2018 Q4 Form 10-Q Financial Statement

#000143853318000032 Filed on November 01, 2018

View on sec.gov

Income Statement

Concept 2018 Q4 2018 Q3 2017 Q4
Revenue $43.77M $40.71M $42.00K
YoY Change 104116.67% 101665.0% -99.89%
Cost Of Revenue $1.600M $1.133M $1.170M
YoY Change 36.75% 22.49% -2.5%
Gross Profit $42.17M $39.57M $41.00M
YoY Change 2.85% -4571.53% 13.51%
Gross Profit Margin 96.34% 97.22% 97619.05%
Selling, General & Admin $21.54M $26.11M $22.40M
YoY Change -3.84% 5.05% -0.8%
% of Gross Profit 51.08% 65.97% 54.63%
Research & Development $31.70M $32.45M $19.49M
YoY Change 62.65% 65.47% -2.55%
% of Gross Profit 75.17% 82.0% 47.54%
Depreciation & Amortization $4.880M $4.800M $4.460M
YoY Change 9.42% 3.9% 6.44%
% of Gross Profit 11.57% 12.13% 10.88%
Operating Expenses $48.76M $76.29M $57.35M
YoY Change -14.99% 49.74% 3.25%
Operating Profit -$4.985M -$35.58M -$15.18M
YoY Change -67.15% 235.44% -16.71%
Interest Expense -$2.370M -$2.533M -$4.230M
YoY Change -43.97% 283.79% 227.91%
% of Operating Profit
Other Income/Expense, Net -$2.470M -$18.52M $4.139M
YoY Change -159.68% 120.22% -169.74%
Pretax Income -$7.455M -$54.10M -$11.04M
YoY Change -32.46% 184.49% -10.17%
Income Tax $0.00 $415.0K $6.580M
% Of Pretax Income
Net Earnings -$7.455M -$54.52M -$17.62M
YoY Change -57.69% 206.37% 104.79%
Net Earnings / Revenue -17.03% -133.93% -41947.62%
Basic Earnings Per Share -$0.18 -$1.34 -$0.45
Diluted Earnings Per Share -$0.18 -$1.34 -$0.55
COMMON SHARES
Basic Shares Outstanding 41.25M shares 40.43M shares 39.31M shares
Diluted Shares Outstanding

Balance Sheet

Concept 2018 Q4 2018 Q3 2017 Q4
SHORT-TERM ASSETS
Cash & Short-Term Investments $311.3M $350.9M $222.7M
YoY Change 39.83% 15.47% -12.98%
Cash & Equivalents $102.9M $154.8M $99.39M
Short-Term Investments $208.5M $196.1M $123.3M
Other Short-Term Assets $5.900M $5.600M $6.000M
YoY Change -1.67% 115.38% -27.71%
Inventory $5.619M $5.129M $5.351M
Prepaid Expenses
Receivables $12.66M $13.45M $13.87M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $495.7M $503.0M $325.8M
YoY Change 52.14% 54.6% -1.97%
LONG-TERM ASSETS
Property, Plant & Equipment $3.146M $3.323M $3.230M
YoY Change -2.6% 22.3% 24.86%
Goodwill $936.0K $936.0K $936.0K
YoY Change 0.0% 0.0% 0.0%
Intangibles $186.7M $184.8M
YoY Change 1.01% 1.52%
Long-Term Investments $15.00M $15.00M $0.00
YoY Change
Other Assets $7.709M $7.393M $5.556M
YoY Change 38.75% 4.11% -24.55%
Total Long-Term Assets $213.5M $213.2M $194.5M
YoY Change 9.74% 9.24% 0.83%
TOTAL ASSETS
Total Short-Term Assets $495.7M $503.0M $325.8M
Total Long-Term Assets $213.5M $213.2M $194.5M
Total Assets $709.2M $716.2M $520.3M
YoY Change 36.29% 37.59% -0.94%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $6.954M $9.314M $18.94M
YoY Change -63.28% 26.38% 151.77%
Accrued Expenses $49.70M $43.35M $36.02M
YoY Change 37.97% 34.4% 8.14%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $22.50M $22.40M
YoY Change
Total Short-Term Liabilities $104.6M $99.87M $85.67M
YoY Change 22.12% 19.03% 2.89%
LONG-TERM LIABILITIES
Long-Term Debt $195.1M $192.8M $45.10M
YoY Change 332.59% 329.4% 1.58%
Other Long-Term Liabilities $17.55M $4.885M $2.472M
YoY Change 609.75% 28.28% -38.35%
Total Long-Term Liabilities $17.55M $4.885M $2.472M
YoY Change 609.75% 28.28% -38.35%
TOTAL LIABILITIES
Total Short-Term Liabilities $104.6M $99.87M $85.67M
Total Long-Term Liabilities $17.55M $4.885M $2.472M
Total Liabilities $390.9M $397.1M $227.2M
YoY Change 72.05% 83.86% 4.46%
SHAREHOLDERS EQUITY
Retained Earnings -$270.0M -$262.6M -$177.7M
YoY Change 51.99% 64.06% 57.14%
Common Stock $589.8M $582.7M $471.8M
YoY Change 25.01% 25.27% 11.98%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $318.3M $319.1M $293.1M
YoY Change
Total Liabilities & Shareholders Equity $709.2M $716.2M $520.3M
YoY Change 36.29% 37.59% -0.94%

Cashflow Statement

Concept 2018 Q4 2018 Q3 2017 Q4
OPERATING ACTIVITIES
Net Income -$7.455M -$54.52M -$17.62M
YoY Change -57.69% 206.37% 104.79%
Depreciation, Depletion And Amortization $4.880M $4.800M $4.460M
YoY Change 9.42% 3.9% 6.44%
Cash From Operating Activities -$3.570M -$3.900M -$860.0K
YoY Change 315.12% -162.9% -89.87%
INVESTING ACTIVITIES
Capital Expenditures -$3.860M -$3.850M -$2.940M
YoY Change 31.29% 2.94% -30.5%
Acquisitions
YoY Change
Other Investing Activities -$44.94M -$157.7M $2.840M
YoY Change -1682.39% -10340.26% -91.82%
Cash From Investing Activities -$48.80M -$161.6M -$110.0K
YoY Change 44263.64% 7310.55% -100.36%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 520.0K 231.0M 1.370M
YoY Change -62.04% 3861.58% -127.13%
NET CHANGE
Cash From Operating Activities -3.570M -3.900M -860.0K
Cash From Investing Activities -48.80M -161.6M -110.0K
Cash From Financing Activities 520.0K 231.0M 1.370M
Net Change In Cash -51.85M 65.51M 400.0K
YoY Change -13062.5% 565.08% -97.64%
FREE CASH FLOW
Cash From Operating Activities -$3.570M -$3.900M -$860.0K
Capital Expenditures -$3.860M -$3.850M -$2.940M
Free Cash Flow $290.0K -$50.00K $2.080M
YoY Change -86.06% -100.5% -148.83%

Facts In Submission

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<div style="font-family:Times New Roman;font-size:10pt;"><div style="line-height:120%;padding-bottom:13px;padding-top:12px;font-size:13pt;"><font style="font-family:Arial;font-size:13pt;color:#000000;font-style:normal;font-weight:bold;text-decoration:none;">DESCRIPTION OF BUSINESS</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:16px;font-size:12pt;"><font style="font-family:Arial;font-size:12pt;color:#133f7f;font-style:normal;font-weight:bold;text-decoration:none;">Organization and Description of Business</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:justify;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Retrophin, Inc. (&#8220;we&#8221;, &#8220;our&#8221;, &#8220;us&#8221;, &#8220;Retrophin&#8221; and the &#8220;Company&#8221;) refers to Retrophin, Inc., a Delaware corporation, as well as our direct and indirect subsidiaries. Retrophin is a 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 rare diseases and that we believe offer attractive growth characteristics.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:12px;font-size:10.5pt;"><font style="font-family:Arial;font-size:10.5pt;color:#424242;font-style:italic;font-weight:bold;text-decoration:none;">The Company is developing the following pipeline products:</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">The Company is developing fosmetpantotenate (RE-024), a novel small molecule, as a potential treatment for </font><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">pantothenate kinase-associated neurodegeneration (&#8220;PKAN&#8221;). PKAN is a genetic neurodegenerative disorder that is typically diagnosed in the first decade of life. Consequences of PKAN include dystonia, dysarthria, rigidity, retinal degeneration, and severe digestive problems. There are currently no viable treatment options for patients with PKAN. Fosmetpantotenate is a phosphopantothenate replacement therapy that aims to restore levels of this key substrate in PKAN patients.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Sparsentan (RE-021) is an investigational product candidate which acts as both a potent </font><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">angiotensin receptor blocker (&#8220;ARB&#8221;), as well as a selective endothelin receptor antagonist (&#8220;ERA&#8221;), with in vitro selectivity toward endothelin receptor type A. The Company secured a license to sparsentan from Ligand Pharmaceuticals, Inc. and Bristol-Myers Squibb Company (who referred to it as DARA). The Company is developing sparsentan as a treatment for:</font></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;" rowspan="1" colspan="1"></td><td rowspan="1" colspan="1"></td></tr><tr><td style="vertical-align:top" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#2c2c2c;font-weight:bold;">&#9642;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#2c2c2c;font-weight:normal;">Focal segmental glomerulosclerosis ("FSGS")</font><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">, which is a leading cause of end-stage renal disease and nephrotic syndrome (&#8220;NS&#8221;). There are no U.S. Food and Drug Administration ("FDA") approved pharmacologic treatments for FSGS and off-label resources are limited to ACE/ARBs, steroids, and immunosuppressant agents, which are effective in only a subset of patients.</font></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;" rowspan="1" colspan="1"></td><td rowspan="1" colspan="1"></td></tr><tr><td style="vertical-align:top" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#2c2c2c;font-weight:bold;">&#9642;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#2c2c2c;font-weight:normal;">Immunoglobulin A nephropathy ("IgAN")</font><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">, which is characterized by hematuria, proteinuria, and variable rates of progressive renal failure. There is no FDA approved treatment for IgAN.</font></div></td></tr></table><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">The Company is a party to a&#160;joint development agreement with&#160;Censa Pharmaceuticals Inc. ("Censa"), a privately held biotechnology company focused on developing therapies for orphan metabolic diseases, to evaluate sepiapterin ("CNSA-001") for the treatment of phenylketonuria ("PKU"). CNSA-001 is an orally bioavailable form of a natural precursor of tetrahydrobiopterin ("BH4") with the potential to provide improved phenylalanine ("Phe") reduction in patients with PKU when compared to BH4.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">PKU is a rare, genetic metabolic condition in which the body cannot breakdown Phe due to a missing or defective phenylalanine hydroxylase ("PAH") enzyme. High Phe levels can lead to developmental and physical growth delay, executive function impairment, seizures, and microcephaly caused by toxic Phe accumulation in the brain.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">The Company is party to a three-way Cooperative Research and Development Agreement ("CRADA")&#160;with the National Institutes of Health&#8217;s National Center for Advancing Translational Sciences and patient advocacy foundation NGLY1.org&#160;to collaborate on research efforts aimed at the identification of potential small molecule therapeutics for N-glycanase deficiency ("NGLY1").</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">NGLY1 is an extremely rare genetic disorder believed to be caused by a deficiency in an enzyme called N-glycanase-1, which is encoded by the gene NGLY1. The condition has been characterized by symptoms such as developmental delays, seizures, complex hyperkinetic movement disorders, diminished reflexes and an inability to produce tears. There are no approved therapeutic options for NGLY1 deficiency, and current therapeutic strategies are limited to symptom management.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;text-align:left;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Liquid ursodeoxycholic acid ("L-UDCA") is a liquid formulation of ursodeoxycholic acid being developed for the treatment of a rare liver disease called primary biliary cholangitis ("PBC"). The Company obtained the rights to L-UDCA in 2016 with the intention of making L-UDCA commercially available to the subset of PBC patients who have difficulty swallowing.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:12px;font-size:10.5pt;"><font style="font-family:Arial;font-size:10.5pt;color:#424242;font-style:italic;font-weight:bold;text-decoration:none;">The Company sells the following </font><font style="font-family:Arial;font-size:10.5pt;color:#424242;font-style:italic;font-weight:bold;text-decoration:none;">three</font><font style="font-family:Arial;font-size:10.5pt;color:#424242;font-style:italic;font-weight:bold;text-decoration:none;"> products:</font></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;" rowspan="1" colspan="1"></td><td rowspan="1" colspan="1"></td></tr><tr><td style="vertical-align:top" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">&#8226;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;text-align:justify;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Chenodal&#174; (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 also been the standard of care for cerebrotendinous xanthomatosis ("CTX") patients for more than three decades and the Company is currently pursuing adding this indication to the label.</font></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;" rowspan="1" colspan="1"></td><td rowspan="1" colspan="1"></td></tr><tr><td style="vertical-align:top" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">&#8226;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;text-align:justify;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Cholbam&#174; (cholic acid capsules) is approved in the United States (approved and marketed in Europe for select indications as Kolbam) 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.</font></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;" rowspan="1" colspan="1"></td><td rowspan="1" colspan="1"></td></tr><tr><td style="vertical-align:top" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;padding-left:24px;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">&#8226;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;text-align:justify;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Thiola&#174; (tiopronin tablets) is approved in the United States for the prevention of cystine (kidney) stone formation in patients with severe homozygous cystinuria.</font></div></td></tr></table></div>

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