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Halozyme Reiterates 2024 Financial Guidance and Raises 2025 and Multi-Year Financial Guidance

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Halozyme (NASDAQ: HALO) has reiterated its 2024 financial guidance and raised its 2025 and multi-year financial outlook. The company projects 2025 total revenue of $1,150-$1,225 million (16-23% YoY growth), adjusted EBITDA of $755-$805 million (24-32% growth), and non-GAAP diluted EPS of $4.95-$5.35 (21-30% growth).

The growth is primarily driven by VYVGART Hytrulo's strong acceptance in generalized myasthenia gravis and CIDP, along with continued growth of Darzalex SC and Phesgo. Three additional products - Ocrevus Zunovo, Tecentriq Hybreza, and Opdivo Qvantig - are expected to contribute modestly in 2025 with meaningful growth from 2026.

The company has also announced a new $250 million accelerated share repurchase program under its previously announced $750 million share repurchase program.

Halozyme (NASDAQ: HALO) ha confermato le sue previsioni finanziarie per il 2024 e ha rivisto al rialzo le previsioni finanziarie per il 2025 e per gli anni successivi. L'azienda prevede un fatturato totale per il 2025 di 1.150-1.225 milioni di dollari (crescita del 16-23% rispetto all'anno precedente), un EBITDA rettificato di 755-805 milioni di dollari (crescita del 24-32%) e un EPS diluito non-GAAP di 4,95-5,35 dollari (crescita del 21-30%).

La crescita è principalmente guidata dalla forte accettazione di VYVGART Hytrulo nella miastenia gravis generalizzata e nella CIDP, insieme alla continua crescita di Darzalex SC e Phesgo. Tre ulteriori prodotti - Ocrevus Zunovo, Tecentriq Hybreza e Opdivo Qvantig - si prevede contribuiscano modestamente nel 2025 con una crescita significativa a partire dal 2026.

L'azienda ha anche annunciato un nuovo programma di riacquisto accelerato di azioni da 250 milioni di dollari nell'ambito del precedente programma di riacquisto di azioni da 750 milioni di dollari.

Halozyme (NASDAQ: HALO) ha reiterado su guía financiera para 2024 y ha actualizado al alza sus proyecciones financieras para 2025 y los años siguientes. La empresa proyecta un ingreso total de 1,150-1,225 millones de dólares para 2025 (crecimiento del 16-23% interanual), un EBITDA ajustado de 755-805 millones de dólares (crecimiento del 24-32%) y un EPS diluido no-GAAP de 4.95-5.35 dólares (crecimiento del 21-30%).

El crecimiento es impulsado principalmente por la fuerte aceptación de VYVGART Hytrulo en miastenia gravis generalizada y CIDP, junto con el crecimiento continuo de Darzalex SC y Phesgo. Se espera que tres productos adicionales - Ocrevus Zunovo, Tecentriq Hybreza y Opdivo Qvantig - contribuyan modestamente en 2025, con un crecimiento significativo desde 2026.

La empresa también ha anunciado un nuevo programa acelerado de recompra de acciones por 250 millones de dólares bajo su programa de recompra de acciones previamente anunciado de 750 millones de dólares.

Halozyme (NASDAQ: HALO)가 2024년 재무 가이던스를 재확인하고 2025년 및 다년 재무 전망을 상향 조정했습니다. 회사는 2025년 총 수익 11억 5천만~12억 2천5백만 달러 (전년 대비 16-23% 성장), 조정된 EBITDA 7억 5천5백만~8억 5백만 달러 (24-32% 성장), 비-GAAP 희석 주당순이익 4.95-5.35 달러 (21-30% 성장)를 예상하고 있습니다.

성장은 주로 VYVGART Hytrulo의 일반화된 중증 근무력증 및 CIDP에서의 강한 수용에 의해 주도되며, Darzalex SC와 Phesgo의 지속적인 성장도 포함됩니다. Ocrevus Zunovo, Tecentriq Hybreza 및 Opdivo Qvantig의 세 가지 추가 제품은 2025년에 소폭 기여할 것으로 예상되며, 2026년부터는 의미 있는 성장이 기대됩니다.

회사는 또한 이전에 발표된 7억 5천만 달러 규모의 자사주매입 프로그램에 따라 2억 5천만 달러 규모의 자사주 매입 가속화 프로그램을 새롭게 발표했습니다.

Halozyme (NASDAQ: HALO) a réitéré son guide financier pour 2024 et a relevé ses prévisions financières pour 2025 et sur plusieurs années. L'entreprise prévoit un chiffre d'affaires total de 1,150-1,225 millions de dollars pour 2025 (croissance de 16-23% par rapport à l'année précédente), un EBITDA ajusté de 755-805 millions de dollars (croissance de 24-32%) et un BPA dilué non-GAAP de 4,95-5,35 dollars (croissance de 21-30%).

La croissance est principalement soutenue par la forte acceptation de VYVGART Hytrulo dans la myasthénie grave généralisée et le CIDP, ainsi que par la croissance continue de Darzalex SC et Phesgo. Trois produits supplémentaires - Ocrevus Zunovo, Tecentriq Hybreza et Opdivo Qvantig - devraient contribuer de manière modeste en 2025, avec une croissance significative à partir de 2026.

L'entreprise a également annoncé un nouveau programme de rachat d'actions accéléré de 250 millions de dollars dans le cadre de son programme de rachat d'actions de 750 millions de dollars précédemment annoncé.

Halozyme (NASDAQ: HALO) hat seine Finanzprognose für 2024 bekräftigt und den Ausblick für 2025 sowie für mehrere Jahre angehoben. Das Unternehmen prognostiziert für 2025 einen Gesamtumsatz von 1.150-1.225 Millionen Dollar (Wachstum von 16-23% im Vergleich zum Vorjahr), ein bereinigtes EBITDA von 755-805 Millionen Dollar (Wachstum von 24-32%) und ein verwässertes EPS nach non-GAAP von 4,95-5,35 Dollar (Wachstum von 21-30%).

Das Wachstum wird hauptsächlich durch die starke Akzeptanz von VYVGART Hytrulo bei generalisierter Myasthenia Gravis und CIDP angetrieben, zusammen mit dem fortgesetzten Wachstum von Darzalex SC und Phesgo. Drei weitere Produkte - Ocrevus Zunovo, Tecentriq Hybreza und Opdivo Qvantig - werden voraussichtlich 2025 einen bescheidenen Beitrag leisten, mit erheblichen Wachstumschancen ab 2026.

Das Unternehmen hat außerdem ein neues 250 Millionen Dollar schweres beschleunigtes Aktienrückkaufprogramm im Rahmen seines zuvor angekündigten Aktienrückkaufprogramms über 750 Millionen Dollar angekündigt.

Positive
  • 2025 revenue guidance raised to $1,150-$1,225 million (16-23% YoY growth)
  • Adjusted EBITDA projected at $755-$805 million (24-32% growth)
  • Royalty revenue expected to grow 30-35% in 2025
  • New $250 million accelerated share repurchase program announced
  • Strong commercial portfolio with nine ENHANZE co-formulated products
Negative
  • None.

Insights

This financial update reveals substantial growth momentum for Halozyme. The revised 2025 guidance showcases impressive metrics with $1,150-$1,225 million in total revenue (16-23% YoY growth) and adjusted EBITDA of $755-$805 million (24-32% YoY growth). The $250 million accelerated share repurchase program signals management's confidence in the company's valuation and future prospects. The royalty revenue projection of $725-$750 million for 2025 (30-35% growth) indicates strong commercial traction of ENHANZE-partnered products, particularly VYVGART Hytrulo and Darzalex SC. Three newly approved products (Ocrevus Zunovo, Tecentriq Hybreza, Opdivo Qvantig) position the company for sustained growth beyond 2025. The projected non-GAAP EPS of $4.95-$5.35 represents robust bottom-line expansion, though investors should note this doesn't factor in potential share repurchases.

Halozyme's ENHANZE technology platform demonstrates strong market penetration and expanding commercial opportunities. The guidance raise reflects accelerating adoption of subcutaneous formulations across multiple therapeutic areas. VYVGART Hytrulo's performance in both myasthenia gravis and CIDP indicates successful market expansion. The portfolio's de-risked nature, with nine commercialized products and multiple growth drivers, provides revenue diversification and reduces dependency on any single product. Early-stage launches of Ocrevus Zunovo, Tecentriq Hybreza and Opdivo Qvantig represent significant future revenue potential, particularly from 2026 onwards. The robust pipeline and continued partner interest suggest sustained long-term growth potential beyond current projections.

Halozyme's business model demonstrates excellent operational leverage with adjusted EBITDA growth outpacing revenue growth. The company's strategy of partnering with major pharmaceutical companies minimizes development risks while maximizing royalty potential. The raised guidance reflects strong execution in commercialization and market penetration. The $250 million ASR program, part of a larger $750 million authorization, indicates strong free cash flow generation and commitment to shareholder returns. The diverse product portfolio across multiple therapeutic areas and partners creates a resilient revenue stream. The company's position as a drug delivery technology leader with proven commercial success should continue attracting new partnership opportunities, supporting long-term growth beyond current projections.

Reports Preliminary 2024 Unaudited Estimated Ranges Consistent with Previous Financial Guidance 

Raises 2025 Financial Guidance Ranges for Total Revenue to $1,150 - $1,225 million, Representing YoY Growth of 16% - 23%, Adjusted EBITDA of $755 - $805 million, Representing YoY Growth of 24% - 32%, and non-GAAP Diluted EPS of $4.95 - $5.35, Representing YoY Growth of 21% - 30%1,2

Announces New $250 million Accelerated Share Repurchase

Conference Call Scheduled Today at 5:30am PT/8:30am ET

SAN DIEGO, Jan. 8, 2025 /PRNewswire/ -- Halozyme Therapeutics, Inc. (NASDAQ: HALO) ("Halozyme" or the "Company") today provided a financial update, reiterating full year 2024 financial guidance and raising full year 2025 and multi-year financial guidance. The Company also announced it has recently entered into a new $250 million accelerated share repurchase (ASR) program under its previously announced $750 million share repurchase program.

"Halozyme is at the forefront of drug delivery innovation, fostering a high-growth and durable business underpinned by our proprietary ENHANZE drug delivery technology. This leadership position is reflected in the global launch of nine ENHANZE co-formulated products, a robust pipeline and continuing interest from potential new partners," said Dr. Helen Torley, president and chief executive officer. "Our 2025 guidance, with projected revenue growth of 16% to 23% and adjusted EBITDA growth of 24% to 32%, is largely driven by VYVGART Hytrulo, which has received strong early acceptance in generalized myasthenia gravis, and is now seeing growing adoption in CIDP following the June 2024 U.S. approval, and by the continued strong growth of Darzalex SC and Phesgo. Three additional products, Ocrevus Zunovo, Tecentriq Hybreza and Opdivo Qvantig, which are in the early stages of commercialization following recent approvals, are projected to contribute modestly in 2025, growing meaningfully from 2026 onwards. The combined continued projected growth of each product in this exciting de-risked portfolio is what resulted in our also raising our multi-year guidance."

Table 1. 2024 Unaudited Preliminary Estimates of Results for the Twelve Months Ended December 31, 2024


2024 Estimate

Total Revenue

$970 to $1,020 million

Royalty Revenue

$550 to $565 million

Net Income

$419 to $443 million

Adjusted EBITDA

$595 to $625 million

GAAP Diluted EPS

$3.22 to $3.40

Non-GAAP Diluted EPS

$4.00 to $4.20


Footnotes:

1

Growth rates calculated from 2024 midpoint to low end of 2025 range and high-end of 2025 range. See "2025 Financial Guidance" below.

2

Adjusted EBITDA and non-GAAP Diluted EPS are non-GAAP financial measures. See "Note Regarding Use of Non-GAAP Financial Measures" below for an explanation of these measures.

Financial Outlook for 2025

The Company is raising its financial guidance for 2025. For the full year 2025, the Company expects:

  • Total revenue of $1,150 million to $1,225 million, representing growth of 16% to 23% over projected 2024 total revenue, primarily driven by increases in royalty revenue and product sales from XYOSTED®.

  • Revenue from royalties of $725 million to $750 million, representing growth of 30% to 35% over 2024.

  • Adjusted EBITDA of $755 million to $805 million, representing growth of 24% to 32% over 2024.

  • Non-GAAP diluted earnings per share of $4.95 to $5.35, representing growth of 21% to 30% over 2024. The Company's earnings per share guidance does not consider the impact of potential future share repurchases.

Table 2. 2025 Financial Guidance



Previous Guidance
Range


New Guidance Range

Expected
YoY Growth1

Total Revenue


$1,095 to $1,170 million


$1,150 to $1,225 million

16% to 23%

Royalty Revenue


$650 to $675 million


$725 to $750 million

30% to 35%

Adjusted EBITDA


$710 to $760 million


$755 to $805 million

24% to 32%

Non-GAAP Diluted EPS


$4.45 to $4.85


$4.95 to $5.35

21% to 30%



Footnote:

1

Growth rates calculated from 2024 midpoint to low end of 2025 range and high-end of 2025 range.

Website and Conference Call
Halozyme will host an Investor Conference Call today, Wednesday, January 8 at 5:30am PT/8:30am ET. On the call, Dr. Helen Torley, President and Chief Executive Officer, and Nicole LaBrosse, Chief Financial Officer, will provide preliminary unaudited full year 2024 results and updated 2025 and multi-year financial guidance. Pre-registration of the live call can be accessed via link here: https://registrations.events/direct/Q4I871904593. A webcast of the live call and presentation materials (which will be available 15 minutes before the start of the call) will be available through the "Investors" section of Halozyme's corporate website at ir.halozyme.com.

About Halozyme

Halozyme is a biopharmaceutical company advancing disruptive solutions to improve patient experiences and outcomes for emerging and established therapies. As the innovators of ENHANZE® drug delivery technology with the proprietary enzyme rHuPH20, Halozyme's commercially-validated solution is used to facilitate the subcutaneous delivery of injected drugs and fluids, with the goal of improving the patient experience with rapid subcutaneous delivery and reduced treatment burden. Having touched more than 800,000 patient lives in post-marketing use in nine commercialized products across more than 100 global markets, Halozyme has licensed its ENHANZE® technology to leading pharmaceutical and biotechnology companies including Roche, Takeda, Pfizer, Janssen, AbbVie, Eli Lilly, Bristol-Myers Squibb, argenx, ViiV Healthcare, Chugai Pharmaceutical and Acumen Pharmaceuticals.

Halozyme also develops, manufactures and commercializes, for itself or with partners, drug-device combination products using its advanced auto-injector technologies that are designed to provide commercial or functional advantages such as improved convenience, reliability and tolerability, and enhanced patient comfort and adherence. The Company has two commercial proprietary products, Hylenex® and XYOSTED®, partnered commercial products and ongoing product development programs with Teva Pharmaceuticals and Idorsia Pharmaceuticals.

Halozyme is headquartered in San Diego, CA and has offices in Ewing, NJ and Minnetonka, MN. Minnetonka is also the site of its operations facility.

For more information visit www.halozyme.com and connect with us on LinkedIn and Twitter.

Note Regarding 2024 Preliminary Results

The financial results presented herein are preliminary, estimated, and unaudited. They are subject to the completion and finalization of the Company's financial and accounting close procedures. They reflect management's estimates based solely upon information available to management as of the date of this press release. Further information learned during the completion and finalization of these procedures may alter the final results. These preliminary estimates should not be considered a substitute for the financial information to be filed with the Securities and Exchange Commission on the Company's Form 10-K for the year ended December 31, 2024 once it becomes available. There is a possibility that the Company's financial results for the twelve months ended December 31, 2024 could vary materially from these preliminary estimates. Accordingly, you should not place undue reliance upon this preliminary information.

Note Regarding Use of Non-GAAP Financial Measures

In addition to disclosing financial measures prepared in accordance with U.S. generally accepted accounting principles ("GAAP"), this press release and the accompanying tables contain certain non-GAAP financial measures. The Company reports earnings before interest, taxes, depreciation, and amortization ("EBITDA"), adjusted EBITDA, Non-GAAP diluted earnings per share and non-GAAP diluted shares and guidance with respect to those measures, in addition to, and not as a substitute for, or superior to, financial measures calculated in accordance with GAAP. The Company calculates non-GAAP diluted earnings per share excluding share-based compensation expense, amortization of debt discounts, intangible asset amortization, one-time changes, if any, such as changes in contingent liabilities, inventory adjustments, impairment charges, and certain adjustments to income tax expense. The Company calculates non-GAAP diluted shares excluding the dilutive impact of convertible notes which is used in calculating non-GAAP diluted earnings. The Company calculates EBITDA excluding interest, taxes, depreciation and amortization. The Company calculates adjusted EBITDA excluding one-time items, if any such as changes in contingent liabilities, inventory adjustments and impairment charges. Reconciliations between GAAP and Non-GAAP financial measures are included at the end of this press release. The Company does not provide reconciliations of forward-looking adjusted measures to GAAP due to the inherent difficulty in forecasting and quantifying certain amounts that are necessary for such reconciliation, including adjustments that could be made for changes in share-based compensation expense and the effects of any discrete income tax items. For the same reasons, the Company is unable to address the probable significance of the unavailable information. The Company provides non-GAAP financial measures that it believes will be achieved, however it cannot accurately predict all of the components of the adjusted calculations and the U.S. GAAP measures may be materially different than the non-GAAP measures.

The Company evaluates other items of income and expense on an individual basis for potential inclusion in the calculation of Non-GAAP financial measures and considers both the quantitative and qualitative aspects of the item, including (i) its size and nature, (ii) whether or not it relates to the Company's ongoing business operations and (iii) whether or not the Company expects it to occur as part of the Company's normal business on a regular basis. Non-GAAP financial measures do not have any standardized meaning and are therefore unlikely to be comparable to similarly titled measures presented by other companies. These non-GAAP financial measures are not meant to be considered in isolation and should be read in conjunction with the Company's consolidated financial statements prepared in accordance with GAAP, and are not prepared under any comprehensive set of accounting rules or principles. In addition, from time to time in the future there may be other items that the Company may exclude for purposes of its non-GAAP financial measures, and the Company may in the future cease to exclude items that it has historically excluded for purposes of its non-GAAP financial measures.

The Company considers these non-GAAP financial measures to be important because they provide useful measures of the operating performance of the Company, exclusive of factors that do not directly affect what the Company considers to be its core operating performance, as well as unusual events. The non-GAAP measures also allow investors and analysts to make additional comparisons of the operating activities of the Company's core business over time and with respect to other companies, as well as assessing trends and future expectations. The Company uses non-GAAP financial information in assessing what it believes is a meaningful and comparable set of financial performance measures to evaluate operating trends, as well as in establishing portions of our performance-based incentive compensation programs.

Safe Harbor Statement

In addition to historical information, the statements set forth in this press release include forward-looking statements including, without limitation, statements concerning the Company's financial performance (including preliminary results for the fiscal year ended December 31, 2024 and the Company's expected financial outlook for 2025) and expectations for future growth, profitability, total revenue, royalty revenue, EBITDA, Adjusted EBITDA, and non-GAAP diluted earnings-per-share. Forward-looking statements regarding the Company's ENHANZE® drug delivery technology may include the possible benefits and attributes of ENHANZE®, its potential application to aid in the dispersion and absorption of other injected therapeutic drugs and facilitating more rapid delivery and administration of higher volumes of injectable medications through subcutaneous delivery. Forward-looking statements regarding the Company's business may include potential growth and receipt of royalty and milestone payments driven by our partners' development and commercialization efforts, potential new clinical trial study starts and clinical data, regulatory submissions and product launches, the size and growth prospects of our partners' drug franchises, potential new or expanded collaborations and collaborative targets and regulatory review, and potential approvals of new partnered or proprietary products, and the potential timing of these events. These forward-looking statements are typically, but not always, identified through use of the words "expect," "believe," "enable," "may," "will," "could," "intends," "estimate," "anticipate," "plan," "predict," "probable," "potential," "preliminary," "possible," "should," "continue," and other words of similar meaning and involve risk and uncertainties that could cause actual results to differ materially from those in the forward-looking statements. Actual results could differ materially from the expectations contained in these forward-looking statements as a result of several factors, including unexpected levels of revenues, expenditures and costs, unexpected results or delays in the growth of the Company's business, or in the development, regulatory review or commercialization of the Company's partnered or proprietary products, regulatory approval requirements, unexpected adverse events or patient outcomes and competitive conditions. These and other factors that may result in differences are discussed in greater detail in the Company's most recent Annual Report on Form 10-K and Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission. Except as required by law, the Company undertakes no duty to update forward-looking statements to reflect events after the date of this release.

Contacts: 
Tram Bui
VP, Investor Relations and Corporate Communications
609-359-3016
tbui@halozyme.com

Samantha Gaspar
Teneo
212-886-9356
samantha.gaspar@teneo.com 

The following tables reconcile, for the twelve months ended December 31, 2024, the Company's estimated ranges of 2024 EBITDA and 2024 Adjusted EBITDA to the Company's estimated ranges of 2024 Net Income, and 2024 Non-GAAP Diluted EPS to the Company's estimated ranges of 2024 GAAP Diluted EPS.

 

Halozyme Therapeutics, Inc. 
GAAP to Non-GAAP Reconciliations
Preliminary Net Income and Diluted EPS
(Unaudited)
(In millions, except per share amounts)




Twelve Months Ended
December 31, 2024

GAAP Net Income


$     419  -  443

Adjustments



Investment and other income


(23)  -  (23)

Interest expense


18  -  18

Income tax


100  -  105

Depreciation and amortization


82  -  82

EBITDA


595  -  625

Adjustments


Adjusted EBITDA


$     595  -  625




GAAP Diluted EPS


$   3.22  -  3.40

Adjustments



Share-based compensation


0.32  -  0.35

Amortization of debt discount


0.06  -  0.06

Amortization of intangible assets


0.55  -  0.55

Income tax effect of above adjustments(1)


(0.15)  -  (0.16)

Non-GAAP Diluted EPS


$    4.00  -  4.20




GAAP Diluted Shares


129.8  -  130.4

Adjustments



Adjustment for dilutive impact of senior 2028 Convertible Notes(2)


(0.4)  -  (0.4)

Non-GAAP Diluted Shares


129.4  -  130.0


Note:  Dollar amounts, as presented, are rounded. Consequently, totals may not add up.



(1)

Adjustments relate to taxes for the reconciling items, as well as excess benefits or tax deficiencies from stock-based compensation, and the quarterly impact of other discrete items.

(2)

Adjustment made for the dilutive effect of our Convertible Senior Notes due 2028 when the effect is not the same on a GAAP and non-GAAP basis for the reporting period.

 

Halozyme Therapeutics, Inc. Logo. (PRNewsFoto/Halozyme Therapeutics, Inc.) (PRNewsfoto/Halozyme Therapeutics, Inc.)

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SOURCE Halozyme Therapeutics, Inc.

FAQ

What is Halozyme's (HALO) projected revenue growth for 2025?

Halozyme projects total revenue growth of 16-23% for 2025, reaching $1,150-$1,225 million.

How much is Halozyme's (HALO) new share repurchase program worth?

Halozyme announced a new $250 million accelerated share repurchase program under its existing $750 million share repurchase program.

What is driving Halozyme's (HALO) growth in 2025?

Growth is primarily driven by VYVGART Hytrulo's acceptance in myasthenia gravis and CIDP, along with continued growth of Darzalex SC and Phesgo.

What is Halozyme's (HALO) expected royalty revenue growth for 2025?

Halozyme expects royalty revenue to grow 30-35% in 2025, reaching $725-750 million.

What is Halozyme's (HALO) projected EPS guidance for 2025?

Halozyme projects non-GAAP diluted EPS of $4.95-$5.35 for 2025, representing 21-30% growth.

Halozyme Therapeutics, Inc.

NASDAQ:HALO

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7.28B
125.89M
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101.82%
7.39%
Biotechnology
Biological Products, (no Disgnostic Substances)
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United States
SAN DIEGO