2020 Q1 Form 10-K Financial Statement

#000162828020003395 Filed on March 11, 2020

View on sec.gov

Income Statement

Concept 2020 Q1 2019 2018 Q4
Revenue $2.754M $6.750M -$6.310M
YoY Change 5.92% -3.96% -430.19%
Cost Of Revenue $66.00K -$566.5K -$2.140M
YoY Change -91.23% -117.37% -436.48%
Gross Profit $2.688M $7.317M -$4.180M
YoY Change 45.5% 94.2% -427.84%
Gross Profit Margin 97.6% 108.39%
Selling, General & Admin $3.353M $11.61M -$2.670M
YoY Change 9.15% 4.98% -166.85%
% of Gross Profit 124.74% 158.64%
Research & Development $4.768M $11.76M $2.010M
YoY Change 40.19% 103.3% 2.5%
% of Gross Profit 177.38% 160.78%
Depreciation & Amortization $453.0K $3.884M $1.220M
YoY Change -58.76% -14.74% 197.56%
% of Gross Profit 16.85% 53.08%
Operating Expenses $8.121M $23.37M -$2.530M
YoY Change -34.69% -59.45% -142.49%
Operating Profit -$31.41M -$16.14M -$1.650M
YoY Change 527.64% -54.39% -64.74%
Interest Expense $10.00K $121.3K $730.0K
YoY Change -66.91% 646.12% 2254.84%
% of Operating Profit
Other Income/Expense, Net $7.101M $147.0K $0.00
YoY Change -26635.87% 167.57%
Pretax Income -$24.31M -$15.99M -$920.0K
YoY Change 383.18% -54.73% -78.9%
Income Tax -$2.200M $280.3K -$140.0K
% Of Pretax Income
Net Earnings -$21.12M -$16.07M -$7.220M
YoY Change 183.3% -59.87% 133.58%
Net Earnings / Revenue -766.78% -238.1%
Basic Earnings Per Share
Diluted Earnings Per Share -$4.70 -$4.498M -$2.11
COMMON SHARES
Basic Shares Outstanding 57.61M shares 40.81M shares
Diluted Shares Outstanding

Balance Sheet

Concept 2020 Q1 2019 2018 Q4
SHORT-TERM ASSETS
Cash & Short-Term Investments $20.37M $11.24M $10.65M
YoY Change 26.36% 5.56% 331.17%
Cash & Equivalents $5.659M $3.609M $10.65M
Short-Term Investments $14.71M $7.629M $0.00
Other Short-Term Assets $840.0K $1.222M $4.880M
YoY Change -36.84% -74.97% 597.14%
Inventory $16.28K $21.33K $317.9K
Prepaid Expenses
Receivables $2.190M $1.002M $820.0K
Other Receivables $2.064M $4.241M $5.262M
Total Short-Term Assets $25.49M $17.72M $21.93M
YoY Change -4.71% -19.19% 105.47%
LONG-TERM ASSETS
Property, Plant & Equipment $1.417M $1.448M $586.5K
YoY Change -4.08% 146.83% 1214.7%
Goodwill $14.41M $14.40M
YoY Change -12.2% 17.17%
Intangibles $2.696M $3.765M
YoY Change -91.06% -78.68%
Long-Term Investments
YoY Change
Other Assets $110.0K $102.0K $29.56M
YoY Change 37.5% -99.66% 22638.46%
Total Long-Term Assets $18.63M $18.38M $48.32M
YoY Change -61.28% -61.95% 50.37%
TOTAL ASSETS
Total Short-Term Assets $25.49M $17.72M $21.93M
Total Long-Term Assets $18.63M $18.38M $48.32M
Total Assets $44.12M $36.11M $70.25M
YoY Change -41.07% -48.6% 64.11%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $2.726M $2.078M $1.446M
YoY Change 118.17% 43.66% 11.33%
Accrued Expenses $6.190M $5.565M $5.370M
YoY Change -43.78% 3.55% -28.69%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $1.050M
YoY Change
Total Short-Term Liabilities $15.33M $12.16M $26.22M
YoY Change -45.51% -53.62% 136.41%
LONG-TERM LIABILITIES
Long-Term Debt $0.00 $0.00 $14.33M
YoY Change -100.0%
Other Long-Term Liabilities $1.094M $2.867M $385.5K
YoY Change -7.99% -87.57% 1488.32%
Total Long-Term Liabilities $1.094M $2.867M $14.71M
YoY Change -92.94% -87.57% 60518.82%
TOTAL LIABILITIES
Total Short-Term Liabilities $15.33M $12.16M $26.22M
Total Long-Term Liabilities $1.094M $2.867M $14.71M
Total Liabilities $18.53M $15.11M $49.34M
YoY Change -64.19% -69.37% 230.11%
SHAREHOLDERS EQUITY
Retained Earnings -$135.4M -$98.22M
YoY Change 28.11% 68.86%
Common Stock $59.56K $40.80K
YoY Change 39.31% 30.5%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $25.59M $21.00M $20.91M
YoY Change
Total Liabilities & Shareholders Equity $44.12M $36.11M $70.25M
YoY Change -41.07% -48.6% 64.11%

Cashflow Statement

Concept 2020 Q1 2019 2018 Q4
OPERATING ACTIVITIES
Net Income -$21.12M -$16.07M -$7.220M
YoY Change 183.3% -59.87% 133.58%
Depreciation, Depletion And Amortization $453.0K $3.884M $1.220M
YoY Change -58.76% -14.74% 197.56%
Cash From Operating Activities -$5.739M -$19.13M -$1.980M
YoY Change 83.85% 511.69% -22.35%
INVESTING ACTIVITIES
Capital Expenditures $0.00 $262.0K $490.0K
YoY Change -100.0% -53.58% 4800.0%
Acquisitions $0.00
YoY Change -100.0%
Other Investing Activities -$181.0K $0.00
YoY Change -112.66% -100.0%
Cash From Investing Activities -$1.251M -$443.0K -$490.0K
YoY Change 653.76% -151.19% -97.41%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $0.00 $8.976M
YoY Change -100.0%
Debt Paid & Issued, Net $0.00 $256.1K
YoY Change -100.0%
Cash From Financing Activities $9.098M $12.56M 6.160M
YoY Change 3.19% 20.72% 61500.0%
NET CHANGE
Cash From Operating Activities -$5.739M -$19.13M -1.980M
Cash From Investing Activities -$1.251M -$443.0K -490.0K
Cash From Financing Activities $9.098M $12.56M 6.160M
Net Change In Cash $2.108M -$7.018M 3.690M
YoY Change -61.88% -186.2% -117.21%
FREE CASH FLOW
Cash From Operating Activities -$5.739M -$19.13M -$1.980M
Capital Expenditures $0.00 $262.0K $490.0K
Free Cash Flow -$5.739M -$19.40M -$2.470M
YoY Change 74.57% 425.29% -3.52%

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<div style="font-family:Times New Roman;font-size:10pt;"><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-style:italic;font-weight:bold;">Concentration of Credit Risk</font></div><div style="line-height:120%;text-align:justify;text-indent:84px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">&#160;</font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">Financial instruments that potentially subject the Company to concentrations of credit risk are primarily cash and cash equivalents. The Company maintains a portion of its cash and cash equivalent balances in the form of a money market account with a financial institution that management believes to be creditworthy. The Company has no financial instruments with off&#8209;balance sheet risk of loss.</font></div></div>
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<div style="font-family:Times New Roman;font-size:10pt;"><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-weight:bold;">Business</font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:left;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;color:#ff0000;"></font><font style="font-family:inherit;font-size:10pt;">Cerecor Inc. (the "Company" or "Cerecor") is a biopharmaceutical company focused on becoming a leader in development and commercialization of treatments for rare pediatric and orphan diseases. The Company is advancing an emerging clinical-stage pipeline of innovative therapies that address unmet patient needs within rare pediatric and orphan diseases. The Company's pediatric rare disease pipeline is led by CERC-801, CERC-802 and CERC-803 ("CERC-800 compounds"), which are therapies for inherited metabolic disorders known as Congenital Disorders of Glycosylation ("CDGs"). The U.S. Food and Drug Administration ("FDA") granted Rare Pediatric Disease designation ("RPDD") and Orphan Drug Designation ("ODD") to all </font><font style="font-family:inherit;font-size:10pt;">three</font><font style="font-family:inherit;font-size:10pt;"> CERC-800 compounds, thus potentially qualifying the Company to receive a Priority Review Voucher ("PRV") upon approval of each New Drug Application ("NDA"). Each PRV may be sold or transferred an unlimited number of times. The Company plans to leverage the 505(b)(2) NDA pathway for all </font><font style="font-family:inherit;font-size:10pt;">three</font><font style="font-family:inherit;font-size:10pt;"> compounds to accelerate development and approval. Additionally, CERC-801 and CERC-802 were granted Fast Track Designation ("FTD") from the FDA, which can help facilitate and potentially expedite development of each compound. </font></div><div style="line-height:120%;text-align:left;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:left;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The Company is also developing CERC-002, CERC-006 and CERC-007. CERC-007 is an anti-IL-18 monoclonal antibody being developed for the treatment of autoimmune inflammatory diseases such as Adult Onset Stills Disease ("AOSD") and Multiple Myeloma. CERC-006 is a dual mTOR inhibitor being developed for the treatment of complex Lymphatic Malformations. CERC-002 is an anti-LIGHT (</font><font style="font-family:inherit;font-size:10pt;font-weight:bold;">L</font><font style="font-family:inherit;font-size:10pt;">ymphotoxin-like, exhibits&#160;</font><font style="font-family:inherit;font-size:10pt;font-weight:bold;">I</font><font style="font-family:inherit;font-size:10pt;">nducible expression, and competes with HSV&#160;</font><font style="font-family:inherit;font-size:10pt;font-weight:bold;">G</font><font style="font-family:inherit;font-size:10pt;">lycoprotein D for&#160;</font><font style="font-family:inherit;font-size:10pt;font-weight:bold;">H</font><font style="font-family:inherit;font-size:10pt;">VEM, a receptor expressed by&#160;</font><font style="font-family:inherit;font-size:10pt;font-weight:bold;">T</font><font style="font-family:inherit;font-size:10pt;">&#160;lymphocytes) monoclonal antibody being developed for the treatment of Pediatric-onset Crohn's Disease. </font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The Company continues to explore strategic alternatives for its non-core assets, including CERC-301, as well as its sole commercialized product, Millipred</font><font style="font-family:inherit;font-size:10pt;"><sup style="vertical-align:top;line-height:120%;font-size:7pt">&#174;</sup></font><font style="font-family:inherit;font-size:10pt;">, an oral prednisolone indicated across a wide variety of inflammatory conditions.</font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">On February 3, 2020, the Company consummated its two-step merger (the "Merger") with Aevi Genomic Medicine, Inc. ("Aevi") in accordance with the terms of the Agreement and Plan of Merger and Reorganization (the "Merger Agreement") dated December 5, 2019. The Merger consideration included stock valued at approximately </font><font style="font-family:inherit;font-size:10pt;">$15.6 million</font><font style="font-family:inherit;font-size:10pt;">, resulting in the issuance of approximately </font><font style="font-family:inherit;font-size:10pt;">3.9 million</font><font style="font-family:inherit;font-size:10pt;"> shares of Cerecor common stock to Aevi stockholders, forgiveness of a </font><font style="font-family:inherit;font-size:10pt;">$4.1 million</font><font style="font-family:inherit;font-size:10pt;"> loan that Cerecor loaned Aevi in December 2019 (the "Aevi Loan"), and contingent value rights ("CVRs") for up to an additional </font><font style="font-family:inherit;font-size:10pt;">$6.5 million</font><font style="font-family:inherit;font-size:10pt;"> in subsequent payments based on clinical and/or regulatory milestones. As part of the Merger, Cerecor acquired CERC-002, CERC-006 and CERC-007, expanding Cerecor's pipeline to </font><font style="font-family:inherit;font-size:10pt;">six</font><font style="font-family:inherit;font-size:10pt;"> clinical stage assets being developed for rare pediatric and orphan diseases. Effective upon the consummation of the Merger, Cerecor entered into an employment agreement with Mike Cola for him to serve as Cerecor's Chief Executive Officer, an employment agreement with Dr. Garry Neil for him to serve as Cerecor's Chief Medical Officer and appointed Mike Cola and Sol J. Barer, Ph.D. to the Company's Board of Directors. See Note 17 for more information. </font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">During the fourth quarter of 2019, the Company entered into, and closed on, an asset purchase agreement (the "Aytu Purchase Agreement") with Aytu BioScience, Inc. (&#8220;Aytu&#8221;) to sell the Company&#8217;s rights, title and interest in, assets relating to its pediatric portfolio, namely Aciphex</font><font style="font-family:inherit;font-size:10pt;"><sup style="vertical-align:top;line-height:120%;font-size:7pt">&#174; </sup></font><font style="font-family:inherit;font-size:10pt;">Sprinkle&#8482;, Cefaclor for Oral Suspension, Karbinal&#8482; ER, Flexichamber&#8482;, Poly-Vi-Flor</font><font style="font-family:inherit;font-size:10pt;"><sup style="vertical-align:top;line-height:120%;font-size:7pt">&#174;</sup></font><font style="font-family:inherit;font-size:10pt;"> and Tri-Vi-Flor&#8482; (the "Pediatric Portfolio"), as well as the corresponding commercial infrastructure consisting of the right to offer employment to Cerecor&#8217;s sales force and the assignment of supporting commercial contracts (the "Aytu Divestiture"). Aytu paid consideration of </font><font style="font-family:inherit;font-size:10pt;">$4.5 million</font><font style="font-family:inherit;font-size:10pt;"> in cash and approximately </font><font style="font-family:inherit;font-size:10pt;">9.8 million</font><font style="font-family:inherit;font-size:10pt;"> shares of Aytu convertible preferred stock (the "Investment"), and assumed certain of the Company&#8217;s liabilities, including the Company&#8217;s payment obligations payable to Deerfield CSF, LLC of $</font><font style="font-family:inherit;font-size:10pt;">15.1 million</font><font style="font-family:inherit;font-size:10pt;"> and other liabilities of </font><font style="font-family:inherit;font-size:10pt;">$11.0 million</font><font style="font-family:inherit;font-size:10pt;">. The Company recognized a gain of </font><font style="font-family:inherit;font-size:10pt;">$8.0 million</font><font style="font-family:inherit;font-size:10pt;"> upon the closing of the Aytu Divestiture. As a result of the sale of the Pediatric Portfolio, the Pediatric Portfolio met all conditions required in order to be classified as discontinued operations. Therefore, operating results from the Pediatric Portfolio are reported within income (loss) from discontinued operations, net of tax (inclusive of gain on sale) for all periods presented and the gain recognized as a result of the sale is reported within income from discontinued operations, net of tax (inclusive of gain on sale) for the year ended December 31, 2019. In addition, assets and liabilities related to the Pediatric Portfolio are reported as assets and liabilities of discontinued operations in the accompanying consolidated balance sheets as of December 31, 2019 and 2018. See Note 3 for more information regarding the Aytu Divestiture and its accounting treatment.</font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">Cerecor was incorporated in 2011, commenced operations in the second quarter of 2011 and completed an initial public offering in October 2015.</font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-style:italic;font-weight:bold;">Liquidity</font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-style:italic;font-weight:bold;"></font><font style="font-family:inherit;font-size:10pt;">During the first quarter of 2019, the Company closed on an underwritten public offering of common stock for </font><font style="font-family:inherit;font-size:10pt;">1,818,182</font><font style="font-family:inherit;font-size:10pt;"> shares of common stock of the Company, at a price to the public of </font><font style="font-family:inherit;font-size:10pt;">$5.50</font><font style="font-family:inherit;font-size:10pt;"> per share ("public price"). Armistice Capital Master Fund Ltd. ("Armistice"), the Company's largest stockholder, participated in the offering by purchasing </font><font style="font-family:inherit;font-size:10pt;">363,637</font><font style="font-family:inherit;font-size:10pt;"> shares of common stock of the Company at the public price. Cerecor director, Steven J. Boyd, is Armistice's Chief Investment Officer. The net proceeds of the offering were approximately </font><font style="font-family:inherit;font-size:10pt;">$9.0 million</font><font style="font-family:inherit;font-size:10pt;">. During the third quarter of 2019, the Company entered into a securities purchase agreement with Armistice, pursuant to which, the Company sold </font><font style="font-family:inherit;font-size:10pt;">1,200,000</font><font style="font-family:inherit;font-size:10pt;"> shares of its common stock for a purchase price of </font><font style="font-family:inherit;font-size:10pt;">$3.132</font><font style="font-family:inherit;font-size:10pt;"> per share. Net proceeds of the private placement were approximately </font><font style="font-family:inherit;font-size:10pt;">$3.7 million</font><font style="font-family:inherit;font-size:10pt;">. During the fourth quarter of 2019, the Company entered into, and subsequently closed on, the Aytu Purchase Agreement to sell the Company's rights, title and interest in, assets relating to its Pediatric Portfolio and related commercial infrastructure for a combination of cash and preferred stock (</font><font style="font-family:inherit;font-size:10pt;">$4.5 million</font><font style="font-family:inherit;font-size:10pt;"> in cash, and approximately </font><font style="font-family:inherit;font-size:10pt;">9.8 million</font><font style="font-family:inherit;font-size:10pt;"> shares of Aytu convertible preferred stock) and the assumption of certain of the Company's liabilities including the Company&#8217;s payment obligations payable to Deerfield of </font><font style="font-family:inherit;font-size:10pt;">$15.1 million</font><font style="font-family:inherit;font-size:10pt;"> and certain other liabilities of approximately </font><font style="font-family:inherit;font-size:10pt;">$11.0 million</font><font style="font-family:inherit;font-size:10pt;">. During the first quarter of 2020, the Company closed on a registered direct offering with institutional investors of </font><font style="font-family:inherit;font-size:10pt;">1,306,282</font><font style="font-family:inherit;font-size:10pt;"> shares of the Company's common stock at a purchase price of </font><font style="font-family:inherit;font-size:10pt;">$3.98</font><font style="font-family:inherit;font-size:10pt;"> per share. Armistice participated in the offering by purchasing </font><font style="font-family:inherit;font-size:10pt;">1,256,282</font><font style="font-family:inherit;font-size:10pt;"> shares of common stock from the Company. The net proceeds of the offering were approximately </font><font style="font-family:inherit;font-size:10pt;">$5.0 million</font><font style="font-family:inherit;font-size:10pt;">.</font></div><div style="line-height:120%;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">In order to meet its cash flow needs, the Company applies a disciplined decision-making methodology as it evaluates the optimal allocation of the Company's resources between investing in the Company's existing pipeline assets and acquisitions or in-licensing of new assets. For the year ended December 31, 2019, Cerecor generated a net loss of </font><font style="font-family:inherit;font-size:10pt;">$16.1 million</font><font style="font-family:inherit;font-size:10pt;"> and negative cash flow from operations of </font><font style="font-family:inherit;font-size:10pt;">$19.1 million</font><font style="font-family:inherit;font-size:10pt;">. As of December 31, 2019, Cerecor had an accumulated deficit of </font><font style="font-family:inherit;font-size:10pt;">$114.3 million</font><font style="font-family:inherit;font-size:10pt;"> and </font><font style="font-family:inherit;font-size:10pt;">$3.6 million</font><font style="font-family:inherit;font-size:10pt;"> in cash and cash equivalents. </font></div><div style="line-height:120%;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The accompanying consolidated financial statements have been prepared assuming the Company will continue as a going concern; however, the Company expects to incur additional losses in the future in connection with research and development activities and will require additional financing to fund its operations and to continue to execute its strategy. The Company plans to use its current cash on hand and the anticipated cash flows from the Company's profits from Millipred product sales and/or the potential proceeds from the out-license or sale of Millipred to a third party to offset costs related to its orphan disease pipeline assets, business development, and costs associated with its organizational infrastructure; however, Cerecor expects to continue to incur significant expenses and operating losses for the immediate future as it continues to invest in the Company's pipeline assets. The Company&#8217;s ability to continue as a going concern through 2020 is dependent upon the Company&#8217;s ability to raise additional equity and/or debt capital; however, there can be no assurance that such capital will be available in sufficient amounts or on terms acceptable to the Company. </font></div><div style="line-height:120%;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">Over the long term, the Company's ultimate ability to achieve and maintain profitability is dependent on, among other things, the development, regulatory approval, and commercialization of its pipeline assets, and the potential sale of any PRVs it receives, all being adequate to support its cost structure and pipeline asset development.</font></div><div style="line-height:120%;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:left;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">These conditions raise substantial doubt about its ability to continue as a going concern within one year after the date that the financial statements are issued. To alleviate these conditions, the Company is evaluating the potential out-licensing or sale of Millipred to a third party and some combination of rights to future PRV sales, equity or debt financings, collaborations, out-licensing arrangements, strategic alliances, federal and private grants, marketing, distribution or licensing arrangements, the sale of current or future assets or possible monetization of the Company's holdings of Aytu equity. If the Company raises additional funds through collaborations, strategic alliances or licensing arrangements with third parties, the Company might have to relinquish valuable rights to its technologies, future revenue streams, research programs or product candidates. If the Company is not able to secure adequate additional funding, the Company may be forced to make reductions in spending, extend payment terms with suppliers, liquidate assets where possible or suspend or curtail planned programs. Due to the uncertainty regarding future financings and/or other potential options to raise additional funds, management has concluded that substantial doubt exists with respect to the Company&#8217;s ability to continue as a going concern within one year after the date that the financial statements are issued.</font></div></div>
CY2019 us-gaap Use Of Estimates
UseOfEstimates
<div style="font-family:Times New Roman;font-size:10pt;"><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-style:italic;font-weight:bold;">Use of Estimates</font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;font-style:italic;font-weight:bold;">&#160;&#160;&#160;&#160;</font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">The preparation of consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets, liabilities, revenues, expenses, and related disclosures. On an ongoing basis, management evaluates its estimates, including estimates related to but not limited to, revenue recognition, cost of product sales, stock-based compensation, fair value measurements (including those relating to contingent consideration, equity Investment in Aytu, and guaranteed liabilities), cash flows used in management's going concern assessment, income taxes, goodwill and other intangible assets, and clinical trial accruals. The Company bases its estimates on historical experience and other market&#8209;specific or other relevant assumptions that it believes to be reasonable under the circumstances. Actual results may differ from those estimates or assumptions.</font></div><div style="line-height:120%;text-align:justify;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div><div style="line-height:120%;text-align:justify;text-indent:48px;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;">Certain estimates related specifically to the Pediatric Portfolio, such as revenue, cost of product sales, fair value measurement (including those relating to contingent consideration), goodwill, and other intangible assets have been reclassified under discontinued operations and included in assets and liabilities of discontinued operations. </font></div><div style="line-height:120%;text-align:left;font-size:10pt;"><font style="font-family:inherit;font-size:10pt;"><br clear="none"/></font></div></div>

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