2023 Q1 Form 10-K Financial Statement

#000107008123000011 Filed on February 21, 2023

View on sec.gov

Income Statement

Concept 2023 Q1 2022 Q4 2022
Revenue $220.4M $167.4M $698.8M
YoY Change 48.17% 1.32% 29.75%
Cost Of Revenue $14.14M $10.89M $44.68M
YoY Change 39.56% 16.79% 38.2%
Gross Profit $206.2M $156.5M $654.1M
YoY Change 48.8% 0.4% 29.21%
Gross Profit Margin 93.58% 93.49% 93.61%
Selling, General & Admin $86.91M $92.72M $326.0M
YoY Change 18.62% 7.13% 14.08%
% of Gross Profit 42.14% 59.24% 49.84%
Research & Development $195.1M $188.7M $651.5M
YoY Change 39.3% 25.93% 20.49%
% of Gross Profit 94.61% 120.56% 99.6%
Depreciation & Amortization $42.83M $38.87M $128.8M
YoY Change 62.75% 106.61% 100.89%
% of Gross Profit 20.76% 24.83% 19.7%
Operating Expenses $338.0M $323.5M $1.146B
YoY Change 43.67% 34.43% 25.54%
Operating Profit -$117.6M -$167.0M -$447.4M
YoY Change 35.94% 97.05% 19.49%
Interest Expense -$27.33M -$39.70M -$90.87M
YoY Change 16.23% -4.11% 5.64%
% of Operating Profit
Other Income/Expense, Net $9.956M $50.35M -$49.21M
YoY Change -183.98% -503.56% -14.98%
Pretax Income -$135.0M -$189.7M -$587.5M
YoY Change 10.75% 36.86% 13.34%
Income Tax $3.969M -$18.80M -$28.47M
% Of Pretax Income
Net Earnings -$139.0M -$170.9M -$559.0M
YoY Change 9.65% 19.28% 6.7%
Net Earnings / Revenue -63.05% -102.08% -80.0%
Basic Earnings Per Share -$1.88 -$7.79
Diluted Earnings Per Share -$1.88 -$2.35 -$7.79
COMMON SHARES
Basic Shares Outstanding 73.82M 71.88M 71.73M
Diluted Shares Outstanding 73.73M 71.73M

Balance Sheet

Concept 2023 Q1 2022 Q4 2022
SHORT-TERM ASSETS
Cash & Short-Term Investments $286.3M $410.7M $410.7M
YoY Change -51.29% -46.89% -46.89%
Cash & Equivalents $167.5M $279.8M $279.8M
Short-Term Investments $118.8M $130.9M $130.9M
Other Short-Term Assets $98.57M $105.7M $105.7M
YoY Change 232.49% 93.23% 93.23%
Inventory $26.65M $21.81M $21.81M
Prepaid Expenses
Receivables $201.9M $155.6M $155.6M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $613.4M $693.8M $693.8M
YoY Change -20.75% -27.3% -27.3%
LONG-TERM ASSETS
Property, Plant & Equipment $79.49M $72.59M $175.0M
YoY Change 34.53% 38.04% 34.62%
Goodwill $82.30M $82.34M
YoY Change 0.0% 0.0%
Intangibles $686.2M $705.9M
YoY Change -10.14% -2.61%
Long-Term Investments
YoY Change
Other Assets $47.88M $48.58M $48.58M
YoY Change 7.85% 4.48% 4.48%
Total Long-Term Assets $995.4M $1.012B $1.012B
YoY Change -2.94% 2.86% 2.86%
TOTAL ASSETS
Total Short-Term Assets $613.4M $693.8M $693.8M
Total Long-Term Assets $995.4M $1.012B $1.012B
Total Assets $1.609B $1.706B $1.706B
YoY Change -10.6% -11.99% -11.99%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $26.31M $27.27M $91.06M
YoY Change 43.27% 18.39% 295.32%
Accrued Expenses $82.02M $126.1M $126.1M
YoY Change 3.15% 19.35% 19.35%
Deferred Revenue $214.0K $1.351M
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $99.73M $75.15M $75.15M
YoY Change -33.39% -49.75% -64.52%
Total Short-Term Liabilities $441.6M $406.2M $406.2M
YoY Change -7.37% -20.24% -20.24%
LONG-TERM LIABILITIES
Long-Term Debt $572.1M $571.7M $1.276B
YoY Change 102.74% 102.81% 30.67%
Other Long-Term Liabilities $141.0K $2.641M $267.5M
YoY Change -99.95% -99.16% -14.68%
Total Long-Term Liabilities $572.2M $574.4M $1.544B
YoY Change 102.79% 103.75% 19.65%
TOTAL LIABILITIES
Total Short-Term Liabilities $441.6M $406.2M $406.2M
Total Long-Term Liabilities $572.2M $574.4M $1.544B
Total Liabilities $2.066B $2.053B $2.053B
YoY Change 9.32% 5.99% 5.99%
SHAREHOLDERS EQUITY
Retained Earnings -$2.796B -$2.657B
YoY Change 25.68% 26.65%
Common Stock $73.00K $72.00K
YoY Change 2.82% 1.41%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity -$457.6M -$347.1M -$347.1M
YoY Change
Total Liabilities & Shareholders Equity $1.609B $1.706B $1.706B
YoY Change -10.6% -11.99% -11.99%

Cashflow Statement

Concept 2023 Q1 2022 Q4 2022
OPERATING ACTIVITIES
Net Income -$139.0M -$170.9M -$559.0M
YoY Change 9.65% 19.28% 6.7%
Depreciation, Depletion And Amortization $42.83M $38.87M $128.8M
YoY Change 62.75% 106.61% 100.89%
Cash From Operating Activities -$29.49M -$166.0M -$356.7M
YoY Change -69.72% 141.09% 41.91%
INVESTING ACTIVITIES
Capital Expenditures $10.27M $8.622M $32.02M
YoY Change 10.29% -198.81% 13.48%
Acquisitions
YoY Change
Other Investing Activities -$18.70M $41.06M $322.2M
YoY Change -132.05% -46.67% 30.24%
Cash From Investing Activities -$28.97M $32.44M $290.2M
YoY Change -159.07% -52.49% 32.39%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 4.094M 302.9M 168.0M
YoY Change 250.51% 6857.23% 704.48%
NET CHANGE
Cash From Operating Activities -29.49M -166.0M -356.7M
Cash From Investing Activities -28.97M 32.44M 290.2M
Cash From Financing Activities 4.094M 302.9M 168.0M
Net Change In Cash -62.33M 169.4M 98.71M
YoY Change 36.87% 4371.86% -616.95%
FREE CASH FLOW
Cash From Operating Activities -$29.49M -$166.0M -$356.7M
Capital Expenditures $10.27M $8.622M $32.02M
Free Cash Flow -$39.76M -$174.6M -$388.7M
YoY Change -62.74% 190.42% 39.04%

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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;text-indent:18pt;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. PTC’s ability to innovate to identify new therapies and to globally commercialize products is the foundation that drives investment in a robust and diversified pipeline of transformative medicines. PTC’s mission is to provide access to best-in-class treatments for patients who have little to no treatment options. PTC’s strategy is to leverage its strong scientific and clinical expertise and global commercial infrastructure to bring therapies to patients.  PTC believes that this allows it to maximize value for all of its stakeholders.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt 0pt 12pt 0pt;">The Company has two products, Translarna™ (ataluren) and Emflaza<sup style="font-size:7.5pt;line-height:100%;top:0pt;vertical-align:top;">®</sup> (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 Russia for the treatment of nmDMD in patients aged two years and older. 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. Translarna also has marketing authorization in Brazil for the treatment of nmDMD in ambulatory patients two years and older and for continued treatment of patients that become non-ambulatory. 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;text-indent:18pt;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. The marketing authorization in the EEA was last renewed in June 2022 and is effective, unless extended, through August 5, 2023. In September 2022, the Company submitted a Type II variation to the EMA to support conversion of the conditional marketing authorization for Translarna to a standard marketing authorization, which included a report on the placebo-controlled trial of Study 041 and data from the open-label extension. The Company expects an opinion from the Committee for Medicinal Products for Human Use in the first half of 2023.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt 0pt 12pt 0pt;">Translarna is an investigational new drug in the United States. Following the Company’s announcement of top-line results from the placebo-controlled trial of Study 041 in June 2022, the Company submitted a meeting request to the U.S. Food and Drug Administration (“FDA”) to gain clarity on the regulatory pathway for a potential re-submission of New Drug Application (“NDA”) for Translarna. The FDA provided initial written feedback that Study 041 does not provide substantial evidence of effectiveness to support NDA re-submission. The Company recently had an informal meeting with the FDA, during which the Company discussed the potential path to an NDA re-submission for Translarna. Based on the meeting discussion, the Company plans to request an additional Type C meeting with the FDA in the near future to review the totality of data collected to date, including dystrophin and other mechanistic data as well as additional analyses that could support the benefit of Translarna.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt;">The Company has a pipeline of gene therapy product candidates for rare monogenic diseases that affect the central nervous system (“CNS”) including Upstaza (eladocagene exuparvovec) 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 July 2022, the European Commission approved Upstaza for the treatment of AADC deficiency for patients 18 months and older within the EEA. In November 2022, the Medicines and Healthcare Products Regulatory Agency approved Upstaza for the treatment of AADC deficiency for patients 18 months and older within the United Kingdom. The Company is also preparing a biologics license application </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">(“BLA”) for Upstaza for the treatment of AADC deficiency in the United States and it expects to submit a BLA to the FDA in the first half of 2023.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt 0pt 12pt 0pt;">The Company holds the rights for the commercialization of Tegsedi<sup style="font-size:7.5pt;line-height:100%;top:0pt;vertical-align:top;">®</sup> (inotersen) and Waylivra<sup style="font-size:7.5pt;line-height:100%;top:0pt;vertical-align:top;">®</sup> (volanesorsen) for the treatment of rare diseases in countries in Latin America and the Caribbean pursuant to the Collaboration and License Agreement (the “Tegsedi-Waylivra Agreement”), dated August 1, 2018, by and between the Company and Akcea Therapeutics, Inc. (“Akcea”), a subsidiary of Ionis Pharmaceuticals, Inc. 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”). The Company began to make commercial sales of Tegsedi for the treatment of hATTR amyloidosis in Brazil in the second quarter of 2022 and it continues to make Tegsedi available in certain other countries within Latin America and the Caribbean through early access programs (“EAP Programs”). In August 2021, ANVISA, the Brazilian health regulatory authority, approved Waylivra as the first treatment for familial chylomicronemia syndrome (“FCS”) in Brazil and the Company began to make commercial sales of Waylivra in Brazil in the third quarter of 2022 while continuing to make Waylivra available in certain other countries within Latin America and the Caribbean through EAP Programs. In December 2022, ANVISA approved Waylivra for the treatment of familial partial lipodystrophy, or FPL. Waylivra has also received marketing authorization in the EU for the treatment of FCS.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;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<sup style="font-size:7.5pt;line-height:100%;top:0pt;vertical-align:top;">®</sup> (risdiplam), which was approved by the 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 May 2022, the FDA approved a label expansion for Evrysdi to include infants under two months old with SMA and the Company expects the European Medicines Agency (“EMA”) to make a regulatory decision on approval for a label expansion for Evrysdi to include infants under two months old with SMA in 2023. 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 initiated a Phase 2 study of PTC518 for the treatment of HD in the first quarter of 2022, which consists of an initial 12-week placebo-controlled phase focused on safety, pharmacology and pharmacodynamic effects followed by a nine-month placebo-controlled phase focused on PTC518 biomarker effect. Enrollment in the Phase 2 study remains active and ongoing outside of the United States. Enrollment within the United States is paused as the FDA has requested additional data to allow the Phase 2 study to proceed; discussions are ongoing with the FDA to allow the resumption of U.S. enrollment. The Company expects data from the initial 12-week phase of the Phase 2 study in the <span style="background:#ffffff;">second quarter</span> of 2023.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin: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 utreloxastat. The Company initiated a registration-directed Phase 2/3 placebo-controlled trial of vatiquinone in children with mitochondrial disease associated seizures in the third quarter of 2020. The Company has completed enrollment in this trial after previously experiencing delays in enrollment due to the COVID-19 pandemic.  The Company anticipates results from the Phase 2/3 trial to be available in the second quarter of 2023. 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 results from this trial to be available in the second quarter of 2023. In the third quarter of 2021, the Company completed a Phase 1 trial in healthy volunteers to evaluate the safety and pharmacology of utreloxastat. Utreloxastat was found to be well-tolerated with no </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;margin:0pt 0pt 12pt 0pt;">reported serious adverse events while demonstrating predictable pharmacology. The Company initiated a Phase 2 trial of utreloxastat for amyotrophic lateral sclerosis in the first quarter of 2022 <span style="background:#ffffff;">and </span>enrollment is ongoing<span style="background:#ffffff;">.</span></p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt 0pt 12pt 0pt;">The most advanced molecule in the Company’s metabolic platform is sepiapterin, a precursor to intracellular tetrahydrobiopterin, which is a critical enzymatic cofactor involved in metabolism and synthesis of numerous metabolic products. The Company initiated a registration-directed Phase 3 trial for sepiapterin for PKU in the third quarter of 2021 with the primary endpoint in the study of achieving statistically-significant reduction in blood Phe level. The primary analysis population includes those patients who have a greater than 30% reduction in blood Phe levels during the Part 1 run-in phase of the trial. In January 2023, the Company announced preliminary data from the Part 1 run-in phase of this trial, including that the mean reduction in blood Phe levels in an initial cohort of subjects during the Part 1 would be recognized as clinically meaningful if maintained in Part 2 of the trial. The Company now expects results from Part 2 of this trial to be available in May 2023 as the trial is overenrolled and additional time is required for the entirety of the primary analysis population to complete the study.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt 0pt 12pt 0pt;">Unesbulin is the Company’s most advanced oncology agent. The Company completed its Phase 1 trials evaluating unesbulin in leiomyosarcoma (“LMS”) and diffuse intrinsic pontine glioma (“DIPG”) in the fourth quarter of 2021. The Company initiated a registration-directed Phase 2/3 trial of unesbulin for the treatment of LMS in the first quarter of 2022 and enrollment is ongoing. The initiation of the Company’s registration-directed Phase 2/3 trial of unesbulin for DIPG was delayed as it continued to track the progress of patients in its Phase 1 trial and analyze the corresponding data. The Company now expects to initiate a registration-directed Phase 2/3 trial of unesbulin for the treatment of DIPG in the fourth quarter of 2023.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;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 for rare diseases.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-align:justify;text-indent:18pt;margin:0pt 0pt 12pt 0pt;">As of 2022, the Company had an accumulated deficit of approximately $2,657.0 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 (see Note 8), public offerings of common stock in February 2014, October 2014, April 2018, January 2019, and September 2019, “at the market offering” of its common stock, its initial public offering of common stock in June 2013, proceeds from the 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), net proceeds from our borrowings under our credit agreement with Blackstone (see Note 8), private placements of its convertible preferred stock and common stock, collaborations, bank and institutional lender debt, other convertible 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. On August 15, 2022, the Company repaid the outstanding principal amount and accrued interest, totaling $152.3 million, of the 3.00% convertible senior notes due August 15, 2022 (the “2022 Convertible Notes”) that was due upon maturity in accordance with the terms of the notes. 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 since 2014, Emflaza for the treatment of DMD in the United States since 2017 and Upstaza for the treatment of AADC deficiency in the EEA since May 2022. 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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CY2022Q4 us-gaap Finance Lease Liability Payments Due Year Two
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CY2022Q4 us-gaap Finance Lease Liability Payments Due Year Three
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CY2022Q4 us-gaap Lessee Operating Lease Liability Payments Due Year Four
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CY2022Q4 us-gaap Finance Lease Liability Payments Due Year Four
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CY2022Q4 ptct Lessee Operating Lease Liability Payments Due Year Fiveand Thereafter
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CY2022Q4 ptct Finance Lease Liability Payments Due Year Five And After
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18000000
CY2022Q4 us-gaap Lessee Operating Lease Liability Payments Due
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CY2022Q4 us-gaap Finance Lease Liability Payments Due
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30000000
CY2022Q4 us-gaap Lessee Operating Lease Liability Undiscounted Excess Amount
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157807000
CY2022Q4 us-gaap Finance Lease Liability Undiscounted Excess Amount
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CY2022Q4 us-gaap Operating Lease Liability
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CY2022Q4 us-gaap Finance Lease Liability
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CY2021Q4 us-gaap Accounts Payable Current
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12054000
CY2021Q4 us-gaap Other Accrued Liabilities Current
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320366000
CY2021Q4 us-gaap Accounts Payable And Accrued Liabilities Current
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CY2020Q3 ptct Proceeds From Sale Of Future Royalties
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650000000.0
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CY2021Q4 ptct Liability Sale Of Future Royalties
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733985000
CY2022 ptct Liability Sale Of Future Royalties Royalty Revenue Payable
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48738000
CY2022 ptct Liability Sale Of Future Royalties Interest Expense
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72639000
CY2022Q4 ptct Liability Sale Of Future Royalties
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757886000
CY2022Q4 us-gaap Debt Instrument Interest Rate Effective Percentage
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542470
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53.37
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28100000
CY2022 us-gaap Sale Of Stock Number Of Shares Issued In Transaction
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CY2021Q2 us-gaap Common Stock Shares Authorized
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250000000
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CY2021 us-gaap Net Income Loss Available To Common Stockholders Basic
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CY2021 us-gaap Net Income Loss Available To Common Stockholders Diluted
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CY2020 us-gaap Net Income Loss Available To Common Stockholders Basic
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CY2020 us-gaap Net Income Loss Available To Common Stockholders Diluted
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CY2022 us-gaap Weighted Average Number Of Diluted Shares Outstanding
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CY2021 us-gaap Weighted Average Number Of Shares Outstanding Basic
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CY2021 us-gaap Weighted Average Number Of Diluted Shares Outstanding
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70466393
CY2020 us-gaap Weighted Average Number Of Shares Outstanding Basic
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CY2020 us-gaap Weighted Average Number Of Diluted Shares Outstanding
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CY2022 us-gaap Earnings Per Share Diluted
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CY2021 us-gaap Earnings Per Share Basic
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CY2021 us-gaap Earnings Per Share Diluted
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CY2020 us-gaap Earnings Per Share Basic
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CY2020 us-gaap Earnings Per Share Diluted
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CY2021Q4 us-gaap Contract With Customer Asset Net
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0
CY2022Q4 us-gaap Contract With Customer Asset Net
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CY2021 us-gaap Contract With Customer Liability Revenue Recognized
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4000000.0
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1400000
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14018753
CY2021 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
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12292413
CY2020 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
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10645735
CY2022 us-gaap Allocated Share Based Compensation Expense
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110333000
CY2021 us-gaap Allocated Share Based Compensation Expense
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103513000
CY2020 us-gaap Allocated Share Based Compensation Expense
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70325000
CY2022Q4 us-gaap Employee Service Share Based Compensation Nonvested Awards Total Compensation Cost Not Yet Recognized
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176100000
CY2022 us-gaap Employee Service Share Based Compensation Nonvested Awards Total Compensation Cost Not Yet Recognized Period For Recognition1
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P2Y2M8D
CY2022Q4 us-gaap Contract With Customer Liability
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CY2021Q4 us-gaap Contract With Customer Liability
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CY2021Q4 us-gaap Revenue Remaining Performance Obligation
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0
CY2022Q4 us-gaap Revenue Remaining Performance Obligation
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0
CY2021Q4 us-gaap Deferred Tax Assets Tax Deferred Expense Reserves And Accruals Accrued Liabilities
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8208000
CY2022 us-gaap Income Loss From Continuing Operations Before Income Taxes Domestic
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CY2021 us-gaap Income Loss From Continuing Operations Before Income Taxes Domestic
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CY2020 us-gaap Income Loss From Continuing Operations Before Income Taxes Domestic
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CY2022 us-gaap Income Loss From Continuing Operations Before Income Taxes Foreign
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CY2021 us-gaap Income Loss From Continuing Operations Before Income Taxes Foreign
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CY2020 us-gaap Income Loss From Continuing Operations Before Income Taxes Foreign
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CY2022 us-gaap Income Loss From Continuing Operations Before Income Taxes Extraordinary Items Noncontrolling Interest
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CY2021 us-gaap Income Loss From Continuing Operations Before Income Taxes Extraordinary Items Noncontrolling Interest
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CY2020 us-gaap Income Loss From Continuing Operations Before Income Taxes Extraordinary Items Noncontrolling Interest
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CY2022 us-gaap Current Federal Tax Expense Benefit
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CY2021 us-gaap Current Federal Tax Expense Benefit
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0
CY2020 us-gaap Current Federal Tax Expense Benefit
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CY2022 us-gaap Current State And Local Tax Expense Benefit
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CY2021 us-gaap Current State And Local Tax Expense Benefit
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CY2020 us-gaap Current State And Local Tax Expense Benefit
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CY2022 us-gaap Current Foreign Tax Expense Benefit
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CY2021 us-gaap Current Foreign Tax Expense Benefit
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CY2020 us-gaap Current Foreign Tax Expense Benefit
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CY2022 us-gaap Deferred Federal Income Tax Expense Benefit
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CY2021 us-gaap Deferred Federal Income Tax Expense Benefit
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CY2020 us-gaap Deferred Federal Income Tax Expense Benefit
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CY2022 us-gaap Deferred State And Local Income Tax Expense Benefit
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CY2021 us-gaap Deferred State And Local Income Tax Expense Benefit
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CY2020 us-gaap Deferred State And Local Income Tax Expense Benefit
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CY2022 us-gaap Deferred Foreign Income Tax Expense Benefit
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CY2021 us-gaap Deferred Foreign Income Tax Expense Benefit
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CY2020 us-gaap Deferred Foreign Income Tax Expense Benefit
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CY2022 us-gaap Income Tax Expense Benefit
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CY2021 us-gaap Income Tax Expense Benefit
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CY2020 us-gaap Income Tax Expense Benefit
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CY2022Q4 ptct Deferred Tax Assets Amortization
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52532000
CY2021Q4 ptct Deferred Tax Assets Amortization
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CY2022Q4 ptct Deferred Tax Assets Tax Credit Federal
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CY2022 us-gaap Effective Income Tax Rate Reconciliation At Federal Statutory Income Tax Rate
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CY2021 us-gaap Effective Income Tax Rate Reconciliation At Federal Statutory Income Tax Rate
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CY2020 us-gaap Effective Income Tax Rate Reconciliation At Federal Statutory Income Tax Rate
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CY2022 us-gaap Effective Income Tax Rate Reconciliation State And Local Income Taxes
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CY2021 us-gaap Effective Income Tax Rate Reconciliation State And Local Income Taxes
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CY2020 us-gaap Effective Income Tax Rate Reconciliation State And Local Income Taxes
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CY2022 ptct Effective Income Tax Rate Reconciliation Permanent Differences
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CY2021 ptct Effective Income Tax Rate Reconciliation Permanent Differences
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CY2020 ptct Effective Income Tax Rate Reconciliation Permanent Differences
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CY2022 us-gaap Effective Income Tax Rate Reconciliation Nondeductible Expense Research And Development
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CY2021 us-gaap Effective Income Tax Rate Reconciliation Nondeductible Expense Research And Development
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CY2020 us-gaap Effective Income Tax Rate Reconciliation Nondeductible Expense Research And Development
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CY2022 us-gaap Effective Income Tax Rate Reconciliation Change In Deferred Tax Assets Valuation Allowance
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CY2021 us-gaap Effective Income Tax Rate Reconciliation Change In Deferred Tax Assets Valuation Allowance
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CY2020 us-gaap Effective Income Tax Rate Reconciliation Change In Deferred Tax Assets Valuation Allowance
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CY2022 ptct Effective Income Tax Rate Reconciliation Change In Deferred Tax Assets Percent
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CY2021 ptct Effective Income Tax Rate Reconciliation Change In Deferred Tax Assets Percent
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CY2020 ptct Effective Income Tax Rate Reconciliation Change In Deferred Tax Assets Percent
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CY2022 us-gaap Effective Income Tax Rate Reconciliation Foreign Income Tax Rate Differential
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CY2021 us-gaap Effective Income Tax Rate Reconciliation Foreign Income Tax Rate Differential
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CY2020 us-gaap Effective Income Tax Rate Reconciliation Foreign Income Tax Rate Differential
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CY2022 us-gaap Effective Income Tax Rate Reconciliation Change In Enacted Tax Rate
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CY2021 us-gaap Effective Income Tax Rate Reconciliation Change In Enacted Tax Rate
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CY2020 us-gaap Effective Income Tax Rate Reconciliation Change In Enacted Tax Rate
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CY2021 ptct Effective Income Tax Rate Reconciliation Change In Uncertain Tax Positions Percent
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CY2020 ptct Effective Income Tax Rate Reconciliation Change In Uncertain Tax Positions Percent
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CY2021 us-gaap Effective Income Tax Rate Reconciliation Other Adjustments
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CY2020 us-gaap Effective Income Tax Rate Reconciliation Other Adjustments
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CY2022 us-gaap Effective Income Tax Rate Continuing Operations
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CY2021 us-gaap Effective Income Tax Rate Continuing Operations
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CY2020 us-gaap Effective Income Tax Rate Continuing Operations
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CY2022Q4 us-gaap Deferred Tax Liabilities Goodwill And Intangible Assets Intangible Assets
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102834000
CY2021Q4 us-gaap Deferred Tax Liabilities Goodwill And Intangible Assets Intangible Assets
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137110000
CY2022Q4 us-gaap Deferred Tax Liabilities
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102834000
CY2021Q4 us-gaap Deferred Tax Liabilities
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CY2022Q4 us-gaap Deferred Tax Assets Tax Deferred Expense Reserves And Accruals Accrued Liabilities
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2124000
CY2021Q4 ptct Deferred Tax Assets Tax Credit Federal
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CY2022Q4 ptct Deferred Tax Assets Tax Credit State
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9787000
CY2021Q4 ptct Deferred Tax Assets Tax Credit State
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CY2022Q4 us-gaap Deferred Tax Assets Operating Loss Carryforwards Domestic
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CY2021Q4 us-gaap Deferred Tax Assets Operating Loss Carryforwards Domestic
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CY2022Q4 us-gaap Deferred Tax Assets Operating Loss Carryforwards State And Local
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CY2021Q4 us-gaap Deferred Tax Assets Operating Loss Carryforwards State And Local
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CY2022Q4 us-gaap Deferred Tax Assets Operating Loss Carryforwards Foreign
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CY2021Q4 us-gaap Deferred Tax Assets Operating Loss Carryforwards Foreign
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CY2022Q4 ptct Deferred Tax Assets Deferred Expense Capitalized Research And Development Costs
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CY2021Q4 ptct Deferred Tax Assets Deferred Expense Capitalized Research And Development Costs
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CY2022Q4 us-gaap Deferred Tax Assets Other
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CY2021Q4 us-gaap Deferred Tax Assets Other
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CY2022Q4 us-gaap Deferred Tax Assets Deferred Income
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CY2021Q4 us-gaap Deferred Tax Assets Deferred Income
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CY2022Q4 ptct Deferred Tax Assets Noncash Interest Expense
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CY2021Q4 ptct Deferred Tax Assets Noncash Interest Expense
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26040000
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CY2021Q4 ptct Other Comprehensive Gain Loss Net
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CY2022Q4 us-gaap Deferred Tax Assets Gross
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CY2021Q4 us-gaap Deferred Tax Assets Gross
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CY2022Q4 us-gaap Deferred Tax Assets Valuation Allowance
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CY2021Q4 us-gaap Deferred Tax Assets Valuation Allowance
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CY2021Q4 us-gaap Deferred Tax Assets Net
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549000
CY2022Q4 us-gaap Deferred Tax Liabilities Property Plant And Equipment
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CY2021Q4 us-gaap Deferred Tax Liabilities Property Plant And Equipment
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CY2022Q4 us-gaap Deferred Tax Liabilities Goodwill And Intangible Assets Intangible Assets
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102834000
CY2021Q4 us-gaap Deferred Tax Liabilities Goodwill And Intangible Assets Intangible Assets
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CY2022Q4 us-gaap Deferred Income Tax Liabilities
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CY2021Q4 us-gaap Deferred Income Tax Liabilities
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CY2022Q4 us-gaap Deferred Tax Liabilities
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CY2021Q4 us-gaap Deferred Tax Liabilities
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CY2022 ptct Taxable Income Before Net Operating Loss
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CY2022 us-gaap Current State And Local Tax Expense Benefit
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CY2022Q4 us-gaap Deferred Tax Assets Valuation Allowance
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CY2021Q4 us-gaap Deferred Tax Assets Valuation Allowance
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CY2022 us-gaap Valuation Allowance Deferred Tax Asset Change In Amount
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CY2021 us-gaap Valuation Allowance Deferred Tax Asset Change In Amount
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CY2022Q4 us-gaap Deferred Tax Assets Tax Credit Carryforwards General Business
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CY2020 ptct Operating Loss Carryforwards Utilized
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364100000
CY2021 ptct Operating Loss Carryforwards Utilized
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0
CY2022 ptct Operating Loss Carryforwards Utilized
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CY2021 us-gaap Effective Income Tax Rate Reconciliation At Federal Statutory Income Tax Rate
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CY2022 us-gaap Effective Income Tax Rate Reconciliation At Federal Statutory Income Tax Rate
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CY2022 ptct Change In Taxable Income Change In Tax Code Qualifying Research And Development Costs
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450100000
CY2022Q4 us-gaap Unrecognized Tax Benefits
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27200000
CY2022Q4 us-gaap Liability For Uncertain Tax Positions Current
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CY2022Q4 us-gaap Undistributed Earnings Of Foreign Subsidiaries
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CY2021Q4 us-gaap Unrecognized Tax Benefits
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27217000
CY2022Q4 us-gaap Unrecognized Tax Benefits
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27217000
CY2022 us-gaap Number Of Operating Segments
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1
CY2022Q4 us-gaap Assets
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CY2022Q4 us-gaap Property Plant And Equipment Net
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CY2022 us-gaap Revenue From Contract With Customer Excluding Assessed Tax
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CY2021Q4 us-gaap Assets
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CY2021Q4 us-gaap Property Plant And Equipment Net
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52585000
CY2021 us-gaap Revenue From Contract With Customer Excluding Assessed Tax
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CY2020 us-gaap Defined Contribution Plan Employer Matching Contribution Percent Of Match
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1
CY2021 us-gaap Defined Contribution Plan Employer Matching Contribution Percent Of Match
DefinedContributionPlanEmployerMatchingContributionPercentOfMatch
1
CY2022 us-gaap Defined Contribution Plan Employer Matching Contribution Percent Of Match
DefinedContributionPlanEmployerMatchingContributionPercentOfMatch
1
CY2020 us-gaap Defined Contribution Plan Employer Matching Contribution Percent
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CY2021 us-gaap Defined Contribution Plan Employer Matching Contribution Percent
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0.06
CY2022 us-gaap Defined Contribution Plan Employer Matching Contribution Percent
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CY2022 us-gaap Defined Contribution Plan Cost Recognized
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8400000
CY2021 us-gaap Defined Contribution Plan Cost Recognized
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6600000
CY2020 us-gaap Defined Contribution Plan Cost Recognized
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5300000
CY2022 us-gaap Amortization Of Intangible Assets
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116600000
CY2021 us-gaap Amortization Of Intangible Assets
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54800000
CY2020 us-gaap Amortization Of Intangible Assets
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36900000
CY2022Q4 us-gaap Finite Lived Intangible Assets Amortization Expense Next Twelve Months
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142324000
CY2022Q4 us-gaap Finite Lived Intangible Assets Amortization Expense Year Two
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30609000
CY2022Q4 us-gaap Finite Lived Intangible Assets Amortization Expense Year Three
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9352000
CY2022Q4 us-gaap Finite Lived Intangible Assets Amortization Expense Year Four
FiniteLivedIntangibleAssetsAmortizationExpenseYearFour
9352000
CY2022Q4 ptct Finite Lived Intangible Assets Amortization Expense Year Five And Thereafter
FiniteLivedIntangibleAssetsAmortizationExpenseYearFiveAndThereafter
60688000
CY2022Q4 us-gaap Finite Lived Intangible Assets Net
FiniteLivedIntangibleAssetsNet
252325000
CY2022Q4 us-gaap Intangible Assets Net Excluding Goodwill
IntangibleAssetsNetExcludingGoodwill
705891000

Files In Submission

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FilingSummary.xml Edgar Link unprocessable
0001070081-23-000011-index-headers.html Edgar Link pending
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