2019 Q2 Form 10-Q Financial Statement

#000143853319000011 Filed on May 07, 2019

View on sec.gov

Income Statement

Concept 2019 Q2 2019 Q1 2018 Q1
Revenue $44.71M $39.57M $38.43M
YoY Change 8.15% 2.96% 14.31%
Cost Of Revenue $979.0K $1.017M $1.613M
YoY Change -16.89% -36.95% 127.5%
Gross Profit $43.73M $38.55M $36.82M
YoY Change 8.89% 4.71% 11.87%
Gross Profit Margin 97.81% 97.43% 95.8%
Selling, General & Admin $38.97M $32.67M $26.47M
YoY Change 55.26% 23.43% 14.51%
% of Gross Profit 89.12% 84.74% 71.89%
Research & Development $37.93M $33.44M $24.64M
YoY Change 10.08% 35.75% 18.1%
% of Gross Profit 86.75% 86.75% 66.91%
Depreciation & Amortization $4.840M $4.901M $4.348M
YoY Change 4.31% 12.72% 1.49%
% of Gross Profit 11.07% 12.71% 11.81%
Operating Expenses $81.24M $77.80M $56.34M
YoY Change 29.16% 38.08% 17.31%
Operating Profit -$36.53M -$38.23M -$17.91M
YoY Change 69.43% 113.42% 24.32%
Interest Expense -$4.817M -$4.865M -$1.155M
YoY Change 355.72% 321.21% 775.0%
% of Operating Profit
Other Income/Expense, Net -$2.103M -$2.348M -$237.0K
YoY Change 249.34% 890.72% -118.9%
Pretax Income -$38.63M -$40.58M -$18.15M
YoY Change 74.32% 123.57% 37.97%
Income Tax $69.00K $401.0K $229.0K
% Of Pretax Income
Net Earnings -$38.70M -$40.98M -$18.38M
YoY Change 73.32% 122.97% 65.72%
Net Earnings / Revenue -86.57% -103.56% -47.82%
Basic Earnings Per Share -$0.99 -$0.46
Diluted Earnings Per Share -$922.3K -$0.99 -$0.46
COMMON SHARES
Basic Shares Outstanding 41.44M shares 41.41M shares 39.66M shares
Diluted Shares Outstanding 41.41M shares 39.66M shares

Balance Sheet

Concept 2019 Q2 2019 Q1 2018 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $298.4M $270.7M $264.0M
YoY Change 16.7% 2.52% 6.39%
Cash & Equivalents $75.66M $69.84M $61.12M
Short-Term Investments $222.7M $200.8M $202.9M
Other Short-Term Assets $10.60M $9.600M $4.600M
YoY Change 92.73% 108.7% -33.33%
Inventory $5.050M $5.571M $5.142M
Prepaid Expenses
Receivables $15.50M $12.71M $12.98M
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $457.0M $475.5M $286.8M
YoY Change 63.85% 65.8% -11.04%
LONG-TERM ASSETS
Property, Plant & Equipment $3.015M $2.995M $3.042M
YoY Change -12.74% -1.55% 25.29%
Goodwill $936.0K $936.0K $936.0K
YoY Change 0.0% 0.0% 0.0%
Intangibles
YoY Change
Long-Term Investments $15.00M $15.00M $15.00M
YoY Change 0.0% 0.0%
Other Assets $12.70M $13.47M $6.457M
YoY Change 137.38% 108.63% 76.37%
Total Long-Term Assets $190.6M $192.2M $214.0M
YoY Change -10.21% -10.2% 13.84%
TOTAL ASSETS
Total Short-Term Assets $457.0M $475.5M $286.8M
Total Long-Term Assets $190.6M $192.2M $214.0M
Total Assets $647.6M $667.7M $500.8M
YoY Change 31.85% 33.32% -1.88%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $12.52M $7.627M $9.423M
YoY Change 59.54% -19.06% 101.73%
Accrued Expenses $50.56M $46.62M $31.64M
YoY Change 43.34% 47.32% 4.81%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $0.00 $22.50M
YoY Change -100.0%
Total Short-Term Liabilities $90.59M $104.1M $56.53M
YoY Change -12.47% 84.12% -26.16%
LONG-TERM LIABILITIES
Long-Term Debt $199.9M $197.5M $45.20M
YoY Change 336.95% 1.35%
Other Long-Term Liabilities $22.10M $23.41M $4.617M
YoY Change 352.91% 407.08% 19.7%
Total Long-Term Liabilities $22.10M $23.41M $4.617M
YoY Change 352.91% 407.08% 19.7%
TOTAL LIABILITIES
Total Short-Term Liabilities $90.59M $104.1M $56.53M
Total Long-Term Liabilities $22.10M $23.41M $4.617M
Total Liabilities $370.5M $382.0M $201.3M
YoY Change 82.37% 89.73% -3.88%
SHAREHOLDERS EQUITY
Retained Earnings -$349.7M -$311.0M -$185.7M
YoY Change 68.09% 67.46% 43.95%
Common Stock $626.0M $596.6M $486.7M
YoY Change 25.91% 22.59% 13.09%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $277.1M $285.7M $299.5M
YoY Change
Total Liabilities & Shareholders Equity $647.6M $667.7M $500.8M
YoY Change 31.85% 33.32% -1.88%

Cashflow Statement

Concept 2019 Q2 2019 Q1 2018 Q1
OPERATING ACTIVITIES
Net Income -$38.70M -$40.98M -$18.38M
YoY Change 73.32% 122.97% 65.72%
Depreciation, Depletion And Amortization $4.840M $4.901M $4.348M
YoY Change 4.31% 12.72% 1.49%
Cash From Operating Activities -$19.11M -$20.49M -$14.73M
YoY Change 592.39% 39.08% 332.08%
INVESTING ACTIVITIES
Capital Expenditures -$3.390M $19.00K $39.00K
YoY Change -9.12% -51.28% -95.35%
Acquisitions
YoY Change
Other Investing Activities $28.62M -$7.430M -$12.60M
YoY Change -9.57% -41.03% -249.29%
Cash From Investing Activities $25.23M -$11.41M -$20.85M
YoY Change -9.6% -45.27% -604.87%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities -320.0K -$1.110M -$2.702M
YoY Change -110.39% -58.92% -1901.33%
NET CHANGE
Cash From Operating Activities -19.11M -$20.49M -$14.73M
Cash From Investing Activities 25.23M -$11.41M -$20.85M
Cash From Financing Activities -320.0K -$1.110M -$2.702M
Net Change In Cash 5.800M -$33.04M -$38.28M
YoY Change -79.45% -13.69% -4499.66%
FREE CASH FLOW
Cash From Operating Activities -$19.11M -$20.49M -$14.73M
Capital Expenditures -$3.390M $19.00K $39.00K
Free Cash Flow -$15.72M -$20.51M -$14.77M
YoY Change -1720.62% 38.84% 247.76%

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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:#006ebf;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:#666666;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;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;)</font><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">. PKAN is a genetic neurodegenerative disorder that is typically diagnosed in the first decade of life.</font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Sparsentan</font><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;font-style:italic;">,</font><font 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, a potent angiotensin receptor blocker (&#8220;ARB&#8221;) and selective endothelin receptor antagonist (&#8220;ERA&#8221;), with in vitro selectivity toward endothelin receptor type A. Sparsentan is currently being evaluated in two pivotal Phase 3 clinical studies in the following indications:</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:#4c4c4c;font-weight:bold;">&#8226;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Focal segmental glomerulosclerosis ("FSGS") is a rare kidney disease characterized by proteinuria where the glomeruli become progressively scarred. FSGS is a leading cause of end-stage renal disease.</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:#4c4c4c;font-weight:bold;">&#8226;</font></div></td><td style="vertical-align:top;" rowspan="1" colspan="1"><div style="line-height:120%;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">Immunoglobulin A nephropathy ("IgAN") 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.</font></div></td></tr></table><div style="line-height:120%;padding-bottom:8px;padding-top:4px;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). </font></div><div style="line-height:120%;padding-bottom:8px;padding-top:4px;font-size:9.5pt;"><font style="font-family:Arial Narrow;font-size:9.5pt;color:#000000;">In September 2017, the Company entered into a three-way Cooperative Research and Development Agreement ("CRADA")&#160;with the National Institutes of Health&#8217;s National Center for Advancing Translational Sciences (NCATS) and patient advocacy foundation NGLY1.org&#160;to collaborate on research efforts aimed at the identification of potential small molecule therapeutics for NGLY1 deficiency.</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:#666666;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:#666666;font-style:italic;font-weight:bold;text-decoration:none;">three</font><font style="font-family:Arial;font-size:10.5pt;color:#666666;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 (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 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 (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.</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 (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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