OPKO Health Reports First Quarter 2025 Business Highlights and Financial Results
OPKO Health reports Q1 2025 financial results with key developments in its business portfolio. The company signed a definitive agreement to sell BioReference's oncology testing assets to Labcorp for up to $225 million. OPKO partnered with Entera Bio to develop an oral GLP-1/glucagon tablet for obesity treatment, with OPKO holding a 60% stake.
Financial highlights include consolidated revenues of $149.9 million, down from $173.7 million in Q1 2024. The company posted a net loss of $67.6 million ($0.10 per share), improving from $81.8 million ($0.12 per share) year-over-year.
Notable progress includes Merck's Phase 1 trial of an Epstein-Barr virus vaccine and ModeX's advancement of four clinical candidates. The Board authorized an additional $100 million for stock repurchase, bringing total capacity to $200 million. Cash position stands strong at $449.7 million as of March 31, 2025.
OPKO Health presenta i risultati finanziari del primo trimestre 2025 con sviluppi chiave nel suo portafoglio aziendale. La società ha firmato un accordo definitivo per la vendita degli asset di test oncologici di BioReference a Labcorp per un massimo di 225 milioni di dollari. OPKO ha collaborato con Entera Bio per sviluppare una compressa orale di GLP-1/glucagone per il trattamento dell'obesità, detenendo una quota del 60%.
I dati finanziari mostrano ricavi consolidati di 149,9 milioni di dollari, in calo rispetto ai 173,7 milioni del primo trimestre 2024. La società ha registrato una perdita netta di 67,6 milioni di dollari (0,10 dollari per azione), migliorando rispetto agli 81,8 milioni (0,12 dollari per azione) dell'anno precedente.
Tra i progressi rilevanti, il trial di Fase 1 di Merck per un vaccino contro il virus di Epstein-Barr e l'avanzamento di quattro candidati clinici da parte di ModeX. Il Consiglio di Amministrazione ha autorizzato un ulteriore riacquisto di azioni per 100 milioni di dollari, portando la capacità totale a 200 milioni. La posizione di cassa è solida, con 449,7 milioni di dollari al 31 marzo 2025.
OPKO Health informa los resultados financieros del primer trimestre de 2025 con desarrollos clave en su cartera de negocios. La compañía firmó un acuerdo definitivo para vender los activos de pruebas oncológicas de BioReference a Labcorp por hasta 225 millones de dólares. OPKO se asoció con Entera Bio para desarrollar una tableta oral de GLP-1/glucagón para el tratamiento de la obesidad, con OPKO manteniendo una participación del 60%.
Los aspectos financieros incluyen ingresos consolidados de 149,9 millones de dólares, una disminución respecto a los 173,7 millones del primer trimestre de 2024. La compañía registró una pérdida neta de 67,6 millones de dólares (0,10 dólares por acción), mejorando desde los 81,8 millones (0,12 dólares por acción) año tras año.
Progresos destacados incluyen el ensayo de Fase 1 de Merck para una vacuna contra el virus de Epstein-Barr y el avance de cuatro candidatos clínicos de ModeX. La Junta autorizó una recompra adicional de acciones por 100 millones de dólares, elevando la capacidad total a 200 millones. La posición de efectivo se mantiene sólida con 449,7 millones de dólares al 31 de marzo de 2025.
OPKO Health가 2025년 1분기 재무 실적과 사업 포트폴리오의 주요 발전 사항을 보고했습니다. 회사는 BioReference의 종양 검사 자산을 Labcorp에 최대 2억 2,500만 달러에 매각하는 최종 계약을 체결했습니다. OPKO는 Entera Bio와 협력하여 비만 치료를 위한 경구용 GLP-1/글루카곤 정제를 개발 중이며, OPKO가 60% 지분을 보유하고 있습니다.
재무 하이라이트로는 2024년 1분기 1억 7,370만 달러에서 감소한 1억 4,990만 달러의 통합 매출을 기록했습니다. 순손실은 6,760만 달러(주당 0.10달러)로, 전년 동기 8,180만 달러(주당 0.12달러) 대비 개선되었습니다.
주목할 만한 진전으로는 머크의 1상 에프스타인-바 바이러스 백신 임상시험과 ModeX의 네 개 임상 후보물질 진전이 포함됩니다. 이사회는 주식 재매입을 위해 추가 1억 달러를 승인하여 총 재매입 한도를 2억 달러로 늘렸습니다. 2025년 3월 31일 기준 현금 보유액은 4억 4,970만 달러로 견고한 상태입니다.
OPKO Health publie ses résultats financiers du premier trimestre 2025 avec des développements clés dans son portefeuille d’activités. La société a signé un accord définitif pour vendre les actifs de tests oncologiques de BioReference à Labcorp pour un montant pouvant atteindre 225 millions de dollars. OPKO s’est associé à Entera Bio pour développer un comprimé oral GLP-1/glucagon pour le traitement de l’obésité, détenant une participation de 60 %.
Les points financiers majeurs incluent des revenus consolidés de 149,9 millions de dollars, en baisse par rapport à 173,7 millions au premier trimestre 2024. La société a enregistré une perte nette de 67,6 millions de dollars (0,10 dollar par action), une amélioration par rapport à 81,8 millions (0,12 dollar par action) d’une année sur l’autre.
Les progrès notables comprennent l’essai de phase 1 de Merck pour un vaccin contre le virus Epstein-Barr et l’avancement de quatre candidats cliniques par ModeX. Le conseil d’administration a autorisé un rachat d’actions supplémentaire de 100 millions de dollars, portant la capacité totale à 200 millions. La trésorerie reste solide à 449,7 millions de dollars au 31 mars 2025.
OPKO Health berichtet über die Finanzergebnisse des ersten Quartals 2025 mit wichtigen Entwicklungen im Geschäftsportfolio. Das Unternehmen unterzeichnete eine endgültige Vereinbarung zum Verkauf der Onkologie-Test-Assets von BioReference an Labcorp für bis zu 225 Millionen US-Dollar. OPKO ging eine Partnerschaft mit Entera Bio ein, um eine orale GLP-1/Glucagon-Tablette zur Behandlung von Adipositas zu entwickeln, wobei OPKO einen Anteil von 60 % hält.
Finanzielle Highlights umfassen konsolidierte Umsätze von 149,9 Millionen US-Dollar, ein Rückgang von 173,7 Millionen US-Dollar im ersten Quartal 2024. Das Unternehmen verzeichnete einen Nettoverlust von 67,6 Millionen US-Dollar (0,10 US-Dollar pro Aktie), eine Verbesserung gegenüber 81,8 Millionen US-Dollar (0,12 US-Dollar pro Aktie) im Vorjahresvergleich.
Bemerkenswerte Fortschritte umfassen Mercks Phase-1-Studie eines Epstein-Barr-Virus-Impfstoffs und ModeX’ Fortschritte bei vier klinischen Kandidaten. Der Vorstand genehmigte eine zusätzliche Aktienrückkaufmaßnahme von 100 Millionen US-Dollar, wodurch die Gesamtkapazität auf 200 Millionen US-Dollar steigt. Die Barposition ist mit 449,7 Millionen US-Dollar zum 31. März 2025 solide.
- Sale of BioReference oncology assets to Labcorp for up to $225M, with $192.5M at closing
- Strategic collaboration with Entera Bio for oral GLP-1/glucagon tablet development with 60% ownership
- Phase 1 EBV vaccine trial with Merck triggered milestone payment
- Board authorized additional $100M for stock repurchase, total $200M (14% of shares)
- BARDA contract revenue increased to $7.0M from $2.2M YoY
- Higher clinical test reimbursement rates in diagnostics segment
- Strong cash position of $449.7M as of March 31, 2025
- Q1 2025 consolidated revenues declined to $149.9M from $173.7M YoY
- Operating loss of $67.2M in Q1 2025
- Net loss of $67.6M ($0.10 per share) in Q1 2025
- Product revenue decreased to $34.8M from $38.1M YoY
- Rayaldee sales declined to $6.3M from $6.9M YoY
- NGENLA profit share payments decreased to $4.5M from $5.6M YoY
- Diagnostics revenue dropped to $102.8M from $126.9M YoY
- Convertible notes exchange resulted in significant share dilution (121.4M new shares)
Insights
OPKO's asset sale to Labcorp and narrowing losses show strategic restructuring, but revenue decline continues amid pipeline investments.
OPKO Health's Q1 2025 results present a mixed financial picture with strategic moves to reshape operations. The
While total revenue declined to
The Board's authorization of an additional
OPKO advances multiple clinical assets with strategic collaboration in high-value GLP-1 space and progress in oncology/vaccine programs.
OPKO's pipeline is showing meaningful progression across multiple therapeutic areas. The collaboration with Entera Bio to develop an oral GLP-1/glucagon tablet for obesity represents a strategic entry into one of pharma's most competitive and lucrative therapeutic spaces. The 60/40 ownership structure favors OPKO, who also made a
The Merck-partnered Epstein-Barr virus (EBV) vaccine trial has commenced patient dosing in a Phase 1 study evaluating safety and tolerability in up to 200 healthy adults. This triggered a milestone payment to OPKO's ModeX division and validates their ferritin nanoparticle vaccine platform technology.
In immuno-oncology, the lead MDX2001 tetraspecific antibody targeting CMet-Trop2/CD3-CD28 has advanced to the fourth dose level in Phase 1, with Phase 1B studies in targeted solid tumors planned for early 2026. Three additional clinical candidates are approaching human trials in 2025-2026, including the MDX2003 tetraspecific for lymphoma/leukemia and MDX2004 immune rejuvenator.
The BARDA-supported development of multispecific antibodies for COVID and influenza continues to progress, generating
Conference call begins at 4:30 p.m. Eastern time today
MIAMI, April 30, 2025 (GLOBE NEWSWIRE) -- OPKO Health, Inc. (NASDAQ: OPK) reports business highlights and financial results for the three months ended March 31, 2025.
Highlights from the first quarter of 2025 and recent weeks include the following:
- Signed definitive agreement with Labcorp to sell oncology and related clinical testing assets of BioReference Health (BioReference). The transaction includes the sale of BioReference’s laboratory testing businesses focused on oncology and oncology-related clinical testing services for up to
$225 million , including$192.5 million payable at closing and up to$32.5 million in an earnout based on performance. BioReference will continue to offer urology diagnostic services nationwide, as well as maintain its core clinical testing operations in New York and New Jersey, which represented approximately$300 million in revenue for 2024. The transaction is anticipated to close in the second half of 2025. - Entered into collaboration agreement with Entera Bio to advance oral GLP-1/glucagon tablet candidate into the clinic to treat obesity and metabolic disorders. This program combines OPKO’s proprietary long-acting oxyntomodulin analog (OPK-88006) and Entera’s proprietary N-Tab™ technology. Under the terms of the agreement, OPKO and Entera will hold
60% and40% ownership interests, respectively, in the orally administered product and will be responsible for60% and40% , respectively, of the program’s development costs. In connection with the execution of the agreement, OPKO purchased approximately 3.7 million ordinary shares of Entera for a purchase price equal to$2.17 per share. Entera agreed to utilize the proceeds from this share purchase to fund its40% share of the program's development costs through the completion of Phase 1. - Enrollment and dosing underway by Merck in the Phase 1 Epstein-Barr virus (EBV) vaccine trial. Dosing of patients commenced for the Phase 1 study (NCT06655324) of an EBV vaccine candidate being developed in collaboration with Merck. The investigational vaccine, based on ModeX’s ferritin nanoparticle vaccine platform, is being evaluated for safety and tolerability in up to 200 healthy adults. Commencement of this study triggered a milestone payment to ModeX.
- ModeX continued to advance its immuno-oncology and immunology portfolio with four potential clinical candidates progressing in the pipeline. The MDX2001 CMet-Trop2/CD3-CD28 tetraspecific antibody advanced to the fourth dose level in its Phase 1 clinical trial, with Phase 1B studies in selected solid tumors expected in early 2026. The MDX2003 tetraspecific antibody for lymphoma/leukemia and the MDX2004 immune rejuvenator are expected to begin human trials in late 2025/early 2026. Development of multispecific antibodies for immune impaired patients at risk for COVID and influenza A and B continues to progress with support from the Biomedical Advanced Research and Development Authority (BARDA).
- OPKO’s Board of Directors authorized an additional
$100 million for its common stock repurchase program, bringing total capacity to$200 million . Approximately$40.2 million of OPKO’s common stock has been repurchased under the prior program since its authorization in July 2024. This increased authorization, along with the prior authorization, represents approximately14% of OPKO’s common shares outstanding at the current stock price.
First Quarter Financial Results
- Consolidated: Consolidated total revenues for the first quarter of 2025 were
$149.9 million compared with$173.7 million for the comparable period of 2024. Operating loss for the first quarter of 2025 was$67.2 million compared with$71.5 million for the 2024 quarter. The first quarter of 2025 included a realized gain of$3.9 million from the sale of shares of GeneDx Holdings Corp. (GeneDx) compared with$22.7 million in the year-ago period primarily reflecting an unrealized gain in the fair value of GeneDx. In addition, other expense in the first quarter of 2024 included a non-cash, non-recurring expense of$26.3 million related to an embedded derivative as part of the 2029 convertible debt. Net loss for the first quarter of 2025 was$67.6 million , or$0.10 per share, compared with net loss of$81.8 million , or$0.12 per share, for the 2024 quarter. - Pharmaceuticals: Revenue from products in the first quarter of 2025 was
$34.8 million compared with$38.1 million in the first quarter of 2024, reflecting unfavorable foreign currency exchange rates and a decrease in Rayaldee sales. Revenue from sales of Rayaldee was$6.3 million compared with$6.9 million in the same period in 2024. Revenue from the transfer of intellectual property and other was$12.3 million in the first quarter of 2025 compared with$8.7 million in the 2024 period. This increase was driven by revenue from the BARDA contract of$7.0 million in 2025 compared with$2.2 million in 2024. This increase was partially offset by a decrease in gross profit share payments for NGENLA, which totaled$4.5 million in the 2025 period compared with$5.6 million in the 2024 period. Total costs and expenses increased to$81.9 million in the first quarter of 2025 from$74.5 million in the prior-year period, primarily due to higher research and development expenses related to increased activity within the ModeX development programs. Operating loss was$34.8 million in the first quarter of 2025, which included$17.8 million of depreciation and amortization expense, compared with$27.7 million in the first quarter of 2024, which included$18.0 million of depreciation and amortization expense. - Diagnostics: Revenue from services in the first quarter of 2025 was
$102.8 million compared with$126.9 million in the prior-year period, with the decrease primarily due to lower clinical test volume principally as a result of the sale of certain BioReference assets, partially offset by higher clinical test reimbursement rates. Total costs and expenses were$126.8 million in the first quarter of 2025, which included$7.3 million of non-recurring facility closure and severance costs, compared with$161.3 million in the first quarter of 2024. The decrease was primarily attributable to the assets sold and continued cost-reduction initiatives at BioReference. Operating loss was$23.9 million in the first quarter of 2025 compared with a loss of$34.4 million in the 2024 period. The first quarter of 2025 included revenue of$25.1 million and costs and expenses of$32.4 million from the oncology assets pending sale to Labcorp. Both periods include$5.7 million and$7.9 million of depreciation and amortization expense, respectively, within the operating loss. - Cash, cash equivalents, marketable securities and restricted cash: Cash, cash equivalents and restricted cash were
$449.7 million as of March 31, 2025, including the receipt of$51.7 million from the sale of all of OPKO’s remaining GeneDx shares. Subsequent to the first quarter of 2025, OPKO completed an exchange agreement with certain institutional holders to purchase$159.2 million of the Company’s outstanding convertible notes, including accrued and unpaid interest, for 121.4 million shares and approximately$63.5 million in cash.
Conference Call and Webcast Information
OPKO’s senior management will provide a business update, discuss first quarter financial results, provide financial guidance and answer questions during a conference call and live audio webcast today beginning at 4:30 p.m. Eastern time. Participants are encouraged to pre-register for the conference call here. Callers who pre-register will receive a unique PIN to gain immediate access to the call and bypass the live operator. Participants may register at any time, including up to and after the call start time. Those unable to pre-register may participate by dialing 833-630-0584 (U.S.) or 412-317-1815 (International). A webcast of the call can also be accessed at OPKO’s Investor Relations page and here.
A telephone replay will be available until May 7, 2025, by dialing 877-344-7529 (U.S.) or 412-317-0088 (International) and providing the passcode 3746692. A webcast replay will be available beginning approximately one hour after the completion of the live conference call here.
About OPKO Health
OPKO is a multinational biopharmaceutical and diagnostics company that seeks to establish industry-leading positions in large, rapidly growing markets by leveraging its discovery, development, and commercialization expertise and novel and proprietary technologies. For more information, visit www.opko.com.
Cautionary Statement Regarding Forward Looking Statements
This press release contains "forward-looking statements," as that term is defined under the Private Securities Litigation Reform Act of 1995 (PSLRA), which statements may be identified by words such as "expects," "plans," "projects," "will," "may," "anticipates," "believes," "should," "intends," "estimates," and other words of similar meaning, including statements regarding expected financial performance and expectations regarding the market for and sales of our products, whether the anticipated sale of assets to Labcorp will close and the remaining BioReference business will be successful, whether we will be able to submit an Investigational New Drug application for the oral GLP-1/glucagon and the timing of that submission, in addition to whether we will have a successful collaboration with Entera Bio, whether our product development efforts will be successful and whether the expected benefits of our products will be realized, including the timing for when clinical trials for MDX2003 and MDX 2004 will commence and whether they will be successful, whether the trial for MDX2001 will continue to progress and whether the data will be positive for all trials, including the EBV Vaccine trial, whether we will receive additional funding from BARDA, whether the relationship with our commercial and strategic partners will be successful, whether our commercial and strategic partners will be able to commercialize our products and successfully utilize our technologies, whether our partner will be able to continue to successfully commercialize NGENLA and the NGENLA profits will provide adequate upside, whether we will continue to repurchase shares under a buyback program, our ability to market and sell any of our products in development, whether we will continue to successfully advance products in our pipeline and whether they can be commercialized, as well as other non-historical statements about our expectations, beliefs or intentions regarding our business, technologies and products, financial condition, strategies or prospects. Many factors could cause our actual activities or results to differ materially from the activities and results anticipated in forward-looking statements. These factors include those described in our Annual Reports on Form 10-K filed and to be filed with the Securities and Exchange Commission and under the heading “Risk Factors” in our other filings with the Securities and Exchange Commission, as well as the continuation and success of our relationship with our commercial partners, liquidity issues and the risks inherent in funding, developing and obtaining regulatory approvals of new, commercially-viable and competitive products and treatments. In addition, forward-looking statements may also be adversely affected by general market factors, competitive product development, product availability, federal and state regulations and legislation, the regulatory process for new products and indications, manufacturing issues that may arise, patent positions and litigation, among other factors. The forward-looking statements contained in this press release speak only as of the date the statements were made, and we do not undertake any obligation to update forward-looking statements. We intend that all forward-looking statements be subject to the safe-harbor provisions of the PSLRA.
Contacts:
Alliance Advisors IR
Yvonne Briggs, 310-691-7100
ybriggs@allianceadvisors.com
or
Bruce Voss, 310-691-7100
bvoss@allianceadvisors.com
—Tables to Follow—
OPKO Health, Inc. and Subsidiaries Condensed Consolidated Balance Sheets (in millions) Unaudited | |||||||
As of | |||||||
March 31, 2025 | December 31, 2024 | ||||||
Assets: | |||||||
Cash and cash equivalents | $ | 436.0 | $ | 431.9 | |||
Assets held for sale | 87.0 | 0.0 | |||||
Other current assets | 214.6 | 230.2 | |||||
Total current assets | 737.6 | 662.1 | |||||
In-process research and development and goodwill | 671.7 | 724.3 | |||||
Other assets | 719.1 | 813.8 | |||||
Total Assets | $ | 2,128.4 | $ | 2,200.2 | |||
Liabilities and Equity: | |||||||
Accounts payable | $ | 59.4 | $ | 47.1 | |||
Accrued expenses | 113.2 | 118.4 | |||||
Current portion of convertible notes | 101.2 | 0.2 | |||||
Other current liabilities | 22.1 | 27.4 | |||||
Total current liabilities | 295.9 | 193.1 | |||||
Long-term portion of convertible notes | 77.2 | 173.6 | |||||
Senior secured notes | 245.8 | 245.6 | |||||
Deferred tax liabilities, net | 129.4 | 140.8 | |||||
Other long-term liabilities, principally leases | 68.4 | 81.7 | |||||
Total Liabilities | 816.7 | 834.8 | |||||
Equity | 1,311.7 | 1,365.4 | |||||
Total Liabilities and Equity | $ | 2,128.4 | $ | 2,200.2 |
OPKO Health, Inc. and Subsidiaries Condensed Consolidated Statements of Operations (in millions, except share and per share data) Unaudited | ||||||||
For the three months ended March 31, | ||||||||
2025 | 2024 | |||||||
Revenues | ||||||||
Revenue from services | $ | 102.8 | $ | 126.9 | ||||
Revenue from products | 34.8 | 38.1 | ||||||
Revenue from transfer of intellectual property | 12.3 | 8.7 | ||||||
Total revenues | 149.9 | 173.7 | ||||||
Costs and expenses | ||||||||
Cost of service revenues | 84.5 | 109.9 | ||||||
Cost of product revenues | 22.8 | 21.8 | ||||||
Selling, general and administrative | 59.1 | 70.2 | ||||||
Research and development | 30.8 | 21.9 | ||||||
Amortization of intangible assets | 19.9 | 21.4 | ||||||
Total costs and expenses | 217.1 | 245.2 | ||||||
Operating loss | (67.2 | ) | (71.5 | ) | ||||
Other expense, net | (6.2 | ) | (11.7 | ) | ||||
Loss before income taxes and investment losses | (73.4 | ) | (83.2 | ) | ||||
Income tax benefit | 5.8 | 1.4 | ||||||
Net loss before investment losses | (67.6 | ) | (81.8 | ) | ||||
Loss from investments in investees | (0.0 | ) | (0.0 | ) | ||||
Net loss | $ | (67.6 | ) | $ | (81.8 | ) | ||
Loss per share, basic and diluted | $ | (0.10 | ) | $ | (0.12 | ) | ||
Weighted average common shares outstanding, basic and diluted | 671,577,429 | 706,882,189 |
