2020 Q4 Form 10-K Financial Statement

#000162828021003283 Filed on February 25, 2021

View on sec.gov

Income Statement

Concept 2020 Q4 2020 Q3 2020 Q2
Revenue $56.70M $59.99M $90.14M
YoY Change -18.53% -34.78% -10.58%
Cost Of Revenue $63.23M $30.35M $174.6M
YoY Change 65.76% -20.69% 363.55%
Gross Profit -$300.0K $29.64M -$84.47M
YoY Change -100.76% -44.81% -233.8%
Gross Profit Margin -0.53% 49.41% -93.71%
Selling, General & Admin $40.30M $40.17M $35.48M
YoY Change -10.24% 17.53% -1.62%
% of Gross Profit 135.52%
Research & Development $37.60M $46.86M $52.82M
YoY Change -53.23% -37.11% -38.36%
% of Gross Profit 158.07%
Depreciation & Amortization $7.730M $500.0K $500.0K
YoY Change -20.23% -16.67% -16.67%
% of Gross Profit 1.69%
Operating Expenses $78.87M $87.74M $89.35M
YoY Change -37.55% -19.96% -27.16%
Operating Profit -$85.40M -$58.10M -$173.8M
YoY Change -10.0% 3.92% 192.02%
Interest Expense -$2.300M -$2.274M -$2.308M
YoY Change 187.5% -1097.37% -575.88%
% of Operating Profit
Other Income/Expense, Net -$1.597M -$1.864M -$1.932M
YoY Change 18.82% -4434.88% -480.31%
Pretax Income -$87.00M -$59.96M -$175.8M
YoY Change -9.56% 7.33% 197.81%
Income Tax $0.00 $0.00 $0.00
% Of Pretax Income
Net Earnings -$87.00M -$59.96M -$175.8M
YoY Change -7.92% 9.85% 202.13%
Net Earnings / Revenue -153.44% -99.95% -194.97%
Basic Earnings Per Share -$0.42 -$1.28
Diluted Earnings Per Share -$599.2K -$0.42 -$1.28
COMMON SHARES
Basic Shares Outstanding 144.5M shares 143.3M shares
Diluted Shares Outstanding 143.3M shares

Balance Sheet

Concept 2020 Q4 2020 Q3 2020 Q2
SHORT-TERM ASSETS
Cash & Short-Term Investments $268.7M $269.3M $295.3M
YoY Change 81.93% 84.94% 115.92%
Cash & Equivalents $228.7M $169.3M $245.4M
Short-Term Investments $40.00M $100.0M $49.90M
Other Short-Term Assets $14.90M $9.000M $10.00M
YoY Change 125.76% 15.38% -65.03%
Inventory $61.02M $88.24M $104.6M
Prepaid Expenses
Receivables $26.85M $24.47M $39.12M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $371.4M $391.0M $449.1M
YoY Change 20.0% 30.77% 41.94%
LONG-TERM ASSETS
Property, Plant & Equipment $8.622M $8.821M $9.380M
YoY Change -16.94% -31.08% -13.97%
Goodwill $55.10M $55.10M $55.10M
YoY Change 0.0% 0.09% 0.09%
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $37.98M $44.17M $47.27M
YoY Change -50.02% -54.89% -52.98%
Total Long-Term Assets $272.7M $285.1M $296.1M
YoY Change -40.93% -42.54% -41.62%
TOTAL ASSETS
Total Short-Term Assets $371.4M $391.0M $449.1M
Total Long-Term Assets $272.7M $285.1M $296.1M
Total Assets $644.1M $676.1M $745.2M
YoY Change -16.48% -14.97% -9.51%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $41.31M $40.40M $29.41M
YoY Change 5.33% -37.23% 52.23%
Accrued Expenses $130.6M $123.0M $142.8M
YoY Change 1.2% -2.86% 13.38%
Deferred Revenue $15.21M $18.03M $23.53M
YoY Change -61.8% -43.89% -41.64%
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $0.00
YoY Change
Total Short-Term Liabilities $187.1M $181.5M $195.8M
YoY Change -10.08% -18.68% 5.47%
LONG-TERM LIABILITIES
Long-Term Debt $96.38M $76.61M $76.34M
YoY Change 27.14%
Other Long-Term Liabilities $60.61M $40.97M $41.51M
YoY Change 100.55% 36.3% 38.83%
Total Long-Term Liabilities $157.0M $117.6M $117.8M
YoY Change 48.06% 291.15% 294.16%
TOTAL LIABILITIES
Total Short-Term Liabilities $187.1M $181.5M $195.8M
Total Long-Term Liabilities $157.0M $117.6M $117.8M
Total Liabilities $396.5M $358.2M $374.9M
YoY Change 5.33% 9.32% 23.26%
SHAREHOLDERS EQUITY
Retained Earnings -$1.178B -$1.091B -$1.031B
YoY Change 48.29% 55.88% 59.78%
Common Stock $1.425B $1.408B $1.401B
YoY Change 19.88% 20.31%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $247.6M $318.0M $370.3M
YoY Change
Total Liabilities & Shareholders Equity $644.1M $676.1M $745.2M
YoY Change -16.48% -14.97% -9.51%

Cashflow Statement

Concept 2020 Q4 2020 Q3 2020 Q2
OPERATING ACTIVITIES
Net Income -$87.00M -$59.96M -$175.8M
YoY Change -7.92% 9.85% 202.13%
Depreciation, Depletion And Amortization $7.730M $500.0K $500.0K
YoY Change -20.23% -16.67% -16.67%
Cash From Operating Activities -$30.78M -$27.24M $37.22M
YoY Change -66.59% -347.86% -197.0%
INVESTING ACTIVITIES
Capital Expenditures -$320.0K $50.00K -$50.00K
YoY Change 45.45% -101.98% -97.47%
Acquisitions
YoY Change
Other Investing Activities $60.00M -$49.98M -$49.96M
YoY Change 166.67% -285.66% -189.2%
Cash From Investing Activities $59.69M -$49.94M -$50.00M
YoY Change 167.91% -304.76% -192.52%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 30.51M 1.050M 142.8M
YoY Change -67.69% 452.63% 1521.0%
NET CHANGE
Cash From Operating Activities -30.78M -27.24M 37.22M
Cash From Investing Activities 59.69M -49.94M -50.00M
Cash From Financing Activities 30.51M 1.050M 142.8M
Net Change In Cash 59.42M -76.13M 130.0M
YoY Change 141.84% -314.03% 431.17%
FREE CASH FLOW
Cash From Operating Activities -$30.78M -$27.24M $37.22M
Capital Expenditures -$320.0K $50.00K -$50.00K
Free Cash Flow -$30.46M -$27.29M $37.27M
YoY Change -66.86% -301.85% -202.42%

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Nature of Organization and Operations<div style="margin-top:6pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">Akebia Therapeutics, Inc., referred to as Akebia or the Company, was incorporated in the State of Delaware in 2007. Akebia is a biopharmaceutical company with the purpose of bettering the lives of people living with kidney disease. Akebia’s lead investigational product candidate, vadadustat, is an oral therapy in Phase 3 development for the treatment of anemia due to chronic kidney disease, or CKD. Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor, or HIF-PHI, designed to mimic the physiologic effect of altitude on oxygen availability. At higher altitudes, the body responds to lower oxygen availability with stabilization of hypoxia-inducible factor, or HIF, which can lead to red blood cell, or RBC, production and improved oxygen delivery to tissues. Vadadustat is approved and marketed in Japan as a treatment for anemia due to CKD in both dialysis-dependent and non-dialysis dependent adult patients under the trade name Vafseo</span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:6.5pt;font-weight:400;line-height:120%;position:relative;top:-3.5pt;vertical-align:baseline">TM</span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">. In addition, the Company has a commercial product, Auryxia, which is currently approved by the U.S. Food and Drug Administration, or FDA, and marketed for two indications in the United States, the control of serum phosphorus levels in adult patients with CKD on dialysis, or DD-CKD, and the treatment of iron deficiency anemia, or IDA, in adult patients with CKD not on dialysis, or NDD-CKD. Ferric citrate is also approved and marketed in Japan as an oral treatment for the improvement of hyperphosphatemia in patients with DD-CKD and NDD-CKD under the trade name Riona.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">On November 11, 2019, the Company, with Keryx Biopharmaceuticals, Inc., or Keryx, as guarantor, entered into a loan agreement, or the Loan Agreement, with Biopharma Credit plc as collateral agent and lender, or the Collateral Agent, and Biopharma Credit Investments V (Master) LP as lender, pursuant to which term loans in an aggregate principal amount of $100 million were available to the Company in two tranches, subject to certain terms and conditions, or the Term Loans. BioPharma Credit PLC subsequently transferred its interest in the Term Loans, solely in its capacity as a lender, to its affiliate, BPCR Limited Partnership. The Collateral Agent and the lenders are collectively referred to as Pharmakon.</span><span style="color:#000000;font-family:'Calibri',sans-serif;font-size:11pt;font-weight:400;line-height:120%"> </span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">The first tranche of $80.0 million, or Tranche A, was drawn on November 25, 2019 and the second tranche of $20.0 million, or Tranche B, was drawn on December 10, 2020. Refer to Note 11 to our consolidated financial statements in Part II, Item 8 – Financial Statements and Supplementary Data for additional details on the Loan Agreement.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">On December 12, 2018, the Company completed a merger with Keryx Biopharmaceuticals, Inc., or Keryx, or the Merger. Pursuant to the terms and conditions of the Agreement and Plan of Merger, or the Merger Agreement, each share of Keryx common stock, or Keryx Share, issued and outstanding immediately prior to the effective time of the Merger, or the Effective Time, was cancelled and converted into 0.37433, or the Exchange Multiplier, fully paid and non-assessable shares of Akebia common stock, or Akebia Shares, resulting in the issuance of an aggregate of 59,270,410 Akebia Shares.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">Since inception, the Company has devoted most of its resources to research and development, including its preclinical and clinical development activities, and providing general and administrative support for these operations. The Company began recording revenue from the U.S. sales of Auryxia and revenue from sublicensing rights to Auryxia in Japan to the Company’s Japanese partners Japan Tobacco, Inc. and its subsidiary Torii Pharmaceutical Co., Ltd., collectively JT and Torii, on December 12, 2018. Additionally, following regulatory approval of vadadustat in Japan, the Company began recognizing royalty revenues from Mitsubishi Tanabe Pharma Corporation, or MTPC, from the sale of Vafseo in August 2020. The Company has not generated a profit to date and may never generate profits from product sales. Vadadustat and the Company’s other potential product candidates are subject to long development cycles, and the Company may be unsuccessful in its efforts to develop, obtain marketing approval for or market vadadustat and its other potential product candidates. If the Company does not successfully commercialize Auryxia, vadadustat or any other potential product candidate, it may be unable to achieve profitability.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">The Company is subject to a number of risks including, but not limited to, the need to obtain adequate additional funding, including the resources necessary to fund the continued development and commercialization of Auryxia, and the development, regulatory activities and potential commercialization of vadadustat, risks relating to integration following the Merger, risks relating to market acceptance, coverage and reimbursement of Auryxia and vadadustat, if approved, risks related to maintaining the Company’s commercial organization and capabilities, risks relating to potential generic entrants, risks of clinical trial failures, the risk of relying on third parties, the risk that the Company never achieves profitability, protection of proprietary technology, compliance with governmental regulations, and dependence on key personnel, and the impact of legal, regulatory and administrative proceedings.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">In December 2015, the Company entered into a collaboration agreement with MTPC to develop and commercialize vadadustat in Japan and certain other countries in Asia, collectively, the MTPC Territory, for total payments of up to $245.0 million, </span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">comprised of a $20.0 million upfront payment, up to $50.0 million in specified development and regulatory milestones, and up to $175.0 million in specified commercial milestones, as well as tiered royalty payments ranging from 13% to 20% on annual net sales of vadadustat in the MTPC Territory, subject to a reduction upon launch of a generic product on a country-by-country basis. The Company began receiving royalty payments from MTPC during the year ended December 31, 2020 when MTPC commenced commercial sales of vadadustat in Japan under the trade name, Vafseo</span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:6.5pt;font-weight:400;line-height:120%;position:relative;top:-3.5pt;vertical-align:baseline">TM</span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">, in August 2020 (Note 4).</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">In December 2016, the Company entered into a collaboration and license agreement with Otsuka Pharmaceutical Co. Ltd., or Otsuka, to develop and commercialize vadadustat in the United States. In December 2016, the Company received $125.0 million upfront payment, and in March 2017, Otsuka reimbursed the Company approximately $33.8 million for global expenses previously incurred by us for the global development program for vadadustat in DD-CKD and NDD-CKD adult patients. The agreement also provides for additional funding for the global development program for vadadustat, totaling $319.0 million or more, depending on the actual global development costs incurred. In addition, as of December 31, 2020, Akebia is eligible to receive from Otsuka up to $65.0 million in specified regulatory milestones and up to $575.0 million in specified commercial milestones. The Company will share with Otsuka the costs of developing and commercializing vadadustat in the United States and the profits from sales of vadadustat in the United States after approval by the FDA and commercial launch (Note 4).</span></div><div><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:6pt;font-weight:400;line-height:120%"> </span></div><div style="margin-top:6pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">In April 2017, the Company entered into a collaboration and license agreement with Otsuka to develop and commercialize vadadustat in Europe, Russia, China, Canada, Australia, the Middle East and certain other territories. In April 2017, the Company received a $73.0 million upfront payment and $0.2 million for global expenses previously incurred by the Company in implementing the current global Phase 3 development plan for vadadustat in DD-CKD and NDD-CKD adult patients in excess of a specified threshold during the quarter-ended March 31, 2017. The agreement also provides for additional funding for the global development program for vadadustat, totaling $226.2 million or more, depending on the actual global development costs incurred. In addition, as of December 31, 2020, Akebia is eligible to receive from Otsuka up to $52.0 million in specified regulatory milestones and up to $525.0 million in specified commercial milestones (Note 4).</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">From inception through December 31, 2020, the Company has raised approximately $704.3 million of net proceeds from the sale of equity, including $519.8 million from several underwritten public offerings, $134.5 million from at-the-market offerings, or ATM offerings, pursuant to sales agreements with Cantor Fitzgerald &amp; Co. and $50.0 million from the sale of 3,571,429 shares of common stock to Vifor (International) Ltd., or Vifor Pharma. During the year ended December 31, 2020, the Company completed an underwritten public offering of our common stock with aggregate net proceeds of $142.4 million and raised $67.3 million of net proceeds from ATM offerings. In November 2019, the Company received net proceeds of $77.3 million from Tranche A of the Loan Agreement with Pharmakon. In December 2020, the Company received net proceeds of $20.0 million from Tranche B of the Loan Agreement with Pharmakon. Subsequent to December 31, 2020 and through the date of this Annual Report on Form 10-K, the Company raised $15.9 million in net proceeds from ATM offerings. At the inception of the Company’s collaboration agreements with Otsuka and MTPC, they committed to an aggregate of approximately $573.0 million or more in cost-share funding, of which the Company received approximately $272.0 million at the onset of the collaborations, and the remainder of which the Company generally continues to receive on a quarterly prepaid basis, and via license payments.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">The Company's management completed its going concern assessment in accordance with ASC 205-40, </span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-style:italic;font-weight:400;line-height:120%">Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern</span><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">, or ASC 205-40. The Company believes that its cash resources will be sufficient to allow the Company to fund its current operating plan through at least the next twelve months from the filing of the Company’s 2020 Annual Report on Form 10-K, as required by ASC 205-40. There can be no assurance, however, that the current operating plan will be achieved in the time frame anticipated by the Company, or that its cash resources will fund the Company’s operating plan for the period anticipated by the Company or that additional funding will be available on terms acceptable to the Company, or at all. The Company will require additional capital to pursue development and commercial activities related to Auryxia and vadadustat or any additional products and product candidates, including those that may be in-licensed or acquired. The Company expects to finance future cash needs through product revenue, public or private equity or debt transactions, payments from its collaborators, royalty transactions, strategic transactions, or a combination of these approaches. However, adequate additional financing may not be available to the Company on acceptable terms, or at all. If the Company is unable to raise capital in sufficient amounts when needed or on attractive terms, it may not be able to pursue development and commercial activities related to Auryxia and vadadustat or any additional products and product candidates, including those that may be in-licensed or acquired.</span></div>
us-gaap Proceeds From Issuance Or Sale Of Equity
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704300000 USD
CY2020 us-gaap Number Of Operating Segments
NumberOfOperatingSegments
1 segment
CY2020 us-gaap Use Of Estimates
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<div style="margin-top:18pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:700;line-height:120%">Use of Estimates</span></div><div style="margin-top:6pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">The preparation of 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 disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results may differ from those estimates. Management considers many factors in selecting appropriate financial accounting policies and controls, and in developing the estimates and assumptions that are used in the preparation of these financial statements. Management must apply significant judgment in this process. In addition, other factors may affect estimates, including expected business and operational changes, sensitivity and volatility associated with the assumptions used in developing estimates, and whether historical trends are expected to be representative of future trends. The estimation process often may yield a range of potentially reasonable estimates of the ultimate future outcomes, and management must select an amount that falls within that range of reasonable estimates. Estimates are used in the following areas, among others: prepaid and accrued research and development expense, operating lease assets and liabilities, derivative liabilities, other non-current liabilities, including the excess purchase commitment liability, stock-based compensation expense, product and collaboration revenues including various rebates and reserves related to product sales, inventories, income taxes, intangible assets and goodwill. The Company has made estimates of the impact of COVID-19 within the consolidated financial statements and there may be changes to those estimates in future periods including changes to sales, payer mix, reserves and allowances, intangible assets and goodwill. </span></div><div style="margin-top:6pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">Although the Company regularly assesses these estimates, actual results could differ materially from these estimates. Changes in estimates are recorded in the period they become known. The Company bases its estimates on historical experience and various other assumptions that it believes to be reasonable under the circumstances.</span></div>
CY2020Q4 us-gaap Cash And Cash Equivalents At Carrying Value
CashAndCashEquivalentsAtCarryingValue
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CY2019Q4 us-gaap Cash And Cash Equivalents At Carrying Value
CashAndCashEquivalentsAtCarryingValue
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CY2018Q4 us-gaap Cash And Cash Equivalents At Carrying Value
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CY2017Q4 us-gaap Cash And Cash Equivalents At Carrying Value
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CY2020Q4 us-gaap Cash Cash Equivalents Restricted Cash And Restricted Cash Equivalents
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CY2019Q4 us-gaap Cash Cash Equivalents Restricted Cash And Restricted Cash Equivalents
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CY2018Q4 us-gaap Cash Cash Equivalents Restricted Cash And Restricted Cash Equivalents
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CY2017Q4 us-gaap Cash Cash Equivalents Restricted Cash And Restricted Cash Equivalents
CashCashEquivalentsRestrictedCashAndRestrictedCashEquivalents
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CY2020 us-gaap Concentration Risk Credit Risk
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<div style="margin-top:18pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:700;line-height:120%">Concentrations of Credit Risk and Off-Balance Sheet Risk</span></div><div style="margin-top:6pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">Cash, cash equivalents, investments, and accounts receivable are the only financial instruments that potentially subject the Company to concentrations of credit risk. The Company maintains its cash, cash equivalents, and investments with high quality, accredited financial institutions and, accordingly, such funds are subject to minimal credit risk. The Company’s investment </span></div><div style="margin-top:6pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">policy includes guidelines on the quality of the institutions and financial instruments and defines allowable investments that the Company believes minimizes the exposure to concentration of credit risk. The Company has no significant off-balance sheet concentrations of credit risk, such as foreign currency exchange contracts, option contracts or other hedging arrangements.</span></div><div style="margin-top:12pt"><span style="color:#000000;font-family:'Times New Roman',sans-serif;font-size:10pt;font-weight:400;line-height:120%">Accounts receivable represent amounts due from the Company’s Customers and collaboration partners. As part of its credit management policy, the Company performs ongoing credit evaluations of its Customers and generally does not require collateral from any customer. The Company also monitors economic conditions of its collaboration partners to identify facts or circumstances that may indicate that any of its accounts receivable are at risk of collection.</span></div>
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CY2019Q4 us-gaap Property Plant And Equipment Gross
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CY2019Q4 us-gaap Property Plant And Equipment Net
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CY2020 us-gaap Depreciation
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CY2018Q4 us-gaap Valuation Allowances And Reserves Balance
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CY2020Q4 us-gaap Available For Sale Debt Securities Accumulated Gross Unrealized Loss Before Tax
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CY2020Q4 us-gaap Available For Sale Securities Debt Securities
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CY2020Q4 us-gaap Available For Sale Debt Securities Accumulated Gross Unrealized Gain Before Tax
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CY2020Q4 us-gaap Available For Sale Debt Securities Accumulated Gross Unrealized Loss Before Tax
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CY2019Q4 us-gaap Cash And Cash Equivalents At Carrying Value
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CY2019Q4 us-gaap Cash And Cash Equivalents Fair Value Disclosure
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CY2019Q4 us-gaap Available For Sale Debt Securities Accumulated Gross Unrealized Loss Before Tax
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CY2019Q4 us-gaap Available For Sale Securities Debt Securities
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CY2019Q4 us-gaap Available For Sale Debt Securities Accumulated Gross Unrealized Loss Before Tax
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CY2020Q4 us-gaap Available For Sale Securities Debt Maturities Single Maturity Date
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CY2020 us-gaap Debt Securities Available For Sale Realized Gain Loss
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CY2019Q4 us-gaap Inventory Work In Process Net Of Reserves
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CY2020 us-gaap Fair Value Measurement With Unobservable Inputs Reconciliation Recurring Basis Liability Purchases
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CY2020Q4 us-gaap Inventory Finished Goods Net Of Reserves
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CY2019Q4 us-gaap Inventory Finished Goods Net Of Reserves
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CY2020Q4 akba Inventory Net Current And Non Current
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CY2019Q4 akba Inventory Net Current And Non Current
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CY2020Q4 us-gaap Inventory Net
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CY2019Q4 us-gaap Inventory Net
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CY2020 us-gaap Goodwill Impairment Loss
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CY2020Q4 us-gaap Inventory Noncurrent
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CY2019Q4 us-gaap Inventory Noncurrent
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CY2020 us-gaap Inventory Write Down
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CY2019 us-gaap Inventory Write Down
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CY2018Q4 us-gaap Inventory Write Down
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CY2020Q4 us-gaap Finite Lived Intangible Assets Amortization Expense Year Three
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CY2020Q4 us-gaap Finite Lived Intangible Assets Amortization Expense After Year Five
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CY2020Q4 us-gaap Goodwill
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CY2019Q4 us-gaap Goodwill
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CY2020Q4 us-gaap Goodwill
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CY2019Q4 us-gaap Accrued Royalties Current
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CY2020Q4 us-gaap Line Of Credit Facility Remaining Borrowing Capacity
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CY2019Q4 us-gaap Line Of Credit Facility Remaining Borrowing Capacity
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CY2020Q4 us-gaap Long Term Debt Maturities Repayments Of Principal In Year Four
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CY2020Q4 us-gaap Long Term Debt
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CY2019Q4 us-gaap Line Of Credit Facility Maximum Borrowing Capacity
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CY2020Q4 us-gaap Line Of Credit
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CY2020Q2 us-gaap Common Stock Shares Authorized
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CY2020Q4 us-gaap Common Stock Shares Authorized
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CY2020Q4 us-gaap Common Stock Shares Authorized
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CY2020Q4 us-gaap Common Stock Shares Outstanding
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CY2020Q4 us-gaap Common Stock Shares Issued
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CY2019Q4 us-gaap Common Stock Shares Outstanding
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CY2019Q4 us-gaap Common Stock Shares Issued
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CY2020Q4 us-gaap Preferred Stock Shares Authorized
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CY2019Q4 us-gaap Preferred Stock Shares Issued
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CY2020Q4 us-gaap Preferred Stock Shares Issued
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CY2020Q4 us-gaap Preferred Stock Shares Outstanding
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CY2019Q4 us-gaap Preferred Stock Shares Outstanding
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CY2019Q4 us-gaap Common Stock Capital Shares Reserved For Future Issuance
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5.63
CY2019 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Equity Instruments Other Than Options Grants In Period Weighted Average Grant Date Fair Value
ShareBasedCompensationArrangementByShareBasedPaymentAwardEquityInstrumentsOtherThanOptionsGrantsInPeriodWeightedAverageGrantDateFairValue
3.85
CY2018 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Equity Instruments Other Than Options Grants In Period Weighted Average Grant Date Fair Value
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7.12
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400000 USD
CY2019 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercises In Period Total Intrinsic Value
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1300000 USD
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1200000 USD
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6800000 USD
CY2019 us-gaap Sharebased Compensation Arrangement By Sharebased Payment Award Options Vested In Period Fair Value1
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4300000 USD
CY2018 us-gaap Sharebased Compensation Arrangement By Sharebased Payment Award Options Vested In Period Fair Value1
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13600000 USD
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CY2020 us-gaap Current Income Tax Expense Benefit
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CY2018 us-gaap Current Federal Tax Expense Benefit
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23000 USD
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0 USD
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0 USD
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CY2020 us-gaap Deferred Income Tax Expense Benefit
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0.020
CY2018 us-gaap Effective Income Tax Rate Reconciliation Tax Credits Research
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CY2020 us-gaap Effective Income Tax Rate Reconciliation Nondeductible Expense Share Based Compensation Cost
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0
CY2019 us-gaap Effective Income Tax Rate Reconciliation Nondeductible Expense Share Based Compensation Cost
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0
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CY2019 us-gaap Effective Income Tax Rate Reconciliation Change In Enacted Tax Rate
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CY2020 akba Effective Income Tax Rate Reconciliation Prior Year Adjustment State And Local Jurisdiction Deferred Tax Assets Operating Loss Carryforward Percent
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0
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0
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0
CY2020 us-gaap Effective Income Tax Rate Continuing Operations
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0
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2132000 USD
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806000 USD
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109352000 USD
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0 USD
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34178000 USD
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75940000 USD
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25494000 USD
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CY2019Q4 us-gaap Deferred Income Tax Liabilities
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CY2020Q4 us-gaap Deferred Tax Liabilities
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CY2019Q4 us-gaap Deferred Tax Liabilities
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CY2020 akba Term Of Change In Ownership Of Stockholders
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1300000 USD
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CY2019 us-gaap Operating Lease Payments
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6900000 USD
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1797000 USD
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4799000 USD
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7322000 USD
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307000 USD
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5739000 USD
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0 USD
CY2020Q4 akba Lessee Operating Lease Liability Payments Due Net Year Four
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CY2020Q4 us-gaap Lessor Operating Lease Payments To Be Received Thereafter
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CY2020Q4 akba Lessee Operating Lease Liability Payments Due Net After Year Five
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CY2020Q4 us-gaap Lessee Operating Lease Liability Payments Due
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CY2020Q4 us-gaap Lessee Operating Lease Liability Payments Due
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35596000 USD
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5672000 USD
CY2020Q4 us-gaap Operating Lease Liability
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29924000 USD
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14700000 USD
CY2020 us-gaap Research And Development Arrangement Contract To Perform For Others Costs Incurred Gross
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155900000 USD
CY2020Q1 us-gaap Cost Of Revenue
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CY2019 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
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CY2020Q4 us-gaap Operating Expenses
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CY2020Q3 us-gaap Nonoperating Income Expense
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CY2020Q4 us-gaap Nonoperating Income Expense
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CY2020Q1 us-gaap Income Tax Expense Benefit
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CY2020Q4 us-gaap Income Tax Expense Benefit
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CY2019Q3 us-gaap Operating Expenses
OperatingExpenses
109619000 USD
CY2019Q4 us-gaap Operating Expenses
OperatingExpenses
126299000 USD
CY2019Q1 us-gaap Operating Income Loss
OperatingIncomeLoss
-75969000 USD
CY2020Q3 us-gaap Net Income Loss
NetIncomeLoss
-59959000 USD
CY2020Q4 us-gaap Net Income Loss
NetIncomeLoss
-87000000 USD
CY2020Q1 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.47
CY2020Q2 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-1.28
CY2020Q3 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.42
CY2020Q4 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.60
CY2020Q1 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
128395163 shares
CY2020Q2 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
136906968 shares
CY2020Q3 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
143314729 shares
CY2020Q4 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
145111415 shares
CY2019Q1 us-gaap Cost Of Revenue
CostOfRevenue
31257000 USD
CY2019Q2 us-gaap Cost Of Revenue
CostOfRevenue
37669000 USD
CY2019Q3 us-gaap Cost Of Revenue
CostOfRevenue
38263000 USD
CY2019Q4 us-gaap Cost Of Revenue
CostOfRevenue
38147000 USD
CY2019Q1 us-gaap Operating Expenses
OperatingExpenses
117378000 USD
CY2019Q2 us-gaap Operating Expenses
OperatingExpenses
122657000 USD
CY2019Q3 us-gaap Net Income Loss
NetIncomeLoss
-54585000 USD
CY2019Q4 us-gaap Net Income Loss
NetIncomeLoss
-94483000 USD
CY2019Q1 us-gaap Nonoperating Income Expense
NonoperatingIncomeExpense
791000 USD
CY2019Q2 us-gaap Nonoperating Income Expense
NonoperatingIncomeExpense
508000 USD
CY2019Q3 us-gaap Nonoperating Income Expense
NonoperatingIncomeExpense
43000 USD
CY2019Q4 us-gaap Nonoperating Income Expense
NonoperatingIncomeExpense
-1344000 USD
CY2019Q1 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
-2757000 USD
CY2019Q2 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
-845000 USD
CY2019Q3 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
-1277000 USD
CY2019Q4 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
-1752000 USD
CY2019Q1 us-gaap Net Income Loss
NetIncomeLoss
-72421000 USD
CY2019Q2 us-gaap Net Income Loss
NetIncomeLoss
-58170000 USD
CY2019Q1 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.62
CY2019Q2 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.49
CY2019Q3 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.46
CY2019Q4 us-gaap Earnings Per Share Basic And Diluted
EarningsPerShareBasicAndDiluted
-0.79
CY2019Q1 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
117063352 shares
CY2019Q2 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
118268832 shares
CY2019Q3 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
118863063 shares
CY2019Q4 us-gaap Weighted Average Number Of Share Outstanding Basic And Diluted
WeightedAverageNumberOfShareOutstandingBasicAndDiluted
119358081 shares

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