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Published: 2023-05-09 00:00:00 ET
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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 March 31, 2023

 

 

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

 

For the transition period from         to

 

Commission File Number 001-14027

 

Anika Therapeutics, Inc.

(Exact Name of Registrant as Specified in Its Charter)

 

Delaware04-3145961
(State or Other Jurisdiction of Incorporation or Organization)(I.R.S. Employer Identification No.)

 

32 Wiggins Avenue, Bedford, Massachusetts 01730

(Address of Principal Executive Offices) (Zip Code)

 

(781) 457-9000

(Registrant’s Telephone Number, Including Area Code)

 

N/A

(Former Name, Former Address and Former Fiscal Year, if Changed Since Last Report)

 

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

 

Title of Each ClassTrading SymbolName of Each Exchange on Which Registered
Common Stock, par value $0.01 per shareANIKNASDAQ Global Select Market

 

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

 

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐

 

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

Emerging growth

   

company

company

     

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition 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 ☒

 

APPLICABLE ONLY TO CORPORATE ISSUERS:

 

As of April 30, 2023, there were 14,757,151 outstanding shares of Common Stock, par value $0.01 per share.

 

 

 

 

ANIKA THERAPEUTICS, INC.

TABLE OF CONTENTS

 

   

Page

Part I

Financial Information

3

Item 1.

Condensed Consolidated Financial Statements (unaudited):

3

 

Condensed Consolidated Balance Sheets as of March 31, 2023 and December 31, 2022

3

 

Condensed Consolidated Statement of Operations and Comprehensive Income for the three months ended March 31, 2023 and 2022

4

 

Condensed Consolidated Statements of Stockholders’ Equity for the three months ended March 31, 2023 and 2022

5

 

Condensed Consolidated Statements of Cash Flows for the three months ended March 31, 2023 and 2022

6

 

Notes to Condensed Consolidated Financial Statements

7

Item 2.

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

16

Item 3.

Quantitative and Qualitative Disclosures About Market Risk

25

Item 4.

Controls and Procedures

25

Part II

Other Information

25

Item 1.

Legal Proceedings

25

Item 1A.

Risk Factors

25

Item 2.

Unregistered Sales of Equity Securities and Use of Proceeds

26

Item 6.

Exhibits

27

Signatures

 

28

 

References in this Quarterly Report on Form 10-Q to “we,” “us,” “our,” “our company,” and other similar references refer to Anika Therapeutics, Inc. and its subsidiaries unless the context otherwise indicates.

 

ANIKA, ANIKA THERAPEUTICS, ANIKAVISC, ARTHROSURFACE, CINGAL, HYAFF, HYVISC, MONOVISC, ORTHOVISC, OVOMOTION, PARCUS MEDICAL, REVOMOTION, TACTOSET, WRISTMOTION and XTWIST are our registered trademarks that appear in this Quarterly Report on Form 10-Q. For convenience, these trademarks appear in this Quarterly Report on Form 10-Q without ® and ™ symbols, but that practice does not mean that we will not assert, to the fullest extent under applicable law, our rights to the trademarks. This Quarterly Report on Form 10-Q also contains trademarks and trade names that are the property of other companies and licensed to us.

 

 

 

 

 

 

 

 

 

PART I:

FINANCIAL INFORMATION

 

 

ITEM 1.

FINANCIAL STATEMENTS

 

 

Anika Therapeutics, Inc. and Subsidiaries

Condensed Consolidated Balance Sheets

(in thousands, except per share data)

(unaudited)

 

  

March 31,

  

December 31,

 
ASSETS 

2023

  

2022

 

Current assets:

        

Cash and cash equivalents

 $79,737  $86,327 

Accounts receivable, net

  30,629   34,627 

Inventories, net

  41,319   39,765 

Prepaid expenses and other current assets

  8,646   8,828 

Total current assets

  160,331   169,547 

Property and equipment, net

  48,803   48,279 

Right-of-use assets

  30,175   30,696 

Other long-term assets

  18,131   17,219 

Deferred tax assets

  1,519   1,449 

Intangible assets, net

  72,653   74,599 

Goodwill

  7,462   7,339 

Total assets

 $339,074  $349,128 
         
LIABILITIES AND STOCKHOLDERS EQUITY        
         

Current liabilities:

        

Accounts payable

 $8,948  $9,074 

Accrued expenses and other current liabilities

  19,745   18,840 

Total current liabilities

  28,693   27,914 

Other long-term liabilities

  399   398 

Deferred tax liability

  4,114   6,436 

Lease liabilities

  28,280   28,817 

Commitments and contingencies (Note 9)

          

Stockholders’ equity:

        

Preferred stock, $0.01 par value; 1,250 shares authorized, no shares issued and outstanding at March 31, 2023 and December 31, 2022, respectively

  -   - 

Common stock, $0.01 par value; 90,000 shares authorized, 14,741 and 14,625 shares issued and outstanding at March 31, 2023 and December 31, 2022, respectively

  147   146 

Additional paid-in-capital

  83,243   81,141 

Accumulated other comprehensive loss

  (6,171)  (6,443)

Retained earnings

  200,369   210,719 

Total stockholders’ equity

  277,588   285,563 

Total liabilities and stockholders’ equity

 $339,074  $349,128 

 

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

3

 

 

Anika Therapeutics, Inc. and Subsidiaries

Condensed Consolidated Statements of Operations and Comprehensive Income (Loss)

(in thousands, except per share data)

(unaudited)

 

   

Three Months Ended March 31,

 
   

2023

   

2022

 

Revenue

  $ 37,924     $ 36,693  

Cost of revenue

    15,081       14,889  

Gross Profit

    22,843       21,804  
                 

Operating expenses:

               

Research and development

    8,400       6,157  

Selling, general and administrative

    26,996       19,201  

Total operating expenses

    35,396       25,358  

Loss from operations

    (12,553 )     (3,554 )

Interest and other income (expense), net

    539       (154 )

Loss before income taxes

    (12,014 )     (3,708 )

Benefit from income taxes

    (1,664 )     (775 )

Net loss

  $ (10,350 )   $ (2,933 )
                 

Net (loss) per share:

               

Basic

  $ (0.71 )   $ (0.20 )

Diluted

  $ (0.71 )   $ (0.20 )
                 

Weighted average common shares outstanding:

               

Basic

    14,653       14,466  

Diluted

    14,653       14,466  
                 

Net loss

  $ (10,350 )   $ (2,933 )

Foreign currency translation adjustment

    272       (81 )

Comprehensive loss

  $ (10,078 )   $ (3,014 )

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

 

4

 

 

Anika Therapeutics, Inc. and Subsidiaries

Condensed Consolidated Statements of Stockholders' Equity

(in thousands, except per share data)

(unaudited)

 

            Three Months Ended March 31, 2023
        Common Stock            

Accumulated

         
                    Additional            

Other

   

Total

 
   

Number of

   

$.01 Par

   

Paid

   

Retained

   

Comprehensive

   

Stockholders'

 
   

Shares

   

Value

   

in Capital

   

Earnings

   

Loss

   

Equity

 

Balance, January 1, 2023

    14,625     $ 146     $ 81,141     $ 210,719     $ (6,443 )   $ 285,563  

Issuance of common stock for equity awards

    1       -       7       -       -       7  

Vesting of restricted stock units

    177       2       (2 )     -       -       -  

Stock-based compensation expense

    -       -       3,717       -       -       3,717  

Retirement of common stock for minimum tax withholdings

    (62 )     (1 )     (1,620 )     -       -       (1,621 )

Net loss

    -       -       -       (10,350 )     -       (10,350 )

Other comprehensive loss

    -       -       -       -       272       272  

Balance, March 31, 2023

    14,741     $ 147     $ 83,243     $ 200,369     $ (6,171 )   $ 277,588  

 

            Three Months Ended March 31, 2022  
        Common Stock            

Accumulated

         
                    Additional            

Other

   

Total

 
   

Number of

   

$.01 Par

   

Paid

   

Retained

   

Comprehensive

   

Stockholders'

 
   

Shares

   

Value

   

in Capital

   

Earnings

   

Loss

   

Equity

 

Balance, January 1, 2022

    14,441     $ 144     $ 67,081     $ 225,578     $ (5,718 )   $ 287,085  

Issuance of common stock for equity awards

    1       -       15       -       -       15  

Vesting of restricted stock units

    106       1       (1 )     -       -       -  

Stock-based compensation expense

    -       -       2,545       -       -       2,545  

Retirement of common stock for minimum tax withholdings

    (30 )     -       (844 )     -       -       (844 )

Net loss

    -       -       -       (2,933 )     -       (2,933 )

Other comprehensive loss

    -       -       -       -       (81 )     (81 )

Balance, March 31, 2022

    14,518     $ 145     $ 68,796     $ 222,645     $ (5,799 )   $ 285,787  

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

5

 

 

Anika Therapeutics, Inc. and Subsidiaries

Condensed Consolidated Statements of Cash Flows

(in thousands)

(unaudited)

 

  

Three Months Ended March 31,

 
  

2023

  

2022

 

Cash flows from operating activities:

        

Net loss

 $(10,350) $(2,933)

Adjustments to reconcile net income to net cash provided by operating activities:

        

Depreciation

  1,605   1,671 

Amortization of acquisition related intangible assets

  1,946   1,946 

Non-cash operating lease cost

  542   403 

Stock-based compensation expense

  3,717   2,545 

Deferred income taxes

  (2,373)  (273)

Provision for credit losses

  24   5 

Provision for inventory

  629   586 

Changes in operating assets and liabilities:

        

Accounts receivable

  4,057   383 

Inventories

  (3,063)  (602)

Prepaid expenses, other current and long-term assets

  (462)  (1,189)

Accounts payable

  (713)  (473)

Operating lease liabilities

  (523)  (387)

Accrued expenses, other current and long-term liabilities

  665   (2,929)

Income taxes

  681   (622)

Net cash used in operating activities

  (3,618)  (1,869)
         

Cash flows from investing activities:

        

Purchases of property and equipment

  (1,389)  (1,326)

Net cash used in investing activities

  (1,389)  (1,326)
         

Cash flows from financing activities:

        

Cash paid for tax withheld on vested restricted stock awards

  (1,620)  (846)

Proceeds from exercises of equity awards

  7   15 

Payments made on finance leases

  -   (31)

Net cash used in financing activities

  (1,613)  (862)
         

Exchange rate impact on cash

  30   (4)
         

Decrease in cash and cash equivalents

  (6,590)  (4,061)

Cash and cash equivalents at beginning of period

  86,327   94,386 

Cash and cash equivalents at end of period

 $79,737  $90,325 

Supplemental disclosure of cash flow information:

        

Non-cash investing activities:

        

Purchases of property and equipment included in accounts payable and accrued expenses

 $729  $728 

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

6

 

Anika Therapeutics, Inc. and Subsidiaries

Notes to Condensed Consolidated Financial Statements

(amounts in thousands, except share and per share amounts or as otherwise noted)

(unaudited)

 

 

1.

Nature of Business

 

Anika Therapeutics, Inc. (the “Company”) is a global joint preservation company that creates and delivers meaningful advancements in early intervention orthopedic care, including in the areas of osteoarthritis (“OA”) pain management, regenerative solutions, sports medicine and Arthrosurface joint solutions.

 

In early 2020, the Company expanded its overall technology platform through its strategic acquisitions of Parcus Medical, LLC (“Parcus Medical”), a sports medicine implant and instrumentation solutions provider focused on sports medicine and soft tissue repair, and Arthrosurface, Inc. (“Arthrosurface”), a company specializing in less invasive, bone preserving partial and total joint replacement solutions. These acquisitions broadened the Company's product portfolio, developed over its 30 years of expertise in hyaluronic acid technology, into joint preservation and restoration space with higher market potential, added new revenue streams, increased and accelerated its commercial capabilities, diversified its revenue base, and expanded its product pipeline and research and development expertise.

 

The Company is subject to risks common to companies in the life sciences industry including, but not limited to, development by the Company or its competitors of new technological innovations, dependence on key personnel, protection of proprietary technology, commercialization of existing and new products, and compliance with U.S. Food and Drug Administration (“FDA”) and foreign regulations and approval requirements, as well as the ability to grow the Company’s business through appropriate commercial strategies.

 

 

2.

Basis of Presentation

 

The accompanying unaudited condensed consolidated financial statements and related notes have been prepared by the Company pursuant to the rules and regulations of the Securities and Exchange Commission (the “SEC”) and in accordance with accounting principles generally accepted in the United States (“U.S. GAAP”). The financial statements include the accounts of Anika Therapeutics, Inc. and its subsidiaries. Inter-company transactions and balances have been eliminated. Certain information and footnote disclosures normally included in annual financial statements prepared in accordance with U.S. GAAP have been or omitted pursuant to SEC rules and regulations relating to interim financial statements. The December 31, 2022 balances reported herein were derived from the audited consolidated financial statements. In the opinion of management, these unaudited condensed consolidated financial statements contain all adjustments (consisting only of normal recurring adjustments) necessary to fairly state the condensed consolidated financial statements.

 

The accompanying unaudited condensed consolidated financial statements and related notes should be read in conjunction with the Company’s annual financial statements filed with its Annual Report on Form 10-K for the year ended December 31, 2022. The results of operations for the three-month period ended March 31, 2023 are not indicative of the results to be expected for the year ending December 31, 2023.

 

Segment Information

 

Operating segments are components of an enterprise about which separate financial information is available that is evaluated regularly by the chief operating decision maker, or decision-making group, in deciding how to allocate resources and in assessing performance. The Company’s chief operating decision maker as of March 31, 2023 was its President and Chief Executive Officer. Based on the criteria established by Accounting Standards Codification 280, Segment Reporting, the Company has one operating and reportable segment.

 

7

 
 

3.

Accounts Receivable

 

The Company estimates an allowance for credit losses with its accounts receivable resulting from the inability of its customers to make required payments, which is included in selling, general and administrative expenses in the accompanying consolidated statements of operations. In determining the adequacy of the allowance, management specifically analyzes individual accounts receivable, historical bad debts, customer concentrations, customer creditworthiness, current and reasonable and supportable forecasts of future economic conditions, accounts receivable aging trends, and changes in the Company’s customer payment terms.

 

The components of the Company’s accounts receivable are as follows:

 

  

As of

  

As of

 
  

March 31,

  December 31, 
  

2023

  

2022

 

Accounts Receivable

 $32,166  $36,235 

Allowance for credit losses

  1,537   1,608 

Net balance, end of period

  30,629   34,627 

 

A summary of activity in the allowance for credit losses is as follows:

 

  

As of March 31,

 
  

2023

  

2022

 

Balance, beginning of the period

 $1,608  $1,442 

Amounts provided

  102   33 

Amounts recovered

  (78)  (28)

Amounts written off

  (106)  (79)

Translation adjustments

  11   (18)

Balance, end of period

 $1,537  $1,350 

 

8

 
 

4.

Fair Value Measurements

 

The Company has certain cash equivalents in money market funds that are classified within Level 1 of the fair value hierarchy and are valued based on quoted prices in active markets. For cash, accounts receivables, accounts payable, and accrued interest, the carrying amounts approximate fair value, because of the short maturity of these instruments, and therefore fair value information is not included in the table below. There were no transfers between fair value levels during the three-month periods ended March 31, 2023 or 2022.

 

The classification of the Company’s cash equivalents within the fair value hierarchy was as follows:

 

 

  March 31,  Active
Markets
for Identical
Assets
  Significant
Other
Observable
Inputs
  Significant
Unobservable
Inputs
  Amortized 
  

2023

  

(Level 1)

  

(Level 2)

  

(Level 3)

  

Cost

 

Cash equivalents:

                    

Money Market Funds

 $63,450  $63,450  $-  $-  $63,450 

 

 

  December 31,  Active
Markets
for Identical
Assets
  Significant
Other
Observable
Inputs
  Significant
Unobservable
Inputs
   Amortized 
  

2022

  

(Level 1)

  

(Level 2)

  

(Level 3)

  

Cost

 

Cash equivalents:

                    

Money Market Funds

 $67,801  $67,801  $-  $-  $67,801 

 

 
5. 

Inventories

 

Inventories consist of the following:

 

  

March 31,

  

December 31,

 
  

2023

  

2022

 

Raw materials

 $19,027  $20,535 

Work-in-process

  14,974   10,648 

Finished goods

  24,946   25,306 

Total

 $58,947  $56,489 
         
         

Inventories

 $41,319  $39,765 

Other long-term assets

  17,628   16,724 

Total

 $58,947  $56,489 

 

Inventories are stated net of inventory reserves of approximately $11.3 million and $9.9 million, as of March 31, 2023 and December 31, 2022, respectively.

 

9

 
 

6.

Intangible Assets

 

Intangible assets as of March 31, 2023 and December 31, 2022 consisted of the following:

 

                  

December 31,

     
      

Three Months Ended March 31, 2023

  

2022

     
      

Less:

                 
      

Accumulated

              

Weighted

 
      

Currency

  

Less:

          

Average

 
  

Gross

  

Translation

  

Accumulated

  

Net Book

  

Net Book

  

Useful

 
  

Value

  

Adjustment

  

Amortization

  

Value

  

Value

  

Life

 

Developed technology

 $89,580  $(1,608) $(25,135) $62,837  $64,286   15 

IPR&D

  2,656   (1,006)  -   1,650   1,650  

Indefinite

 

Customer relationships

  9,000   -   (2,852)  6,148   6,373   10 

Distributor relationships

  4,700   (415)  (4,285)  -   -   5 

Patents

  1,000   (189)  (692)  119   131   16 

Tradenames

  5,200   -   (3,301)  1,899   2,159   5 

Total

 $112,136  $(3,218) $(36,265) $72,653  $74,599   13 

 

The aggregate amortization expense related to intangible assets was $1.9 million for the three-month periods ended March 31, 2023 and 2022.

 

7.

Goodwill

 

The Company assesses goodwill for impairment annually, or, under certain circumstances, more frequently, such as when events or changes in circumstances indicate there may be impairment.

 

Changes in the carrying value of goodwill for the three-month ended March 31, 2023 were as follows:

 

  

Three Months Ended
March 31,

 
  

2023

 

Balance, beginning of period

 $7,339 

Effect of foreign currency adjustments

  123 

Balance, ending of period

 $7,462 
 
8.

Accrued Expenses

 

Accrued expenses consist of the following:

 

  

March 31,

  

December 31,

 
  

2023

  

2022

 

Compensation and related expenses

 $7,715  $11,303 

Professional fees

  4,152   3,145 

Parcus arbitration settlement

  3,250   - 

Operating lease liability - current

  2,105   2,073 

Clinical trial costs

  1,059   999 

Income taxes payable

  889   810 

Other

  575   510 

Total

 $19,745  $18,840 
 

9.

Commitments and Contingencies

 

In certain of its contracts, the Company warrants to its customers that the products it manufactures conform to the product specifications as in effect at the time of delivery of the specific product. The Company may also warrant that the products it manufactures do not infringe, violate, or breach any U.S. or international patent or intellectual property right, trade secret, or other proprietary information of any third party. On occasion, the Company contractually indemnifies its customers against any and all losses arising out of, or in any way connected with, any claim or claims of breach of its warranties or any actual or alleged defect in any product caused by the negligent acts or omissions of the Company. The Company maintains a products liability insurance policy that limits its exposure to these risks. Based on the Company’s historical activity, in combination with its liability insurance coverage, the Company believes the estimated fair value of these indemnification agreements is immaterial. The Company had no accrued warranties as of March 31, 2023 or December 31, 2022 and has no history of claims paid.

 

10

 

The Company is also involved from time-to-time in various legal proceedings arising in the normal course of business. Although the outcomes of these legal proceedings are inherently difficult to predict, the Company does not expect the resolution of these occasional legal proceedings to have a material adverse effect on its financial position, results of operations, or cash flow.

 

On October 21, 2021, the Company received notice that the former unitholders of Parcus Medical had filed an arbitration request regarding the earnout provisions of up to $60 million, of which the Company paid $4.3 million, agreed to in the Parcus Medical Merger Agreement. On April 20, 2023, the Company and the former unitholders of Parcus Medical entered into a settlement agreement to end the arbitration case. The Company recorded a liability of $3.25 million at March 31, 2023 which was paid to the former unitholders of Parcus Medical in April 2023.

 

10.

Revenue and Geographic Information

 

Revenue by product family is as follows:

 

  

Three Months Ended March 31,

 
  

2023

  

2022

 

OA Pain Management

 $22,633  $20,964 

Joint Preservation and Restoration

  13,453   12,139 

Non-Orthopedic

  1,838   3,590 

Total

 $37,924  $36,693 

 

Effective January 1, 2023, the Company beganto report revenue from product sales to veterinary customers within the Non-Orthopedic product family whereas such revenue had been previously reported within the OA Pain Management product family. Revenue from product sales to veterinary customers amounted to $0.5 million and $1.8 million for the three months ended March 31, 2023 and 2022, respectively, and are included within the Non-Orthopedic product family for all periods presented. Accordingly, revenue from product sales to veterinary customers in the prior period have been reclassified to conform to the current period presentation.

 

Revenue from the Company’s sole significant customer, DePuy Synthes Mitek Sports Medicine, part of the Johnson & Johnson Medical Companies, as a percentage of the Company’s total revenue was 43% and 39% for the three months ended March 31, 2023 and 2022, respectively.

 

Total revenue by geographic location based on the location of the customer in total and as a percentage of total revenue were as follows:

 

     Three Months Ended March 31, 
  

2023

  

2022

 
      

Percentage of

      

Percentage of

 
  

Revenue

  

Revenue

  

Revenue

  

Revenue

 

Geographic Location:

                

United States

 $27,288   72% $26,773   73%

Europe

  5,662   15%  5,796   16%

Other

  4,974   13%  4,124   11%

Total

 $37,924   100% $36,693   100%

 

11

 
 

11.

Equity Incentive Plan

 

Equity Incentive Plan

 

The Anika Therapeutics, Inc. 2017 Omnibus Incentive Plan (the “2017 Plan”) was approved by the Company’s stockholders on June 13, 2017 and subsequently amended on June 18, 2019, June 16, 2020, June 16, 2021 and June 8, 2022. On June 8, 2022, the Company’s stockholders approved an amendment to the 2017 Plan increasing the number of shares by 250,000 shares from 4.6 million shares to 4.85 million shares. The 2017 Plan provides for the grant of incentive stock options, nonqualified stock options, stock appreciation rights (“SARs”), restricted stock awards, performance restricted stock units (“PSUs”), restricted stock units (“RSUs”), total shareholder return options (“TSRs”) and performance options that may be settled in cash, stock, or other property. In accordance with the 2017 Plan approved by the Company’s stockholders, including the amendments thereto, each share award other than stock options or SARs will reduce the number of total shares available for grant by two shares. Subject to adjustment for specified types of changes in the Company’s capitalization, no more than 4.85 million shares of common stock may be issued under the 2017 Plan. There were 0.4 million shares available for future grant at March 31, 2023 under the 2017 Plan.

 

The Anika Therapeutics, Inc. 2021 Inducement Plan (the “Inducement Plan”) was adopted by the Company’s board of directors on November 4, 2021. The Inducement Plan reserves 125,000 shares of common stock for issuance pursuant to equity-based awards granted under the Inducement Plan. Such awards may be granted only to an individual who was not previously the Company’s employee or director with the Company. The Inducement Plan provides for the grant of awards under terms substantially similar to the 2017 Plan (as amended). There were 4,883 shares available for future grant at March 31, 2023 under the Inducement Plan.

 

The Company may satisfy the awards upon exercise, or upon fulfillment of the vesting requirements for other equity-based awards, with either newly issued shares or shares reacquired by the Company. Stock-based awards are granted with an exercise price equal to or greater than the market price of the Company’s stock on the date of grant. Awards contain service conditions or service and performance conditions, and they generally become exercisable ratably over three years with a maximum contractual term of ten years.

 

The Company presents the expenses related to stock-based compensation awards in the same expense line items as cash compensation paid to each of its employees as follows (in thousands):

 

  

Three Months Ended March 31,

 
  

2023

  

2022

 
         

Cost of revenue

 $184  $176 

Research and development

  517   367 

Selling, general and administrative

  3,016   2,002 

Total stock-based compensation expense

 $3,717  $2,545 

 

Stock Options

 

Stock options are granted to purchase common shares at prices that are equal to the fair market value of the shares on the date the options are granted or, in the case of premium options, are granted with an exercise price at 110% of the market price of the Company’s common stock on the date of grant. Options generally vest in equal annual installments over a period of three years and expire 10 years after the date of grant. The grant-date fair value of options is recognized as expense on a straight-line basis over the requisite service period, which is generally the vesting period.

 

12

 

The following summarizes the activity under the Company’s stock option plans:

 

          

Weighted

     
          

Average

  

 

 
      

Weighted

  

Remaining

  

Aggregate

 
      

Average

  

Contractual

  

Intrinsic

 
  

Number of

  

Exercise

  

Term

  

Value

 
  

Options

  

Price

  

(in years)

  

(in thousands)

 

Outstanding as of December 31, 2022

  1,530,703  $34.93         

Granted

  339,145  $29.68         

Exercised

  (637) $10.87      $13 

Forfeited and canceled

  (11,212) $39.77         

Outstanding as of March 31, 2023

  1,857,999  $33.95   8.2  $632 

Vested, March 31, 2023

  915,798  $37.08   7.4  $82 

Vested or expected to vest, March 31, 2023

  1,857,999  $33.95   8.2  $632 

 

The aggregate intrinsic value of options exercised for the three-month period ended March 31, 2023 was immaterial. The Company granted 339,145 stock options during the three-month ended March 31, 2023.

 

The Company uses the Black-Scholes pricing model to determine the fair value of options granted. The calculation of the fair value of stock options is affected by the stock price on the grant date, the expected volatility of the Company’s common stock over the expected term of the award, the expected life of the award, the risk-free interest rate and the dividend yield.

 

The assumptions used in the Black-Scholes pricing model for options granted during the three months ended March 31, 2023 and 2022, along with the weighted-average grant-date fair values, were as follows:

 

  Three Months Ended 
  March 31, 
 

2023

  

2022

 

Risk free interest rate

 3.5%  -   4.3%  1.3%  -  1.9%

Expected volatility

 48.7%  -   49.4%  53.8%  -  54.6%

Expected life (years)

     4.5           4.5    

Expected dividend yield

     0.0%          0.0%   

Fair value per option

     $11.71  $        $11.37    

 

As of March 31, 2023, there was $9.9 million of unrecognized compensation cost related to unvested stock options. This expense is expected to be recognized over a weighted average period of 2.1 years.

 

Restricted Stock Units

 

RSUs generally vest in equal annual installments over a three-year period. The grant-date fair value of RSUs is recognized as expense on a straight-line basis over the requisite service period, which is generally the vesting period. The Company determines the fair value of RSUs based on the closing price of its common stock on the date of grant.

 

RSU activity for the three-month period ended March 31, 2023 was as follows:

 

      

Weighted

 
  

Number of

  

Average

 
  

Shares

  

Fair Value

 

Outstanding as of December 31, 2022

  675,405  $28.40 

Granted

  368,169  $26.91 

Vested

  (177,611) $28.98 

Forfeited and cancelled

  (15,010) $27.34 

Outstanding as of March 31, 2023

  850,953  $27.65 

 

13

 

The weighted-average grant-date fair value per share of RSUs granted was $26.91 and $25.75 for the three-month periods ended March 31, 2023 and 2022, respectively. The total fair value of RSUs vested was $5.7 million and $3.3 million for the three-month periods ended March 31, 2023 and 2022, respectively.

 

As of March 31, 2023, there was $19.4 million of unrecognized compensation cost related to time-based RSUs, which was expected to be recognized over a weighted-average period of 2.3 years.

 

Performance Stock Units

 

PSU activity for the three-month ended March 31, 2023 was as follows:

 

  

Number of

Shares

  

Weighted

Average

Fair Value

 

Outstanding as of December 31, 2022

  117,897  $34.98 

Forfeited and cancelled

  (117,897) $34.98 

Outstanding as of March 31, 2023

  -  $- 

 

The total fair value of PSUs vested was $0 and $0.6 million for the three-month period ended March 31, 2023 and 2022. As of March 31, 2023, there are no outstanding PSUs.

 

 

 

 

 

 

14

 
 

12.

Income Taxes

 

The Company recorded an income tax benefit of $1.7 million for the three-month period ended March 31, 2023, resulting in an effective tax rate of 13.9%. The income tax benefit was $0.8 million for the three-month period ended March 31, 2022, resulting in an effective tax rate of 20.9%. The net change in the effective tax rate for the three-month period ended March 31, 2023, as compared to the same period in 2022, was primarily due to a valuation allowance being recorded against domestic deferred tax assets.

 

The Company recognizes deferred tax assets to the extent that it believes that these assets are more likely than not to be realized. In making such a determination, the Company considers all available positive and negative evidence, including future reversals of existing taxable temporary differences, projected future taxable income, tax-planning strategies, carryback potential if permitted under the tax law, and results of recent operations. At December 31, 2022, the Company determined that its domestic deferred tax assets were realizable based upon future reversals of existing taxable temporary differences. The Company expects to incur an operating loss for 2023. As a result, the Company anticipates that deferred tax assets originating during the year ended December 31, 2023 will exceed the availability of reversing taxable temporary differences. Due to significant negative evidence, including the Company’s current and prior year operating losses, the Company concluded its anticipated net deferred tax assets in the U.S. are not more likely than not to be realizable. Accordingly, the estimated annual effective tax rate used to compute the income tax provision for the three-month period ended March 31, 2023 includes an adjustment for the valuation allowance required against the U.S deferred tax assets. As of March 31, 2023, the Company continues to believe its foreign deferred tax assets are realizable based upon future reversals of existing taxable temporary differences and projected future taxable income.

 

The Company files income tax returns in the United States on a federal basis, in certain U.S. states, and in certain foreign jurisdictions. The associated tax filings remain subject to examination by applicable tax authorities for a certain length of time following the tax year to which those filings relate, which varies by jurisdiction.

 

13.

Earnings Per Share (EPS)

 

Basic EPS is calculated by dividing net income (loss) by the weighted average number of shares outstanding during the period. Unvested restricted shares, although legally issued and outstanding, are not considered outstanding for purposes of calculating basic EPS. Diluted EPS is calculated by dividing net income by the weighted average number of shares outstanding plus the dilutive effect, if any, of outstanding share-based awards using the treasury stock method.

 

The following table provides share information used in the calculation of the Company's basic and diluted earnings per share (in thousands):

 

 

  

Three Months Ended March 31,

 
  

2023

  

2022

 

Shares used in the calculation of basic EPS

  14,653   14,466 

Effect of dilutive securities:

        

Share based awards

  -   - 

Diluted shares used in the calculation of EPS

  14,653   14,466 

 

The Company had a net loss during the three-month ended March 31, 2023 and 2022, respectively, and therefore all potential common shares would have been anti-dilutive and accordingly were excluded from the computation of diluted EPS. Stock options of 1.9 million shares and 1.5 million shares were outstanding for the three-month periods ended March 31, 2023 and 2022, respectively. Restricted stock units and performance stock units totaling 0.9 million and 0.8 million were outstanding for the three-month periods ended March 31, 2023 and 2022, respectively. These securities were not included in the computation of diluted EPS because the awards’ impact on EPS would have been anti-dilutive.

 

14.

Subsequent Event

 

On April 13, 2023, the Company entered into a Cooperation Agreement (the “Cooperation Agreement”) with Caligan Partners LP (collectively with each of their respective affiliates and associates, the “Investor Group”). Pursuant to the Cooperation Agreement, the Company has agreed to increase the size of the board of directors to eight directors and appointed an additional independent director.

 

The Company also agreed to commit to a return of capital program, subject to market conditions, applicable legal requirements and other relevant factors, by establishing a share repurchase program for an aggregate purchase price equal to $20,000,000 to occur within twelve months from the date of the Cooperation Agreement as follows: (i) the first $5,000,000 of which will be effected through an accelerated stock repurchase program with an investment bank commencing with the Company’s next open trading window, which will open on or before May 12, 2023, (ii) the second $5,000,000 of which to be purchased in the open market, and (iii) the remaining $10,000,000 of which to be purchased in the open market subject to positive cash flow.

 

 

15

 
 

ITEM 2.

MANAGEMENTS DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

 

You should read the following discussion in conjunction with our financial statements and related notes appearing elsewhere in this report and our audited consolidated financial statements and related notes contained in our Annual Report on Form 10-K for the year ended December 31, 2022, or our 2022 Form 10-K. In addition to historical information, this report contains "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 concerning our business, consolidated financial condition, and results of operations. The Securities and Exchange Commission, or the SEC, encourages companies to disclose forward-looking statements so that investors can better understand a companys future prospects and make informed investment decisions. Forward-looking statements are subject to risks and uncertainties, many of which are outside our control, which could cause actual results to differ materially from these statements. Therefore, you should not rely on any of these forward-looking statements. Forward-looking statements can be identified by such words as "will," "likely," "may," "believe," "expect," "anticipate," "intend," "seek," "designed," "develop," "would," "future," "can," "could," and other expressions that are predictions of or indicate future events and trends and that do not relate to historical matters. All statements other than statements of historical facts included in this report regarding our strategies, prospects, financial condition, operations, costs, plans, and objectives are forward-looking statements. Examples of forward-looking statements include, among others, statements regarding the effect of COVID-19 and related impacts on our business, operations, and financial results, expected future operating results, expectations regarding the timing and receipt of regulatory results, anticipated levels of capital expenditures, and expectations of the effect on our financial condition of claims, litigation, and governmental and regulatory proceedings.

 

Please also refer to “Item 1A. Risk Factors” of our 2022 Form 10-K for important factors that we believe could cause actual results to differ materially from those in our forward-looking statements. Any forward-looking statement made by us in this report is based only on information currently available to us and speaks only as of the date on which it is made. We undertake no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

 

Management Overview

 

We are a global joint preservation company that creates and delivers meaningful advancements in early intervention orthopedic care. Based on our collaborations with clinicians to understand what they need most to treat their patients, we develop minimally invasive products that restore active living for people around the world. We are committed to leading in high opportunity spaces within orthopedics, including osteoarthritis, or OA, pain management, regenerative solutions, sports medicine and Arthrosurface joint solutions (previously Bone Preserving Joint Technologies).

 

We have over thirty years of global expertise developing, manufacturing and commercializing products our hyaluronic acid, or HA, technology platform. HA is a naturally occurring polymer found throughout the body that is vital for proper joint health and tissue function. Our proprietary technologies for modifying the HA molecule allow product properties to be tailored specifically to multiple uses, including enabling longer residence time to support OA pain management and creating a solid form of HA called Hyaff, which is a platform utilized in our regenerative solutions portfolio.

 

In early 2020, we expanded our overall technology platform, product portfolio, and significantly expanded our commercial infrastructure, especially in the United States, through our strategic acquisitions of Parcus Medical, LLC, or Parcus Medical, a sports medicine and instrumentation solutions provider, and Arthrosurface, Inc, or Arthrosurface, a company specializing in bone preserving partial and total joint replacement solutions. These acquisitions have ignited the transformation of our company by augmenting our HA-based OA pain management and regenerative products with a broad suite of products and capabilities focused on early intervention joint preservation primarily in upper and lower extremities such as shoulder, foot/ankle, knee and hand/wrist.

 

 

16

 

As we look forward, our business is positioned to capture value within our target markets in joint preservation. We believe our future success will be driven by our:

 

 

Decades of experience in HA-based regenerative solutions and early intervention orthopedics combined under new seasoned leadership with a strong financial foundation for future investment in meaningful solutions for our customers and their patients;

 

 

Utilizing HA-based technology and manufacturing expertise to provide new and differentiated solutions for the faster growing joint preservation and regenerative medicine markets;

 

 

Robust network of stakeholders in our target markets that will allow us to identify evolving unmet patient treatment needs;

 

 

Prioritized investment in differentiated pipeline of regenerative solutions, bone preserving implants and sports medicine solutions;

 

 

Global commercial expertise, which we will leverage to drive growth across our product portfolio, including an intentional site of care focus in ambulatory surgery centers in the United States and continued international expansion;

 

 

Pursuit of strategic inorganic growth opportunities, including potential partnerships and smaller acquisitions and technology licensing, by leveraging our strong financial foundation and operational capabilities; and

 

 

Energized and experienced team focused on strong values, talent, and culture.

 

COVID-19 Pandemic

 

In March 2020, the World Health Organization declared the spread of the COVID-19 virus a pandemic. This pandemic has caused an economic downturn globally, which created volatility in our results due to the worldwide cancellation or delay of elective procedures, staffing shortages and supply chain disruptions, as well as the impact on timelines associated with certain clinical studies. Please see the section captioned “Part I. Item 1A. Risk Factors” of our Annual Report on Form 10-K for additional information with respect to the risks faced by our business in light of the COVID-19 pandemic. While the impact has been limited to these items to date, we caution that there continues to be a possibility for potential future implementation of certain additional restrictions or other challenges associated with infections, staffing shortages or supply chain disruptions due to COVID-19 and current or new variants in certain jurisdictions. The impact of these challenges is currently unknown but could be significant and we continue to take precautions so as not to disrupt our business.

 

Products

 

OA Pain Management

 

Our OA Pain Management product family consists of Monovisc and Orthovisc, our single- and multi-injection, HA-based viscosupplement offerings that are indicated to provide pain relief from osteoarthritis conditions; and Cingal, our novel, next-generation, single-injection OA Pain Management product consisting of our proprietary cross-linked HA material combined with a fast-acting steroid, designed to provide both short- and long-term pain relief, which is currently sold outside the United States in over 35 countries.

 

17

 

Joint Preservation and Restoration

 

Our Joint Preservation and Restoration product family consists of: (a) Our portfolio of orthopedic regenerative solutions products, including Hyalofast and Tactoset; (b) our line of sports medicine solutions used to repair and reconstruct damaged ligaments and tendons due to sports injuries, trauma and disease; and (c) our portfolio of over 150 bone preserving joint technologies, including partial joint replacement, joint resurfacing, and minimally invasive and bone sparing implants, designed to treat upper and lower extremity orthopedic conditions caused by trauma, injury and arthritic disease.

 

Non-Orthopedic

 

Our Non-Orthopedic product family consists of legacy HA-based products that are marketed principally for non-orthopedic applications, including our anti-adhesion barrier product, advanced wound care products, our ear, nose and throat products, and our ophthalmic products. We have also reclassified Hyvisc, our high molecular weight injectable HA veterinary product approved for the treatment of joint dysfunction in horses due to non-infectious synovitis associated with equine OA. Hyvisc was previously reported in the OA Pain Management product family but has been reclassified to the Non-Orthopedic product family.

 

 

 

 

 

 

 

 

 

 

 

 

18

 

Results of Operations

 

Three Months Ended March 31, 2023 Compared to Three Months Ended March 31, 2022

 

      Three Months Ended March 31,  
   

2023

   

2022

   

$ Change

   

% Change

 
        (in thousands, except percentages)    

Revenue

  $ 37,924     $ 36,693     $ 1,231       3 %

Cost of revenue

    15,081       14,889       192       1 %

Gross profit

    22,843       21,804       1,039       5 %

Gross margin

    60 %     59 %                

Operating expenses:

                               

Research and development

    8,400       6,157       2,243       36 %

Selling, general and administrative

    26,996       19,201       7,795       41 %

Total operating expenses

    35,396       25,358       10,038       40 %

Loss from operations

    (12,553 )     (3,554 )     (8,999 )     253 %

Interest and other income (expense), net

    539       (154 )     693       (450 %)

Loss before income taxes

    (12,014 )     (3,708 )     (8,306 )     224 %

Benefit from for income taxes

    (1,664 )     (775 )     (889 )     115 %

Net loss

  $ (10,350 )   $ (2,933 )   $ (7,417 )     253 %

 

Revenue

 

The following table presents revenue by product family for the three-month period ended March 31, 2023 and 2022 as follows:

 

      Three Months Ended March 31,  
   

2023

   

2022

   

$ Change

   

% Change

 
        (in thousands, except percentages)  

OA Pain Management

  $ 22,633     $ 20,964     $ 1,669       8 %

Joint Preservation and Restoration

    13,453       12,139       1,314       11 %

Non-Orthopedic

    1,838       3,590       (1,752 )     (49 %)
    $ 37,924     $ 36,693     $ 1,231       3 %

 

Revenue from our OA Pain Management product family increased 8% for the three-month period ended March 31, 2023, as compared to the same period in 2022, due primarily to favorable strategic partner ordering patterns and sales growth on increasing customer demand, offset in part by unfavorable international distributor ordering patterns as strategic partner and distributor ordering patterns can vary significantly on a quarterly basis.

 

Revenue from our Joint Preservation and Restoration product family increased 11% for the three-month period ended March 31, 2023, as compared to the same period in 2022, due primarily due to improving elective procedure volumes and rapidly growing commercial adoption of our newest products.

 

Revenue from our Non-Orthopedic product family decreased 49% for the three-month ended March 31, 2023, as compared to the same period in 2022, primarily due to unfavorable timing of distributor ordering patterns as well as due to end of life of certain legacy products.

 

19

 

Gross Profit and Margin

 

Gross profit for the three-month period ended March 31, 2023 increased $1.0 million to $22.8 million, representing a 60% gross margin for the period as compared to 59% in the prior year. The increase in gross profit for the three-month period ended March 31, 2023, as compared to the same period in 2022, was primarily resulted from increased revenue. Gross margin for the three-month period ended March 31, 2023, increased compared to the same period of prior year due primarily to improved production volumes.

 

Research and Development

 

Research and development expenses for the three-month period ended March 31, 2023 were $8.4 million, an increase of $2.2 million as compared to the same period in 2022. The increase was primarily related to increased costs to comply with growing regulatory requirements globally as well as new product development associated with our research and development pipeline and scale-up manufacturing activities.

 

Selling, General and Administrative

 

Selling, general and administrative expenses for the three-month period ended March 31, 2023 were $27.0 million, an increase of $7.8 million, as compared to the same period in 2022. This increase for the three-month period ended March 31, 2023 was primarily due to $5.8 million of non-recurring costs incurred during the quarter related to the Parcus Medical unitholder arbitration settlement, shareholder activism and other non-recurring corporate costs. The growth in SG&A expenses also reflects expansion of our commercial capabilities and marketing activities, as well as higher stock-based compensation expense in part driven by forfeitures in the first quarter of 2022.

 

Income Taxes

 

The benefit from income taxes was $1.7 million for the three-month period ended March 31, 2023, resulting in an effective tax rate of 13.9%. The benefit from income taxes was $0.8 million for the three-month period ended March 31, 2022, resulting in an effective tax rate of 20.9%. The net change in the effective tax rate for the three-month period ended March 31, 2023, as compared to the same period in 2022, was primarily due to a valuation allowance in 2023 being recorded against domestic deferred tax assets.

 

Net Loss

 

For the three-month period ended March 31, 2023, net loss was $10.4 million, or $0.71 per diluted share, compared to net income of $2.9 million, or $0.20 per diluted share, for the same period in prior year. The decrease in net income and diluted earnings per share was primarily due to the non-recurring expenses related to the Parcus Medical arbitration settlement, shareholder activism and other non-recurring corporate costs.

 

Non-GAAP Financial Measures

 

We present certain information with respect to adjusted gross profit and adjusted gross margin, adjusted Earnings Before Interest, Tax, Depreciation and Amortization, or EBITDA, adjusted net income, adjusted diluted earnings per share or adjusted EPS, which are financial measures not based on any standardized methodology prescribed by accounting principles generally accepted in the United States, or GAAP, and is not necessarily comparable to similarly titled measures presented by other companies.

 

20

 

We have presented adjusted gross profit and adjusted gross margin, adjusted EBITDA, adjusted net income, adjusted EPS, because they are key measures used by our management and board of directors to understand and evaluate our operating performance and to develop operational goals for managing our business. We believe these financial measures help identify underlying trends in our business that could otherwise be masked by the effect of the expenses that we exclude. In particular, we believe that the exclusion of these items in calculating these measures can provide a useful tool for period-to-period comparisons of our core operating performance. Accordingly, we believe that these measures provide useful information to investors and others in understanding and evaluating our operating results, enhancing the overall understanding of our past performance and future prospects and allowing for greater transparency with respect to key financial metrics used by our management in their financial and operational decision-making.

 

Adjusted Gross Profit and Adjusted Gross Margin

 

We define adjusted gross profit as our gross profit excluding amortization of certain acquired intangible assets, the impact of inventory fair-value step up associated with our recent acquisitions and certain product rationalization charges. The amortized assets contribute to revenue generation, and the amortization of such assets will likely continue in future periods until such assets are fully amortized. These assets include the fair value of certain identified assets acquired in acquisitions, including developed technology and acquired tradenames. We define adjusted gross margin as adjusted gross profit divided by total revenue.

 

The following is a reconciliation of adjusted gross profit to gross profit for the three-month periods ended March 31, 2023 and 2022, respectively:

 

    Three-Month Periods Ended March 31,  
   

2023

   

2022

 
Gross profit   $ 22,843     $ 21,804  
Acquisition related intangible asset amortization     1,562       1,562  
Adjusted gross profit   $ 24,405     $ 23,366  
Adjusted gross margin     64 %     64 %

 

Adjusted gross profit for the three-month period ended March 31, 2023 increased $1.0 million to $24.4 million representing adjusted gross margin of 64%. Adjusted gross profit for the three-month period ended March 31, 2022 was $23.4 million, or adjusted gross margin of 64%. There was no change in adjusted gross margin for the three-month period ended March 31, 2023 as compared to 2022, as the impact of improved production volumes was offset by unfavorable product mix in 2023.

 

Adjusted EBITDA

 

We present information below with respect to adjusted EBITDA, which we define as our net income (loss) excluding interest and other expense, net, income tax benefit, depreciation and amortization, stock-based compensation, and acquisition-related expenses.

 

Adjusted EBITDA is not prepared in accordance with US GAAP, and should not be considered in isolation of, or as an alternative to, measures prepared in accordance with US GAAP. There are a number of limitations related to the use of adjusted EBITDA rather than net (loss) income, which is the nearest US GAAP equivalent. Some of these limitations are:

 

 

adjusted EBITDA excludes depreciation and amortization, and, although these are non-cash expenses, the assets being depreciated or amortized may have to be replaced in the future, the cash requirements for which are not reflected in adjusted EBITDA;

 

 

we exclude stock-based compensation expense from adjusted EBITDA although (a) it has been, and will continue to be for the foreseeable future, a significant recurring expense for our business and an important part of our compensation strategy and (b) if we did not pay out a portion of our compensation in the form of stock-based compensation, the cash salary expense included in operating expenses would be higher, which would affect our cash position;

 

21

 

 

we exclude acquisition related expenses, including, amortization and depreciation of acquired assets in recent acquisitions, and the impact of inventory fair-value step up on cost of revenue;

 

 

the expenses and other items that we exclude in our calculation of adjusted EBITDA may differ from the expenses and other items, if any, that other companies may exclude from adjusted EBITDA when they report their operating results;

 

The following is a reconciliation of adjusted EBITDA to net loss for the three-month periods ended March 31, 2023 and 2022, respectively:

 

   

Three Months Ended March 31,

 
   

2023

   

2022

 
   

(in thousands)

 

Net loss

  $ (10,350 )   $ (2,933 )

Interest and other (income) expense, net

    (539 )     154  

Benefit from income taxes

    (1,664 )     (775 )

Depreciation and amortization

    1,764       1,830  

Share-based compensation

    3,717       2,545  

Arbitration settlement

    3,250       -  

Acquisition related intangible asset amortization

    1,787       1,787  

Costs of shareholder activism

    831       -  

Adjusted EBITDA

  $ (1,204 )   $ 2,608  

 

Adjusted EBITDA in the three-month period ended March 31, 2023 decreased $3.8 million as compared with the same period in 2022. The decrease in adjusted EBITDA for the period was primarily due to an increase in operating expenses largely attributable to costs to comply with growing regulatory requirements globally, expansion of our operational capabilities to support our continued growth as well as certain non-recurring corporate costs.

 

Adjusted Net (Loss) Income and Adjusted EPS

 

We present information below with respect to adjusted net (loss) income and adjusted EPS. We define adjusted net (loss) income as our net (loss) income excluding amortization and depreciation of acquired assets, the impact of inventory fair-value step up on cost of revenue and changes in the fair value of contingent consideration, on a tax effected basis. The amortized assets contribute to revenue generation, and the amortization of such assets will recur in future periods until such assets are fully amortized. These assets include the estimated fair value of certain identified assets acquired in acquisitions, including in-process research and development, developed technology, customer relationships and acquired tradenames. We define adjusted EPS as GAAP diluted earnings per share excluding the above adjustments to net (loss) income used in calculating adjusted net (loss) income, each on a per share and tax effected basis.

 

The following is a reconciliation of adjusted net (loss) income to net (loss) income for the three-month periods ended March 31, 2023 and 2022, respectively:

 

   

Three Months Ended March 31,

 
   

2023

   

2022

 
   

(in thousands)

 

Net loss

  $ (10,350 )   $ (2,933 )

Arbitration settlement, tax effected

    2,776       -  

Acquisition related intangible asset amortization, tax effected

    1,526       1,345  

Costs of shareholder activism, tax effected

    710       -  

Adjusted net loss

  $ (5,338 )   $ (1,588 )

 

22

 

The following is a reconciliation of adjusted diluted EPS to diluted EPS for the three-month periods ended March 31, 2023 and 2022, respectively:

 

   

Three Months Ended March 31,

 
   

2023

   

2022

 

Diluted loss per share

  $ (0.71 )   $ (0.20 )

Arbitration settlement, tax effected

    0.19       -  

Acquisition related intangible asset amortization, tax effected

    0.11       0.09  

Costs of shareholder activism, tax effected

    0.05       -  

Adjusted diluted loss per share

  $ (0.36 )   $ (0.11 )

 

Adjusted net loss and adjusted diluted loss per share in the three-month period ended March 31, 2023 increased $3.8 million and $0.25, respectively, as compared with the same period in 2022. The increase for the period was primarily due to an increase in operating expenses largely attributable to expansion of our operational capabilities to support our growing business needs as well as non-recurring expenses related to the Parcus Medical arbitration settlement, shareholder activism and other non-recurring corporate costs.

 

Liquidity and Capital Resources

 

We require cash to fund our operating activities and to make capital expenditures and other investments in the business. We expect that our requirements for cash to fund these uses will increase as our operations expand. We continue to generate cash from operating activities and believe that our operating cash flows, cash currently on our condensed consolidated balance sheet and availability under our credit facility will be sufficient to allow us to continue to invest in our existing business, to manage our capital structure on a short and long-term basis, and to meet our anticipated operating cash needs. Cash, cash equivalents, and investments aggregated $79.7 million and $86.3 million, and working capital totaled $131.6 million and $141.6 million, at March 31, 2023 and December 31, 2022, respectively. We are closely monitoring our liquidity and capital resources for any potential impact that the COVID-19 pandemic may have on our operations.

 

On November 12, 2021, we entered into a Third Amendment to Credit Agreement with Bank of America N.A. as administrative agent, which amended our existing revolving line of credit agreement dated October 24, 2017 which provides up to $75.0 million in the form of a senior revolving line of credit. Subject to certain conditions, we may request up to an additional $75.0 million for a maximum aggregate commitment of $150.0 million. As of March 31, 2023, and December 31, 2022, there were no outstanding borrowings, and we are in compliance with the terms of the credit facility.

 

Summary of Cash Flows (in thousands):

 

   

Three Months Ended March 31,

 
   

2023

   

2022

 

Cash provided by (used in)

               

Operating activities

  $ (3,618 )   $ (1,869 )

Investing activities

    (1,389 )     (1,326 )

Financing activities

    (1,613 )     (862 )

Effect of exchange rate changes on cash

    30       (4 )

Net decrease in cash and cash equivalents

  $ (6,590 )   $ (4,061 )

 

The following changes contributed to the net change in cash and cash equivalents in the three-month period ended March 31, 2023 as compared to the same period in 2022.

 

Operating Activities

 

Cash used in operating activities was $3.6 million for the three-month period ended March 31, 2023, as compared to cash used in operating activities of $1.9 million for the same period in 2022. The increase in cash used in operating activities in 2023 was primarily due to a higher net loss and an increase in inventories.

 

For the foreseeable future, we expect to continue to invest substantial resources in research and development as well as continued investment in our commercial and operational infrastructure to support our growth strategy. These costs will be funded with a combination of cash on hand and cash expected to be generated from future operations.

 

23

 

Investing Activities

 

Cash used in investing activities was $1.4 million for the three-month period ended March 31, 2023, as compared to cash used in investing activities of $1.3 million for the same period in 2022. The change was primarily due to an increase in capital expenditures to support commercial growth of the business in the three-month period ended March 31, 2023.

 

Financing Activities

 

Cash used in financing activities was $1.6 million for the three-month period ended March 31, 2023, as compared to cash used in financing activities of $0.9 million for the same period in 2022. In both periods, the cash used in financing activities was primarily attributable to utilization of cash for employee tax withholding in exchange for shares surrendered by equity award holders.

 

Critical Accounting Policies and Estimates

 

The preparation of our condensed consolidated financial statements in conformity with GAAP requires management to use judgment in making estimates and assumptions that affect the reported amounts of assets, liabilities, revenue and expenses, and related disclosure of contingent assets and liabilities. We believe that our accounting policies for revenue recognition, accounts receivable and allowance for credit losses, goodwill, acquired in-process research and development, inventory and contingencies are based on, among other things, judgments and assumptions made by management that include inherent risks and uncertainties. There have been no significant changes to the above critical accounting policies or in the underlying accounting assumptions and estimates used in such policies from those disclosed in our annual consolidated financial statements and accompanying notes included in our 2022 Form 10-K for the year ended December 31, 2022. We monitor our estimates on an ongoing basis for changes in facts and circumstances, and material changes in these estimates could occur in the future. Changes in estimates are recorded in the period in which they become known. We base our estimates on historical experience and other assumptions that we believe to be reasonable under the circumstances. Actual results may differ from our estimates if past experience or other assumptions do not turn out to be substantially accurate.

 

Recent Accounting Pronouncements

 

A discussion of Recent Accounting Pronouncements is included in our 2022 Form 10-K for the fiscal year ended December 31, 2022 and is updated in the Notes to the condensed consolidated financial statements included in this report.

 

Contractual Obligations and Other Commercial Commitments

 

Our contractual obligations and other commercial commitments are summarized in the section captioned “Part II, Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations—Liquidity and Capital Resources—Contractual Obligations and Other Commercial Commitments” in our 2022 Form 10-K for the year ended December 31, 2022. There were no material changes to our contractual obligations reported in our 2022 Form 10-K during the three months ended March 31, 2023. For additional discussion, see Note 9 to the condensed consolidated financial statements included in this report.

 

To the extent that funds generated from our operations, together with our existing capital resources, are insufficient to meet future requirements, we will be required to obtain additional funds through equity or debt financings, strategic alliances with corporate partners and others, or through other sources. No assurance can be given that any additional financing will be made available to us or will be available on acceptable terms should such a need arise.

 

24

 

ITEM 3.

QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

 

Our market risks and the ways we manage them are summarized in the section captioned “Part II, Item 7A. Quantitative and Qualitative Disclosures About Market Risk” in our Annual Report on Form 10-K for the year ended December 31, 2022. There have been no material changes in the first three months of 2023 to our market risks or to our management of such risks.

 

ITEM 4.

CONTROLS AND PROCEDURES

 

(a) Evaluation of disclosure controls and procedures.

 

Under the supervision and with the participation of our management, including our chief executive officer and chief financial officer, we have evaluated the effectiveness of the design and operation of our disclosure controls and procedures as defined by Rules 13a-15(e) and 15d-15(e) of the Securities Exchange Act of 1934, as amended, as of the end of the period covered by this report. Based upon that evaluation, the chief executive officer and chief financial officer have concluded as of March 31, 2023 that our disclosure controls and procedures were not effective because of the material weaknesses in our internal control over financial reporting that were disclosed in our Annual Report on Form 10-K for the year ended December 31, 2022 (the “2022 Form 10-K”).

 

(b) Changes in internal controls over financial reporting.

 

Except for the material weaknesses discussed in Part II, Item 9A of the 2022 Form 10-K, there were no material changes in our internal control over financial reporting during the quarter ended March 31, 2023, that have materially affected, or were reasonably likely to materially affect, our internal control over financial reporting.

 

We are in the process of remediating the material weaknesses in our internal control over financial reporting as noted in Part II, Item 9A of the 2022 Form 10-K. We have undertaken a number of measures designed to directly address, or contribute to, the remediation of our material weaknesses and the enhancement of our internal control over financial reporting including establishment of additional review procedures and monitoring activities at a centralized level in order to verify that process level controls are present and functioning as designed. In addition, we have begun training finance personnel on internal control over financial reporting, the importance of monitoring control activities, and fraud risk assessment. The material weaknesses will not be considered remediated until the applicable remedial controls operate for a sufficient period of time and management has concluded, through testing, that these controls are operating effectively.

 

PART II:

OTHER INFORMATION

 

ITEM 1.

LEGAL PROCEEDINGS

 

We are involved from time-to-time in various legal proceedings arising in the normal course of business. Although the outcomes of these legal proceedings are inherently difficult to predict, we do not expect the resolution of these occasional legal proceedings to have a material adverse effect on our financial position, results of operations, or cash flow. There have been no material changes to the information provided in the section captioned “Part I, Item 3. Legal Proceedings” in our Annual Report on Form 10-K for the year ended December 31, 2022.

 

ITEM 1A.

RISK FACTORS

 

Except as set forth below, there have been no material changes to the risk factors described in the section captioned “Part I, Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2022. In addition to the other information set forth in this report, you should carefully consider the factors discussed in the section captioned “Part I, Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2022, which could materially affect our business, financial condition, or future results. The risks described in our Annual Report on Form 10-K are not the only risks we face. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial also may have a material adverse effect on our business, financial condition, and/or operating results.

 

25

 

We have been, and may continue to be, subject to the actions of activist stockholders, which could cause us to incur substantial costs, divert managements and the boards attention and resources, and have an adverse effect on our business and stock price.

 

From time to time, we may be subject to proposals by activist stockholders urging us to take certain corporate actions or to nominate certain individuals to our board of directors. For example, we received a notice from Caligan Partners LP, or Caligan, of its intent to nominate two directors for election to the board of directors at our 2023 annual meeting of stockholders. We subsequently entered into a cooperation agreement with Caligan on April 13, 2023 and pursuant to the cooperation agreement, Caligan withdrew its director nominations. If activist stockholder activities, such as those by Caligan or other stockholders, ensue, our business could be adversely affected, as responding to proxy contests and reacting to other actions by activist stockholders can be costly and time-consuming, disrupt our operations and divert the attention of management and our board of directors. For example, we retained, and may be required to retain in the future, the services of various professionals to advise us on activist stockholder matters, including legal, financial, and communications advisors, the costs of which negatively impact our financial results. In addition, perceived uncertainties as to our future direction, strategy or leadership created as a consequence of activist stockholder initiatives may result in the loss of potential business opportunities, harm our ability to attract new investors, customers, and employees, and cause our stock price to experience periods of volatility or stagnation.

 

ITEM 2.

UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

 

Issuer Purchases of Equity Securities

 

On May 2, 2019, we announced that our board of directors approved a $50.0 million share repurchase program with $30.0 million tobe utilized for an accelerated share repurchase program, which was completed in January 2020, and $20.0 million reserved for open market repurchases which represents the maximum value of shares that may yet be purchased. No open market repurchases were made during the three-month period ended March 31, 2023, and this repurchase program was canceled in April 2023.

 

On April 13, 2023, we announced the establishment of a share repurchase program for an aggregate purchase price equal to $20,000,000 to occur within twelve months from the date of the share repurchase program as follows: (i) the first $5,000,000 of which will be effected through an accelerated stock repurchase program with an investment bank commencing with the Company’s next open trading window, which will open on or before May 12, 2023, (ii) the second $5,000,000 of which to be purchased in the open market, and (iii) the remaining $10,000,000 of which to be purchased in the open market subject to positive cash flow.  This share repurchase program replaces the program that was announced in May 2019.

 

 

 

 

 

 

 

 

 

26

 

ITEM 6.

EXHIBITS

 

Exhibit No.

Description

 

 

3.1

Certificate of Incorporation of Anika Therapeutics, Inc. (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K (File No. 001-14027) filed by the Registrant on June 6, 2018)

 

 

3.2

Bylaws of Anika Therapeutics, Inc., effective as of June 6, 2018 (incorporated by reference to Exhibit 3.2 to the Current Report on Form 8-K (File No. 001-14027) filed by the Registrant on June 6, 2018)

 

 

(31)

Rule 13a-14(a)/15d-14(a) Certifications

 

 

*31.1

Certification of Dr. Cheryl R. Blanchard, pursuant to Rules 13a-15(e) and 15d-15(e), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

 

 

*31.2

Certification of Michael Levitz, pursuant to Rules 13a-15(e) and 15d-15(e), as adopted pursuant to Section 302 of the Sarbanes-Oxley Actof 2002.

 

 

(32)

Section 1350 Certifications

 

 

**32.1

Certification of Dr. Cheryl R. Blanchard, and Michael Levitz, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

 

 

(101)

XBRL

 

 

*101

The following materials from Anika Therapeutics, Inc.’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2023 as filed with the SEC on May 9, 2023, formatted in Inline XBRL (eXtensible Business Reporting Language), as follows:

 

 

i.

Condensed Consolidated Balance Sheets as of March 31, 2023 (unaudited) and December 31, 2022 (unaudited)

 

 

ii.

Condensed Consolidated Statements of Operations and Comprehensive Income for the Three Months Ended March 31, 2023 and March 31, 2022 (unaudited)

 

 

iii.

Condensed Consolidated Statements of Stockholders’ Equity for the Three Months Ended March 31, 2023 and March 31, 2022 (unaudited)

 

 

iv.

Condensed Consolidated Statements of Cash Flows for the Three Months Ended March 31, 2023 and March 31, 2022 (unaudited)

 

 

v.

Notes to Condensed Consolidated Financial Statements (unaudited)

 

104

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

 

*

Filed herewith.

**

Furnished herewith.

 

 

27

 

SIGNATURES

 

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

 

   

ANIKA THERAPEUTICS, INC.

 
   

(Registrant)

 
       

Date: May 9, 2023

By:

/s/ MICHAEL LEVITZ  
   

Michael Levitz

 
   

Executive Vice President, Chief Financial Officer and Treasurer

   

(Authorized Officer and Principal Financial Officer)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

28