2020 Q1 Form 10-Q Financial Statement

#000143853320000011 Filed on May 11, 2020

View on sec.gov

Income Statement

Concept 2020 Q1 2019 Q1
Revenue $47.77M $39.57M
YoY Change 20.72% 2.96%
Cost Of Revenue $1.370M $1.017M
YoY Change 34.71% -36.95%
Gross Profit $46.40M $38.55M
YoY Change 20.35% 4.71%
Gross Profit Margin 97.13% 97.43%
Selling, General & Admin $33.14M $32.67M
YoY Change 1.44% 23.43%
% of Gross Profit 71.42% 84.74%
Research & Development $30.25M $33.44M
YoY Change -9.55% 35.75%
% of Gross Profit 65.19% 86.75%
Depreciation & Amortization $5.656M $4.901M
YoY Change 15.41% 12.72%
% of Gross Profit 12.19% 12.71%
Operating Expenses $62.84M $77.80M
YoY Change -19.23% 38.08%
Operating Profit -$15.07M -$38.23M
YoY Change -60.59% 113.42%
Interest Expense -$4.887M -$4.865M
YoY Change 0.45% 321.21%
% of Operating Profit
Other Income/Expense, Net -$3.101M -$2.348M
YoY Change 32.07% 890.72%
Pretax Income -$18.17M -$40.58M
YoY Change -55.22% 123.57%
Income Tax -$19.00M $401.0K
% Of Pretax Income
Net Earnings $808.0K -$40.98M
YoY Change -101.97% 122.97%
Net Earnings / Revenue 1.69% -103.56%
Basic Earnings Per Share $0.02 -$0.99
Diluted Earnings Per Share $0.02 -$0.99
COMMON SHARES
Basic Shares Outstanding 43.12M shares 41.41M shares
Diluted Shares Outstanding 43.59M shares 41.41M shares

Balance Sheet

Concept 2020 Q1 2019 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $269.9M $270.7M
YoY Change -0.3% 2.52%
Cash & Equivalents $67.02M $69.84M
Short-Term Investments $202.8M $200.8M
Other Short-Term Assets $5.300M $9.600M
YoY Change -44.79% 108.7%
Inventory $6.593M $5.571M
Prepaid Expenses
Receivables $18.10M $12.71M
Other Receivables $20.20M $0.00
Total Short-Term Assets $406.6M $475.5M
YoY Change -14.49% 65.8%
LONG-TERM ASSETS
Property, Plant & Equipment $2.617M $2.995M
YoY Change -12.62% -1.55%
Goodwill $936.0K $936.0K
YoY Change 0.0% 0.0%
Intangibles
YoY Change
Long-Term Investments $15.00M
YoY Change 0.0%
Other Assets $6.803M $13.47M
YoY Change -49.5% 108.63%
Total Long-Term Assets $166.4M $192.2M
YoY Change -13.39% -10.2%
TOTAL ASSETS
Total Short-Term Assets $406.6M $475.5M
Total Long-Term Assets $166.4M $192.2M
Total Assets $573.1M $667.7M
YoY Change -14.17% 33.32%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $9.966M $7.627M
YoY Change 30.67% -19.06%
Accrued Expenses $41.59M $46.62M
YoY Change -10.79% 47.32%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00
YoY Change
Long-Term Debt Due $22.50M
YoY Change
Total Short-Term Liabilities $68.09M $104.1M
YoY Change -34.58% 84.12%
LONG-TERM LIABILITIES
Long-Term Debt $207.4M $197.5M
YoY Change 5.01% 336.95%
Other Long-Term Liabilities $13.31M $23.41M
YoY Change -43.14% 407.08%
Total Long-Term Liabilities $13.31M $23.41M
YoY Change -43.14% 407.08%
TOTAL LIABILITIES
Total Short-Term Liabilities $68.09M $104.1M
Total Long-Term Liabilities $13.31M $23.41M
Total Liabilities $347.3M $382.0M
YoY Change -9.07% 89.73%
SHAREHOLDERS EQUITY
Retained Earnings -$415.6M -$311.0M
YoY Change 33.65% 67.46%
Common Stock $642.9M $596.6M
YoY Change 7.75% 22.59%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $225.7M $285.7M
YoY Change
Total Liabilities & Shareholders Equity $573.1M $667.7M
YoY Change -14.17% 33.32%

Cashflow Statement

Concept 2020 Q1 2019 Q1
OPERATING ACTIVITIES
Net Income $808.0K -$40.98M
YoY Change -101.97% 122.97%
Depreciation, Depletion And Amortization $5.656M $4.901M
YoY Change 15.41% 12.72%
Cash From Operating Activities -$29.16M -$20.49M
YoY Change 42.28% 39.08%
INVESTING ACTIVITIES
Capital Expenditures $208.0K $19.00K
YoY Change 994.74% -51.28%
Acquisitions
YoY Change
Other Investing Activities $44.17M -$7.430M
YoY Change -694.48% -41.03%
Cash From Investing Activities $39.55M -$11.41M
YoY Change -446.57% -45.27%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $100.0M
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities -$5.773M -$1.110M
YoY Change 420.09% -58.92%
NET CHANGE
Cash From Operating Activities -$29.16M -$20.49M
Cash From Investing Activities $39.55M -$11.41M
Cash From Financing Activities -$5.773M -$1.110M
Net Change In Cash $4.583M -$33.04M
YoY Change -113.87% -13.69%
FREE CASH FLOW
Cash From Operating Activities -$29.16M -$20.49M
Capital Expenditures $208.0K $19.00K
Free Cash Flow -$29.36M -$20.51M
YoY Change 43.16% 38.84%

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DESCRIPTION OF BUSINESS<div style="line-height:120%;padding-bottom:8px;padding-top:16px;font-size:12pt;"><span style="font-family:Arial;font-size:12pt;color:#006ebf;font-style:normal;font-weight:bold;text-decoration:none;">Organization and Description of Business</span></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:justify;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Retrophin, Inc. (“we”, “our”, “us”, “Retrophin” and the “Company”) refers to Retrophin, Inc., a Delaware corporation, as well as our direct and indirect subsidiaries. Retrophin 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 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="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:justify;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">On January 30, 2020, the World Health Organization (“WHO”) declared that the recent novel coronavirus (COVID-19) outbreak was a global health emergency, which prompted national governments to begin putting actions in place to slow the spread of COVID-19. In March 2020, the WHO classified the COVID-19 outbreak as a pandemic. The outbreak of COVID-19 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 fiscal quarter ended March 31, 2020, these governmental actions 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="line-height:120%;padding-bottom:8px;padding-top:12px;font-size:10.5pt;"><span style="font-family:Arial;font-size:10.5pt;color:#666666;font-style:italic;font-weight:bold;text-decoration:none;">Clinical Programs:</span></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Sparsentan</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;font-style:italic;">,</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;"> also known as RE-021, is an investigational product candidate with a dual mechanism of action, selective endothelin receptor antagonist (“ERA”), with in vitro selectivity toward endothelin receptor type A, and a potent angiotensin receptor blocker (“ARB”). Sparsentan is currently being evaluated in two pivotal Phase 3 clinical studies in the following indications:</span></div><table cellpadding="0" cellspacing="0" style="padding-top:12px;padding-bottom:4px;font-family:Times New Roman; font-size:10pt;"><tr><td style="width:48px;"/><td/></tr><tr><td style="vertical-align:top"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#4c4c4c;font-weight:bold;">•</span></div></td><td style="vertical-align:top;"><div style="line-height:120%;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;font-weight:bold;">Focal segmental glomerulosclerosis ("FSGS")</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;"> is a rare kidney disease characterized by proteinuria where the glomeruli become progressively scarred. FSGS is a leading cause of end-stage renal disease.</span></div></td></tr></table><table cellpadding="0" cellspacing="0" style="padding-top:12px;padding-bottom:4px;font-family:Times New Roman; font-size:10pt;"><tr><td style="width:48px;"/><td/></tr><tr><td style="vertical-align:top"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#4c4c4c;font-weight:bold;">•</span></div></td><td style="vertical-align:top;"><div style="line-height:120%;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;font-weight:bold;">Immunoglobulin A nephropathy ("IgAN")</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;"> is an immune-complex-mediated glomerulonephritis characterized by hematuria, proteinuria, and variable rates of progressive renal failure. IgAN is the most common primary glomerular disease.</span></div></td></tr></table><div style="line-height:120%;padding-bottom:8px;padding-top:4px;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;"><br/></span></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Chenodal® has been recognized as the standard of care for cerebrotendinous xanthomatosis (“CTX”) patients for more than three decades but is not currently labeled for this indication. In January 2020, we randomized the first patients in a Phase 3 clinical trial to evaluate the effects of Chenodal in adult and pediatric patients with CTX. The pivotal study, known as the RESTORE study, is intended to support a new drug application (“NDA”) submission for marketing authorization of Chenodal for CTX in the United States.</span></div><div style="line-height:120%;padding-bottom:8px;padding-top:12px;font-size:10.5pt;"><span style="font-family:Arial;font-size:10.5pt;color:#666666;font-style:italic;font-weight:bold;text-decoration:none;">Cooperative Research and Development Agreements ("CRADAs"):</span></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">The Company is a participant in two CRADAs, which form a multi-stakeholder approach to pool resources with leading experts, and incorporates the patient perspective early in the identification and development process. Retrophi</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">n has partnered with the </span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">National Institutes of Health’s National Center for Advancing Translational Sciences ("NCATS")</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;"> and leading patients advocacy organizations, NGLY1.org and </span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Alagille Syndrome Alliance ("ALGSA")</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">, aimed at the identification of potential small molecule therapeutics for NGLY1 deficiency and Alagille syndrome, respectively. There are no treatment options currently approved for these diseases.</span></div><div style="line-height:120%;padding-bottom:8px;padding-top:12px;text-align:justify;font-size:10.5pt;"><span style="font-family:Arial;font-size:10.5pt;color:#666666;font-style:italic;font-weight:bold;text-decoration:none;">Approved products:</span></div><table cellpadding="0" cellspacing="0" style="padding-top:4px;padding-bottom:8px;font-family:Times New Roman; font-size:10pt;"><tr><td style="width:48px;"/><td/></tr><tr><td style="vertical-align:top"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">•</span></div></td><td style="vertical-align:top;"><div style="line-height:120%;text-align:justify;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">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. Chenodal has been the standard of care for CTX patients for more than three decades.</span></div></td></tr></table><table cellpadding="0" cellspacing="0" style="padding-top:4px;padding-bottom:8px;font-family:Times New Roman; font-size:10pt;"><tr><td style="width:48px;"/><td/></tr><tr><td style="vertical-align:top"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">•</span></div></td><td style="vertical-align:top;"><div style="line-height:120%;text-align:justify;font-size:9.5pt;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Cholbam</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">® </span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">(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></td></tr></table><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">•</span></div><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Thiola</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">® </span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">and Thiola EC</span><span style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">® </span>(tiopronin tablets) are approved in the United States for the prevention of cystine (kidney) stone formation in patients with severe homozygous cystinuria.
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CY2020Q1 us-gaap Debt Instrument Repurchase Amount
DebtInstrumentRepurchaseAmount
23400000 USD
CY2019Q2 us-gaap Stock Issued During Period Shares Conversion Of Convertible Securities
StockIssuedDuringPeriodSharesConversionOfConvertibleSecurities
1300000 shares
CY2020Q1 rtrx Government Rebates Payable
GovernmentRebatesPayable
7945000 USD
CY2019Q4 rtrx Government Rebates Payable
GovernmentRebatesPayable
6584000 USD
CY2020Q1 us-gaap Accrued Salaries Current
AccruedSalariesCurrent
7830000 USD
CY2019Q4 us-gaap Accrued Salaries Current
AccruedSalariesCurrent
14045000 USD
CY2020Q1 rtrx Accrued Royaltyand Contingent Consideration
AccruedRoyaltyandContingentConsideration
7199000 USD
CY2019Q4 rtrx Accrued Royaltyand Contingent Consideration
AccruedRoyaltyandContingentConsideration
7272000 USD
CY2020Q1 rtrx Accrued Liabilities Researchand Development Current
AccruedLiabilitiesResearchandDevelopmentCurrent
12481000 USD
CY2019Q4 rtrx Accrued Liabilities Researchand Development Current
AccruedLiabilitiesResearchandDevelopmentCurrent
16067000 USD
CY2020Q1 rtrx Accrued Liabilities Selling Generaland Administrative Current
AccruedLiabilitiesSellingGeneralandAdministrativeCurrent
4363000 USD
CY2019Q4 rtrx Accrued Liabilities Selling Generaland Administrative Current
AccruedLiabilitiesSellingGeneralandAdministrativeCurrent
3552000 USD
CY2020Q1 rtrx Accrued Liabilities Miscellaneous
AccruedLiabilitiesMiscellaneous
1772000 USD
CY2019Q4 rtrx Accrued Liabilities Miscellaneous
AccruedLiabilitiesMiscellaneous
4225000 USD
CY2020Q1 us-gaap Accrued Liabilities Current
AccruedLiabilitiesCurrent
41590000 USD
CY2019Q4 us-gaap Accrued Liabilities Current
AccruedLiabilitiesCurrent
51745000 USD
CY2020Q1 us-gaap Weighted Average Number Of Shares Outstanding Basic
WeightedAverageNumberOfSharesOutstandingBasic
43122897 shares
CY2020Q1 us-gaap Net Income Loss
NetIncomeLoss
808000 USD
CY2020Q1 us-gaap Earnings Per Share Basic
EarningsPerShareBasic
0.02
CY2019Q1 us-gaap Weighted Average Number Of Shares Outstanding Basic
WeightedAverageNumberOfSharesOutstandingBasic
41410314 shares
CY2019Q1 us-gaap Net Income Loss
NetIncomeLoss
-40977000 USD
CY2019Q1 us-gaap Earnings Per Share Basic
EarningsPerShareBasic
-0.99
CY2020Q1 rtrx Dilutive Securities Effecton Basic Earnings Per Share Employee Stock Purchase Plan
DilutiveSecuritiesEffectonBasicEarningsPerShareEmployeeStockPurchasePlan
16636 shares
CY2019Q1 rtrx Dilutive Securities Effecton Basic Earnings Per Share Employee Stock Purchase Plan
DilutiveSecuritiesEffectonBasicEarningsPerShareEmployeeStockPurchasePlan
0 shares
CY2020Q1 rtrx Dilutive Securities Effecton Basic Earnings Per Share Restricted Stock
DilutiveSecuritiesEffectonBasicEarningsPerShareRestrictedStock
75044 shares
CY2019Q1 rtrx Dilutive Securities Effecton Basic Earnings Per Share Restricted Stock
DilutiveSecuritiesEffectonBasicEarningsPerShareRestrictedStock
0 shares
CY2020Q1 rtrx Dilutive Securities Effecton Basic Earnings Per Share Options
DilutiveSecuritiesEffectonBasicEarningsPerShareOptions
377922 shares
CY2019Q1 rtrx Dilutive Securities Effecton Basic Earnings Per Share Options
DilutiveSecuritiesEffectonBasicEarningsPerShareOptions
0 shares
CY2020Q1 us-gaap Weighted Average Number Of Diluted Shares Outstanding
WeightedAverageNumberOfDilutedSharesOutstanding
43592499 shares
CY2020Q1 us-gaap Net Income Loss
NetIncomeLoss
808000 USD
CY2020Q1 us-gaap Earnings Per Share Diluted
EarningsPerShareDiluted
0.02
CY2019Q1 us-gaap Earnings Per Share Diluted
EarningsPerShareDiluted
-0.99
CY2019Q1 us-gaap Weighted Average Number Of Diluted Shares Outstanding
WeightedAverageNumberOfDilutedSharesOutstanding
41410314 shares
CY2019Q1 us-gaap Net Income Loss
NetIncomeLoss
-40977000 USD
CY2020Q1 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
14807564000 shares
CY2019Q1 us-gaap Antidilutive Securities Excluded From Computation Of Earnings Per Share Amount
AntidilutiveSecuritiesExcludedFromComputationOfEarningsPerShareAmount
16614304000 shares
CY2020Q1 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercisable Number
ShareBasedCompensationArrangementByShareBasedPaymentAwardOptionsExercisableNumber
5200000 shares
CY2020Q1 us-gaap Share Based Compensation Arrangement By Share Based Payment Award Options Exercisable Weighted Average Exercise Price
ShareBasedCompensationArrangementByShareBasedPaymentAwardOptionsExercisableWeightedAverageExercisePrice
19.11
CY2020Q1 us-gaap Allocated Share Based Compensation Expense
AllocatedShareBasedCompensationExpense
5910000 USD
CY2019Q1 us-gaap Allocated Share Based Compensation Expense
AllocatedShareBasedCompensationExpense
6520000 USD
CY2020Q1 us-gaap Income Tax Expense Benefit
IncomeTaxExpenseBenefit
-19000000.0 USD
CY2020Q1 us-gaap Inventory Raw Materials Net Of Reserves
InventoryRawMaterialsNetOfReserves
3085000 USD
CY2019Q4 us-gaap Inventory Raw Materials Net Of Reserves
InventoryRawMaterialsNetOfReserves
2713000 USD
CY2020Q1 us-gaap Inventory Finished Goods Net Of Reserves
InventoryFinishedGoodsNetOfReserves
3508000 USD
CY2019Q4 us-gaap Inventory Finished Goods Net Of Reserves
InventoryFinishedGoodsNetOfReserves
3369000 USD
CY2020Q1 us-gaap Inventory Net
InventoryNet
6593000 USD
CY2019Q4 us-gaap Inventory Net
InventoryNet
6082000 USD
CY2020Q1 us-gaap Inventory Valuation Reserves
InventoryValuationReserves
3200000 USD
CY2019Q4 us-gaap Inventory Valuation Reserves
InventoryValuationReserves
3100000 USD
CY2020Q1 us-gaap Accounts Receivable Net Current
AccountsReceivableNetCurrent
18100000 USD
CY2019Q4 us-gaap Accounts Receivable Net Current
AccountsReceivableNetCurrent
18000000.0 USD
CY2016Q2 us-gaap Payments To Acquire Businesses Gross
PaymentsToAcquireBusinessesGross
500000 USD
CY2016Q2 us-gaap Business Combination Contingent Consideration Liability
BusinessCombinationContingentConsiderationLiability
25000000.0 USD
CY2016 us-gaap Business Combination Contingent Consideration Arrangements Change In Amount Of Contingent Consideration Liability1
BusinessCombinationContingentConsiderationArrangementsChangeInAmountOfContingentConsiderationLiability1
-2300000 USD
CY2017 us-gaap Business Combination Contingent Consideration Arrangements Change In Amount Of Contingent Consideration Liability1
BusinessCombinationContingentConsiderationArrangementsChangeInAmountOfContingentConsiderationLiability1
-5700000 USD
CY2018 us-gaap Business Combination Contingent Consideration Arrangements Change In Amount Of Contingent Consideration Liability1
BusinessCombinationContingentConsiderationArrangementsChangeInAmountOfContingentConsiderationLiability1
1000000.0 USD
CY2019Q1 us-gaap Impairment Of Intangible Assets Finitelived
ImpairmentOfIntangibleAssetsFinitelived
25500000 USD
CY2019Q1 rtrx Write Off Of Contingent Consideration
WriteOffOfContingentConsideration
18000000.0 USD
CY2019Q1 us-gaap Disposal Group Not Discontinued Operation Gain Loss On Disposal
DisposalGroupNotDiscontinuedOperationGainLossOnDisposal
-7500000 USD
CY2020Q1 rtrx At The Market Equity Offering Program Maximum Amount Authorized
AtTheMarketEquityOfferingProgramMaximumAmountAuthorized
100000000.0 USD
CY2020Q1 us-gaap Sale Of Stock Number Of Shares Issued In Transaction
SaleOfStockNumberOfSharesIssuedInTransaction
0 shares

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