2019 Q2 Form 10-Q Financial Statement

#000119312519144237 Filed on May 10, 2019

View on sec.gov

Income Statement

Concept 2019 Q2 2019 Q1 2018 Q1
Revenue $7.210M $2.012M $928.0K
YoY Change 908.39% 116.81% 57.29%
Cost Of Revenue $706.0K $330.0K
YoY Change
Gross Profit $6.504M $1.682M
YoY Change 809.65%
Gross Profit Margin 90.21% 83.6%
Selling, General & Admin $12.10M $11.92M $2.280M
YoY Change 111.08% 422.85% -6.17%
% of Gross Profit 186.02% 708.74%
Research & Development $3.955M $3.797M $3.325M
YoY Change -17.0% 14.2% 0.03%
% of Gross Profit 60.81% 225.74%
Depreciation & Amortization $650.0K $44.00K $43.00K
YoY Change 0.0% 2.33% -79.52%
% of Gross Profit 9.99% 2.62%
Operating Expenses $17.38M $16.66M $5.606M
YoY Change 65.52% 197.24% -2.5%
Operating Profit -$10.17M -$14.65M -$4.678M
YoY Change 3.92% 213.19% -9.34%
Interest Expense $1.599M $1.020M -$2.300M
YoY Change 122.08% -144.35% -11600.0%
% of Operating Profit
Other Income/Expense, Net -$1.333M -$4.587M -$2.300M
YoY Change -94.59% 99.43% -11600.0%
Pretax Income -$11.50M -$19.24M -$6.980M
YoY Change -66.6% 175.64% 35.8%
Income Tax $0.00
% Of Pretax Income
Net Earnings -$11.50M -$19.24M -$6.978M
YoY Change -66.6% 175.7% 35.76%
Net Earnings / Revenue -159.47% -956.16% -751.94%
Basic Earnings Per Share
Diluted Earnings Per Share -$1.083M -$2.015M -$1.531M
COMMON SHARES
Basic Shares Outstanding 106.1M 45.26M shares
Diluted Shares Outstanding

Balance Sheet

Concept 2019 Q2 2019 Q1 2018 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $44.20M $43.40M $16.30M
YoY Change 13.92% 166.26% 5.84%
Cash & Equivalents $44.16M $43.38M $16.35M
Short-Term Investments
Other Short-Term Assets $3.100M $1.800M $900.0K
YoY Change 287.5% 100.0% 12.5%
Inventory $1.670M $886.0K
Prepaid Expenses
Receivables $9.600M $2.300M $500.0K
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $58.57M $48.37M $17.68M
YoY Change 46.77% 173.67% 7.32%
LONG-TERM ASSETS
Property, Plant & Equipment $417.0K $425.0K $250.0K
YoY Change 64.82% 70.0% 3.73%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $200.0K $200.0K $300.0K
YoY Change 0.0% -33.33% 0.0%
Total Long-Term Assets $32.76M $33.48M $32.48M
YoY Change 3.14% 3.08% 3038.45%
TOTAL ASSETS
Total Short-Term Assets $58.57M $48.37M $17.68M
Total Long-Term Assets $32.76M $33.48M $32.48M
Total Assets $91.33M $81.85M $50.16M
YoY Change 27.43% 63.19% 186.54%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $6.066M $6.318M $2.760M
YoY Change 106.33% 128.91% 272.47%
Accrued Expenses $4.214M $2.924M $3.215M
YoY Change 13.19% -9.05% -18.46%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due
YoY Change
Total Short-Term Liabilities $10.72M $24.66M $21.22M
YoY Change -50.51% 16.23% 329.45%
LONG-TERM LIABILITIES
Long-Term Debt $46.25M $31.95M $12.85M
YoY Change 167.2% 148.65%
Other Long-Term Liabilities $3.000M $2.100M $938.0K
YoY Change 143.7% 123.88% 838.0%
Total Long-Term Liabilities $49.25M $34.05M $13.79M
YoY Change 165.64% 146.97% 13688.0%
TOTAL LIABILITIES
Total Short-Term Liabilities $10.72M $24.66M $21.22M
Total Long-Term Liabilities $49.25M $34.05M $13.79M
Total Liabilities $63.12M $61.98M $41.96M
YoY Change 5.23% 47.7% 740.04%
SHAREHOLDERS EQUITY
Retained Earnings -$439.2M -$427.7M -$329.6M
YoY Change 20.67% 29.79% 8.2%
Common Stock $466.6M $446.8M $336.9M
YoY Change 24.48% 32.6% 6.53%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $28.21M $19.88M $8.198M
YoY Change
Total Liabilities & Shareholders Equity $91.33M $81.85M $50.16M
YoY Change 27.43% 63.19% 186.54%

Cashflow Statement

Concept 2019 Q2 2019 Q1 2018 Q1
OPERATING ACTIVITIES
Net Income -$11.50M -$19.24M -$6.978M
YoY Change -66.6% 175.7% 35.76%
Depreciation, Depletion And Amortization $650.0K $44.00K $43.00K
YoY Change 0.0% 2.33% -79.52%
Cash From Operating Activities -$17.11M -$13.33M -$4.819M
YoY Change 181.41% 176.7% 6.15%
INVESTING ACTIVITIES
Capital Expenditures -$30.00K $182.0K $0.00
YoY Change -40.0% -100.0%
Acquisitions $0.00 $15.07M
YoY Change -100.0%
Other Investing Activities $0.00 $0.00 -$15.07M
YoY Change -100.0% -100.0% -549.85%
Cash From Investing Activities -$30.00K -$182.0K -$15.07M
YoY Change -98.29% -98.79% -552.61%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $0.00 $9.266M
YoY Change -100.0%
Debt Paid & Issued, Net $20.00M
YoY Change
Cash From Financing Activities 17.92M 11.63M 23.36M
YoY Change -40.78% -50.2% 877.45%
NET CHANGE
Cash From Operating Activities -17.11M -13.33M -4.819M
Cash From Investing Activities -30.00K -182.0K -15.07M
Cash From Financing Activities 17.92M 11.63M 23.36M
Net Change In Cash 780.0K -1.882M 3.470M
YoY Change -96.52% -154.24% 194.07%
FREE CASH FLOW
Cash From Operating Activities -$17.11M -$13.33M -$4.819M
Capital Expenditures -$30.00K $182.0K $0.00
Free Cash Flow -$17.08M -$13.52M -$4.819M
YoY Change 183.25% 180.47% 6.38%

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CY2019Q1 dei Document Type
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CY2019Q1 dei Amendment Flag
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2019-03-31
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2019
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CY2019Q1 dei Entity Registrant Name
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EyePoint Pharmaceuticals, Inc.
CY2019Q1 dei Entity Central Index Key
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0001314102
CY2019Q1 dei Current Fiscal Year End Date
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--12-31
CY2019Q1 dei Entity Filer Category
EntityFilerCategory
Accelerated Filer
CY2019Q1 dei Trading Symbol
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EYPT
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CY2019Q1 us-gaap Nature Of Operations
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<div><table style="border: none;border-collapse: collapse;margin-bottom: .001pt;width: 100%;"><tr><td style="border-bottom: none;border-left: none;border-right: none;border-top: none;padding-bottom: 0pt;padding-left: 0;padding-right: 0;padding-top: 0pt;vertical-align: top;width: 4.0%;"><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; line-height: normal;"><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;"><div style="font-weight:bold;display:inline;">1.</div></div></div></td><td style="border-bottom: none;border-left: none;border-right: none;border-top: none;padding-bottom: 0pt;padding-left: 0;padding-right: 0;padding-top: 0pt;vertical-align: top;"><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; margin-bottom: 0px; margin-top: 0px; line-height: normal;"><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;"><div style="font-weight:bold;display:inline;">Operations and Basis of Presentation </div></div></div></td></tr></table><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div><div style="clear: both; max-height: 0px;"></div></div><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; margin-bottom: 0px; margin-top: 6pt; text-indent: 0in;"><div style="font-weight:bold;display:inline;">Overview </div></div><div style="font-family: 'times new roman', 'serif';font-size: 10pt;margin-bottom: 0;margin-top: 6pt;text-indent: 0.79in;"><div style="font-size: 10pt; letter-spacing: 0px; top: 0px;;display:inline;">The accompanying condensed consolidated financial statements of EyePoint Pharmaceuticals, Inc. and subsidiaries (collectively, the &#8220;Company&#8221;) as of March&#160;31, 2019 and for the three months ended March&#160;31, 2019 and 2018 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 Transition Report on Form&#160;10-K&#160;for the six months ended December&#160;31, 2018. 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 six months ended December&#160;31, 2018, 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)&#160;reported amounts of assets and liabilities; (ii)&#160;disclosure of contingent assets and liabilities at the date of the consolidated financial statements; and (iii)&#160;reported amounts of revenues and expenses during the reporting period. The results of operations for the three months ended March&#160;31, 2019 are not necessarily indicative of the results that may be expected for the entire fiscal year or any future period.</div><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;"> </div></div><div style="margin: 12pt 0in 0.0001pt; text-indent: 0.79in; font-family: &quot;times new roman&quot;, serif; font-size: 10pt;">The Company is a specialty biopharmaceutical company committed to developing and commercializing innovative ophthalmic products for the treatment of eye diseases. The Company has two products, YUTIQ&#8482; and DEXYCU&#8482;, which were approved by the U.S. Food and Drug Administration (&#8220;FDA&#8221;) in October 2018 and February 2018, respectively.</div><div style="font-family: 'times new roman', 'serif';font-size: 10pt;margin-bottom: 0;margin-top: 12pt;text-indent: 0.79in;"><div style="font-size: 10pt; letter-spacing: 0px; top: 0px;;display:inline;">YUTIQ&#160;(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&#160;non-infectious&#160;uveitis affecting the posterior segment of the eye, which affects between 55,000 to 120,000 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<div style="color: rgb(0, 0, 0); font-family: &quot;times new roman&quot;; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 4%; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; background-color: rgb(255, 255, 255); text-decoration-style: initial; text-decoration-color: initial; font-size: 10pt; vertical-align: top;;vertical-align: super;font-size: smaller;display:inline;">&#8482;</div>&#160;sustained-release drug delivery technology platform, which can deliver drugs for predetermined periods of time ranging from months to years.</div></div><div style="font-family: 'times new roman', 'serif';font-size: 10pt;margin-bottom: 0;margin-top: 12pt;text-indent: 0.79in;">DEXYCU&#160;(dexamethasone intraocular suspension) 9%, for intraocular administration, was launched directly in the U.S. in March 2019. Indicated for the treatme<div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;">nt of post-operative ocular inflammation, DEXYCU 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<div style="vertical-align: super;font-size: smaller;display:inline;">&#174;</div> drug-delivery platform, which allows for a single intraocular injection that releases dexamethasone, a corticosteroid, over time. There were approximately 4.8&#160;million cataract surgeries performed during 2018 in the U.S., with growth projected at an estimated annual rate of 8%, 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. </div></div><div style="font-size:10pt; color:#000000; font-family:'times new roman'; font-style:normal; font-variant-ligatures:normal; font-variant-caps:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-transform:none; white-space:normal; widows:2; word-spacing:0px; -webkit-text-stroke-width:0px; text-decoration-style:initial; text-decoration-color:initial; margin-top:12pt; margin-bottom:0pt; text-indent:4%">ILUVIEN<div style="font-size:11.3333px; vertical-align:top;vertical-align: super;font-size: smaller;display:inline;">&#174;</div>&#160;for diabetic macular edema (&#8220;DME&#8221;), the Company&#8217;s lead licensed product, is sold directly in the U.S. and several European Union (&#8220;EU&#8221;) countries by Alimera Sciences, Inc. (&#8220;Alimera&#8221;).&#160;In&#160;July&#160;2017,&#160;the&#160;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. Retisert&#174;, one of the Company&#8217;s earlier generation products, was approved in 2005 by the FDA for the treatment of chronic&#160;non-infectious&#160;uveitis affecting the posterior segment of the eye&#160;and is sold in the U.S. by Bausch&#160;&amp; Lomb Incorporated (&#8220;Bausch&#160;&amp; Lomb&#8221;). The Company&#8217;s development programs are focused primarily on developing sustained release products that utilize its Durasert and Verisome technology platforms to deliver approved drugs to treat chronic diseases. The Company&#8217;s strategy includes developing products independently while continuing to leverage its technology platforms through collaborations and license agreements.</div><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; margin-bottom: 0px; margin-top: 13.5pt; text-indent: 0in; line-height: 12pt;"><div style="font-weight:bold;display:inline;">Liquidity </div></div><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; margin-bottom: 0px; margin-top: 6pt; text-indent: 0.79in; line-height: 12pt;">The Company has a history of operating losses and has not had significant recurring cash inflows from revenue. The Company&#8217;s operations have been financed primarily from sales of its equity securities, issuance of debt and a combination of royalty income and other fees received from collaboration partners. In February 2019, the Company refinanced its then existing $20.0&#160;million term loan and made an initial draw of $35.0&#160;million from a new term loan agreement (the &#8220;CRG Loan Agreement&#8221;) with CRG Servicing LLC (&#8220;CRG&#8221;) (see Note 9), resulting in incremental net proceeds of approximately $11.4&#160;million. In addition to total cash and cash equivalents of $43.4&#160;million at March&#160;31, 2019, the Company received net proceeds of $18.6&#160;million on April&#160;1, 2019 from the issuance of common stock (&#8220;Common Stock&#8221;) (excluding approximately $300,000 of additional unpaid share issue costs) (see Note 15). During April 2019, the Company exercised its option to draw an additional $15.0&#160;million under the CRG Loan Agreement and paid a $15.0&#160;million development milestone that was due to the former Icon security holders following the first commercial sale of DEXYCU (see Note 3). At April&#160;30, 2019, the Company had $56.9&#160;million of cash and cash equivalents.</div><div style="margin: 12pt 0in 0.0001pt; text-indent: 0.79in; font-family: &quot;times new roman&quot;, serif; font-size: 10pt;">During the three months ended March&#160;31, 2019, the Company commenced the U.S. launch of its first two commercial products, YUTIQ and DEXYCU. Executing a phased launch approach specifically for DEXYCU, many early patients have been injected at the end of cataract surgery through the Company&#8217;s non-revenue samples program that has facilitated physician training. Overall, early sales of these products have been encouraging, and the Company is optimistic that existing cash and cash equivalents at April&#160;30, 2019 and cash inflows from anticipated YUTIQ and DEXYCU product sales will be sufficient to fund the Company&#8217;s current and planned operations through to the generation of positive cash flow in 2020.</div><div style="margin: 12pt 0in 0.0001pt; text-indent: 0.79in; font-family: &quot;times new roman&quot;, serif; font-size: 10pt;">The Company, however, has no history of direct commercialization of its products and management does not yet have sufficient historical evidence to assert that it is probable that the Company will receive sufficient revenues from its sales of YUTIQ and DEXYCU to fund 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. 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.</div><div style="font-family: 'times new roman', 'serif';font-size: 10pt;margin-bottom: 0;margin-top: 18pt;"><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;"><div style="font-weight:bold;display:inline;">Recently Adopted and Recently Issued Accounting Pronouncements </div></div></div><div style="font-family: 'times new roman', 'serif';font-size: 10pt;margin-bottom: 0;margin-top: 6pt;text-indent: 0.79in;"><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;">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. </div></div><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; margin-bottom: 0px; margin-top: 9pt; text-indent: 0.79in; line-height: 12pt;">In February 2016, the FASB issued Accounting Standards Update (&#8220;ASU&#8221;) No.&#160;2016-02, <div style="font-style:italic;display:inline;;font-style:italic;display:inline;">Leases</div> (<div style="font-style:italic;display:inline;;font-style:italic;display:inline;">Topic 842</div>) (&#8220;ASU 2016-02&#8221;). In July 2018, the FASB issued ASU No.&#160;2018-11, Leases (Topic 842), Targeted Improvements, which contains certain amendments to ASU 2016-02 intended to provide relief in implementing the new standard. The new standard establishes a right-of-use (&#8220;ROU&#8221;) model that requires a lessee to record a ROU asset and a lease liability on the balance sheet for all operating leases, with an exception provided for leases with a duration of one year or less. The Company adopted ASU 2016-02 on January&#160;1, 2019 using the modified retrospective transition approach which, pursuant to ASU 2018-11, allows companies to recognize existing leases at the adoption date without requiring comparable period presentation. Comparative periods are presented in accordance with the previous guidance in Accounting Standards Codification (&#8220;ASC&#8221;) 840, Leases.</div><div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; margin-bottom: 0px; margin-top: 9pt; text-indent: 0.79in; line-height: 12pt;">In adopting the new standard, the Company elected to utilize the available package of practical expedients permitted under the transition guidance within the new standard, which does not require the reassessment of the following: (i)&#160;whether existing or expired arrangements are or contain a lease, (ii)&#160;the lease classification of existing or expired leases, and (iii)&#160;whether previous initial direct costs would qualify for capitalization under the new lease standard. Additionally, the Company elected to combine lease and non-lease components and to exclude leases with a term of 12 months or less. The adoption of this accounting standard resulted in recording operating lease ROU assets for three real estate operating lease arrangements and corresponding operating lease liabilities of $3.5&#160;million and $3.7&#160;million, respectively, as of January&#160;1, 2019. The operating lease assets at adoption were lower than the operating lease liabilities because the balance of the Company&#8217;s deferred rent liabilities at December&#160;31, 2018, which represented lease incentives, was reclassified into operating lease assets. The adoption of the standard did not have a material effect on the Company&#8217;s consolidated statements of operations or consolidated statements of cash flows.<div style="font-family: &quot;times new roman&quot;, serif; font-size: 10pt; color: rgb(0, 0, 0); letter-spacing: 0px; top: 0px;;display:inline;"> </div></div><div style="margin: 9pt 0in 0.0001pt; text-indent: 0.79in; font-family: &quot;times new roman&quot;, serif; font-size: 10pt; line-height: 12pt;">Under Topic 842, the Company determines whether the arrangement is or contains a lease at inception. Operating leases are recognized on the consolidated balance sheets as ROU assets, current portion of lease liabilities and long-term lease liabilities. ROU assets represent the Company&#8217;s right to use an underlying asset for the lease term and lease liabilities represent the Company&#8217;s obligation to make lease payments arising from the lease. Operating lease liabilities and their corresponding ROU assets are recorded based on the present value of lease payments over the expected remaining lease term. For this purpose, the Company considers only payments that are fixed and determinable at the time of commencement. The operating lease ROU assets also include any lease payments made and adjustments for prepayments and lease incentives. The interest rate implicit in lease contracts is typically not readily determinable. As a result, the Company utilized its incremental borrowing rate, which is the rate incurred to borrow on a collateralized basis over a similar term an amount equal to the lease payments in a similar economic environment. Lease terms may include options to extend or terminate the lease when it is reasonably certain that the Company will exercise that option. Lease expense for lease payments is recognized on a straight-line basis over the lease term.</div> <table border="0" style="width:100%; table-layout:fixed;" cellspacing="0" cellpadding="0"><tr><td></td></tr></table>
CY2018Q1 eypt Transaction Costs Allocated To Derivative Liabilities Expensed As Change In Fair Value Of Derivative
TransactionCostsAllocatedToDerivativeLiabilitiesExpensedAsChangeInFairValueOfDerivative
171000
CY2018Q1 eypt Percentage Of Partnering Income Received Payable As Earnout Consideration
PercentageOfPartneringIncomeReceivedPayableAsEarnoutConsideration
0.20

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