2015 Q1 Form 10-K Financial Statement

#000119312515060006 Filed on February 24, 2015

View on sec.gov

Income Statement

Concept 2015 Q1 2014 2013 Q4
Revenue $1.658M $9.843M $1.524M
YoY Change 29.06% -34.39% -9.62%
Cost Of Revenue $24.43M $340.0K $70.00K
YoY Change 34800.0% 70.0% -99.27%
Gross Profit -$22.77M $9.500M $1.450M
YoY Change -1966.39% -35.81% -118.49%
Gross Profit Margin -1373.34% 96.52% 95.14%
Selling, General & Admin $3.530M $11.04M $2.980M
YoY Change 24.73% -2.21% 3.47%
% of Gross Profit 116.21% 205.52%
Research & Development $4.719M $13.66M $2.960M
YoY Change 50.0% 5.67% -68.84%
% of Gross Profit 143.78% 204.14%
Depreciation & Amortization $40.00K $160.0K $40.00K
YoY Change 0.0% 14.29% 0.0%
% of Gross Profit 1.68% 2.76%
Operating Expenses $4.719M $13.66M $5.940M
YoY Change 50.0% 5.67% -37.47%
Operating Profit -$31.02M -$15.86M -$4.483M
YoY Change 552.64% 68.45% -74.15%
Interest Expense $866.9K $3.749M $290.0K
YoY Change -8.84% -2.41% -72.64%
% of Operating Profit
Other Income/Expense, Net -$826.7K -$2.866M
YoY Change 1.98% -1.35%
Pretax Income -$31.85M -$18.73M -$4.200M
YoY Change 472.84% 52.03% -66.05%
Income Tax $0.00
% Of Pretax Income
Net Earnings -$31.85M -$18.73M -$4.198M
YoY Change 472.4% 52.0% -66.07%
Net Earnings / Revenue -1920.87% -190.28% -275.44%
Basic Earnings Per Share
Diluted Earnings Per Share -$1.475M -$1.090M -$245.2K
COMMON SHARES
Basic Shares Outstanding 103.2M shares 85.80M shares
Diluted Shares Outstanding

Balance Sheet

Concept 2015 Q1 2014 2013 Q4
SHORT-TERM ASSETS
Cash & Short-Term Investments $100.0M $49.80M $58.20M
YoY Change 73.01% -14.43% 4.86%
Cash & Equivalents $23.47M $7.700M $9.591M
Short-Term Investments $76.50M $42.00M $48.60M
Other Short-Term Assets $800.0K $500.0K $500.0K
YoY Change 60.0% 0.0% 25.0%
Inventory
Prepaid Expenses
Receivables $1.769M $2.000M $1.477M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $102.6M $52.20M $60.17M
YoY Change 71.93% -13.29% 5.83%
LONG-TERM ASSETS
Property, Plant & Equipment $364.0K $400.0K $445.7K
YoY Change -10.92% 0.0% 2.65%
Goodwill $8.982M $8.982M
YoY Change 0.0% 0.0%
Intangibles
YoY Change
Long-Term Investments $7.200M $800.0K $10.70M
YoY Change 18.03% -92.52% 234.38%
Other Assets $60.87K $200.0K $104.0K
YoY Change -33.23% -33.33% -34.09%
Total Long-Term Assets $16.76M $10.40M $20.42M
YoY Change 6.62% -49.02% 58.13%
TOTAL ASSETS
Total Short-Term Assets $102.6M $52.20M $60.17M
Total Long-Term Assets $16.76M $10.40M $20.42M
Total Assets $119.3M $62.60M $80.59M
YoY Change 58.31% -22.33% 15.51%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $2.782M $2.300M $2.037M
YoY Change 9.33% 15.0% -18.66%
Accrued Expenses $1.365M $2.000M $1.911M
YoY Change 9.5% 5.26% 29.63%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $5.584M $5.700M $2.610M
YoY Change 64.61% 119.23%
Total Short-Term Liabilities $9.731M $10.10M $6.559M
YoY Change 24.62% 53.03% 64.84%
LONG-TERM LIABILITIES
Long-Term Debt $21.80M $22.60M $27.95M
YoY Change -18.74% -19.0% -6.35%
Other Long-Term Liabilities $168.3K $200.0K $196.7K
YoY Change -13.56% -77.78% 0.93%
Total Long-Term Liabilities $21.96M $22.80M $28.14M
YoY Change -18.71% -20.83% -6.3%
TOTAL LIABILITIES
Total Short-Term Liabilities $9.731M $10.10M $6.559M
Total Long-Term Liabilities $21.96M $22.80M $28.14M
Total Liabilities $31.69M $32.80M $35.42M
YoY Change -8.99% -7.34% -0.24%
SHAREHOLDERS EQUITY
Retained Earnings -$811.4M -$760.8M
YoY Change 5.87% 1.65%
Common Stock $900.5M $870.8K
YoY Change 103208.08% 7.42%
Preferred Stock
YoY Change
Treasury Stock (at cost) $1.524M $1.524M
YoY Change 0.0% 70.99%
Treasury Stock Shares 1.223M shares 1.223M shares
Shareholders Equity $87.62M $29.80M $45.17M
YoY Change
Total Liabilities & Shareholders Equity $119.3M $62.60M $80.59M
YoY Change 58.31% -22.33% 15.51%

Cashflow Statement

Concept 2015 Q1 2014 2013 Q4
OPERATING ACTIVITIES
Net Income -$31.85M -$18.73M -$4.198M
YoY Change 472.4% 52.0% -66.07%
Depreciation, Depletion And Amortization $40.00K $160.0K $40.00K
YoY Change 0.0% 14.29% 0.0%
Cash From Operating Activities -$7.760M -$16.81M -$5.510M
YoY Change 46.14% 76.24% -59.81%
INVESTING ACTIVITIES
Capital Expenditures $14.96K $92.00K -$20.00K
YoY Change -39.87% -66.67%
Acquisitions
YoY Change
Other Investing Activities -$40.57M $16.37M -$5.910M
YoY Change -1279.36% -221.62% -49.4%
Cash From Investing Activities -$40.58M $16.27M -$5.930M
YoY Change -1279.65% -219.5% -49.45%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $64.60M $0.00
YoY Change 35703.16% -100.0%
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 64.06M -$1.304M 7.250M
YoY Change 35488.89% -106.52% -76.14%
NET CHANGE
Cash From Operating Activities -7.760M -$16.81M -5.510M
Cash From Investing Activities -40.58M $16.27M -5.930M
Cash From Financing Activities 64.06M -$1.304M 7.250M
Net Change In Cash 15.72M -$1.844M -4.190M
YoY Change -1030.18% -41.58% -184.65%
FREE CASH FLOW
Cash From Operating Activities -$7.760M -$16.81M -$5.510M
Capital Expenditures $14.96K $92.00K -$20.00K
Free Cash Flow -$7.775M -$16.91M -$5.490M
YoY Change 46.42% 74.41% -59.78%

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The Company has agreed to make each of the following one-time payments to Debiopharm (i) $3,000,000 within 30 days after the first dosing of the first patient in the first Phase 3 clinical trial of Debio 0932; and (ii) $10,000,000 within 30 days after receipt of the first marketing approval for Debio 0932 in the United States of America or any specified major European market (whichever occurs first);
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10-K
CY2014 dei Entity Registrant Name
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CURIS INC
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CY2014 dei Trading Symbol
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CRIS
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CY2014 us-gaap Nature Of Operations
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<div> <table style="BORDER-COLLAPSE: collapse" cellspacing="0" cellpadding="0" width="100%" border="0"> <tr> <td valign="top" width="4%" align="left"><font style="FONT-FAMILY: Times New Roman" size="2"><b>(1)</b></font></td> <td valign="top" align="left"><font style="FONT-FAMILY: Times New Roman" size="2"><b>OPERATIONS</b></font></td> </tr> </table> <!-- xbrl,body --> <p style="MARGIN-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">Curis, Inc. is a biotechnology company seeking to develop and commercialize innovative drug candidates for the treatment of human cancers. As used throughout these consolidated financial statements, the term &#x201C;the Company&#x201D; refers to the business of Curis, Inc. and its wholly owned subsidiaries, except where the context otherwise requires, and the term &#x201C;Curis&#x201D; refers to Curis, Inc.</font></p> <p style="MARGIN-BOTTOM: 0px; PADDING-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">The Company conducts its research and development programs both internally and through strategic collaborations. The Company is leveraging its experience in targeting signaling pathways to develop drug candidates including CUDC-907, a dual histone deacetylase, or HDAC and phosphoinositide-3 kinase, or PI3K, inhibitor, CUDC-427, a small molecule antagonist of the inhibitor of apoptosis, or IAP, proteins, and CUDC-305, a Heat Shock Protein 90, or HSP90, inhibitor. Erivedge<font style="FONT-FAMILY: Times New Roman" size="1"><sup style="VERTICAL-ALIGN: baseline; POSITION: relative; BOTTOM: 0.8ex">&#xAE;</sup></font>, the first and only approved medicine for the treatment of advanced basal cell carcinoma, or BCC, is being commercialized by F. Hoffmann-La Roche Ltd., or Roche, and Genentech Inc., or Genentech, a member of the Roche Group, under a collaboration agreement between Curis and Genentech.</font></p> <p style="MARGIN-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">In January 2015, the Company entered into an exclusive collaboration agreement focused on immuno-oncology and selected precision oncology targets with Aurigene Discovery Technologies Limited, or Aurigene, a specialized, discovery stage biotechnology company developing novel therapies to treat cancer and inflammatory diseases. The collaboration provides for inclusion of multiple programs, with Curis having the option to exclusively license compounds once a development candidate is nominated within each respective program. The first two programs under the collaboration are orally-available small molecule antagonists of programmed death ligand-1 (PD-L1) in the immuno-oncology field and orally-available small molecule inhibitors of Interleukin-1 receptor-associated kinase 4 (IRAK4) in the precision oncology field.</font></p> <p style="MARGIN-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">The Company operates in a single reportable segment, which is the research and development of innovative cancer therapeutics. The Company expects that any products that are successfully developed and commercialized would be used in the health care industry and would be regulated in the United&#xA0;States by the Food and Drug Administration, or FDA, and in overseas markets by similar regulatory authorities.</font></p> <p style="MARGIN-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">The Company is subject to risks common to companies in the biotechnology industry as well as risk factors that are specific to the Company&#x2019;s business, including, but not limited to: the Company&#x2019;s reliance on Genentech and Roche to successfully commercialize Erivedge in the approved indication of advanced BCC and to progress it&#x2019;s clinical development in indications other than BCC; the Company&#x2019;s reliance on Aurigene to successfully discover and preclinically develop drug candidates under the parties&#x2019; collaboration agreement, the Company&#x2019;s ability to advance and expand its research and development programs; the Company&#x2019;s ability to obtain adequate financing to fund its operations; the ability of the Company&#x2019;s wholly owned subsidiary, Curis Royalty, LLC, or Curis Royalty, to satisfy the terms of its loan agreement with BioPharma Secured Debt Fund II Sub, S.&#xE0; r.l., a Luxembourg limited liability company managed by Pharmakon Advisors, or BioPharma-II; the Company&#x2019;s ability to obtain and maintain necessary intellectual property protection; development by the Company&#x2019;s competitors of new or better technological innovations; dependence on key personnel; the Company&#x2019;s ability to comply with regulatory requirements; and the Company&#x2019;s ability to execute on its overall business strategies.</font></p> <p style="MARGIN-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">The Company&#x2019;s future operating results will largely depend on the magnitude of payments that it receives and makes under its current and potential future corporate collaborators and the progress of drug candidates currently in its development pipeline. The results of the Company&#x2019;s operations will vary significantly from year to year and quarter to quarter and depend on a number of factors, including, but not limited to: Roche and Genentech&#x2019;s ability to successfully commercialize Erivedge; positive results in Genentech&#x2019;s ongoing clinical trials; Aurigene&#x2019;s ability to successfully discover and develop preclinically programs under the Company&#x2019;s collaboration with Aurigene, as well as the Company&#x2019;s decision to exclusively license and further develop programs under this collaboration; the timing, outcome and cost of the Company&#x2019;s preclinical studies and clinical trials for its drug candidates; and the Company&#x2019;s ability to successfully enter into one or more material outlicensing or collaboration agreements for its proprietary drug candidates.</font></p> <p style="MARGIN-BOTTOM: 0px; MARGIN-LEFT: 8%; MARGIN-TOP: 6px"> <font style="FONT-FAMILY: Times New Roman" size="2">The Company anticipates that existing cash, cash equivalents and investments at December&#xA0;31, 2014 should enable it to maintain current and planned operations into 2016. The Company&#x2019;s ability to continue funding its planned operations beyond this period is dependent upon, among other things, the success of its collaborations with Genentech and the Leukemia&#xA0;&amp; Lymphoma Society, or LLS, including its receipt of additional contingent cash payments under these collaborations; its ability to control expenses and its ability to raise additional funds through equity or debt financings, new collaborations or other sources of financing. The Company may not be able to successfully raise additional funds or enter into or continue any corporate collaborations and the timing, amount and likelihood of the Company receiving payments under such collaborations is highly uncertain. If the Company is unable to obtain adequate financing, the Company may be required to reduce or delay spending on its research and/or development programs.</font></p> </div>
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<div> <table style="FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; BORDER-COLLAPSE: collapse" cellspacing="0" cellpadding="0" width="100%" border="0"> <tr> <td width="4%">&#xA0;</td> <td valign="top" width="4%" align="left">(a)</td> <td valign="top" align="left">USE OF ESTIMATES</td> </tr> </table> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-LEFT: 8%; MARGIN-TOP: 6pt"> The preparation of the Company&#x2019;s consolidated financial statements in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the reported amounts and disclosure of revenue, expenses and certain assets and liabilities at the balance sheet date. Such estimates include revenue recognition, including estimates of the performance obligations under the Company&#x2019;s collaboration agreements; the estimated repayment term of the Company&#x2019;s debt and related short- and long-term classification; the collectibility of receivables; the carrying value of property and equipment and intangible assets; the assumptions used in the Company&#x2019;s valuation of stock-based compensation and the value of certain investments and liabilities, including our warrant liability. Actual results may differ from such estimates.</p> </div>
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2014-12-31
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2014
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FY
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CY2014 us-gaap Concentration Risk Credit Risk
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<div> <table style="FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; BORDER-COLLAPSE: collapse" cellspacing="0" cellpadding="0" width="100%" border="0"> <tr> <td width="4%">&#xA0;</td> <td valign="top" width="4%" align="left">(m)</td> <td valign="top" align="left">CONCENTRATION OF RISK</td> </tr> </table> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-LEFT: 8%; MARGIN-TOP: 6pt"> Financial instruments, which potentially subject the Company to concentrations of credit risk, consist principally of cash and cash equivalents, short- and long-term investments. The Company invests directly in commercial paper of financial institutions and corporations with A-/Aa3 or better long-term ratings and A-1/P-1 short term debt ratings and U.S. Treasury securities. The Company maintains deposits in federally insured financial institutions in excess of federally insured limits. Management believes that the Company is not exposed to significant credit risk due to the financial position of the depository institutions in which those deposits are held. The Company&#x2019;s credit risk related to investments is reduced as a result of the Company&#x2019;s policy to limit the amount invested in any one issue.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-LEFT: 8%; MARGIN-TOP: 6pt"> The Company&#x2019;s accounts receivable at December&#xA0;31, 2014, represents amounts due from collaborators, primarily for royalties earned on sales of Erivedge by Genentech and Roche.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-LEFT: 8%; MARGIN-TOP: 6pt"> The Company relies on third parties to supply certain raw materials necessary to produce its drug candidates, including CUDC-907 and CUDC-427, for preclinical studies and clinical trials. There are a small number of suppliers for certain raw materials that the Company uses to manufacture its drug candidates.</p> </div>
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