— First Quarter Revenues of $306.5 Million —

— GAAP Net Income of $22.5 Million and Diluted GAAP Earnings per Share of $0.13 —

— Company Reiterates 2025 Financial Expectations —

DUBLIN, May 1, 2025 /PRNewswire/ -- Alkermes plc (Nasdaq: ALKS) today reported financial results for the first quarter of 2025.

"Our first quarter financial performance provides a solid foundation to deliver on our financial guidance for the year. We are in a strong position in this dynamic macroeconomic environment and remain focused on executing on the strategic objectives that we believe will drive the future value of the company," said Richard Pops, Chief Executive Officer of Alkermes. "We recently achieved an important milestone in the program for ALKS 2680, our novel, investigational, oral orexin 2 receptor agonist, completing enrollment in our first phase 2 study in the program, Vibrance-1, in narcolepsy type 1. We now expect topline results from Vibrance-1 early in the third quarter. We expect to complete enrollment in the Vibrance-2 phase 2 study, in narcolepsy type 2, mid-year, with topline data from that study expected in the fall. Enrollment in Vibrance-3, our phase 2 study in idiopathic hypersomnia, is now also underway. Across the ALKS 2680 development program, we have strong momentum and are preparing for the phase 3 program. With the potential to transform the treatment of central disorders of hypersomnolence, orexin 2 receptor agonists are one of the most exciting new therapeutic categories in development."

Key Financial Highlights

Revenues (In millions) Three Months Ended 
March  31, 2025 2024 Total Revenues $ 306.5 $ 350.4 Total Proprietary Net Sales $ 244.5 $ 233.5 VIVITROL® $ 101.0 $ 97.7 ARISTADA®i $ 73.5 $ 78.9 LYBALVI® $ 70.0 $ 57.0  Profitability (In millions) Three Months Ended 
March 31, 2025 2024 GAAP Net Income From Continuing Operations $ 22.5 $ 38.9 GAAP Net Income (Loss) From Discontinued Operations $ -- $ (2.1) GAAP Net Income  $ 22.5 $ 36.8  EBITDA From Continuing Operations $ 22.8 $ 51.5 EBITDA From Discontinued Operations $ -- $ (2.5) EBITDA $ 22.8 $ 49.0  Adjusted EBITDA $ 45.6 $ 81.8

Revenue Highlights

LYBALVI

Revenues for the quarter were $70.0 million. Revenues and total prescriptions for the quarter grew 23% and 22%, respectively, compared to the first quarter of 2024.

ARISTADAi

Revenues for the quarter were $73.5 million.

VIVITROL

Revenues for the quarter were $101.0 million.

Story Continues

Manufacturing & Royalty Revenues

VUMERITY® manufacturing and royalty revenues for the quarter were $27.8 million. Royalty revenues from XEPLION®, INVEGA TRINZA®/TREVICTA® and INVEGA HAFYERA®/BYANNLI® for the quarter were $17.7 million.

Key Operating Expenses

Please see Note 1 below for details regarding discontinued operations.

(In millions)          Three Months Ended 
March 31, 2025 2024 R&D Expense – Continuing Operations          $ 71.8 $ 67.6 R&D Expense – Discontinued Operations          $ -- $ 2.5  SG&A Expense – Continuing Operations          $ 171.7 $ 179.7 SG&A Expense – Discontinued Operations          $ -- $ --

Balance Sheet

At March 31, 2025, the company recorded cash, cash equivalents and total investments of $916.2 million, compared to $824.8 million at Dec. 31, 2024.

Financial Expectations for 2025 Alkermes reiterates its financial expectations for 2025, as set forth in its press release dated Feb. 12, 2025.

Notes and Explanations 1. The company determined that upon the separation of its former 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, 2024.

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 Thursday, May 1, 2025, 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 and idiopathic hypersomnia. 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 EBITDA and Adjusted 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.

EBITDA represents earnings before interest, tax, depreciation and amortization. Adjusted EBITDA excludes share-based compensation expense in addition to the components of EBITDA from earnings.

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, EBITDA and Adjusted 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, EBITDA and Adjusted 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, including expected value drivers; and the company's expectations regarding development plans, activities and timelines for, and the potential therapeutic and commercial value of, ALKS 2680. 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 achieve its financial expectations; 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 or may make adverse decisions regarding the company's products; the unfavorable outcome of arbitration, litigation, or other proceedings or disputes related to the company's products or products using the company's proprietary technologies; 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, 2024 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 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, 2025  March 31, 2024 Revenues:  Product sales, net  $                 244,493  $                 233,536 Manufacturing and royalty revenues  62,017  116,833 Research and development revenue  —  3 Total Revenues  306,510  350,372 Expenses:  Cost of goods manufactured and sold  49,197  58,644 Research and development  71,817  67,611 Selling, general and administrative  171,704  179,749 Amortization of acquired intangible assets  —  1,059 Total Expenses  292,718  307,063 Operating Income  13,792  43,309 Other Income, net:  Interest income  10,141  9,399 Interest expense  —  (5,978) Other income, net  1,556  182 Total Other Income, net  11,697  3,603 Income Before Income Taxes  25,489  46,912 Income Tax Provision   3,025  7,964 Net Income From Continuing Operations  22,464  38,948 Loss from Discontinued Operations — Net of Tax  —  (2,120) Net Income — GAAP  $                   22,464  $                   36,828  GAAP Earnings (Loss) Per Share - Basic:  From continuing operations  $                       0.14  $                       0.23 From discontinued operations  —  (0.01) Earnings per share  $                       0.14  $                       0.22  GAAP Earnings (Loss) Per Share - Diluted:  From continuing operations  $                       0.13  $                       0.23 From discontinued operations  —  (0.01) Earnings per share  $                       0.13  $                       0.21  Weighted Average Number of Ordinary Shares Outstanding:  Basic  — GAAP  163,407  167,984 Diluted — GAAP  168,737  172,981   Condensed Consolidated Statements of Operations - GAAP (Continued)  Three Months Ended  Three Months Ended (In thousands, except per share data)  March 31, 2025  March 31, 2024 An itemized reconciliation between net income from continuing operations on a GAAP basis and Adjusted EBITDA is as follows:  Net Income from Continuing Operations  $                   22,464  $                   38,948 Adjustments:  Depreciation and amortization expense  7,421  8,056 Interest income   (10,141)  (9,399) Interest expense  —  5,978 Income tax provision  3,025  7,964 EBITDA from Continuing Operations  22,769  51,547 EBITDA from Discontinued Operations  —  (2,516) EBITDA  22,769  49,031 Share-based compensation  22,810  32,755 Adjusted EBITDA  $                   45,579  $                   81,786  Alkermes plc and Subsidiaries Selected Financial Information (Unaudited)  Condensed Consolidated Balance Sheets  March 31,  December 31, (In thousands)  2025  2024 Cash, cash equivalents and total investments  $                 916,206  $                 824,816 Receivables  318,703  389,733 Inventory  183,438  182,887 Contract assets  3,049  4,990 Prepaid expenses and other current assets  89,843  86,077 Property, plant and equipment, net  233,920  227,564 Intangible assets, net and goodwill  83,899  83,917 Deferred tax assets  152,144  154,835 Other assets  100,775  100,748 Total Assets  $              2,081,977  $              2,055,567 Accrued sales discounts, allowances and reserves  $                 249,795  $                 272,452 Other current liabilities  193,935  192,747 Other long-term liabilities  126,664  125,391 Total shareholders' equity  1,511,583  1,464,977 Total Liabilities and Shareholders' Equity  $              2,081,977  $              2,055,567  Ordinary shares outstanding (in thousands)  164,853  162,177  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, 2025, which the company intends to file in May 2025.

Alkermes Contacts:  For Investors:  Sandy Coombs  +1 781 609 6377 For Media:  Katie Joyce  +1 781 249 8927Alkermes plc Logo (PRNewsfoto/Alkermes plc)Cision

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