2020 Q1 Form 10-Q Financial Statement

#000156459020020617 Filed on May 04, 2020

View on sec.gov

Income Statement

Concept 2020 Q1 2019 Q1
Revenue $0.00 $0.00
YoY Change
Cost Of Revenue
YoY Change
Gross Profit
YoY Change
Gross Profit Margin
Selling, General & Admin $4.190M $4.710M
YoY Change -11.04% 9.79%
% of Gross Profit
Research & Development $8.080M $11.61M
YoY Change -30.4% 37.4%
% of Gross Profit
Depreciation & Amortization $4.367K $4.367K
YoY Change 0.0%
% of Gross Profit
Operating Expenses $12.27M $16.31M
YoY Change -24.77% 28.04%
Operating Profit -$12.27M -$16.31M
YoY Change -24.77% 28.0%
Interest Expense $120.0K $480.0K
YoY Change -75.0% -779.42%
% of Operating Profit
Other Income/Expense, Net
YoY Change
Pretax Income -$12.15M -$15.83M
YoY Change -23.25% 27.46%
Income Tax
% Of Pretax Income
Net Earnings -$12.15M -$15.83M
YoY Change -23.23% 27.45%
Net Earnings / Revenue
Basic Earnings Per Share
Diluted Earnings Per Share -$310.1K -$406.2K
COMMON SHARES
Basic Shares Outstanding
Diluted Shares Outstanding

Balance Sheet

Concept 2020 Q1 2019 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $37.50M $79.20M
YoY Change -52.65% -34.55%
Cash & Equivalents $30.04M $30.61M
Short-Term Investments $7.500M $48.60M
Other Short-Term Assets $1.000M $1.200M
YoY Change -16.67% -72.09%
Inventory
Prepaid Expenses $851.9K
Receivables
Other Receivables
Total Short-Term Assets $38.47M $80.30M
YoY Change -52.1% -35.91%
LONG-TERM ASSETS
Property, Plant & Equipment $11.64K $400.0K
YoY Change -97.09%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $14.81K $14.81K
YoY Change 0.0%
Total Long-Term Assets $30.33M $49.50M
YoY Change -38.72% 0.61%
TOTAL ASSETS
Total Short-Term Assets $38.47M $80.30M
Total Long-Term Assets $30.33M $49.50M
Total Assets $68.80M $129.8M
YoY Change -47.0% -25.62%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $3.000M $3.000M
YoY Change 0.0% 7.14%
Accrued Expenses $4.100M $3.900M
YoY Change 5.13% 62.5%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00
YoY Change
Long-Term Debt Due
YoY Change
Total Short-Term Liabilities $7.100M $6.900M
YoY Change 2.9% -12.66%
LONG-TERM LIABILITIES
Long-Term Debt $0.00 $0.00
YoY Change
Other Long-Term Liabilities $41.20M $41.40M
YoY Change -0.48% 0.49%
Total Long-Term Liabilities $41.20M $41.40M
YoY Change -0.48% 0.49%
TOTAL LIABILITIES
Total Short-Term Liabilities $7.100M $6.900M
Total Long-Term Liabilities $41.20M $41.40M
Total Liabilities $50.20M $52.40M
YoY Change -4.2% -1.5%
SHAREHOLDERS EQUITY
Retained Earnings
YoY Change
Common Stock
YoY Change
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $18.62M $77.42M
YoY Change
Total Liabilities & Shareholders Equity $68.80M $129.8M
YoY Change -47.0% -25.62%

Cashflow Statement

Concept 2020 Q1 2019 Q1
OPERATING ACTIVITIES
Net Income -$12.15M -$15.83M
YoY Change -23.23% 27.45%
Depreciation, Depletion And Amortization $4.367K $4.367K
YoY Change 0.0%
Cash From Operating Activities -$9.202M -$9.601M
YoY Change -4.15% -12.18%
INVESTING ACTIVITIES
Capital Expenditures
YoY Change
Acquisitions
YoY Change
Other Investing Activities $17.03M -$10.55M
YoY Change -261.42% -133.68%
Cash From Investing Activities $17.03M -$10.55M
YoY Change -261.38% -133.69%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 797.6K 525.0K
YoY Change 51.93% -140.7%
NET CHANGE
Cash From Operating Activities -9.202M -9.601M
Cash From Investing Activities 17.03M -10.55M
Cash From Financing Activities 797.6K 525.0K
Net Change In Cash 8.624M -19.63M
YoY Change -143.94% -202.79%
FREE CASH FLOW
Cash From Operating Activities -$9.202M -$9.601M
Capital Expenditures
Free Cash Flow
YoY Change

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<p style="margin-bottom:0pt;margin-top:0pt;text-indent:0%;font-weight:bold;font-size:10pt;font-family:Times New Roman;font-style:normal;text-transform:none;font-variant: normal;">NOTE&#160;1&#160;&#8212; NATURE OF OPERATIONS AND LIQUIDITY </p> <p style="margin-bottom:0pt;margin-top:12pt;margin-left:2.27%;text-indent:0%;font-weight:bold;font-style:italic;font-size:10pt;font-family:Times New Roman;text-transform:none;font-variant: normal;">Nature of Operations </p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:0%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">Minerva Neurosciences, Inc. (&#8220;Minerva&#8221; or the &#8220;Company&#8221;) is a clinical-stage biopharmaceutical company focused on the development and commercialization of a portfolio of product candidates to treat patients suffering from central nervous system diseases. The Company has acquired or in-licensed four development-stage proprietary compounds that it believes have innovative mechanisms of action and therapeutic profiles that may potentially address the unmet needs of patients with these diseases. The Company&#8217;s lead product candidate is roluperidone (also known as MIN-101), a compound the Company is developing for the treatment of schizophrenia. In addition, the Company&#8217;s portfolio includes seltorexant (also known as MIN-202 or JNJ-42847922), a compound the Company is co-developing with Janssen Pharmaceutica NV (&#8220;Janssen&#8221;) for the treatment of insomnia disorder and major depressive disorder (&#8220;MDD&#8221;); and MIN-301, a compound the Company is developing for the treatment of Parkinson&#8217;s disease.</p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:0%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">In November&#160;2013, the Company merged with Sonkei Pharmaceuticals&#160;Inc. (&#8220;Sonkei&#8221;), a clinical-stage biopharmaceutical company and, in February&#160;2014, the Company acquired Mind-NRG, a pre-clinical-stage biopharmaceutical company. The Company refers to these transactions as the Sonkei Merger and Mind-NRG Acquisition, respectively. The Company holds licenses to roluperidone and MIN-117 from Mitsubishi Tanabe Pharma Corporation (&#8220;MTPC&#8221;) with the rights to develop, sell and import roluperidone and MIN-117 globally, excluding most of Asia. With the acquisition of Mind-NRG, the Company obtained exclusive rights to develop and commercialize MIN-301. The Company has also entered into a co-development and license agreement with Janssen, for the exclusive right to commercialize, and the co-exclusive right (with Janssen and its affiliates) to use and develop seltorexant in the European Union, Switzerland, Liechtenstein, Iceland and Norway (the &#8220;Minerva Territory&#8221;), subject to certain royalty payments to Janssen, and royalty rights for any sales outside the Minerva Territory. </p> <p style="margin-bottom:0pt;margin-top:12pt;margin-left:2.27%;text-indent:0%;font-weight:bold;font-style:italic;font-size:10pt;font-family:Times New Roman;text-transform:none;font-variant: normal;">Liquidity </p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:0%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The accompanying condensed consolidated financial statements have been prepared as though the Company will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business. The Company has limited capital resources and has incurred recurring operating losses and negative cash flows from operations since inception. As of March 31, 2020, the Company has an accumulated deficit of approximately <font style="color:#000000;">$298.9</font><font style="font-size:12pt;">&#160;</font><font style="color:#000000;">million </font>and net cash used in operating activities was approximately $9.2 million during the three months ended March 31, 2020. The Company&#8217;s management team expects to continue to incur operating losses and negative cash flows from operations. The Company has financed its operations to date from proceeds from the sale of common stock, warrants, loans and convertible promissory notes.</p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:0%;color:#000000;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">As of March 31, 2020, the Company had cash, cash equivalents, restricted cash, and marketable securities of $37.6 million. <font style="color:#000000;">The Company believes that its existing cash, cash equivalents, restricted cash and marketable securities will be sufficient to meet its cash commitments for at least the next 12 months after the date that the condensed consolidated financial statements are issued. The process of drug development can be costly and the timing and outcomes of clinical trials is uncertain.&#160;The assumptions upon which the Company has based its estimates are routinely evaluated and may be subject to change.&#160;The actual amount of the Company&#8217;s expenditures will vary depending upon a number of factors including but not limited to the design, timing and duration of future clinical trials, the progress of the Company&#8217;s research and development programs, the resolution of the Company&#8217;s dispute with Janssen as described in Notes 5 and 8, the infrastructure to support a commercial enterprise, the cost of a commercial product launch, and the level of financial resources available. If it is determined that the Company is required to make a significant payment to Janssen, it may not have sufficient cash to make such payment and may be required to incur additional indebtedness or to raise additional funds via an equity financing in order to make such payment to Janssen. The Company has the ability to adjust its operating plan spending levels based on the timing of future clinical trials which will be predicated upon adequate funding to complete the trials.</font></p> <p style="margin-top:12pt;margin-bottom:0pt;text-indent:0%;font-family:Times New Roman;font-size:10pt;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">The Company will need to raise additional capital in order to continue to fund operations and fully fund later stage clinical development programs. The Company believes that it will be able to obtain additional working capital through equity financings or other arrangements to fund future operations; however, there can be no assurance that such additional financing, if available, can be obtained on terms acceptable to the Company. If the Company is unable to obtain such additional financing, future operations would need to be scaled back or discontinued.</p>
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<p style="margin-bottom:0pt;margin-top:12pt;text-indent:0%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">Concentration of credit risk</p> <p style="margin-bottom:0pt;margin-top:12pt;text-indent:0%;font-size:10pt;font-family:Times New Roman;font-weight:normal;font-style:normal;text-transform:none;font-variant: normal;">Financial instruments that potentially subject the Company to concentrations of credit risk are primarily cash, cash equivalents and marketable securities. The Company maintains its cash and cash equivalent balances in the form of business checking accounts and money market accounts, the balances of which, at times, may exceed federally insured limits. Exposure to cash and cash equivalents credit risk is reduced by placing such deposits with major financial institutions and monitoring their credit ratings. Marketable securities consist primarily of corporate bonds, with fixed interest rates. Exposure to credit risk of marketable securities is reduced by maintaining a diverse portfolio and monitoring their credit ratings.</p>
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