2021 Q3 Form 10-Q Financial Statement

#000107008121000029 Filed on July 29, 2021

View on sec.gov

Income Statement

Concept 2021 Q3 2021 Q2 2020 Q2
Revenue $138.7M $116.7M $75.24M
YoY Change 17.18% 55.07% -12.02%
Cost Of Revenue $6.539M $7.358M $5.300M
YoY Change 39.13% 38.83% 65.06%
Gross Profit $132.2M $109.3M $69.90M
YoY Change 16.27% 56.39% -15.08%
Gross Profit Margin 95.29% 93.69% 92.9%
Selling, General & Admin $69.25M $68.88M $53.66M
YoY Change 19.73% 28.36% 9.03%
% of Gross Profit 52.38% 63.01% 76.77%
Research & Development $130.8M $125.5M $176.5M
YoY Change 40.7% -28.92% 194.31%
% of Gross Profit 98.97% 114.79% 252.54%
Depreciation & Amortization $16.75M $14.98M $10.21M
YoY Change 43.9% 46.75% 32.6%
% of Gross Profit 12.67% 13.71% 14.61%
Operating Expenses $231.8M $215.2M $262.5M
YoY Change 33.59% -18.03% 111.23%
Operating Profit -$93.08M -$98.49M -$187.3M
YoY Change 68.83% -47.41% 383.19%
Interest Expense -$21.80M -$22.56M -$5.379M
YoY Change 3.63% 319.39% 159.35%
% of Operating Profit
Other Income/Expense, Net -$18.78M $3.170M $11.31M
YoY Change -165.29% -71.97% -6279.78%
Pretax Income -$133.7M -$117.9M -$181.3M
YoY Change 181.96% -35.0% 342.14%
Income Tax -$36.00K $488.0K $84.00K
% Of Pretax Income
Net Earnings -$133.6M -$118.4M -$181.4M
YoY Change 91.74% -34.76% 334.15%
Net Earnings / Revenue -96.31% -101.45% -241.13%
Basic Earnings Per Share -$1.89 -$1.68
Diluted Earnings Per Share -$1.893M -$1.68 -$2.782M
COMMON SHARES
Basic Shares Outstanding 70.60M 70.41M 62.88M shares
Diluted Shares Outstanding 70.59M 70.41M

Balance Sheet

Concept 2021 Q3 2021 Q2 2020 Q2
SHORT-TERM ASSETS
Cash & Short-Term Investments $867.9M $947.1M $498.9M
YoY Change -23.93% 89.83% 37.25%
Cash & Equivalents $189.8M $177.3M $158.5M
Short-Term Investments $678.1M $769.7M $340.4M
Other Short-Term Assets $30.94M $23.91M $34.10M
YoY Change 15.01% -29.88% 95.98%
Inventory $15.61M $16.44M $18.37M
Prepaid Expenses
Receivables $96.65M $78.80M $53.60M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $1.011B $1.066B $605.0M
YoY Change -18.73% 76.23% 27.38%
LONG-TERM ASSETS
Property, Plant & Equipment $46.35M $42.91M $26.81M
YoY Change 64.72% 60.08% 74.17%
Goodwill $82.34M $82.34M $82.30M
YoY Change 0.05% 0.05% 0.0%
Intangibles $723.3M $717.1M $708.8M
YoY Change 1.51% 1.17% 0.87%
Long-Term Investments
YoY Change
Other Assets $65.53M $69.41M $48.80M
YoY Change 133.21% 42.24% 741.38%
Total Long-Term Assets $996.2M $992.4M $871.6M
YoY Change 6.33% 13.86% 6.74%
TOTAL ASSETS
Total Short-Term Assets $1.011B $1.066B $605.0M
Total Long-Term Assets $996.2M $992.4M $871.6M
Total Assets $2.007B $2.059B $1.477B
YoY Change -7.97% 39.42% 14.33%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $21.46M $20.82M $15.47M
YoY Change 37.02% 34.63% 51.34%
Accrued Expenses $82.05M $76.58M $51.10M
YoY Change 20.66% 49.86% 43.14%
Deferred Revenue $0.00 $7.702M
YoY Change -100.0% -3.79%
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $149.4M $46.46M $18.33M
YoY Change 153.4% -8.34%
Total Short-Term Liabilities $465.3M $291.0M $201.8M
YoY Change 83.3% 44.15% 16.03%
LONG-TERM LIABILITIES
Long-Term Debt $281.6M $430.5M $297.0M
YoY Change -7.05% 44.93% 118.91%
Other Long-Term Liabilities $1.376M $1.392M $26.68M
YoY Change -30.08% -94.78% 216.99%
Total Long-Term Liabilities $283.0M $431.9M $323.7M
YoY Change -7.2% 33.42% 124.64%
TOTAL LIABILITIES
Total Short-Term Liabilities $465.3M $291.0M $201.8M
Total Long-Term Liabilities $283.0M $431.9M $323.7M
Total Liabilities $1.902B $1.862B $904.1M
YoY Change 13.91% 105.95% 12.61%
SHAREHOLDERS EQUITY
Retained Earnings -$1.955B -$1.821B -$1.485B
YoY Change 25.74% 22.65% 41.03%
Common Stock $70.00K $70.00K $67.00K
YoY Change 2.94% 4.48% 15.52%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $104.9M $196.6M $572.5M
YoY Change
Total Liabilities & Shareholders Equity $2.007B $2.059B $1.477B
YoY Change -7.97% 39.42% 14.33%

Cashflow Statement

Concept 2021 Q3 2021 Q2 2020 Q2
OPERATING ACTIVITIES
Net Income -$133.6M -$118.4M -$181.4M
YoY Change 91.74% -34.76% 334.15%
Depreciation, Depletion And Amortization $16.75M $14.98M $10.21M
YoY Change 43.9% 46.75% 32.6%
Cash From Operating Activities -$51.19M -$31.14M -$74.81M
YoY Change -292.08% -58.37% 145.12%
INVESTING ACTIVITIES
Capital Expenditures -$5.844M -$7.973M -$2.160M
YoY Change 76.56% 269.12% 9.09%
Acquisitions
YoY Change
Other Investing Activities $70.55M $64.03M $144.2M
YoY Change -118.05% -55.6% -498.51%
Cash From Investing Activities $64.70M $56.05M $142.1M
YoY Change -116.41% -60.54% -472.15%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 2.976M 4.017M -32.92M
YoY Change -99.54% -112.2% -1255.09%
NET CHANGE
Cash From Operating Activities -51.19M -31.14M -74.81M
Cash From Investing Activities 64.70M 56.05M 142.1M
Cash From Financing Activities 2.976M 4.017M -32.92M
Net Change In Cash 16.49M 28.93M 34.32M
YoY Change -94.01% -15.71% -152.13%
FREE CASH FLOW
Cash From Operating Activities -$51.19M -$31.14M -$74.81M
Capital Expenditures -$5.844M -$7.973M -$2.160M
Free Cash Flow -$45.35M -$23.17M -$72.65M
YoY Change -251.36% -68.11% 154.56%

Facts In Submission

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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.        The Company</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">PTC Therapeutics, Inc. (the “Company” or “PTC”) is a science-driven global biopharmaceutical company focused on the discovery, development and commercialization of clinically differentiated medicines that provide benefits to patients with rare disorders. The Company’s ability to globally commercialize products is the foundation that drives its continued investment in a robust diversified pipeline of transformative medicines and its mission to provide access to best-in-class treatments for patients who have an unmet medical need. The Company’s strategy is to leverage its strong scientific expertise and global commercial infrastructure to maximize value for its patients and other stakeholders.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The Company has two products, Translarna™ (ataluren) and Emflaza™ (deflazacort), for the treatment of Duchenne muscular dystrophy (“DMD”), a rare, life threatening disorder. Translarna has marketing authorization in the European Economic Area (the “EEA”) for the treatment of nonsense mutation Duchenne muscular dystrophy (“nmDMD”) in ambulatory patients aged 2 years and older and in Brazil for the treatment of nmDMD in ambulatory patients aged 5 years and older, subject to annual renewal and other conditions. In July 2020, the European Commission approved the removal of the statement “efficacy has not been demonstrated in non-ambulatory patients” from the indication statement for Translarna. Emflaza is approved in the United States for the treatment of DMD in patients two years and older.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The Company holds the rights for the commercialization of Tegsedi™ (inotersen) and Waylivra™ (volanesorsen) for the treatment of rare diseases in countries in Latin America and the Caribbean pursuant to the Collaboration and License Agreement (the “Akcea Collaboration and License Agreement”), dated August 1, 2018, by and between the Company and Akcea Therapeutics, Inc. (“Akcea”). Tegsedi has received marketing authorization in the United States, the European Union (the “EU”) and Brazil for the treatment of stage 1 or stage 2 polyneuropathy in adult patients with hereditary transthyretin amyloidosis (“hATTR amyloidosis”). While the Company is in the process of initiating its<span style="background-color:#ffffff;"> commercial launch for Tegsedi for the treatment of hATTR amyloidosis in Latin America, it continues to make Tegsedi available in certain countries within Latin America and the Caribbean through early access programs. </span>Waylivra has received marketing authorization in the EU for the treatment of familial chylomicronemia syndrome (“FCS”). The Company filed for marketing authorization for Waylivra for the treatment of FCS with ANVISA, the Brazilian health regulatory authority, in June 2020 and, subject to further potential delays in the review process related to the COVID-19 pandemic, expects a regulatory decision on approval from ANVISA in the fourth quarter of 2021.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The Company also has a spinal muscular atrophy (“SMA”) collaboration with F. Hoffman-La Roche Ltd and Hoffman-La Roche Inc. (referred to collectively as “Roche”) and the Spinal Muscular Atrophy Foundation (“SMA Foundation”). The SMA program has one approved product, Evrysdi™ (risdiplam), which was approved by the United States Food and Drug Administration (“FDA”) in August 2020 for the treatment of SMA in adults and children two months and older and by the European Commission in March 2021 for the treatment of 5q SMA in patients two months and older with a clinical diagnosis of SMA Type 1, Type 2 or Type 3 or with one to four SMN2 copies. Evrysdi also received marketing authorization for the treatment of SMA in Brazil in October 2020 and Japan in June 2021. In addition to the Company’s SMA program, the Company’s splicing platform also includes PTC518, which is being developed for the treatment of Huntington’s disease (“HD”). The Company announced preliminary results from its ongoing Phase 1 study of PTC518 in healthy volunteers in April 2021 demonstrating dose-dependent lowering of huntingtin messenger ribonucleic acid levels and that PTC518 was well tolerated with no safety-related findings. The Company expects to announce results from additional cohorts for this Phase 1 study in the third quarter of 2021 and is planning to initiate a Phase 2 study of PTC518 by the end of 2021.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt;">The Company has a pipeline of gene therapy product candidates for rare monogenic diseases that affect the central nervous system (“CNS”) including PTC-AADC for the treatment of Aromatic L-Amino Acid Decarboxylase (“AADC”) deficiency (“AADC deficiency”), a rare CNS disorder arising from reductions in the enzyme AADC that results from mutations in the dopa decarboxylase gene. In January 2020, the Company submitted an MAA to the European Medicines Agency </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">(“EMA”) for PTC-AADC for the treatment of AADC deficiency in the EEA, and the Company expects an opinion from the <span style="background-color:#ffffff;">Committee for Medicinal Products for Human Use (“CHMP”)</span> in the fourth quarter of 2021. The Company is also preparing a biologics license application (“BLA”) for PTC-AADC for the treatment of AADC deficiency in the United States and expects to submit a BLA to the FDA by the end of 2021. </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The Company’s Bio-e platform consists of small molecule compounds that target oxidoreductase enzymes that regulate oxidative stress and inflammatory pathways central to the pathology of a number of CNS diseases. The two most advanced molecules in the Company’s Bio-e platform are vatiquinone and PTC857. The Company initiated a registration-directed Phase 2/3 placebo-controlled trial of vatiquinone in children with mitochondrial disease and associated refractory epilepsy in the third quarter of 2020 and anticipates data from this trial to be available in the third quarter of 2022.  The Company also initiated a registration-directed Phase 3 trial of vatiquinone in children and young adults with Friedreich ataxia in the fourth quarter of 2020 and anticipates data from this trial to be available in 2023. In the second quarter of 2020, the Company initiated a Phase 1 trial in healthy volunteers to evaluate the safety and pharmacology of PTC857. This Phase 1 trial was recently completed and PTC857 was found to be well-tolerated with no reported serious adverse events while demonstrating predictable pharmacology. The Company expects to initiate a Phase 2 trial of PTC857 for amyotrophic lateral sclerosis in the first quarter of 2022.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">On May 29, 2020, the Company completed its acquisition of Censa Pharmaceuticals, Inc. (“Censa”) pursuant to an Agreement and Plan of Merger, dated as of May 5, 2020 (the "Censa Merger Agreement"), by and among the Company, Hydro Merger Sub, Inc., the Company’s wholly owned, indirect subsidiary, and, solely in its capacity as the representative, agent and attorney-in-fact of the securityholders of Censa, Shareholder Representative Services LLC (the "Censa Merger"). The transaction was accounted for as an asset acquisition. In connection with the Censa Merger, the Company acquired PTC923, an oral formulation of synthetic sepiapterin, a precursor to intracellular tetrahydrobiopterin, which is a critical enzymatic cofactor involved in metabolism and synthesis of numerous metabolic products. The Company expects to initiate a registration-directed Phase 3 trial for PTC923 for phenylketonuria (“PKU”) in the third quarter of 2021. </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">In June 2020, the Company initiated a Phase 2/3 clinical trial evaluating the efficacy and safety of emvododstat, formerly known as PTC299, a dihydroorotate dehydrogenase inhibitor that the Company has also been developing in oncological indications, in patients hospitalized with COVID-19. The Company expects this trial to be completed by the end of 2021.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">In addition, the Company has a pipeline of product candidates and discovery programs that are in early clinical, pre-clinical and research and development stages focused on the development of new treatments for multiple therapeutic areas, including rare diseases and oncology.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The Company’s marketing authorization for Translarna in the EEA is subject to annual review and renewal by the European Commission following reassessment by the EMA of the benefit-risk balance of the authorization, which the Company refers to as the annual EMA reassessment. This marketing authorization is further subject to the specific obligation to conduct and submit the results of a multi-center, randomized, double-blind, 18 month, placebo-controlled trial, followed by an 18 month open-label extension, according to an agreed protocol, in order to confirm the efficacy and safety of Translarna. The final report on the trial and open-label extension is to be submitted by the Company to the EMA by the end of the third quarter of 2022. The Company refers to the trial and open-label extension together as Study 041.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The marketing authorization in the EEA was last renewed in June 2021 and is effective, unless extended, through August 5, 2022. The renewal was based on the Company’s commitment to conduct Study 041 and the totality of the clinical data available from its trials and studies of Translarna for the treatment of nmDMD, including the safety and efficacy results of the Phase 2b and Phase 3 clinical trials. The primary efficacy endpoint was not achieved in either trial within the pre-specified level of statistical significance.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt;">Translarna is an investigational new drug in the United States. During the first quarter of 2017, the Company filed a New Drug Application (“NDA”) over protest with the FDA, for which the FDA granted a standard review. In October 2017, the Office of Drug Evaluation I of the FDA issued a complete response letter for the NDA, stating that it was unable to approve the application in its current form. In response, the Company filed a formal dispute resolution request with the Office of New Drugs of the FDA. In February 2018, the Office of New Drugs of the FDA denied the Company’s appeal of the Complete Response Letter. In its response, the Office of New Drugs recommended a possible path forward for the </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">ataluren NDA submission based on the accelerated approval pathway. This would involve a re-submission of an NDA containing the current data on effectiveness of ataluren with new data to be generated on dystrophin production in nmDMD patients’ muscles. The Company followed the FDA’s recommendation and collected, using newer technologies via procedures and methods that the Company designed, such dystrophin data in a new study, Study 045, and announced the results of Study 045 in February 2021. Study 045 did not meet its pre-specified primary endpoint. While the Company plans to discuss the Study 045 dystrophin results and the totality of existing clinical and real-world data with the FDA to determine if there is a potential path to approval based on these results and data, there is substantial risk that the FDA will determine that the results from the Company’s clinical trials and existing real-world data are not sufficient to support a marketing approval for Translarna for the treatment of nmDMD in the United States. The Company also expects to have data for Study 041 in the third quarter of 2022, and subject to a positive outcome in that study, the Company expects to re-submit the NDA at that time.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt;">As of June 30, 2021, the Company had an accumulated deficit of approximately $1,821.1 million. The Company has financed its operations to date primarily through the private offerings in September 2019 of 1.50% convertible senior notes due 2026 and in August 2015 of 3.00% convertible senior notes due 2022 (collectively, the “Convertible Notes”) (see Note 9), public offerings of common stock in February 2014, October 2014, April 2018, January 2019, and September 2019, "at the market offerings" of its common stock, its initial public offering of common stock in June 2013, proceeds from a Royalty Purchase Agreement dated as of July 17, 2020, by and among the Company, RPI 2019 Intermediate Finance Trust (“RPI”), and, solely for the limited purposes set forth therein, Royalty Pharma PLC (the “Royalty Purchase Agreement”) (see Note 2), private placements of its convertible preferred stock, collaborations, bank and institutional lender debt, grant funding and clinical trial support from governmental and philanthropic organizations and patient advocacy groups in the disease area addressed by the Company’s product candidates. Since 2014, the Company has also relied on revenue generated from net sales of Translarna for the treatment of nmDMD in territories outside of the United States, and since May 2017, the Company has generated revenue from net sales of Emflaza for the treatment of DMD in the United States. The Company has also relied on revenue associated with milestone and royalty payments from Roche pursuant to the License and Collaboration Agreement (the “SMA License Agreement”) dated as of November 23, 2011, by and among the Company, Roche and, for the limited purposes set forth therein, the SMA Foundation, under its SMA program. The Company expects that cash flows from the sales of its products, together with the Company’s cash, cash equivalents and marketable securities, will be sufficient to fund its operations for at least the next twelve months.  </p>
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<p style="font-family:'Times New Roman','Times','serif';font-size:10pt;font-weight:bold;margin:0pt 0pt 12pt 0pt;">Use of estimates</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the amounts reported in the financial statements and accompanying notes. Significant estimates in these consolidated financial statements have been made in connection with the calculation of net product sales, royalty revenue, certain accruals related to the Company’s research and development expenses, valuation procedures for liability for sale of future royalties, valuation procedures for convertible notes, fair value of the contingent consideration, and the provision for or benefit from income taxes. Actual results could differ from those estimates. Changes in estimates are reflected in reported results in the period in which they become known.</p>
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ProceedsFromSaleOfFutureRoyalties
650000000.0
CY2020Q3 us-gaap Debt Instrument Interest Rate Effective Percentage
DebtInstrumentInterestRateEffectivePercentage
0.110
CY2020Q4 ptct Liability Sale Of Future Royalties
LiabilitySaleOfFutureRoyalties
679762000
ptct Liability Sale Of Future Royalties Royalty Revenue Payable
LiabilitySaleOfFutureRoyaltiesRoyaltyRevenuePayable
8681000
ptct Liability Sale Of Future Royalties Interest Expense
LiabilitySaleOfFutureRoyaltiesInterestExpense
38083000
CY2021Q2 ptct Liability Sale Of Future Royalties
LiabilitySaleOfFutureRoyalties
709164000
CY2021Q2 us-gaap Debt Instrument Interest Rate Effective Percentage
DebtInstrumentInterestRateEffectivePercentage
0.115
us-gaap Number Of Operating Segments
NumberOfOperatingSegments
1
CY2021Q2 ptct Numberofdistributors
Numberofdistributors
2
CY2020Q2 ptct Numberofdistributors
Numberofdistributors
2
ptct Numberofdistributors
Numberofdistributors
2
ptct Numberofdistributors
Numberofdistributors
3
CY2020Q4 us-gaap Contract With Customer Liability
ContractWithCustomerLiability
4200000
CY2021Q2 us-gaap Contract With Customer Liability Revenue Recognized
ContractWithCustomerLiabilityRevenueRecognized
1900000
us-gaap Contract With Customer Liability Revenue Recognized
ContractWithCustomerLiabilityRevenueRecognized
4000000.0
CY2020Q2 us-gaap Contract With Customer Liability Revenue Recognized
ContractWithCustomerLiabilityRevenueRecognized
2000000.0
us-gaap Contract With Customer Liability Revenue Recognized
ContractWithCustomerLiabilityRevenueRecognized
4000000.0
CY2020Q4 us-gaap Revenue Remaining Performance Obligation
RevenueRemainingPerformanceObligation
4200000
CY2021Q2 us-gaap Amortization Of Intangible Assets
AmortizationOfIntangibleAssets
12800000
CY2020Q2 us-gaap Amortization Of Intangible Assets
AmortizationOfIntangibleAssets
8700000
us-gaap Amortization Of Intangible Assets
AmortizationOfIntangibleAssets
24000000.0
us-gaap Amortization Of Intangible Assets
AmortizationOfIntangibleAssets
16700000
CY2021Q2 us-gaap Finite Lived Intangible Assets Amortization Expense Remainder Of Fiscal Year
FiniteLivedIntangibleAssetsAmortizationExpenseRemainderOfFiscalYear
25496000
CY2021Q2 us-gaap Finite Lived Intangible Assets Amortization Expense Next Twelve Months
FiniteLivedIntangibleAssetsAmortizationExpenseNextTwelveMonths
50992000
CY2021Q2 us-gaap Finite Lived Intangible Assets Amortization Expense Year Two
FiniteLivedIntangibleAssetsAmortizationExpenseYearTwo
50992000
CY2021Q2 us-gaap Finite Lived Intangible Assets Amortization Expense Year Three
FiniteLivedIntangibleAssetsAmortizationExpenseYearThree
8482000
CY2021Q2 ptct Finite Lived Intangible Assets Amortization Expense Year Four And Thereafter
FiniteLivedIntangibleAssetsAmortizationExpenseYearFourAndThereafter
4617000
CY2021Q2 us-gaap Finite Lived Intangible Assets Net
FiniteLivedIntangibleAssetsNet
140579000
us-gaap Indefinitelived Intangible Assets Acquired
IndefinitelivedIntangibleAssetsAcquired
576500000
us-gaap Indefinite Lived Intangible Assets Period Increase Decrease
IndefiniteLivedIntangibleAssetsPeriodIncreaseDecrease
0
CY2018Q3 us-gaap Goodwill
Goodwill
82300000
us-gaap Goodwill Period Increase Decrease
GoodwillPeriodIncreaseDecrease
0
CY2021Q2 us-gaap Goodwill Period Increase Decrease
GoodwillPeriodIncreaseDecrease
0

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