2017 Q1 Form 10-K Financial Statement

#000156459017005798 Filed on March 31, 2017

View on sec.gov

Income Statement

Concept 2017 Q1 2016 Q4 2016 Q3
Revenue $1.192M $766.0K $0.00
YoY Change
Cost Of Revenue
YoY Change
Gross Profit
YoY Change
Gross Profit Margin
Selling, General & Admin $200.0K $190.0K $10.00K
YoY Change -93.59% -93.38% -99.66%
% of Gross Profit
Research & Development $4.651M $3.184M $7.089M
YoY Change -52.4% -55.51% -0.04%
% of Gross Profit
Depreciation & Amortization $66.00K
YoY Change 8.2%
% of Gross Profit
Operating Expenses $6.738M $5.274M $5.963K
YoY Change -47.72% -47.41% -99.94%
Operating Profit -$5.963K
YoY Change
Interest Expense $797.0K $457.0K $521.0K
YoY Change 20.21% -33.67% 2.36%
% of Operating Profit
Other Income/Expense, Net -$793.0K -$437.0K -$496.0K
YoY Change 21.25% -36.39% -1.78%
Pretax Income -$240.0K -$200.0K -$20.00K
YoY Change -98.23% -98.13% -99.81%
Income Tax
% Of Pretax Income
Net Earnings -$6.339M -$4.945M -$9.959M
YoY Change -53.19% -53.85% -5.61%
Net Earnings / Revenue -531.8% -645.56%
Basic Earnings Per Share
Diluted Earnings Per Share -$263.7K -$227.3K -$24.39K
COMMON SHARES
Basic Shares Outstanding 29.02M 27.44M 820.0K
Diluted Shares Outstanding 830.5K

Balance Sheet

Concept 2017 Q1 2016 Q4 2016 Q3
SHORT-TERM ASSETS
Cash & Short-Term Investments $12.03M $40.00K $38.06M
YoY Change -80.12% -99.95% -50.97%
Cash & Equivalents $94.02K $44.61K $14.07K
Short-Term Investments
Other Short-Term Assets $2.450M
YoY Change
Inventory
Prepaid Expenses
Receivables $1.139M $823.0K $1.150M
Other Receivables $0.00 $0.00
Total Short-Term Assets $15.61M $36.79M $39.20M
YoY Change -74.86% -52.41% -50.47%
LONG-TERM ASSETS
Property, Plant & Equipment $114.0K $668.0K $700.0K
YoY Change -83.48% 15.97% 100.0%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $230.0K $12.68K $230.0K
YoY Change 0.0% -96.35% -62.3%
Total Long-Term Assets $344.0K $898.0K $930.0K
YoY Change -62.61% -2.71% -4.12%
TOTAL ASSETS
Total Short-Term Assets $15.61M $36.79M $39.20M
Total Long-Term Assets $344.0K $898.0K $930.0K
Total Assets $15.95M $37.69M $40.13M
YoY Change -74.69% -51.82% -49.91%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $644.0K $1.446M $1.780M
YoY Change -70.59% -35.04% -17.59%
Accrued Expenses $3.538M $4.611M $5.920M
YoY Change -36.37% -28.61% 34.55%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $700.0K $0.00
YoY Change
Long-Term Debt Due $0.00 $8.190M
YoY Change -100.0% 103.23%
Total Short-Term Liabilities $6.682M $755.2K $15.89M
YoY Change -57.11% -95.38% 49.76%
LONG-TERM LIABILITIES
Long-Term Debt $0.00 $0.00 $6.550M
YoY Change -100.0% -100.0% -37.8%
Other Long-Term Liabilities $162.0K $1.206M $1.080M
YoY Change -78.96% 154.97% 217.65%
Total Long-Term Liabilities $1.530M $7.638M $7.630M
YoY Change -86.65% -41.89% -29.81%
TOTAL LIABILITIES
Total Short-Term Liabilities $6.682M $755.2K $15.89M
Total Long-Term Liabilities $1.530M $7.638M $7.630M
Total Liabilities $8.212M $755.2K $23.51M
YoY Change -69.63% -97.44% 9.5%
SHAREHOLDERS EQUITY
Retained Earnings -$207.0M -$727.8K
YoY Change -99.55%
Common Stock $214.8M $17.21K
YoY Change -99.99%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $7.741M -$710.6K $16.62M
YoY Change
Total Liabilities & Shareholders Equity $15.95M $44.61K $40.13M
YoY Change -74.69% -99.94% -49.91%

Cashflow Statement

Concept 2017 Q1 2016 Q4 2016 Q3
OPERATING ACTIVITIES
Net Income -$6.339M -$4.945M -$9.959M
YoY Change -53.19% -53.85% -5.61%
Depreciation, Depletion And Amortization $66.00K
YoY Change 8.2%
Cash From Operating Activities -$50.00K -$160.0K $24.29M
YoY Change -99.62% -98.05% -404.77%
INVESTING ACTIVITIES
Capital Expenditures
YoY Change
Acquisitions
YoY Change
Other Investing Activities $0.00
YoY Change -100.0%
Cash From Investing Activities $0.00
YoY Change -100.0%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $62.00K
YoY Change 51.22%
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 100.0K 200.0K 3.860M
YoY Change -105.29% -96.97% 2473.33%
NET CHANGE
Cash From Operating Activities -50.00K -160.0K 24.29M
Cash From Investing Activities 0.000
Cash From Financing Activities 100.0K 200.0K 3.860M
Net Change In Cash 50.00K 40.00K 28.15M
YoY Change -100.32% -102.33% -458.6%
FREE CASH FLOW
Cash From Operating Activities -$50.00K -$160.0K $24.29M
Capital Expenditures
Free Cash Flow
YoY Change

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<div> <div align="left"> <table border="0" cellspacing="0" cellpadding="0" style="border-collapse:collapse; width:100%;"> <tr> <td valign="top" style="width:4.54%;white-space:nowrap"> <p style="margin-bottom:0pt;margin-top:12pt;font-family:Times New Roman;font-size:10pt;font-weight:bold;">1.</p></td> <td valign="top"> <p style="margin-bottom:0pt;margin-top:12pt;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">NATURE OF BUSINESS AND OPERATIONS </p></td></tr></table></div> <p style="margin-bottom:0pt;margin-top:12pt;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;text-indent:4.54%;">Nature of Business<font style="font-weight:normal;"> &#8212; Cerulean Pharma Inc. (the &#8220;Company&#8221;) was incorporated on November&#160;28, 2005, as a Delaware corporation and is located in Waltham, Massachusetts. The Company was formed to develop novel, nanotechnology-based therapeutics in the areas of oncology and other diseases. In 2013, the Company formed a wholly owned subsidiary, Cerulean Pharma Australia Pty&#160;Ltd as an Australian-based proprietary limited company to perform clinical activities in Australia. </font></p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company's operations have consisted primarily of raising capital, product research and development, and initial market development.</p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company has not generated any revenue related to its primary business purpose to date and is subject to a number of risks common to other development stage life science companies, including dependence on key individuals, competition from other companies, the need for development of commercially viable products, and the need to obtain adequate additional financing to fund the development of product candidates. The Company is also subject to a number of risks similar to other companies in the industry, including rapid technological change, regulatory approval of products, uncertainty of market acceptance of products, competition from substitute products and larger companies, the need to obtain additional financing, compliance with government regulations, protection of proprietary technology, dependence on third parties, product liability and dependence on key individuals.</p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company has an accumulated deficit of $200.7 million at December 31, 2016. The Company has financed its operations primarily through private placements of its preferred stock, proceeds from borrowings, an initial public offering completed in 2014 and a follow-on offering completed in 2015.&nbsp;&nbsp;In October 2016 the Company entered into a collaboration with Novartis Institutes for BioMedical Research, Inc. (&#8220;Novartis&#8221;) to develop nanoparticle-drug conjugates combining the Company&#8217;s proprietary Dynamic Tumor Targeting technology with Novartis&#8217; proprietary compounds.&nbsp;&nbsp;Under this collaboration the Company received important funding to support its research program.&nbsp;&nbsp;The Company has not completed development of any product candidate and has devoted substantially all of its financial resources and efforts to research and development, including preclinical and clinical development. Accordingly, the Company will continue to depend on its ability to raise capital through equity and debt issuances and/or through strategic partnerships. The Company expects to continue to incur significant expenses and increasing operating losses for at least several years.</p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">As of December 31, 2016, the Company had cash and cash equivalents of $35.0 million.&nbsp;&nbsp;The Company has no other sources of significant liquidity in place as of December 31, 2016.&nbsp;&nbsp;The Company expects that its existing cash and cash equivalents will fund its operations into the second half of 2017 based on the Company&#8217;s 2017 operating plan.&nbsp;&nbsp;The Company has undertaken a strategic review of potential financing alternatives such as the sale of the company, a merger, a business combination, a strategic investment into the company, or a sale, license or disposition of assets of the Company.&nbsp;&nbsp;If the Company is unable to obtain additional funding on a timely basis, it may be required to curtail or terminate research and development activities under its collaboration agreement with Novartis, or to scale back, suspend or terminate its business operations.</p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">As more fully discussed in Note 17 Subsequent Events, pursuant to management&#8217;s plans, in March 2017 the Company entered into a series of transactions including the payoff of its note payable to Hercules Capital for $12.4 million.&nbsp;&nbsp;The Company sold and assigned all of its right, title and interest in and to its clinical product candidates CRLX101 and CRLX301 for proceeds of $1.5 million.&nbsp;&nbsp;The Company also <font style="Background-color:#FFFFFF;">agreed to sell and assign to Novartis all of its right, title and interest in and to the patent rights, know-how and third-party license agreements relating to </font>its Dynamic Tumor Targeting Platform technology for proceeds of $6.0 million, whereby the proceeds from this asset sale are to be received upon closing of the transaction.&nbsp;&nbsp;The Company also entered into a Stock Purchase Agreement with Dar&#233; Biosciences, Inc., which if approved by the shareholders, will be consummated by an exchange of common stock shares and no cash consideration paid or received.</p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">With exception of the payoff of the note payable and the sale of the clinical product candidates, these transactions are subject to certain closing conditions.&nbsp;&nbsp;There can be no assurances that these transactions will be consummated prior to the exhaustion of the Company&#8217;s cash and cash equivalent resources, if at all.</p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The foregoing matters give rise to substantial doubt about the Company&#8217;s ability to continue as a going concern. The accompanying financial statements do not include any adjustments that might result from the outcome of this uncertainty. </p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;">&nbsp;</p></div>
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<div> <p style="margin-bottom:0pt;margin-top:12pt;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;text-indent:4.54%;">Use of Estimates<font style="font-weight:normal;"> &#8212; </font><font style="color:#000000;font-weight:normal;">The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period.</font></p> <p style="Background-color:#FFFFFF;margin-top:12pt;margin-bottom:0pt;text-indent:4.54%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">On an ongoing basis, the Company's management evaluates its estimates, including estimates related to clinical trial accruals, stock-based compensation expense, and reported amounts of revenues and expenses during the reported period. The Company bases its estimates on historical experience and other market-specific or other relevant assumptions that it believes to be reasonable under the circumstances. Although the Company regularly assesses these estimates, actual results could differ from those estimates. Changes in estimates are recorded in the period in which they become known.</p></div>
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<div> <p style="margin-bottom:0pt;margin-top:12pt;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;text-indent:4.54%;">Concentrations of Credit Risk<font style="font-weight:normal;"> &#8212; Financial instruments that subject the Company to significant concentrations of credit risk consist primarily of cash and cash equivalents. Substantially all of the Company&#8217;s cash and cash equivalents are held at one financial institution that management believes to be of high-credit quality. Deposits with this financial institution may exceed the amount of insurance provided on such deposits; however these deposits may be redeemed upon demand and, therefore, bear minimal risk. </font></p></div>
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<div> <p style="margin-bottom:0pt;margin-top:12pt;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;text-indent:4.54%;">Guarantees and Indemnification<font style="font-weight:normal;"> &#8212;&#160;As permitted under Delaware law, the Company indemnifies its officers and directors employees for certain events or occurrences while the officer or director is, or was serving at the Company&#8217;s request in such a capacity.&#160;The term of the indemnification is for the officer&#8217;s or director&#8217;s lifetime. During the year ended December 31, 2016, the Company </font><font style="font-weight:normal;">did not experience any losses related to these indemnification obligations. The Company does not expect significant claims related to these indemnification obligations, and consequently, has concluded the fair value of these obligations is not material. Accordingly, as of December 31, 2016 no amounts have been accrued related to such indemnification provisions.</font></p></div>
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