2024 Q2 Form 10-Q Financial Statement

#000143853324000020 Filed on May 06, 2024

View on sec.gov

Income Statement

Concept 2024 Q2 2024 Q1
Revenue $54.12M $41.37M
YoY Change -9.35% -27.41%
Cost Of Revenue $2.061M $1.504M
YoY Change 3.57% -70.65%
Gross Profit $52.06M $39.87M
YoY Change -9.79% -23.13%
Gross Profit Margin 96.19% 96.36%
Selling, General & Admin $64.78M $64.22M
YoY Change 2.64% -11.1%
% of Gross Profit 124.44% 161.08%
Research & Development $54.33M $49.42M
YoY Change -18.9% 558.93%
% of Gross Profit 104.37% 123.95%
Depreciation & Amortization $10.35M $9.880M
YoY Change -25.6% 3.51%
% of Gross Profit 19.87% 24.78%
Operating Expenses $119.1M $113.6M
YoY Change -18.02% 42.51%
Operating Profit -$67.70M -$139.2M
YoY Change -22.7% 59.96%
Interest Expense $1.632M $2.800M
YoY Change -26.39% -3.45%
% of Operating Profit
Other Income/Expense, Net -$1.863M $3.470M
YoY Change 826.87% 337.58%
Pretax Income -$69.57M -$135.8M
YoY Change -18.7% 57.41%
Income Tax $85.00K $191.0K
% Of Pretax Income
Net Earnings -$70.41M -$136.1M
YoY Change -17.78% 57.6%
Net Earnings / Revenue -130.11% -328.86%
Basic Earnings Per Share -$0.91 -$1.76
Diluted Earnings Per Share -$0.91 -$1.76
COMMON SHARES
Basic Shares Outstanding 76.13M shares 76.10M shares
Diluted Shares Outstanding 77.50M shares 77.14M shares

Balance Sheet

Concept 2024 Q2 2024 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $253.9M $284.6M
YoY Change -48.32% -35.38%
Cash & Equivalents $32.29M $43.25M
Short-Term Investments $221.7M $241.4M
Other Short-Term Assets $13.14M $12.77M
YoY Change 13.7% -15.67%
Inventory $42.98M $42.31M
Prepaid Expenses
Receivables $24.50M $22.70M
Other Receivables $0.00 $0.00
Total Short-Term Assets $369.0M $481.1M
YoY Change -31.93% -20.47%
LONG-TERM ASSETS
Property, Plant & Equipment $6.580M $6.943M
YoY Change -76.61% -23.93%
Goodwill $800.0K $800.0K
YoY Change -11.11% -11.11%
Intangibles $105.2M $101.2M
YoY Change -31.91% -37.88%
Long-Term Investments $0.00
YoY Change
Other Assets $16.92M $19.30M
YoY Change 43.52% 75.02%
Total Long-Term Assets $182.1M $182.5M
YoY Change -6.29% -10.26%
TOTAL ASSETS
Total Short-Term Assets $369.0M $481.1M
Total Long-Term Assets $182.1M $182.5M
Total Assets $551.1M $663.5M
YoY Change -25.16% -17.9%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $25.84M $16.73M
YoY Change 29.77% -0.01%
Accrued Expenses $79.64M $139.6M
YoY Change 22.23% 62.75%
Deferred Revenue $5.378M $6.460M
YoY Change -47.5% -41.14%
Short-Term Debt $0.00 $0.00
YoY Change
Long-Term Debt Due
YoY Change
Total Short-Term Liabilities $121.3M $173.2M
YoY Change -10.64% 32.6%
LONG-TERM LIABILITIES
Long-Term Debt $378.1M $377.7M
YoY Change 0.46% 0.46%
Other Long-Term Liabilities $16.64M $16.38M
YoY Change -84.57% 80.62%
Total Long-Term Liabilities $16.64M $16.38M
YoY Change -96.56% 80.62%
TOTAL LIABILITIES
Total Short-Term Liabilities $121.3M $173.2M
Total Long-Term Liabilities $16.64M $16.38M
Total Liabilities $536.0M $589.5M
YoY Change -13.54% -4.78%
SHAREHOLDERS EQUITY
Retained Earnings -$1.332B -$1.262B
YoY Change 12.3% 14.64%
Common Stock $8.000K $8.000K
YoY Change 14.29% 14.29%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $15.15M $74.07M
YoY Change
Total Liabilities & Shareholders Equity $551.1M $663.5M
YoY Change -25.16% -17.9%

Cashflow Statement

Concept 2024 Q2 2024 Q1
OPERATING ACTIVITIES
Net Income -$70.41M -$136.1M
YoY Change -17.78% 57.6%
Depreciation, Depletion And Amortization $10.35M $9.880M
YoY Change -25.6% 3.51%
Cash From Operating Activities -$40.24M -$119.0M
YoY Change -41.93% 46.71%
INVESTING ACTIVITIES
Capital Expenditures $76.99M $0.00
YoY Change 1907.12% -100.0%
Acquisitions
YoY Change
Other Investing Activities $105.6M $111.4M
YoY Change -635.59% -1327.56%
Cash From Investing Activities $28.61M $104.9M
YoY Change -221.47% -383.21%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 782.0K -$525.0K
YoY Change -65.49% -100.24%
NET CHANGE
Cash From Operating Activities -40.24M -$119.0M
Cash From Investing Activities 28.61M $104.9M
Cash From Financing Activities 782.0K -$525.0K
Net Change In Cash -10.85M -$14.93M
YoY Change -88.02% -114.97%
FREE CASH FLOW
Cash From Operating Activities -$40.24M -$119.0M
Capital Expenditures $76.99M $0.00
Free Cash Flow -$117.2M -$119.0M
YoY Change 60.31% 45.58%

Facts In Submission

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NatureOfOperations
DESCRIPTION OF BUSINESS<div style="margin-bottom:6pt;margin-top:12pt"><span style="color:#006ebf;font-family:'Arial',sans-serif;font-size:12pt;font-weight:700;line-height:120%">Organization and Description of Business</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">Travere Therapeutics, Inc. (“we”, “our”, “us”, “Travere” and the “Company”) refers to Travere Therapeutics, Inc., a Delaware corporation, as well as its subsidiaries. Travere is a fully integrated biopharmaceutical company headquartered in San Diego, California focused on identifying, developing and delivering life-changing therapies to people living with rare kidney and metabolic diseases. The Company regularly evaluates and, where appropriate, acts on opportunities to expand its product pipeline through licenses and acquisitions of products in areas that will serve patients with serious </span><span style="background-color:#ffffff;color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">unmet medical need</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%"> and that the Company believes offer attractive growth characteristics.</span></div><div style="margin-bottom:6pt;margin-top:6pt"><span style="color:#006ebf;font-family:'Arial Narrow',sans-serif;font-size:10pt;font-weight:700;line-height:120%">Discontinued Operations - Sale of Bile Acid Product Portfolio</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">In July 2023, Travere entered into an Asset Purchase Agreement (the “Purchase Agreement”) with Mirum Pharmaceuticals, Inc. ("Mirum Pharmaceuticals" or “Mirum”), pursuant to which Mirum agreed to purchase from Travere substantially all of the assets primarily related to Travere’s business of development, manufacture (including synthesis, formulation, finishing or packaging) and commercialization of Chenodal and Cholbam (also known as Kolbam, and together with Chenodal, the “Products”), collectively, the "bile acid business". On August 31, 2023, the Company and Mirum consummated the transactions contemplated by the Purchase Agreement (the “Closing”). In connection with the Closing, Mirum paid Travere an upfront cash payment of $210.0 million. Pursuant to the Purchase Agreement, after the Closing, Travere is eligible to receive up to $235.0 million upon the achievement of certain milestones based on specified amounts of annual net sales (tiered from $125.0 million to $500.0 million) of the Products. The Company has reflected the bile acid business as a discontinued operation in the unaudited consolidated financial statements for all periods presented. See Note 18 for further discussion. </span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">Unless otherwise noted, amounts and disclosures throughout the Notes to the unaudited consolidated financial statements relate to the Company's continuing operations.</span></div><div style="margin-bottom:6pt;margin-top:9pt;text-align:justify"><span style="color:#666666;font-family:'Arial',sans-serif;font-size:10pt;font-style:italic;font-weight:700;line-height:120%">Approved Products:</span></div><div style="margin-bottom:6pt;margin-top:6pt"><span style="color:#006ebf;font-family:'Arial Narrow',sans-serif;font-size:10pt;font-weight:700;line-height:120%">FILSPARI® (sparsentan)</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">On February 17, 2023, the U.S. Food and Drug Administration (the "FDA") granted accelerated approval of FILSPARI® (sparsentan) to reduce proteinuria in adults with primary IgAN at risk of rapid disease progression, generally a UPCR ≥1.5 gram/gram. FILSPARI, a once-daily, oral medication is designed to selectively target two critical pathways (endothelin 1 and angiotensin-II) in the disease progression of IgAN. </span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">This indication was granted under accelerated approval based on reduction in proteinuria. The continued approval of FILSPARI may be contingent upon confirmation of a clinical benefit in the Company's Phase 3 clinical trial of sparsentan for the treatment of IgAN (the "PROTECT Study"). In September 2023, the Company announced topline two-year confirmatory secondary endpoint results from the PROTECT Study and in December 2023, the Company announced the completion of a successful pre-NDA meeting with the FDA for FILSPARI in IgAN. In March 2024, the Company submitted a supplemental New Drug Application (sNDA) for conversion of the existing U.S. accelerated approval of FILSPARI to full approval. In May 2024, the Company announced that the FDA has accepted and granted Priority Review of its sNDA to convert FILSPARI from accelerated approval to full approval for the treatment of IgAN in the U.S. The FDA assigned a Prescription Drug User Fee Act (“PDUFA”) target action date of September 5, 2024.</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">In April 2024, the Company and Vifor (International) Ltd. ("CSL Vifor"), with whom the Company entered into a license and collaboration agreement ("License Agreement") in September 2021, announced that the European Commission has granted conditional marketing authorization (“CMA”) for FILSPARI (sparsentan) for the treatment of adults with primary IgAN with a urine protein excretion ≥1.0 g/day (or urine protein-to-creatinine ratio ≥0.75 g/g). The CMA is granted for all member states of the European Union, as well as in Iceland, Liechtenstein and Norway. The European Commission's decision follows the positive opinion from the Committee for Medicinal Products for Human Use (“CHMP”) in February 2024, based on results from the pivotal Phase 3 PROTECT Study of FILSPARI in IgAN. Under the terms of the License Agreement, the Company will be entitled to receive a regulatory milestone payment of $17.5 million upon receipt of full regulatory approval by the European Commission for IgAN, and an additional milestone payment upon achievement of market access initiatives in certain countries. The Company also expects to make a milestone payment of $5.8 million to Ligand Pharmaceuticals in the second quarter of 2024.</span></div><div style="margin-bottom:6pt;margin-top:6pt"><span style="color:#006ebf;font-family:'Arial Narrow',sans-serif;font-size:10pt;font-weight:700;line-height:120%">Thiola® and Thiola EC® (tiopronin tablets)</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%"> </span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">Thiola® and Thiola EC® (tiopronin tablets) are approved in the United States for the prevention of cystine (kidney) stone formation in patients with severe homozygous cystinuria.</span></div><div style="margin-bottom:6pt;margin-top:9pt;text-align:justify"><span style="color:#666666;font-family:'Arial',sans-serif;font-size:10pt;font-style:italic;font-weight:700;line-height:120%">Clinical-Stage Programs:</span></div><div style="margin-bottom:6pt;margin-top:6pt;text-align:justify"><span style="color:#006ebf;font-family:'Arial Narrow',sans-serif;font-size:10pt;font-weight:700;line-height:120%">Sparsentan for the treatment of FSGS</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">Sparsentan remains a novel investigational product candidate which has been granted Orphan Drug Designation for the treatment of focal segmental glomerulosclerosis (FSGS) in the U.S. and the EEA. In December 2023, the Company announced that it had completed its planned Type C meeting with the FDA to discuss previously reported results from the Phase 3 DUPLEX Study of sparsentan in FSGS. The FDA acknowledged the high unmet need for approved therapies as well as the challenges in studying FSGS but indicated that the two-year results from the Phase 3 DUPLEX Study alone were not sufficient to support an sNDA submission. Together with CSL Vifor, the Company also plans to engage with the EMA to determine the potential for a subsequent variation to the CMA of sparsentan for the treatment of FSGS, subject to a review decision on the pending application for CMA of sparsentan in </span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">IgAN. The Company is conducting additional analyses of FSGS data and intends to engage with regulators to evaluate potential regulatory pathways for a sparsentan FSGS indication.</span></div><div style="margin-bottom:6pt;margin-top:6pt;text-align:justify"><span style="color:#006ebf;font-family:'Arial Narrow',sans-serif;font-size:10pt;font-weight:700;line-height:120%">Pegtibatinase</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">Pegtibatinas</span><span style="background-color:#ffffff;color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">e is a novel investigational human enzyme replacement candidate being evaluated for the treatment of classical homocystinuria (HCU). Pegtibatinase has been granted Rare Pediatric Disease, Fast Track and Breakthrough Therapy designations by the FDA, as well as orphan drug designation in the United States and European Union. In May 2023, the Company announced positive topline results from cohort 6 in the Phase 1/2 COMPOSE Study. </span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">In December 2023, the Company initiated the pivotal Phase 3 HARMONY Study to support the potential approval of pegtibatinase for the treatment of classical HCU. The HARMONY Study is a global, randomized, multi-center, double-blind, placebo-controlled Phase 3 clinical trial designed to evaluate the efficacy and safety of pegtibatinase as a novel treatment to reduce total homocysteine (tHcy) levels. In the beginning of 2024, the first patients were dosed in the HARMONY Study. Topline results from the HARMONY Study are expected in 2026. </span><span style="background-color:#ffffff;color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">The Company</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%"> acquired pegtibatinase as part of the November 2020 acquisition of Orphan Technologies Limited.</span></div><div style="margin-bottom:6pt;margin-top:9pt"><span style="color:#666666;font-family:'Arial',sans-serif;font-size:10pt;font-style:italic;font-weight:700;line-height:120%">Preclinical Programs:</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">The Company is a participant in a Cooperative Research and Development Agreement ("CRADA"), which forms a multi-stakeholder approach to pool resources with leading experts and incorporate the patient perspective early in the therapeutic identification and development process. The Company is partnering with the National Institutes of Health’s National Center for Advancing Translational Sciences ("NCATS") and a leading patient advocacy organization, Alagille Syndrome Alliance, aimed at the identification of potential small molecule therapeutics for Alagille syndrome ("ALGS"). There are no treatment options currently approved for ALGS.</span></div><div style="margin-bottom:6pt;margin-top:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">The Company is party to a collaboration agreement with PharmaKrysto Limited and their early-stage cystinuria discovery program, whereby the Company is responsible for funding all research and development expenses for the pre-clinical activities associated with the cystinuria program.</span></div>
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RevenuePerformanceObligationDescriptionOfTiming
For FILSPARI, sales are recognized upon delivery of the product to the specialty pharmacies. The Company receives payments from its FILSPARI sales based on terms that are generally 30 days from shipment of the product to the specialty pharmacy. For the Company's other products, product sales are recognized upon delivery to the patient. The Company receives payments from sales of its other products, primarily through third party payers, based on terms that generally are within 30 days of delivery of product to the patient.
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3400000 usd
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2800000 usd
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2900000 usd
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20861000 usd
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26006000 usd
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18715000 usd
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29908000 usd
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6686000 usd
CY2023Q4 us-gaap Accrued Royalties Current
AccruedRoyaltiesCurrent
6991000 usd
CY2024Q1 tvtx Accrued Liabilities Selling Generaland Administrative Current
AccruedLiabilitiesSellingGeneralandAdministrativeCurrent
5893000 usd
CY2023Q4 tvtx Accrued Liabilities Selling Generaland Administrative Current
AccruedLiabilitiesSellingGeneralandAdministrativeCurrent
7190000 usd
CY2024Q1 us-gaap Restructuring Reserve Current
RestructuringReserveCurrent
1204000 usd
CY2023Q4 us-gaap Restructuring Reserve Current
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11421000 usd
CY2024Q1 tvtx Transition Services Accrual Current
TransitionServicesAccrualCurrent
605000 usd
CY2023Q4 tvtx Transition Services Accrual Current
TransitionServicesAccrualCurrent
12282000 usd
CY2024Q1 tvtx Accrued Liabilities Miscellaneous Current
AccruedLiabilitiesMiscellaneousCurrent
8983000 usd
CY2023Q4 tvtx Accrued Liabilities Miscellaneous Current
AccruedLiabilitiesMiscellaneousCurrent
11463000 usd
CY2024Q1 us-gaap Accrued Liabilities Current
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CY2023Q4 us-gaap Accrued Liabilities Current
AccruedLiabilitiesCurrent
118991000 usd
CY2024Q1 tvtx Weighted Average Number Of Shares Outstanding Diluted Continuing Operations
WeightedAverageNumberOfSharesOutstandingDilutedContinuingOperations
77136493 shares
CY2024Q1 tvtx Weighted Average Number Of Shares Outstanding Basic Continuing Operations
WeightedAverageNumberOfSharesOutstandingBasicContinuingOperations
77136493 shares
CY2024Q1 us-gaap Income Loss From Continuing Operations
IncomeLossFromContinuingOperations
-135958000 usd
CY2024Q1 us-gaap Income Loss From Continuing Operations Per Diluted Share
IncomeLossFromContinuingOperationsPerDilutedShare
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CY2024Q1 us-gaap Income Loss From Continuing Operations Per Basic Share
IncomeLossFromContinuingOperationsPerBasicShare
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CY2023Q1 tvtx Weighted Average Number Of Shares Outstanding Basic Continuing Operations
WeightedAverageNumberOfSharesOutstandingBasicContinuingOperations
68174099 shares
CY2023Q1 tvtx Weighted Average Number Of Shares Outstanding Diluted Continuing Operations
WeightedAverageNumberOfSharesOutstandingDilutedContinuingOperations
68174099 shares
CY2023Q1 us-gaap Income Loss From Continuing Operations
IncomeLossFromContinuingOperations
-96564000 usd
CY2023Q1 us-gaap Income Loss From Continuing Operations Per Basic Share
IncomeLossFromContinuingOperationsPerBasicShare
-1.42
CY2023Q1 us-gaap Income Loss From Continuing Operations Per Diluted Share
IncomeLossFromContinuingOperationsPerDilutedShare
-1.42
CY2024Q1 tvtx Weighted Average Number Of Shares Outstanding Diluted Discontinued Operations
WeightedAverageNumberOfSharesOutstandingDilutedDiscontinuedOperations
77136493 shares
CY2024Q1 tvtx Weighted Average Number Of Shares Outstanding Basic Discontinued Operations
WeightedAverageNumberOfSharesOutstandingBasicDiscontinuedOperations
77136493 shares
CY2024Q1 us-gaap Income Loss From Discontinued Operations Net Of Tax Attributable To Reporting Entity
IncomeLossFromDiscontinuedOperationsNetOfTaxAttributableToReportingEntity
-103000 usd
CY2024Q1 us-gaap Income Loss From Discontinued Operations Net Of Tax Per Basic Share
IncomeLossFromDiscontinuedOperationsNetOfTaxPerBasicShare
0
CY2024Q1 us-gaap Income Loss From Discontinued Operations Net Of Tax Per Diluted Share
IncomeLossFromDiscontinuedOperationsNetOfTaxPerDilutedShare
0
CY2023Q1 tvtx Weighted Average Number Of Shares Outstanding Basic Discontinued Operations
WeightedAverageNumberOfSharesOutstandingBasicDiscontinuedOperations
68174099 shares
CY2023Q1 tvtx Weighted Average Number Of Shares Outstanding Diluted Discontinued Operations
WeightedAverageNumberOfSharesOutstandingDilutedDiscontinuedOperations
68174099 shares
CY2023Q1 us-gaap Income Loss From Discontinued Operations Net Of Tax Attributable To Reporting Entity
IncomeLossFromDiscontinuedOperationsNetOfTaxAttributableToReportingEntity
10233000 usd
CY2023Q1 us-gaap Income Loss From Discontinued Operations Net Of Tax Per Basic Share
IncomeLossFromDiscontinuedOperationsNetOfTaxPerBasicShare
0.15
CY2023Q1 us-gaap Income Loss From Discontinued Operations Net Of Tax Per Diluted Share
IncomeLossFromDiscontinuedOperationsNetOfTaxPerDilutedShare
0.15
CY2024Q1 us-gaap Allocated Share Based Compensation Expense
AllocatedShareBasedCompensationExpense
9758000 usd
CY2024Q1 us-gaap Weighted Average Number Of Shares Outstanding Basic
WeightedAverageNumberOfSharesOutstandingBasic
77136493 shares
CY2024Q1 us-gaap Weighted Average Number Of Diluted Shares Outstanding
WeightedAverageNumberOfDilutedSharesOutstanding
77136493 shares
CY2024Q1 us-gaap Net Income Loss Available To Common Stockholders Diluted
NetIncomeLossAvailableToCommonStockholdersDiluted
-136061000 usd
CY2024Q1 us-gaap Net Income Loss Available To Common Stockholders Basic
NetIncomeLossAvailableToCommonStockholdersBasic
-136061000 usd
CY2024Q1 us-gaap Earnings Per Share Diluted
EarningsPerShareDiluted
-1.76
CY2024Q1 us-gaap Earnings Per Share Basic
EarningsPerShareBasic
-1.76
CY2023Q1 us-gaap Weighted Average Number Of Diluted Shares Outstanding
WeightedAverageNumberOfDilutedSharesOutstanding
68174099 shares
CY2023Q1 us-gaap Weighted Average Number Of Shares Outstanding Basic
WeightedAverageNumberOfSharesOutstandingBasic
68174099 shares
CY2023Q1 us-gaap Net Income Loss Available To Common Stockholders Diluted
NetIncomeLossAvailableToCommonStockholdersDiluted
-86331000 usd
CY2023Q1 us-gaap Net Income Loss Available To Common Stockholders Basic
NetIncomeLossAvailableToCommonStockholdersBasic
-86331000 usd
CY2023Q1 us-gaap Earnings Per Share Basic
EarningsPerShareBasic
-1.27
CY2023Q1 us-gaap Earnings Per Share Diluted
EarningsPerShareDiluted
-1.27
CY2024Q1 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
26395000 shares
CY2023Q1 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
25523529 shares
CY2024Q1 tvtx In Process Research And Development Expense
InProcessResearchAndDevelopmentExpense
65200000 usd
CY2024Q1 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercisable Number
ShareBasedCompensationArrangementByShareBasedPaymentAwardOptionsExercisableNumber
8200000 shares
CY2024Q1 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercisable Weighted Average Exercise Price
ShareBasedCompensationArrangementByShareBasedPaymentAwardOptionsExercisableWeightedAverageExercisePrice
20.99
CY2023Q1 us-gaap Allocated Share Based Compensation Expense
AllocatedShareBasedCompensationExpense
13471000 usd
CY2024Q1 us-gaap Inventory Raw Materials Net Of Reserves
InventoryRawMaterialsNetOfReserves
29838000 usd
CY2023Q4 us-gaap Inventory Raw Materials Net Of Reserves
InventoryRawMaterialsNetOfReserves
33790000 usd
CY2024Q1 us-gaap Inventory Work In Process Net Of Reserves
InventoryWorkInProcessNetOfReserves
9329000 usd
CY2023Q4 us-gaap Inventory Work In Process Net Of Reserves
InventoryWorkInProcessNetOfReserves
4727000 usd
CY2024Q1 us-gaap Inventory Finished Goods Net Of Reserves
InventoryFinishedGoodsNetOfReserves
3139000 usd
CY2023Q4 us-gaap Inventory Finished Goods Net Of Reserves
InventoryFinishedGoodsNetOfReserves
2387000 usd
CY2024Q1 us-gaap Inventory Net
InventoryNet
42306000 usd
CY2023Q4 us-gaap Inventory Net
InventoryNet
40904000 usd
CY2024Q1 us-gaap Inventory Gross
InventoryGross
4532000 usd
CY2023Q4 us-gaap Inventory Gross
InventoryGross
9410000 usd
CY2024Q1 us-gaap Inventory Noncurrent
InventoryNoncurrent
37774000 usd
CY2023Q4 us-gaap Inventory Noncurrent
InventoryNoncurrent
31494000 usd
CY2024Q1 us-gaap Inventory Net
InventoryNet
42306000 usd
CY2023Q4 us-gaap Inventory Net
InventoryNet
40904000 usd
CY2024Q1 us-gaap Accounts Receivable Net Current
AccountsReceivableNetCurrent
22700000 usd
CY2023Q4 us-gaap Accounts Receivable Net Current
AccountsReceivableNetCurrent
21200000 usd
CY2024Q1 tvtx Transition Services Accruals Current
TransitionServicesAccrualsCurrent
600000 usd
CY2024Q1 ecd Non Rule10b51 Arr Adopted Flag
NonRule10b51ArrAdoptedFlag
false
CY2024Q1 ecd Non Rule10b51 Arr Trmntd Flag
NonRule10b51ArrTrmntdFlag
false

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