2017 Q4 Form 10-Q Financial Statement

#000119312517336444 Filed on November 08, 2017

View on sec.gov

Income Statement

Concept 2017 Q4 2017 Q3 2016 Q3
Revenue $1.193M $305.0K $305.0K
YoY Change 291.15% 0.0% 0.0%
Cost Of Revenue
YoY Change
Gross Profit
YoY Change
Gross Profit Margin
Selling, General & Admin $4.080M $3.560M $3.270M
YoY Change 37.37% 8.87% 2.19%
% of Gross Profit
Research & Development $16.60M $12.19M $12.27M
YoY Change 95.88% -0.7% 313.54%
% of Gross Profit
Depreciation & Amortization $150.0K $150.0K
YoY Change 66.67%
% of Gross Profit
Operating Expenses $20.68M $15.75M $15.54M
YoY Change 80.69% 1.34% 152.2%
Operating Profit -$19.49M -$15.45M -$15.24M
YoY Change 74.93% 1.37% 160.12%
Interest Expense $460.0K $411.0K $268.0K
YoY Change 70.37% 53.36% -217.03%
% of Operating Profit
Other Income/Expense, Net $385.0K $358.0K $269.0K
YoY Change 18.1% 33.09% -114.36%
Pretax Income -$19.10M -$15.09M -$14.97M
YoY Change 76.52% 0.8% 93.66%
Income Tax $0.00 $0.00
% Of Pretax Income
Net Earnings -$19.10M -$15.09M -$14.97M
YoY Change 76.64% 0.79% 93.62%
Net Earnings / Revenue -1601.34% -4946.89% -4907.87%
Basic Earnings Per Share
Diluted Earnings Per Share -$796.5K -$678.5K -$836.3K
COMMON SHARES
Basic Shares Outstanding 24.39M shares 22.22M shares 17.78M shares
Diluted Shares Outstanding

Balance Sheet

Concept 2017 Q4 2017 Q3 2016 Q3
SHORT-TERM ASSETS
Cash & Short-Term Investments $131.3M $121.5M $116.0M
YoY Change 22.71% 4.74% 15.42%
Cash & Equivalents $35.17M $20.73M $12.75M
Short-Term Investments $96.10M $100.8M $103.2M
Other Short-Term Assets $1.800M $1.900M $1.000M
YoY Change 50.0% 90.0% 100.0%
Inventory
Prepaid Expenses
Receivables
Other Receivables
Total Short-Term Assets $133.4M $124.0M $117.3M
YoY Change 22.98% 5.72% 15.76%
LONG-TERM ASSETS
Property, Plant & Equipment $267.0K $286.0K $283.0K
YoY Change 2.69% 1.06% 183.0%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments $3.200M
YoY Change
Other Assets $231.0K $236.0K $179.0K
YoY Change -4.94% 31.84% -88.07%
Total Long-Term Assets $3.744M $522.0K $462.0K
YoY Change 644.33% 12.99% -69.2%
TOTAL ASSETS
Total Short-Term Assets $133.4M $124.0M $117.3M
Total Long-Term Assets $3.744M $522.0K $462.0K
Total Assets $137.2M $124.5M $117.7M
YoY Change 25.84% 5.75% 14.52%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $2.232M $2.246M $2.010M
YoY Change -6.02% 11.74% 67.5%
Accrued Expenses $12.00M $10.70M $5.900M
YoY Change 76.47% 81.36% 118.52%
Deferred Revenue $1.573M
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due
YoY Change
Total Short-Term Liabilities $15.80M $14.21M $9.147M
YoY Change 52.4% 55.32% -32.24%
LONG-TERM LIABILITIES
Long-Term Debt $0.00 $0.00 $0.00
YoY Change
Other Long-Term Liabilities $310.0K $267.0K $223.0K
YoY Change 7.64% 19.73% -98.8%
Total Long-Term Liabilities $17.07M $13.57M $14.75M
YoY Change 17.65% -7.97% -20.71%
TOTAL LIABILITIES
Total Short-Term Liabilities $15.80M $14.21M $9.147M
Total Long-Term Liabilities $17.07M $13.57M $14.75M
Total Liabilities $32.87M $27.78M $23.90M
YoY Change 32.13% 16.25% -25.56%
SHAREHOLDERS EQUITY
Retained Earnings -$366.1M -$347.0M -$294.5M
YoY Change 19.92% 17.84%
Common Stock $470.6M $443.7M $388.2M
YoY Change 20.85% 14.29%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $104.3M $96.71M $93.83M
YoY Change
Total Liabilities & Shareholders Equity $137.2M $124.5M $117.7M
YoY Change 25.84% 5.75% 14.52%

Cashflow Statement

Concept 2017 Q4 2017 Q3 2016 Q3
OPERATING ACTIVITIES
Net Income -$19.10M -$15.09M -$14.97M
YoY Change 76.64% 0.79% 93.62%
Depreciation, Depletion And Amortization $150.0K $150.0K
YoY Change 66.67%
Cash From Operating Activities -$12.72M -$10.18M -$11.45M
YoY Change 22.07% -11.09% 121.04%
INVESTING ACTIVITIES
Capital Expenditures -$40.00K -$40.00K -$50.00K
YoY Change -20.0% 400.0%
Acquisitions
YoY Change
Other Investing Activities $1.590M $6.960M $8.110M
YoY Change -92.55% -14.18% -209.59%
Cash From Investing Activities $1.550M $6.920M $8.050M
YoY Change -92.73% -14.04% -208.64%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $24.90M
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 25.61M 1.010M 1.710M
YoY Change 14964.71% -40.94% -97.15%
NET CHANGE
Cash From Operating Activities -12.72M -10.18M -11.45M
Cash From Investing Activities 1.550M 6.920M 8.050M
Cash From Financing Activities 25.61M 1.010M 1.710M
Net Change In Cash 14.44M -2.250M -1.690M
YoY Change 30.32% 33.14% -103.56%
FREE CASH FLOW
Cash From Operating Activities -$12.72M -$10.18M -$11.45M
Capital Expenditures -$40.00K -$40.00K -$50.00K
Free Cash Flow -$12.68M -$10.14M -$11.40M
YoY Change 21.69% -11.05% 120.5%

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<div> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt"> <b>1. Nature of Business</b></p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 6pt; TEXT-INDENT: 4%"> Syndax Pharmaceuticals, Inc. (the &#x201C;Company&#x201D;) is a clinical stage biopharmaceutical company developing an innovative pipeline of combination therapies in multiple cancer indications. The Company&#x2019;s lead product candidate, entinostat, is currently being evaluated in a Phase 3 clinical trial for advanced hormone receptor positive, human epidermal growth factor receptor 2 negative breast cancer. The U.S. Food and Drug Administration granted Breakthrough Therapy designation to entinostat when given in combination with exemestane following positive results from the Company&#x2019;s ENCORE 301 Phase 2b clinical trial. Given its potential ability to block the function of immune suppressive cells in the tumor microenvironment, the Company is evaluating entinostat as a combination therapeutic in Phase 1b/2 clinical trials with Merck&#xA0;&amp; Co., Inc. for <font style="WHITE-SPACE: nowrap">non-small</font> cell lung cancer, melanoma and microsatellite stable colorectal cancer; with Genentech, Inc. for triple negative breast cancer; and with Merck KGaA, Darmstadt, Germany, and Pfizer Inc. for ovarian cancer. The Company&#x2019;s second product candidate, SNDX-6352, is a monoclonal antibody that targets the colony stimulating <font style="WHITE-SPACE: nowrap">factor-1</font> receptor to enhance the body&#x2019;s immune response against tumors that have shown sensitivity to immunotherapy. The Company is evaluating SNDX-6352 in a multiple ascending dose Phase 1 clinical trial in cancer patients. The Company plans to continue to leverage the technical and business expertise of our management team and scientific collaborators to license, acquire and develop additional cancer therapies to expand our pipeline.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> On October&#xA0;13, 2017, the Company entered into a license agreement with Vitae Pharmaceuticals, Inc., a subsidiary of Allergan plc (&#x201C;Allergan&#x201D;), under which Allergan granted to the Company a worldwide, sublicenseable, exclusive license to a portfolio of preclinical, orally-available, small molecule inhibitors of the interaction of Menin with the Mixed Lineage Leukemia (&#x201C;MLL&#x201D;) protein (the &#x201C;Menin Assets&#x201D;). Concurrent with the development of entinostat and SNDX-6352, the Company is also developing the Menin Assets to potentially treat MLL-r driven malignancies. The Company believes that the Menin Assets have the potential to be used to treat a genetically-defined subset of acute leukemias with chromosomal rearrangements in the MLL gene (&#x201C;MLL-r&#x201D;). The Company expects to begin preclinical studies of the Menin Assets during the fourth quarter of 2017.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> On October&#xA0;17, 2017, the Company entered into a purchase agreement with Biotech Value Fund, L.P. (&#x201C;BVF&#x201D;) and certain entities affiliated with BVF (the &#x201C;Purchase Agreement&#x201D;). Pursuant to the Purchase Agreement, the Company issued directly to BVF in a registered direct offering (the &#x201C;Offering&#x201D;), 2,021,018 shares of the Company&#x2019;s common stock at a price of $12.37 per share, representing the closing price of the Company&#x2019;s shares on the Nasdaq Global Select Market on Friday, October&#xA0;13, 2017. The net proceeds from the Offering, after deducting estimated expenses, are expected to be approximately $24.8&#xA0;million.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> In March 2016, the Company completed its initial public offering (&#x201C;IPO&#x201D;) whereby it sold 4,809,475 shares of common stock at the initial public offering price of $12.00 per share, which included 409,475 shares issued pursuant to the underwriters&#x2019; partial exercise of their over-allotment option to purchase additional shares of common stock. The aggregate net proceeds received by the Company from the offering were $50.5&#xA0;million, net of underwriting discounts and commissions of $4.0&#xA0;million and offering expenses of $3.1&#xA0;million. Upon the closing of the IPO, all outstanding shares of the Company&#x2019;s outstanding convertible preferred stock converted into 12,872,551 shares of common stock; and the Company&#x2019;s outstanding warrant liability to purchase 357,840 shares of the Company&#x2019;s common stock valued at $4.6&#xA0;million was reclassified to additional <font style="WHITE-SPACE: nowrap">paid-in</font> capital. In connection with the closing of the Company&#x2019;s IPO, the Company filed an amended and restated certificate of incorporation and adopted amended and restated bylaws, both of which were approved by the Company&#x2019;s board of directors and stockholders on September&#xA0;28, 2015 and February&#xA0;24, 2016, respectively. Pursuant to the amended and restated certificate of incorporation, the Company is now authorized to issue 100,000,000 shares of common stock and 10,000,000 shares of preferred stock.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> In May 2017, the Company completed a <font style="WHITE-SPACE: nowrap">follow-on</font> public offering whereby the Company sold 3,950,190 shares of common stock at a price of $13.25 per share, which included 200,190 shares issued pursuant to the underwriters&#x2019; partial exercise of their option to purchase additional shares of common stock. The aggregate net proceeds received by the Company from the offering were approximately $48.7&#xA0;million, net of underwriting discounts and commissions and estimated offering expenses payable by the Company.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> In April 2017, the Company entered into a sales agreement with Cowen and Company, LLC (&#x201C;Cowen&#x201D;) under which the Company may issue and sell shares of our common stock having aggregate sales proceeds of up to $50.0&#xA0;million from time to time through Cowen, acting as agent, in a series of one or more <font style="WHITE-SPACE: nowrap"><font style="WHITE-SPACE: nowrap">at-the-market</font></font> (&#x201C;ATM&#x201D;) equity offerings. Cowen is not required to sell any specific amount, but acts as our sales agent using commercially reasonable efforts consistent with its normal trading and sales practices. Shares sold pursuant to the sales agreement will be sold pursuant to a shelf registration statement, which became effective on April&#xA0;20, 2017. Our common stock will be sold at prevailing market prices at the time of the sale; and as a result, prices may vary. We will pay Cowen up to 3% of the gross proceeds from any common stock sold through the sales agreement. During the three months ended September&#xA0;30, 2017, the Company sold 92,511 shares of Common Stock pursuant to the ATM program, at an average price of $12.49 per share for gross proceeds of $1.2&#xA0;million, resulting in net proceeds of $1.1&#xA0;million after deducting sales commissions and offering expenses. As of September&#xA0;30, 2017, $48.8&#xA0;million of Common Stock remained available for sale under the ATM program.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> Since its inception, the Company has devoted its efforts principally to research and development and raising capital. The Company is subject to risks common to companies in the development stage, including, but not limited to, successful development of therapeutics, obtaining additional funding, protection of proprietary therapeutics, compliance with government regulations, fluctuations in operating results, dependence on key personnel and collaborative partners, and risks associated with industry changes. The Company&#x2019;s long-term success is dependent upon its ability to successfully develop and market its product candidates, expand its oncology drug pipeline, earn revenue, obtain additional capital when needed, and ultimately, achieve profitable operations. The Company anticipates that it may be two or more years before any of our product candidates are approved, if ever, and the Company begins to generate revenue from sales of any of our product candidates. Accordingly, management expects to incur substantial losses on the ongoing development of our product candidates and does not expect to achieve positive cash flow from operations for the foreseeable future, if ever. As a result, the Company will continue to require additional capital to move forward with its business plan. While certain amounts of this additional capital were raised in the past, there can be no assurance that funds necessary beyond these amounts will be available in amounts or on terms sufficient to ensure ongoing operations.</p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 12pt; TEXT-INDENT: 4%"> The Company&#x2019;s management believes that the cash, cash equivalents and short-term investments balances as of September&#xA0;30, 2017 should enable the Company to maintain its planned operations for at least the next 12&#xA0;months. The Company&#x2019;s ability to fund all of its planned operations internally beyond that date, including the completion of its ongoing and planned clinical trial activities, may be substantially dependent upon whether the Company can obtain sufficient funding on terms acceptable to the Company. Proceeds from additional capital transactions would allow the Company to accelerate and/or expand its planned research and development activities. In the event that sufficient funds were not available, the Company may be required to delay or reduce expenditures to conserve cash, which could involve scaling back or curtailing development and general and administrative activities.</p> </div>
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dei Trading Symbol
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us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
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<div> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-LEFT: 4%; MARGIN-TOP: 0pt"> <i>Use of Estimates</i></p> <p style="MARGIN-BOTTOM: 0pt; FONT-SIZE: 10pt; FONT-FAMILY: Times New Roman; MARGIN-TOP: 6pt; TEXT-INDENT: 4%"> The preparation of condensed consolidated financial statements in conformity with U.S. GAAP 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 condensed consolidated financial statements and the reported amounts of costs and expenses during the reporting period. The Company bases estimates and assumptions on historical experience when available and on various factors that it believes to be reasonable under the circumstances. The Company evaluates its estimates and assumptions on an ongoing basis. The Company&#x2019;s actual results may differ from these estimates under different assumptions or conditions.</p> </div>
sndx Stock Issued During Period Value New Issues Under The At The Market Program
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sndx Vesting Of Restricted Stock Value
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sndx Recent Accounting Standards Expected Date Of Adoption
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sndx Number Of Revenue Arrangement
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us-gaap Allocated Share Based Compensation Expense
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us-gaap Available For Sale Securities Gross Realized Gain Loss Net
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us-gaap Increase Decrease In Deferred Revenue
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us-gaap Income Tax Expense Benefit
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us-gaap Increase Decrease In Accounts Payable
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us-gaap Increase Decrease In Accrued Liabilities And Other Operating Liabilities
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us-gaap Increase Decrease In Prepaid Deferred Expense And Other Assets
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us-gaap Increase Decrease In Restricted Cash
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us-gaap Interest Income Expense Nonoperating Net
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us-gaap Interest Paid
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us-gaap Licenses Revenue
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us-gaap Net Cash Provided By Used In Investing Activities Continuing Operations
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us-gaap Share Based Compensation
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us-gaap Temporary Equity Dividends Adjustment
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us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
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us-gaap Operating Expenses
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sndx Fair Value Adjustment Of Warrants And Derivative Liabilities
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sndx Reclassification Of Common Stock Warrant Liability To Additional Paid In Capital
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sndx Issuance Costs Included In Accounts Payable And Accrued Expenses
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sndx Vesting Of Restricted Stock Value
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CY2017Q2 sndx Payment Specified Percentage Of Gross Proceeds From Sale Of Shares
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