2015 Q3 Form 10-Q Financial Statement

#000156459015010330 Filed on November 10, 2015

View on sec.gov

Income Statement

Concept 2015 Q3 2014 Q3
Revenue $7.167M $16.05M
YoY Change -55.35% 3072.33%
Cost Of Revenue
YoY Change
Gross Profit
YoY Change
Gross Profit Margin
Selling, General & Admin $10.20M $4.000M
YoY Change 155.0% 66.67%
% of Gross Profit
Research & Development $68.22M $18.50M
YoY Change 268.83% 274.87%
% of Gross Profit
Depreciation & Amortization $700.0K $192.0K
YoY Change 264.58% 90.1%
% of Gross Profit
Operating Expenses $78.38M $22.48M
YoY Change 248.76% 208.34%
Operating Profit -$71.22M -$6.423M
YoY Change 1008.78% -5.31%
Interest Expense $33.00K $1.000K
YoY Change 3200.0% -99.95%
% of Operating Profit
Other Income/Expense, Net -$235.0K -$1.490M
YoY Change -84.23% -88.27%
Pretax Income -$71.50M -$7.900M
YoY Change 805.06% -63.26%
Income Tax $0.00
% Of Pretax Income
Net Earnings -$71.33M -$7.872M
YoY Change 806.17% -63.34%
Net Earnings / Revenue -995.31% -49.04%
Basic Earnings Per Share -$1.86
Diluted Earnings Per Share -$1.86 -$237.2K
COMMON SHARES
Basic Shares Outstanding 38.43M 4.624M
Diluted Shares Outstanding 38.43M

Balance Sheet

Concept 2015 Q3 2014 Q3
SHORT-TERM ASSETS
Cash & Short-Term Investments $153.7M $100.9M
YoY Change 52.33%
Cash & Equivalents $153.7M $100.9M
Short-Term Investments
Other Short-Term Assets $35.10M $18.10M
YoY Change 93.92%
Inventory
Prepaid Expenses $17.95M
Receivables
Other Receivables
Total Short-Term Assets $189.3M $118.9M
YoY Change 59.24%
LONG-TERM ASSETS
Property, Plant & Equipment $8.652M $3.680M
YoY Change 135.11%
Goodwill $943.0K $943.0K
YoY Change 0.0%
Intangibles $2.620M $2.620M
YoY Change 0.0%
Long-Term Investments
YoY Change
Other Assets $800.0K $3.064M
YoY Change -73.89%
Total Long-Term Assets $13.00M $10.31M
YoY Change 26.11%
TOTAL ASSETS
Total Short-Term Assets $189.3M $118.9M
Total Long-Term Assets $13.00M $10.31M
Total Assets $202.3M $129.2M
YoY Change 56.6%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $25.20M $4.411M
YoY Change 471.3%
Accrued Expenses $25.20M $7.700M
YoY Change 227.27%
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 $82.50M $48.08M
YoY Change 71.6%
LONG-TERM LIABILITIES
Long-Term Debt $0.00 $0.00
YoY Change
Other Long-Term Liabilities $79.80M $130.0K
YoY Change 61284.62%
Total Long-Term Liabilities $79.80M $130.0K
YoY Change 61284.62%
TOTAL LIABILITIES
Total Short-Term Liabilities $82.50M $48.08M
Total Long-Term Liabilities $79.80M $130.0K
Total Liabilities $161.7M $120.0M
YoY Change 34.75%
SHAREHOLDERS EQUITY
Retained Earnings -$157.6M
YoY Change
Common Stock $1.000K
YoY Change
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $40.60M -$151.8M
YoY Change
Total Liabilities & Shareholders Equity $202.3M $129.2M
YoY Change 56.6%

Cashflow Statement

Concept 2015 Q3 2014 Q3
OPERATING ACTIVITIES
Net Income -$71.33M -$7.872M
YoY Change 806.17% -63.34%
Depreciation, Depletion And Amortization $700.0K $192.0K
YoY Change 264.58% 90.1%
Cash From Operating Activities -$59.70M -$5.100M
YoY Change 1070.59% -123.72%
INVESTING ACTIVITIES
Capital Expenditures -$2.400M -$800.0K
YoY Change 200.0%
Acquisitions
YoY Change
Other Investing Activities -$800.0K $0.00
YoY Change
Cash From Investing Activities -$3.200M -$800.0K
YoY Change 300.0%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 10.50M -1.800M
YoY Change -683.33% -118.0%
NET CHANGE
Cash From Operating Activities -59.70M -5.100M
Cash From Investing Activities -3.200M -800.0K
Cash From Financing Activities 10.50M -1.800M
Net Change In Cash -52.40M -7.700M
YoY Change 580.52% -124.44%
FREE CASH FLOW
Cash From Operating Activities -$59.70M -$5.100M
Capital Expenditures -$2.400M -$800.0K
Free Cash Flow -$57.30M -$4.300M
YoY Change 1232.56% -120.0%

Facts In Submission

Frame Concept Type Concept / XBRL Key Value Unit
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us-gaap Interest Expense
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us-gaap Depreciation And Amortization
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us-gaap Increase Decrease In Accrued Liabilities And Other Operating Liabilities
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us-gaap Increase Decrease In Deferred Revenue
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us-gaap Nature Of Operations
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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:0pt;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">1.</p></td> <td valign="top"> <p style="margin-bottom:0pt;margin-top:0pt;font-weight:bold;font-style:normal;text-transform:none;font-variant: normal;font-family:Times New Roman;font-size:10pt;">Organization and Operations<font style="font-weight:normal;"> </font></p></td></tr></table></div> <p style="margin-bottom:0pt;margin-top:6pt;text-indent:0%;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">Description of the Business </p> <p style="margin-bottom:0pt;margin-top:6pt;text-indent:4.54%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">Coherus BioSciences, Inc. (the &#8220;Company&#8221;, &#8220;Coherus&#8221;, &#8220;we&#8221;, &#8220;our&#8221; or &#8220;us&#8221;) was incorporated in the state of Delaware as BioGenerics, Inc. in September&#160;2010 and changed its name to Coherus BioSciences, Inc. in April 2012. The Company is a late-stage clinical biologics platform company, focused on the global biosimilar market. The Company&#8217;s headquarters and laboratories are located in Redwood City, California and in Camarillo, California, respectively. The Company operates in one segment. </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&#8217;s clinical stage pipeline consists of a long-acting form of granulocyte colony-stimulating factor (&#8220;G-CSF&#8221;), and two anti-inflammatory agents targeting tumor necrosis factor (&#8220;TNF&#8221;): </p> <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:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">&nbsp;</p></td> <td valign="top" style="width:4.54%;white-space:nowrap"> <p style="margin-bottom:0pt;margin-top:6pt;font-family:'Symbol';font-size:10pt;">&#183;</p></td> <td valign="top"> <p style="margin-bottom:0pt;margin-top:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company&#8217;s long-acting G-CSF product candidate, CHS-1701, is being developed as a pegfilgrastim (Neulasta) biosimilar. In October 2015, the Company completed a pivotal pharmacokinetic (PK) and pharmacodynamics (PD) study for CHS-1701 in the United States (U.S.), which the Company believes will support the planned filing of a biologics license application (&#8220;BLA&#8221;) in the U.S. An additional immunogenicity study is underway in healthy volunteers pursuant to this BLA, which is projected to be submitted to the U.S. Food and Drug Administration (&#8220;FDA&#8221;) in the first quarter of 2016.</p></td></tr></table></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:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">&nbsp;</p></td> <td valign="top" style="width:4.54%;white-space:nowrap"> <p style="margin-bottom:0pt;margin-top:6pt;font-family:'Symbol';font-size:10pt;">&#183;</p></td> <td valign="top"> <p style="margin-bottom:0pt;margin-top:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company&#8217;s most clinically advanced anti-TNF product candidate, CHS-0214, is being developed as an etanercept (Enbrel) biosimilar that the Company has partnered with Baxalta Incorporated, Baxalta US Inc., and Baxalta GmbH, (collectively &#8220;Baxalta&#8221;) and Daiichi Sankyo Company, Limited (&#8220;Daiichi Sankyo&#8221;) to develop and commercialize in key markets outside of the U.S. In October 2015, the Company completed part 1 of a Phase 3 clinical study in psoriasis comparing CHS-0214 to Enbrel.&nbsp;&nbsp;This study is on-going, but this study met all its primary efficacy endpoints. There were no clinically important safety issues in either treatment group. The Company expects that results from these studies, if positive, combined with data from our Phase 1 studies and Phase 3 study in psoriasis, will support the expected filing of a marketing application in Europe and Japan in 2016. The Company has retained the development and commercial rights to this product in the U.S. However, the therapeutic protein in etanercept is subject to certain originator-controlled U.S. patents expiring in 2028 and 2029. Assuming these patents are valid and enforceable, and that the Company would be unable to obtain a license to them, the Company does not expect to commercialize CHS-0214 in the U.S. prior to their expiration.</p></td></tr></table></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:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">&nbsp;</p></td> <td valign="top" style="width:4.54%;white-space:nowrap"> <p style="margin-bottom:0pt;margin-top:6pt;font-family:'Symbol';font-size:10pt;">&#183;</p></td> <td valign="top"> <p style="margin-bottom:0pt;margin-top:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company&#8217;s second anti-TNF product candidate, CHS-1420, is being developed as an adalimumab (Humira) biosimilar. This product successfully completed a pivotal Phase 1 PK study in August 2014 by meeting the primary study endpoint. The Company initiated a Phase 3 study in psoriasis in August 2015 to support the planned filing of a marketing application in the U.S. in 2016 and the E.U. in 2017. A bridging PK study comparing the Phase 3 CHS-1420 material to adalimumab (Humira) is planned for during the first half of 2016.</p></td></tr></table></div> <p style="margin-bottom:0pt;margin-top:18pt;text-indent:0%;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">Need to Raise Additional Capital</p> <p style="margin-bottom:0pt;margin-top:6pt;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 September 30, 2015, the Company had an accumulated deficit of $357.6 million and cash and cash equivalents of $153.7 million. The Company believes that its current available cash and cash equivalents, together with funding it expects to receive under its license agreements with Daiichi Sankyo and Baxalta, will be sufficient to fund its planned expenditures and meet the Company&#8217;s obligations through at least the next twelve months. However, if the anticipated operating results are not achieved in future periods, the planned expenditures may need to be reduced in order to extend the time period over which the then-available resources would be able to fund the operations. The Company will need to raise additional funds in the future, however there can be no assurance that such efforts will be successful or that, in the event that they are successful, the terms and conditions of such financing will be favorable. </p></div>
us-gaap Use Of Estimates
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<div> <p style="margin-bottom:0pt;margin-top:8pt;text-indent:0%;font-weight:bold;font-family:Times New Roman;font-size:10pt;font-style:normal;text-transform:none;font-variant: normal;">Use of Estimates </p> <p style="margin-bottom:0pt;margin-top:6pt;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;text-indent:4.54%;">The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the amounts and disclosures reported in the financial statements. Management uses significant judgment when making estimates related to its common stock valuation and related stock-based compensation, the valuations of the convertible preferred stock warrant liability and embedded derivative instruments, valuation of deferred tax assets, impairment of goodwill and long-lived assets, the valuation of acquired intangible assets, clinical trial accruals, revenue recognition period, as well as certain accrued liabilities. Management bases its estimates on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results could differ from these estimates. </p></div>
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chrs Lease Initiation Date
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214734
us-gaap Weighted Average Number Of Shares Common Stock Subject To Repurchase Or Cancellation
WeightedAverageNumberOfSharesCommonStockSubjectToRepurchaseOrCancellation
4825
us-gaap Weighted Average Number Of Shares Common Stock Subject To Repurchase Or Cancellation
WeightedAverageNumberOfSharesCommonStockSubjectToRepurchaseOrCancellation
432431
us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
7924249
us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
27421663

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