statements. We assume no obligation to update or supplement forward-looking statements, except as may be required under applicable law.

 

This Quarterly Report on Form 10-Q includes trademarks, such as Aytu, Karbinal®, Natesto®, Poly-Vi-Flor®, Tuzistra®, and ZolpiMist®, and the recently acquired consumer health products such as DiabaSens®, FlutiCare®, UriVarx® and Vesele®, as well as Beyond Human-®, a specialty marketing platform, which are protected under applicable intellectual property laws and we own or have the rights to. Solely for convenience, our trademarks and trade names referred to in this Quarterly Report on Form 10-Q may appear without the ® or TM symbols, but such references are not intended to indicate in any way that we will not assert, to the fullest extent under applicable law, our rights to these trademarks and trade names.

 

3

 

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

Condensed Consolidated Balance Sheets

 

   

December 31,

   

June 30,

 
   

2020

   

2020

 
   

(Unaudited)

         

Assets

 

Current assets

               

Cash and cash equivalents

  $ 62,032,642     $ 48,081,715  

Restricted cash

    251,964       251,592  

Accounts receivable, net

    7,001,068       5,175,924  

Inventory, net

    6,571,254       9,999,441  

Prepaid expenses and other

    6,081,766       5,715,089  

Other current assets

    10,598,771       5,742,011  

Total current assets

    92,537,465       74,965,772  

Fixed assets, net

    89,663       258,516  

Right-of-use asset

    310,479       634,093  

Licensed assets, net

    15,449,281       16,586,847  

Patents and tradenames, net

    10,197,112       11,081,048  

Product technology rights, net

    20,051,666       21,186,666  

Deposits

    16,023       32,981  

Goodwill

    28,090,407       28,090,407  

Total long-term assets

    74,204,631       77,870,558  

Total assets

  $ 166,742,096     $ 152,836,330  

 

See the accompanying Notes to the Condensed Consolidated Financial Statements

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

Condensed Consolidated Balance Sheets, contd

 

   

December 31,

   

June 30,

 
   

2020

   

2020

 
   

(Unaudited)

         

Liabilities

 

Current liabilities

               

Accounts payable and other

  $ 7,157,208     $ 11,824,560  

Accrued liabilities

    8,877,715       7,849,855  

Accrued compensation

    2,540,353       3,117,177  

Debt

    41,318       982,076  

Contract liability

    475,680       339,336  

Current lease liability

    100,263       300,426  

Current portion of fixed payment arrangements

    1,937,476       2,340,166  

Current portion of CVR liabilities

    977,475       839,734  

Current portion of contingent consideration

    3,705,931       713,251  

Total current liabilities

    25,813,419       28,306,581  

Long-term contingent consideration, net of current portion

    12,573,916       12,874,351  

Long-term lease liability, net of current portion

    211,056       725,374  

Long-term fixed payment arrangements, net of current portion

    9,945,554       11,171,491  

Long-term CVR liabilities, net of current portion

    5,494,112       4,731,866  

Other long-term liabilities

    11,371       11,371  

Total liabilities

    54,049,428       57,821,034  

Commitments and contingencies (Note 10)

               

Stockholders' equity

               

Preferred Stock, par value $.0001; 50,000,000 shares authorized; shares issued and outstanding 0 and 0, respectively as of December 31, 2020 and June 30, 2020, respectively.

    -       -  

Common Stock, par value $.0001; 200,000,000 shares authorized; shares issued and outstanding 17,882,893 and 12,583,736, respectively as of December 31, 2020 and June 30, 2020.

    1,788       1,259  

Additional paid-in capital

    246,532,284       215,024,216  

Accumulated deficit

    (133,841,404 )     (120,010,179 )

Total stockholders' equity

    112,692,668       95,015,296  

Total liabilities and stockholders' equity

  $ 166,742,096     $ 152,836,330  

 

See accompanying Notes to the Condensed Consolidated Financial Statements

 

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

 

Condensed Consolidated Statements of Operations

(unaudited)

 

   

Three Months Ended

   

Six Months Ended

 
   

December 31,

   

December 31,

 
   

2020

   

2019

   

2020

   

2019

 

Revenues

                               

Product revenue, net

  $ 15,147,034     $ 3,175,236     $ 28,667,280     $ 4,615,062  
                                 

Operating expenses

                               

Cost of sales

    5,998,389       606,046       9,817,545       981,766  

Research and development

    286,572       66,675       469,437       144,695  

Selling, general and administrative

    12,852,614       6,516,160       24,342,983       11,662,603  

Amortization of intangible assets

    1,584,580       953,450       3,169,161       1,528,567  

Total operating expenses

    20,722,155       8,142,331       37,799,126       14,317,631  

Loss from operations

    (5,575,121 )     (4,967,095 )     (9,131,846 )     (9,702,569 )

Other (expense) income

                               

Other (expense), net

    (378,958 )     (446,958 )     (1,130,499 )     (642,344 )

Loss from change in fair value of contingent consideration

    (3,313,656 )     -       (3,311,320 )     -  

Gain from derecognition of contingent consideration

    -       5,199,806       -       5,199,806  

Gain from warrant derivative liability

    -       -       -       1,830  

Loss on debt exchange

    (257,559 )     -       (257,559 )     -  

Total other (expense) income

    (3,950,173 )     4,752,848       (4,699,378 )     4,559,292  

Net loss

  $ (9,525,294 )   $ (214,247 )   $ (13,831,224 )   $ (5,143,277 )

Weighted average number of common shares outstanding

    13,281,904       1,753,815       12,717,180       1,642,599  

Basic and diluted net loss per common share

  $ (0.72 )   $ (0.12 )   $ (1.09 )   $ (3.13 )

 

See the accompanying Notes to the Condensed Consolidated Financial Statements.

 

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

 

Condensed Consolidated Statement of Stockholders Equity

(unaudited unless indicated otherwise)

 

   

Preferred Stock

   

Common Stock

   

Additional paid-in

   

Accumulated

   

Total Stockholders'

 
   

Shares

   

Amount

   

Shares

   

Amount

   

capital

   

Deficit

   

Equity

 

BALANCE - June 30, 2019 (audited)

    3,594,981     $ 359       1,753,808     $ 176     $ 113,476,783     $ (106,389,500 )   $ 7,087,818  

Stock-based compensation

    -       -       -       -       165,171       -       165,171  

Preferred stock converted in common stock

    (443,833 )     (44 )     44,384       5       39       -       -  

Net loss

    -       -       -       -       -       (4,929,030 )     (4,929,030 )
BALANCE - September 30, 2019     3,151,148     $ 315       1,798,192     $ 181     $ 113,641,993     $ (111,318,530 )   $ 2,323,959  
                                                         
Stock-based compensation           $ -       -     $ -     $ 162,264     $ -     $ 162,264  
Issuance of Series F preferred stock from October 2019 private placement financing, net of $741,650 issuance costs     10,000       1       -       -       5,249,483       -       5,249,484  
Warrants issued in connection with the private placement      -       -       -       -       4,008,866       -       4,008,866  
Issuance of Series G preferred stock due to acquisition of the Cerecor portfolio of pediatrics therapeutics     9,805,845       981                       5,558,933               5,559,914  
Preferred stock converted in common stock     (2,751,148 )     (275 )     275,115       28       247       -       -  
Net loss             -       -       -       -       (214,247 )   $ (214,247 )

BALANCE - December 30, 2019

    10,215,845     $ 1,022       2,073,307     $ 209     $ 128,621,786     $ (111,532,777 )   $ 17,090,240  

 

   

Preferred Stock

   

Common Stock

   

Additional paid-in

   

Accumulated

   

Total Stockholders'

 
   

Shares

   

Amount

   

Shares

   

Amount

   

capital

   

Deficit

   

Equity

 

BALANCE - June 30, 2020 (audited)

    -     $ -       12,583,736     $ 1,259     $ 215,024,216     $ (120,010,179 )   $ 95,015,296  

Stock-based compensation

    -       -       -       -       454,918       -       454,918  

Issuance costs

    -       -       -       -       (101,537 )     -       (101,537 )

Net loss

    -       -       -       -       -       (4,305,931 )     (4,305,931 )
BALANCE - September 30, 2020     -     $ -       12,583,736     $ 1,259     $ 215,377,597     $ (124,316,110 )   $ 91,062,746  
                                                         
Stock-based compensation     -     $ -       -     $ -     $ 508,059     $ -     $ 508,059  
Exchange of debt for common stock     -       -       130,081       13       1,057,546       -       1,057,559  
Issuance of common stock, net of issue costs and warrants     -       -       5,169,076       516       28,316,928       -       28,317,444  
Warrants issued in connection with common stock offering     -       -                       1,272,154               1,272,154  
      -       -                                          
Net loss      -       -       -       -       -       (9,525,294 )     (9,525,294 )

BALANCE - December 31, 2020

    -     $ -       17,882,893     $ 1,788     $ 246,532,284     $ (133,841,404 )   $ 112,692,668  

 

See the accompanying Notes to the Condensed Consolidated Financial Statements

 

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

 

Condensed Consolidated Statements of Cash Flows

(unaudited)

 

   

Six Months Ended

 
   

December 31,

 
   

2020

   

2019

 
                 

Operating Activities

               

Net loss

  $ (13,831,224 )   $ (5,143,277 )

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

               

Depreciation, amortization and accretion

    4,012,909       2,157,540  

Stock-based compensation expense

    962,977       327,435  
Loss from change in fair value of contingent consideration     2,411,333          

(Gain) from derecognition of contingent consideration

    -       (5,199,806 )

Loss on sale of equipment

    112,110       -  

(Gain) on termination of lease

    (343,185 )     -  
Loss on debt exchange     257,559          

Changes in allowance for bad debt

    147,627       -  

Loss from change in fair value of CVR

    899,987       -  

Derivative income

            (1,830 )

Changes in operating assets and liabilities:

               

Increase in accounts receivable

    (1,965,271 )     (3,456,364 )

Increase in inventory

    (3,615,662 )     (132,199 )

Increase in prepaid expenses and other

    (379,337 )     (171,430 )

Decrease (increase) in other current assets

    2,295,055       (136,694 )

(Decrease) increase in accounts payable and other

    (3,136,163 )     2,806,973  

Increase in accrued liabilities

    1,711,466       145,467  

Decrease in accrued compensation

    (576,824 )     (62,729 )
Decrease in fixed payment arrangements     -       (216,150 )

Increase in contract liability

    136,344       -  

Decrease in deferred rent

    -       (3,990 )

Net cash used in operating activities

    (10,900,299 )     (9,087,054 )
                 

Investing Activities

               

Deposit

    (3,923 )     -  

Contingent consideration payment

    (42,760 )     (104,635 )
Note receivable     -       (1,350,000 )
Purchase of assets     -       (4,500,000 )

Net cash used in investing activities

    (46,683 )     (5,954,635 )
                 

Financing Activities

               
Issuance of preferred, common stock and warrants     32,249,652       10,000,000  

Issuance cost related to registered offering

    (4,292,781 )     (741,650 )

Payments made to borrowings

    (272,727 )     -  

Payments made to fixed payment arrangements

    (2,785,863 )     -  

Net cash provided by financing activities

    24,898,281       9,258,350  
                 

Net change in cash, restricted cash and cash equivalents

    13,951,299       (5,783,339 )

Cash, restricted cash and cash equivalents at beginning of period

    48,333,307       11,294,227  

Cash, restricted cash and cash equivalents at end of period

  $ 62,284,606     $ 5,510,888  

 

See the accompanying Notes to the Condensed Consolidated Financial Statements.

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

 

Condensed Consolidated Statements of Cash Flows, contd

(unaudited)

 

   

Six Months Ended

 
   

December 31,

 

Supplemental disclosures of cash and non-cash investing and financing transactions

 

2020

   

2019

 

Warrants issued to underwriters

  $ 356,139     $ -  

Cash paid for interest

    306,752       3,390  

Fair value of right-to-use asset and related lease liability

    43,082       412,691  

Contingent consideration included in accounts payable

    -       3,430  
Debt exchange     1,057,559       -  

Fixed payment arrangements included in accrued liabilities

    1,050,000       -  
Inventory swap     7,043,849       -  

Acquisition costs included in accounts payable

    -       59,014  

Exchange of convertible preferred stock into common stock

  $ -     $ 44  

 

See the accompanying Notes to the Condensed Consolidated Financial Statements

 

 

AYTU BIOSCIENCE, INC. AND SUBSIDIARIES

 

Notes to Condensed Consolidated Financial Statements

(unaudited)

 

 

 

 

 1. Nature of Business, Financial Condition, Basis of Presentation

 

 

Nature of Business. Aytu BioScience, Inc. (“Aytu”, the “Company” or “we”) is a commercial-stage specialty pharmaceutical company focused on commercializing novel products that address significant healthcare needs in both prescription and consumer health categories. The Company currently operates its Aytu BioScience business, consisting of the primary care product portfolio (the “Primary Care Portfolio”), the prescription pediatric portfolio (the “Pediatric Portfolio”), and its Aytu consumer healthcare products business (the “Consumer Health Portfolio”). The Aytu BioScience business is focused on commercializing prescription pharmaceutical products treating hypogonadism (low testosterone), cough and upper respiratory symptoms, insomnia, male infertility, and various pediatric conditions. The Aytu Consumer Health business is focused on commercializing consumer healthcare products. The Company plans to expand into other therapeutic areas as opportunities arise. The Company was incorporated as Rosewind Corporation on August 9, 2002 in the State of Colorado. Aytu was re-incorporated in the state of Delaware on June 8, 2015.

 

The Primary Care Portfolio consists of (i) Natesto, the only FDA-approved nasal formulation of testosterone for men with hypogonadism (low testosterone, or "Low T"), (ii) ZolpiMist, the only FDA-approved oral spray prescription sleep aid, and (iii) Tuzistra XR, the only FDA-approved 12-hour codeine-based antitussive syrup.

 

The Pediatric Care Portfolio, acquired on November 1, 2019, (the “Pediatric Portfolio”), includes (i) Poly-Vi-Flor and Tri-Vi-Flor, two complementary prescription fluoride-based supplement product lines containing combinations of fluoride and vitamins in various formulations for infants and children with fluoride deficiency, (ii) Cefaclor, a second-generation cephalosporin antibiotic suspension; and (iii) Karbinal ER, an extended-release carbinoxamine (antihistamine) suspension indicated to treat numerous allergic conditions.

 

On February 14, 2020, the Company acquired Innovus Pharmaceuticals Inc. (“Innovus”), a specialty pharmaceutical company licensing, developing and commercializing safe and effective consumer healthcare products designed to improve health and vitality. Innovus commercializes over twenty consumer health products competing in large healthcare categories including diabetes, men's health, sexual wellness and respiratory health. The Consumer Health Portfolio is commercialized through direct-to- consumer marketing channels utilizing Innovus’s proprietary Beyond Human® marketing and sales platform and on e-commerce platforms.

 

On December 10, 2020, the Company and Neutron Acquisition Sub, Inc., a wholly owned subsidiary of the Company (“Merger Sub”), entered into an Agreement and Plan of Merger (the “Merger Agreement”) with Neos Therapeutics, Inc. (“Neos”). The Merger Agreement provides, among other things, that on the terms and subject to the conditions set forth therein, Merger Sub will merge with and into Neos, with Neos surviving as a wholly owned subsidiary of the Company (the “Neos Merger”). The Neos Merger is subject to the approval of both the shareholders of the Company and Neos. Based on the number of shares of the Company’s common stock anticipated to be immediately issued to Neos stockholders upon closing of the merger (which could be impacted by changes in Neos stock price leading to the exercise of options not otherwise being assumed by the Company) and the number of shares of the Company’s common stock outstanding as of December 31, 2020, it is expected that, immediately after completion of the merger, former Neos stockholders will own approximately 24% of the outstanding shares of the Company’s common stock. Existing Company stockholders are expected to own approximately 76% of the outstanding shares of the Company’s common stock. In addition, each unvested option to acquire shares of Neos common stock that is outstanding as of immediately prior to the close of the Neos Merger (the "Effective Time") with an exercise price equal to or less than $0.95 shall be assumed by the Company and converted into an option to acquire shares of the Company’s common stock on the same terms and conditions. The number of shares of Company’s common stock subject to each such assumed option shall be equal to (i) the number of shares of Neos common stock subject to the corresponding assumed option immediately prior to the close multiplied by (ii) 0.1088 (the "Exchange Ratio"), rounded down, if necessary, to the nearest whole share of the Company’s common stock, and such assumed option shall have an exercise price per share (rounded up to the nearest whole cent) equal to (A) the exercise price per share of Neos common stock otherwise purchasable pursuant to the corresponding assumed option divided by (B) the Exchange Ratio. As of February 5, 2021, the total estimated shares to be issued in connection with this merger totaled approximately 5.4 million with an estimated fair value of $44.2 million.

 

In connection with the execution of the Merger Agreement, the Company and Neos have entered into a Commitment Letter (the “Bridge Commitment Letter”) for the Company to provide financing to Neos under an unsecured convertible note, in an aggregate amount of up to $5,000,000, subject to the terms set forth therein (the "Bridge Financing"). Interest accrues on the principal amount outstanding under the note at a rate of 6.0% per annum, compounding monthly and commencing if and when such Bridge Financing is provided. If an event of default has occurred and is continuing, the interest rate then in effect will be increased by 2.0% per annum, and all overdue obligations under the note will bear interest at the interest rate in effect at such time plus the additional 2.0% per annum. The Company's rights under the note, including rights to payment, are subordinated to the rights of Neos’s existing senior lenders. The maturity date of the note is the earlier of the acceleration of the obligations evidenced thereby and November 7, 2022. In the event that Neos draws down on the note, the exchange ratio will be adjusted downward by an amount equal to 0.00011 for every $100,000 of financing funded to Neos under the note.

 

In April of 2020, the Company entered into a licensing agreement with Cedars-Sinai Medical Center to secure worldwide rights to various potential uses of Healight, an investigational medical device platform technology. Healight has demonstrated safety and efficacy in pre-clinical studies, and we plan to advance this technology and assess its safety and efficacy in human studies, initially focused on COVID-19 patients.

 

The Company recently established a purchasing relationship with a U.S. supplier of Emergency Use Authorization (EUA) authorized antigen tests. Antigen tests rapidly detect the presence of the SARS-CoV-2 virus antigen via a nasopharyngeal swab and are used without laboratory equipment. Demand for rapid antigen tests has increased in recent months across the U.S.

 

The Company’s strategy is to continue building its portfolio of revenue-generating products, leveraging its commercial team’s expertise to build leading brands within large therapeutic markets.

 

Financial Condition. As of December 31, 2020, the Company had approximately $62.3 million of cash, cash equivalents and restricted cash. The Company’s operations have historically consumed cash and are expected to continue to require cash, but at a declining rate.

 

Revenues for the three- and six- months ended December 31, 2020were $15.1 million and $28.7 million, compared to $3.2 million and $4.6 million for the same periods ended December 31, 2019, an increase of approximately 377% and 521%,  respectively. Revenue is expected to increase over time, which will allow the Company to rely less on the Company's existing cash balance and proceeds from financing transactions. Cash used by operations during the six-months ended December 31, 2020 was $10.9 million compared to $9.1 million for the six-months ended December 31, 2019. The increase is due primarily to an increase in working capital and pay down of other liabilities.

 

 

As of the date of this Report, the Company expects costs for its current operations to increase modestly as the Company continues to integrate the acquisition of the Pediatrics Portfolio, Innovus and if approved by the Company's and Neos' shareholders, the Neos Merger, continues to focus on revenue growth through increasing product sales and additional acquisitions. The Company’s current assets totaling approximately $92.5 million as of December 31, 2020 plus the proceeds expected from ongoing product sales will be used to fund existing operations. The Company may continue to access the capital markets from time-to-time when market conditions are favorable. The timing and amount of capital that may be raised is dependent on the terms and conditions upon which investors would require to provide such capital. There is no guarantee that capital will be available on terms favorable to the Company and its stockholders, or at all. The Company raised approximately $29.6 million, net during the three months ended December 31, 2020, from the sale of approximately 0.4 million shares using the Company’s at-the-market facility and from the issuance of approximately 4.8 million shares of the Company's common stock and 0.3 million placement agent warrants on December 15, 2020. On December 10, 2020, the Company exchanged $0.8 million of debt into 0.1 million shares of the Company's common stock, eliminating the use cash to satisfy this obligation (see Note 15). Between December 31, 2020, and the filing date of this quarterly report on Form 10-Q, the Company has not issued common stock under the Company’s at-the-market offering program.  As of the date of this report, the Company has adequate capital resources to complete its near-term operating objectives. 

 

Since the Company has sufficient cash on-hand as of December 31, 2020 to cover potential net cash outflows for the twelve months following the filing date of this Quarterly Report, the Company reports that there exists no indication of substantial doubt about its ability to continue as a going concern.

 

If the Company is unable to raise adequate capital in the future when it is required, the Company's management can adjust its operating plans to reduce the magnitude of the capital need under its existing operating plan. Some of the adjustments that could be made include delays of and reductions to commercial programs, reductions in headcount, narrowing the scope of the Company’s commercial plans, or reductions to its research and development programs. Without sufficient operating capital, the Company could be required to relinquish rights to products or renegotiate to maintain such rights on less favorable terms than it would otherwise choose. This may lead to impairment or other charges, which could materially affect the Company’s balance sheet and operating results.

 

Basis of Presentation. The unaudited consolidated financial statements contained in this report represent the financial statements of the Company and its wholly-owned subsidiaries, Aytu Women’s Health, LLC, Innovus Pharmaceuticals, Inc., and Aytu Therapeutics, LLC. The unaudited consolidated financial statements should be read in conjunction with the Company's Annual Report on Form 10-K for the year ended June 30, 2020, which included all disclosures required by generally accepted accounting principles in the United States (“GAAP”). In the opinion of management, these unaudited consolidated financial statements contain all adjustments necessary to present fairly the financial position of the Company and the results of operations and cash flows for the interim periods presented. The results of operations for the period ended December 31, 2020 are not necessarily indicative of expected operating results for the full year. The information presented throughout this report, as of and for the three and six-month periods ended December 31, 2020, and 2019, is unaudited. 

 

On December 8, 2020, the Company effected a reverse stock split in which each common stockholder received one share of common stock for every 10 shares held (herein referred to collectively as the “Reverse Stock Split”). All share and per share amounts in this report have been adjusted to reflect the effect of the Reverse Stock Split.

 

Interim Unaudited Condensed Consolidated Financial Statements. The accompanying condensed consolidated balance sheet as of December 31, 2020, and the condensed consolidated statements of operations, stockholders’ equity, for the three- and six- months ended, and the interim condensed consolidated statements of cash flows for the six-months ended December 31, 2020 and 2019, are unaudited. The condensed consolidated balance sheet as of June 30, 2020 was derived from audited financial statements but does not include all disclosures required by U.S. GAAP. The interim unaudited condensed consolidated financial statements have been prepared on a basis consistent with the annual consolidated financial statements and, in the opinion of management, reflect all adjustments, which include only normal recurring adjustments, necessary to state fairly the Company’s financial condition, its operations and cash flows for the periods presented. The historical results are not necessarily indicative of future results, and the results of operations for the three and six-months ended December 31, 2020 are not necessarily indicative of the results to be expected for the full year or any other period.

 

Use of Estimates

 

The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent consideration, contingent value rights ("CVRs"), and fixed payment obligations at the date of the financial statements and the reported amounts of revenue and expenses for the reporting period. On an ongoing basis, the Company evaluates its estimates, including, but not limited to, those related to the determination of the fair value of equity awards, the fair value of identified assets and liabilities acquired in business combinations, the useful lives of property and equipment, intangible assets, impairment of long-lived and intangible assets, including goodwill, provisions for doubtful accounts receivable, certain accrued expenses, and the discount rate used in measuring lease liabilities. These estimates and assumptions are based on the Company’s historical results and management’s future expectations. Actual results could differ from those estimates.

 

 

Significant Accounting Policies

 

The Company’s significant accounting policies are discussed in Note 2—Summary of Significant Accounting Policies and Recent Accounting Pronouncements in the Annual Report. There have been no significant changes to these policies that have had a material impact on the Company’s unaudited condensed consolidated financial statements and related notes during the three months ended December 31, 2020.

 

Adoption of New Accounting Pronouncements

 

Fair Value Measurements (ASU 2018-13). In August 2018, the FASB issued ASU 2018-13, “Fair Value Measurement (Topic 820) Disclosure Framework-Changes to the Disclosure Requirements for Fair Value Measurement.” The amendments in the standard apply to all entities that are required, under existing GAAP, to make disclosures about recurring or nonrecurring fair value measurements. ASU 2018-13 removes, modifies, and adds certain disclosure requirements in ASC 820, Fair Value Measurement. The standard is effective for all entities for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2019.

 

The amendments on changes in unrealized gains and losses, the range and weighted average of significant unobservable inputs used to develop Level 3 fair value measurements, and the narrative description of measurement uncertainty should be applied prospectively for only the most recent interim or annual period presented in the initial fiscal year of adoption. All other amendments should be applied retrospectively to all periods presented upon their effective date. The Company adopted this as of July 1, 2020, the beginning of the Company’s fiscal year-ended June 30, 2021. The most relevant component of ASU 2018-13 to the Company’s financial statements relates to the need to disclose the range and weighted-average of significant unobservable inputs used in Level 3 fair value measurements. However, the Company discloses on a discrete basis all significant inputs for all Level 3 Fair Value measurements.

 

Recent Accounting Pronouncements

 

Financial Instruments Credit Losses (ASU 2016-13). In June 2016, the FASB issued ASU 2016-13, “Financial Instruments – Credit Losses” to require the measurement of expected credit losses for financial instruments held at the reporting date based on historical experience, current conditions and reasonable forecasts. The main objective of this ASU is to provide financial statement users with more decision-useful information about the expected credit losses on financial instruments and other commitments to extend credit held by a reporting entity at each reporting date. The standard was effective for interim and annual reporting periods beginning after December 15, 2019. However, in October 2019, the FASB approved deferral of the adoption date for smaller reporting companies for fiscal periods beginning after December 15, 2022. Accordingly, the Company’s fiscal year of adoption will be the fiscal year ended June 30, 2024. Early adoption is permitted for interim and annual reporting periods beginning after December 15, 2018, but the Company did not elect to early adopt. The Company is currently assessing the impact that ASU 2016-13 will have on its consolidated financial statements, but no conclusion has been reached.

 

This Quarterly Report on Form 10-Q does not discuss recent pronouncements that are not anticipated to have an impact on or are unrelated to the Company’s financial condition, results of operations, cash flows or disclosures.

 

 

2. Acquisitions

 

The Pediatric Portfolio

 

On October 10, 2019, the Company entered into the Purchase Agreement with Cerecor, Inc. (“Cerecor”) to acquire the Pediatric Portfolio, which closed on November 1, 2019. The Pediatric Portfolio consists of four main prescription products (i) Cefaclor™ for Oral Suspension, (iii) Karbinal® ER (iii) Poly-Vi-Flor®, and (iv) Tri-Vi-Flor™.

Total consideration transferred to Cerecor consisted of $4.5 million cash and approximately 980 thousand shares of Series G Convertible Preferred Stock. The Company also assumed certain of Cerecor’s financial and royalty obligations, and not more than $2.7 million of Medicaid rebates and up to $0.8 million of product returns, of which $3.5 million has been incurred. The Company also hired the majority of Cerecor’s workforce focused on sales, commercial contracts and customer relationships.

 

 

In addition, the Company assumed Cerecor obligations due to an investor that include fixed and variable payments aggregating to $25.6 million. The Company assumed fixed monthly payments equal to $0.1 million from November 2019 through January 2021 plus $15 million due in January 2021. Monthly variable payments due to the same investor are equal to 15% of net revenue generated from a subset of the Pediatric Portfolio, subject to an aggregate monthly minimum of $0.1 million, except for January 2020, when a one-time payment of $0.2 million was paid to the investor. The variable payment obligation continues until the earlier of: (i) aggregate variable payments of approximately $9.5 million have been made, or (ii) February 12, 2026. In June 2020, the Company paid down a $15 million balloon payment originally owed in January 2021 to reduce the fixed liability.

 

Further, certain of the products in the Pediatric Portfolio require royalty payments ranging from 12% to 15% of net revenue. One of the products in the Product Portfolio requires the Company to generate minimum annual sales sufficient to represent annual royalties of approximately $1.8 million, in the event the minimum sales volume is not satisfied.

 

 

While no equity was acquired by the Company, the transaction was accounted for as a business combination under the acquisition method of accounting pursuant to Topic 805. Accordingly, the tangible and identifiable intangible assets acquired, and liabilities assumed were recorded at fair value as of the date of acquisition, with the remainder of the aggregate purchase price recorded as goodwill. The goodwill recognized is attributable primarily to strategic opportunities related to an expanded commercial footprint and diversified product portfolio that is expected to provide revenue and cost synergies.

 

The following table summarized the fair value of assets acquired and liabilities assumed at the date of acquisition. 

 

   

As of

 
   

November 1, 2019

 

Consideration

       

Cash and cash equivalents

  $ 4,500,000  

Fair value of Series G Convertible Preferred Stock

       

Total shares issued

    9,805,845  

Estimated fair value per share of Aytu common stock

  $ 0.567  

Estimated fair value of equity consideration transferred

    5,559,914  

Total consideration transferred

  $ 10,059,914  

Recognized amounts of identifiable assets acquired and liabilities assumed

       

Inventory

  $ 459,123  

Prepaid assets

    1,743,555  

Other current assets

    2,525,886  

Intangible assets - product marketing rights

    22,700,000  

Accrued liabilities

    (300,000 )

Accrued product program liabilities

    (6,683,932 )

Assumed fixed payment obligations

  $ (29,837,853 )

Total identifiable net assets

    (9,393,221 )

Goodwill

  $ 19,453,135  

 

The fair values of intangible assets, including product technology rights were determined using variations of the income approach. Varying discount rates were also applied to the projected net cash flows. The Company believes the assumptions are representative of those a market participant would use in estimating fair value (see Note 9).

 

The fair value of the net identifiable asset acquired was determined to be $22.7 million, which is being amortized over ten years.

 

Innovus Merger (Consumer Health Portfolio)

 

On February 14, 2020, the Company completed the Merger with Innovus Pharmaceuticals after approval by the stockholders of both companies on February 13, 2020. Upon the effectiveness of the Merger, a subsidiary of the Company merged with and into Innovus, and all outstanding Innovus common stock was exchanged for approximately 380 thousand shares of the Company’s common stock and up to $16 million of Contingent Value Rights (“CVRs”). The outstanding Innovus warrants with cash out rights were exchanged for approximately 200 thousand shares of Series H Convertible Preferred stock of the Company and retired. The remaining Innovus warrants outstanding, those without ‘cash- out’ rights, at the time of the Merger, continue to be outstanding, and upon exercise, retain the right to the merger consideration offered to Innovus stockholders, including any remaining claims represented by CVRs at the time of exercise. Innovus is now a 100% wholly-owned subsidiary of the Company, (“Aytu Consumer Health”).

 

On March 31, 2020, the Company paid out the first CVR Milestone in the form of approximately 120 thousand shares of the Company’s common stock to satisfy the $2.0 million obligation as a result of Innovus achieving the $24 million revenue milestone for the calendar year ended December 31, 2019. As a result of this, the Company recognized a gain of approximately $0.3 million.

 

In addition, as part of the Merger, the Company assumed approximately $3.1 million of notes payable, $0.8 million in lease liabilities, and other assumed liabilities associated with Innovus. Of the $3.1 million of notes payable, approximately $2.2 million was converted into approximately 180 thousand shares of the Company’s common stock since February 14, 2020. Approximately $41 thousand remained outstanding as of December 31, 2020.

 

 

The following table summarized the preliminary fair value of assets acquired and liabilities assumed at the date of acquisition. These estimates are preliminary, pending final evaluation of certain assets and liabilities, and therefore, are subject to revisions that may result in adjustments to the values presented below:

 

   

As of

 
   

February 14, 2020

 

Consideration

       

Fair Value of Aytu Common Stock

       

Total shares issued at close

    3,810,393  

Estimated fair value per share of Aytu common stock

  $ 0.756  

Estimated fair value of equity consideration transferred

  $ 2,880,581  

Fair value of Series H Convertible Preferred Stock

       

Total shares issued

    1,997,736  

Estimated fair value per share of Aytu common stock

  $ 0.756  

Estimated fair value of equity consideration transferred

  $ 1,510,288  

Fair value of former Innovus warrants

  $ 15,315  

Fair value of Contingent Value Rights

  $ 7,049,079  

Forgiveness of Note Payable owed to the Company

  $ 1,350,000  

Total consideration transferred

  $ 12,805,263  

 

   

As of

 
   

February 14, 2020

 

Total consideration transferred

  $ 12,805,263  

Recognized amounts of identified assets acquired and liabilities assumed

       

Cash and cash equivalents

  $ 390,916  

Accounts receivable

    278,826  

Inventory

    1,149,625  

Prepaid expenses and other current assets

    1,692,133  

Other long-term assets

    36,781  

Right-to-use assets

    328,410  

Property, plant and equipment

    190,393  

Trademarks and patents

    11,744,000  

Accounts payable and accrued other expenses

    (7,202,309 )

Other current liabilities

    (629,601 )

Notes payable

    (3,056,361 )

Lease liability

    (754,822 )

Total identifiable assets

  $ 4,167,991  

Goodwill

  $ 8,637,272  

 

The fair values of intangible assets, including product distribution rights were determined using variations of the income approach, specifically the relief-from-royalties method. It also includes customer lists using an income approach utilizing a discounted cash flow model. Varying discount rates were also applied to the projected net cash flows. The CVRs were valued using a Monte-Carlo model. The Company believes the assumptions are representative of those a market participant would use in estimating fair value (see Note 10).

 

The fair value of the net identifiable assets acquired was determined to be $11.7 million, which is being amortized over a range between 1.5 to 10 years.

 

 

Unaudited Pro Forma Information

 

The following supplemental unaudited proforma financial information presents the Company’s results as if the following acquisitions had occurred on July 1, 2019:

 

 

Acquisition of the Pediatric Portfolio, effective November 1, 2019;

 

Merger with Innovus effective February 14, 2020.

 

The unaudited pro forma results have been prepared based on estimates and assumptions, which management believes are reasonable, however, the results are not necessarily indicative of the consolidated results of operations had the acquisition occurred on July 1, 2019, or of future results of operations:

 

 

   

Three Months Ended

   

Six Months Ended

 
   

December 31, 2020

   

December 31, 2019

   

December 31, 2020

   

December 31, 2019

 
   

Actual

   

Pro forma

   

Actual

   

Pro forma

 
   

(Unaudited)

   

(Unaudited)

   

(Unaudited)

   

(Unaudited)

 

Total revenues, net

  $ 15,147,034     $ 8,929,802     $ 28,667,280     $ 20,541,401  

Net (loss)

    (9,525,294 )     (2,450,247 )     (13,831,224 )     (11,255,247 )

Net (loss) per share (aa)

  $ (0.72 )   $ (1.40 )   $ (1.09 )   $ (6.85 )

 

(aa) Pro forma net loss per share calculations excluded the impact of the issuance of the (i) Series G Convertible Preferred Stock and the, (ii) Series H Convertible Preferred Stock under the assumption those shares would continue to remain non-participatory during the periods reported above.

 

 

3. Revenue Recognition

 

Revenues by Geographic location. The following table reflects our product revenues by geographic location as determined by the billing address of our customers:

 

   

Three Months Ended

   

Six Months Ended

 
   

December 31,

   

December 31,

 
   

2020

   

2019

   

2020

   

2019

 
   

(unaudited)

   

(unaudited)

   

(unaudited)

   

(unaudited)

 

U.S.

  $ 13,757,000     $ 3,047,000     $ 25,901,000     $ 4,309,000  

International

    1,390,000       128,000       2,766,000       306,000  

  Total net revenue

  $ 15,147,000     $ 3,175,000     $ 28,667,000     $ 4,615,000  

 

Revenues by Product Portfolio. Net revenue disaggregated by significant product portfolio for the three and six-months ended December 31, 2020 and December 31, 2019 were as follows:

 

   

Three Months Ended December 31,

   

Six Months Ended December 31,

 
   

2020

   

2019

   

2020

   

2019

 
                                 

Primary care and devices portfolio

  $ 4,097,000     $ 1,190,000     $ 7,130,000     $ 2,630,000  

Pediatric portfolio

    3,115,000       1,985,000       5,834,000       1,985,000  

Consumer Health portfolio

    7,935,000       -       15,703,000       -  

  Total net revenue

  $ 15,147,000     $ 3,175,000     $ 28,667,000     $ 4,615,000  

 

 

 

4. Inventories

 

Inventories consist of raw materials and finished goods and are recorded at the lower of cost or net realizable value, with cost determined on a first-in, first-out basis. Aytu periodically reviews the composition of its inventories to identify obsolete, slow-moving or otherwise unsaleable items. If unsaleable items are observed and there are no alternate uses for the inventory, Aytu will record a write-down to net realizable value in the period that the impairment is first recognized. The Company wrote down $0.1 million and $0.2 million of inventory during the three and six-months ended December 31, 2020, respectively. There was no inventory written down for the three and six-months ended December 31, 2019, respectively.

 

Inventory balances consist of the following:

 

   

As of

   

As of

 
   

December 31,

   

June 30,

 
   

2020

   

2020

 

Raw materials

  $ 590,000     $ 397,000  

Finished goods, net

    5,981,000       9,603,000  
    $ 6,571,000     $ 10,000,000  

 

 

5. Fixed Assets

 

Fixed assets are recorded at cost and once placed in service, are depreciated on a straight-line basis over the estimated useful lives. Leasehold improvements are amortized over the shorter of the estimated economic life or related lease term. Fixed assets consist of the following:

 

         

As of

   

As of

 
   

Estimated

   

December 31,

   

June 30,

 
   

Useful Lives in years

   

2020

   

2020

 

Manufacturing equipment

  2 - 5     $ 112,000     $ 112,000  

Leasehold improvements

  3       111,000       229,000  

Office equipment, furniture and other

  2 - 5       281,000       312,000  

Lab equipment

  3 - 5       90,000       90,000  

Less accumulated depreciation and amortization

          (504,000 )     (484,000 )

Fixed assets, net

        $ 90,000     $ 259,000  

 

During the six months ended December 31, 2020, the Company recognized a loss of $0.1 million on sale of equipment due to termination of leases.

 

        Depreciation and amortization expense totaled $18,000 and $16,000 for the three-months ended December 31, 2020 and 2019, respectively, and $51,000 and $32,000 for the six-months ended December 31, 2020 and 2019, respectively.

 

 

6. Leases, Right-to-Use Assets and Related Liabilities

 

The Company previously adopted the FASB issued ASU 2016-02, “Leases (Topic 842)” as of July 1, 2019. With the adoption of ASU 2016-02, the Company recorded an operating right-of-use asset and an operating lease liability on its balance sheet associated with the lease of its corporate headquarters. The right-of-use asset represents the Company’s right to use the underlying asset for the lease term, and the lease obligation represents the Company’s commitment to make the lease payments arising from the lease. Right-of-use lease assets and obligations were recognized at the later of the commencement date or July 1, 2019; the date of adoption of Topic 842; based on the present value of remaining lease payments over the lease term. As the Company’s lease does not provide an implicit rate, the Company used an estimated incremental borrowing rate based on the information available at the commencement date in determining the present value of the lease payments. Rent expense is recognized on a straight-line basis over the lease term, subject to any changes in the lease or expectations regarding the terms. The lease liability is classified as current or long-term on the balance sheet.

 

 

As of December 31, 2020, the maturities of the Company’s future minimum lease payments were as follows:

 

 

   

Operating

   

Finance

 

2021 (remaining 6 months)

  $ 37,000     $ 61,000  

2022

    18,000       124,000  

2023

    -       127,000  

2024

    -       35,000  

2025

    -       3,000  

Total lease payments

    55,000       350,000  

Less: Imputed interest

            (39,000 )

Lease liabilities

          $ 311,000  

 

Cash paid for amounts included in the measurement of finance lease liabilities for the six months ended December 31, 2020 and 2019 was $147,000 and $63,000, respectively, and was included in net cash used in operating activities in the consolidated statements of cash flows.

 

As of December 31, 2020, the weighted average remaining lease term is 2.28 years, and the weighted average discount rate used to determine operating lease liabilities was 8.0%. Rent expense for the three-months ended December 31, 2020 and 2019 totaled $90,000 and $30,000. Rent expense for the six-months ended December 31, 2020 and 2019 totaled $160,000 and $63,000, respectively.

 

On August 28, 2020, the Company’s Innovus subsidiary signed a lease termination agreement with its lessor to terminate its lease effective September 30, 2020. The original lease termination date was April 30, 2023. As part of the agreement, Innovus agreed to make a cash payment to the landlord the equivalent of two additional months’ rent aggregating to $44,306 plus $125,000 less the security deposit of $20,881. The fair value of the lease liability related to this facility lease was approximately $0.7 million as of June 30, 2020. The Company recognized a gain of approximately $343,000 during the six months ended December 31, 2020.

       

       On October 1, 2020, the Company's Innovus subsidiary entered into a short-term lease for warehouse space in Carlsbad, CA. The lease term is for one-year with an option to terminate after six months with ninety days' notice. This lease is accounted for as a short-term lease and is not included as a component of the Company's right-to-use assets and related liability.

 

 

 

 

7. Intangible Assets Amortizable

 

The Company currently holds the following intangible asset portfolios as of December 31, 2020: (i) Licensed assets, which consist of pharmaceutical product assets that were acquired prior to July 1, 2020; (ii) Product technology rights, acquired from the November 1, 2019 acquisition of the Pediatric Portfolio from Cerecor; and, as a result of the Merger with Innovus on February 14, 2020, both, (iii) the Acquired product distribution rights; consisting of patents and trade names, and the Acquired customer lists.

 

If acquired in an asset acquisition, the Company capitalized the acquisition cost of each licensed patent or tradename, which can include a combination of both upfront consideration, as well as the estimated future contingent consideration estimated at the acquisition date. If acquired in a business combination, the Company capitalizes the estimated fair value of the intangible asset or assets acquired, based primarily on a discounted cash flow model approach or relief-from-royalties model.

 

The following table provides the summary of the Company’s intangible assets as of December 31, 2020 and June 30, 2020, respectively.

 

   

December 31, 2020

 
   

Gross Carrying Amount

   

Accumulated Amortization

   

Impairment

   

Net Carrying Amount

    Weighted-Average Remaining Life (in years)  

Licensed assets

  $ 23,649,000     $ (8,200,000 )   $ -     $ 15,449,000       11.72  

Acquired product technology right

    22,700,000       (2,648,000 )     -       20,052,000       8.84  

Acquired product distribution rights

    11,354,000       (1,319,000 )     -       10,035,000       7.27  

Acquired customer lists

    390,000       (227,000 )     -       163,000       0.62  
    $ 58,093,000     $ (12,394,000 )   $ -     $ 45,699,000       9.44  

 

   

June 30, 2020

 
   

Gross Carrying Amount

   

Accumulated Amortization

   

Impairment

   

Net Carrying Amount

    Weighted-Average Remaining Life (in years)  

Licensed assets

  $ 23,649,000     $ (7,062,000 )   $ -     $ 16,587,000       11.88  

MiOXSYS Patent

    380,000       (185,000 )     (195,000 )     -       -  

Acquired product technology right

    22,700,000       (1,513,000 )     -       21,187,000       9.34  

Acquired product distribution rights

    11,354,000       (565,000 )     -       10,789,000       7.78  

Acquired customer lists

    390,000       (98,000 )     -       292,000       1.12  
    $ 58,473,000     $ (9,423,000 )   $ (195,000 )   $ 48,855,000       9.11  

 

 

The following table summarizes the estimated future amortization expense to be recognized over the next five years and periods thereafter:

 

   

Amortization

 

2021

  $ 3,157,000  

2022

    6,085,000  

2023

    6,045,000  

2024

    6,033,000  

2025

    4,480,000  

Thereafter

    19,899,000  
    $ 45,699,000  

 

Certain of the Company’s amortizable intangible assets include renewal options, extending the expected life of the asset. The renewal periods range between approximately 1 to 20 years depending on the license, patent, or other agreement. Renewals are accounted for when they are reasonably assured. Intangible assets are amortized using the straight-line method over the estimated useful lives. Amortization expense of intangible assets was $1.6 million and $0.9 million for the three months ended December 31, 2020 and 2019, respectively. Amortization expense of intangible assets was $3.2 million and $1.5 million for the six months ended December 31, 2020 and 2019, respectively.

 

 

8. Accrued liabilities

 

Accrued liabilities consist of the following:

 

   

As of

   

As of

 
   

December 31,

   

June 30,

 
   

2020

   

2020

 

Accrued settlement expense

  $ 150,000     $ 315,000  

Accrued program liabilities

    1,386,000       959,000  

Accrued product-related fees

    2,332,000       2,471,000  

Credit card liabilities

    712,000       510,000  

Medicaid liabilities

    2,094,000       1,842,000  

Return reserve

    1,656,000       1,329,000  

Sales taxes payable

    175,000       175,000  

Other accrued liabilities*

    373,000       249,000  

Total accrued liabilities

  $ 8,878,000     $ 7,850,000  

 

* Other accrued liabilities consist of franchise tax, accounting fee, interest payable, merchant services charges, none of which individually represent greater than five percent of total current liabilities.

 

 

9. Fair Value Considerations

 

The Company’s asset and liability classified financial instruments include cash and cash equivalents, restricted cash, accounts receivable, accounts payable, accrued liabilities, warrant derivative liability, and contingent consideration. The carrying amounts of financial instruments, including cash and cash equivalents, restricted cash, accounts receivable, accounts payable, and accrued liabilities approximate their fair value due to their short maturities. The fair value of acquisition-related contingent consideration is based on Monte-Carlo models. The valuation policies are determined by management, and the Company’s Board of Directors is informed of any policy change.

 

 

Authoritative guidance defines fair value as the price that would be received to sell an asset or paid to transfer a liability (an exit price) in an orderly transaction between market participants at the measurement date. The guidance establishes a hierarchy for inputs used in measuring fair value that maximizes the use of observable inputs and minimizes the use of unobservable inputs by requiring that the most observable inputs be used when available. Observable inputs are inputs that market participants would use in pricing the asset or liability developed based on market data obtained from sources independent of the Company. Unobservable inputs are inputs that reflect the Company’s assumptions of what market participants would use in pricing the asset or liability developed based on the best information available in the circumstances. The hierarchy is broken down into three levels based on reliability of the inputs as follows:

 

Level 1: Inputs that reflect unadjusted quoted prices in active markets that are accessible to Aytu for identical assets or liabilities;

 

Level 2: Inputs that include quoted prices for similar assets and liabilities in active or inactive markets or that are observable for the asset or liability either directly or indirectly; and

 

Level 3: Unobservable inputs that are supported by little or no market activity.

 

The Company’s assets and liabilities which are measured at fair value are classified in their entirety based on the lowest level of input that is significant to their fair value measurement. The Company’s policy is to recognize transfers in and/or out of fair value hierarchy as of the date in which the event or change in circumstances caused the transfer. Aytu has consistently applied the valuation techniques discussed below in all periods presented.

 

Recurring Fair Value Measurements

 

The following table presents the Company’s financial liabilities that were accounted for at fair value on a recurring basis as of  December 31, 2020 and June 30, 2020, by level within the fair value hierarchy.

 

           

Fair Value Measurements at December 31, 2020

 
   

Fair Value at December 31, 2020

   

Quoted Priced in Active Markets for Identical Assets (Level 1)

   

Significant Other Observable Inputs (Level 2)

   

Significant Unobservable Inputs (Level 3)

 

Recurring:

                               

Contingent consideration

    16,280,000                   16,280,000  

CVR liability

    6,472,000                   6,472,000  
    $ 22,752,000                 $ 22,752,000  

 

           

Fair Value Measurements at June 30, 2020

 
   

Fair Value at June 30, 2020

   

Quoted Priced in Active Markets for Identical Assets
(Level 1)

   

Significant Other Observable Inputs
(Level 2)

   

Significant Unobservable Inputs
(Level 3)

 

Recurring:

                               

Contingent consideration

    13,588,000                   13,588,000  

CVR liability

  $ 5,572,000                 $ 5,572,000  
    $ 19,160,000                 $ 19,160,000  

 

Contingent Consideration. The Company classifies its contingent consideration liability in connection with the acquisition of Tuzistra XR, ZolpiMist and Innovus, within Level 3 as factors used to develop the estimated fair value are unobservable inputs that are not supported by market activity. The Company estimates the fair value of our contingent consideration liability based on projected payment dates, discount rates, probabilities of payment, and projected revenues. Projected contingent payment amounts are discounted back to the current period using a discounted cash flow methodology.

 

As of November 2, 2018, the contingent consideration, related to this Tuzistra XR, was valued at $8.8 million using a Monte Carlo simulation. As of December 31,2020, the contingent consideration was revalued at $15.8 million using the same Monte Carlo simulation methodology, and based on current interest rates, expected sales potential, and Aytu stock trading variables.  As of December 31, 2020, none of the milestones had been achieved, and therefore, no milestone payment was made. However, approximately $3.0 million is expected to be paid in November 2021, as this milestone will be satisfied.

 

 

The contingent consideration related to the ZolpiMist royalty payments was valued at $2.6 million using a Monte Carlo simulation, as of June 11, 2018. As of December 31, 2020, the contingent consideration was revalued at $0.3 million using the same Monte Carlo simulation methodology, and based on current interest rates, expected sales potential, and Aytu stock trading variables. The Company reevaluates the contingent consideration on a quarterly basis for changes in the fair value recognized after the acquisition date, such as measurement period adjustments.  As of December 31, 2020, none of the milestones had been achieved, and therefore, no milestone payment was made.

 

The Company recognized approximately $0.2 million in product related contingent consideration as a result of the February 14, 2020 Innovus Merger. The fair value was based on a discounted value of the future contingent payment using a 30% discount rate based on the estimates risk that the milestones are achieved. The contingent consideration accretion expense for the three and six-months ended December 31, 2020 and 2019 was $15,000, and $28,000, respectively. There was no material change in this valuation as of December 31, 2020.

 

Contingent value rights. Contingent value rights (“CVRs”) represent contingent additional consideration of up to $16 million payable to satisfy future performance milestones related to the Innovus Merger. Consideration can be satisfied in up to 470 thousand shares of the Company’s common stock, or cash either upon the option of the Company or in the event there are insufficient shares available to satisfy such obligations. The fair value of the contingent value rights was based on a Monte Carlo model which takes into account current interest rates and expected sales potential. On March 31, 2020, the Company paid out approximately 120 thousand shares of the Company’s common stock to satisfy the first $2 million milestone, which relates to the Innovus achievement of $24 million in revenues during the 2019 calendar year. The unrealized loss for the three and six-months ended December 31, 2020 and 2019was $0.1 million and $0.8 million, respectively. The CVR's did not exist until after December 31, 2019. 

 

Summary of Level 3 Input Changes

 

The following table sets forth a summary of changes to those fair value measures using Level 3 inputs for the three months ended December 31, 2020:

 

   

CVR Liability

   

Contingent Consideration

 

Balance as of June 30, 2020

  $ 5,572,000     $ 13,588,000  

Transfers into Level 3

           

Transfer out of Level 3

           

Total gains, losses, amortization or accretion in period

           

Included in earnings

  $ 900,000     $ 2,735,000  

Included in other comprehensive income

           

Purchases, issues, sales and settlements

           

Purchases

           

Issues

           

Sales

           

Settlements

        $ (43,000 )

Balance as of December 31, 2020

  $ 6,472,000     $ 16,280,000  

 

 

Significant Assumptions

 

Contingent consideration. The Company estimates the fair value of the Contingent Consideration at each reporting date using management's forecast as the baseline for developing a Monte-Carlo model. The other significant assumptions used in the Monte Carlo Simulation as of December 31, 2020, were as follows: 

 

 

   

As of December 31, 2020

Contingent Consideration

   

Credit risk assumption

 

19.10%

Sales volatility

 

45.00%

Credit spread

 

4.00%

Time steps per year

 

1

Number of iterations

 

500

 

Contingent value rights. The Company estimates the fair value of the Contingent Value Rights at each reporting date using management's forecast as the baseline for developing a Monte-Carlo model. The other significant assumptions used in the Monte Carlo Simulation as of December 31, 2020 were as follows:

 

 

   

As of December 31, 2020

Contingent Value Rights

   

Credit risk assumption

 

9.6%

Time steps per year

 

30.00

Number of iterations

 

10,000

 

 

 

10. Commitments and Contingencies

 

Commitments and contingencies are described below and summarized by the following as of December 31, 2020:

 

   

Total

   

2021

   

2022

   

2023

   

2024

   

2025

   

Thereafter

 

Prescription database

  $ 1,278,000     $ 545,000     $ 733,000       -       -       -       -  

Pediatric portfolio fixed payments and product minimums

    15,825,000       1,650,000       3,300,000       3,300,000       3,300,000       3,300,000       975,000  

Inventory purchase commitment

    1,717,000       981,000       736,000       -       -       -       -  

CVR liability

    14,000,000       2,000,000       2,000,000       5,000,000       5,000,000       -       -  

Product contingent liability

    2,500,000       -       -       -       -       -       2,500,000  

Product milestone payments

    3,000,000       -       3,000,000       -       -       -       -  
                                                         
    $ 38,320,000     $ 5,176,000     $ 9,769,000     $ 8,300,000     $ 8,300,000     $ 3,300,000     $ 3,475,000  

 

Prescription Database

 

In May 2016, the Company entered into an agreement with a vendor that will provide it with prescription database information. The Company agreed to pay approximately $1.6 million over three years for access to the database of prescriptions written for Natesto. In January 2020, the Company amended the agreement and agreed to pay additional $0.6 million to add access to the database of prescriptions written for the Pediatric Portfolio. The payments have been broken down into quarterly payments.

 

Pediatric Portfolio Fixed Payments and Product Milestone

 

The Company assumed two fixed, periodic payment obligations to an investor (the “Fixed Obligation”). Beginning November 1, 2019 through January 2021, the Company will pay monthly payments of $86,840, with a balloon payment of $15,000,000 due in January 2021. A second fixed obligation requires the Company pay a minimum of $100,000 monthly through February 2026, except for $210,767 paid in January 2020. 

 

On May 29, 2020, the Company entered into an Early Payment Agreement and Escrow Instruction (the “Early Payment Agreement”) pursuant to which the Company agreed to pay $15.0 million to the investor in early satisfaction of the Balloon Payment Obligation. The parties to the Early Payment Agreement acknowledged and agreed that the remaining fixed payments other than the Balloon Payment Obligation remain due and payable pursuant to the terms of the Agreement, and that nothing in the Early Payment Agreement alters, amends, or waives any provisions or obligations in the Waiver or the Investor agreement other than as expressly set forth therein.

 

In addition, the Company acquired a Supply and Distribution Agreement with Tris Pharma, Inc. ("TRIS"), (the “Karbinal Agreement”), under which the Company is granted the exclusive right to distribute and sell the product in the United States. The initial term of the Karbinal Agreement was 20 years. The Company will pay TRIS a royalty equal to 23.5% of net sales. A third party agreed to offset the 23.5% royalty payable by 8.5%, for a net royalty equal to 15%, in fiscal year 2018 and 2019 for net sales of Karbinal.

 

The Karbinal Agreement make-whole payment is capped at $2,100,000 each year. The Karbinal Agreement also contains minimum unit sales commitments, which is based on a commercial year that spans from August 1 through July 31, of 70,000 units through 2025. The Company is required to pay TRIS a royalty make whole payment of $30 for each unit under the 70,000-unit annual minimum sales commitment through 2025. The annual payment is due in August of each year. The Karbinal Agreement also has multiple commercial milestone obligations that aggregate up to $3.0 million based on cumulative net sales, the first of which is triggered at $40.0 million of net revenues.

 

Inventory Purchase Commitment

 

On May 1, 2020, the Company's Innovus subsidiary entered into a Settlement Agreement and Release (the “Settlement Agreement”) with Hikma Pharmaceuticals USA, Inc. (“Hikma”). Pursuant to the settlement agreement, Innovus has agreed to purchase and Hikma has agreed to manufacture a minimum amount of our branded fluticasone propionate nasal spray USP, 50 mcg per spray (FlutiCare®), under Hikma’s FDA approved ANDA No. 207957 in the U.S. The commitment requires Innovus to purchase three batches of product through fiscal year 2022 each of which amount to $1.0 million.

 

CVR Liability

 

On February 14, 2020, the Company closed on the Merger with Innovus Pharmaceuticals after approval by the stockholders of both companies on February 13, 2020. Upon closing the Merger, a subsidiary of the Company merged with and into Innovus and entered into a Contingent Value Rights Agreement (the “CVR Agreement”). Each CVR entitles its holder to receive its pro rata share, payable in cash or stock, at the option of Aytu, of certain payment amounts if the targets are met. If any of the payment amounts is earned, they are to be paid by the end of the first quarter of the calendar year following the year in which they are earned. Multiple revenue milestones can be earned in one year.

 

On March 31, 2020, the Company paid out the first CVR Milestone in the form of approximately 120 thousand shares of the Company’s common stock to satisfy the $2.0 million obligation as a result of Innovus achieving the $24.0 million revenue milestone for calendar year ended December 31, 2019. As a result of this, the Company recognized a gain of approximately $0.3 million during the fiscal year ended June 30, 2020. No additional milestone payments have been paid as of December 31, 2020.

 

 

Product Contingent Liability

 

In February 2015, Innovus acquired Novalere, which included the rights associated with distributing FlutiCare. As part of the Merger, Innovus is obligated to make 5 additional payments of $0.5 million each when certain levels of FlutiCare sales are achieved. The discounted value as of December 31, 2020, is approximately $0.2 million.

 

 

Product Milestone Payments

 

In connection with the Company’s intangible assets, Aytu has certain milestone payments, totaling $3.0 million, payable at a future date, are not directly tied to future sales, but upon other events certain to happen. These obligations are included in the valuation of the Company’s contingent consideration (see Note 9).

 

 

11. Capital Structure

 

The Company has 200 million shares of common stock authorized with a par value of $0.0001 per share and 50 million shares of preferred stock authorized with a par value of $0.0001 per share. On December 31, 2020 and June 30, 2020, Aytu had 17,882,893 and 12,583,736 common shares outstanding, respectively, and zero preferred shares outstanding, respectively.

 

Included in the common stock outstanding are 365,869 shares of restricted stock issued to executives, directors, employees, and consultants.

 

In June 2020, the Company initiated an at-the-market offering program, which allows the Company to sell and issue shares of our common stock from time-to-time. The company issued 430,230 shares of common stock, with total gross proceeds of $6.8 million before deducting underwriting discounts, commissions and other offering expenses payable by the Company of $0.2 million through December 31, 2020. The Company did not issue any shares of common stock under the at-the-market offering program during the three months ended September 30, 2020. During the three months ended December 31, 2020, the Company issued 352,912 shares of common stock, with total gross proceeds of approximately $3.6 million before deducting underwriting discounts, commissions, and other offering expenses payable by the Company of $0.1 million.

 

In July 2020, the Company paid $1.5 million issuance cost in cash related to the March 10, 12, and 19 offerings (the “March Offerings”) and issued 92,302 warrants to purchase 92,302 shares of the Company's common stock with an weighted-average exercise price of $15.99 to an investment bank conjunction with the March 2020 offerings. The warrants have a term of one year from the issuance date. These warrants had at issuance a fair value of approximately $356,000 and were valued using a Black-Scholes model.

 

On December 10, 2020, the Company entered into an exchange agreement to exchange the $0.8 million of debt outstanding for 130,081 shares of the Company's common stock (see Note 15).

 

    On December 10, 2020, the Company entered into an underwriting agreement with H.C. Wainwright & Co., LLC (“Wainwright”) (as amended and restated, the “Underwriting Agreement”). Pursuant to the Underwriting Agreement, the Company agreed to sell, in an upsized firm commitment offering, 4,166,667 shares (the “Shares”) of the Company’s common stock, $0.0001 par value per share (the “Common Stock”), to Wainwright at an offering price to the public of $6.00 per share, less underwriting discounts and commissions. In addition, pursuant to the Underwriting Agreement, the Company has granted Wainwright a 30-day option to purchase up to an additional 625,000 shares of Common Stock at the same offering price to the public, less underwriting discounts and commissions. Wainwright exercised their over-allotment option in full, purchasing total common stock of 4,791,667 shares. In connection with the offering, the Company issued 311,458 underwriter warrants to purchase up 311,458 shares of common stock. The exercise price per share of the underwriter warrants is $7.50 (equal to 125% of the public offering price per share for the shares of common stock sold in the offering) and the underwriter warrants have a term of five years from the date of effectiveness of the offering. The underwriter warrants will be exercisable immediately.

 

 

 

12. Equity Incentive Plan

 

Share-based Compensation Plans

 

On June 1, 2015, the Company’s stockholders approved the Aytu BioScience 2015 Stock Option and Incentive Plan (the “2015 Plan”), which, as amended in July 2017, provides for the award of stock options, stock appreciation rights, restricted stock and other equity awards for up to an aggregate of 3.0 million shares of common stock. The shares of common stock underlying any awards that are forfeited, canceled, reacquired by Aytu prior to vesting, satisfied without any issuance of stock, expire or are otherwise terminated (other than by exercise) under the 2015 Plan will be added back to the shares of common stock available for issuance under the 2015 Plan. On February 13, 2020, the Company’s stockholders approved an increase to 5.0 million total shares of common stock in the 2015 Plan. As of December 31, 2020, we have 4,560,864 shares that are available for grant under the 2015 Plan.

 

 

Stock Options

 

Employee Stock Options:

 

The fair value of the options is calculated using the Black-Scholes option pricing model. In order to calculate the fair value of the options, certain assumptions are made regarding components of the model, including the estimated fair value of the underlying common stock, risk-free interest rate, volatility, expected dividend yield and expected option life. Changes to the assumptions could cause significant adjustments to valuation. Aytu estimates the expected term based on the average of the vesting term and the contractual term of the options. The risk-free interest rate is based on the U.S. Treasury yield in effect at the time of the grant for treasury securities of similar maturity. There were no grants of stock options to employees during the three- and six-months ended December 31, 2020 and 2019

 

Stock option activity is as follows:

 

   

Number of Options

   

Weighted Average Exercise Price

   

Weighted Average Remaining Contractual Life in Years

   

Aggregate Intrinsic Value

 
Outstanding June 30, 2020     76,614     $ 19.39       9.67     $ -  

Granted

    -       -                  

Exercised

    -       -                  

Forfeited/Cancelled

    (3,187 )     -                  

Expired

    (2 )     -                  

Outstanding December 31, 2020

    73,425       19.71       9.08       -  

Exercisable at December 31, 2020

    9,095     $ 67.62       7.81     $ -  

 

As of December 31, 2020, there was $494,000 unrecognized option-based compensation expense related to non-vested stock options. The Company expects to recognize this expense over a weighted-average period of 2.68 years.

 

Restricted Stock

 

Restricted stock activity is as follows:

 

   

Number of Shares

    Weighted Average Grant Date Fair Value    

Weighted Average Remaining Contractual Life in Years

 

Unvested at June 30, 2020

    418,454     $ 14.69       6.4  

Granted

                       

Vested

    (52,743 )                

Forfeited

                       

Unvested at December 31, 2020

    365,711     $ 15.66       6.3  

 

Under the 2015 Plan, there was $4.3 million of total unrecognized stock-based compensation expense related to the non-vested restricted stock as of December 31, 2020. The Company expects to recognize this expense over a weighted-average period of 6.3 years. The Company previously issued 158 shares of restricted stock outside the Company’s 2015 Plan, which vest in July 2026. The unrecognized expense related to these shares was $1.1 million as of December 31, 2020 and is expected to be recognized over the weighted average period of 5.5 years.

 

Stock-based compensation expense related to the fair value of stock options and restricted stock was included in the statements of operations as selling, general and administrative expenses as set forth in the table below:

 

   

Three Months Ended December 31,

   

Six Months Ended December 31,

 

Selling, general and administrative:

 

2020

   

2019

   

2020

   

2019

 

Stock options

  $ 94,000     $ 2,000     $ 166,000     $ 7,000  

Restricted stock

    414,000       160,000       797,000       320,000  

Total stock-based compensation expense

  $ 508,000     $ 162,000     $ 963,000     $ 327,000  

 

 

 

13. Warrants

 

In July 2020, the Company issued 92,302 shares of warrants with a weighted average exercise price of $15.99 in connection with the March Offerings. The warrants have a term of one year from the issuance date. These warrants have a fair value of $356,000 and are classified within stockholders' equity.

 

On December 15, 2020, the Company issued 311,458 shares of warrants with an exercise price of $7.50 in connection with the December 15, 2020 offering. These warrants have a fair value of approximately $1.3 million and are classified within stockholders' equity.

 

Significant assumptions in valuing the warrants issued during the quarter are as follows:

 

   

Warrants Issued Three Months Ended December 31, 2020

 

Expected volatility

    100 %

Equivalent term (years)

    5.0  

Risk-free rate

    37 %

Dividend yield

    0.00 %

 

A summary of equity-based warrants is as follows:

 

   

Number of Warrants

   

Weighted Average Exercise Price

   

Weighted Average Remaining Contractual Life in Years

 

Outstanding June 30, 2020

    2,288,528     $ 30.26       2.00  

Warrants issued

    403,760                  

Warrants expired

    (842 )                

Warrants exercised

    -                  

Outstanding December 31, 2020

    2,691,446     $ 26.94       1.65  

 

 

14. Net Loss per Common Share

 

Basic income (loss) per common share is calculated by dividing the net income (loss) available to the common shareholders by the weighted average number of common shares outstanding during that period. Diluted net loss per share reflects the potential of securities that could share in the net loss of the Company. For each three-month period presented, the basic and diluted loss per share were the same for 2020 and 2019, as they were not included in the calculation of the diluted net loss per share because they would have been anti-dilutive.

 

The following table sets-forth securities that could be potentially dilutive, but as of the three and six-months ended December 31, 2020 and 2019 are anti-dilutive, and therefore excluded from the calculation of diluted earnings per share.

 

     

Three Months Ended

 
     

December 31,

 
     

2020

   

2019

 

Warrants to purchase common stock - liability classified

    24,105       24,105  

Warrant to purchase common stock - equity classified

(Note 13)

    2,691,446       1,621,891  

Employee stock options

(Note 12)

    73,425       156  

Employee unvested restricted stock

(Note 12)

    365,869       234,261  

Convertible preferred stock

(Note 11)

    -       315,115  
        3,154,845       2,195,528  

 

 

 

15. Notes Payable

 

The Aytu BioScience Note. On February 27, 2020, the Company issued a $0.8 million promissory note (the “Note”) and received consideration of approximately $0.6 million. The Note had an eight-month term with principal and interest payable on November 1, 2020, and the recognition of approximately $0.2 million of debt discount related to the issuance of promissory notes. The discount was amortized over the life of the promissory notes through the fourth quarter of calendar 2020. During the three and six-months ended months ended December 31, 2020 and 2019 the Company recorded approximately $15,000 and $70,000, respectively, of related amortization. There was no amortization for the same period in 2019. On December 10, 2020, the Company agreed to exchange the Note for 130,081 shares of the Company's common stock. The Company recognized a non-cash loss of approximately $0.3 million as a result of this exchange, saving the Company $0.8 million in cash that otherwise would have been used to satisfy this obligation on December 31, 2020.

 

The Innovus Notes. On January 9, 2020, prior to the completion of the merger, Innovus Pharmaceuticals, Inc., entered into a note agreement upon which it received gross proceeds of $0.4 million with a principal amount of $0.5 million. The note requires twelve equal monthly payments of approximately $45,000. As of December 31, 2020, the net balance of the note was $41,000.

 

 

16. Segment reporting

 

The Company’s chief operating decision maker (the “CODM”), who is the Company’s Chief Executive Officer, allocates resources and assesses performance based on financial information of the Company. The CODM reviews financial information presented for each reportable segment for purposes of making operating decisions and assessing financial performance.

 

The Company manages and aggregates its operational and financial information in accordance with two reportable segments: Aytu BioScience and Aytu Consumer Health. The Aytu BioScience segment consists of the Company’s prescription products. The Aytu Consumer Health segment contains the Company’s consumers healthcare products, which was the result of the Innovus Merger. Select financial information for these segments is as follows:

 

   

Three months Ended December 31,

   

Six Months Ended December 31,

 
   

2020

   

2019

   

2020

   

2019

 

Consolidated revenue:

                               

Aytu BioScience

  $ 7,212,000     $ 3,175,000     $ 13,000,000     $ 4,615,000  

Aytu Consumer Health

    7,935,000       -       16,000,000       -  

Consolidated revenue

    15,147,000       3,175,000       29,000,000       4,615,000  
                                 

Consolidated net loss:

                               

Aytu BioScience

    (8,267,000 )     (214,000 )     (11,218,000 )     (5,143,000 )

Aytu Consumer Health

    (1,258,000 )     -       (2,613,000 )     -  

Consolidated net loss

    (9,525,000 )     (214,000 )     (13,831,000 )     (5,143,000 )

 

   

As of

   

As of

 
   

December 31,

   

June 30,

 
   

2020

   

2020

 

Total assets:

               

Aytu BioScience

  $ 140,647,000     $ 126,267,000  

Aytu Consumer Health

    26,095,000       26,569,000  

Total assets

  $ 166,742,000     $ 152,836,000  

 

 

17. Related Party Transactions

 

Tris Pharma, Inc.

 

On November 2, 2018, the Company entered into a License, Development, Manufacturing and Supply Agreement (the “Tris License Agreement”). On November 1, 2019, the Company acquired the rights to Karbinal as a result of the acquisition of the Pediatric Portfolio from Cerecor, Inc. (See Notes 2 and 10). Mr. Ketan Mehta serves as a Director on the Board of Directors of the Company and is also the Chief Executive Officer of TRIS. The Company paid TRIS approximately $1.9 million and $0.2 million during the three months ended December 31, 2020 and 2019, respectively for a combination of royalty payments, inventory purchases and other payments as contractually required. The Company’s liabilities, including accrued royalties, contingent consideration and fixed payment obligations were $24.1 million and $24.8 million as of December 31, 2020 and 2019, respectively. In October 2020, the Company paid Tris approximately $1.6 million related to its Karbinal fixed payment obligation.

 

 

25

 

 

18. Subsequent Events

 

Except for below, see Footnote 1 for information relating to certain events occurring between December 31, 2020, and the filing of this report Form 10-Q, impacting information disclosed above.

 

MiOXSYS® Licensing Agreement

 

On January 20, 2021, the Company signed an Exclusive License Agreement (the “ MiOXSYS Agreement”) to exclusively license the intellectual property surrounding the use of the Company's rapid in vitro diagnostic test that accurately measures seminal oxidative stress, including all components of the MiOXSYS® commercial system (the “Product”). The Agreement has been entered into with Avrio Genetics, LLC (“Avrio Genetics”), a Pennsylvania-based limited liability company focused on reproductive health.

 

Under the MiOXSYS Agreement, Avrio Genetics will purchase existing inventory, commercialize, and market the Product under a royalty on Product net sales with a minimum annual payment fee structure for a term of ten (10) years, with the term continuing in perpetuity with a fixed percentage royalty rate based on Product sales payable annually to the Company. The Company will continue to own the intellectual property in the Product, with Avrio Genetics bearing all related patent maintenance and prosecution fees, commercial expenses, and regulatory fees. Further, Avrio Genetics will foster and expand all related customer, manufacturing, marketing, and distribution relationships in their effort to increase the commercialization of the Product. With Avrio’s assumption of the Product-related expenses and management of the Product programs, the Company expects to eliminate expenses associated the Product while maintain future revenue potential in the form of royalty and minimum annual payments from Avrio Genetics.

 

 

 

 

 

 

Item 2. Managements Discussion and Analysis of Financial Condition and Results of Operations.

 

This discussion should be read in conjunction with Aytu BioScience, Inc.s Annual Report on Form 10-K for the year ended June 30, 2020, filed on October 6, 2020. The following discussion and analysis contain forward-looking statements that involve risks and uncertainties. Actual results could differ materially from those projected in the forward-looking statements. For additional information regarding these risks and uncertainties, please see the risk factors included in Aytus Form 10-K filed with the Securities and Exchange Commission on October 6, 2020.

 

Overview

 

We are a commercial-stage specialty pharmaceutical company focused on commercializing novel products that address significant healthcare needs in both prescription and consumer health categories. We are currently operate our Aytu BioScience business, consisting of the Primary Care Portfolio (the “Primary Care Portfolio”) and Pediatric Care Portfolio (the “Pediatric Portfolio”), and our Aytu Consumer Health business (the “Consumer Health Portfolio”). Our Aytu BioScience business is focused on prescription pharmaceutical products treating hypogonadism (low testosterone), cough and upper respiratory symptoms, insomnia, male infertility, and various pediatric conditions. Our Consumer Health business is focused on consumer health products. We plan to expand into other therapeutic areas as opportunities arise. Aytu was incorporated as Rosewind Corporation on August 9, 2002 in the State of Colorado. Aytu was re-incorporated in the state of Delaware on June 8, 2015.

 

The primary care portfolio includes (i) Natesto, the only FDA-approved nasal formulation of testosterone for men with hypogonadism (low testosterone, or "Low T"), (ii) ZolpiMist, the only FDA-approved oral spray prescription sleep aid, and (iii) Tuzistra XR, the only FDA- approved 12-hour codeine-based antitussive syrup.

 

The pediatric care portfolio, acquired on November 1, 2019, (the “Pediatric Portfolio”), includes (i) Poly-Vi-Flor and Tri-Vi-Flor, two complementary prescription fluoride-based supplement product lines containing combinations of fluoride and vitamins in various formulations for infants and children with fluoride deficiency, (ii) Cefaclor, a second-generation cephalosporin antibiotic suspension; and (iii) Karbinal ER, an extended-release carbinoxamine (antihistamine) suspension indicated to treat numerous allergic conditions.

 

On February 14, 2020 we acquired Innovus Pharmaceuticals (“Innovus”), a specialty pharmaceutical company licensing, developing and commercializing safe and effective consumer healthcare products designed to improve health and vitality. Innovus commercializes over twenty consumer health products competing in large healthcare categories including diabetes, men's health, sexual wellness and respiratory health. The Innovus product portfolio is commercialized through direct-to-consumer marketing channels utilizing the Innovus’s proprietary Beyond Human® marketing and sales platform and on e-commerce platforms.

 

On December 10, 2020, Aytu and Neutron Acquisition Sub, Inc., our wholly owned subsidiary (“Merger Sub”), entered into an Agreement and Plan of Merger (the “Merger Agreement”) with Neos Therapeutics, Inc. (“Neos”). The Merger Agreement provides, among other things, that on the terms and subject to the conditions set forth therein, Merger Sub will merge with and into Neos, with Neos surviving as a wholly owned subsidiary of Aytu (the “Neos Merger”). The Neos Merger is subject to the approval of both the shareholders of Aytu and Neos. Based on the number of shares of our common stock anticipated to be immediately issued to Neos stockholders upon closing of the merger (which could be impacted by changes in Neos stock price leading to exercise of options not otherwise being assumed by Aytu or by additional issuances of Neos common stock that we may consent to) and the number of shares of our common stock outstanding as of December 31, 2020, it is expected that, immediately after completion of the merger, former Neos stockholders are expected to own approximately 24% of the outstanding shares of the our common stock and existing Aytu stockholders are expected to own approximately 76% of the outstanding shares of our common stock. In addition, each unvested option to acquire shares of Neos common stock that is outstanding as of immediately prior to the close of the Neos Merger  (the "Effective Time") with an exercise price equal to or less than $0.95 shall be assumed by Aytu and converted into an option to acquire shares of our common stock on the same terms and conditions. The number of shares of our common stock subject to each such assumed option shall be equal to (i) the number of shares of Neos common stock subject to the corresponding assumed option immediately prior to the Effective Time multiplied by (ii) 0.1088 (the "Exchange Ratio"), rounded down, if necessary, to the nearest whole share of our common stock, and such assumed option shall have an exercise price per share (rounded up to the nearest whole cent) equal to (A) the exercise price per share of Neos common stock otherwise purchasable pursuant to the corresponding assumed option divided by (B) the Exchange Ratio. As of February 5, 2021, the total estimated shares to be issued as consideration in connection with this merger totaled approximately 5.4 million with an estimated fair value of $44.2 million. 

 

In connection with the execution of the Merger Agreement, Aytu and Neos have entered into a Commitment Letter (the “Bridge Commitment Letter”) for us to provide financing to Neos under an unsecured convertible note, in an aggregate amount of up to $5,000,000, subject to the terms set forth therein (the "Bridge Financing"). Interest accrues on the principal amount outstanding under the note at a rate of 6.0% per annum, compounding monthly and commencing if and when such Bridge Financing is provided. If an event of default has occurred and is continuing, the interest rate then in effect will be increased by 2.0% per annum, and all overdue obligations under the note will bear interest at the interest rate in effect at such time plus the additional 2.0% per annum. Our rights under the note, including rights to payment, are subordinated to the rights of Neos’s existing senior lenders. The maturity date of the note is the earlier of the acceleration of the obligations evidenced thereby and November 7, 2022. In the event that Neos draws down on the note, the exchange ratio will be adjusted downward by an amount equal to 0.00011 for every $100,000 of financing funded to Neos under the note.

 

In April of 2020, the Company entered into a licensing agreement with Cedars-Sinai Medical Center to secure worldwide rights to various potential uses of Healight, an investigational medical device platform technology. Healight has demonstrated safety and efficacy in pre-clinical studies, and we plan to advance this technology and assess its safety and efficacy in human studies, initially focused on COVID-19 patients.

 

We recently established a purchasing relationship with a U.S. supplier of Emergency Use Authorization (EUA) authorized antigen tests. Antigen tests rapidly detect the presence of the SARS-CoV-2 virus antigen via a nasopharyngeal swab and are used without laboratory equipment. Demand for rapid antigen tests has increased in recent months across the U.S.

Our strategy is to continue building our portfolio of revenue-generating products, leveraging our focused commercial team and expertise to build leading brands within large therapeutic markets.

 

Strategic Growth Initiatives

 

Pursuant to our strategy of identifying and acquiring complimentary assets and companies, we expect to substantially increase our revenue generating capacity and provide opportunities to reduce our combined operating losses through a combination of our recent acquisitions during the twelve months ended June 30, 2020, coupled with the December 10, 2020 announcement of our planto merge with Neos. The combined impact of these transactions on revenue and operating expenses is expected to position us to achieve positive cash flow earlier than previously expected.

 

 Strategic Rx Acquisitions. On December 10, 2020, we entered in a Merger Agreement with Neos Therapeutics, Inc. The merger is subject the approval by shareholders of both Aytu and Neos. The merger can accelerate our path to profitability, with estimated annualized cost synergies of up to approximately $15M beginning FY 2022. Neos’ established, multi-brand ADHD portfolio, will enhance our footprint in pediatrics and expanding our presence in adjacent specialty care segments. Opportunity to leverage and further enhance Neos RxConnect, a best-in-class patient support program, for our product portfolio of best-in-class prescription therapeutics, and potentially, our consumer health products.

 

On November 1 2019, we acquired the Cerecor, Inc.'s ("Cerecor") portfolio of prescription pediatric therapeutics (the “Pediatric Portfolio”). The Pediatric Portfolio consists of four pharmaceutical and other prescription products consisting of (i) Cefaclor for Oral Suspension, (ii) Karbinal ER, (iii) Poly- Vi-Flor, and (iv) Tri-Vi-Flor. . Total consideration transferred consisted of $4.5 million cash and approximately 9.8 million shares of Series G Convertible Preferred Stock, plus the assumption not more than $3.5 million of Medicaid rebates and products returns. In addition, we hired the majority of the Cerecor’s workforce focused on commercial sales, commercial contracts, and customer relationships.

 

 

 

We have assumed obligations due to an investor including fixed and variable payments. We assumed fixed monthly payments equal to $0.1 million from November 2019 through January 2021 plus $15 million due in January 2021. Monthly variable payments due to the same investor are equal to 15% of net revenue generated from a subset of the Product Portfolio, subject to an aggregate monthly minimum of $0.1 million, except for January 2020, when a one-time payment of $0.2 million was due and paid. The variable payment obligation continues until the earlier of: (i) aggregate variable payments of approximately $9.5 million have been made, or (ii) February 12, 2026. The Company subsequently paid down the $15 million balloon payment early in June 2020, removing this obligation from our balance sheet.

 

Further, certain of the products in the Pediatric Portfolio require royalty payments ranging from 15% to 38.0% of net revenue. One of the products in the Pediatric Portfolio requires us to generate minimum annual sales sufficient to represent annual royalties of approximately $1.75 million.

 

Consumer Health Acquisitions. On February 14, 2020, we closed on the merger with Innovus Pharmaceuticals after approval by the stockholders of both companies on February 13, 2020. The acquisition of Innovus has enabled the company to expand into the consumer healthcare market with Innovus’ over-the-counter medicines and other consumer health products. We expect Innovus to continue to develop additional consumer healthcare products and expand its product portfolio. This, we expect, will drive additional revenue for the consumer health subsidiary and contribute meaningfully to the company's overall revenue growth.

 

Additionally, we expect to continue to participate in the U.S. COVID-19 testing market. We have purchased 1,600,000 COVID-19 IgG/IgM rapid antibody tests from Zhejiang Orient Gene Biotech Limited via our distribution agreement with L.B. Resources, Ltd. We also signed an exclusive license with Cedars-Sinai Medical Center for rights to a medical device technology platform that is a prospective treatment for COVID-19 for seriously ill patients in the ICU. We expect to advance this technology through development and, if proven clinically effective and able to be manufactured at scale, expect to commercialize this product in the future.

 

In the near-term, we expect to create value for shareholders by implementing a focused strategy of increasing sales of our prescription therapeutics while leveraging our commercial infrastructure. Further, we expect to increase sales of our consumer healthcare product portfolio. Additionally, we expect to expand both our Rx and consumer health product portfolios through continuous business and product development. Finally, we expect to identify operational efficiencies identified through our recent transactions and implement expense reductions accordingly.

 

ACCOUNTING POLICIES

 

Significant Accounting Policies and Estimates

 

Our consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America. The preparation of the consolidated financial statements requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities at the date of the consolidated financial statements, and the reported amounts of expenses during the reporting period. On an ongoing basis, management evaluates its estimates and judgments, including those related to recoverability and useful lives of long-lived assets, stock compensation, valuation of derivative instruments, allowances, contingent consideration, contingent value rights ("CVR"), fixed payment arrangements and going concern. Management bases its estimates and judgments on historical experience and on various other factors, including COVID-19, that the Company believes to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions. The methods, estimates, and judgments used by us in applying these critical accounting policies have a significant impact on the results we report in our consolidated financial statements. Our significant accounting policies and estimates are included in our Annual Report on Form 10-K for the fiscal year ended June 30, 2020, filed with the SEC on October 6, 2020.

 

Information regarding our accounting policies and estimates can be found in the Notes to the consolidated Financial Statements.

 

Newly Issued Accounting Pronouncements

 

Information regarding the recently issued accounting standards (adopted and pending adoption as of December 31, 2020) are presented in Note 1 to the condensed consolidated financial statements.

 

 

RESULTS OF OPERATIONS

 

Results of Operations Three and Six Months Ended December 31, 2020 compared to the Three and Six Months Ended December 31, 2019

 

  

   

Three months Ended December 31,

                 
   

2020

   

2019

   

Change

    %  
                                 

Revenues

                               

Product and service revenue, net

  $ 15,147,034     $ 3,175,236     $ 11,971,798       377 %

Operating expenses

                               

Cost of sales

    5,998,389       606,046       5,392,343       890 %

Research and development

    286,572       66,675       219,897       330 %

Selling, general and administrative

    12,852,614       6,516,160       6,336,454       97 %

Amortization of intangible assets

    1,584,581       953,450       631,131       66 %

Total operating expenses

    20,722,156       8,142,331       12,579,825       154 %

Loss from operations

    (5,575,122 )     (4,967,095 )     (608,027 )     12 %

Other (expense) income

                               

Other (expense), net

    (378,958 )     (446,958 )     68,000       -15 %

Loss from change in fair value of contingent consideration

    (3,313,656 )     -       (3,313,656 )      
Gain from derecognition of contingent consideration     -       5,199,806       (5,199,806 )     -100 %
Loss on debt exchange     (257,559 )     -       (257,559 )      
Total other (expense) income     (3,950,173 )     4,752,848       (8,703,021 )     -183 %
Net loss   $ (9,525,295 )   $ (214,247 )   $ (9,311,048 )     4346 %
                                 
                                 
                                 
                                 
    Six Months Ended December 31,                  
    2020     2019     Change       %
                                 
Revenues                                
Product and service revenue, net   $ 28,667,280     $ 4,615,062     $ 24,052,218       521 %
Operating expenses                                
Cost of sales     9,817,545       981,766       8,835,779       900 %
Research and development     469,437       144,695       324,742       224 %
Selling, general and administrative     24,342,983       11,662,603       12,680,380       109 %
Amortization of intangible assets     3,169,161       1,528,567       1,640,594       107 %

Total operating expenses

    37,799,126       14,317,631       23,481,495       164 %
Loss from operations     (9,131,846 )     (9,702,569 )     570,723       -6 %
Other (expense) income                                
Other (expense), net     (1,130,499 )     (642,344 )     (488,155 )     76 %
Loss from change in fair value of contingent consideration     (3,311,320 )     -       (3,311,320 )      
Gain from derecognition of contingent consideration     -       5,199,806       (5,199,806 )     -100 %

Gain from warrant derivative liability

    -       1,830       (1,830 )     -100 %
Loss on debt exchange     (257,559 )     -       (257,559 )      
Total other (expense) income     (4,699,378 )     4,559,292       (9,258,670 )     -203 %

Net loss

  $ (13,831,224 )   $ (5,143,277 )   $ (8,687,947 )     169 %

 

Product revenue. We recognized net revenue from product sales of approximately $15.1 million and $3.2 million for the three months ended December 31, 2020 and 2019, respectively. We recognized net revenue from product sales of approximately $28.7 and $4.6 million for the six months ended December 31, 2020, and 2019, respectively. The increase was primarily driven by the acquisition of the Pediatric Portfolio on November 1, 2019 and Consumer Health Portfolio on February 14, 2020, as well as additional revenues from COVID-19 test kit sales. 

 

Cost of sales. We incurred the cost of sales of $6.0 million and $0.6 million recognized for the three months ended December 31, 2020 and 2019, respectively. We incurred the cost of sales $9.8 million and $1.0 million for the six months ended December 31, 2020 and 2019, respectively. The increase was primarily driven by the acquisition of the Pediatric Portfolio on November 1, 2019 and Innovus (a/k/a Consumer Health Portfolio) on February 14, 2020, as well as additional sales from COVID-19 test kit sales. 

 

Research and Development. Research and development expenses increased $0.2 million, or 230%, for the three months ended December 31, 2020, compared to the three months ended December 31, 2019. Research and development expenses increased approximately $0.3 million, or 224% for the six months ended December 31, 2020, compared to the six months ended December 31, 2019. The increase was due primarily to costs associated with the Company’s Healight Platform license and initial development and clinical costs.

 

Selling, General and Administrative. Selling, general and administrative costs increased $6.3 million, or 97%, for the three months ended December 31, 2020, compared the three months ended December 31, 2019. Selling, general and administrative costs increased $12.7 million, or approximately 109% for the six months ended December 31, 2020. The increase was primarily due to the Pediatric Portfolio and Innovus acquisition that occurred in the prior year ended June 30, 2020, of which, only the Pediatric Portfolio was a component of our financial results for November and December of 2019.

 

 

Amortization of Intangible Assets. Amortization expense for the remaining intangible assets was approximately $1.6 million and $1.0 million for the for the three months ended December 31, 2020 and 2019, respectively. Amortization expense for the remaining intangible assets was approximately $3.2 million and $1.5 million, respectively, for the six months ended December 31, 2020. This expense is related to corresponding amortization of our finite-lived intangible assets. The increase of this expense is due to the Pediatric Portfolio acquisition from Cerecor and Innovus Merger that occurred in the 2020 fiscal year ended June 30, 2020.

 

Interest (expense) income, net. Interest (expense) income, net for the three months ended December 31, 2020, was expense of approximately $0.4 million, compared to expenses of $0.5 million for the three months ended December 31, 2019. Interest (expense) income, net for the six months ended December 31, 2020, was expense of approximately $1.1 million, compared to interest expense of $0.6 million for the three months ended December 31, 2019. The increase was primarily due to the accretion and interest expense resulting from the assumed fixed payment obligations and other long-term liabilities that arose from the (i) November 1, 2019 acquisition of the Pediatric Portfolio from Cerecor, Inc. and (ii) the February 14, 2020, Merger with Innovus.

 

Loss from change in fair value of contingent consideration. We recognized a loss of approximately $2.5 million from the change in the fair value of the ZolpiMist and Tuzistra contingent consideration liability and a loss of approximately $0.8 million from the change in fair value of the contingent value rights ("CVR's") liability related to the Innovus Merger.

 

Liquidity and Capital Resources

 

As of December 31, 2020, we had approximately $62.3 million of cash, cash equivalents and restricted cash. Our operations have historically consumed cash and are expected to continue to require cash, but at a declining rate.

 

Revenues for the three and six-months ended December 31, 2020, were approximately $15.1 million and $28.7 million, compared to $3.2 million and $4.6 million for the same periods ended December 31, 2019, an increase of 377% and 521%, respectively. Revenues increased 277% and 100% for each of the years ended June 30, 2020 and 2019, respectively. Revenue is expected to increase over time, which will allow us to rely less on our existing cash balance and proceeds from financing transactions. Cash used by operations during the three and six-months ended December 31, 2020 was $10.9 million compared to $9.1 million for the three and six-months ended December 31, 2019. The increase is due primarily to an increase in working capital and pay down of other liabilities.

 

As of the date of this report, we expect costs for current operations to increase modestly as we continue to integrate the acquisition of the Pediatrics Portfolio and Innovus and continue to focus on revenue growth through increasing product sales. Our current assets totaling approximately $92.5 million as of December 31, 2020, plus the proceeds expected from ongoing product sales will be used to fund existing operations. We may continue to access the capital markets from time-to-time when market conditions are favorable. The timing and amount of capital that may be raised is dependent the terms and conditions upon which investors would require to provide such capital. There is no guarantee that capital will be available on terms favorable to us and our stockholders, or at all. We raised approximately $29.6 million, net during the three months ended December 31, 2020, from the sale of approximately 0.4 million shares using the Company’s at-the-market facility and from the issuance of approximately 4.8 million shares of our common stock and 0.3 million placement agent warrants on the December 15, 2020 offering. Finally, on December 10, 2020, we exchanged $0.8 million of debt into 0.1 million shares of our common stock, reducing the need to use cash to satisfy this obligation. Between December 31, 2020, and the filing date of this quarterly report on Form 10-Q, we have not issued any common stock under our at-the-market offering program. As of the date of this report, we have adequate capital resources to complete our near-term operating objectives. 

 

Since we have sufficient cash on-hand as of December 31, 2020, to cover potential net cash outflows for the twelve months following the filing date of this Quarterly Report, we report that there is no indication of substantial doubt about our ability to continue as a going concern.

 

If we are unable to raise adequate capital in the future when it is required, we can adjust our operating plans to reduce the magnitude of the capital needs under our existing operating plan. Some of the adjustments that could be made include delays of and reductions to commercial programs, reductions in headcount, narrowing the scope of our commercial plans, or reductions to its research and development programs. Without sufficient operating capital, we could be required to relinquish rights to products or renegotiate to maintain such rights on less favorable terms than it would otherwise choose. This may lead to impairment or other charges, which could materially affect our balance sheet and operating results.

 

The following table shows cash flows for the three months ended December 31, 2020 and 2019:

 

   

Six Months Ended December 31,

 
   

2020

   

2019

 

Net cash used in operating activities

  $ (10,900,299 )   $ (9,087,054 )

Net cash used in investing activities

    (46,683 )     (5,954,635 )

Net cash provided by financing activities

  $ 24,898,281     $ 9,258,350  

 

 

Net Cash Used in Operating Activities

 

During the six-months ended December 31, 2020, our operating activities used $10.9 million in cash, which was less than the net loss of $13.8 million, primarily due to the non-cash depreciation, amortization and accretion, stock-based compensation, and loss from change in fair value of contingent consideration and CVR, a decrease in inventory and an increase in accrued liabilities. These charges were offset by increases in accounts receivable, prepaid expenses, and other current assets and decreases in accounts payables and accrued compensation.

 

During the six-months ended December 31, 2019, our operating activities used $9.1 million in cash, which was greater than the net loss of $5.1 million, primarily as a result of derecognition of contingent consideration and an increase in accounts receivable, offset by the non-cash depreciation, amortization and accretion, stock-based compensation charges to earnings, coupled with an increase in accounts payable.

 

Net Cash Used in Investing Activities

 

During the six-months ended December 31, 2020, we made a payment of $0.05 million in contingent consideration.

 

During the six-months ended December 31, 2019, we issued a note receivable to Innovus totaling $1.4 million. We also used $4.5 million for the Cerecor acquisition and we paid $105,000 in contingent consideration.

 

Net Cash from Financing Activities

 

Net cash provided by financing activities in the six-months ended December 31, 2020, was $24.9 million. This was primarily related to the December 2020 offering for gross proceeds cost of $28.8 million offset by the offering cost of $2.6 million. We also completed the ATM offering with gross proceeds of $3.5 million, which was offset by the offering cost of $1.7 million, driven by a one-time payment in July 2020 of approximately $1.5 million. We paid approximately $2.8 million related to fixed payment obligation and $0.3 million of debt. 

 

Net cash provided by financing activities in the six-months ended December 31, 2019, was $9.3 million. This was primarily related to the October 2019 Offering for gross proceeds of $10.0 million, offset by the offering cost of $0.7 million which was paid in cash.

 

Off Balance Sheet Arrangements

 

We do not have off-balance sheet arrangements, financings, or other relationships with unconsolidated entities or other persons, also known as “variable interest entities.”

 

Contractual Obligations and Commitments

 

Information regarding our Contractual Obligations and Commitments is contained in Note 10 to the Financial Statements.

 

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

 

We are not currently exposed to material market risk arising from financial instruments, changes in interest rates or commodity prices, or fluctuations in foreign currencies. We have not identified a need to hedge against any of the foregoing risks and therefore currently engage in no hedging activities.

 

Item 4. Controls and Procedures.

 

As of the end of the period covered by this Quarterly Report on Form 10-Q, an evaluation was carried out by our management, with the participation of the Chief Executive Officer and Chief Financial Officer, of the effectiveness of our disclosure controls and procedures, as defined in Rule 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended, or the Exchange Act. Based on such evaluation, the Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures are effective to ensure that information required to be disclosed in the reports we file or submit under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms, and are operating in an effective manner.

 

Changes in Internal Control over Financial Reporting

 

There were no changes in our internal controls over financial reporting, except as described below, known to the Chief Executive Officer or the Chief Financial Officer that occurred during the period covered by this Report that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

The Company’s assessment over changes in our internal controls over financial reporting excluded those processes or controls that exist at our Aytu Consumer Health reporting unit which we acquired from the February 14, 2020, Innovus Merger are being evaluated internally, and any changes as a result of that evaluation will be disclosed in future filings. 

 

 

 

PART II. OTHER INFORMATION

 

Item 1. Legal Proceedings.

 

 

Hikma. On May 8, 2017, Innovus entered into a Supply Agreement with Hikma (formerly West-Ward Pharmaceuticals Corp.) for the supply of FlutiCare®, a branded fluticasone propionate nasal spray. During the second year of the Supply Agreement, Innovus received multiple shipments of FlutiCare® products containing non-compliant labelling due to defective label adhesive. Following that Hikma and Innovus began negotiations to settle the issues relating to the defective products and the status of the Supply Agreement. On May 1, 2020, Hikma and Innovus (now a Company subsidiary) entered into the Settlement Agreement requiring Innovus to purchase three batches of FlutiCare® through the fiscal year 2022 at a price of $1 million per batch in exchange for Hikma agreeing to a product quality threshold and inspection and qualification of the product by a third party.

 

Marin County DA. On August 24, 2018, Innovus received a letter from the Marin County District Attorney’s Office (the “Marin DA”) demanding substantiation for certain advertising claims made by Innovus related to DiabaSens®, and Apeaz®, which were sold and marketed in Marin County, California. The Marin DA is part of a larger Northern California task force comprising of district attorney offices from ten counties that agree to handle customer protection matters. Innovus responded to the Marin DA through its regulatory counsel in November 2018 and continued to exchange correspondence with the Marin DA through April 2019. In June 2019, Innovus met with the Northern California task force. In March 2020, Innovus (now a Company subsidiary) entered into a Stipulation for Entry of Final Judgement (the “Stipulation”), pursuant to which Innovus agreed to the following: (i) certain injunctive relief relating the advertising and sale of DiabaSens®, and Apeaz®; (ii) to pay a civil penalty of $150,000; (iii) to reimburse investigative costs of $11,500; and (iv) to pay restitution of $43,000. In May 2020, the Marin DA filed the judgement with the Superior Court for the County of Monterrey and the parties are waiting for the judge to approve the stipulation.

 

 

Pliscott. Between November 20, 2019 and December 17, 2019, four putative class action lawsuits were filed in Delaware state and federal courts in connection with: (i) Aytu’s proposal to approve, in accordance with Nasdaq Marketplace Rule 5635(d), the convertibility of the Company’s Series F convertible preferred stock and the exercisability of certain warrants, in each case, issued in a private placement offering that closed on October 16, 2019 (the “Nasdaq Rule 5635(d) Proposal”); (ii) Aytu’s proposal to approve an amendment to its Certificate of Incorporation to increase the number of its authorized shares of common stock from 100,000,000 to 120,000,000 shares of common stock (the “Authorized Share Increase Proposal”); and (iii) Aytu’s proposal to approve the adjournment of the special meeting, if necessary, to continue to solicit votes for the Nasdaq Rule 5635(d) Proposal and/or the Authorized Share Increase Proposal (“Adjournment Proposal” and, together with the Nasdaq Rule 5635(d) Proposal and the Authorized Share Increase Proposal, the “Proposal”). Three lawsuits were filed in the Court of Chancery of the State of Delaware: Carl Pliscott v. Joshua R. Disbrow, et al. , Case No. 2019-0933, filed on November 20, 2019 (the “Pliscott Action”); Adam Kirschenbaum v. Aytu Bioscience, Inc., et al. , Case No. 2019-0984, filed on December 10, 2019 (the “Kirschenbaum lawsuit”); and Michael Sebree v. Josh Disbrow, et al. , Case No. 2019-1011, filed on December 17, 2019 (the “Sebree Action”). The Kirschenbaum Action and Sebree Action were both assigned to Chancellor Andre G. Bouchard. The Pliscott Action was removed to the United States District Court for the District of Delaware on December 5, 2019, captioned as Carl Pliscott v. Joshua R. Disbrow, et al., Case No. 19-cv-02228-UNA, but was remanded to the Court of Chancery and assigned to Chancellor Andre G. Bouchard on January 14, 2020. One lawsuit was filed in the United States District Court for the District of Delaware and assigned to Chief Judge Leonard P. Stark: Adam Franchi v. Aytu Bioscience, Inc., et al., Case No. 19-cv-02204- LPS, filed on November 26, 2019 (the “Franchi Action”). The Pliscott Action, Kirschenbaum Action, and Sebree Action alleged that the members of the Aytu board breached their fiduciary duties to Aytu stockholders by failing to disclose all information material to the Proposals. The Franchi Action alleged that Aytu and the individual members of the Aytu board violated Sections 14(a) and 20(a) of the Securities Exchange Act of 1934 (and Rule 14a-9, promulgated thereunder) by virtue of allegedly false and misleading statements contained in the proxy statement filed by Aytu on November 21, 2019. All four lawsuits sought, among other things, declaratory relief allowing the action to be maintained as a class action, injunctive relief prohibiting any stockholder vote on the Proposals or other consummation of the Proposals, damages, attorneys’ fees and costs, and other and further relief. The Sebree Action further sought injunctive relief prohibiting consummation of the Asset Purchase Agreement, dated October 10, 2019. Aytu and the board have asserted that all claims asserted are meritless and vigorously defended against the four lawsuits. On January 30, 2020, the parties in the Pliscott Action, Kirschenbaum Action, and Sebree Action filed a stipulation voluntarily dismissing the cases as moot, with plaintiffs reserving the right to seek mootness fees. On February 5, 2020, the Chancery Court dismissed the cases while retaining jurisdiction to adjudicate anticipated mootness fee motions. No mootness fee motion has been filed to date. At this stage, it is not otherwise possible to predict the effect of lawsuits on Aytu.

 

Item 1A. Risk Factors.

 

In addition to other information set forth in this report, you should carefully consider the risk factors discussed in Part I, Item 1A. “Risk Factors” in our Annual Report, which could materially affect our business, financial condition, cash flows, and/or future results. The risk factors in our Annual Report are not the only risks facing our Company. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial also may materially adversely affect our business, financial condition, and/or future results. There are no additional risk factors other than those contained in our Annual Report.

 

Risks Related to the Merger

 

            Because the Exchange Ratio is fixed and the market price of Aytu common stock may fluctuate, Neos stockholders cannot be certain of the precise value of the stock consideration they may receive in the merger.

 

         The Exchange Ratio is fixed and will only be adjusted in certain limited circumstances (including the Bridge Note Adjustment, recapitalizations, reclassifications, stock splits or combinations, exchanges, mergers, consolidations or readjustments of shares, or stock dividends or similar transactions involving Aytu or Neos) and the value of the stock consideration will depend on the market price of Aytu common stock at the time the transaction is completed. Time will elapse from the date of the Merger Agreement, when the Exchange Ratio was established, until each of the date of this joint proxy statement/prospectus, the date on which Neos stockholders vote to approve the Merger Agreement at the Neos special meeting, the date the Aytu stockholders approve the merger consideration, including the Common Stock Issuance, at the Aytu special meeting and the date on which Neos stockholders entitled to receive shares of Aytu common stock under the Merger Agreement actually receive such shares. The market value of Aytu common stock may fluctuate during these periods as a result of a variety of factors, including, among others, general market and economic conditions, changes in Aytu’s businesses, operations and prospects and regulatory considerations, federal, state and local legislation, governmental regulation and legal developments in the businesses in which Aytu operates, any potential stockholder litigation related to the merger, market assessments of the likelihood that the transaction will be completed, the timing of the transaction and the anticipated dilution to holders of Aytu common stock as a result of the issuance of the merger consideration. Many of these factors are outside of the control of Aytu and Neos. The closing trading price per share of Neos common stock as of December 9, 2020, the last trading date before the public announcement of the Merger Agreement, was $0.55, and the closing trading price per share has fluctuated as high as $0.933 and as low as $0.625 between that date and February 5, 2021. The closing trading price per share of Aytu common stock as of December 9, 2020, the last trading date before the public announcement of the Merger Agreement, was $6.83 and the closing trading price per share has fluctuated as high as $8.35 and as low as $5.98 between that date and February 5, 2021. Consequently, at the time Neos stockholders must decide whether to approve the Merger Agreement, they will not know the actual market value of the shares of Aytu common stock they may receive when the merger is completed. The actual value of the shares of Aytu common stock to be issued to Neos stockholders who receive stock consideration will depend on the market value of shares of Aytu common stock on the date of issuance. This value will not be known at the time of the Neos special meeting and may be more or less than the current price of Aytu common stock or the price of Aytu common stock at the time of the Neos special meeting. Neos stockholders should obtain current stock quotations for shares of Aytu common stock before voting their shares of Neos common stock. For additional information about the merger consideration, see the section entitled “The Merger Agreement — Merger Consideration.” 

 

The market price of shares of Aytu common stock after the merger will continue to fluctuate and may be affected by factors different from those that are currently affecting or historically have affected the market price of shares of Neos common stock or Aytu common stock.

 

              Upon completion of the merger, holders of shares of Neos common stock will become holders of shares of Aytu common stock. The market price of Aytu common stock may fluctuate significantly following completion of the merger, and holders of shares of Neos common stock could lose the value of their investment in Aytu common stock if, among other things, the combined company is unable to achieve the expected growth in earnings, or if the operational cost savings estimates in connection with the integration of the Neos and Aytu business are not realized, or if the transaction costs relating to the merger are greater than expected. The market price also may decline if the combined company does not achieve the perceived benefits of the merger as rapidly or to the extent anticipated by financial or industry analysts or if the effect of the merger on the combined company’s financial position, results of operations or cash flows is not consistent with the expectations of financial or industry analysts. The issuance of shares of Aytu common stock in the merger could on its own have the effect of depressing the market price for Aytu common stock. In addition, many Neos stockholders may decide not to hold the shares of Aytu common stock they receive as a result of the merger. Other Neos stockholders, such as funds with limitations on their permitted holdings of stock in individual issuers, may be required to sell the shares of Aytu common stock they receive as a result of the merger. Any such sales of Aytu common stock could have the effect of depressing the market price for Aytu common stock.  In addition, in the future Aytu may issue additional securities to raise capital. Aytu may also acquire interests in other companies by issuing Aytu common stock to finance the acquisition, in whole or in part. Aytu may also issue securities convertible into Aytu common stock.  Moreover, general fluctuations in stock markets could have a material adverse effect on the market for, or liquidity of, the Aytu common stock, regardless of Aytu’s actual operating performance.

 

The businesses of Aytu differ from those of Neos in important respects and, accordingly, the results of operations of the combined company after the merger, as well as the market price of shares of Aytu common stock, may be affected by factors different from those that are currently affecting, historically have affected or would in the future affect the results of operations of Neos and Aytu as stand-alone public companies, as well as the market price of shares of Neos common stock and Aytu common stock prior to completion of the merger.

 

Current Aytu and Neos stockholders will have a reduced ownership and voting interest in Aytu after the merger. 

 

Upon the completion of the merger, each Neos stockholder who receives shares of Aytu common stock will become a stockholder of Aytu with a percentage ownership of Aytu that is substantially smaller than the stockholder’s current percentage ownership of Neos. Accordingly, the former Neos stockholders would exercise significantly less influence over Aytu after the merger relative to their influence over Neos prior to the merger, and thus would have a less significant impact on the approval or rejection of future Aytu proposals submitted to a stockholder vote. Immediately upon consummation of the merger, pre-closing Neos stockholders (other than Aytu and its subsidiaries) are expected to own approximately 24% of the outstanding shares of Aytu common stock and pre-closing Aytu stockholders are expected to own approximately 76% of the outstanding shares of Aytu common stock.

 

Aytu and Neos are subject to restrictive interim operating covenants during the pendency of the merger.

 

Until the merger is completed, the Merger Agreement restricts each of Aytu and Neos from taking specified actions without the consent of the other party, and requires each of Aytu and Neos to operate in the ordinary course of business consistent with past practice. Neos is subject to a number of customary interim operating covenants relating to, among other things, its capital expenditures, incurrence of indebtedness, entry into or amendment of certain types of agreements, issuances of securities and changes in director, officer, employee and independent contractor compensation. Although less restrictive than those imposed on Neos, the Merger Agreement also imposes certain restrictive interim operating covenants on Aytu. These restrictions may prevent Aytu and/or Neos from making appropriate changes to their respective businesses or pursuing financing transactions or attractive business opportunities that may arise prior to the completion of the merger. See the section entitled “The Merger Agreement – Conduct of Business Pending the Merger” for a description of the restrictive covenants applicable to Aytu and Neos, respectively.

 

Aytu and Neos directors and officers have interests in the merger that may be different from, or in addition to, the interests of Aytu stockholders and Neos stockholders.

 

Certain executive officers of Aytu participated in the negotiation of the terms of the Merger Agreement. The Aytu Board approved the Merger Agreement and the merger consideration, including the Common Stock Issuance, and determined that the Merger Agreement and the transactions contemplated thereby, including the merger consideration, are advisable and in the best interests of Aytu and its stockholders. The Neos Board approved the Merger Agreement and determined that the Merger Agreement, the merger and the other transactions contemplated by the Merger Agreement are fair to, advisable and in the best interests of Neos and its stockholders. In considering these facts and the other information contained in this joint proxy statement/prospectus, you should be aware that certain of Aytu’s directors and executive officers and certain of Neos’ directors and executive officers have interests in the merger that may be different from, or in addition to, the interests of Aytu’s or Neos’ stockholders. For example, some Neos directors will serve as Aytu directors. These interests are described in more detail in the sections entitled “Interests of Neos’ Directors and Executive Officers in the Merger.

 

Certain officers and directors of Aytu and Neos, have agreed to vote in favor of the merger consideration and the Merger Agreement, as applicable, regardless of how other Aytu and Neos stockholders vote.

 

Concurrently with the execution and delivery of the Merger Agreement, certain officers and directors of Aytu and Neos holding approximately 2% and 1%, respectively, of the companies’ outstanding voting shares entered into voting agreements with Neos and Aytu, as applicable (the “Voting Agreements”). Pursuant to the Voting Agreements, each of the stockholders of Aytu and Neos, as applicable, have agreed, among other things, to vote their shares of Aytu common stock, or Neos common stock, as applicable, that such stockholder owns in favor of the issuance of shares of Aytu common stock in connection with the merger, or the merger proposal, as applicable. Accordingly, the Voting Agreements make it more likely that the necessary Aytu and Neos stockholder approval will be received for the merger consideration and the Merger Agreement than would be the case in the absence of the voting agreements.

 

The Aytu Board and the Neos Board have not requested, and do not anticipate requesting, an updated opinion from their respective financial advisors reflecting changes in circumstances that may have occurred since the signing of the Merger Agreement.

 

The opinions rendered to the respective boards of directors of Aytu and Neos by Cowen and MTS, respectively, were provided in connection with the Aytu Board’s and the Neos Board’s respective evaluation of the merger. Neither the Aytu Board nor the Neos Board has obtained an updated opinion from Cowen or MTS, respectively, as of the date of this joint proxy statement/prospectus or as of any other date, and the Aytu Board and the Neos Board have not requested, and do not anticipate requesting, an updated opinion from their respective financial advisors reflecting changes in circumstances that may have occurred since the signing of the Merger Agreement. As a result, neither the Aytu Board nor the Neos Board will receive an updated, revised or reaffirmed opinion prior to the consummation of the merger. Changes in the operations and prospects of Aytu or Neos, general market and economic conditions and other factors that may be beyond the control of Aytu or Neos, including the social, political and economic impact of the COVID-19 pandemic, may significantly alter the value of Aytu or Neos or the prices of Aytu common stock or Neos common stock by the time the merger is consummated. The opinions of Cowen and MTS speak as of the date each opinion was rendered, and do not speak as of the time the merger will be consummated or as of any date other than the date of each such opinion. The opinions of Cowen and MTS do not address the fairness of the Exchange Ratio, from a financial point of view, at any time other than the time each such opinion was delivered.

 

               Failure to consummate the merger could negatively impact respective future stock prices, operations and financial results of Aytu and Neos.

 

If the merger is not consummated for any reason, the ongoing businesses of Aytu and/or Neos may be adversely affected, and Aytu and Neos will be subject to a number of risks, including the following:

 

 

 

being required to pay a termination fee to the other party under certain circumstances provided in the Merger Agreement;

 

 

having to pay certain costs related to the merger, including, but not limited to, fees paid to legal, accounting and financial advisors, filing fees and printing costs;

 

 

declines in the stock prices of Aytu common stock and Neos common stock to the extent that the current market prices reflect a market assumption that the merger will be consummated; and

 

 

any negative impact of having the focus of management of each of Aytu and Neos on the merger, which may have the effect of diverting management’s attention and potentially causing Aytu or Neos, as applicable, not to pursue opportunities that could have been beneficial to Aytu or Neos, as applicable.

 

 

If the merger is not completed, Aytu and Neos cannot assure their stockholders that these risks will not materialize and will not materially adversely affect the business, financial results and stock prices of Aytu or Neos. In addition, if the merger with Aytu does not close, Neos may be required to seek other strategic alternatives, including but not limited to, strategic partnerships, a potential business combination or a sale of Neos or its business, or otherwise reduce its operations. There can be no assurance that Neos would be able to take any of these actions or that any effort to sell additional debt or equity securities would be successful or would raise sufficient funds to meet its financial obligations, including the May 2021 debt payment of $15.0 million due to Deerfield. If additional financing is not available when required or is not available on acceptable terms, Neos may need to curtail, delay, modify or abandon its commercialization plans for its marketed products, reduce its investment in the development of its product candidate and Neos may be unable to take advantage of business opportunities or respond to competitive pressures, which could have a material adverse effect on Neos’ revenue, results of operations and financial condition. To preserve Neos’ cash resources, it may be required to reorganize its operations, such as through a reduction in force with respect to one or more functions within Neos or across Neos. If Neos is unable to fund its operations without additional external financing and therefore cannot sustain future operations, it may be required to cease its operations and/or seek bankruptcy protection.

 

In addition, if the merger does not close, Neos may be required to effectuate a reverse stock split of its common stock to increase the per-share market price of Neos common stock to satisfy the Minimum Bid Price Rule under the Nasdaq rules so that Neos common stock, which will remain outstanding and registered under the Exchange Act, will be able to regain compliance with the applicable continued listing standards of Nasdaq and avoid being delisted from Nasdaq Global.

 

The merger may disrupt the attention of Aytu’s management or Neos’ management from ongoing business operations.

 

Each of Aytu and Neos has expended, and expects to continue to expend, significant management resources to complete the merger. Their respective management’s attention may be diverted away from the day-to-day operations of their respective businesses, implementing initiatives to improve performance and executing existing business plans in an effort to complete the merger. This diversion of management resources could disrupt their respective operations and may have an adverse effect on their respective businesses, financial conditions and results of operations.

Aytu and Neos stockholders will not be entitled to appraisal or dissenters’ rights in the merger.

 

Appraisal rights are statutory rights that, if applicable under law, enable stockholders to dissent from an extraordinary transaction, such as a merger, and to demand that the corporation pay the fair value for their shares as determined by a court in a judicial proceeding instead of receiving the consideration offered to stockholders in connection with the extraordinary transaction. Appraisal rights are not available in all circumstances, and exceptions to these rights are provided under the DGCL. In the merger, because Neos common stock is listed on the Nasdaq, and because Neos stockholders are not required to accept in the merger any consideration in exchange for their shares of Neos common stock other than shares of Aytu common stock, which is listed on the Nasdaq, and cash in lieu of fractional shares (if applicable), holders of Neos common stock will not be entitled to any appraisal rights in connection with the merger with respect to their shares of Neos common stock.

 

Under Delaware law, Aytu stockholders are also not entitled to appraisal or dissenters’ rights in connection with the Aytu share issuance proposal.

 

Aytu and Neos may have difficulty attracting, motivating and retaining executives and other key employees in light of the merger. 

 

Aytu’s success after the transaction will depend in part on the ability of Aytu to retain key executives and other employees of Neos. Uncertainty about the effect of the merger on Aytu and Neos employees may have an adverse effect on each of Aytu and Neos separately and consequently the combined business. This uncertainty may impair Aytu’s and/or Neos’ ability to attract, retain and motivate key personnel. Employee retention may be particularly challenging during the pendency of the merger, as employees of Aytu and Neos may experience uncertainty about their future roles in the combined business.

 

Furthermore, if key employees of Aytu or Neos depart or are at risk of departing, including because of issues relating to the uncertainty and difficulty of integration, financial security or a desire not to become employees of the combined business, Aytu may have to incur significant costs in retaining such individuals or in identifying, hiring and retaining replacements for departing employees and may lose significant expertise and talent, and the combined company’s ability to realize the anticipated benefits of the merger may be materially and adversely affected. No assurance can be given that the combined company will be able to attract or retain key employees to the same extent that Neos has been able to attract or retain employees in the past.

 

Completion of the merger is subject to a number of other conditions, and if these conditions are not satisfied or waived, the merger will not be completed. 

 

The obligations of Aytu and Neos to complete the merger are subject to satisfaction or waiver of a number of conditions including (1) the approval of the merger proposal by a majority of the holders of the outstanding shares of Neos common stock, (2) approval of the issuance of Aytu common stock by a majority of the votes cast by Aytu stockholders on the matter, (3) that the conditions to the Debt Facility Letters have been satisfied as of the time of closing, and that the lenders do not dispute the satisfaction thereof, (4) accuracy of each party’s representations and warranties, subject to certain materiality standards set forth in the Merger Agreement, (5) the absence of a material adverse effect of either party and (6) compliance in all material respects with each party’s obligations under the Merger Agreement and certain other conditions. There can be no assurance that the conditions to closing the merger will be satisfied or waived or that the merger will be completed within the expected time frame, or at all.

 

Aytu will assume a significant amount of debt in the merger, which, together with Aytu’s other debt, could limit Aytu’s operational flexibility or otherwise adversely affect Aytu’s financial condition. 

 

If the merger closes, Aytu will indirectly assume approximately $30.6 million of term debt currently owed by Neos, of which $15.0 million will be due upon the closing of the merger, $0.6 will come due in April 2021, and $15.0 million which is due in May 2022. If Aytu fails to meet its obligations under the debt Aytu assumes in the merger, the lenders would be entitled to foreclose on all or some of the collateral securing such debt which could have a material adverse effect on Aytu and its ability to make expected distributions, and could threaten Aytu’s continued viability.

 

Aytu is subject to the risks normally associated with debt financing, including the following risks:

 

 

Aytu’s cash flow may be insufficient to meet required payments of principal and interest, or require Aytu to dedicate a substantial portion of its cash flow to pay its debt and the interest associated with its debt rather than to other areas of its business;

 

 

it may be more difficult for Aytu to obtain additional financing in the future for its operations, working capital requirements, capital expenditures, debt service or other general requirements;

 

 

Aytu may be more vulnerable in the event of adverse economic and industry conditions or a downturn in its business;

 

 

Aytu may be placed at a competitive disadvantage compared to its competitors that have less debt; and

 

 

Aytu may not be able to refinance at all or on favorable terms, as its debt matures.

 

If any of the above risks occurred, Aytu’s financial condition and results of operations could be materially adversely affected.

 

Aytu and Neos may be targets of transaction related lawsuits which could result in substantial costs and may delay or prevent the merger from being completed. If the merger is completed, Aytu will also assume Neos’ risks arising from various legal proceedings. 

 

Securities class action lawsuits and derivative lawsuits are often brought against public companies that have entered into Merger Agreements. Even if the lawsuits are without merit, defending against these claims can result in substantial costs and divert management time and resources. An adverse judgment could result in monetary damages, which could have a negative impact on Aytu’s and Neos’ respective liquidity and financial condition. Additionally, if a plaintiff is successful in obtaining an injunction prohibiting completion of the merger, then that injunction may delay or prevent the merger from being completed, which may adversely affect Aytu’s and Neos’ respective business, financial position and results of operation. There can be no assurance that no complaints will be filed with respect to the merger, or that any additional complaints will be filed with respect to the Aytu’s acquisition of a portfolio of pediatric primary care products from Cerecor, Inc. (“Cerecor”) in 2019 (the “Cerecor Transaction”). Currently, with regard to the merger, Aytu and Neos are not aware of any securities class action lawsuits or derivative lawsuits being filed with respect to the merger.

 

Aytu and Neos have incurred, and will incur, substantial direct and indirect costs as a result of the merger.

 

Aytu and Neos have incurred and expect to incur additional material non-recurring expenses in connection with the merger and completion of the transactions contemplated by the Merger Agreement. Both parties have incurred significant legal, advisory and financial services fees in connection with the process of negotiating and evaluating the terms of the merger. Additional significant unanticipated costs may be incurred in the course of coordinating the businesses of Neos and Aytu after completion of the merger.

 

Even if the merger is not completed, Aytu and Neos will each need to pay certain costs relating to the merger incurred prior to the date the merger was abandoned, such as legal, accounting, financial advisory, filing and printing fees. Such costs may be significant and could have an adverse effect on Aytu’s and Neos’ respective plans.

 

If the merger is completed, Aytu may fail to realize the anticipated benefits and cost savings of the merger, which could adversely affect the value of shares of Aytu common stock.

 

The success of the merger will depend, in part, on Aytu’s ability to realize the anticipated benefits and cost savings from combining the businesses of Aytu and Neos. Aytu’s ability to realize these anticipated benefits and cost savings is subject to certain risks, including, among others:

 

 

Aytu’s ability to successfully combine the businesses of Aytu and Neos;

 

 

the risk that the combined businesses will not perform as expected;

 

 

the extent to which Aytu will be able to realize the expected synergies, which include potential savings from re-assessing priority assets and aligning investments, eliminating duplication and redundancy, adopting an optimized operating model between both companies and leveraging scale, and value creation resulting from the combination of the businesses of Aytu and Neos;

 

 

the possibility that Aytu paid more for Neos than the value it will derive from the merger;

 

 

the assumption of known and unknown liabilities of Neos;

 

 

the possibility of a decline of the credit ratings of the combined company following the completion of the merger; and

 

 

the possibility of costly litigation challenging the merger.

 

               If Aytu is not able to successfully combine the businesses of Aytu and Neos within the anticipated time frame, or at all, the anticipated cost savings and other benefits of the merger may not be realized fully or may take longer to realize than expected, the combined businesses may not perform as expected and the value of the shares of Aytu common stock may be adversely affected.

 

Aytu and Neos have operated and, until completion of the merger will continue to operate, independently, and there can be no assurances that their businesses can be integrated successfully. It is possible that the integration process could result in the loss of key Aytu or Neos employees, the disruption of either company’s or both companies’ ongoing businesses or in unexpected integration issues, higher than expected integration costs and an overall post-completion integration process that takes longer than originally anticipated. Specifically, issues that must be addressed in integrating the operations of Neos and Aytu in order to realize the anticipated benefits of the merger so the combined business performs as expected include, among others:

 

 

 

combining the companies’ separate operational, financial, reporting and corporate functions;

 

 

integrating the companies’ technologies, products and services;

 

 

identifying and eliminating redundant and underperforming operations and assets;

 

 

harmonizing the companies’ operating practices, employee development, compensation and benefit programs, internal controls and other policies, procedures and processes;

 

 

addressing possible differences in corporate cultures and management philosophies;

 

 

maintaining employee morale and retaining key management and other employees;

 

 

attracting and recruiting prospective employees;

 

 

 

consolidating the companies’ corporate, administrative and information technology infrastructure;

 

 

coordinating sales, distribution and marketing efforts;

 

 

managing the movement of certain businesses and positions to different locations;

 

 

maintaining existing agreements with customers and vendors and avoiding delays in entering into new agreements with prospective customers and vendors;

 

 

coordinating geographically dispersed organizations; and

 

 

effecting potential actions that may be required in connection with obtaining regulatory approvals.

 

 

In addition, at times, the attention of certain members of each company’s management and each company’s resources may be focused on completion of the merger and the integration of the businesses of the two companies and diverted from day-to-day business operations, which may disrupt each company’s ongoing business and the business of the combined company.

 

The Merger Agreement contains provisions that make it more difficult for Aytu and Neos to pursue alternatives to the merger and may discourage other companies from trying to acquire Neos for greater consideration than what Aytu has agreed to pay. 

 

The Merger Agreement contains provisions that make it more difficult for Neos to sell its business to a party other than Aytu, or for Aytu to sell its business. These provisions include a general prohibition on each party soliciting any acquisition proposal. Further, there are only limited exceptions to each party’s agreement that its board of directors will not withdraw or modify in a manner adverse to the other party the recommendation of its board of directors in favor of the merger proposal, in the case of Neos, or the approval of the merger consideration, in the case of Aytu, and the other party generally has a right to match any acquisition proposal that may be made. However, at any time prior to the approval of the merger proposal by Neos stockholders, in the case of Neos, or the approval of the merger consideration by Aytu stockholders, in the case of Aytu, such party’s board of directors is permitted to make an adverse recommendation change if it determines in good faith that the failure to take such action would be reasonably likely to be inconsistent with its fiduciary duties under applicable law. In the event that either the Neos Board or the Aytu Board make an adverse recommendation change and the Merger Agreement is terminated, then such party may be required to pay a $2,000,000 termination fee.

 

The parties believe these provisions are reasonable and not preclusive of other offers, but these restrictions might discourage a third party that has an interest in acquiring all or a significant part of either Neos or Aytu from considering or proposing an acquisition proposal, even if that party were prepared to pay consideration with a higher per-share value than the currently proposed merger consideration, in the case of Neos, or that party were prepared to enter into an agreement that may be favorable to Aytu or its stockholders, in the case of Aytu. Furthermore, the termination fees described above may result in a potential competing acquirer proposing to pay a lower per-share price to acquire the applicable party than it might otherwise have proposed to pay because of the added expense of the termination fee that may become payable by such party in certain circumstances. 

 

The indebtedness of the combined company following completion of the merger will be greater than Aytu’s indebtedness on a stand-alone basis. This increased level of indebtedness could adversely affect the combined company’s business flexibility, and increase its borrowing costs. Any resulting downgrades in Aytu’s credit ratings could adversely affect Aytu’s and/or the combined company’s respective businesses, cash flows, financial condition and operating results.

 

              As of January 26, 2021, the current outstanding indebtedness of Neos is $38.3 million, which is subject to change between January 29, 2021 and the closing. As a result of the merger, Aytu will assume the outstanding indebtedness of Neos at the closing. The amount of cash required to service Aytu’s increased indebtedness levels and thus the demands on Aytu’s cash resources will be greater than the amount of cash flows required to service the indebtedness of Aytu individually prior to the merger. The increased levels of indebtedness could also reduce funds available to fund Aytu’s efforts to combine its business with Neos and realize expected benefits of the merger and/or engage in investments in product development, capital expenditures, and other activities and may create competitive disadvantages for Aytu relative to other companies with lower debt levels. While Aytu successfully raised net proceeds of $26.1 million in a common stock financing after announcement of the merger in December 2020, Aytu may be required to raise additional financing for working capital, capital expenditures, acquisitions or other general corporate purposes. Aytu’s ability to arrange additional financing or refinancing will depend on, among other factors, Aytu’s financial position and performance, as well as prevailing market conditions and other factors beyond Aytu’s control. Aytu cannot assure you that it will be able to obtain additional financing or refinancing on terms acceptable to Aytu or at all.

 

Aytu may not be able to service all of the combined company’s indebtedness and may be forced to take other actions to satisfy Aytu’s obligations under Aytu’s indebtedness, which may not be successful. Aytu’s failure to meet its debt service obligations could have a material adverse effect on the combined company’s business, financial condition and results of operations. 

 

Aytu depends on cash on hand and revenue from operations to make scheduled debt payments. Aytu expects to be able to meet the estimated cash interest payments on the combined company’s debt following the merger through the expected revenue from operations of the combined company. However, Aytu’s ability to generate sufficient revenue from operations of the combined company and to utilize other methods to make scheduled payments will depend on a range of economic, competitive and business factors, many of which are outside of Aytu’s control. There can be no assurance that these sources will be adequate. If Aytu is unable to service Aytu’s indebtedness and fund Aytu’s operations, Aytu will be forced to reduce or delay capital expenditures, seek additional capital, sell assets or refinance Aytu’s indebtedness. Any such action may not be successful and Aytu may be unable to service Aytu’s indebtedness and fund Aytu’s operations, which could have a material adverse effect on the combined company’s business, financial condition or results of operations.

 

Aytu will incur significant transaction and integration-related costs in connection with the merger. In addition, the merger may not be accretive, and may be dilutive, to Aytu’s earnings per share, which may negatively affect the market price of shares of Aytu’s common stock. 

 

Aytu expects to incur a number of non-recurring costs associated with the merger and combining the operations of the two companies. Aytu will incur significant transaction costs related to the merger. Aytu also will incur significant integration-related fees and costs related to formulating and implementing integration plans, including facilities and systems consolidation costs and employment-related costs. Aytu continues to assess the magnitude of these costs, and additional unanticipated costs may be incurred in the merger and the integration of the two companies’ businesses. While Aytu has assumed that a certain level of transaction expenses will be incurred, factors beyond Aytu’s control, such as certain of Neos’ expenses, could affect the total amount or the timing of these expenses. Although Aytu expects that the elimination of duplicative costs, as well as the realization of other efficiencies related to the integration of the businesses, should allow Aytu to offset integration-related costs over time, this net benefit may not be achieved in the near term, or at all.

 

Following the closing of the merger, there is a risk that a significant amount of the combined company’s total assets will be related to acquired intangible assets and goodwill, which are subject to annual impairment reviews, or more frequent reviews if events or circumstances indicate that the carrying value may not be recoverable. Because of the significance of these assets, any charges for impairment as well as amortization of intangible assets could have a material adverse effect on the combined company’s results of operations and financial condition.

 

The combined company will be subject to the risks that Neos faces, in addition to the risks faced by Aytu. In particular, the success of the combined company will depend on its ability to obtain, commercialize and protect intellectual property. 

 

Neos and Aytu currently have a limited number of products and the combined company may not be successful in marketing and commercializing these products. In addition, following the merger Aytu may seek to develop current or new product candidates of both Aytu and Neos. The testing, manufacturing and marketing of these product candidates would require regulatory approvals, including approval from the FDA and similar bodies in other countries. To the extent the combined company seeks to develop product candidates, the future growth of the combined company would be negatively affected if Aytu, Neos or the combined company fails to obtain requisite regulatory approvals within the expected time frames, or at all, in the United States and internationally for products in development and approvals for Aytu’s existing products for additional indications.

 

The future results of the combined company may be adversely impacted if the combined company does not effectively manage its expanded operations following completion of the merger. 

 

Following completion of the merger, the size of the combined company’s business will be significantly larger than the current size of either Aytu’s or Neos’ respective businesses. The combined company’s ability to successfully manage this expanded business will depend, in part, upon management’s ability to implement an effective integration of the two companies and its ability to manage a combined business with significantly larger size and scope with the associated increased costs and complexity. There can be no assurances that the management of the combined company will be successful or that the combined company will realize the expected operating efficiencies, cost savings and other benefits currently anticipated from the merger.

 

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

 

None.

 

Item 3. Defaults Upon Senior Securities.

 

None.

 

Item 4. Mine Safety Disclosures.

 

Not Applicable.

 

Item 5. Other Information.

 

 

Item 6. Exhibits.

 

Exhibit No.

 

Description

 

Registrants Form

 

Date Filed

 

Exhibit Number

 

Filed Herewith

                       
2.1  

Agreement and Plan of Merger, dated as of September 12, 2019, by and among Aytu BioScience, Inc., Aytu Acquisition Sub, Inc. and Innovus Pharmaceuticals, Inc.

 

8-K

 

9/18/19

    2.1    
                       
2.2  

Asset Purchase Agreement, dated October 10, 2019

 

8-K

 

10/15/19

    2.1    
                       
2.3   Agreement and Plan of Merger, dated as of December 10, 2020, by and among Aytu BioScience, Inc., Neutron Acquisition Sub, Inc. and Neos Therapeutics, Inc.   8-K   12/10/2020     2.1    
                       
3.1  

Certificate of Incorporation effective June 3, 2015

 

8-K

 

6/09/15

    3.1    
                       
3.2  

Certificate of Amendment of Certificate of Incorporation effective June 1, 2016

 

8-K

 

6/02/16

    3.1    
                       
3.3  

Certificate of Amendment of Certificate of Incorporation, effective June 30, 2016

 

8-K

 

7/01/16

    3.1    
                       
3.4  

Certificate of Designation of Preferences, Rights and Limitations of Series A Convertible Preferred Stock, filed on August 11, 2017

 

8-K

 

8/16/17

    3.1    
                       
3.5  

Certificate of Amendment of Certificate of Incorporation, effective August 25, 2017

 

8-K

 

8/29/17

    3.1    
                       
3.6  

Certificate of Designation of Preferences, Rights and Limitations of Series B Convertible Preferred Stock filed on March 2, 2018

 

S-1/A

 

2/27/18

    3.6    
                       
3.7  

Certificate of Amendment to the Restated of Certificate of Incorporation, effective August 10, 2018

 

8-K

 

8/10/18

    3.1    
                       
3.8  

Amended and Restated Bylaws

 

8-K

 

6/09/15

    3.2    
                       
3.9  

Certificate of Designation of Preferences, Rights and Limitations of Series E Convertible Preferred Stock

 

10-Q

 

2/7/19

    10.4    
                       
3.10  

Certificate of Designation of Preferences, Rights and Limitations of Series F Convertible Preferred Stock

 

8-K

 

10/15/19

    3.1    
                       
3.11  

Certificate of Designation of Preferences, Rights and Limitations of Series G Convertible Preferred Stock

 

8-K

 

11/4/19

    3.1    
                       
3.12   Certificate of Amendment to the Restated Certificate of Incorporation, effective December 7, 2020   8-K   12/8/2020     3.1    
                       
4.1  

Form of Placement Agent Warrant issued in 2015 Convertible Note Financing

 

8-K

 

7/24/15

    4.2    
                       
4.2  

Warrant Agent Agreement, dated May 6, 2016 by and between Aytu BioScience, Inc. and VStock Transfer, LLC

 

8-K

 

5/6/16

    4.1    
                       
4.3  

First Amendment to May 6, 2016 Warrant Agent Agreement between Aytu BioScience, Inc. and VStock Transfer LLC

 

S-1

 

9/21/16

    4.5    
                       
4.4  

Warrant Agent Agreement, dated November 2, 2016 by and between Aytu BioScience, Inc. and VStock Transfer, LLC

 

8-K

 

11/2/16

    4.1    
                       
4.5  

Form of Amended and Restated Underwriters Warrant (May 2016 Financing)

 

8-K

 

3/1/17

    4.1    
                       
4.6  

Form of Amended and Restated Underwriters Warrant (October 2016 Financing)

 

8-K

 

3/1/17

    4.2    
                       
4.7  

Form of Common Stock Purchase Warrant issued on August 15, 2017

 

8-K

 

8/16/17

    4.1    
                       
4.8  

Form of Common Stock Purchase Warrant for March 2018 Offering

 

S-1

 

2/27/18

    4.8    
                       
4.9  

Form of Pre-Funded Purchase Warrant

 

8-K

 

3/13/20

    4.1    
                       
4.10  

Form of Placement Agents Warrant

 

8-K

 

3/13/20

    4.2    
                       
4.11  

Form of Warrant

 

8-K

 

3/13/20

    4.1    
                       
4.12  

Form of Placement Agents Warrant

 

8-K

 

3/13/20

    4.2    
                       
4.13  

Form of Warrant

 

8-K

 

3/20/20

    4.1    
                       
4.14  

Form of Placement Agents Warrants

 

8-K

 

3/20/20

    4.2    
                       
4.15  

Form of Wainwright Warrant

 

8-K

 

7/2/20

    4.1    
                       
4.16   Form of Underwriter's Warrant   8-K   12/14/2020     4.1    
                       
10.1  

Amended Employment Agreement with Joshua R. Disbrow dated July 1, 2020

 

10-K

 

10/6/20

    10.62    
                       
10.2  

Amended Employment Agreement with David A. Green dated July 1, 2020

 

10-K

 

10/6/20

    10.63    

 

 

                       
10.3   License Agreement with Avrio Genetics, LLC, dated January 20, 2020*                 X
                       
31.1  

Certificate of the Chief Executive Officer of Aytu BioScience, Inc. pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

               

X

                       
31.2  

Certificate of the Chief Executive Officer and the Chief Financial Officer of Aytu BioScience, Inc. pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

               

X

                       
32.1   Certificate of Chief Executive Officer and Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002*.                 X
                       
101  
XBRL (extensible Business Reporting Language). The following materials from Aytu BioScience, Inc.’s Quarterly Report on Form 10-Q for the quarter ended December 31, 2020 formatted in XBRL: (i) the Consolidated Balance Sheet, (ii) the Consolidated Statement of Operations, (iii) the Consolidated Statement of Stockholders’ Equity (Deficit), (iv) the Consolidated Statement of Cash Flows, and (v) the Consolidated Notes to the Financial Statements.
               

 

X

 

Indicates is a management contract or compensatory plan or arrangement.

 

*

Information in this exhibit identified by brackets is confidential and has been excluded pursuant to Item 601(b)(10)(iv) of Regulation S-K because it is not material and would likely cause competitive harm to the Company if publicly disclosed. An unredacted copy of this exhibit will be furnished to the Securities and Exchange Commission on a supplemental basis upon request.

 

 
 

 

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

Ex. 10.1

 

 

EXCLUSIVE LICENSE AGREEMENT

 

This Exclusive License Agreement (“Agreement”) is entered into as of this 20th day of January 2021 (“Effective Date”) by and between Aytu BioScience, Inc. a Delaware corporation with offices at 373 Inverness Pkwy, Suite 206, Englewood, CO 80112 (“AYTU”), and Avrio Genetics, LLC, a Pennsylvania limited liability corporation with offices at ____________________________ (“Licensee”). AYTU and Licensee are sometimes referred to herein individually as a “Party” or collectively as the “Parties”.

 

A.     Aytu owns certain Patent Rights, Trademark Rights and Technical Information (as defined below) invented and/or developed in connection with a rapid in vitro diagnostic semen analysis test that accurately measures oxidative stress.

 

B.     Aytu desires to have the Patent Rights, Trademark Rights and Technical Information used and commercialized in the Field of Use (as defined below) by Licensee, and Licensee desires to obtain an exclusive license in the Field of Use within the Territory, and to manufacture, make, have made, use, have used, offer for sale, sell, have sold and/or import Products (as defined below) in the Field of Use, using the Patent Rights, Trademark Rights and Technical Information in accordance with the terms of this Agreement.

 

Now, Therefore, in consideration of the mutual covenants and premises contained herein, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereby agree as follows:

 

1.

Definitions

 

1.1     “Affiliate” or “Affiliates” means any corporation, person or entity, which controls, is controlled by, or is under common control with, a Party without regard to stock or other equity ownership. For purposes hereof, the terms “control” and “controls” mean the possession, direct or indirect, of the power to direct or cause the direction of the management and policies of a corporation, person or entity, whether through the ownership of voting securities, by contract or otherwise.

 

1.2     “Confidential Information” means any confidential or proprietary information furnished by one Party (the “Disclosing Party”) to the other Party (the “Receiving Party”) in connection with this Agreement, including, without limitation, all specifications, know-how, trade secrets, technical information, drawings, software, models and business information pertaining to the Patent Rights, Trademark Rights and Technical Information, as further provided in Article 10 hereof.

 

1.3     “Field of Use” means human reproductive health.

 

1.4     “Improvements” means any and all know-how, invention or discovery (and all intellectual property claiming or covering such invention or discovery) conceived, discovered, or made by Licensee its Affiliates, or its or their agents, sublicensees, or contractors (other than Aytu) during the term of this Agreement, whether patentable or not, to the extent directly related to the Patent Rights, Trademark Rights and/or Technical Information. For the avoidance of doubt, “Improvements” excludes any and all Patent Rights, Trademark Rights and Technical Information, which shall at all times be owned by Aytu.

 

1.5     “Net Sales means the gross amounts invoiced and received by Licensee, its Affiliates, or sublicensees for any and all sales or transfers of any Product, less the following amounts to the extent actually incurred or paid by Licensee, its Affiliates, or sublicensees with respect to such sales or transfers:

 

 

1

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

 

(a)     trade, cash and quantity discounts, charge backs or rebates actually allowed or taken, including discounts or rebates to governmental agencies/entities; wholesalers and other distributors; pharmacies and other retailers; buying groups; health care insurance carriers; pharmacy benefit management companies; regulatory authorities; third parties associated with patient assistance programs; or managed care organizations;

 

(b)     credits or allowances actually given or made for rejection of, or return of previously sold Products;

 

(c)     any charges for insurance, freight, and other transportation costs directly related to the delivery of Product to the extent included in the gross invoiced price;

 

(d)     any tax, tariff, duty or governmental charge levied on the sales, transfer, transportation or delivery of the Product (including any tax such as a value added or similar tax or government charge) borne by the seller thereof, other than franchise or income tax of any kind whatsoever; and

 

(e)     any import or export duties or their equivalent borne by the seller;

 

All aforementioned deductions shall only be allowable to the extent they are commercially reasonable and shall be determined, on a country-by-country basis, as incurred in the ordinary course of business in type and amount consistent with the Party’s, the Affiliate’s, or sublicensee’s (as the case may be) business practices consistently applied across its product lines and accounting standards and verifiable based on conventional industry practices. All such discounts, allowances, credits, rebates, and other deductions shall be fairly and equitably allocated to Product and other products of the Party and its Affiliates and sublicensees such that a Product does not bear a disproportionate portion of such deductions. The transfer of the Product between or among Licensee, its Affiliates and sublicensees will not be considered a sale, provided, that in the event an Affiliate or sublicensee is the end-user of Product, the transfer of Product to such Affiliate or sublicensee shall be included in the calculation of Net Sales at the average selling price charged in an arm’s length sale to a third party who is not an Affiliate or sublicensee in the relevant period. Net Sales includes the cash consideration received on a sale and the fair market value of all non-cash consideration. Disposition of Product for, or use of the Product in, clinical trials or other scientific testing, as free samples, or under compassionate use, named patient sales, patient assistance, or test marketing programs or other similar programs or studies where the Product is supplied without charge shall not result in any Net Sales, however if Licensee or any of its Affiliates or sublicensees charges for such Product, the amount billed will be included in the calculation of Net Sales.

 

If a Product is sold and not invoiced separately in the form of a combination or bundled product containing both the Product and one or more independent products, then Net Sales, for the purpose of calculating royalties owed under this Agreement for sales of such Product, shall be determined as follows: first, Licensee shall determine the actual Net Sales of the combination or bundled product; such amount shall then be multiplied by the fraction A/(A+B), where A is the invoice price of the Product, if sold separately, and B is the total, aggregate invoice price of any other product(s) included in the combination or bundle. If the other product(s) is/are not sold separately, Net Sales shall be calculated by multiplying actual Net Sales of such combination or bundled product by the fraction A/C where A is the invoice price of the Product if sold separately and C is the invoice price of the combination or bundled product. If neither method can be used to accurately determine the Net Sales of a Product in a combination or bundled product, the adjustment to Net Sales shall be determined by the Parties in good faith to reasonably reflect the fair market value of the contribution of the Product in the combination or bundled product to the total fair market value of such combination or bundled product.

 

1.6     “Patent Rights” means the rights associated with the issued patents and pending patent applications shown on Exhibit A attached hereto. All right, title and interest in and to the Patent Rights are owned by Aytu.

 

1.7     “Product” or “Products” shall mean any and all components of the MiOXSYS® commercial system including, without limitation, MiOXSYS® Analyzers, MiOXSYS® Sensors, MiOXSYS® Connectors, MiOXSYS® Calibration Verification Key (CVK), and MiOXSYS® External Control Solutions, as well as any and all products and/or services in the Field of Use that, except for the license granted hereunder, would infringe a Valid Claim of the Patent Rights.

 

2

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

 

1.8     “Technical Information” means any and all know-how, inventions, discoveries, unpatented and proprietary ideas, trade secrets, specifications, instructions, processes, formulae, materials, methods, protocols, expertise and other technology applicable to the MiOXSYS® commercial system or its manufacture, registration, use or marketing or to methods of testing components of the MiOXSYS® commercial system or processes for their manufacture, and including all biological, chemical, pharmacological, biochemical, toxicological, pharmaceutical, physical and analytical, safety, quality control, manufacturing, preclinical and clinical data, instructions, processes, formula, and expertise relating thereto. All right, title and interest in and to the Technical Information is owned by Aytu.

 

1.9     The “Territory” is world-wide.

 

1.10     “Trademark Rights” means, collectively: (a) the word mark “MIOXSYS”, U.S. Registration Number 86724491, which was registered in the U.S. principal register on February 7, 2017; (b) marks that include or incorporate the “MIOXSYS” word mark; (c) any variants or formatives thereof; (d) any and all printed matter, devices, products, articles or merchandise on or in connection with which the Trademark Rights are used including, without limitation, marketing materials, packaging and other materials containing Product branding; and (e) the MiOXSYS® website (https://mioxsys.com/) and all of the information contained therein; each as used on, for and in connection with the marketing and sale of Products.

 

(a)     Licensee shall take no actions that derogate or devalue the Trademark Rights, and agrees to make reasonable efforts to maintain the goodwill of the Trademark Rights, as well as any registrations therefor, as set forth herein.

 

(b)     Licensee acknowledges that Aytu is the sole and exclusive owner of all right, title and interest in and to the Trademark Rights. Licensee agrees that any goodwill in the Trademark Rights resulting from Licensee’s use of the Trademark Rights under this Agreement will inure solely to the benefit of Aytu and will not create any right, title or interest of Licensee (including any ownership right by Licensee) in or to the Trademark Rights. Except in the event of a successful purchase of the Trademark rights by Licensee pursuant to Section 4.5 hereof, upon termination of this Agreement Licensee shall take all steps reasonably necessary to assign any and all goodwill in the Trademark Rights resulting from Licensee’s use of the Trademark Rights under this Agreement to Aytu.

 

1.11     “Valid Claim” means a claim of an issued patent included within the Patent Rights, which has not (a) lapsed, been canceled or become abandoned, (b) been declared invalid or unenforceable by a non-appealable decision or judgment of a court or other appropriate body or authority of competent jurisdiction, or (c) been admitted to be invalid or unenforceable through reissue, disclaimer or otherwise.

 

2.

License

 

2.1     Grant of Exclusive Rights. Subject to the terms of this Agreement, Aytu hereby grants to Licensee, and Licensee hereby accepts from Aytu, the exclusive right and license, with the right to grant sublicenses (subject to the terms of Section 2.2), under and to the Patent Rights, Trademark Rights and Technical Information during the term of this Agreement to manufacture, make, have made, use, have used, offer for sale, sell, have sold and/or import Products in the Field of Use within the Territory. The foregoing grant is made expressly subject to the following:

 

(a)     All applicable laws and regulations, including, without limitation, the requirements of federal law as pertains to the manufacture of products within the United States;

 

(b)     With respect to the Trademark Rights, Licensee agrees to furnish to Aytu, from time to time as requested, representative samples of Products to which it affixes the Trademark Rights. Aytu, or its authorized representative, shall also have the right at any time or times to conduct, during regular business hours, an examination of the Products and of the facility(-ies) and processes for making the Products. If, at any time, any Products made or assembled by or for Licensee and bearing the Trademark Rights shall, in the sole opinion of Aytu, fail to conform to the standards of quality set by Aytu, Licensee shall promptly remove the Trademark Rights from such non-conforming Products in its possession and shall replace, at its own cost, any such non-conforming Products held by the trade with Products containing conforming Trademark Rights.

 

3

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

 

(d)     Notwithstanding any other provision hereof to the contrary, all rights to the Patent Rights, Trademark Rights, Technical Information and Improvements outside of the Field of Use are retained by Aytu. Furthermore, this Agreement confers no license or rights by implication, estoppel, or otherwise under any patent applications or patents of Aytu other than the Patent Rights, regardless of whether such patents are dominant or subordinate to the Patent Rights.

 

2.2     Sublicensing. Licensee shall have the right to grant sublicenses under the exclusive right and license granted to it under Section 2.1. Any sublicensee shall be subject in all respects to the provisions contained in this Agreement and Licensee will remain primarily liable to Aytu for, and shall be responsible for monitoring and enforcing, performance of all of Licensee’s obligations hereunder by any sublicensee. Without limiting the generality of the foregoing, as an express condition of any sublicense granted by Licensee, a sublicensee shall be required to agree in writing to be bound by commercially reasonable reporting and record keeping, indemnification and inspection provisions, and the applicable provisions of this Agreement, including, without limitation, those pertaining to the use of the Patent Rights, Trademark Rights and Technical Information, indemnification of Aytu and the use of Aytu’s Confidential Information. Sublicensees may not further sublicense without Aytu’s prior written consent, which consent may be withheld in Aytu’s sole discretion. Licensee shall promptly forward to Aytu a copy of any and all fully executed sublicense agreements, any subsequent amendments, and all copies of sublicensees’ profit sharing or royalty reports, in no event more than thirty (30) days following execution or receipt thereof, as applicable. Licensee shall also keep Aytu reasonably informed with respect to the progress of any relations entered into with any sublicensees. If Licensee shall conduct one or more audits of its sublicensees hereunder during the term hereof, Licensee shall provide copies of all audit reports to Aytu on a timely basis. The covenants pertaining to the use of Aytu’s Patent Rights, Trademark Rights and Technical Information, the indemnification of Aytu and the use of Aytu’s Confidential Information in any sublicense or assignment shall inure to the benefit of Aytu, who shall be expressly stated as a third-party beneficiary thereof with respect to the covenants set forth in this Agreement. Licensee understands and agrees that none of its permitted sublicenses hereunder shall reduce in any manner any of its obligations set forth in this Agreement.

 

(a)     Royalty-Free Sublicenses. Licensee shall not grant any royalty-free or non-cash sublicense or cross-license until such time as Licensee had paid all of the minimum royalty payments due to Aytu hereunder.

 

2.3     Improvements. Licensee shall own all right, title and interest in and to any Improvements generated under this Agreement made by its employees, agents or contractors, subject to the following:

 

(a)     It shall be Licensee’s responsibility to determine ownership responsibilities for any Improvements generated under this Agreement made by any Affiliate or sublicensee.

 

(b)     Regardless of the source of any Improvement, within thirty (30) days of the conception or reduction to practice, as appropriate, of any Improvement, Licensee shall provide written notification of the Improvement to Aytu, such written notification to include a clear and concise description of the Improvement and Licensee’s initial determination as to whether or not such Improvement falls within the scope of the Patent Rights, Trademark Rights and/or Technical Information. Aytu shall then have thirty (30) days to make its own determination as to whether or not such Improvement falls within the scope of the Patent Rights, Trademark Rights and/or Technical Information and shall provide written notification of its determination to Licensee. In the event the Parties disagree as to the nature of any Improvement, they shall negotiate in good faith until such time as a mutually agreeable decision is reached with respect to the same.

 

(c)     In the event any Improvement falls within the scope of any of the Patent rights, such Improvement shall automatically become part of the exclusive right and license granted to Licensee under Section 2.1; Licensee shall then owe Aytu a royalty on all Net Sales of such Improvement, beginning on the date of the first sale of the Improvement.

 

2.4     Commercialization. Licensee acknowledges that it is important to Aytu that Licensee pursue the commercialization and marketing of Products and otherwise exercise commercially reasonable efforts to maximize the value of this Agreement to Aytu. Licensee will use commercially reasonable efforts to commercialize Products as soon as practicable, consistent with sound business practices and judgment.

 

4

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

(a)     Licensee will not utilize Aytu’s corporate name or logo when commercializing Products. Commercialization will occur exclusively with use of the Trademark Rights and Licensee’s corporate name and logo; Aytu shall never be identified as the source of any Product during the term of this Agreement.

 

(b)     Together with each annual royalty report (see Section 3.5(a)), Licensee shall prepare and deliver to Aytu a written report (certified by an officer of Licensee) indicating its compliance with the obligations in this section.

 

(c)     Licensee’s failure to perform under this Section 2.4 shall be grounds for termination of this Agreement by Aytu.

 

3.

Consideration

 

In consideration of the execution and delivery by Aytu of this Agreement, Licensee agrees as follows:

 

3.1     Royalties and Non-Royalty Revenue.

 

(a)     Minimum Running Royalties for Products. In order to maintain this Agreement, Licensee agrees to pay and shall pay to Aytu, once every calendar year, a minimum, running royalty of either:

 

(1) [*] on Net Sales of all Products and Improvements made, used, sold or otherwise distributed by Licensee, its Affiliates and/or any sublicensee hereunder, or

 

(2) US [*]

 

whichever is greater, until such time as Licensee has paid Aytu a total of US [*] (i.e., for a maximum of ten (10) years). All minimum, running royalty payments under this Section 3.1(a) shall be due and payable thirty (30) days following each twelve (12) month anniversary of the Effective Date. Minimum, running royalty payments will be made in U.S. Dollars via wire transfer, as indicated in Section 3.5 herein. Together with every minimum, running royalty payment, Licensee shall deliver the report specified in Section 3.5(a).

 

(b)     Ongoing Running Royalty Obligations. Once Licensee has paid Aytu a total of {$1,000,000,} the minimum, running royalty obligation under Section 3.21(a) will no longer be required. Thereafter, Licensee agrees to pay and shall pay to Aytu, once every calendar year, a running royalty as follows:

 

(1)     for a period of five (5) years after the date of reaching the [*] milestone, or until the fifteenth (15th) anniversary of the Effective Date, whichever is longer, [*] on Net Sales of all Products and Improvements made, used, sold or otherwise distributed by Licensee, its Affiliates and/or any sublicensee hereunder; and

 

(2)     thereafter, [*] on Net Sales of all Products and Improvements made, used, sold or otherwise distributed by Licensee, its Affiliates and/or any sublicensee hereunder for the remainder of the term of this Agreement.

 

All running royalty payments under this Section 3.1(b) shall be due and payable thirty (30) days following each twelve (12) month anniversary of the Effective Date. Running royalty payments will be made in U.S. Dollars to the bank account, via wire transfer, as indicated in Section 3.5 herein. Together with every minimum, running royalty payment, Licensee shall deliver the report specified in Section 3.5(a).

 

3.2     Arm’s-Length Transactions. On sales of Products and/or Improvements that are made in other than an arms’-length transaction, the value of the Net Sales attributed under this Section 3.1 to such a transaction shall be that which would have been received in an arm’s-length transaction, based on sales of like quality and quantity products on or about the time of such transaction.

 

5

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

3.3     Duration of Royalty Obligations. The royalty obligations of Licensee as to each Product shall terminate with the termination or expiration of this Agreement.

 

3.5     Payment and Accounting.

 

(a)     Reports. Each payment of royalties shall be accompanied by a report in the form attached as Exhibit B hereto, which sets forth in reasonable detail the number and each type of Product and/or Improvement sold, the calculation of Net Sales applicable thereto, and such additional details as may be reasonably requested by Aytu for the determination of royalties payable hereunder. Products and/or Improvements shall be considered as being sold for the purpose of the calculation of royalties under this Agreement when the Products and/or Improvements have been invoiced. Copies of such reports shall be sent to Aytu pursuant to Section 12.1 of this Agreement. All amounts due hereunder shall be paid in United States dollars and shall be made without setoff and free and clear of (and without any deduction or withholding for) any taxes, duties, levies, imposts or similar fees or charges. Licensee agrees to pay and shall pay to Aytu all royalties resulting from the activities of its Affiliates and/or sublicensees.

 

(b)     Wire Transfer Instructions. All payments due hereunder shall be made by Licensee to Aytu in accordance with the following wire transfer instructions:

 

[*]

 

(c)     Termination for Uncured Late Payment. If payment of any minimum, running royalty payment set forth in Section 3.1(a) or any ongoing running royalty payment set forth in Section 3.1(b) is not timely made, Licensee will be in breach of this Agreement. Licensee will have a period of sixty (60) days in which to cure such breach by making payment, in full, of all outstanding amounts owed to Aytu. If payment has not been made by the end of this sixty (60) day cure period, Aytu shall have the right, in its discretion, to terminate this Agreement, such termination to proceed pursuant to Section 7.2(c) of this Agreement.

 

(1)     Service Charges. A service charge of two percent (2%) per month, not to exceed the maximum rate allowed by applicable law, shall be payable by Licensee on any portion of Licensee’s minimum, running royalty payment set forth in Section 3.1(a) or any ongoing running royalty payment set forth in Section 3.1(b) balance, or any other amount payable by Licensee hereunder, that is past due and must be paid during the sixty (60) day cure period.

 

(d)     Records and Audits. Licensee shall create and maintain complete and accurate records and documentation concerning all sales of Products and/or Improvements by Licensee, its Affiliates and sublicensees, in sufficient detail to enable the royalties that are payable hereunder to be determined. Licensee shall retain such records and documentation for not less than seven (7) years from the date of their creation. During the term of this Agreement and for a period of three (3) years thereafter, Aytu and its representatives shall have the right to audit such records and documentation in order to confirm the amounts of royalties paid to Aytu hereunder. Aytu and its representatives shall have reasonable access during regular business hours to Licensee’s offices and the relevant records, files and books of account, and shall have the right to examine any other records reasonably necessary to determine the accuracy of the calculations provided by Licensee. The costs of any such audit shall be borne by Aytu, unless as a result of such inspection it is determined that the amounts payable by Licensee for any one calendar year are in error and underpaid by greater than five percent (5%), in which case the costs of such audit shall be borne by Licensee. Aytu shall report the results of any such audit to Licensee within forty-five (45) days of completion. Thereafter, Licensee shall promptly pay to Aytu the amount of any underpayment discovered in such audit, or Aytu shall credit to Licensee against future royalty payments the amount of any overpayment discovered in such audit, as the case may be. In addition, Licensee shall pay interest on any underpayment at the rate that is the lower of (i) two percent (2%) over the rate of interest announced by Bank of America in Los Angeles, California (or any successor in interest thereto or any commercially equivalent financial institution if no such successor exists) to be its “prime rate”, or (ii) the highest rate permitted by applicable law, from the date such amount was underpaid to the date payment is actually received.

 

6

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

(e)     Currency Transfer Restrictions. If any restrictions on the transfer of currency exist in any country or other jurisdiction so as to prevent Licensee from making payments to Aytu, Licensee shall take all commercially reasonable steps to obtain a waiver of such restrictions or to otherwise enable Licensee to make such payments. If Licensee is unable to do so, Licensee shall make such payments to Aytu in a bank account or other depository designated by Aytu in such country or jurisdiction, which payments shall be in the local currency of such country or jurisdiction, unless payment in United States dollars is permitted. Any payment by Licensee to Aytu in currencies other than United States dollars shall be calculated using the appropriate foreign exchange rate for such currency quoted in the California edition of The Wall Street Journal for the close of business of the last banking day of the calendar quarter in which such payment is being made.

 

(f)     Taxes. Licensee shall pay, or cause to be paid, any and all taxes required to be paid or withheld on any sales, licenses or other transfers for value of Products, Improvements and/or Patent Rights (other than taxes imposed on the income or revenues of Aytu); provided, however, that under no circumstances shall the amounts of such taxes be deducted from the total amount of payments otherwise due to Aytu hereunder. Upon Aytu’s request, Licensee shall secure and send to Aytu proof of any such taxes withheld and paid by Licensee, its Affiliates or sublicensees.

 

4.

Licensee Obligations and Option to Purchase

 

4.1     Purchase of Existing Inventory. Within thirty (30) days after the Effective Date, Licensee shall purchase all of the Product inventory in Aytu’s possession at Aytu's cost. An accounting of the inventory, together with the total Licensee purchase price, is provided in Exhibit C.

 

(a)     Payment for Aytu’s existing inventory shall be made pursuant to the terms provided in Section 3.5(b) hereof. Payment in full must be received by Aytu before possession of Aytu’s existing inventory will pass to Licensee. Once payment in full has been received by Aytu, the parties will make mutually agreeable arrangements for Licensee to obtain possession of Aytu’s existing inventory.

 

4.2     Distribution Agreements. Concurrently with the execution of this Agreement, Licensee shall assume, in full, all of Aytu’s obligations under all Product distribution agreements Aytu has entered into with third party distributors shown in Exhibit D. Aytu will assign all of its obligations under all such distribution agreements to Licensee, effective as of the Effective Date. The foregoing expressly includes, without limitation, Licensee assuming all of Aytu’s warranty obligations under such distribution agreements. Aytu will take all steps reasonably necessary to assist Licensee with the assumption of such responsibilities including, without limitation, obtaining approval for the assignment of such distribution agreements to Licensee as may be necessary. Licensee acknowledges and agrees to such assignment and shall take commercially reasonable steps to fully comply with all of the terms of all existing Aytu Product distribution agreements.

 

4.3     MiOXSYS® Analyzer. Within twelve (12) months after the Effective Date, Licensee shall take all action necessary in order to transfer all of the rights and responsibilities for the manufacturing of the Product analyzer (i.e., the MiOXSYS® Analyzer) from {[*] to another ISO 13485 Certified manufacturer. For the sake of clarity, “ISO 13485 Certified” means a manufacturing entity that has implemented an International Organization for Standard (ISO) 13485 Quality Management System and has successfully met all of the requirements in ISO 13485 (where ISO 13485 = ISO 9001 + Additional Medical Device Requirements).

 

(a)     Upon successful transfer, Licensee shall provide Aytu with written evidence confirming the transfer and such additional information as Aytu may reasonably require.

 

4.4     Customer Relationships. Licensee acknowledges and agrees that a stated purpose of this Agreement is for Licensee to assume all of Aytu’s responsibilities with respect to Aytu’s existing Product customer relationships. Licensee shall take all steps necessary to assume Aytu’s role in all such Product customer relationships and to ensure that all such relationships are maintained in good standing during the term of this Agreement. Without limiting the generality of the foregoing, Licensee hereby agrees to assume full responsibility for all customer complaints, all adverse event reporting, all Product warranty responsibilities, and all other customer-related responsibilities associated with the marketing and sales of all Products that Aytu has heretofore assumed. Aytu shall take reasonable steps to introduce Licensee to all existing customers and to facilitate Licensee’s assumption of Aytu’s responsibilities in all such customer relationships.

 

7

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

4.5     Option to Purchase. After the full amount of the [*] minimum, running royalty recited in Section 3.1(a) has been paid to Aytu by Licensee, Licensee shall have the option, but not the obligation, to purchase all of the Patent rights, Trademark Rights and Technical Information from Aytu. This right shall be ongoing and available to Licensee on a year-to-year basis, concurrently with the payment of the ongoing running royalty payments recited in Section 3.1(b).

 

(a)     In order to exercise this option to purchase, Licensee shall, concurrently with the payment of an ongoing running royalty pursuant to Section 3.1(b), provide Aytu with a commercially reasonable written offer for the purchase of all of the Patent rights, Trademark Rights and Technical Information. Upon receipt of such written offer by Aytu, the Parties will negotiate such purchase in good faith. Should the Parties settle upon mutually agreeable terms of purchase, the Parties shall enter into a separate purchase agreement which will include provisions for the termination of this Agreement.

 

(1)     To be proper, the purchase offer must be for all of the Patent rights, Trademark Rights and Technical Information; offers to purchase only a portion of such rights will not be entertained by Aytu.

 

(b)     For clarity, the option to purchase granted to Licensee after payment in full of the [*] minimum, running royalty of Section 3.1(a) shall be available to Licensee each year for the remainder of the term of this Agreement as a matter of right. Failure by Licensee to exercise this option in any given year shall not preclude Licensee from exercising this option in any subsequent year. Additionally, the failure of the Parties to reach mutually agreeable purchase terms in any given year shall not preclude Licensee from making further purchase offers in subsequent years.

 

5.

Representations And Warranties

 

5.1     Mutual. Each of Aytu and Licensee hereby represents and warrants to the other that the representing and warranting Party is duly organized in its jurisdiction of incorporation; that the representing and warranting Party has the full power and authority to enter into this Agreement; that this Agreement is binding upon the representing and warranting Party; and that this Agreement has been duly authorized by all requisite corporate action within the representing and warranting Party.

 

5.2     Rights to Technology. Aytu represents and warrants to Licensee that, to the best of its actual, current knowledge (without investigation outside of Aytu as to such representations and warranties) (a) it has the right to grant the licenses in this Agreement, (b) it has not granted licenses to the Patent Rights, Trademark Rights or Technical Information to any other party that would restrict the rights granted hereunder, and (c) there are no claims, judgments or settlements to be paid by Aytu with respect the Patent Rights, Trademark Rights or Technical Information or pending claims or litigation relating to the Patent Rights, Trademark rights or Technical Information. Aytu is not aware that any additional rights or licenses are necessary for Licensee to exercise its licensed rights granted by Aytu under this Agreement.

 

5.3     Limited Warranty; Certain Damages.

 

(a)     Limited Warranty. AYTU makes no representation or warranty other than those expressly specified in this Agreement. Licensee accepts the Patent Rights, Trademark Rights, Technical Information and Products on an “AS-IS” basis. AYTU MAKES NO OTHER WARRANTIES CONCERNING PATENT RIGHTS, TRADEMARK RIGHTS, TECHNICAL INFORMATION OR PRODUCT COVERED BY THIS AGREEMENT, INCLUDING WITHOUT LIMITATION, ANY EXPRESS OR IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. AYTU MAKES NO WARRANTY OR REPRESENTATION AS TO THE VALIDITY OR SCOPE OF PATENT RIGHTS OR TRADEMARK RIGHTS, OR THAT ANY PRODUCT WILL BE FREE FROM AN INFRINGEMENT ON PATENTS OR OTHER INTELLECTUAL PROPERTY RIGHTS OF THIRD PARTIES, OR THAT NO THIRD PARTIES ARE IN ANY WAY INFRINGING PATENT RIGHTS OR TRADEMARK RIGHTS COVERED BY THIS AGREEMENT. LICENSEE HEREBY AGREES THAT LICENSEE WILL NOT GIVE, AND SHALL NOT PERMIT ANY AFFILIATES OR SUBLICENSEES OR AFFILIATES THEREOF TO GIVE, ANY SUCH WARRANTY OR REPRESENTATION TO THIRD PARTIES ON BEHALF OF AYTU.

 

8

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

(b)     Certain Damages. EXCEPT FOR THE BREACH OF THE CONFIDENTIALITY PROVISIONS IN ARTICLE 10 OR IN ACCORDANCE WITH THE OBLIGATION TO INDEMNIFY SET FORTH IN ARTICLE 9, IN NO EVENT SHALL AYTU BE LIABLE FOR ANY INDIRECT, SPECIAL OR CONSEQUENTIAL DAMAGES (INCLUDING, WITHOUT LIMITATION, DAMAGES FOR LOSS OF PROFITS OR EXPECTED SAVINGS OR OTHER ECONOMIC LOSSES, OR FOR INJURY TO PERSONS OR PROPERTY) ARISING OUT OF OR IN CONNECTION WITH THIS AGREEMENT OR ITS SUBJECT MATTER, REGARDLESS OF WHETHER AYTU KNOWS OR SHOULD KNOW OF THE POSSIBILITY OF SUCH DAMAGES. EXCEPT FOR THE BREACH OF THE CONFIDENTIALITY PROVISIONS IN ARTICLE 10 OR IN ACCORDANCE WITH THE OBLIGATION TO INDEMNIFY SET FORTH IN ARTICLE 9, AYTU’S AGGREGATE LIABILITY FOR ALL DAMAGES OF ANY KIND RELATING TO THIS AGREEMENT OR ITS SUBJECT MATTER SHALL NOT EXCEED THE AMOUNT PAID BY LICENSEE TO AYTU UNDER THIS AGREEMENT. THE FOREGOING EXCLUSIONS AND LIMITATIONS SHALL APPLY TO ALL CLAIMS AND ACTIONS OF ANY KIND, WHETHER BASED ON CONTRACT, TORT (INCLUDING, BUT NOT LIMITED TO NEGLIGENCE), OR ANY OTHER GROUNDS.

 

5.4     Compliance. Licensee, its Affiliates and sublicensees shall comply in all material respects with all applicable laws in the commercialization of the Products and performance of its obligations under this Agreement, including the statutes, regulations and written directives of the FDA, the EMA and any regulatory authority having jurisdiction in the Territory, the FD&C Act, the Federal Health Care Programs Anti-Kickback Law, 42 USAC. 1320a-7b(b), the statutes, regulations and written directives of Medicare, Medicaid and all other health care programs, as defined in 42 USAC. § 1320a-7b(f), and the Foreign Corrupt Practices Act of 1977, each as may be amended from time to time.

 

6.

Patent Rights, Trademark Rights

 

6.1     Maintenance. Commencing on the Effective Date, Licensee shall assume, in coordination with Aytu, full responsibility for the maintenance of the Patent Rights and the Trademark Rights in the Territory, including, but not limited to, payment of all renewal fees, annuities, maintenance fees, and other costs, fees and expenses related thereto. Licensee shall use commercially reasonable efforts to maintain the Patent Rights and the Trademark Rights to the benefit of Aytu. Aytu shall be reimbursed for all reasonable out-of-pocket expenses associated with such maintenance, as such expenses are incurred. Upon Aytu’s request, Licensee shall secure and send to Aytu proof of such maintenance paid by Licensee, its Affiliates or sublicensees.

 

6.2     Abandonment, Disclaimers, etc. Licensee is not authorized to abandon, disclaim, withdraw, seek reissue, seek reexamination or allow to lapse any patent or patent application within the Patent Rights or any of the Trademark Rights. In the event that Licensee would like to abandon, disclaim, withdraw, seek reissue, seek reexamination or allow to lapse any patent or patent application within the Patent Rights or any of the Trademark Rights, Licensee shall notify Aytu of the same at least sixty (60) days before a final due date which would result in any of the same. In such event, Aytu may, at its sole option and expense, reassume the maintenance of the patent application, patent or trademark at which point Licensee’s rights in and to such patent application, patent or trademark shall immediately terminate. Aytu may also, at its sole option, authorize the abandonment, disclaimer, withdrawal, seeking reissue, seeking reexamination or allowing to lapse of the patent, patent application or trademark at issue, which will cease to be a part of the terms of this Agreement upon formal notification of abandonment by its respective patent office.

 

7.

Term And Termination

 

7.1     Term. Unless earlier terminated as provided in Section 3.5(c) hereof, the term of this Agreement shall commence on the Effective Date and shall continue in perpetuity until terminated pursuant to this Article 7.

 

9

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

7.2     Termination. Except as provided by Section 7.3 hereof, and in addition to the termination provisions of Section 3.5(c), this Agreement shall terminate upon the earliest to occur of the following:

 

(a)     Automatically if Licensee shall enter into a liquidating bankruptcy, be adjudged insolvent, liquidate, dissolve and/or if the business of Licensee shall be placed in the hands of a receiver, assignee, or trustee, whether by voluntary act of Licensee or otherwise; provided, however, that if any such action is involuntary, termination shall not take place unless the action is not reversed within thirty (30) days. Licensee shall give Aytu at least sixty (60) days’ prior written notice before Licensee initiates any bankruptcy proceeding, and Aytu shall have the right to terminate this Agreement immediately upon receipt of such notice;

 

(b)     Automatically if the performance by either party to this Agreement of any term, covenant, condition or provision hereof is deemed illegal or unethical by any recognized governmental agency or body. Upon such occurrence, Aytu shall provide written notice to Licensee setting forth the reason for such termination and the parties shall work in good faith to attempt to revise the terms of this Agreement to mitigate the issue(s). If the parties cannot, within thirty (30) days following Aytu’s delivery of the written notice, resolve the issue(s) through a revision to the terms of this Agreement which is reasonably satisfactory to Aytu, Aytu may immediately terminate this Agreement upon written notice to Licensee;

 

(c)     Immediately upon written notice from Aytu to Licensee of non-payment of any royalty payment required by Sections 3.1(a) and 3.1(b) hereof that has not been cured within the stated sixty (60) day cure period of Section 3.5(c);

 

(d)     In addition to, but exclusive of, the remedy provided in Section 7.2(c), supra, upon ninety (90) days’ written notice from Aytu if, within such 90-day period, Licensee shall fail to cure fully any breach or default of any material obligation under this Agreement as described in such written notice detailing the facts of such breach with reasonable specificity; provided, however, that Licensee may avoid such termination if, before the end of such 75-day period, such breach or default has been cured by Licensee to the reasonable satisfaction of Aytu;

 

(e)     Upon ninety (90) days’ written notice from Licensee if, within such 90- day period, Aytu shall fail to cure fully any breach or default of any material obligation under this Agreement as described in such written notice detailing the facts of such breach with reasonable specificity; provided, however, that Aytu may avoid such termination if, before the end of such 90-day period, such breach or default has been cured by Aytu to the reasonable satisfaction of Licensee; and

 

(f)     Upon the mutual written agreement of the parties hereto (such termination to be effective as of the date mutually agreed upon in such written agreement).

 

7.3     Obligations Upon Termination. Upon any termination of this Agreement pursuant to Section 7.2, nothing herein shall be construed to release any party from any liability for any obligation incurred through the effective date of termination (e.g., confidentiality, payment of any royalty, payment of patent maintenance expenses incurred prior to such date, etc.) or for any breach of this Agreement prior to the effective date of such termination. Upon any termination of this Agreement pursuant to Section 6.2 hereof, all unpaid royalties owed by Licensee to Aytu under Sections 3.1(a) and 3.1(b) of this Agreement which are outstanding as of the effective date of termination (including any interest that has accrued thereon) shall become immediately due and payable, and Licensee shall pay the full outstanding amounts to Aytu within five (5) business days of the effective date of such termination. Licensee may, for a period of one (1) year after the effective date of such termination, sell all tangible Products customarily classified as “inventory” that it has on hand at the date of termination, subject to payment by Licensee to Aytu of the applicable royalty.

 

7.4     Effect of Termination. In the event of any termination of this Agreement pursuant to Section 7.2 hereof, where such termination has not been caused by any action or inaction on the part of any sublicensee of Licensee or by any breach by such sublicensee of its obligations under its sublicense from Licensee, such termination of this Agreement shall be without prejudice to the rights of each non-breaching sublicensee of Licensee and each non-breaching sublicensee shall be deemed to be a licensee of Aytu thereunder, and Aytu shall be entitled to all rights, but shall not be subject to any obligations (other than the grant of license and appurtenant obligations under this Agreement to the extent provided for in such sublicense) of Licensee thereunder.

 

10

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

7.5     Right to Institute Legal Actions. Notwithstanding the provisions of Section 7.2 hereof, Aytu, on the one hand, and Licensee, on the other hand, may institute any other legal action or pursue any other remedy against the other Party permitted by applicable law if the other Party does not substantially cure any breach or default of any material obligation as provided herein.

 

7.6     Reversion of Rights. Notwithstanding anything to the contrary set forth herein, full responsibility for maintenance of the Patent Rights and the Trademark rights shall, at the option of Aytu (exercisable in its sole and absolute discretion), revert to Aytu upon any termination of this Agreement, at Aytu’s sole expense from the date of reversion.

 

7.7     Return of Technical Information, Confidential Information and Data. In the event of any termination of this Agreement, Licensee shall promptly return all Technical Information and Aytu Confidential Information in its possession. Licensee shall not be entitled to retain any copies, even for archival purposes. Licensee shall also provide Aytu with copies of all data, information and materials obtained or generated by or on behalf of Licensee in the course of marketing and commercializing Products using the Patent Rights, Trademark rights and the Technical Information.

 

8.

Infringement By Third Parties

 

8.1     Enforcement. Licensee shall have the first right and the obligation to enforce, at its sole expense, any Patent Rights and/or the Trademark Rights to the extent licensed hereunder against infringement by third parties and shall notify Aytu in writing in advance of all such enforcement efforts. Aytu shall reasonably cooperate in any such enforcement and, as necessary, join as a party therein and Licensee shall reimburse Aytu for all expenses, including reasonable attorneys’ fees, incurred in connection with any such enforcement. Any damages or other recovery from an infringement action undertaken by Licensee shall first be used to reimburse the parties, on a pro rata pari passu basis, for the costs and expenses incurred in such action, and shall thereafter be allocated between the parties as follows{: (i) [*] to Aytu and (ii) [*] to Licensee.}

 

(a)     In the event that Licensee does not file suit against, or commence settlement negotiations with, a substantial infringer of the Patent Rights or the Trademark Rights within ninety (90) days of receipt of a written demand from Aytu that Licensee bring suit, then Aytu shall have the right (but not the obligation), at its own expense, to enforce any Patent Rights or Trademark Rights licensed hereunder on behalf of itself and Licensee. Any damages or other recovery, net of the Parties’ costs and expenses incurred in such infringement action, shall be the sole property of Aytu.

 

8.2     Defense. In the event that any Patent Rights or the Trademark rights are the subject of a legal action seeking invalidation and/or declaratory relief or of any reexamination or opposition proceeding instituted by a third party, the Parties agree to promptly consult with each other concerning the defense of such actions or proceedings. If the Parties agree that such defense should be undertaken, then Licensee shall bear the expenses, including attorneys’ fees, associated with such defense and in any recoupment of expenses. If the Parties disagree, then the Party desiring to defend the action or proceeding may proceed with such defense and will bear its own expenses, and be entitled to all sums recovered.

 

9.

Indemnification

 

9.1     Indemnification by Licensee. Subject to Section 9.2 hereof, Licensee shall hold harmless, defend and indemnify Aytu and each of its officers, directors, employees and agents (each, an “Indemnified Party”, and collectively, the “Indemnified Parties”) from and against any and all claims, damages, losses, liabilities, costs and expenses (including reasonable attorneys’ fees and expenses and costs of investigation, whether or not suit is filed) suffered or incurred by any of the Indemnified Parties in any action, suit, litigation, arbitration or dispute of any kind (“Action”) arising or resulting from any negligence or willful acts or omissions on the part of Licensee, its Affiliates or sublicensees in connection with their use of the Patent Rights, Trademark Rights and/or Technical Information; and/or the exercise of their rights hereunder or under any sublicense, including, but not limited to the manufacture, sale, use, marketing, or other disposition of Products manufactured, sold, marketed, used or otherwise disposed of under this Agreement, including the existing Product inventory (see, Section 4.1).

 

11

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

(a)     As part of its obligations hereunder, Licensee shall defend any Action brought against any of the Indemnified Parties with counsel of its own choosing and reasonably acceptable to Aytu, and neither Aytu nor any other Indemnified Party shall enter into any settlement of any such Action without first obtaining prior approval of Licensee. Licensee shall pay all costs, including attorney’s fees, incurred in enforcing this indemnification provision.

 

(b)     Should Aytu or any other Indemnified Party not afford Licensee the right to defend any such Action, or should Aytu or any other Indemnified Party not obtain the approval of Licensee to any such settlement, Licensee shall have no obligation to indemnify Aytu or any other Indemnified Party hereunder.

 

(c)     Should Licensee fail to provide a defense for the Indemnified Parties as required hereunder, then Licensee shall reimburse Aytu for its out-of-pocket expenses (including, without limitation, reasonable attorneys’ fees and expenses and costs of investigation) which are incurred as a result of any investigation, defense or settlement relating to the foregoing, which reimbursement shall be made immediately to Aytu upon receipt by Licensee of invoices reflecting in reasonable detail such expenses incurred by Aytu.

 

(d)     Within one hundred and twenty (120) days following the Effective Date, Licensee shall obtain and maintain insurance policies (including products liability and general liability policies at such time as is appropriate) which are reasonable and necessary to cover its activities and to comply with the indemnification obligations set forth above. Such insurance policies shall name Aytu as an additional insured party and shall provide a minimum of [*] in coverage per occurrence. Licensee shall provide Aytu with prompt written notice of any material change in coverage under such policies. If Aytu determines that evidence of Licensee’s insurance coverage is necessary and appropriate, within thirty (30) days of the Effective Date (subject to extension if reasonably required) and annually thereafter, Licensee shall provide Aytu with a certificate of insurance issued by the appropriate insurance company evidencing the insurance coverage required by this Section 9.1, together with copies of the endorsement which specifies Aytu as an additional insured and the declarations page for each such insurance policy.

 

9.2     Notice of Claim. Aytu shall promptly notify Licensee in writing of any claim or Action or material threat thereof brought against any Indemnified Party in respect of which indemnification may be sought and, to the extent allowed by law, shall reasonably cooperate with Licensee in defending or settling any such claim or Action. No settlement of any claim, Action or threat thereof received by Aytu and for which Aytu intends to seek indemnification (for itself or on behalf of any other Indemnified Party) shall be made without the prior joint written approval of Licensee and Aytu.

 

10.

Confidentiality

 

10.1     Non-Disclosure. The Parties shall keep the terms of this Agreement and all business and scientific discussions relating to the business of the parties strictly confidential. It may, from time to time, be necessary for the Parties, in connection with performance under this Agreement, to disclose Confidential Information (including know-how) to each other. Should that become necessary, all such information that is intended to be confidential shall be reasonably identified as “Confidential Information”. In such an event, the Receiving Party shall keep in strictest confidence the Confidential Information of the Disclosing Party, using the standard of care it normally uses for information of like character, and shall not disclose the Confidential Information to any third party or use it except as expressly authorized by the prior written consent of the Disclosing Party or as otherwise permitted by this Agreement; provided, however, that Licensee may disclose Aytu’s Confidential Information to its Affiliates and sublicensees as shall be reasonably necessary to carry out the intent of this Agreement or any sublicense granted by Licensee as contemplated by this Agreement if, and only if, such Affiliates and/or sublicensees each execute a legally binding agreement containing confidentiality provisions no less restrictive than those contained in this Section 10. The Receiving Party’s obligation hereunder shall not apply to Confidential Information that the Receiving Party can show:

 

(a)     Is or later becomes part of the public domain through no fault or neglect of the Receiving Party;

 

(b)     Is received in good faith from a third party having no obligations of confidentiality to the Disclosing Party, provided that the Receiving Party complies with any restrictions imposed by the third party;

 

12

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

(c)     Is independently developed by the Receiving Party without use of the Disclosing Party’s Confidential Information; or

 

(d)     Is required by law or regulation to be disclosed, provided that the Receiving Party uses reasonable efforts to restrict disclosure and to obtain confidential treatment.

 

10.2     Limits on Permitted Disclosures. Each Party agrees that any disclosure or distribution of the other party’s Confidential Information within its own organization shall be made only as is reasonably necessary to carry out the intent of this Agreement. The Parties further agree that all of their respective officers, employees, agents, representatives or approved sublicensees to whom any Confidential Information is disclosed or distributed shall have agreed to maintain its confidentiality.

 

10.3     Legally Required Disclosures. If a subpoena or other legal process concerning Confidential Information is served upon any Party pertaining to the subject matter hereof, the Party served shall notify the other party immediately, the other Party shall cooperate with the Party served, at the other Party’s expense, in any effort to contest the validity of such subpoena or other legal process. This Section 10.3 shall not be construed in any way to limit any Party’s ability to satisfy any disclosure of its relationship with the other Party required by any governmental authority.

 

10.4     Technical Information as Confidential Information. The Technical Information is understood by Licensee to be the Confidential Information of Aytu to the extent it is unpublished or otherwise not publicly available. As such, Licensee’s confidentiality obligations hereunder automatically extend to any and all Technical Information.

 

10.5     Remedies. Both Parties acknowledge and agree that it would be difficult to measure damages for breach by either Party of the covenants set forth in this Section 10, that injury from any such breach would be incalculable, and that money damages would therefore be an inadequate remedy for any such breach. Accordingly, either Party shall be entitled, in addition to all other remedies available hereunder or under law or equity, to injunctive or such other equitable relief as a court may deem appropriate to restrain or remedy any breach of such covenants.

 

11.

Patent Marking

 

In the event any Product is the subject of a patent under the Patent Rights, Licensee shall actually or virtually mark all Products made, sold or otherwise disposed of by or on behalf of it or any of its Permitted Sublicensees as set forth under Title 35, Section 287(a) of the United States Code and shall respond to any request or disclosure under Title 35, Section 287(b)(4)(B) of the United States Code by notifying Aytu of the request for disclosure.

 

12.

Miscellaneous

 

12.1     Notices. Any notice, request, instruction or other document required by this Agreement shall be in writing and shall be deemed to have been given (a) if sent via electronic mail or secure electronic file transfer, return receipt requested, at the time of receipt by the intended recipient, (b) if mailed with the United States Postal Service by prepaid, first class, certified mail, return receipt requested, at the time of receipt by the intended recipient, (c) if sent by Federal Express or other overnight carrier, signature of delivery required, at the time of receipt by the intended recipient, or (c) if sent by facsimile transmission, when so sent and when receipt has been acknowledged by appropriate telephone or facsimile receipt, addressed as follows:

 

In the case of Aytu to:

 

Aytu Bioscience, Inc.
373 Inverness Parkway, Suite 206
Englewood, Colorado 80112
Attention: Jake Siciliano, Corporate and Intellectual Property Counsel (jsiciliano@aytubio.com)

 

with a copy to Josh Disbrow, Chairman & Chief Executive Officer (Josh.Disbrow@aytubio.com)

 

13

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

or in the case of Licensee to:

 

[To be completed]

Attention: _________________

 

or to such other physical or electronic mail address or to such other person(s) as may be given from time to time under the terms of this Section 12.1.

 

12.2     Compliance with Laws. Each Party shall comply with all applicable federal, state and local laws and regulations in connection with its activities pursuant to this Agreement.

 

12.3     Governing Law. For any dispute between the Parties to this Agreement which arises from or relates to this Agreement, the Agreement shall be construed and enforced in accordance with the laws of the United States of America and of the State of Delaware, irrespective of choice of laws provisions. The Parties agree that Wilmington, Delaware shall be the situs of any legal proceeding arising out of or relating to this Agreement. Each Party hereby waives any right it may have to assert the doctrine of forum non conveniens or similar doctrine or to object to venue with respect to any proceeding brought in accordance with this Section, and stipulates that the state and federal courts located in Wilmington, Delaware shall have in personam jurisdiction and venue over each of them for the purpose of litigating any dispute, controversy, or proceeding arising out of or related to this Agreement. Each Party hereby authorizes and accepts service of process sufficient for personal jurisdiction in any action against it as contemplated by this Section by registered or certified mail, return receipt requested, postage prepaid, to its address for the giving of notices as set forth in this Agreement.

 

12.4     Waiver. Failure of any Party to enforce a right under this Agreement shall not act as a waiver of that right or the ability to assert that right relative to the particular situation involved.

 

12.5     Enforceability. If any provision of this Agreement shall be found by a court of competent jurisdiction to be void, invalid or unenforceable, the same shall be reformed to comply with applicable law or stricken if not so conformable, so as not to affect the validity or enforceability of the remainder of this Agreement.

 

12.6     Modification. No change, modification, or addition or amendment to this Agreement, or waiver of any term or condition of this Agreement, is valid or enforceable unless in writing and signed and dated by the Parties.

 

12.7     Entire Agreement. This Agreement and the Exhibits hereto (which are incorporated herein by this reference as if fully set forth herein) constitute the entire agreement between the Parties with respect to the subject matter hereof and thereof, and replace and supersede as of the date hereof and thereof any and all prior agreements and understandings, whether oral or written, between the Parties with respect to the subject matter of such agreements.

 

12.8     Construction. This Agreement has been prepared, examined, negotiated and revised by each Party and their respective attorneys, and no implication shall be drawn and no provision shall be construed against any Party by virtue of the purported identity of the drafter of this Agreement or any portion thereof.

 

12.9     Counterparts. This Agreement may be executed simultaneously in one or more counterparts, each of which shall constitute one and the same instrument. This Agreement may be executed by facsimile or in another suitable electronic format (i.e., .pdf).

 

12.10     Assignment; Successors.

 

(a)     Subject to Section 12.10(b), Licensee may assign this Agreement as part of a sale of substantially all of its assets, regardless of whether such a sale occurs through an asset sale, stock sale, merger or other combination, or any other transfer of Licensee’s entire business, or that part of Licensee’s business that exercises all rights granted under this Agreement. In the event of a bankruptcy, assignment is permitted only to a party that can provide adequate assurance of future performance, including diligent marketing and sales of Products.

 

14

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

(b)     Prior to any assignment permitted under Section 12.10(a): (i) Licensee must give Aytu thirty (30) days prior written notice of the assignment, including the new assignee’s contact information, and (ii) the new assignee must agree in writing to Aytu to be bound by this Agreement.

 

(c)     Licensee may assign this Agreement to any Affiliate of Licensee, subject to the prior written consent of Aytu, such consent not to be unreasonably withheld. Prior to such permitted assignment, Licensee must give Aytu the Affiliate’s contact information and the Affiliate must agree in writing to Aytu to be bound by this Agreement.

 

(d)     Subject to the limitations on assignment herein, this Agreement shall be binding upon and inure to the benefit of any successors in interest and assigns of Aytu and Licensee. Any attempt to assign this Agreement by Licensee that is not in accordance with this Section 12.10 is null and void. Aytu shall have the right to assign its rights hereunder as part of any reorganization or bond financing.

 

12.11     Further Assurances. At any time and from time to time after the Effective Date, each Party shall do, execute, acknowledge and deliver, and cause to be done, executed, acknowledged or delivered, all such further acts, transfers, conveyances, assignments or assurances as may be reasonably required to consummate the transactions contemplated by this Agreement.

 

12.12     Survival. The following portion of this Agreement shall survive any expiration or earlier termination of this Agreement: Sections 3.5(a), 3.5(b), 3.5(d), 3.5(e), 3.5(f), 5.3, 7.3, 7.4 and 7.7 and Articles 9, 10 and 12.

 

 

 

[signature page follows]

 

15

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

In Witness Whereof, the Parties have caused their duly authorized representatives to execute this Agreement and the same shall be effective as of the Effective Date, supra.

 

LICENSEE:

 

Avrio Genetics, LLC

 

By:                                              

Name:                                              
Title:                                              

 

 

 

AYTU:

 

Aytu Bioscience, Inc.

 

By:                                              

Name:                                              
Title:                                              

 

16

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

 

 

 

Exhibit A

 

Patent Rights

 

 

 

 

 

 

 

 

 

 

 

 

 

Exhibit B

 

Royalty Reporting Form

 

Licensee name: Avrio Genetics, LLC

Reporting period: 

Date of report: 

 

Royalty Report

Product* (list products* by name)

No. units sold

Invoiced price per unit

Net sales

Country of sale/foreign currency/ conversion rate

Product name

       

Product name

       

Product name

       

Total

       

 

Total Net sales

$

Royalty rate

 

Royalty due

$

 

Total royalty due: $___________________________

Due date:                               

 

Report prepared by:

Title:

Date:

 

Please send report via electronic mail or other file transfer protocol to:

Aytu Bioscience, Inc.
373 Inverness Parkway, Suite 206
Englewood, Colorado 80112
Attention: Jake Siciliano, Corporate and Intellectual Property Counsel (jsiciliano@aytubio.com)

 

with a copy to Josh Disbrow, Chairman & Chief Executive Officer (Josh.Disbrow@aytubio.com)

 

* - if the Royalty is for an Improvement, note that it is in Improvement and list the Improvement by name

17

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

Exhibit C

 

Aytu Product Inventory

 

 

MiOXSYS® Component Name

Part #

Inventory

Unit COG*

Total COG*'s

[*]

 

 

 

 

18

Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10). Such excluded information is not material and would likely cause competitive harm to the registrant if publicly disclosed. We have designated such excluded information in this Exclusive License Agreement with [*]

 

 

Exhibit D

 

Aytu Distribution Agreements

 

 

[*]

 

 

 

19
 
 

 

Exhibit 31.1

 

AYTU BIOSCIENCE, INC.

Certification by Chief Executive Officer

Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

 

 

 

I, Joshua R. Disbrow, certify that:

 

1.

I have reviewed this report on Form 10-Q for the three months ended December 31, 2020 of Aytu BioScience, Inc.;

 

2.

Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

 

3.

Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

 

4.

The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a—15(e) and 15d—15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a—15(f) and 15d—15(f)) for the registrant and have:

 

 

a)

Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant is made known to us by others within those entities particularly during the period in which this report is being prepared;

 

 

b)

Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

 

 

c)

Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

 

 

d)

Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting.

 

5.

The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of registrant’s board of directors (or persons performing the equivalent functions):

 

 

a)

All significant deficiencies or material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

 

 

b)

Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

 

 

                                                                                                                                                                                                                                                                                       

 Date: February 11, 2021 

 

 

 

 

 

 

 

 

 

 

 

By:

/s/ Joshua R. Disbrow

 

 

 

 Joshua R. Disbrow

 

 

 

 Chief Executive Officer (Principal Executive Officer)

 

 

 

 

 


 

 

 

 

Exhibit 31.2

 

AYTU BIOSCIENCE, INC.

Certification by Chief Financial Officer

Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

 

 

 

I, David A. Green, certify that:

 

1.

I have reviewed this report on Form 10-Q for the three months ended December 31, 2020 of Aytu BioScience, Inc.;

 

2.

Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

 

3.

Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

 

4.

The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a—15(e) and 15d—15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a—15(f) and 15d—15(f)) for the registrant and have:

 

 

a)

Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant is made known to us by others within those entities particularly during the period in which this report is being prepared;

 

 

b)

Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

 

 

c)

Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

 

 

d)

Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting.

 

5.

The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of registrant’s board of directors (or persons performing the equivalent functions):

 

 

a)

All significant deficiencies or material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

 

 

b)

Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

 

 

                                                                                                                                                                                                                                                                                          

 Date: February 11, 2021 

 

 

 

 

 

 

 

 

 

 

 

By:

/s/ David A. Green

 

 

 

 David A. Green

 

 

 

 Chief Financial Officer (Principal Financial Officer and Principal Accounting Officer)

 

 

 

 


 

 

Ex. 32.1

 

CERTIFICATION OF THE 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

 

In connection with the filing of the quarterly report on Form 10-Q for the quarter ended December 31, 2020 (the “Report”) by Aytu BioScience, Inc. (the “Company”), each of the undersigned hereby certifies that:

 

1.

The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended, and

 

2.

The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

 

 

 

 Date: February 11, 2021

 

 

 

 

 

 

 

 

 

 

 

By:

/s/ Joshua R. Disbrow

 

 

 

 Joshua R. Disbrow

 

 

 

 Chief Executive Officer (Principal Executive Officer)

 

                                                                                                                                                                                                                                                                                                                                                                                       

 

 

     

 Date: February 11, 2021 

 

 

 

 

 

 

 

 

 

 

 

By:

/s/ David A. Green

 

 

 

 David A. Green

 

 

 

 Chief Financial Officer (Principal Financial Officer and Principal Accounting Officer)