2020 Q1 Form 10-Q Financial Statement

#000156459020023640 Filed on May 08, 2020

View on sec.gov

Income Statement

Concept 2020 Q1 2019 Q1
Revenue $7.490M $2.012M
YoY Change 272.27% 116.81%
Cost Of Revenue $980.0K $330.0K
YoY Change 196.97%
Gross Profit $6.510M $1.682M
YoY Change 287.04%
Gross Profit Margin 86.92% 83.6%
Selling, General & Admin $12.49M $11.92M
YoY Change 4.73% 422.85%
% of Gross Profit 191.78% 708.74%
Research & Development $4.853M $3.797M
YoY Change 27.81% 14.2%
% of Gross Profit 74.55% 225.74%
Depreciation & Amortization $33.00K $44.00K
YoY Change -25.0% 2.33%
% of Gross Profit 0.51% 2.62%
Operating Expenses $18.93M $16.66M
YoY Change 13.62% 197.24%
Operating Profit -$11.44M -$14.65M
YoY Change -21.89% 213.19%
Interest Expense $1.784M $1.020M
YoY Change 74.9% -144.35%
% of Operating Profit
Other Income/Expense, Net -$1.730M -$4.587M
YoY Change -62.28% 99.43%
Pretax Income -$13.17M -$19.24M
YoY Change -31.55% 175.64%
Income Tax
% Of Pretax Income
Net Earnings -$13.17M -$19.24M
YoY Change -31.52% 175.7%
Net Earnings / Revenue -175.89% -956.16%
Basic Earnings Per Share
Diluted Earnings Per Share -$1.140M -$2.015M
COMMON SHARES
Basic Shares Outstanding
Diluted Shares Outstanding

Balance Sheet

Concept 2020 Q1 2019 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $26.30M $43.40M
YoY Change -39.4% 166.26%
Cash & Equivalents $26.45M $43.38M
Short-Term Investments
Other Short-Term Assets $5.600M $1.800M
YoY Change 211.11% 100.0%
Inventory $3.400M $886.0K
Prepaid Expenses
Receivables $14.40M $2.300M
Other Receivables $0.00 $0.00
Total Short-Term Assets $49.70M $48.37M
YoY Change 2.75% 173.67%
LONG-TERM ASSETS
Property, Plant & Equipment $3.400M $425.0K
YoY Change 700.0% 70.0%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $200.0K $200.0K
YoY Change 0.0% -33.33%
Total Long-Term Assets $30.60M $33.48M
YoY Change -8.61% 3.08%
TOTAL ASSETS
Total Short-Term Assets $49.70M $48.37M
Total Long-Term Assets $30.60M $33.48M
Total Assets $80.30M $81.85M
YoY Change -1.9% 63.19%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $5.200M $6.318M
YoY Change -17.7% 128.91%
Accrued Expenses $5.100M $2.924M
YoY Change 74.42% -9.05%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00
YoY Change
Long-Term Debt Due $0.00
YoY Change
Total Short-Term Liabilities $10.30M $24.66M
YoY Change -58.23% 16.23%
LONG-TERM LIABILITIES
Long-Term Debt $47.80M $31.95M
YoY Change 49.6% 148.65%
Other Long-Term Liabilities $5.800M $2.100M
YoY Change 176.19% 123.88%
Total Long-Term Liabilities $53.60M $34.05M
YoY Change 57.41% 146.97%
TOTAL LIABILITIES
Total Short-Term Liabilities $10.30M $24.66M
Total Long-Term Liabilities $53.60M $34.05M
Total Liabilities $63.80M $61.98M
YoY Change 2.94% 47.7%
SHAREHOLDERS EQUITY
Retained Earnings -$427.7M
YoY Change 29.79%
Common Stock $446.8M
YoY Change 32.6%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $16.47M $19.88M
YoY Change
Total Liabilities & Shareholders Equity $80.30M $81.85M
YoY Change -1.9% 63.19%

Cashflow Statement

Concept 2020 Q1 2019 Q1
OPERATING ACTIVITIES
Net Income -$13.17M -$19.24M
YoY Change -31.52% 175.7%
Depreciation, Depletion And Amortization $33.00K $44.00K
YoY Change -25.0% 2.33%
Cash From Operating Activities -$16.35M -$13.33M
YoY Change 22.58% 176.7%
INVESTING ACTIVITIES
Capital Expenditures $16.00K $182.0K
YoY Change -91.21%
Acquisitions $0.00
YoY Change -100.0%
Other Investing Activities $0.00
YoY Change -100.0%
Cash From Investing Activities -$16.00K -$182.0K
YoY Change -91.21% -98.79%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $20.29M $0.00
YoY Change -100.0%
Debt Paid & Issued, Net $20.00M
YoY Change
Cash From Financing Activities 20.45M 11.63M
YoY Change 75.74% -50.2%
NET CHANGE
Cash From Operating Activities -16.35M -13.33M
Cash From Investing Activities -16.00K -182.0K
Cash From Financing Activities 20.45M 11.63M
Net Change In Cash 4.085M -1.882M
YoY Change -317.06% -154.24%
FREE CASH FLOW
Cash From Operating Activities -$16.35M -$13.33M
Capital Expenditures $16.00K $182.0K
Free Cash Flow -$16.36M -$13.52M
YoY Change 21.05% 180.47%

Facts In Submission

Frame Concept Type Concept / XBRL Key Value Unit
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CY2019Q1 us-gaap Other Comprehensive Income Loss Foreign Currency Transaction And Translation Adjustment Net Of Tax
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CY2020Q1 us-gaap Adjustments To Additional Paid In Capital Sharebased Compensation Requisite Service Period Recognition Value
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CY2020Q1 us-gaap Nature Of Operations
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<div align="left"> <table border="0" cellspacing="0" cellpadding="0" style="border-collapse:collapse; width:100%;"> <tr> <td valign="top" style="width:5.24%;white-space:nowrap"> <p style="margin-top:10pt;margin-bottom:0pt;font-weight:bold;color:#000000;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;"><font style="font-weight:bold;color:#000000;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">1.</font></p></td> <td valign="top"> <p style="margin-top:10pt;margin-bottom:0pt;font-weight:bold;color:#000000;font-style:normal;text-transform:none;font-variant: normal;font-family:Times New Roman;font-size:10pt;">Operations and Basis of Presentation&#160;&#160;</p></td></tr></table></div> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:0%;font-weight:bold;color:#000000;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">Overview</p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The accompanying condensed consolidated financial statements of EyePoint Pharmaceuticals, Inc. and subsidiaries (collectively, the &#8220;Company&#8221;) as of March 31, 2020 and for the three months ended March 31, 2020 and 2019 are unaudited. Certain information in the footnote disclosures of these financial statements has been condensed or omitted in accordance with the rules and regulations of the Securities and Exchange Commission (the &#8220;SEC&#8221;). These financial statements should be read in conjunction with the Company&#8217;s audited consolidated financial statements and footnotes included in the Company&#8217;s Annual Report on Form 10-K for the year ended December 31, 2019. In the opinion of management, these statements have been prepared on the same basis as the audited consolidated financial statements as of and for the year ended December 31, 2019, and include all adjustments, consisting only of normal recurring adjustments, that are necessary for the fair presentation of the Company&#8217;s financial position, results of operations, comprehensive loss and cash flows for the periods indicated. The preparation of financial statements in accordance with United States (&#8220;U.S.&#8221;) generally accepted accounting principles (&#8220;GAAP&#8221;) requires management to make assumptions and estimates that affect, among other things, (i) reported amounts of assets and liabilities; (ii) disclosure of contingent assets and liabilities at the date of the consolidated financial statements; and (iii) reported amounts of revenues and expenses during the reporting period. The results of operations for the three months ended March 31, 2020 are not necessarily indicative of the results that may be expected for the entire fiscal year or any future period. </p> <p style="Background-color:#FFFFFF;margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company is a pharmaceutical company committed to developing and commercializing innovative ophthalmic products for the treatment of serious eye disorders. <font style="Background-color:#FFFFFF;color:#000000;">The Company has two products, YUTIQ</font><font style="color:#000000;"><sup style="font-size:85%;line-height:120%;vertical-align:top">&#174;</sup></font><font style="Background-color:#FFFFFF;color:#000000;"> and DEXYCU</font><font style="color:#000000;"><sup style="font-size:85%;line-height:120%;vertical-align:top">&#174;</sup></font><font style="Background-color:#FFFFFF;color:#000000;">, which were approved by the U.S. Food and Drug Administration (&#8220;FDA&#8221;) in 2018.</font></p> <p style="Background-color:#FFFFFF;margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;"><font style="Background-color:#FFFFFF;">YUTIQ (fluocinolone acetonide intravitreal implant) 0.18 mg for intravitreal injection, was launched directly in the U.S. in February 2019. YUTIQ is indicated for the treatment of chronic </font>non-infectious<font style="Background-color:#FFFFFF;"> uveitis affecting the posterior segment of the eye, which affects between 60,000 to 100,000 people in the U.S. each year and causes approximately 30,000 new cases of blindness every year, making it the third leading cause of blindness. Injected into the eye in an office visit, YUTIQ is a micro-insert that delivers a micro-dose of a corticosteroid to the back of the eye on a sustained constant (zero order release) basis for up to 36 months. YUTIQ is based on the Company&#8217;s proprietary Durasert</font><font style="color:#000000;"><sup style="font-size:85%;line-height:120%;vertical-align:top">&#174;</sup></font><font style="Background-color:#FFFFFF;"> sustained-release drug delivery technology platform, which can deliver drugs for predetermined periods of time ranging from months to years.</font></p> <p style="margin-bottom:0pt;margin-top:10pt;text-indent:5.24%;color:#000000;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;"><font style="Background-color:#FFFFFF;">DEXYCU (dexamethasone intraocular suspension) 9%, </font>for intraocular administration, was launched directly in the U.S. in March 2019.&nbsp;&nbsp;Indicated for the treatment of post-operative ocular inflammation, DEXYCU <font style="Background-color:#FFFFFF;">is administered as a single dose at the end of ocular surgery and is the first long-acting intraocular product approved by the FDA for this indication. DEXYCU utilizes the Company&#8217;s proprietary Verisome</font><sup style="font-size:85%;line-height:120%;vertical-align:top">&#174;</sup><font style="Background-color:#FFFFFF;"> drug-delivery platform, which allows for a single intraocular injection that releases dexamethasone, a corticosteroid, over time. There were approximately 3.8&#160;million cataract surgeries performed during 2018 in the U.S.</font><font style="font-size:12pt;color:#000000;">&#160;</font><font style="Background-color:#FFFFFF;">and the Company launched DEXYCU with a primary focus on its use following cataract surgery. The Company acquired DEXYCU in connection with its acquisition of Icon Bioscience, Inc. (&#8220;Icon&#8221;) in March 2018 (the Icon Acquisition&#8221;). </font></p> <p style="Background-color:#FFFFFF;margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">ILUVIEN<sup style="font-size:85%;line-height:120%;vertical-align:top">&#174;</sup>&#160;for diabetic macular edema (&#8220;DME&#8221;), the Company&#8217;s licensed product, is sold directly in the U.S. and several European Union (&#8220;EU&#8221;) countries by Alimera Sciences, Inc. (&#8220;Alimera&#8221;). In July 2017, the Company expanded its license agreement with Alimera to include the uveitis indication utilizing the Durasert technology in Europe, the Middle East and Africa (&#8220;EMEA&#8221;), which received European regulatory approval in March 2019 and, subject to obtaining pricing and reimbursement in each applicable country, will be marketed as ILUVIEN. </p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;"><font style="Background-color:#FFFFFF;">EYP-1901, 6-Month bioerodible Durasert Vorolanib &#8211; Tyrosine Kinase Inhibitor (&#8220;TKI&#8221;) is being advanced as a potential treatment for wet age-related macular degeneration (&#8220;wAMD&#8221;) with potential in diabetic retinopathy (&#8220;DR&#8221;) and retinal vein occlusion (&#8220;RVO&#8221;). The Company has completed initial animal pharmacokinetic and toxicology studies before 2020 and initiated GLP toxicology studies in March 2020 to support the anticipated filing of an Investigational New Drug application with the FDA later this year, </font>with a Phase 1 clinical trial scheduled to follow shortly afterwards<font style="Background-color:#FFFFFF;">.</font>&#160;&#160;<font style="Background-color:#FFFFFF;color:#000000;"> </font>&#160;<font style="Background-color:#FFFFFF;color:#000000;"> </font></p> <p style="margin-bottom:0pt;margin-top:10pt;text-indent:0%;font-weight:bold;color:#000000;font-size:10pt;font-family:Times New Roman;font-style:normal;text-transform:none;font-variant: normal;">Liquidity</p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;"><font style="Background-color:#FFFFFF;">The Company has a history of operating losses and has not had significant recurring cash inflows from revenue.</font><font style="color:#000000;"> The Company&#8217;s operations have been financed primarily from sales of its equity securities, issuance of debt and a combination of license fees, milestone payments, royalty income and other fees received from its collaboration partners</font><font style="Background-color:#FFFFFF;">.</font><font style="color:#000000;"> In the first quarter of 2019, the Company commenced the U.S. launch of its first two commercial products, YUTIQ and DEXYCU. However, management does not yet have sufficient historical evidence to assert that it is probable that the Company will receive sufficient revenues from its product sales to fund operations. As of March 31, 2020, the Company has had recurring operating losses since its inception and has an accumulated deficit of approximately $478.5 million and working capital of $39.4 million. The Company had cash and cash equivalents of $26.3 million at March 31, 2020. </font></p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">Accordingly, the foregoing conditions, taken together, continue to raise substantial doubt about the Company&#8217;s ability to continue as a going concern for one year from the issuance of these financial statements. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.</p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:4.81%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company&#8217;s plans that are intended to mitigate those conditions include continuing to fulfill its funding needs through cash inflows from revenue of YUTIQ and DEXYCU product sales, licensing arrangements, additional capital raises or other arrangements. <font style="Background-color:#FFFFFF;color:#000000;">The Company&#8217;s plans also include a restructuring plan and curtailing expenses to conserve cash in response to a significant decline in product demand associated with shut-downs of customer facilities and postponements of elective surgical procedures and physician office visits in response to the COVID-19 coronavirus pandemic (the &#8220;Pandemic&#8221;).&#160;</font> On April 8, 2020, the Company submitted an application through Silicon Valley Bank for the Paycheck Protection Program Loan (the &#8220;PPP Loan&#8221;) <font style="Background-color:#FFFFFF;color:#000000;">that is administered by the U.S. Small Business Administration (the &#8220;SBA&#8221;),</font><font style="Background-color:#FFFFFF;color:#212529;"> under </font>the Coronavirus Aid, Relief, and Economic Security Act (the &#8220;CARES Act&#8221;)<font style="Background-color:#FFFFFF;color:#000000;">. </font>On April 22, 2020, the Company received the PPP Loan proceeds of $2.0 million. The Company believes that its cash and cash equivalents of $26.3&#160;million at March 31, 2020, the PPP Loan proceeds of $2.0 million received on April 22, 2020, and expected cash inflows under its product sales and royalty agreements coupled with cash conservation activities will enable the Company to fund its current and planned operations into 2021 under current assumptions for the duration of the COVID-19-related closures across the U.S. Although the Company believes such plans, if executed, should provide the Company sufficient financing to meet its needs, there is no assurance that additional funding will be achieved and that the Company will succeed in its future operations. Actual cash requirements could differ from management&#8217;s projections due to many factors, including the success of commercialization for YUTIQ and DEXYCU, the actual costs of these commercialization efforts, additional investments in research and development programs, competing technological and market developments and the costs of any strategic acquisitions and/or development of complementary business opportunities. </p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:0%;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">Recently Adopted and Recently Issued Accounting Pronouncements</p> <p style="margin-top:10pt;margin-bottom:0pt;text-indent:5.24%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">New accounting pronouncements are issued periodically by the Financial Accounting Standards Board (&#8220;FASB&#8221;) and are adopted by the Company as of the specified effective dates. Unless otherwise disclosed below, the Company believes that recently issued and adopted accounting pronouncements will not have a material impact on the Company&#8217;s financial position, results of operations and cash flows or do not apply to the Company&#8217;s operations.</p> <p style="margin-bottom:0pt;margin-top:10pt;text-indent:5.24%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">In June 2016, the FASB issued ASU No. 2016-13, <font style="font-style:italic;">Financial Instruments - Credit Losses (Topic 326)</font><font style="color:#000000;"> (&#8220;ASU 2016-13&#8221;)</font><font style="font-style:italic;">: Measurement of Credit Losses on Financial Instruments,</font> to replace the current incurred loss impairment methodology for financial assets measured at amortized cost with a methodology that reflects expected credit losses and requires consideration of a broader range of reasonable and supportable information, including forecasted information, to develop credit loss estimates. ASU 2016-13 is effective for fiscal years beginning after December 15, 2019, and interim periods within those fiscal years. Early adoption is permitted for fiscal years beginning after December 15, 2018. The Company adopted ASU 2016-13 on January 1, 2020. The adoption of this standard did not have<font style="color:#000000;"> a material impact on its consolidated financial statements. </font></p> <p style="margin-bottom:0pt;margin-top:10pt;text-indent:5.24%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">In December 2019, the FASB issued ASU No. 2019-12, <font style="font-style:italic;">Income Taxes (Topic 740)</font><font style="color:#000000;"> (&#8220;ASU 2019-12&#8221;)</font><font style="font-style:italic;">: Simplifying the Accounting for Income Taxes.</font>&#160;The amendments simplify the accounting for income taxes by removing certain exceptions for recognizing deferred taxes for investments, performing intraperiod allocation and calculating income taxes in interim periods. The ASU also adds guidance to reduce complexity in certain areas, including recognizing deferred taxes for tax goodwill and allocating taxes to members of a consolidated group ASU 2019-12 is effective for fiscal years beginning after December 15, 2020, and interim periods within those fiscal years. Early adoption is permitted, including adoption in interim or annual periods for which financial statements have not yet been issued. This standard will be effective for the Company in the first quarter of its fiscal year ending December 31, 2021. The Company is<font style="color:#000000;"> currently evaluating the impact the adoption of this update will have on its consolidated financial statements.</font></p>
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