Alkermes plc Reports First Quarter 2024 Financial Results
— First Quarter Revenues of $350.4 Million —
— GAAP Net Income from Continuing Operations of $38.9 Million and Diluted GAAP Earnings per Share from Continuing Operations of $0.23 —
— Company Reiterates 2024 Financial Expectations —
DUBLIN, May 1, 2024 /PRNewswire/ -- Alkermes plc (Nasdaq: ALKS) today reported financial results for the first quarter of 2024.
"The first quarter of 2024 marks our first full quarter as a profitable, pure-play neuroscience company. During the quarter, we continued to advance our strategic priorities across the business, highlighted by solid underlying prescription growth for LYBALVI® and advancement of ALKS 2680, our novel, investigational, oral orexin 2 receptor (OX2R) agonist in development as a once-daily treatment for narcolepsy," said Richard Pops, Chief Executive Officer of Alkermes. "For ALKS 2680, we recently initiated our Vibrance-1 phase 2 study in narcolepsy type 1 and announced positive topline phase 1b results in narcolepsy type 2. With these new data now in hand, we plan to initiate a phase 2 study in narcolepsy type 2 in the second half of 2024. In an area where there remains significant unmet patient need, orexin 2 biology represents an important new potential approach to treating disorders characterized by excessive daytime sleepiness. ALKS 2680 is the first candidate from our orexin portfolio to advance in the clinic and we plan to share details regarding our other orexin development programs later this year."
Key Financial Highlights
Revenues | ||||
(In millions) | Three Months Ended | |||
2024 | 2023 | |||
Total Revenues | $ | 350.4 | $ | 287.6 |
Total Proprietary Net Sales | $ | 233.5 | $ | 214.7 |
VIVITROL® | $ | 97.7 | $ | 96.7 |
ARISTADA®i | $ | 78.9 | $ | 80.1 |
LYBALVI® | $ | 57.0 | $ | 38.0 |
Profitability | ||||
(In millions) | Three Months Ended | |||
2024 | 2023 | |||
GAAP Net Income (Loss) From Continuing Operations | $ | 38.9 | $ | (12.1) |
GAAP Net Loss From Discontinued Operations | $ | (2.1) | $ | (29.8) |
GAAP Net Income (Loss) | $ | 36.8 | $ | (41.8) |
Non-GAAP Net Income From Continuing Operations | $ | 76.2 | $ | 30.1 |
Non-GAAP Net Loss From Discontinued Operations | $ | (2.1) | $ | (27.6) |
Non-GAAP Net Income | $ | 74.1 | $ | 2.4 |
EBITDA From Continuing Operations | $ | 51.5 | $ | 7.2 |
EBITDA From Discontinued Operations | $ | (2.5) | $ | (36.0) |
EBITDA | $ | 49.0 | $ | (28.8) |
Revenue Highlights
LYBALVI
- Revenues for the quarter were $57.0 million.
- Revenues and total prescriptions for the quarter grew 50% and 56%, respectively, compared to the first quarter of 2023.
- Inventory in the channel decreased by approximately $2.3 million during the quarter.
ARISTADAi
- Revenues for the quarter were $78.9 million.
- Inventory in the channel decreased by approximately $3.6 million during the quarter.
VIVITROL
- Revenues for the quarter were $97.7 million.
- Inventory in the channel decreased by approximately $4.3 million during the quarter.
Manufacturing & Royalty Revenues
- Royalty revenues from INVEGA SUSTENNA®/XEPLION®, INVEGA TRINZA®/TREVICTA® and INVEGA HAFYERA®/BYANNLI® for the quarter were $62.7 million.
- VUMERITY® manufacturing and royalty revenues for the quarter were $31.3 million.
Key Operating Expenses
Please see Note 1 below for details regarding discontinued operations.
(In millions) | Three Months Ended | |||
2024 | 2023 | |||
R&D Expense – Continuing Operations | $ | 67.6 | $ | 63.8 |
R&D Expense – Discontinued Operations | $ | 2.5 | $ | 29.9 |
SG&A Expense – Continuing Operations | $ | 179.7 | $ | 167.8 |
SG&A Expense – Discontinued Operations | $ | - | $ | 6.6 |
- Year-over-year increase in R&D expense related to continuing operations was driven primarily by investment in the ALKS 2680 development program and approximately $3.2 million of non-recurring share-based compensation expenses.
- Year-over-year increase in SG&A expense related to continuing operations was driven primarily by investment in the LYBALVI direct-to-consumer advertising campaign and approximately $6.2 million of non-recurring share-based compensation expenses.
Balance Sheet
At March 31, 2024, the company recorded cash, cash equivalents and total investments of $807.8 million, compared to $813.4 million at Dec. 31, 2023. The company's total debt outstanding as of March 31, 2024 was $290.1 million.
Financial Expectations for 2024
Alkermes reiterates its financial expectations for 2024, as set forth in its press release dated Feb. 15, 2024.
Recent Events
- In March 2024, the company announced the appointment of new independent director Nancy S. Lurker to the company's board of directors.
- In April 2024, the company presented data from its long-term safety study of LYBALVI (olanzapine and samidorphan) at the 2024 Congress of the Schizophrenia International Research Society (SIRS).
- In April 2024, the company announced positive topline results from the narcolepsy type 2 and idiopathic hypersomnia cohorts in its phase 1b study of ALKS 2680, the company's novel, investigational orexin 2 receptor (OX2R) agonist in development as a once-daily treatment for narcolepsy.
- In April 2024, the company announced initiation of the Vibrance-1 phase 2 study of ALKS 2680 in patients with narcolepsy type 1.
Notes and Explanations
1. The company determined that upon the separation of its oncology business, completed on Nov. 15, 2023, the oncology business met the criteria for discontinued operations in accordance with Financial Accounting Standards Board Accounting Standards Codification 205, Discontinued Operations. Accordingly, the accompanying selected financial information has been updated to present the results of the oncology business as discontinued operations for the three months ended March 31, 2023.
Conference Call
Alkermes will host a conference call and webcast presentation with accompanying slides at 8:00 a.m. ET (1:00 p.m. BST) on Wednesday, May 1, 2024, to discuss these financial results and provide an update on the company. The webcast may be accessed on the Investors section of Alkermes' website at www.alkermes.com. The conference call may be accessed by dialing +1 877 407 2988 for U.S. callers and +1 201 389 0923 for international callers. In addition, a replay of the conference call may be accessed by visiting Alkermes' website.
About Alkermes plc
Alkermes plc is a global biopharmaceutical company that seeks to develop innovative medicines in the field of neuroscience. The company has a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia and bipolar I disorder, and a pipeline of clinical and preclinical candidates in development for neurological disorders, including narcolepsy. Headquartered in Ireland, Alkermes also has a corporate office and research and development center in Massachusetts and a manufacturing facility in Ohio. For more information, please visit Alkermes' website at www.alkermes.com.
Non-GAAP Financial Measures
This press release includes information about certain financial measures that are not prepared in accordance with generally accepted accounting principles in the U.S. (GAAP), including non-GAAP net income and EBITDA. These non-GAAP measures are not based on any standardized methodology prescribed by GAAP and are not necessarily comparable to similar measures presented by other companies.
Non-GAAP net income adjusts for certain one-time and non-cash charges by excluding from GAAP results: share-based compensation expense; amortization; depreciation; non-cash net interest expense; change in the fair value of contingent consideration; certain other one-time or non-cash items; and the income tax effect of these reconciling items. EBITDA represents earnings before interest, tax, depreciation and amortization; earnings include share-based compensation expense.
The company's management and board of directors utilize these non-GAAP financial measures to evaluate the company's performance. The company provides these non-GAAP financial measures of the company's performance to investors because management believes that these non-GAAP financial measures, when viewed with the company's results under GAAP and the accompanying reconciliations, are useful in identifying underlying trends in ongoing operations. However, non-GAAP net income and EBITDA are not measures of financial performance under GAAP and, accordingly, should not be considered as alternatives to GAAP measures as indicators of operating performance. Further, non-GAAP net income and EBITDA should not be considered measures of the company's liquidity.
A reconciliation of GAAP to non-GAAP financial measures has been provided in the tables included in this press release.
Note Regarding Forward-Looking Statements
Certain statements set forth in this press release constitute "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, but not limited to, statements concerning: the company's expectations concerning its future financial and operating performance, business plans or prospects; the company's expectations regarding advancement of its development pipeline, including plans and expected timelines for the ALKS 2680 clinical development program; and the therapeutic and commercial potential of ALKS 2680 and the company's other development programs. The company cautions that forward-looking statements are inherently uncertain. The forward-looking statements are neither promises nor guarantees and they are necessarily subject to a high degree of uncertainty and risk. Actual performance and results may differ materially from those expressed or implied in the forward-looking statements due to various risks and uncertainties. These risks and uncertainties include, among others: whether the company is able to sustain profitability; the unfavorable outcome of arbitration or litigation, including so-called "Paragraph IV" litigation and other patent litigation which may lead to competition from generic drug manufacturers, or other disputes related to the company's products or products using the company's proprietary technologies; clinical development activities may not be completed on time or at all; the results of the company's development activities may not be positive, or predictive of final results from such activities, results of future development activities or real-world results; the U.S. Food and Drug Administration (FDA) or regulatory authorities outside the U.S. may not agree with the company's regulatory approval strategies; the FDA or regulatory authorities outside the U.S. may make adverse decisions regarding the company's products; the company and its licensees may not be able to continue to successfully commercialize their products or support revenue growth from such products; there may be a reduction in payment rate or reimbursement for the company's products or an increase in the company's financial obligations to government payers; the company's products may prove difficult to manufacture, be precluded from commercialization by the proprietary rights of third parties, or have unintended side effects, adverse reactions or incidents of misuse; and those risks and uncertainties described under the heading "Risk Factors" in the company's Annual Report on Form 10-K for the year ended Dec. 31, 2023 and in subsequent filings made by the company with the U.S. Securities and Exchange Commission (SEC), which are available on the SEC's website at www.sec.gov. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Except as required by law, the company disclaims any intention or responsibility for updating or revising any forward-looking statements contained in this press release.
VIVITROL® is a registered trademark of Alkermes, Inc.; ARISTADA®, ARISTADA INITIO® and LYBALVI® are registered trademarks of Alkermes Pharma Ireland Limited, used by Alkermes, Inc. under license; BYANNLI®, INVEGA HAFYERA®, INVEGA SUSTENNA®, INVEGA TRINZA®, TREVICTA® and XEPLION® are registered trademarks of Johnson & Johnson or its affiliated companies; and VUMERITY® is a registered trademark of Biogen MA Inc., used by Alkermes under license.
i | The term "ARISTADA" as used in this press release refers to ARISTADA and ARISTADA INITIO®, unless the context indicates otherwise. |
Alkermes plc and Subsidiaries | ||||
Selected Financial Information (Unaudited) | ||||
Condensed Consolidated Statements of Operations - GAAP | Three Months Ended | Three Months Ended | ||
(In thousands, except per share data) | March 31, 2024 | March 31, 2023 | ||
Revenues: | ||||
Product sales, net | $ 233,536 | $ 214,727 | ||
Manufacturing and royalty revenues | 116,833 | 72,862 | ||
Research and development revenue | 3 | 6 | ||
Total Revenues | 350,372 | 287,595 | ||
Expenses: | ||||
Cost of goods manufactured and sold | 58,644 | 58,164 | ||
Research and development | 67,611 | 63,770 | ||
Selling, general and administrative | 179,749 | 167,833 | ||
Amortization of acquired intangible assets | 1,059 | 8,800 | ||
Total Expenses | 307,063 | 298,567 | ||
Operating Income (Loss) | 43,309 | (10,972) | ||
Other Income (Expense), net: | ||||
Interest income | 9,399 | 4,966 | ||
Interest expense | (5,978) | (5,288) | ||
Other income (expense), net | 182 | (39) | ||
Total Other Income (Expense), net | 3,603 | (361) | ||
Income (Loss) Before Income Taxes | 46,912 | (11,333) | ||
Income Tax Provision | 7,964 | 717 | ||
Net Income (Loss) From Continuing Operations | 38,948 | (12,050) | ||
Loss from Discontinued Operations — Net of Tax | (2,120) | (29,795) | ||
Net Income (Loss) — GAAP | $ 36,828 | $ (41,845) | ||
GAAP Earnings (Loss) Per Share - Basic: | ||||
From continuing operations | $ 0.23 | $ (0.07) | ||
From discontinued operations | (0.01) | (0.18) | ||
Earnings (loss) per share | $ 0.22 | $ (0.25) | ||
GAAP Earnings (Loss) Per Share - Diluted: | ||||
From continuing operations | $ 0.23 | $ (0.07) | ||
From discontinued operations | (0.01) | (0.18) | ||
Earnings (loss) per share | $ 0.21 | $ (0.25) | ||
Weighted Average Number of Ordinary Shares Outstanding: | ||||
Basic — GAAP | 167,984 | 165,085 | ||
Diluted — GAAP | 172,981 | 165,085 | ||
Diluted — Non-GAAP | 172,981 | 170,270 | ||
Condensed Consolidated Statements of Operations - GAAP (Continued) | Three Months Ended | Three Months Ended | ||
(In thousands, except per share data) | March 31, 2024 | March 31, 2023 | ||
An itemized reconciliation between net income (loss) from continuing operations on a GAAP basis and EBITDA is as follows: | ||||
Net Income (Loss) from Continuing Operations | $ 38,948 | $ (12,050) | ||
Adjustments: | ||||
Depreciation expense | 6,997 | 9,384 | ||
Amortization expense | 1,059 | 8,800 | ||
Interest income | (9,399) | (4,966) | ||
Interest expense | 5,978 | 5,288 | ||
Income tax provision | 7,964 | 717 | ||
EBITDA from Continuing Operations | 51,547 | 7,173 | ||
EBITDA from Discontinued Operations | (2,516) | (35,992) | ||
EBITDA | $ 49,031 | $ (28,819) | ||
An itemized reconciliation between net income (loss) from continuing operations on a GAAP basis and non-GAAP net income is as follows: | ||||
Net Income (Loss) from Continuing Operations | $ 38,948 | $ (12,050) | ||
Adjustments: | ||||
Share-based compensation expense | 32,755 | 21,023 | ||
Depreciation expense | 6,997 | 9,384 | ||
Amortization expense | 1,059 | 8,800 | ||
Non-cash net interest expense | 114 | 116 | ||
Separation expense | 427 | 3,783 | ||
Income tax effect related to reconciling items | (4,121) | (995) | ||
Non-GAAP Net Income from Continuing Operations | 76,179 | 30,061 | ||
Non-GAAP Net Loss from Discontinued Operations | (2,120) | (27,645) | ||
Non-GAAP Net Income | $ 74,059 | $ 2,416 | ||
Non-GAAP diluted earnings per share from continuing operations | $ 0.44 | $ 0.18 | ||
Non-GAAP diluted loss per share from discontinued operations | (0.01) | (0.16) | ||
Non-GAAP diluted earnings per share | $ 0.43 | $ 0.01 | ||
Alkermes plc and Subsidiaries | ||||
Selected Financial Information (Unaudited) | ||||
Condensed Consolidated Balance Sheets | March 31, | December 31, | ||
(In thousands) | 2024 | 2023 | ||
Cash, cash equivalents and total investments | $ 807,830 | $ 813,378 | ||
Receivables | 315,848 | 332,477 | ||
Inventory | 198,369 | 186,406 | ||
Contract assets | 1,229 | 706 | ||
Prepaid expenses and other current assets | 111,539 | 98,166 | ||
Property, plant and equipment, net | 224,590 | 226,943 | ||
Intangible assets, net and goodwill | 83,959 | 85,018 | ||
Assets held for sale | 96,792 | 94,260 | ||
Deferred tax assets | 182,536 | 195,888 | ||
Other assets | 101,204 | 102,981 | ||
Total Assets | $ 2,123,896 | $ 2,136,223 | ||
Long-term debt — current portion | $ 3,000 | $ 3,000 | ||
Other current liabilities | 455,977 | 512,678 | ||
Long-term debt | 287,095 | 287,730 | ||
Liabilities from discontinued operations | — | 4,542 | ||
Other long-term liabilities | 123,061 | 125,587 | ||
Total shareholders' equity | 1,254,763 | 1,202,686 | ||
Total Liabilities and Shareholders' Equity | $ 2,123,896 | $ 2,136,223 | ||
Ordinary shares outstanding (in thousands) | 169,185 | 166,980 | ||
This selected financial information should be read in conjunction with the consolidated financial statements and notes thereto included in Alkermes plc's Quarterly Report on Form 10-Q for the quarter ended March 31, 2024, which the company intends to file in May 2024. | ||||
Alkermes plc and Subsidiaries | |||
Amounts included in Discontinued Operations | |||
(In thousands) | Three Months | ||
Cost of goods manufactured and sold | $ - | ||
Research and development | 2,516 | ||
Selling, general and administrative | |||
Income tax benefit | (396) | ||
Loss from discontinued operations, net of tax | $ 2,120 | ||
(In thousands) | Three Months | ||
Cost of goods manufactured and sold | $ 11 | ||
Research and development | 29,867 | ||
Selling, general and administrative | 6,644 | ||
Income tax benefit | (6,727) | ||
Loss from discontinued operations, net of tax | $ 29,795 | ||
Alkermes Contacts:
For Investors: Sandy Coombs +1 781 609 6377
For Media: Katie Joyce +1 781 249 8927
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SOURCE Alkermes plc
