2022 Q3 Form 10-Q Financial Statement

#000155837022013274 Filed on August 11, 2022

View on sec.gov

Income Statement

Concept 2022 Q3 2022 Q2 2022 Q1
Revenue $3.165M $3.918M $3.492M
YoY Change -0.43% 16.05% 13.23%
Cost Of Revenue $740.0K $731.0K $694.0K
YoY Change -16.81% 2.38% 0.0%
Gross Profit $2.425M $3.187M $2.798M
YoY Change 5.94% 19.72% 17.07%
Gross Profit Margin 76.62% 81.34% 80.13%
Selling, General & Admin $6.713M $6.902M $12.50M
YoY Change 38.7% 57.62% 140.92%
% of Gross Profit 276.82% 216.57% 446.89%
Research & Development $4.512M $5.219M $4.728M
YoY Change 0.55% 13.58% -21.9%
% of Gross Profit 186.06% 163.76% 168.98%
Depreciation & Amortization $1.128M $1.006M $947.0K
YoY Change -27.02% -36.52% -41.14%
% of Gross Profit 46.52% 31.57% 33.85%
Operating Expenses $4.512M $5.219M $4.728M
YoY Change 0.55% 13.58% -21.9%
Operating Profit -$8.831M -$8.970M -$14.47M
YoY Change 24.74% 41.17% 60.78%
Interest Expense $620.0K $542.0K $478.0K
YoY Change 202.28% 167.0% 218.67%
% of Operating Profit
Other Income/Expense, Net -$261.0K -$477.0K -$1.471M
YoY Change 29.7% 140.91% 708.24%
Pretax Income -$9.092M -$9.447M -$15.94M
YoY Change 24.87% 44.2% 73.67%
Income Tax $0.00
% Of Pretax Income
Net Earnings -$9.092M -$9.447M -$15.94M
YoY Change 24.87% 44.18% 73.61%
Net Earnings / Revenue -287.27% -241.12% -456.56%
Basic Earnings Per Share -$0.14 -$0.15 -$0.30
Diluted Earnings Per Share -$0.14 -$0.15 -$0.30
COMMON SHARES
Basic Shares Outstanding 64.36M 62.18M 52.47M
Diluted Shares Outstanding 64.46M 62.18M 52.47M

Balance Sheet

Concept 2022 Q3 2022 Q2 2022 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $98.32M $103.8M $57.79M
YoY Change 53.5% 52.95% 7.74%
Cash & Equivalents $98.32M $103.8M $57.80M
Short-Term Investments
Other Short-Term Assets $1.602M $907.0K $874.0K
YoY Change 326.4% 106.38% 7.9%
Inventory
Prepaid Expenses
Receivables $3.136M $3.753M $3.287M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $103.1M $108.5M $61.96M
YoY Change 52.72% 52.13% 12.48%
LONG-TERM ASSETS
Property, Plant & Equipment $3.943M $4.219M $4.614M
YoY Change -27.68% -28.25% -26.72%
Goodwill $3.903M $3.903M $3.903M
YoY Change -0.01% -0.01% -0.01%
Intangibles $3.812M $4.041M $4.225M
YoY Change -15.67% -16.77% -18.85%
Long-Term Investments
YoY Change
Other Assets $15.67M $16.15M $16.49M
YoY Change -4.86% 1.7% 7.26%
Total Long-Term Assets $29.51M $30.58M $31.57M
YoY Change -10.08% -7.5% -5.4%
TOTAL ASSETS
Total Short-Term Assets $103.1M $108.5M $61.96M
Total Long-Term Assets $29.51M $30.58M $31.57M
Total Assets $132.6M $139.1M $93.53M
YoY Change 32.17% 33.24% 5.74%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $1.140M $1.412M $1.666M
YoY Change -29.16% -44.55% -44.54%
Accrued Expenses $6.089M $5.144M $5.976M
YoY Change 18.7% 25.59% 31.34%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $231.0K $281.0K $334.0K
YoY Change -29.02% -14.98% 1.21%
Total Short-Term Liabilities $7.460M $6.837M $7.976M
YoY Change 5.6% -1.95% 1.18%
LONG-TERM LIABILITIES
Long-Term Debt $19.74M $19.61M $19.48M
YoY Change 91.07% 91.21% 91.38%
Other Long-Term Liabilities $10.14M $10.31M $10.44M
YoY Change 6.56% 35.1% 51.26%
Total Long-Term Liabilities $19.74M $19.61M $19.48M
YoY Change 91.07% 91.21% 91.38%
TOTAL LIABILITIES
Total Short-Term Liabilities $7.460M $6.837M $7.976M
Total Long-Term Liabilities $19.74M $19.61M $19.48M
Total Liabilities $37.53M $36.98M $38.14M
YoY Change 37.31% 45.8% 49.3%
SHAREHOLDERS EQUITY
Retained Earnings -$344.1M -$335.0M -$325.5M
YoY Change 15.47% 15.24% 14.53%
Common Stock $64.00K $64.00K $53.00K
YoY Change 23.13% 23.14% 22.27%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $95.03M $102.1M $55.39M
YoY Change
Total Liabilities & Shareholders Equity $132.6M $139.1M $93.53M
YoY Change 32.17% 33.24% 5.74%

Cashflow Statement

Concept 2022 Q3 2022 Q2 2022 Q1
OPERATING ACTIVITIES
Net Income -$9.092M -$9.447M -$15.94M
YoY Change 24.87% 44.18% 73.61%
Depreciation, Depletion And Amortization $1.128M $1.006M $947.0K
YoY Change -27.02% -36.52% -41.14%
Cash From Operating Activities -$5.774M -$8.429M -$9.782M
YoY Change -0.97% 2.1% -21.02%
INVESTING ACTIVITIES
Capital Expenditures -$94.00K -$7.000K $0.00
YoY Change -81.2% -100.0%
Acquisitions
YoY Change
Other Investing Activities $0.00 $5.000K
YoY Change
Cash From Investing Activities -$94.00K -$2.000K $0.00
YoY Change -94.63% -100.0%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net $10.50M
YoY Change 1.42%
Cash From Financing Activities 348.0K 54.48M 10.08M
YoY Change -82.55% 141.62% 1228.33%
NET CHANGE
Cash From Operating Activities -5.774M -8.429M -9.782M
Cash From Investing Activities -94.00K -2.000K 0.000
Cash From Financing Activities 348.0K 54.48M 10.08M
Net Change In Cash -5.520M 46.05M 300.0K
YoY Change 43.91% 223.06% -102.57%
FREE CASH FLOW
Cash From Operating Activities -$5.774M -$8.429M -$9.782M
Capital Expenditures -$94.00K -$7.000K $0.00
Free Cash Flow -$5.680M -$8.422M -$9.782M
YoY Change -2.58% 2.47% -21.35%

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<p style="font-family:'Times New Roman','Times','serif';font-size:10pt;font-weight:bold;margin:0pt 0pt 12pt 0pt;">1. Business</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;font-weight:bold;margin:0pt 0pt 12pt 0pt;">Description of the Business</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">Liquidia Corporation (“Liquidia” or the “Company”) is a biopharmaceutical company focused on the development, manufacture, and commercialization of products that address unmet patient needs, with current focus directed towards the treatment of pulmonary hypertension (“PH”). Liquidia Corporation operates through its wholly owned operating subsidiaries, Liquidia Technologies, Inc. (“Liquidia Technologies”) and Liquidia PAH, LLC (“Liquidia PAH”), formerly known as RareGen, LLC (“RareGen”).</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">The Company generates revenue primarily pursuant to a promotion agreement between Liquidia PAH and Sandoz Inc. (“Sandoz”), dated as of August 1, 2018, as amended (the “Promotion Agreement”), sharing profit derived from the sale of the first-to-file fully substitutable generic treprostinil injection (“Treprostinil Injection”) in the United States. Liquidia PAH has the exclusive rights to conduct commercial activities to encourage the appropriate use of Treprostinil Injection. The Company employs a targeted sales force calling on physicians and hospital pharmacies involved in the treatment of pulmonary arterial hypertension (PAH) in the United States, as well as key stakeholders involved in the distribution and reimbursement of Treprostinil Injection. Strategically, the Company believes that its commercial presence in the field will enable an efficient base to expand from for the launch of YUTREPIA upon final approval, leveraging existing relationships and further validating its reputation as a company committed to supporting PAH patients.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">The Company conducts research, development and manufacturing of novel products by applying its proprietary PRINT® technology, a particle engineering platform, to enable precise production of uniform drug particles designed to improve the safety, efficacy and performance of a wide range of therapies. </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">The Company’s lead product candidate, for which it holds worldwide commercial rights, is YUTREPIA for the treatment of PAH. YUTREPIA is an inhaled dry powder formulation of treprostinil designed to improve the therapeutic profile of treprostinil by enhancing deep lung delivery and achieving higher dose levels than current inhaled therapies. The Company’s New Drug Application (NDA) for YUTREPIA was tentatively approved by the FDA in November 2021.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;font-weight:bold;margin:0pt 0pt 12pt 0pt;">Risks and Uncertainties</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;padding-bottom:12pt;margin:0pt;">The Company is subject to risks and uncertainties common to companies in the biotechnology industry, including, but not limited to, development by competitors of new technological innovations, dependence on third parties and key personnel, protection of proprietary technology, compliance with government regulations, and the ability to secure additional capital to fund operations.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;">The current global macro-economic environment is volatile, which may result in supply chain constraints and elevated rates of inflation. In addition, the Company operates in a dynamic and highly competitive industry and believes that changes in any of the following areas could have a material adverse effect on the Company’s future financial position, results of operations, or cash flows: the ability to obtain future financing; advances and trends in new technologies and industry standards; results of clinical trials; regulatory approval and market acceptance of the Company’s products; development of sales channels; certain strategic relationships; litigation or claims against the Company related to intellectual property, product, regulatory, or other matters; and the Company’s ability to attract and retain employees necessary to support its growth.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:36pt;background:#ffffff;margin:0pt;"><span style="font-size:13.5pt;visibility:hidden;">​</span></p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;">Product candidates developed by the Company require approval from the FDA and/or other international regulatory agencies prior to commercial sales. There can be no assurance that the Company's product candidates will receive the necessary approvals. If the Company is denied approval, approval is delayed, or the Company is unable to maintain approval, it could have a material adverse impact on the Company.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;">The Company relies on single source manufacturers and suppliers for the supply of its product candidates. This adds to the manufacturing risks faced by the Company, which could be left without backup facilities in the event of any failure by a supplier. Any disruption from these manufacturers or suppliers could have a negative impact on the Company’s business, financial position and results of operations.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;"><span style="font-size:13.5pt;visibility:hidden;">​</span></p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;">The COVID-19 pandemic continues to adversely affect global economies, financial markets and the overall environment.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;">The Company does not believe its financial results were materially affected by the COVID-19 pandemic during the six months ended June 30, 2022.  However, the extent to which the COVID-19 pandemic may affect the Company’s future financial results and operations will depend on future developments which are highly uncertain and cannot be predicted, including new information which may emerge concerning the pandemic, the availability and effectiveness of vaccines and treatment options, and current or future domestic and international actions to contain it and treat it. The Company continues to evaluate the potential impact of the COVID-19 pandemic on its business, including the potential impact of the pandemic on the potential commercial launch of YUTREIPA and any potential supply-chain challenges.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;background:#ffffff;margin:0pt;"><span style="visibility:hidden;">​</span></p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;font-weight:bold;margin:0pt 0pt 12pt 0pt;">Liquidity</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">The Company expects to incur significant expenses and operating losses for the foreseeable future as it seeks regulatory approval and pursues commercialization of any approved product candidates. In addition, if the Company obtains marketing approval for any of its current or future product candidates, it would incur significant commercialization expenses related to product manufacturing, marketing, sales and distribution. These efforts require significant amounts of capital, adequate personnel and infrastructure, and extensive compliance-reporting capabilities. Even if the Company's development efforts are successful, it is uncertain when, if ever, the Company will realize significant revenue from product sales. If the Company determines it requires but is unable to obtain funding, the Company could be required to delay, reduce, or eliminate research and development programs, product portfolio expansion, or future commercialization efforts, which could adversely affect its business prospects.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">In accordance with Accounting Standards Update (“ASU”) 2014-15,<i style="font-style:italic;"> Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern (Subtopic 205-40)</i>, the Company has evaluated whether there are conditions and events, considered in the aggregate, that raise substantial doubt about the Company’s ability to continue as a going concern within one year after the date that the condensed consolidated financial statements are issued. The Company has financed its growth and operations through a combination of funds generated from revenues, the issuance of convertible preferred stock and common stock, finance leases, bank borrowings, bank borrowings with warrants and the issuance of convertible notes and warrants. Since inception, the Company has incurred recurring losses, including net loss of $25.4 million for the six months ended June 30, 2022 and the Company had an accumulated deficit of $335.0 million as of June 30, 2022. Although the Company expects to continue to generate operating losses for the foreseeable future, management anticipates that cash and cash equivalents will be sufficient to fund operations and remain in compliance with financial covenants into 2024. The Company has based these estimates on assumptions that may differ from actual results, and it could use its available resources sooner than expected.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;"><span style="background:#ffffff;">The Company expects that its cash and cash equivalents will be sufficient to fund its operating expenses and capital expenditure requirements for at least twelve months from the issuance date of these unaudited interim condensed consolidated financial statements</span><span style="background:#ffffff;">.</span></p>
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<p style="font-family:'Times New Roman','Times','serif';font-size:10pt;font-style:italic;font-weight:bold;margin:0pt 0pt 12pt 0pt;">Use of Estimates</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;"><span style="background:#ffffff;">The preparation of financial statements in accordance with 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 financial statements, as well as the reported amounts of revenues and expenses during the period. The Company evaluates its estimates on an ongoing basis, including those related to the valuation of stock-based awards and certain accruals, and makes changes to the estimates and related disclosures as experience develops or new information becomes known. These estimates are based on historical experience and various other assumptions believed reasonable under the circumstances. Actual results will most likely differ from those estimates.</span></p>
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CY2022Q2 us-gaap Long Term Debt Maturities Repayments Of Principal In Year Two
LongTermDebtMaturitiesRepaymentsOfPrincipalInYearTwo
10000000
CY2022Q2 us-gaap Long Term Debt Maturities Repayments Of Principal In Year Three
LongTermDebtMaturitiesRepaymentsOfPrincipalInYearThree
10000000
CY2022Q2 us-gaap Debt Instrument Carrying Amount
DebtInstrumentCarryingAmount
20000000
CY2022Q2 us-gaap Debt Instrument Unamortized Discount Premium And Debt Issuance Costs Net
DebtInstrumentUnamortizedDiscountPremiumAndDebtIssuanceCostsNet
394000
CY2022Q2 us-gaap Long Term Debt Noncurrent
LongTermDebtNoncurrent
19606000

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