Item 1. Financial Statements
Item 1. Financial Statements
ACLARIS THERAPEUTICS, IN C.
CONDENSED CONSOLIDATED BALANCE SHEET S
(Unaudited)
(In thousands, except share and per share data)
September 30,
December 31,
2021
2020
Assets
Current assets:
Cash and cash equivalents
$
53,602
$
22,063
Short-term marketable securities
144,280
32,068
Accounts receivable, net
811
772
Prepaid expenses and other current assets
7,089
2,590
Total current assets
205,782
57,493
Marketable securities
45,735
—
Property and equipment, net
1,170
1,654
Intangible assets
7,067
7,123
Other assets
3,740
4,514
Total assets
$
263,494
$
70,784
Liabilities and Stockholders’ Equity
Current liabilities:
Accounts payable
$
7,564
$
5,254
Accrued expenses
7,408
5,906
Current portion of lease liabilities
669
603
Discontinued operations - current liabilities
2,198
3,111
Total current liabilities
17,839
14,874
Other liabilities
2,507
3,179
Long-term debt, net
—
10,653
Contingent consideration
26,200
4,061
Deferred tax liability
367
367
Total liabilities
46,913
33,134
Commitments and contingencies (Note 17)
Stockholders’ Equity:
Preferred stock, $ 0.00001 par value; 10,000,000 shares authorized and no shares issued or outstanding at September 30, 2021 and December 31, 2020
—
—
Common stock, $ 0.00001 par value; 100,000,000 shares authorized at September 30, 2021 and December 31, 2020; 61,226,750 and 45,109,314 shares issued and outstanding at September 30, 2021 and December 31, 2020, respectively
1
—
Additional paid‑in capital
789,186
542,286
Accumulated other comprehensive loss
( 3 )
( 94 )
Accumulated deficit
( 572,603 )
( 504,542 )
Total stockholders’ equity
216,581
37,650
Total liabilities and stockholders’ equity
$
263,494
$
70,784
The accompanying notes are an integral part of these condensed consolidated financial statements.
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ACLARIS THERAPEUTICS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(Unaudited)
(In thousands, except share and per share data)
Three Months Ended
Nine Months Ended
September 30,
September 30,
2021
2020
2021
2020
Revenues:
Contract research
$
1,415
$
1,331
$
4,556
$
4,373
Other revenue
244
118
704
529
Total revenue
1,659
1,449
5,260
4,902
Costs and expenses:
Cost of revenue
1,099
1,189
3,564
3,847
Research and development
13,976
6,240
29,711
20,382
General and administrative
5,979
3,859
16,676
15,632
Revaluation of contingent consideration
900
626
22,139
2,393
Total costs and expenses
21,954
11,914
72,090
42,254
Loss from operations
( 20,295 )
( 10,465 )
( 66,830 )
( 37,352 )
Other expense, net
( 851 )
( 194 )
( 1,231 )
( 205 )
Loss from continuing operations
( 21,146 )
( 10,659 )
( 68,061 )
( 37,557 )
Loss from discontinued operations
—
—
—
( 285 )
Net loss
$
( 21,146 )
$
( 10,659 )
$
( 68,061 )
$
( 37,842 )
Net loss per share, basic and diluted
$
( 0.35 )
$
( 0.25 )
$
( 1.23 )
$
( 0.90 )
Weighted average common shares outstanding, basic and diluted
61,219,321
42,802,582
55,215,037
42,187,140
Other comprehensive income (loss):
Unrealized gain (loss) on marketable securities, net of tax of $ 0
$
5
$
( 24 )
$
( 5 )
$
( 1 )
Foreign currency translation adjustment
176
( 36 )
96
22
Total other comprehensive income (loss)
181
( 60 )
91
21
Comprehensive loss
$
( 20,965 )
$
( 10,719 )
$
( 67,970 )
$
( 37,821 )
The accompanying notes are an integral part of these condensed consolidated financial statements.
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ACLARIS THERAPEUTICS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF
STOCKHOLDERS’ EQUITY
(Unaudited)
(In thousands, except share data)
Accumulated
Common Stock
Additional
Other
Total
Par
Paid ‑ in
Comprehensive
Accumulated
Stockholders’
Shares
Value
Capital
Loss
Deficit
Equity
Balance at December 31, 2020
45,109,314
$
—
$
542,286
$
( 94 )
$
( 504,542 )
$
37,650
Issuance of common stock in connection with exercise of stock options and warrants and vesting of restricted stock units
666,144
—
( 2,579 )
—
—
( 2,579 )
Issuance of common stock in connection with public offering, net of offering costs of $ 7,011
6,306,271
—
103,348
—
—
103,348
Unrealized loss on marketable securities
—
—
—
( 35 )
—
( 35 )
Foreign currency translation adjustment
—
—
—
( 11 )
—
( 11 )
Stock-based compensation expense
—
—
2,675
—
—
2,675
Net loss
—
—
—
—
( 28,754 )
( 28,754 )
Balance at March 31, 2021
52,081,729
$
—
$
645,730
$
( 140 )
$
( 533,296 )
$
112,294
Issuance of common stock in connection with exercise of stock options and vesting of restricted stock units
1,024,666
—
1,041
—
—
1,041
Issuance of common stock in connection with public offering, net of offering costs of $ 8,899
8,098,592
1
134,851
—
—
134,852
Unrealized gain on marketable securities
—
—
—
25
—
25
Foreign currency translation adjustment
—
—
—
( 69 )
—
( 69 )
Stock-based compensation expense
—
—
3,833
—
—
3,833
Net loss
—
—
—
—
( 18,161 )
( 18,161 )
Balance at June 30, 2021
61,204,987
$
1
$
785,455
$
( 184 )
$
( 551,457 )
$
233,815
Issuance of common stock in connection with vesting of restricted stock units
21,763
—
29
—
—
29
Unrealized gain on marketable securities
—
—
—
5
—
5
Foreign currency translation adjustment
—
—
—
176
—
176
Stock-based compensation expense
—
—
3,702
—
—
3,702
Net loss
—
—
—
—
( 21,146 )
( 21,146 )
Balance at September 30, 2021
61,226,750
$
1
$
789,186
$
( 3 )
$
( 572,603 )
$
216,581
Accumulated
Common Stock
Additional
Other
Total
Par
Paid ‑ in
Comprehensive
Accumulated
Stockholders’
Shares
Value
Capital
Income (Loss)
Deficit
Equity
Balance at December 31, 2019
41,485,638
$
—
$
523,505
$
( 66 )
$
( 453,527 )
$
69,912
Issuance of common stock in connection with vesting of restricted stock units
346,582
—
( 121 )
—
—
( 121 )
Fair value of warrants issued
—
—
378
—
—
378
Unrealized gain on marketable securities
—
—
—
60
—
60
Foreign currency translation adjustment
—
—
—
53
—
53
Stock-based compensation expense
—
—
3,453
—
—
3,453
Net loss
—
—
—
—
( 15,586 )
( 15,586 )
Balance at March 31, 2020
41,832,220
$
—
$
527,215
$
47
$
( 469,113 )
$
58,149
Issuance of common stock in connection with vesting of restricted stock units
858,894
—
( 463 )
—
—
( 463 )
Unrealized loss on marketable securities
—
—
—
( 37 )
—
( 37 )
Foreign currency translation adjustment
—
—
—
5
—
5
Stock-based compensation expense
—
—
3,309
—
—
3,309
Net loss
—
—
—
—
( 11,597 )
( 11,597 )
Balance at June 30, 2020
42,691,114
$
—
$
530,061
$
15
$
( 480,710 )
$
49,366
Issuance of common stock in connection with vesting of restricted stock units
103,689
—
( 95 )
—
—
( 95 )
Issuance of common stock in connection with equity purchase agreement
121,584
—
263
—
—
263
Unrealized loss on marketable securities
—
—
—
( 24 )
—
( 24 )
Foreign currency translation adjustment
—
—
—
( 35 )
—
( 35 )
Stock-based compensation expense
—
—
1,941
—
—
1,941
Net loss
—
—
—
—
( 10,659 )
( 10,659 )
Balance at September 30, 2020
42,916,387
$
—
$
532,170
$
( 44 )
$
( 491,369 )
$
40,757
The accompanying notes are an integral part of these condensed consolidated financial statements.
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ACLARIS THERAPEUTICS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited)
(In thousands)
Nine Months Ended
September 30,
2021
2020
Cash flows from operating activities :
Net loss
$
( 68,061 )
$
( 37,842 )
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
726
1,773
Stock-based compensation expense
10,209
8,703
Revaluation of contingent consideration
22,139
2,393
Loss on extinguishment of debt
752
—
Changes in operating assets and liabilities:
Accounts receivable
( 39 )
4,783
Prepaid expenses and other assets
( 8 )
1,303
Accounts payable
1,293
( 5,448 )
Accrued expenses
( 2,070 )
( 5,441 )
Net cash used in operating activities
( 35,059 )
( 29,776 )
Cash flows from investing activities:
Purchases of property and equipment
( 108 )
( 445 )
Purchases of marketable securities
( 199,862 )
( 39,898 )
Proceeds from sales and maturities of marketable securities
41,514
49,035
Net cash provided by (used in) investing activities
( 158,456 )
8,692
Cash flows from financing activities:
Proceeds from issuance of common stock in connection with public offerings, net of issuance costs
238,200
—
Proceeds from debt financing (including warrants), net of issuance costs
—
10,913
Repayment of debt
( 11,483 )
—
Restricted stock unit employee tax withholdings
( 3,122 )
—
Finance lease payments
—
( 128 )
Deferred issuance costs
—
( 242 )
Proceeds from exercise of employee stock options and the issuance of stock
1,459
—
Net cash provided by financing activities
225,054
10,543
Net increase (decrease) in cash, cash equivalents and restricted cash
31,539
( 10,541 )
Cash, cash equivalents and restricted cash at beginning of period
22,063
35,937
Cash, cash equivalents and restricted cash at end of period
$
53,602
$
25,396
Supplemental disclosure of non-cash investing and financing activities:
Fair value of warrants issued in connection with debt financing
$
—
$
378
Fair value of common stock issued in connection with an equity purchase agreement
$
—
$
263
The accompanying notes are an integral part of these condensed consolidated financial statements.
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ACLARIS THERAPEUTICS, INC.
NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
1. Organization and Nature of Business
Overview
Aclaris Therapeutics, Inc. was incorporated under the laws of the State of Delaware in 2012. In July 2015, Aclaris Therapeutics International Limited (“ATIL”) was established under the laws of the United Kingdom as a wholly-owned subsidiary of Aclaris Therapeutics, Inc. In August 2017, Confluence Life Sciences, Inc. (now known as Aclaris Life Sciences, Inc.) (“Confluence”) was acquired by Aclaris Therapeutics, Inc. and became a wholly-owned subsidiary thereof. Aclaris Therapeutics, Inc., ATIL and Confluence are referred to collectively as the “Company.” The Company is a clinical-stage biopharmaceutical company focused on developing novel drug candidates for immuno-inflammatory diseases. In addition to developing its novel drug candidates, the Company is pursuing strategic alternatives, including identifying and consummating transactions with third-party partners, to further develop, obtain marketing approval for and/or commercialize its novel drug candidates.
Liquidity
The Company’s condensed consolidated financial statements have been prepared on the basis of continuity of operations, realization of assets and the satisfaction of liabilities in the ordinary course of business. As of September 30, 2021, the Company had cash, cash equivalents and marketable securities of $ 243.6 million and an accumulated deficit of $ 572.6 million. Since inception, the Company has incurred net losses and negative cash flows from its operations. Prior to the acquisition of Confluence in August 2017, the Company had never generated revenue. There can be no assurance that profitable operations will ever be achieved, and, if achieved, will be sustained on a continuing basis. In addition, development activities, including clinical and preclinical testing of the Company’s drug candidates, will require significant additional financing. The future viability of the Company is dependent on its ability to successfully develop its drug candidates and to generate revenue from identifying and consummating transactions with third-party partners to further develop, obtain marketing approval for and/or commercialize its development assets or to raise additional capital to finance its operations. The Company will require additional capital to complete the clinical development of zunsemetinib (ATI-450) and ATI-1777, to develop its preclinical compounds, and to support its discovery efforts.
Additional funds may not be available on a timely basis, on commercially acceptable terms, or at all, and such funds, if raised, may not be sufficient to enable the Company to continue to implement its long-term business strategy. The Company’s ability to raise additional capital may be adversely impacted by potential worsening global economic conditions and the recent disruptions to, and volatility in, the credit and financial markets in the United States and worldwide resulting from the ongoing COVID-19 pandemic. If the Company is unable to raise sufficient additional capital or generate revenue from transactions with potential third-party partners for the development and/or commercialization of its drug candidates, it may need to substantially curtail planned operations. The Company’s failure to raise capital as and when needed could have a negative impact on its financial condition and ability to pursue its business strategies.
In accordance with Accounting Standards Update (“ASU”) 2014-15, Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern (Subtopic 205-40), the Company evaluated whether there are conditions and events, considered in the aggregate, that raise substantial doubt about the Company’s ability to continue as a going concern within one year after the date that its condensed consolidated financial statements are issued. As of the report date, the Company does not believe that substantial doubt exists about its ability to continue as a going concern. The Company believes its existing cash, cash equivalents and marketable securities are sufficient to fund its operating and capital expenditure requirements for a period greater than 12 months from the date of issuance of these condensed consolidated financial statements.
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2. Summary of Significant Accounting Policies
Unaudited Interim Financial Information
The accompanying condensed consolidated balance sheet as of September 30, 2021, the condensed consolidated statements of operations and comprehensive loss for the three and nine months ended September 30, 2021 and 2020, the condensed consolidated statement of stockholders’ equity for the three and nine months ended September 30, 2021 and 2020, and the condensed consolidated statements of cash flows for the nine months ended September 30, 2021 and 2020 are unaudited. The unaudited interim condensed consolidated financial statements have been prepared on the same basis as the audited annual financial statements contained in the Company’s annual report on Form 10-K filed with the Securities and Exchange Commission (“SEC”) on February 25, 2021 and, in the opinion of management, reflect all adjustments, which include only normal recurring adjustments necessary for the fair statement of the Company’s financial position as of September 30, 2021, the results of its operations and comprehensive loss for the three and nine months ended September 30, 2021 and 2020, its changes in stockholders’ equity for the three and nine months ended September 30, 2021 and 2020 and its cash flows for the nine months ended September 30, 2021 and 2020. The condensed consolidated balance sheet data as of December 31, 2020 was derived from audited financial statements but does not include all disclosures required by generally accepted accounting principles in the United States (“GAAP”). The financial data and other information disclosed in these notes related to the three and nine months ended September 30, 2021 and 2020 are unaudited. The results for the three and nine months ended September 30, 2021 are not necessarily indicative of results to be expected for the year ending December 31, 2021, any other interim periods, or any future year or period. The unaudited interim financial statements of the Company included herein have been prepared, pursuant to the rules and regulations of the SEC. Certain information and footnote disclosures normally included in financial statements prepared in accordance with GAAP have been condensed or omitted from this report, as is permitted by such rules and regulations. These unaudited condensed consolidated financial statements should be read in conjunction with the audited consolidated financial statements and the notes thereto for the year ended December 31, 2020 included in the Company’s annual report on Form 10-K filed with the SEC on February 25, 2021.
Basis of Presentation
The accompanying condensed consolidated financial statements have been prepared in conformity with GAAP. The condensed consolidated financial statements of the Company include the accounts of the operating parent company, Aclaris Therapeutics, Inc., and its wholly-owned subsidiaries, ATIL and Confluence. All intercompany transactions have been eliminated. Based upon the Company’s revenue, the Company believes that gross profit does not provide a meaningful measure of profitability and, therefore, has not included a line item for gross profit on the condensed consolidated statement of operations.
Use of Estimates
The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting periods. Significant estimates and assumptions reflected in these financial statements include, but are not limited to, research and development expenses, contingent consideration and the valuation of stock-based awards. Estimates are periodically reviewed in light of changes in circumstances, facts and experience. The COVID-19 pandemic has resulted in a global slowdown in economic activity. As of the date of issuance of these financial statements, the Company is not aware of any specific event or circumstance that would require an update to its estimates, assumptions and judgments or revise the carrying value of its assets or liabilities. Actual results could differ from the Company’s estimates.
Reclassifications
Certain prior year amounts have been reclassified to conform to the current year financial statement presentation.
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Significant Accounting Policies
The Company’s significant accounting policies are disclosed in the audited consolidated financial statements for the year ended December 31, 2020 included in the Company’s annual report on Form 10-K filed with the SEC on February 25, 2021. Except as set forth below, there have been no changes to the Company’s significant accounting policies from those disclosed in the annual report.
Contingent Consideration
The Company initially recorded a contingent consideration liability at fair value on the date of acquisition related to future potential payments resulting from the acquisition of Confluence based upon significant unobservable inputs including the achievement of development, regulatory and commercial milestones, as well as estimated future sales levels and the discount rates applied to calculate the present value of the potential payments. Significant judgement was involved in determining the appropriateness of these assumptions. These assumptions are considered Level 3 inputs. Revaluation of the contingent consideration liability can result from changes to one or more of these assumptions. The Company evaluates the fair value estimate of the contingent consideration liability on a quarterly basis with changes, if any, recorded as income or expense in the condensed consolidated statement of operations.
The fair value of contingent consideration is estimated using a probability-weighted expected payment model for regulatory milestone payments and a Monte Carlo simulation model for commercial milestone and royalty payments and then applying a risk-adjusted discount rate to calculate the present value of the potential payments. Significant assumptions used in the Company’s estimates include the probability of achieving regulatory milestones and commencing commercialization, which are based on an asset’s current stage of development and a review of existing clinical data. Probability of success assumptions ranged between 4 % and 40 %. Additionally, estimated future sales levels and the risk-adjusted discount rate applied to the potential payments are also significant assumptions used in calculating the fair value. The discount rate ranged between 5.9 % and 7.8 % depending on the year of each potential payment.
3. Fair Value of Financial Assets and Liabilities
The following tables present information about the fair value measurements of the Company’s financial assets and liabilities which are measured at fair value on a recurring and non-recurring basis, and indicate the level of the fair value hierarchy utilized to determine such fair values:
September 30, 2021
(In thousands)
Level 1
Level 2
Level 3
Total
Assets:
Cash equivalents
$
50,631
$
—
$
—
$
50,631
Marketable securities
—
190,015
—
190,015
Total assets
$
50,631
$
190,015
$
—
$
240,646
Liabilities:
Contingent consideration
$
—
$
—
$
26,200
$
26,200
Total liabilities
$
—
$
—
$
26,200
$
26,200
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December 31, 2020
(In thousands)
Level 1
Level 2
Level 3
Total
Assets:
Cash equivalents
$
14,955
$
1,500
$
—
$
16,455
Marketable securities
—
32,068
—
32,068
Total assets
$
14,955
$
33,568
$
—
$
48,523
Liabilities:
Contingent consideration
$
—
$
—
$
4,061
$
4,061
Total liabilities
$
—
$
—
$
4,061
$
4,061
As of September 30, 2021 and December 31, 2020, the Company’s cash equivalents consisted of a money market fund, which was valued based upon Level 1 inputs. The Company’s cash equivalents as of December 31, 2020 also included commercial paper, which was valued based upon Level 2 inputs. The Company’s marketable securities as of September 30, 2021 and December 31, 2020 consisted of commercial paper and asset-backed and U.S. government agency debt securities, which were valued based upon Level 2 inputs. The Company’s marketable securities as of September 30, 2021 also included corporate debt securities and foreign government agency debt securities, which were valued based upon Level 2 inputs.
In determining the fair value of its Level 2 investments, the Company relied on quoted prices for identical securities in markets that are not active. These quoted prices were obtained by the Company with the assistance of a third-party pricing service based on available trade, bid and other observable market data for identical securities. Quarterly, the Company compares the quoted prices obtained from the third-party pricing service to other available independent pricing information to validate the reasonableness of the quoted prices provided. The Company evaluates whether adjustments to third-party pricing are necessary and, historically, the Company has not made adjustments to quoted prices obtained from the third-party pricing service. During the nine months ended September 30, 2021 and 2020, there were no transfers between Level 1, Level 2 and Level 3.
The increase in contingent consideration of $ 22.1 million during the nine months ended September 30, 2021 resulted from updates to the Company’s probability of achieving regulatory milestones and commencing commercialization and estimated future sales level assumptions as a result of the completion of a Phase 2a clinical trial of zunsemetinib in subjects with moderate to severe rheumatoid arthritis and the inclusion of estimated future sales of zunsemetinib for the potential treatment of psoriatic arthritis and moderate to severe hidradenitis suppurativa, which are additional planned indications for zunsemetinib, as well as a result of the completion of a Phase 2a clinical trial of ATI-1777 in subjects with moderate to severe atopic dermatitis.
As of September 30, 2021 and December 31, 2020, the fair value of the Company’s available for sale marketable securities by type of security was as follows:
September 30, 2021
Gross
Gross
Amortized
Unrealized
Unrealized
Fair
(In thousands)
Cost
Gain
Loss
Value
Marketable securities:
Corporate debt securities
$
36,725
$
3
( 10 )
$
36,718
Commercial paper
81,828
—
—
81,828
Asset-backed debt securities
37,229
3
( 7 )
37,225
Foreign government agency debt securities
4,112
—
( 2 )
4,110
U.S. government agency debt securities
30,124
10
—
30,134
Total marketable securities
$
190,018
$
16
$
( 19 )
$
190,015
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December 31, 2020
Gross
Gross
Amortized
Unrealized
Unrealized
Fair
(In thousands)
Cost
Gain
Loss
Value
Marketable securities:
Commercial paper
$
20,483
$
—
$
—
$
20,483
Asset-backed debt securities
4,036
1
—
4,037
U.S. government agency debt securities
7,547
1
—
7,548
Total marketable securities
$
32,066
$
2
$
—
$
32,068
4. Property and Equipment, Net
Property and equipment, net consisted of the following:
September 30,
December 31,
(In thousands)
2021
2020
Computer equipment
$
1,253
$
1,197
Lab equipment
1,389
1,340
Furniture and fixtures
620
617
Leasehold improvements
1,123
1,123
Property and equipment, gross
4,385
4,277
Accumulated depreciation
( 3,215 )
( 2,623 )
Property and equipment, net
$
1,170
$
1,654
Depreciation expense was $ 0.2 million and $ 0.3 million for the three months ended September 30, 2021 and 2020, respectively, and $ 0.6 million and $ 0.9 million for the nine months ended September 30, 2021 and 2020, respectively.
5. Intangible Assets
Intangible assets consisted of the following:
Gross Cost
Accumulated Amortization
Remaining
September 30,
December 31,
September 30,
December 31,
(In thousands, except years)
Life (years)
2021
2020
2021
2020
Other intangible assets
5.8
$
751
$
751
$
313
$
257
In-process research and development
n/a
6,629
6,629
—
—
Total intangible assets
$
7,380
$
7,380
$
313
$
257
As of September 30, 2021, estimated future amortization expense was as follows:
Year Ending
(In thousands)
December 31,
2021
$
18
2022
75
2023
75
2024
75
2025
75
Thereafter
120
Total
$
438
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6. Accrued Expenses
Accrued expenses consisted of the following:
September 30,
December 31,
(In thousands)
2021
2020
Employee compensation expenses
$
2,845
$
3,971
Research and development expenses
882
761
Litigation settlements (see Note 17)
3,075
—
Other
606
1,174
Total accrued expenses
$
7,408
$
5,906
7. Debt
Loan and Security Agreement – Silicon Valley Bank
In March 2020, the Company entered into a Loan and Security Agreement with Silicon Valley Bank (“SVB”). The Loan and Security Agreement provided for $ 11.0 million in term loans, of which the Company borrowed the entire amount on March 30, 2020. In connection with the Loan and Security Agreement, the Company issued to SVB a warrant to purchase up to 460,251 shares of common stock (the “Warrant”) (see Note 8). The proceeds of the Loan and Security Agreement were allocated to the term loan and Warrant using a relative fair value approach.
In July 2021, the Company repaid in full the $ 11.0 million that was outstanding under the Loan and Security Agreement, together with all accrued and unpaid interest and fees as of the payoff date, for a total payment of $ 11.7 million. Following this repayment, all of the Company’s obligations under the Loan and Security Agreement are deemed to be terminated, except as set forth in the agreement.
8. Stockholders’ Equity
Preferred Stock
As of September 30, 2021 and December 31, 2020, the Company’s amended and restated certificate of incorporation authorized the Company to issue 10,000,000 shares of undesignated preferred stock. There were no shares of preferred stock outstanding as of September 30, 2021 or December 31, 2020.
Common Stock
As of September 30, 2021 and December 31, 2020, the Company’s amended and restated certificate of incorporation authorized the Company to issue 100,000,000 shares of $ 0.00001 par value common stock.
Each share of common stock entitles the holder to one vote on all matters submitted to a vote of the Company’s stockholders. Common stockholders are entitled to receive dividends, as may be declared by the board of directors, if any, subject to any preferential dividend rights of any series of preferred stock that may be outstanding. No dividends have been declared through September 30, 2021.
Warrants
The Warrant issued to SVB in March 2020 had an initial exercise price of $ 0.956 per share, subject to adjustment as provided in the Warrant. The Warrant became immediately exercisable in full upon the funding of the term loan facility. The Company assigned a fair value of $ 0.4 million to the Warrant using a Black-Scholes valuation methodology, and also concluded that the Warrant was indexed to its own stock and therefore classified the Warrant as an equity instrument. In January 2021, SVB net exercised the Warrant in full, and the Company issued to SVB 388,119 shares of common stock.
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Equity Purchase Agreement with Lincoln Park Capital Fund, LLC
In August 2020, the Company entered into an equity purchase agreement (the “Purchase Agreement”) with Lincoln Park Capital Fund, LLC (“Lincoln Park”) which provided that, upon the terms and subject to the conditions and limitations set forth therein, the Company could sell to Lincoln Park, at its discretion, up to $ 15.0 million of shares of its common stock over the 36-month term of the Purchase Agreement. U pon execution of the Purchase Agreement, the Company issued 121,584 shares of its common stock to Lincoln Park as commitment shares in accordance with the closing conditions contained within the Purchase Agreement. The commitment shares were valued using the closing price of the Company’s common stock on the effective date of the Purchase Agreement resulting in an aggregate fair value of $ 0.3 million. Through December 31, 2020, the Company sold 2,111,170 shares of its common stock to Lincoln Park under the Purchase Agreement for net proceeds of $ 7.7 million. The Company terminated the Purchase Agreement in January 2021 in connection with the public offering of common stock described below. The Company did not sell any additional shares prior to terminating the Purchase Agreement.
January 2021 Public Offering
In January 2021, the Company closed a public offering in which it sold 6,306,271 shares of common stock at a price to the public of $ 17.50 per share, for aggregate gross proceeds of $ 110.4 million. The Company paid underwriting discounts and commissions of $ 6.6 million, and also incurred expenses of $ 0.4 million in connection with the offering. As a result, the net offering proceeds received by the Company, after deducting underwriting discounts, commissions and offering expenses, were $ 103.3 million.
June 2021 Public Offering
In June 2021, the Company closed a public offering in which it sold 8,098,592 shares of common stock at a price to the public of $ 17.75 per share, for aggregate gross proceeds of $ 143.8 million. The Company paid underwriting discounts and commissions of $ 8.6 million, and also incurred expenses of $ 0.3 million in connection with the offering. As a result, the net offering proceeds received by the Company, after deducting underwriting discounts, commissions and offering expenses, were $ 134.9 million.
9. Stock-Based Awards
2015 Equity Incentive Plan
In September 2015, the Company’s board of directors adopted the 2015 Equity Incentive Plan (the “2015 Plan”), and the Company’s stockholders approved the 2015 Plan. The 2015 Plan became effective in connection with the Company’s initial public offering in October 2015. Beginning at the time the 2015 Plan became effective, no further grants may be made under the Company’s 2012 Equity Compensation Plan, as amended and restated (the “2012 Plan”). The 2015 Plan provides for the grant of incentive stock options, nonqualified stock options, stock appreciation rights, restricted stock awards, restricted stock unit (“RSU”) awards, performance stock awards, cash-based awards and other stock-based awards. The number of shares initially reserved for issuance under the 2015 Plan was 1,643,872 shares of common stock. The number of shares of common stock that may be issued under the 2015 Plan will automatically increase on January 1 of each year ending on January 1, 2025, in an amount equal to the lesser of (i) 4.0 % of the shares of the Company’s common stock outstanding on December 31st of the preceding calendar year or (ii) an amount determined by the Company’s board of directors. The shares of common stock underlying any awards that expire, are otherwise terminated, settled in cash or repurchased by the Company under the 2015 Plan and the 2012 Plan will be added back to the shares of common stock available for issuance under the 2015 Plan. As of January 1, 2021, the number of shares of common stock that may be issued under the 2015 Plan was increased by 1,804,372 shares. As of September 30, 2021, 2,795,696 shares remained available for grant under the 2015 Plan. The Company had 2,843,205 stock options and 1,458,483 RSUs outstanding as of September 30, 2021 under the 2015 Plan.
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2017 Inducement Plan
In July 2017, the Company’s board of directors adopted the 2017 Inducement Plan (the “2017 Inducement Plan”). The 2017 Inducement Plan is a non-stockholder approved stock plan adopted pursuant to the “inducement exception” provided under Nasdaq listing rules. The Company had 416,375 stock options and 7,480 RSUs outstanding as of September 30, 2021 under the 2017 Inducement Plan. All shares of common stock that were eligible for issuance under the 2017 Inducement Plan after October 1, 2018, including any shares underlying any awards that expire or are otherwise terminated, reacquired to satisfy tax withholding obligations, settled in cash or repurchased by the Company in the future that would have been eligible for re-issuance under the 2017 Inducement Plan, were retired.
2012 Equity Compensation Plan
Upon the 2015 Plan becoming effective, no further grants can be made under the 2012 Plan. The Company granted stock options to purchase a total of 1,140,524 shares under the 2012 Plan, of which 484,145 were outstanding as of September 30, 2021. Stock options granted under the 2012 Plan expire after ten years .
Stock Option Valuation
The weighted average assumptions the Company used to estimate the fair value of stock options granted during the nine months ended September 30, 2021 and 2020 were as follows:
Nine Months Ended
September 30,
2021
2020
Risk-free interest rate
0.90
%
0.87
%
Expected term (in years)
6.2
6.1
Expected volatility
76.60
%
85.19
%
Expected dividend yield
0
%
0
%
The Company recognizes compensation expense for awards over their vesting period. Compensation expense for awards includes the impact of forfeitures in the period when they occur.
Stock Options
The following table summarizes stock option activity for the nine months ended September 30, 2021:
Weighted
Weighted
Average
Average
Remaining
Aggregate
Number
Exercise
Contractual
Intrinsic
(In thousands, except share and per share data and years)
of Shares
Price
Term
Value
(in years)
Outstanding as of December 31, 2020
2,871,498
$
15.16
6.8
$
4,890
Granted
1,013,600
23.73
Exercised
( 115,548 )
12.63
$
1,373
Forfeited and cancelled
( 25,825 )
22.77
Outstanding as of September 30, 2021
3,743,725
$
17.51
7.0
$
18,150
Options vested and expected to vest as of September 30, 2021
3,743,725
$
17.51
7.0
$
18,150
Options exercisable as of September 30, 2021
2,177,823
$
17.85
5.6
$
10,517
The weighted average grant date fair value of stock options granted during the nine months ended September 30, 2021 was $ 15.86 per share.
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Restricted Stock Units
The following table summarizes RSU activity for the nine months ended September 30, 2021:
Weighted
Average
Grant Date
Aggregate
Number
Fair Value
Intrinsic
(In thousands, except share and per share data)
of Shares
Per Share
Value
Outstanding as of December 31, 2020
2,244,157
$
3.83
Granted
629,348
23.72
Vested
( 1,339,625 )
3.18
$
31,486
Forfeited and cancelled
( 67,917 )
10.06
Outstanding as of September 30, 2021
1,465,963
$
12.67
Stock-Based Compensation
Stock-based compensation expense included in total costs and expenses on the condensed consolidated statement of operations included the following:
Three Months Ended
Nine Months Ended
September 30,
September 30,
(In thousands)
2021
2020
2021
2020
Cost of revenue
$
206
$
216
$
787
$
728
Research and development
939
437
2,969
2,192
General and administrative
2,557
1,288
6,453
5,783
Total stock-based compensation expense
$
3,702
$
1,941
$
10,209
$
8,703
As of September 30, 2021, the Company had unrecognized stock-based compensation expense for stock options and RSUs of $ 14.7 million and $ 15.0 million, respectively, each of which is expected to be recognized over a weighted average period of 3.0 years.
10. Net Loss per Share
Basic and diluted net loss per share is summarized in the following table:
Three Months Ended
Nine Months Ended
September 30,
September 30,
(In thousands, except for share and per share data)
2021
2020
2021
2020
Numerator:
Net loss
$
( 21,146 )
$
( 10,659 )
$
( 68,061 )
$
( 37,842 )
Denominator:
Weighted average shares of common stock outstanding, basic and diluted
61,219,321
42,802,582
55,215,037
42,187,140
Net loss per share, basic and diluted
$
( 0.35 )
$
( 0.25 )
$
( 1.23 )
$
( 0.90 )
The Company’s potentially dilutive securities, which included stock options, RSUs and warrants, have been excluded from the computation of diluted net loss per share since the effect would be to reduce the net loss per share. Therefore, the weighted average number of shares of common stock outstanding used to calculate both basic and diluted net loss per share is the same. The following table presents potential shares of common stock excluded from the calculation
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of diluted net loss per share for the three and nine months ended September 30, 2021 and 2020. All share amounts presented in the table below represent the total number outstanding as of September 30, 2021 and 2020.
September 30,
2021
2020
Options to purchase common stock
3,743,725
3,100,763
Restricted stock unit awards
1,465,963
2,308,357
Warrants
—
460,251
Total potential shares of common stock
5,209,688
5,869,371
11. Leases
Operating Leases
Agreements for Office Space
The Company has a sublease agreement with Auxilium Pharmaceuticals, LLC (the “Sublandlord”) pursuant to which it subleases 33,019 square feet of office space for its headquarters in Wayne, Pennsylvania. The sublease has a term that runs through October 2023. If for any reason the lease between Chesterbrook Partners, LP (“Landlord”) and Sublandlord is terminated or expires prior to October 2023, the Company’s sublease will automatically terminate. In December 2020, the Company entered into a sub-sublease agreement under which it sub-subleased 8,115 square feet. The sub-sublease term runs concurrently with the original sublease agreement.
In February 2019, the Company entered into a sublease agreement with a third party for 20,433 square feet of office and laboratory space in St. Louis, Missouri. The lease commenced in June 2019 and has a term that runs through June 2029.
Supplemental balance sheet information related to operating leases is as follows:
September 30,
December 31,
(In thousands)
2021
2020
Operating Leases:
Gross cost
$
5,240
$
5,240
Accumulated amortization
( 1,625 )
( 1,111 )
Other assets
$
3,615
$
4,129
Current portion of lease liabilities
$
669
$
603
Other liabilities
2,383
2,894
Total operating lease liabilities
$
3,052
$
3,497
Amortization expense related to operating lease right-of-use assets and accretion of operating lease liabilities totaled $ 0.3 million for each of the three months ended September 30, 2021 and 2020 and $ 0.8 million for each of the nine months ended September 30, 2021 and 2020.
Finance Leases
Laboratory Equipment
The Company leased laboratory equipment which it used in its laboratory space in St. Louis, Missouri under two finance lease financing arrangements which the Company entered into in August 2017 and October 2017, for which terms ended in October 2020 and December 2020, respectively.
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12. Related Party Transactions
Mallinckrodt plc
In April 2018, Bryan Reasons was appointed to the Company’s board of directors. Subsequently, in March 2019, Mr. Reasons became the Chief Financial Officer of Mallinckrodt plc. Prior to Mr. Reasons joining Mallinckrodt plc, the Company entered into a master services agreement with a subsidiary of Mallinckrodt plc, pursuant to which Confluence provides laboratory services to the subsidiary (“Mallinckrodt”) in the ordinary course of business. Mr. Reasons was not involved in the negotiation or execution of the agreement, but may be deemed to have an interest in the ongoing transactions based on his employment as an executive officer of Mallinckrodt plc. During the nine months ended September 30, 2021 and 2020, the Company invoiced Mallinckrodt for $ 24 thousand and $ 0.3 million, respectively, under the master services agreement. As of September 30, 2021 and December 31, 2020, the Company had $ 0 and $ 24 thousand, respectively, of outstanding accounts receivable balances from Mallinckrodt. Mr. Reasons had no financial interest in these transactions.
13. Agreements Related to Intellectual Property
Asset Purchase Agreement – EPI Health, LLC
In October 2019, the Company sold RHOFADE (oxymetazoline hydrochloride) cream, 1 % (“RHOFADE”) to EPI Health, LLC (“EPI Health”) pursuant to an asset purchase agreement. EPI Health agreed to pay the Company a high single-digit royalty calculated as a percentage of net sales on a country-by-country basis until the date that the patent rights related to RHOFADE have expired or, if later, ten years from the date of the first commercial sale of RHOFADE in such country. The Company recorded royalty income under the asset purchase agreement of $ 0.6 million and $ 0.5 million during the nine months ended September 30, 2021 and 2020, respectively. Royalty income is included in other revenue on the condensed consolidated statements of operations and comprehensive loss. EPI Health has also agreed to pay the Company potential sales milestone payments of up to $ 20.0 million in the aggregate upon the achievement of specified levels of net sales of products covered by the asset purchase agreement, and 25 % of any upfront, license, milestone, maintenance or fixed payment received by EPI Health in connection with any license or sublicense of the assets transferred in the disposition in any territory outside of the United States, subject to specified exceptions.
Agreement and Plan of Merger – Confluence
In August 2017, the Company entered into an Agreement and Plan of Merger, pursuant to which it acquired Confluence (the “Confluence Agreement”). In November 2018, a development milestone specified in the Confluence Agreement was achieved, as a result of which the Company paid the former Confluence equity holders $ 2.5 million in cash and issued 253,208 shares of its common stock with a fair value of $ 2.2 million. Under the Confluence Agreement, the Company also agreed to pay the former Confluence equity holders aggregate remaining contingent consideration of up to $ 75.0 million based upon the achievement of specified regulatory and commercial milestones set forth in the Confluence Agreement. In addition, the Company agreed to pay the former Confluence equity holders future royalty payments calculated as a low single-digit percentage of annual net sales, subject to specified reductions, limitations and other adjustments, until the date that all of the patent rights for that product have expired, as determined on a country-by-country and product-by-product basis or, in specified circumstances, ten years from the first commercial sale of such product. In addition to the payments described above, if the Company sells, licenses or transfers any of the intellectual property acquired from Confluence pursuant to the Confluence Agreement to a third party, the Company will be obligated to pay the former Confluence equity holders a portion of any consideration received from such sale, license or transfer in specified circumstances.
As of September 30, 2021 and December 31, 2020, the balance of the Company’s contingent consideration liability was $ 26.2 million and $ 4.1 million, respectively (see Note 3).
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14. Income Taxes
The Company did not record a federal or state income tax benefit for losses incurred during each of the three and nine months ended September 30, 2021 and 2020. The Company concluded that it is more likely than not that its deferred tax assets will not be realized which resulted in recording a full valuation allowance during those periods.
15. Discontinued Operations
The following table presents information related to liabilities reported as discontinued operations in the Company’s condensed consolidated balance sheet:
September 30,
December 31,
(In thousands)
2021
2020
Accounts payable
$
—
$
1,175
Accrued expenses
2,198
1,936
Discontinued operations - current liabilities
$
2,198
$
3,111
16. Segment Information
The Company has two reportable segments, therapeutics and contract research. The therapeutics segment is focused on identifying and developing innovative therapies to address significant unmet needs for immuno-inflammatory diseases. The contract research segment earns revenue from the provision of laboratory services. Contract research revenue is generally evidenced by contracts with clients which are on an agreed upon fixed-price, fee-for-service basis. Corporate and other includes general and administrative expenses as well as eliminations of intercompany transactions. The Company does not report balance sheet information by segment since it is not reviewed by the chief operating decision maker, and all of the Company’s tangible assets are held in the United States.
The Company’s results of operations by segment for the three and nine months ended September 30, 2021 and 2020 are summarized in the tables below:
(In thousands)
Contract
Corporate
Total
Three Months Ended September 30, 2021
Therapeutics
Research
and Other
Company
Total revenue
$
244
$
3,335
$
( 1,920 )
$
1,659
Cost of revenue
—
2,912
( 1,813 )
1,099
Research and development
14,083
—
( 107 )
13,976
General and administrative
—
837
5,142
5,979
Revaluation of contingent consideration
900
—
—
900
Loss from operations
$
( 14,739 )
$
( 414 )
$
( 5,142 )
$
( 20,295 )
(In thousands)
Contract
Corporate
Total
Three Months Ended September 30, 2020
Therapeutics
Research
and Other
Company
Total revenue
$
118
$
3,015
$
( 1,684 )
$
1,449
Cost of revenue
—
2,765
( 1,576 )
1,189
Research and development
6,347
—
( 107 )
6,240
General and administrative
—
672
3,187
3,859
Revaluation of contingent consideration
626
—
—
626
Loss from operations
$
( 6,855 )
$
( 422 )
$
( 3,188 )
$
( 10,465 )
(In thousands)
Contract
Corporate
Total
Nine Months Ended September 30, 2021
Therapeutics
Research
and Other
Company
Total revenue
$
704
$
10,016
$
( 5,460 )
$
5,260
Cost of revenue
—
8,705
( 5,141 )
3,564
Research and development
30,030
—
( 319 )
29,711
General and administrative
—
2,344
14,332
16,676
Revaluation of contingent consideration
22,139
—
—
22,139
Loss from operations
$
( 51,465 )
$
( 1,033 )
$
( 14,332 )
$
( 66,830 )
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(In thousands)
Contract
Corporate
Total
Nine Months Ended September 30, 2020
Therapeutics
Research
and Other
Company
Total revenue
$
529
$
10,079
$
( 5,706 )
$
4,902
Cost of revenue
—
9,233
( 5,386 )
3,847
Research and development
20,702
—
( 320 )
20,382
General and administrative
—
2,112
13,520
15,632
Revaluation of contingent consideration
2,393
—
—
2,393
Loss from operations
$
( 22,566 )
$
( 1,266 )
$
( 13,520 )
$
( 37,352 )
Loss from discontinued operations
$
( 284 )
$
—
$
( 1 )
$
( 285 )
Intersegment Revenue
Revenue for the contract research segment included $ 1.9 million and $ 1.7 million for services performed on behalf of the therapeutics segment for the three months ended September 30, 2021 and 2020, respectively and $ 5.5 million and $ 5.7 million for the nine months ended September 30, 2021 and 2020, respectively. All intersegment revenue has been eliminated in the Company’s condensed consolidated statement of operations.
17. Legal Proceedings
Securities Class Action
On July 30, 2019, plaintiff Linda Rosi (“Rosi”) filed a putative class action complaint captioned Rosi v. Aclaris Therapeutics, Inc., et al. in the U.S. District Court for the Southern District of New York against the Company and certain of its executive officers. The complaint alleges that the defendants violated federal securities laws by, among other things, failing to disclose an alleged likelihood that regulators would scrutinize advertising materials related to ESKATA and find that the materials minimized the risks or overstated the efficacy of the product. The complaint seeks unspecified compensatory damages on behalf of Rosi and all other persons and entities that purchased or otherwise acquired the Company’s securities between May 8, 2018 and June 20, 2019.
On September 5, 2019, an additional plaintiff, Robert Fulcher (“Fulcher”), filed a substantially identical putative class action complaint captioned Fulcher v. Aclaris Therapeutics, Inc., et al. in the same court against the same defendants.
On November 6, 2019, the court consolidated the Rosi and Fulcher actions (together, the “Consolidated Securities Action”) and appointed Fulcher “lead plaintiff” for the putative class.
On January 24, 2020, Fulcher filed a consolidated amended complaint in the Consolidated Securities Action, naming two additional executive officers as defendants, extending the putative class period to August 12, 2019, and adding allegations concerning, among other things, alleged statements and omissions throughout the putative class period concerning ESKATA’s risks, tolerability and effectiveness. The defendants filed a motion to dismiss the consolidated amended complaint on April 17, 2020. Following briefing and oral argument on February 25, 2021, the motion was granted in part and denied in part on March 29, 2021, and the issues in dispute significantly narrowed. The defendants filed an answer to the remaining aspects of the consolidated amended complaint on April 19, 2021.
In June 2021, the defendants and the plaintiffs agreed to settle the Consolidated Securities Action. The parties signed and filed a settlement agreement in July 2021. On August 18, 2021, the court preliminarily approved the proposed settlement, directed that notice be given to the putative class and scheduled the final approval settlement hearing for November 30, 2021. Notice was subsequently given to the putative class. The proposed settlement is subject to final approval by the court.
The Company had $ 2.65 million accrued as of September 30, 2021 for its estimated financial obligation. The Company expects its financial obligation to be within the limits of its insurance coverage and accordingly recorded a receivable for an insurance recovery equal to the settlement amount. The insurance recovery receivable and the litigation settlement liability are recorded in prepaid expenses and other current assets and accrued expenses, respectively, in the condensed consolidated balance sheet.
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Stockholder Derivative Action
On November 15, 2019, plaintiff Keith Allred (“Allred”) filed a derivative stockholder complaint captioned Allred v. Walker et al. in the U.S. District Court for the Southern District of New York against certain of the Company’s directors and executive officers. The complaint alleges that the defendants, among other things, breached their fiduciary duties as directors and/or officers in connection with the claims alleged in the Consolidated Securities Action. The complaint seeks, among other things, unspecified compensatory damages on behalf of the Company.
On November 25, 2019, an additional plaintiff, Bruce Brown (“Brown”), filed a substantially identical complaint captioned Brown v. Walker et al. in the same court against the same defendants.
On December 12, 2019, the court consolidated the Allred and Brown actions under the caption In re Aclaris Therapeutics, Inc. Derivative Litigation (the “Consolidated Derivative Action”) and directed that future derivative cases filed in or transferred to the court arising out of substantially the same transactions or events be similarly consolidated. Thereafter, on January 11, 2020, the court stayed – subject to certain conditions – all deadlines in the Consolidated Derivative Action pending resolution of the defendants’ then-anticipated motion to dismiss the Consolidated Securities Action. On May 18, 2021, the court extended the stay – subject to certain conditions – until the resolution of a motion for summary judgment in the Consolidated Securities Action, which defendants in that action intended to file had the parties to the Consolidated Securities Action not reached an agreement to settle.
In June 2021, the defendants and the plaintiffs agreed to settle the Consolidated Derivative Action. The agreed terms provide for the Company to implement certain policies and for attorneys’ fees to be paid to plaintiff’s counsel. The parties signed and filed a settlement agreement in July 2021. On August 18, 2021, the court preliminarily approved the proposed settlement, directed that notice be given to the Company’s stockholders and scheduled the final approval settlement hearing for November 30, 2021. Notice was subsequently given to the Company’s stockholders . The proposed settlement is subject to final approval by the court.
The Company had $ 425 thousand accrued as of September 30, 2021 for its estimated financial obligation. The Company expects its financial obligation to be within the limits of its insurance coverage and accordingly recorded a receivable for an insurance recovery equal to the settlement amount. The insurance recovery receivable and the litigation settlement liability are recorded in prepaid expenses and other current assets and accrued expenses, respectively, in the condensed consolidated balance sheet.
Product Liability Lawsuit
On December 18, 2020, plaintiff Daurie Mancini filed an amended complaint under the caption Daurie Mancini v. Aclaris Therapeutics, Inc. et al in the Superior Court of New Jersey Ocean County against the Company and certain third parties alleging injuries as a result of the plaintiff’s alleged treatment with ESKATA in 2019. The amended complaint seeks unspecified compensatory and punitive damages. The Company filed a motion to dismiss the amended complaint on March 15, 2021. The Company’s motion to dismiss was granted on July 9, 2021. The Court dismissed the majority of claims against the Company with prejudice. All remaining claims against the Company were dismissed without prejudice.
18. Subsequent Event
On November 1, 2021, Kamil Ali-Jackson, Co-Founder, Chief Legal Officer, Chief Compliance Officer and Corporate Secretary notified the Company that she will retire from her position effective January 3, 2022. In connection with her retirement, the Company entered into a Severance Agreement containing a release of claims against the Company. Under the Severance Agreement, Ms. Ali-Jackson will receive a lump sum cash payment of $ 615 thousand, equal to her annual base salary, her 2021 target bonus, and accrued but unused paid-time off. She will also receive continuation of health insurance benefits for 12 months, acceleration of vesting of options and restricted stock units, to the extent the award would have vested had she remained employed through March 31, 2022, and acceleration of additional currently outstanding restricted stock units held by her, with respect to a number of shares equal to (i) $ 157 thousand divided by (ii)
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the fair market value of the Company’s common stock on January 3, 2022.
Text extracted from the filing as submitted to EDGAR. Formatting, tables and exhibits are simplified for reading; the original document is authoritative for anything you rely on.