$CRIS
CURIS INC Stock $cris

$cris Overview Financials Valuation SEC Filings Company Website

2018 Q3 Form 10-Q Financial Statement

#000110820518000013 Filed on August 02, 2018

Income Statement

Concept	2018 Q3	2018 Q2	2017 Q2
Revenue	$2.847M	$2.358M	$2.061M
YoY Change	16.49%	14.41%	22.68%
Cost Of Revenue	$150.0K	$130.0K	$100.0K
YoY Change	25.0%	30.0%	0.0%
Gross Profit	$2.690M	$2.220M	$1.970M
YoY Change	15.95%	12.69%	23.9%
Gross Profit Margin	94.49%	94.15%	95.58%
Selling, General & Admin	$4.130M	$3.630M	$3.820M
YoY Change	21.11%	-4.97%	11.05%
% of Gross Profit	153.53%	163.51%	193.91%
Research & Development	$4.983M	$6.451M	$11.26M
YoY Change	-62.76%	-42.68%	27.58%
% of Gross Profit	185.24%	290.59%	571.32%
Depreciation & Amortization	$40.00K	$50.00K	$50.00K
YoY Change	-42.86%	0.0%	-16.67%
% of Gross Profit	1.49%	2.25%	2.54%
Operating Expenses	$4.983M	$6.451M	$11.26M
YoY Change	-62.76%	-42.68%	27.58%
Operating Profit	-$6.417M	-$7.860M	-$13.11M
YoY Change	-55.66%	-40.04%	22.74%
Interest Expense	$972.0K	$993.0K	$1.119M
YoY Change	-12.35%	-11.26%	53.5%
% of Operating Profit
Other Income/Expense, Net	-$806.0K	-$804.0K	-$981.0K
YoY Change	-18.26%	-18.04%	60.82%
Pretax Income	-$7.220M	-$8.660M	-$14.09M
YoY Change	-53.3%	-38.54%	24.8%
Income Tax
% Of Pretax Income
Net Earnings	-$7.223M	-$8.664M	-$14.09M
YoY Change	-53.27%	-38.51%	24.8%
Net Earnings / Revenue	-253.71%	-367.43%	-683.65%
Basic Earnings Per Share
Diluted Earnings Per Share	-$217.7K	-$261.3K	-$489.9K
COMMON SHARES
Basic Shares Outstanding	33.18M shares	165.6M shares	143.8M shares
Diluted Shares Outstanding

Balance Sheet

Concept	2018 Q3	2018 Q2	2017 Q2
SHORT-TERM ASSETS
Cash & Short-Term Investments	$30.80M	$40.40M	$51.00M
YoY Change	-55.49%	-20.78%	-17.34%
Cash & Equivalents	$25.56M	$30.47M	$26.68M
Short-Term Investments	$5.300M	$10.00M	$24.40M
Other Short-Term Assets	$1.100M	$800.0K	$1.200M
YoY Change	-21.43%	-33.33%	20.0%
Inventory
Prepaid Expenses
Receivables	$2.855M	$2.505M	$2.231M
Other Receivables	$0.00	$0.00	$0.00
Total Short-Term Assets	$34.82M	$43.70M	$54.38M
YoY Change	-52.31%	-19.64%	-15.7%
LONG-TERM ASSETS
Property, Plant & Equipment	$312.0K	$352.0K	$426.0K
YoY Change	-18.75%	-17.37%	-5.54%
Goodwill	$8.982M	$8.982M	$8.982M
YoY Change	0.0%	0.0%	0.0%
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets	$3.000K	$3.000K	$3.000K
YoY Change	0.0%	0.0%	0.0%
Total Long-Term Assets	$9.450M	$9.490M	$9.411M
YoY Change	0.86%	0.84%	-1.86%
TOTAL ASSETS
Total Short-Term Assets	$34.82M	$43.70M	$54.38M
Total Long-Term Assets	$9.450M	$9.490M	$9.411M
Total Assets	$44.27M	$53.19M	$63.80M
YoY Change	-46.26%	-16.62%	-13.91%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable	$3.008M	$4.275M	$8.202M
YoY Change	-53.86%	-47.88%	111.66%
Accrued Expenses	$3.300M	$3.263M	$2.480M
YoY Change	30.54%	31.57%	23.26%
Deferred Revenue
YoY Change
Short-Term Debt	$0.00	$0.00	$0.00
YoY Change
Long-Term Debt Due	$6.900M	$6.965M	$3.931M
YoY Change	34.87%	77.18%	-27.59%
Total Short-Term Liabilities	$13.23M	$14.50M	$14.61M
YoY Change	-6.57%	-0.75%	29.14%
LONG-TERM LIABILITIES
Long-Term Debt	$30.20M	$31.53M	$39.95M
YoY Change	-20.02%	-21.08%	141.57%
Other Long-Term Liabilities	$29.00K	$46.00K	$0.00
YoY Change			-100.0%
Total Long-Term Liabilities	$30.23M	$31.58M	$39.95M
YoY Change	-19.94%	-20.96%	140.67%
TOTAL LIABILITIES
Total Short-Term Liabilities	$13.23M	$14.50M	$14.61M
Total Long-Term Liabilities	$30.23M	$31.58M	$39.95M
Total Liabilities	$43.48M	$46.08M	$54.57M
YoY Change	-16.25%	-15.55%	95.46%
SHAREHOLDERS EQUITY
Retained Earnings	-$978.9M	-$971.7M	-$928.8M
YoY Change	3.67%	4.62%	8.09%
Common Stock	$979.7M	$978.8M	$939.5M
YoY Change	0.36%	4.18%	3.6%
Preferred Stock
YoY Change
Treasury Stock (at cost)	$0.00	$0.00	$1.524M
YoY Change	-100.0%	-100.0%	0.0%
Treasury Stock Shares	0.000 shares	0.000 shares	1.223M shares
Shareholders Equity	$782.0K	$7.110M	$9.228M
YoY Change
Total Liabilities & Shareholders Equity	$44.27M	$53.19M	$63.80M
YoY Change	-46.26%	-16.62%	-13.91%

Cashflow Statement

Concept	2018 Q3	2018 Q2	2017 Q2
OPERATING ACTIVITIES
Net Income	-$7.223M	-$8.664M	-$14.09M
YoY Change	-53.27%	-38.51%	24.8%
Depreciation, Depletion And Amortization	$40.00K	$50.00K	$50.00K
YoY Change	-42.86%	0.0%	-16.67%
Cash From Operating Activities	-$8.230M	-$6.940M	-$9.220M
YoY Change	-50.06%	-24.73%	-15.02%
INVESTING ACTIVITIES
Capital Expenditures	-$10.00K	$0.00	-$80.00K
YoY Change	-50.0%	-100.0%	-68.0%
Acquisitions
YoY Change
Other Investing Activities	$4.690M	$13.82M	-$5.940M
YoY Change	-5.44%	-332.66%	-210.61%
Cash From Investing Activities	$4.680M	$13.81M	-$6.010M
YoY Change	-5.07%	-329.78%	-217.15%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities	-1.360M	-1.140M	-510.0K
YoY Change	-103.92%	123.53%	59.38%
NET CHANGE
Cash From Operating Activities	-8.230M	-6.940M	-9.220M
Cash From Investing Activities	4.680M	13.81M	-6.010M
Cash From Financing Activities	-1.360M	-1.140M	-510.0K
Net Change In Cash	-4.910M	5.730M	-15.74M
YoY Change	-121.2%	-136.4%	160.6%
FREE CASH FLOW
Cash From Operating Activities	-$8.230M	-$6.940M	-$9.220M
Capital Expenditures	-$10.00K	$0.00	-$80.00K
Free Cash Flow	-$8.220M	-$6.940M	-$9.140M
YoY Change	-50.06%	-24.07%	-13.77%

Facts In Submission

Frame	Concept Type	Concept / XBRL Key	Value	Unit
	dei	Document Type DocumentType	10-Q
	dei	Entity Central Index Key EntityCentralIndexKey	0001108205
CY2018Q3	dei	Entity Common Stock Shares Outstanding EntityCommonStockSharesOutstanding	33181146	shares
	dei	Entity Filer Category EntityFilerCategory	Accelerated Filer
	dei	Entity Registrant Name EntityRegistrantName	CURIS INC
CY2017Q1	cris	Cash Distribution Paidto Parent Company CashDistributionPaidtoParentCompany	26600000	USD
CY2017Q1	cris	Cash Distribution Paidto Parent Company CashDistributionPaidtoParentCompany	26600000	USD
	cris	Collaboration Agreement Exclusivity Payment CollaborationAgreementExclusivityPayment	10000000	USD
CY2015Q1	cris	Collaborative Arrangement Numberof Optional Additional Terms CollaborativeArrangementNumberofOptionalAdditionalTerms	3	term
CY2015Q1	cris	Collaborative Arrangement Option Fees Numberof Payments CollaborativeArrangementOptionFeesNumberofPayments	2	payment
CY2015Q1	cris	Collaborative Arrangement Option Fees Total CollaborativeArrangementOptionFeesTotal	7500000	USD
CY2015Q1	cris	Collaborative Arrangement Optional Additional Term CollaborativeArrangementOptionalAdditionalTerm	P1Y
	cris	Increase Decrease In Equity Issuance Cost Payable IncreaseDecreaseInEquityIssuanceCostPayable	0	USD
	cris	Increase Decrease In Equity Issuance Cost Payable IncreaseDecreaseInEquityIssuanceCostPayable	8000	USD
	cris	Share Based Compensation Plans ShareBasedCompensationPlans	2	plan
CY2018Q2	cris	Treasury Stock Shares Acquiredto Date TreasuryStockSharesAcquiredtoDate	244569	shares
CY2018Q2	cris	Treasury Stock Value Acquiredto Date Cost Method TreasuryStockValueAcquiredtoDateCostMethod	1500000	USD
	dei	Amendment Flag AmendmentFlag	false
	dei	Current Fiscal Year End Date CurrentFiscalYearEndDate	--12-31
	dei	Document Fiscal Period Focus DocumentFiscalPeriodFocus	Q2
	dei	Document Fiscal Year Focus DocumentFiscalYearFocus	2018
	dei	Document Period End Date DocumentPeriodEndDate	2018-06-30
	dei	Trading Symbol TradingSymbol	CRIS
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CY2018Q2	us-gaap	Accounts Payable Current AccountsPayableCurrent	4275000	USD
CY2017Q4	us-gaap	Accounts Receivable Net Current AccountsReceivableNetCurrent	3073000	USD
CY2018Q2	us-gaap	Accounts Receivable Net Current AccountsReceivableNetCurrent	2505000	USD
	us-gaap	Accretion Amortization Of Discounts And Premiums Investments AccretionAmortizationOfDiscountsAndPremiumsInvestments	49000	USD
	us-gaap	Accretion Amortization Of Discounts And Premiums Investments AccretionAmortizationOfDiscountsAndPremiumsInvestments	128000	USD
CY2017Q4	us-gaap	Accrued Liabilities Current AccruedLiabilitiesCurrent	2793000	USD
CY2018Q2	us-gaap	Accrued Liabilities Current AccruedLiabilitiesCurrent	3263000	USD
CY2017Q4	us-gaap	Accrued Professional Fees Current AccruedProfessionalFeesCurrent	148000	USD
CY2018Q2	us-gaap	Accrued Professional Fees Current AccruedProfessionalFeesCurrent	332000	USD
CY2017Q4	us-gaap	Accrued Salaries Current AccruedSalariesCurrent	2187000	USD
	us-gaap	Amortization Of Financing Costs AmortizationOfFinancingCosts	128000	USD
	us-gaap	Amortization Of Financing Costs AmortizationOfFinancingCosts	16000	USD
CY2018Q2	us-gaap	Accrued Salaries Current AccruedSalariesCurrent	2548000	USD
CY2017Q4	us-gaap	Accumulated Other Comprehensive Income Loss Net Of Tax AccumulatedOtherComprehensiveIncomeLossNetOfTax	-2000	USD
	us-gaap	Repayments Of Debt RepaymentsOfDebt	3074000	USD
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	us-gaap	Costs And Expenses CostsAndExpenses	22594000	USD
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	us-gaap	Nature Of Operations NatureOfOperations	<div style="font-family:Times New Roman;font-size:10pt;"><div style="line-height:120%;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-weight:bold;text-decoration:underline;">Nature of Business</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">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 “the Company” refers to the business of Curis, Inc. and its wholly owned subsidiaries, except where the context otherwise requires, and the term “Curis” refers to Curis, Inc.</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The Company conducts its research and development programs both internally and through strategic collaborations. The Company’s clinical stage drug candidates are fimepinostat (CUDC-907), which is currently in clinical studies in patients with MYC-altered diffuse large B-cell lymphoma (DLBCL) and solid tumors; CA-170, which is currently undergoing testing in a Phase 1 study in patients with advanced solid tumors and lymphomas; and CA-4948, which is being tested in a Phase 1 trial in patients with advanced non-Hodgkin lymphomas, including those with myeloid differentiation primary response 88, or MYD88, alterations. The U.S. Food and Drug Administration, or FDA, granted fimepinostat Orphan Drug Designation in April 2015 and Fast Track Designation in May 2018 for the treatment of DLBCL. The Company’s pipeline also includes CA-327, which is a pre-Investigational New Drug (IND) stage oncology drug candidate. The Company continues work to enable the filing of an IND application with the U.S. FDA for clinical testing of CA-327 in 2018. The Company is party to a collaboration with F. Hoffmann-La Roche Ltd, or Roche, and Genentech Inc., or Genentech, a member of the Roche Group, under which Roche and Genentech are commercializing Erivedge, a first-in-class orally-administered small molecule Hedgehog signaling pathway inhibitor. Erivedge® (vismodegib) is approved for the treatment of advanced basal cell carcinoma, or BCC.</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">In January 2015, and as amended in September 2016, the Company entered into a collaboration, option and license agreement focused on immuno-oncology and selected precision oncology targets with Aurigene Discovery Technologies Limited, or Aurigene.</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The collaboration with Aurigene is comprised of multiple programs, and Curis has the option to exclusively license each program, including data, intellectual property and compounds associated therewith, once a development candidate is nominated within such program. In October 2015, the Company exercised options to license </font><font style="font-family:inherit;font-size:10pt;">two</font><font style="font-family:inherit;font-size:10pt;"> programs under this collaboration. The first licensed program is in the immuno-oncology field and the Company has named CA-170, an orally-available small molecule antagonist of two immune checkpoints, programmed death ligand-1 (PDL1) and V-domain Ig suppressor of T cell activation (VISTA), as the development candidate from this program. The second licensed program is in the precision oncology field and the Company has named CA-4948, an orally-available small molecule inhibitor of Interleukin-1 receptor-associated kinase 4 (IRAK4) as the development candidate. In October 2016, the Company exercised its option to license a third program in the collaboration, and designated CA-327, a distinct orally available small molecule antagonist of two immune checkpoints, PDL1 and T-cell immunoglobulin and mucin domain containing protein-3 (TIM3) as the development candidate from this program. In March 2018, the Company exercised its option to license a fourth program, which is an immuno-oncology program. </font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">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 healthcare industry and would be regulated in the United States by the FDA and in overseas markets by similar regulatory authorities.</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The Company is subject to risks common to companies in the biotechnology industry as well as risks that are specific to the Company’s business, including, but not limited to: the Company’s ability to advance and expand its research and development programs; the Company’s reliance on Aurigene to successfully discover and preclinically develop drug candidates under the parties’ collaboration agreement; the Company’s reliance on Roche and Genentech to successfully commercialize Erivedge in the approved indication of advanced BCC and to progress its clinical development in indications other than BCC; the Company’s ability to obtain adequate financing to fund its operations; the ability of the Company and its wholly-owned subsidiary, Curis Royalty, LLC, or Curis Royalty, to satisfy the terms of its credit agreement with HealthCare Royalty Partners III, L.P., a Delaware limited partnership managed by HealthCare Royalty Management, LLC, or HealthCare Royalty; the Company’s ability to obtain and maintain necessary intellectual property protection; development by the Company’s competitors of new or better technological innovations; the Company's dependence on key personnel; the Company’s ability to comply with regulatory requirements; the Company's ability to obtain and maintain applicable regulatory approvals and commercialize any approved product candidates and the Company’s ability to execute on its overall business strategies.</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The Company’s future operating results will largely depend on the progress of drug candidates currently in its development pipeline and the magnitude of payments that it may receive and make under its current and potential future collaborations. The results of the Company’s operations have varied and will likely continue to vary significantly from year to year and quarter to quarter and depend on a number of factors, including, but not limited to: the timing, outcome and cost of the Company’s preclinical studies and clinical trials for its drug candidates; Aurigene’s ability to successfully discover and develop preclinical programs under the Company’s collaboration with Aurigene, as well as the Company’s decision to exclusively license and further develop programs under this collaboration; Roche and Genentech’s ability to successfully commercialize Erivedge; and positive results in Roche and Genentech’s ongoing clinical trials.</font></div><div style="line-height:120%;padding-top:8px;text-indent:30px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The Company has incurred losses and negative cash flows from operations since its inception. As of </font><font style="font-family:inherit;font-size:10pt;">June 30, 2018</font><font style="font-family:inherit;font-size:10pt;">, the Company had an accumulated deficit of approximately </font><font style="font-family:inherit;font-size:10pt;">$971.7 million</font><font style="font-family:inherit;font-size:10pt;">. The Company anticipates that its </font><font style="font-family:inherit;font-size:10pt;">$40.4 million</font><font style="font-family:inherit;font-size:10pt;"> of existing cash, cash equivalents and investments at </font><font style="font-family:inherit;font-size:10pt;">June 30, 2018</font><font style="font-family:inherit;font-size:10pt;"> should enable it to maintain its planned operations into the second half of 2019. In order to ensure adequate cash resources for 12 months from the issuance date of these financial statements, the Company will reduce or delay spending on its research and development programs and operating expenses to the extent it is unable to raise additional capital through its current at-the-market sale agreement with Cowen and Company, LLC, or Cowen or other potential financing. The Company’s ability to raise additional funds will depend, among other factors, on financial, economic and market conditions, many of which are outside of its control and it may be unable to raise financing in the next 12 months, or on terms favorable to the Company. The Company’s inability to obtain additional funds in the next 12 months would delay, or cause the Company to reduce in scope or eliminate some of its development programs, potentially delaying the time to market for any of its product candidates, and would have a negative impact on the Company’s financial condition and ability to pursue its business strategies.</font></div></div>

Files In Submission

Name	View Source	Status
0001108205-18-000013-index-headers.html	Edgar Link	pending
0001108205-18-000013-index.html	Edgar Link	pending
0001108205-18-000013.txt	Edgar Link	pending
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cris-20180630.xml	Edgar Link	completed
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cris-6302018x10qexx102.htm	Edgar Link	pending
cris-6302018x10qexx311.htm	Edgar Link	pending
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cris-6302018x10qexx322.htm	Edgar Link	pending
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updatedpipeline06302018.jpg	Edgar Link	pending

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$CRIS
CURIS INC Stock $cris

2018 Q3 Form 10-Q Financial Statement

#000110820518000013 Filed on August 02, 2018

Income Statement

Balance Sheet

Cashflow Statement

Facts In Submission

Files In Submission

$CRIS CURIS INC Stock $cris

2018 Q3 Form 10-Q Financial Statement

#000110820518000013 Filed on August 02, 2018

Income Statement

Balance Sheet

Cashflow Statement

Facts In Submission

Files In Submission

$CRIS
CURIS INC Stock $cris