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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
________________________________________________________________________________________
FORM 10-Q
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☒
| Quarterly Report Pursuant to Section 13 or 15 (d) of the Securities Exchange Act of 1934 |
For the quarterly period ended September 30, 2019
or
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☐ | Transition Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 |
For the Transition Period From ______ to ______ .
Commission File Number: 001-33093
LIGAND PHARMACEUTICALS INCORPORATED
(Exact name of registrant as specified in its charter)
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Delaware | 77-0160744 |
(State or other jurisdiction of incorporation or organization) | (I.R.S. Employer Identification No.) |
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3911 Sorrento Valley Boulevard, Suite 110 | |
San Diego | |
CA | 92121 |
(Address of principal executive offices) | (Zip Code) |
(858) 550-7500
(Registrant's Telephone Number, Including Area Code)
Securities registered pursuant to Section 12(b) of the Act:
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Title of each class: | Trading symbol: | Name of each exchange on which registered: |
Common Stock , par value $0.001 per share | LGND | The Nasdaq Global Market |
________________________________________________________________________________________
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and "emerging growth company" in Rule 12b-2 of the Exchange Act. (Check one)
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Large Accelerated Filer | ☒ | | Accelerated Filer | ☐ |
Non-Accelerated Filer | ☐ | | Smaller Reporting Company | ☐ |
Emerging Growth Company | ☐ | | | |
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒
As of November 6, 2019, the registrant had 17,563,389 shares of common stock outstanding.
LIGAND PHARMACEUTICALS INCORPORATED
QUARTERLY REPORT
FORM 10-Q
TABLE OF CONTENTS
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PART I. FINANCIAL INFORMATION | | |
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PART II. OTHER INFORMATION | | |
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GLOSSARY OF TERMS AND ABBREVIATIONS | |
Abbreviation | Definition |
2018 Annual Report | Annual Report on Form 10-K for the year ended December 31, 2018, filed with the SEC on February 28, 2019 |
2019 Notes | $245.0 million aggregate principal amount of convertible senior unsecured notes due 2019 |
2023 Notes | $750.0 million aggregate principal amount of convertible senior unsecured notes due 2023 |
Ab Initio | Ab Initio Biotherapeutics, Inc. |
Abvivo | Abvivo, LLC |
Amgen | Amgen, Inc. |
ANDA | Abbreviated New Drug Application |
ASC | Accounting Standards Codification |
ASU | Accounting Standards Update |
Aziyo | Aziyo Med, LLC |
BeiGene | BeiGene Switzerland GmbH |
BendaRx | BendaRx Corp. |
CE | Captisol-enabled |
CEO | Chief Executive Officer |
Company | Ligand Pharmaceuticals Incorporated, including subsidiaries |
COPD | Chronic obstructive pulmonary disease |
CorMatrix | CorMatrix Cardiovascular, Inc. |
CVR | Contingent value right |
Crystal | Crystal Bioscience, Inc. |
CStone Pharmaceuticals | CStone Pharmaceuticals (Suzhou) Co., Ltd. |
CyDex | CyDex Pharmaceuticals, Inc. |
Dianomi Therapeutics | Dianomi Therapeutics, Inc. |
ESPP | Employee Stock Purchase Plan, as amended and restated |
FASB | Financial Accounting Standards Board |
FDA | Food and Drug Administration |
GAAP | Generally accepted accounting principles in the United States |
GigaGen | GigaGen, Inc. |
GPCR | G-protein coupled receptor |
GRA | Glucagon receptor antagonist |
Hikma | Hikma Pharmaceuticals PLC |
IPR&D | In-process Research and Development |
Kira Pharma | Kira Pharmaceuticals Ltd. |
Ligand | Ligand Pharmaceuticals Incorporated, including subsidiaries |
Marinus Pharmaceuticals | Marinus Pharmaceuticals, Inc. |
Metabasis | Metabasis Therapeutics, Inc. |
Metavant | Metavant Sciences |
Millennium | Millennium Pharmaceuticals, Inc. |
NDA | New Drug Application |
Novan | Novan, Inc. |
Novartis | Novartis AG |
Nucorion Pharmaceuticals | Nucorion Pharmaceuticals, Inc. |
Opthea | Opthea Limited |
OTTI | Other-than-temporary impairment |
PFS | Progression-free Survival |
Pfizer | Pfizer Inc. |
Q3 2018 | The Company's fiscal quarter ended September 30, 2018 |
Q3 2019 | The Company's fiscal quarter ended September 30, 2019 |
Quadriga Bio | Quadriga Biosciences, Inc. |
Retrophin | Retrophin, Inc. |
Roivant | Roivant Sciences GMBH |
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Sage Therapeutics | Sage Therapeutics, Inc. |
SEC | Securities and Exchange Commission |
Seelos Therapeutics | Seelos Therapeutics, Inc. |
Selexis | Selexis, SA |
Sermonix Pharmaceuticals | Sermonix Pharmaceuticals, LLC |
sNDA | Supplemental New Drug Application |
SQ Innovation | SQ Innovation, Inc. |
Takeda | Takeda Pharmaceutical Company |
Talem Therapeutics | Talem Therapeutics LLC |
Teva | Teva Pharmaceuticals USA, Inc., Teva Pharmaceutical Industries Ltd. and Actavis, LLC, collectively |
Vernalis | Vernalis plc |
VDP | Vernalis Design Platform |
Verona Pharma | Verona Pharma plc |
Viking | Viking Therapeutics, Inc. |
WuXi | WuXi Biologics Ireland Limited |
YTD | Year-to-date |
PART I - FINANCIAL INFORMATION
Item 1. Condensed Consolidated Financial Statements
LIGAND PHARMACEUTICALS INCORPORATED
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited, in thousands, except par value)
| | | | | | | | | | | |
| September 30, 2019 | | December 31, 2018 |
ASSETS | | | |
Current assets: | | | |
Cash and cash equivalents | $ | 225,302 | | | $ | 117,164 | |
Short-term investments | 874,383 | | | 601,217 | |
Investment in Viking | 49,856 | | | 55,448 | |
Accounts receivable, net | 21,958 | | | 55,850 | |
Inventory | 6,565 | | | 7,124 | |
Derivative asset | — | | | 22,576 | |
Other current assets | 5,039 | | | 11,161 | |
Total current assets | 1,183,103 | | | 870,540 | |
Deferred income taxes, net | — | | | 46,521 | |
Intangible assets, net | 216,268 | | | 219,793 | |
Goodwill | 93,513 | | | 86,646 | |
Commercial license and other economic rights, net | 35,413 | | | 31,460 | |
Property and equipment, net | 6,411 | | | 5,372 | |
Operating lease right-of-use assets | 10,280 | | | — | |
Other assets | 2,488 | | | 471 | |
Total assets | $ | 1,547,476 | | | $ | 1,260,803 | |
LIABILITIES AND STOCKHOLDERS' EQUITY | | | |
Current liabilities: | | | |
Accounts payable | $ | 2,040 | | | $ | 4,183 | |
Accrued liabilities | 13,060 | | | 19,200 | |
Income tax payable | 16,571 | | | — | |
Current contingent liabilities | 1,794 | | | 5,717 | |
Deferred revenue | 2,230 | | | 3,286 | |
2019 convertible senior notes, net | — | | | 26,433 | |
Derivative liability | — | | | 23,430 | |
Total current liabilities | 35,695 | | | 82,249 | |
2023 convertible senior notes, net | 631,533 | | | 609,864 | |
Long-term contingent liabilities | 7,995 | | | 6,825 | |
Deferred income taxes, net | 3,761 | | | — | |
Long-term operating lease liabilities | 9,932 | | | — | |
Other long-term liabilities | 7,979 | | | 951 | |
Total liabilities | 696,895 | | | 699,889 | |
Commitments and contingencies | | | |
Stockholders' equity: | | | |
Preferred stock, $0.001 par value; 5,000 shares authorized; none issued and outstanding at September 30, 2019 and December 31, 2018 | — | | | — | |
Common stock, $0.001 par value; 60,000 shares authorized; 17,563 and 20,766 shares issued and outstanding at September 30, 2019 and December 31, 2018, respectively | 17 | | | 21 | |
Additional paid-in capital | 444,587 | | | 791,114 | |
Accumulated other comprehensive loss | (1,493) | | | (1,024) | |
Retained earnings (accumulated deficit) | 407,470 | | | (229,197) | |
Total stockholders' equity | 850,581 | | | 560,914 | |
Total liabilities and stockholders' equity | $ | 1,547,476 | | | $ | 1,260,803 | |
See accompanying notes to unaudited condensed consolidated financial statements.
LIGAND PHARMACEUTICALS INCORPORATED
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
(in thousands, except per share amounts)
| | | | | | | | | | | | | | | | | | | | | | | |
| Three months ended | | | | Nine months ended | | |
| September 30, | | | | September 30, | | |
| 2019 | | 2018 | | 2019 | | 2018 |
Revenues: | | | | | | | |
Royalties | $ | 9,767 | | | $ | 36,127 | | | $ | 35,931 | | | $ | 88,343 | |
Material sales | 6,849 | | | 7,027 | | | 24,357 | | | 19,030 | |
License fees, milestones and other revenues | 8,192 | | | 2,509 | | | 32,991 | | | 84,490 | |
Total revenues | 24,808 | | | 45,663 | | | 93,279 | | | 191,863 | |
Operating costs and expenses: | | | | | | | |
Cost of material sales | 3,147 | | | 1,460 | | | 9,410 | | | 3,382 | |
Amortization of intangibles | 3,552 | | | 5,725 | | | 10,560 | | | 12,309 | |
Research and development | 13,742 | | | 5,483 | | | 37,244 | | | 19,023 | |
General and administrative | 9,525 | | | 9,633 | | | 31,607 | | | 26,571 | |
Total operating costs and expenses | 29,966 | | | 22,301 | | | 88,821 | | | 61,285 | |
Gain from sale of Promacta license | — | | | — | | | 812,797 | | | — | |
Income (loss) from operations | (5,158) | | | 23,362 | | | 817,255 | | | 130,578 | |
Other income (expense): | | | | | | | |
Gain (loss) from Viking | (10,520) | | | 62,398 | | | (5,592) | | | 124,206 | |
Interest income | 7,396 | | | 5,474 | | | 22,590 | | | 9,111 | |
Interest expense | (8,993) | | | (11,200) | | | (26,911) | | | (28,133) | |
Other expense, net | (2,596) | | | (808) | | | (2,528) | | | (5,643) | |
Total other income (loss), net | (14,713) | | | 55,864 | | | (12,441) | | | 99,541 | |
Income (loss) before income taxes | (19,871) | | | 79,226 | | | 804,814 | | | 230,119 | |
Income tax benefit (expense) | 4,620 | | | (11,864) | | | (168,147) | | | (44,316) | |
Net income (loss) | $ | (15,251) | | | $ | 67,362 | | | $ | 636,667 | | | $ | 185,803 | |
| | | | | | | |
Basic net income (loss) per share | $ | (0.81) | | | $ | 3.19 | | | $ | 32.51 | | | $ | 8.77 | |
Shares used in basic per share calculations | 18,770 | | | 21,148 | | | 19,586 | | | 21,189 | |
| | | | | | | |
Diluted net income (loss) per share | $ | (0.81) | | | $ | 2.80 | | | $ | 31.29 | | | $ | 7.61 | |
Shares used in diluted per share calculations | 18,770 | | | 24,052 | | | 20,349 | | | 24,430 | |
| | | | | | | |
See accompanying notes to unaudited condensed consolidated financial statements.
LIGAND PHARMACEUTICALS INCORPORATED
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME (LOSS)
(Unaudited)
(in thousands)
| | | | | | | | | | | | | | | | | | | | | | | |
| Three months ended | | | | Nine months ended | | |
| September 30, | | | | September 30, | | |
| 2019 | | 2018 | | 2019 | | 2018 |
Net income (loss): | $ | (15,251) | | | $ | 67,362 | | | $ | 636,667 | | | $ | 185,803 | |
Unrealized net gain (loss) on available-for-sale securities, net of tax | (187) | | | 87 | | | 546 | | | 73 | |
Foreign currency translation | (764) | | | — | | | (1,015) | | | — | |
Comprehensive income (loss) | $ | (16,202) | | | $ | 67,449 | | | $ | 636,198 | | | $ | 185,876 | |
| | | | | | | |
See accompanying notes to unaudited condensed consolidated financial statements.
LIGAND PHARMACEUTICALS INCORPORATED
CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY
(Unaudited)
(in thousands)
| | | | | | | | | | | | | | | | | | | | |
| Common Stock | | Additional paid in capital | Accumulated other comprehensive income (loss) | Retain earnings (Accumulated deficit) | Total stockholders' equity |
| Shares | Amount | | | | |
Balance at January 1, 2019 | 20,765 | | $ | 21 | | $ | 791,114 | | $ | (1,024) | | $ | (229,197) | | $ | 560,914 | |
Issuance of common stock under employee stock compensation plans, net | 135 | | — | | (991) | | — | | — | | (991) | |
Share-based compensation | — | | — | | 5,347 | | — | | — | | 5,347 | |
Repurchase of common stock | (1,236) | | (1) | | (151,584) | | — | | — | | (151,585) | |
Unrealized net gain on available-for-sale securities, net of deferred tax | — | | — | | — | | 230 | | — | | 230 | |
Foreign currency translation adjustment | — | | — | | — | | 291 | | — | | 291 | |
Other tax adjustments | — | | — | | (569) | | — | | — | | (569) | |
Net income | — | | — | | — | | — | | 666,337 | | 666,337 | |
Balance at March 31, 2019 | 19,664 | | $ | 20 | | $ | 643,317 | | $ | (503) | | $ | 437,140 | | $ | 1,079,974 | |
Issuance of common stock under employee stock compensation plans, net | 17 | | — | | 740 | | — | | — | | 740 | |
Share-based compensation | — | | — | | 6,571 | | — | | — | | 6,571 | |
Repurchase of common stock | (291) | | (1) | | (33,716) | | — | | — | | (33,717) | |
Unrealized net gain on available-for-sale securities, net of deferred tax | — | | — | | — | | 503 | | — | | 503 | |
Foreign currency translation adjustment | — | | — | | — | | (542) | | — | | (542) | |
Other tax adjustments | — | | — | | 2,343 | | — | | — | | 2,343 | |
Net loss | — | | — | | — | | — | | (14,419) | | (14,419) | |
Balance at June 30, 2019 | 19,390 | | $ | 19 | | $ | 619,255 | | $ | (542) | | $ | 422,721 | | $ | 1,041,453 | |
Issuance of common stock under employee stock compensation plans, net | 7 | | — | | 199 | | — | | — | | 199 | |
Share-based compensation | — | | — | | 6,297 | | — | | — | | 6,297 | |
Repurchase of common stock | (1,834) | | (2) | | (181,186) | | — | | — | | (181,188) | |
Unrealized net loss on available-for-sale securities, net of deferred tax | — | | — | | — | | (187) | | — | | (187) | |
Foreign currency translation adjustment | — | | — | | — | | (764) | | — | | (764) | |
Other tax adjustments | — | | — | | 22 | | — | | — | | 22 | |
Net loss | — | | — | | — | | — | | (15,251) | | (15,251) | |
Balance at September 30, 2019 | 17,563 | | $ | 17 | | $ | 444,587 | | $ | (1,493) | | $ | 407,470 | | $ | 850,581 | |
| | | | | | | | | | | | | | | | | | | | |
| Common Stock | | Additional paid in capital | Accumulated other comprehensive income (loss) | Accumulated deficit | Total stockholders' equity |
| Shares | Amount | | | | |
Balance at January 1, 2018 | 21,149 | | $ | 21 | | $ | 798,205 | | $ | 2,486 | | $ | (400,924) | | $ | 399,788 | |
Issuance of common stock under employee stock compensation plans, net | 166 | | 1 | | 5,118 | | — | | — | | 5,119 | |
Reclassification of equity component of currently redeemable convertible notes | — | | — | | 2,781 | | — | | — | | 2,781 | |
Share-based compensation | — | | — | | 4,555 | | — | | — | | 4,555 | |
Repurchase of common stock | (13) | | (1) | | (1,894) | | — | | — | | (1,895) | |
Unrealized net loss on available-for-sale securities, net of deferred tax | — | | — | | — | | (110) | | — | | (110) | |
Cumulative-effect adjustment from adoption of ASU 2016-01 | — | | — | | — | | (2,662) | | 2,662 | | — | |
Cumulative-effect adjustment from adoption of ASU 2014-09, net of tax | — | | — | | — | | — | | 25,583 | | 25,583 | |
Net income | — | | — | | — | | — | | 45,279 | | 45,279 | |
Balance at March 31, 2018 | 21,302 | | $ | 21 | | $ | 808,765 | | $ | (286) | | $ | (327,400) | | $ | 481,100 | |
Issuance of common stock under employee stock compensation plans, net | 60 | | — | | 3,296 | | — | | — | | 3,296 | |
Reclassification of equity component of currently redeemable convertible notes | — | | — | | 16,078 | | — | | — | | 16,078 | |
Share-based compensation | — | | — | | 4,812 | | — | | — | | 4,812 | |
Repurchase of common stock | (267) | | — | | (50,832) | | — | | — | | (50,832) | |
Unrealized net loss on available-for-sale securities, net of deferred tax | — | | — | | — | | (495) | | — | | (495) | |
Derivative associated with 2019 Notes and Bond Hedge | — | | — | | (1,559) | | — | | — | | (1,559) | |
Loss on settlement of 2019 Notes | — | | — | | 590 | | — | | — | | 590 | |
Tax effect on 2019 Notes transactions | — | | — | | 67 | | — | | — | | 67 | |
Derivative associated with 2023 Notes and Bond Hedge | — | | — | | (1,807) | | — | | — | | (1,807) | |
Warrant derivative in connection with 2023 Notes | — | | — | | 97,805 | | — | | — | | 97,805 | |
Tax effect for 2023 Notes transactions | — | | — | | (3,240) | | — | | — | | (3,240) | |
Other tax adjustments | — | | — | | 208 | | 630 | | — | | 838 | |
Net income | — | | — | | — | | — | | 73,160 | | 73,160 | |
Balance at June 30, 2018 | 21,095 | | $ | 21 | | $ | 874,183 | | $ | (151) | | $ | (254,240) | | $ | 619,813 | |
Issuance of common stock under employee stock compensation plans, net | 131 | | — | | 6,788 | | — | | — | | 6,788 | |
Share-based compensation | — | | — | | 5,470 | | — | | — | | 5,470 | |
Other comprehensive income | — | | — | | — | | 87 | | — | | 87 | |
Other tax adjustments | — | | — | | (2,964) | | — | | 2,964 | | — | |
Net income | — | | — | | — | | — | | 67,362 | | 67,362 | |
Balance at September 30, 2018 | 21,226 | | 21 | | 883,477 | | (64) | | (183,914) | | 699,520 | |
See accompanying notes to unaudited condensed consolidated financial statements.
LIGAND PHARMACEUTICALS INCORPORATED
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited, in thousands)
| | | | | | | | | | | |
| Nine months ended | | |
| September 30, | | |
| 2019 | | 2018 |
Cash flows from operating activities: | | | |
Net income | $ | 636,667 | | | $ | 185,803 | |
Adjustments to reconcile net income to net cash provided by operating activities: | | | |
Gain from sale of Promacta license | (812,797) | | | — | |
Non-cash change in estimated fair value of contingent liabilities | 762 | | | 3,637 | |
Depreciation and amortization | 12,560 | | | 11,421 | |
Amortization of discount on investments, net | (7,477) | | | (3,780) | |
Amortization of debt discount and issuance fees | 22,562 | | | 25,155 | |
Amortization of other economic rights | 9,135 | | | — | |
Share-based compensation | 18,215 | | | 14,837 | |
Deferred income taxes | 57,766 | | | 44,149 | |
Loss (gain) from investment in Viking | 5,592 | | | (121,679) | |
Other | (1,249) | | | (976) | |
Royalties recorded in retained earnings upon adoption of ASC 606 | — | | | 32,707 | |
Changes in operating assets and liabilities, net of effects from acquisition: | | | |
Accounts receivable, net | 33,892 | | | (21,380) | |
Inventory | (1,500) | | | (3,763) | |
Accounts payable and accrued liabilities | (3,374) | | | (42) | |
Income tax payable | 16,571 | | | — | |
Other economic rights | (12,000) | | | — | |
Other | 2,678 | | | (4,602) | |
Net cash provided by (used in) operating activities | (21,997) | | | 161,487 | |
| | | |
Cash flows from investing activities: | | | |
Proceeds from sale of Promacta license | 812,797 | | | — | |
Purchase of short-term investments | (1,682,586) | | | (1,158,290) | |
Proceeds from sale of short-term investments | 144,182 | | | 75,993 | |
Proceeds from maturity of short-term investments | 1,274,851 | | | 381,690 | |
Cash paid for acquisition, net of cash acquired | (11,840) | | | — | |
Cash paid for equity method investment | (1,000) | | | — | |
Other | (6,307) | | | 2,036 | |
Net cash provided by (used in) investing activities | 530,097 | | | (698,571) | |
| | | |
Cash flows from financing activities: | | | |
Repayment of debt | (27,323) | | | (21,785) | |
Gross proceeds from issuance of 2023 Notes | — | | | 750,000 | |
Payment of debt issuance costs | — | | | (16,900) | |
Proceeds from issuance of warrants | — | | | 90,000 | |
Purchase of convertible bond hedge | — | | | (140,250) | |
Proceeds from convertible bond hedge settlement | 12,401 | | | 52,129 | |
Payments to convert holders for bond conversion | (12,401) | | | — | |
Net proceeds from stock option exercises and ESPP | 2,856 | | | 18,860 | |
Taxes paid related to net share settlement of equity awards | (2,906) | | | (3,657) | |
Share repurchase | (371,106) | | | (52,727) | |
Payments to CVR Holders | (3,000) | | | — | |
Net cash provided by (used in) financing activities | (401,479) | | | 675,670 | |
Effect of exchange rate changes on cash | (88) | | | — | |
Net increase in cash, cash equivalents and restricted cash | 106,533 | | | 138,586 | |
Cash, cash equivalents and restricted cash at beginning of period | 119,780 | | | 20,620 | |
Cash, cash equivalents and restricted cash at end of period | $ | 226,313 | | | $ | 159,206 | |
| | | | | | | | | | | |
Supplemental disclosure of cash flow information: | | | |
Interest paid | $ | 3,015 | | | $ | 1,513 | |
Taxes paid | $ | 93,817 | | | $ | 341 | |
Restricted cash in other current assets | $ | 1,011 | | | $ | — | |
| | | |
Supplemental schedule of non-cash activity: | | | |
| | | |
| | | |
| | | |
Accrued fixed asset purchases | $ | — | | | $ | 4 | |
| | | |
Unrealized gain on AFS investments | $ | 699 | | | $ | — | |
Excess of conversion value over the principal amount of 2019 Notes paid in shares | $ | — | | | $ | (31,571) | |
Value of shares reacquired under convertible bond hedge transaction entered into with 2019 Notes | $ | — | | | $ | 31,571 | |
See accompanying notes to unaudited condensed consolidated financial statements.
LIGAND PHARMACEUTICALS INCORPORATED
Notes to Condensed Consolidated Financial Statements
(Unaudited)
Unless the context requires otherwise, references in this report to “Ligand,” “we,” “us,” the “Company,” and “our” refer to Ligand Pharmaceuticals Incorporated and its consolidated subsidiaries.
1. Basis of Presentation and Summary of Significant Accounting Policies
Basis of Presentation
Our condensed consolidated financial statements include the financial statements of Ligand and its wholly-owned subsidiaries. All significant intercompany accounts and transactions have been eliminated in consolidation. We have included all adjustments, consisting only of normal recurring adjustments, which we considered necessary for a fair presentation of our financial results. These unaudited condensed consolidated financial statements and accompanying notes should be read together with the audited consolidated financial statements included in our 2018 Annual Report. Interim financial results are not necessarily indicative of the results that may be expected for the full year.
Reclassifications
Certain amounts in the prior period consolidated financial statements have been reclassified to conform with the current period presentation. Specifically, our investment in Viking warrants was reclassified from “other current assets” to “investment in Viking” in the audited consolidated balance sheet as of December 31, 2018.
Prior Period Immaterial Error
During the second quarter of 2019, in connection with the preparation of our condensed consolidated statement of cash flows for the six months ended June 30, 2019, an immaterial error was identified in our condensed consolidated statement of cash flows for the three months ended March 31, 2019 by including a $4.6 million accrued liability for the share repurchase as of December 31, 2018 that was paid during the first quarter of 2019 in the cash flows for operating activities instead of financing activities. Our condensed consolidated statement of cash flows for the three months ended March 31, 2019 understated cash flows provided by operating activities by $4.6 million and understated cash flows used in financing activities by $4.6 million. We evaluated the materiality of the error considering both quantitative and qualitative factors as required by authoritative guidance and determined the related impact was not material to our previously issued condensed consolidated financial statements. The immaterial error has been corrected in our condensed consolidated statement of cash flows for the six months ended June 30, 2019 included in our Quarterly Report on Form 10-Q for the quarter ended June 30, 2019. The immaterial error did not impact our condensed consolidated balance sheet as of March 31, 2019, nor did it impact our condensed consolidated statements of operations, comprehensive income or equity for the three months ended March 31, 2019.
Significant Accounting Policies
We have described our significant accounting policies in Note 1, Basis of Presentation and Summary of Significant Accounting Policies, of Notes to Consolidated Financial Statements in our 2018 Annual Report.
Use of Estimates
The preparation of condensed consolidated financial statements in conformity with GAAP requires the use of estimates and assumptions that affect the amounts reported in the condensed consolidated financial statements and the accompanying notes. Actual results may differ from those estimates.
Accounting Standards Recently Adopted
Leases - In February 2016, the FASB issued ASU 2016-02, Leases (Topic 842). This standard requires organizations that lease assets to recognize the assets and liabilities created by those leases. The standard also requires disclosures to help investors and other financial statement users better understand the amount, timing, and uncertainty of cash flows arising from leases. In 2018, the FASB issued guidance that provides an optional transition method for adoption of this standard, which allows organizations to initially apply the new requirements at the effective date, recognize a cumulative effect adjustment to the opening balance of retained earnings, and continue to apply the legacy guidance in ASC 840, Leases (Topic 840), including its disclosure
requirements, in the comparative periods presented. We adopted this standard on January 1, 2019 by applying this optional transition method. For leases with a term of 12 months or less, we elected to not recognize lease assets and lease liabilities and expense the leases over a straight-line basis for the term of those leases. In addition, we elected the available package of practical expedients upon adoption, which allowed us to carry forward our historical assessment of whether existing agreements contained a lease and the classification of our existing operating leases. We did not elect to use the hindsight practical expedient to determine the lease term or evaluate impairment for existing leases. We continue to report our financial position as of December 31, 2018 under Topic 840 in our audited consolidated balance sheet. The adoption of this standards update resulted in the recognition of right-of-use assets of approximately $5.2 million and lease liabilities of approximately $5.9 million on our unaudited condensed consolidated balance as of January 1, 2019, with no material impact to our consolidated statement of operations. See Note 9, Leases, for further information regarding the impact of the adoption of ASU 2016-02 on our financial statements.
Accounting Standards Not Yet Adopted
Financial Instruments - In June 2016, the FASB issued ASU 2016-13, Financial Instruments - Credit Losses: Measurement of Credit Losses on Financial Instruments (Topic 326), which amends the impairment model by requiring entities to use a forward-looking approach based on expected losses to estimate credit losses on certain types of financial instruments, including trade receivables and available for sale debt securities. ASU 2016-13 is effective for us beginning in the first quarter of 2020, with early adoption permitted. We are currently evaluating the impact of this ASU on our consolidated financial statements. This standard includes our financial instruments, such as accounts receivable, investments that are generally of high credit quality, and commercial license rights. Previously, when credit losses were measured under GAAP, an entity generally only considered past events and current conditions in measuring the incurred loss. The new guidance requires us to identify, analyze,
document and support new methodologies for quantifying expected credit loss estimates for our financial instruments, using information such as historical experience and current economic conditions, plus the use of reasonable supportable forecast
information.
Goodwill Impairment Testing - In January 2017, the FASB issued ASU 2017-04, Simplifying the Test for Goodwill Impairment, which eliminates the requirement to perform a hypothetical purchase price allocation to measure goodwill impairment. Under the new standard the goodwill impairment test is performed by comparing the fair value of a reporting unit with its carrying amount, and recognizing an impairment charge for the amount by which the carrying amount of the reporting unit exceeds its fair value, although it cannot exceed the total amount of goodwill allocated to that reporting unit. This standard is effective for us beginning in the first quarter of 2020, with earlier adoption permitted. We do not expect the adoption to have a material impact on our consolidated financial statements.
Fair Value Measurement - In August 2018, the FASB issued ASU 2018-13, Fair Value Measurement: Disclosure Framework—Changes to the Disclosure Requirements for Fair Value Measurement (Topic 820), which modifies the disclosure requirements on fair value measurements. ASU 2018-13 is effective for us beginning in the first quarter of 2020, with earlier adoption permitted. We are currently evaluating the impact of this ASU on our consolidated financial statements.
Collaborative Arrangements - In November 2018, the FASB issued ASU 2018-18, Collaborative Arrangements: Clarifying the Interaction between Topic 808 and Topic 606 (Topic 808). The new standard clarifies that certain transactions between participants in a collaborative arrangement should be accounted for under Topic 606, Revenue from Contracts with Customers, when the counterparty is a customer for a good or service that is a distinct unit of account. The amendments also preclude entities from presenting consideration from transactions with a collaborator that is not a customer together with revenue recognized from contracts with customers. The new standard is effective for fiscal years beginning after December 15, 2019, and interim periods within those fiscal years. Early adoption is permitted in any interim period for entities that have adopted ASC 606. The standard should be applied retrospectively to the period when we initially adopted ASC 606. We do not expect the adoption of this standard to have a material impact on our consolidated financial statements.
We do not believe that any other recently issued, but not yet effective accounting pronouncements, if adopted, would have a material impact on our consolidated financial statements or disclosures.
Revenue
Our revenue is generated primarily from royalties on sales of products commercialized by our partners, Captisol material sales, license fees and development, regulatory and sales based milestone payments, and other service revenue.
Royalties, License Fees and Milestones
We receive royalty revenue on sales by our partners of products covered by patents that we own. We do not have future performance obligations under these license arrangements. We generally satisfy our obligation to grant intellectual property rights on the effective date of the contract. However, we apply the royalty recognition constraint required under the guidance for sales-based royalties which requires a sales-based royalty to be recorded no sooner than the underlying sale. Therefore, royalties on sales of products commercialized by our partners are recognized in the quarter the product is sold. Our partners generally report sales information to us on a one quarter lag. Thus, we estimate the expected royalty proceeds based on an analysis of historical experience and interim data provided by our partners including their publicly announced sales. Differences between actual and estimated royalty revenues are adjusted for in the period in which they become known, typically the following quarter.
Our contracts with customers often will include future contingent milestone based payments. We include contingent milestone based payments in the estimated transaction price when there is a basis to reasonably estimate the amount of the payment. These estimates are based on historical experience, anticipated results and our best judgment at the time. If the contingent milestone based payment is sales-based, we apply the royalty recognition constraint and record revenue when the underlying sale has taken place. Significant judgments must be made in determining the transaction price for our sales of intellectual property. Because of the risk that products in development with our partners will not reach development based milestones or receive regulatory approval, we generally recognize any contingent payments that would be due to us upon or after the development milestone or regulatory approval.
Material Sales
We recognize revenue when control of Captisol material is transferred to our customers in an amount that reflects the consideration we expect to receive from our customers in exchange for those products. This process involves identifying the contract with a customer, determining the performance obligations in the contract, determining the contract price, allocating the contract price to the distinct performance obligations in the contract, and recognizing revenue when the performance obligations have been satisfied. A performance obligation is considered distinct from other obligations in a contract when it provides a benefit to the customer either on its own or together with other resources that are readily available to the customer and is separately identified in the contract. We consider a performance obligation satisfied once we have transferred control of the product, meaning the customer has the ability to use and obtain the benefit of the Captisol material or intellectual property license right. We recognize revenue for satisfied performance obligations only when we determine there are no uncertainties regarding payment terms or transfer of control. Sales tax and other taxes we collect concurrent with revenue-producing activities are excluded from revenue. We expense incremental costs of obtaining a contract when incurred if the expected amortization period of the asset that we would have recognized is one year or less or the amount is immaterial. We did not incur any incremental costs of obtaining a contract during the periods reported.
Depending on the terms of the arrangement, we may also defer a portion of the consideration received because we have to satisfy a future obligation. We use an observable price to determine the stand-alone selling price for separate performance obligations or a cost plus margin approach when one is not available. We have elected to recognize the cost for freight and shipping when control over Captisol material has transferred to the customer as an expense in cost of material sales.
The timing of revenue recognition, billings and cash collections results in billed accounts receivable, unbilled receivables (contract assets), and customer advances and deposits (contract liabilities) on the consolidated balance sheet. Except for royalty revenue and certain service revenue, we generally receive payment at the point we satisfy our obligation or soon after. Therefore, we do not generally carry a contract asset balance. Any fees billed in advance of being earned are recorded as deferred revenue. During the three and nine months ended September 30, 2019, the amount recognized as revenue that was previously deferred was $1.0 million and $5.0 million, respectively. During the three and nine months ended September 30, 2018, the amount recognized as revenue that was previously deferred was not material.
Disaggregation of Revenue
The following table represents disaggregation of Royalties, Material Sales and License fees, milestone and other (in thousands):
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