2022 Q1 Form 10-Q Financial Statement

#000143853322000025 Filed on May 05, 2022

View on sec.gov

Income Statement

Concept 2022 Q1 2021 Q1
Revenue $48.49M $47.41M
YoY Change 2.28% -0.76%
Cost Of Revenue $2.138M $1.645M
YoY Change 29.97% 20.07%
Gross Profit $46.35M $45.76M
YoY Change 1.28% -1.37%
Gross Profit Margin 95.59% 96.53%
Selling, General & Admin $46.79M $36.78M
YoY Change 27.22% 10.98%
% of Gross Profit 100.95% 80.37%
Research & Development $56.61M $47.95M
YoY Change 18.07% 58.5%
% of Gross Profit 122.14% 104.77%
Depreciation & Amortization $7.092M $6.074M
YoY Change 16.76% 7.39%
% of Gross Profit 15.3% 13.27%
Operating Expenses $103.4M $84.72M
YoY Change 22.04% 34.83%
Operating Profit -$66.13M -$47.55M
YoY Change 39.08% 215.58%
Interest Expense -$2.515M -$5.321M
YoY Change -52.73% 8.88%
% of Operating Profit
Other Income/Expense, Net -$9.789M -$6.005M
YoY Change 63.01% 93.65%
Pretax Income -$75.92M -$53.55M
YoY Change 41.76% 194.77%
Income Tax $100.0K $300.0K
% Of Pretax Income
Net Earnings -$75.97M -$53.87M
YoY Change 41.03% -6766.71%
Net Earnings / Revenue -156.68% -113.63%
Basic Earnings Per Share -$1.20 -$0.96
Diluted Earnings Per Share -$1.20 -$0.96
COMMON SHARES
Basic Shares Outstanding 63.13M shares 56.27M shares
Diluted Shares Outstanding 63.13M shares 56.27M shares

Balance Sheet

Concept 2022 Q1 2021 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $529.7M $431.0M
YoY Change 22.89% 59.71%
Cash & Equivalents $256.6M $148.2M
Short-Term Investments $273.1M $282.8M
Other Short-Term Assets $6.507M $6.700M
YoY Change -2.88% 26.42%
Inventory $6.521M $7.183M
Prepaid Expenses
Receivables $14.70M $13.10M
Other Receivables $0.00 $17.10M
Total Short-Term Assets $631.1M $565.0M
YoY Change 11.69% 38.96%
LONG-TERM ASSETS
Property, Plant & Equipment $10.60M $11.70M
YoY Change -9.36% 346.96%
Goodwill $900.0K $936.0K
YoY Change -3.85% 0.0%
Intangibles $153.3M
YoY Change
Long-Term Investments
YoY Change
Other Assets $10.83M $35.03M
YoY Change -69.08% 414.92%
Total Long-Term Assets $197.3M $199.0M
YoY Change -0.85% 19.57%
TOTAL ASSETS
Total Short-Term Assets $631.1M $565.0M
Total Long-Term Assets $197.3M $199.0M
Total Assets $828.4M $764.0M
YoY Change 8.42% 33.33%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $18.43M $15.01M
YoY Change 22.83% 50.59%
Accrued Expenses $69.24M $46.47M
YoY Change 49.01% 11.73%
Deferred Revenue $14.23M
YoY Change
Short-Term Debt $0.00 $0.00
YoY Change
Long-Term Debt Due
YoY Change
Total Short-Term Liabilities $119.5M $85.01M
YoY Change 40.53% 24.85%
LONG-TERM LIABILITIES
Long-Term Debt $374.3M $218.1M
YoY Change 71.63% 5.16%
Other Long-Term Liabilities $10.35M $43.17M
YoY Change -76.02% 224.27%
Total Long-Term Liabilities $10.35M $43.17M
YoY Change -76.02% 224.27%
TOTAL LIABILITIES
Total Short-Term Liabilities $119.5M $85.01M
Total Long-Term Liabilities $10.35M $43.17M
Total Liabilities $620.3M $401.4M
YoY Change 54.54% 15.56%
SHAREHOLDERS EQUITY
Retained Earnings -$811.7M -$639.7M
YoY Change 26.88% 53.92%
Common Stock $6.000K $1.003B
YoY Change -100.0% 55.97%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $208.1M $362.7M
YoY Change
Total Liabilities & Shareholders Equity $828.4M $764.0M
YoY Change 8.42% 33.33%

Cashflow Statement

Concept 2022 Q1 2021 Q1
OPERATING ACTIVITIES
Net Income -$75.97M -$53.87M
YoY Change 41.03% -6766.71%
Depreciation, Depletion And Amortization $7.092M $6.074M
YoY Change 16.76% 7.39%
Cash From Operating Activities -$55.32M -$26.47M
YoY Change 108.96% -9.2%
INVESTING ACTIVITIES
Capital Expenditures $131.0K $4.495M
YoY Change -97.09% 2061.06%
Acquisitions
YoY Change
Other Investing Activities $38.43M -$96.44M
YoY Change -139.85% -318.34%
Cash From Investing Activities $33.17M -$105.7M
YoY Change -131.37% -367.27%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities $113.9M $195.8M
YoY Change -41.81% -3490.84%
NET CHANGE
Cash From Operating Activities -$55.32M -$26.47M
Cash From Investing Activities $33.17M -$105.7M
Cash From Financing Activities $113.9M $195.8M
Net Change In Cash $90.82M $63.46M
YoY Change 43.11% 1284.68%
FREE CASH FLOW
Cash From Operating Activities -$55.32M -$26.47M
Capital Expenditures $131.0K $4.495M
Free Cash Flow -$55.45M -$30.97M
YoY Change 79.05% 5.47%

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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 our direct and indirect subsidiaries. Travere is a fully integrated biopharmaceutical company headquartered in San Diego, California focused on identifying, developing and delivering life-changing therapies to people with rare diseases. We regularly evaluate and, where appropriate, act on opportunities to expand our product pipeline through licenses and acquisitions of products in areas that will serve patients with serious or rare diseases and that we believe offer attractive growth characteristics. </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 ongoing novel coronavirus (COVID-19) pandemic has resulted in travel restrictions, quarantines, “stay-at-home” and “shelter-in-place” orders and extended shutdown of certain businesses around the world. While the impact of the COVID-19 pandemic did not have a material adverse effect on our financial position or results of operations for the three months ended March 31, 2022, these governmental actions and similar actions that may be enacted in the future, and the widespread economic disruption arising from the pandemic, have the potential to materially impact our business and influence our business decisions. The extent and duration of the pandemic is unknown, and the future effects on our business are uncertain and difficult to predict. The Company is continuing to monitor the events and circumstances surrounding the COVID-19 pandemic, which may require adjustments to the Company’s estimates and assumptions in the future.</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 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%">Sparsentan is a novel investigational product candidate and has been granted Orphan Drug Designation for the treatment of focal segmental glomerulosclerois (FSGS) and immunoglobulin A nephropathy (IgAN) in the U.S. and Europe. Sparsentan is currently being evaluated in two pivotal Phase 3 clinical studies in rare kidney diseases.</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%">Pegtibatinase (</span><span style="background-color:#ffffff;color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">TVT-058) is a novel investigational human enzyme replacement candidate being evaluated for the treatment of classical homocystinuria (HCU). Pegtibatinase has been granted Rare Pediatric Disease and Fast Track designations by the U.S. Food and Drug Administration ("FDA"), as well as orphan drug designation in the United States and European Union. Pegtibatinase is currently being evaluated in the Phase 1/2 COMPOSE Study to assess its safety, tolerability, pharmacokinetics, pharmacodynamics and clinical effects in patients with classical HCU. 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:3pt;text-align:justify"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">Chenodal (chenodeoxycholic acid or CDCA) is a naturally occurring bile acid that is approved for the treatment of people with radiolucent stones in the gallbladder. In January 2020, we randomized the first patients in our Phase 3 RESTORE Study to evaluate the effects of Chenodal in adult and pediatric patients with cerebrotendinous xanthomatosis (CTX), and the study enrollment remains open. The pivotal study is intended to support an NDA submission for marketing authorization of Chenodal for CTX in the United States. </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%">We are a participant in two Cooperative Research and Development Agreements ("CRADAs"), which form a multi-stakeholder approach to pool resources with leading experts, and incorporate the patient perspective early in the therapeutic identification and development process. We have partnered with the National Institutes of Health’s National Center for Advancing Translational Sciences ("NCATS") and leading patient advocacy organizations, CDG Care and Alagille Syndrome Alliance, aimed at the identification of potential small molecule therapeutics for NGLY1 deficiency and Alagille syndrome ("ALGS"), respectively. There are no treatment options currently approved for these diseases.</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:3pt;padding-left:36pt;text-align:justify;text-indent:-18pt"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">•</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%;padding-left:15.42pt">Chenodal (chenodiol tablets) is approved in the United States for the treatment of patients suffering from gallstones in whom surgery poses an unacceptable health risk due to disease or advanced age. </span></div><div style="margin-bottom:6pt;margin-top:3pt;padding-left:36pt;text-align:justify;text-indent:-18pt"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">•</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%;padding-left:15.42pt">Cholbam</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:5.85pt;font-weight:400;line-height:120%;position:relative;top:-3.15pt;vertical-align:baseline">®</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%"> (cholic acid capsules) is approved in the United States for the treatment of bile acid synthesis disorders due to single enzyme defects and is further indicated for adjunctive treatment of patients with peroxisomal disorders.</span></div><div style="margin-bottom:6pt;margin-top:3pt;padding-left:36pt;text-align:justify;text-indent:-18pt"><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%">•</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%;padding-left:15.42pt">Thiola</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:5.85pt;font-weight:400;line-height:120%;position:relative;top:-3.15pt;vertical-align:baseline">®</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%"> and Thiola EC</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:5.85pt;font-weight:400;line-height:120%;position:relative;top:-3.15pt;vertical-align:baseline">®</span><span style="color:#000000;font-family:'Arial Narrow',sans-serif;font-size:9pt;font-weight:400;line-height:120%"> (tiopronin tablets) are approved in the United States for the prevention of cystine (kidney) stone formation in patients with severe homozygous cystinuria.</span></div>
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FiniteLivedIntangibleAssetsNet
152400000 USD
CY2022Q1 us-gaap Finite Lived Intangible Assets Gross
FiniteLivedIntangibleAssetsGross
295175000 USD
CY2021Q4 us-gaap Finite Lived Intangible Assets Gross
FiniteLivedIntangibleAssetsGross
283557000 USD
CY2022Q1 us-gaap Finite Lived Intangible Assets Accumulated Amortization
FiniteLivedIntangibleAssetsAccumulatedAmortization
142790000 USD
CY2021Q4 us-gaap Finite Lived Intangible Assets Accumulated Amortization
FiniteLivedIntangibleAssetsAccumulatedAmortization
136058000 USD
CY2022Q1 us-gaap Finite Lived Intangible Assets Net
FiniteLivedIntangibleAssetsNet
152385000 USD
CY2021Q4 us-gaap Finite Lived Intangible Assets Net
FiniteLivedIntangibleAssetsNet
147499000 USD
CY2021Q4 us-gaap Goodwill
Goodwill
900000 USD
CY2022Q1 us-gaap Goodwill
Goodwill
900000 USD
CY2022Q1 us-gaap Amortization Of Intangible Assets
AmortizationOfIntangibleAssets
6556000 USD
CY2021Q1 us-gaap Amortization Of Intangible Assets
AmortizationOfIntangibleAssets
5952000 USD
CY2022Q1 tvtx Debt Instrument Repurchase Amount Including Accrued And Unpaid Interest
DebtInstrumentRepurchaseAmountIncludingAccruedAndUnpaidInterest
213800000 USD
CY2022Q1 us-gaap Gains Losses On Extinguishment Of Debt
GainsLossesOnExtinguishmentOfDebt
-7600000 USD
CY2022Q1 us-gaap Write Off Of Deferred Debt Issuance Cost
WriteOffOfDeferredDebtIssuanceCost
3400000 USD
CY2022Q1 us-gaap Accrued Salaries Current
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23408000 USD
CY2021Q4 us-gaap Accrued Salaries Current
AccruedSalariesCurrent
25998000 USD
CY2022Q1 tvtx Accrued Liabilities Researchand Development Current
AccruedLiabilitiesResearchandDevelopmentCurrent
22058000 USD
CY2021Q4 tvtx Accrued Liabilities Researchand Development Current
AccruedLiabilitiesResearchandDevelopmentCurrent
26841000 USD
CY2022Q1 tvtx Government Rebates Payable
GovernmentRebatesPayable
9351000 USD
CY2021Q4 tvtx Government Rebates Payable
GovernmentRebatesPayable
7493000 USD
CY2022Q1 tvtx Accrued Royaltyand Contingent Consideration
AccruedRoyaltyandContingentConsideration
6694000 USD
CY2021Q4 tvtx Accrued Royaltyand Contingent Consideration
AccruedRoyaltyandContingentConsideration
8402000 USD
CY2022Q1 tvtx Accrued Liabilities Selling Generaland Administrative Current
AccruedLiabilitiesSellingGeneralandAdministrativeCurrent
5349000 USD
CY2021Q4 tvtx Accrued Liabilities Selling Generaland Administrative Current
AccruedLiabilitiesSellingGeneralandAdministrativeCurrent
3144000 USD
CY2022Q1 tvtx Accrued Liabilities Miscellaneous
AccruedLiabilitiesMiscellaneous
2380000 USD
CY2021Q4 tvtx Accrued Liabilities Miscellaneous
AccruedLiabilitiesMiscellaneous
3302000 USD
CY2022Q1 us-gaap Accrued Liabilities Current
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69240000 USD
CY2021Q4 us-gaap Accrued Liabilities Current
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75180000 USD
CY2022Q1 us-gaap Weighted Average Number Of Shares Outstanding Basic
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63132841 shares
CY2022Q1 us-gaap Weighted Average Number Of Diluted Shares Outstanding
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63132841 shares
CY2022Q1 us-gaap Net Income Loss Available To Common Stockholders Basic
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CY2022Q1 us-gaap Net Income Loss Available To Common Stockholders Diluted
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CY2022Q1 us-gaap Earnings Per Share Basic
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-1.20
CY2022Q1 us-gaap Earnings Per Share Diluted
EarningsPerShareDiluted
-1.20
CY2021Q1 us-gaap Weighted Average Number Of Shares Outstanding Basic
WeightedAverageNumberOfSharesOutstandingBasic
56268508 shares
CY2021Q1 us-gaap Weighted Average Number Of Diluted Shares Outstanding
WeightedAverageNumberOfDilutedSharesOutstanding
56268508 shares
CY2021Q1 us-gaap Net Income Loss Available To Common Stockholders Diluted
NetIncomeLossAvailableToCommonStockholdersDiluted
-53867000 USD
CY2021Q1 us-gaap Net Income Loss Available To Common Stockholders Basic
NetIncomeLossAvailableToCommonStockholdersBasic
-53867000 USD
CY2021Q1 us-gaap Earnings Per Share Diluted
EarningsPerShareDiluted
-0.96
CY2021Q1 us-gaap Earnings Per Share Basic
EarningsPerShareBasic
-0.96
CY2022Q1 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
20100996 shares
CY2021Q1 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
17979101 shares
CY2022Q1 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercisable Number
ShareBasedCompensationArrangementByShareBasedPaymentAwardOptionsExercisableNumber
6600000 shares
CY2022Q1 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercisable Weighted Average Exercise Price
ShareBasedCompensationArrangementByShareBasedPaymentAwardOptionsExercisableWeightedAverageExercisePrice
19.76
CY2021Q4 us-gaap Inventory Finished Goods Net Of Reserves
InventoryFinishedGoodsNetOfReserves
2108000 USD
CY2022Q1 us-gaap Allocated Share Based Compensation Expense
AllocatedShareBasedCompensationExpense
8186000 USD
CY2021Q1 us-gaap Allocated Share Based Compensation Expense
AllocatedShareBasedCompensationExpense
7694000 USD
CY2022Q1 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
100000 USD
CY2021Q1 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
300000 USD
CY2022Q1 us-gaap Inventory Raw Materials Net Of Reserves
InventoryRawMaterialsNetOfReserves
4964000 USD
CY2021Q4 us-gaap Inventory Raw Materials Net Of Reserves
InventoryRawMaterialsNetOfReserves
5205000 USD
CY2022Q1 us-gaap Inventory Finished Goods Net Of Reserves
InventoryFinishedGoodsNetOfReserves
1557000 USD
CY2022Q1 us-gaap Inventory Net
InventoryNet
6521000 USD
CY2021Q4 us-gaap Inventory Net
InventoryNet
7313000 USD
CY2022Q1 us-gaap Inventory Valuation Reserves
InventoryValuationReserves
4100000 USD
CY2021Q4 us-gaap Inventory Valuation Reserves
InventoryValuationReserves
4100000 USD
CY2022Q1 us-gaap Accounts Receivable Net Current
AccountsReceivableNetCurrent
14700000 USD
CY2021Q4 us-gaap Accounts Receivable Net Current
AccountsReceivableNetCurrent
15900000 USD
CY2021Q2 us-gaap Common Stock Shares Authorized
CommonStockSharesAuthorized
100000000 shares
CY2021Q2 us-gaap Common Stock Shares Authorized
CommonStockSharesAuthorized
200000000 shares

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