[Ad hoc announcement pursuant to Art. 53 LR] Roche continues strong momentum with 7% growth (CER) in the first half of 2025
Roche (OTCQX:RHHBY) reported strong H1 2025 results with 7% Group sales growth (CER) to CHF 30.9 billion. The Pharmaceuticals Division led growth with a 10% increase to CHF 24.0 billion, driven by key medicines including Phesgo, Xolair, Hemlibra, Vabysmo, and Ocrevus. The Diagnostics Division remained stable despite China pricing reforms.
Core operating profit rose 11% to CHF 12.0 billion, with core EPS up 12% and IFRS net income increasing 23%. Notable regulatory achievements included US approval for Susvimo, EU approvals for Itovebi and Evrysdi, and advancement of key molecules into phase III trials. The company confirmed its 2025 outlook, expecting mid-single-digit sales growth and high-single-digit core EPS growth.
Roche (OTCQX:RHHBY) ha riportato risultati solidi per il primo semestre 2025 con una crescita delle vendite del Gruppo del 7% (CER), raggiungendo 30,9 miliardi di CHF. La Divisione Farmaceutica ha guidato la crescita con un incremento del 10% a 24,0 miliardi di CHF, trainata da farmaci chiave come Phesgo, Xolair, Hemlibra, Vabysmo e Ocrevus. La Divisione Diagnostica è rimasta stabile nonostante le riforme dei prezzi in Cina.
Il profitto operativo core è aumentato dell�11% a 12,0 miliardi di CHF, con un utile per azione core in crescita del 12% e un utile netto IFRS in aumento del 23%. Tra i risultati regolatori degni di nota figurano l’approvazione negli USA per Susvimo, le approvazioni UE per Itovebi ed Evrysdi, e il progresso di molecole chiave nelle sperimentazioni di fase III. L’azienda ha confermato le previsioni per il 2025, prevedendo una crescita delle vendite a una cifra media e una crescita dell’utile per azione core a una cifra alta.
Roche (OTCQX:RHHBY) reportó sólidos resultados en el primer semestre de 2025 con un crecimiento del 7% en ventas del Grupo (CER) hasta 30.9 mil millones de CHF. La División Farmacéutica lideró el crecimiento con un aumento del 10% a 24.0 mil millones de CHF, impulsado por medicamentos clave como Phesgo, Xolair, Hemlibra, Vabysmo y Ocrevus. La División de Diagnósticos se mantuvo estable a pesar de las reformas de precios en China.
El beneficio operativo básico aumentó un 11% hasta 12.0 mil millones de CHF, con una ganancia por acción básica que creció un 12% y un ingreso neto IFRS que subió un 23%. Entre los logros regulatorios destacados están la aprobación en EE. UU. de Susvimo, las aprobaciones en la UE para Itovebi y Evrysdi, y el avance de moléculas clave en ensayos de fase III. La compañía confirmó sus perspectivas para 2025, esperando un crecimiento de ventas de un dígito medio y un crecimiento alto de un dígito en la ganancia por acción básica.
롵ӊ(հϳ:)� 2025� 상반기에 7%� 그룹 매출 성장(CER)� 기록하며 309� 스위� 프랑� 견고� 실적� 보고했습니다. 제약 부�은 페스�, 졸레�, 헴리브라, 바비스모, 오크레버� � 주요 의약품의 견인으로 10% 증가� 240� 스위� 프랑� 달성하며 성장� 주도했습니다. 진단 부�은 중국� 가� 개혁에도 불구하고 안정적인 실적� 유지했습니다.
핵심 영업이익은 11% 증가� 120� 스위� 프랑� 기록했으�, 핵심 주당순이익은 12% 상승했고 IFRS 순이익은 23% 증가했습니다. 주요 규제 성과로는 미국에서� 서스비모 승인, EU에서� 이토베비 � 에브리스� 승인, 그리� 주요 분자� 3� 임상 진전� 포함됩니�. 회사� 2025� 전망� 유지하며 중간 수준� � 자릿� 매출 성장� 높은 � 자릿� 핵심 주당순이� 성장� 기대하고 있습니다.
Roche (OTCQX:RHHBY) a publié de solides résultats pour le premier semestre 2025 avec une croissance des ventes du Groupe de 7% (CER) atteignant 30,9 milliards de CHF. La division Pharmaceutique a porté la croissance avec une augmentation de 10% à 24,0 milliards de CHF, soutenue par des médicaments clés tels que Phesgo, Xolair, Hemlibra, Vabysmo et Ocrevus. La division Diagnostics est restée stable malgré les réformes tarifaires en Chine.
Le bénéfice opérationnel de base a augmenté de 11% pour atteindre 12,0 milliards de CHF, le BPA de base a progressé de 12% et le résultat net IFRS a augmenté de 23%. Parmi les réalisations réglementaires notables figurent l’approbation américaine de Susvimo, les approbations européennes d’Itovebi et d’Evrysdi, ainsi que l’avancement de molécules clés en essais de phase III. La société a confirmé ses prévisions pour 2025, anticipant une croissance des ventes à un chiffre moyen et une croissance du BPA de base à un chiffre élevé.
Roche (OTCQX:RHHBY) meldete starke Ergebnisse für das erste Halbjahr 2025 mit einem 7%igen Wachstum des Konzernumsatzes (CER) auf 30,9 Milliarden CHF. Die Pharma-Sparte führte das Wachstum mit einem Anstieg von 10% auf 24,0 Milliarden CHF an, getrieben von wichtigen Medikamenten wie Phesgo, Xolair, Hemlibra, Vabysmo und Ocrevus. Die Diagnostik-Sparte blieb trotz Preisanpassungen in China stabil.
Das bereinigte Betriebsergebnis stieg um 11% auf 12,0 Milliarden CHF, das bereinigte Ergebnis je Aktie um 12% und der IFRS-Nettogewinn um 23%. Bedeutende regulatorische Erfolge waren die Zulassung von Susvimo in den USA, die Zulassungen von Itovebi und Evrysdi in der EU sowie der Fortschritt wichtiger Moleküle in Phase-III-Studien. Das Unternehmen bestätigte seine Prognose für 2025 und erwartet ein Umsatzwachstum im mittleren einstelligen Bereich sowie ein bereinigtes Ergebnis je Aktie im hohen einstelligen Bereich.
- None.
- Diagnostics Division sales remained flat (0% CER, -3% CHF)
- Asia-Pacific diagnostics sales decreased 15% due to China pricing reforms
- Swiss franc appreciation negatively impacted results in CHF terms
- Continued sales decline in loss of exclusivity (LOE) products
Basel, 24 July 2025
- Group sales grew by
7% 1 at constant exchange rates (CER;4% in CHF), driven by strong demand for medicines. - Pharmaceuticals Division sales rose by
10% (6% in CHF), with Phesgo (breast cancer), Xolair (food allergies), Hemlibra (haemophilia A), Vabysmo (severe eye diseases) and Ocrevus (multiple sclerosis) being the top growth drivers. - Diagnostics Division sales were stable (-
3% in CHF) as strong demand for pathology solutions and blood screening tests offset the impact of healthcare pricing reforms in China. - Core operating profit increased by
11% (6% in CHF), driven by higher sales and effective cost management. - Core earnings per share showed significant growth of
12% (8% in CHF); IFRS net income jumped by23% (17% in CHF). - Outlook for 2025 confirmed.
- Highlights:
- US approval for Susvimo for diabetic retinopathy, a potentially blinding eye disease
- EU approval for Itovebi for a type of advanced breast cancer and Evrysdi tablet for spinal muscular atrophy
- CHMP recommendation for EU label update for Phesgo for breast cancer to allow at-home administration
- Advancement of key molecules into phase III development: prasinezumab for early-stage Parkinsonߴs disease and zosurabalpin for life-threatening bacterial infections
- Positive data on several therapies: Lunsumio and Polivy combination and Columvi for blood cancer, Tecentriq for lung cancer, Itovebi and Perjeta for breast cancer and fenebrutinib for multiple sclerosis and NXT007 for haemophiliaA
- Introduction of innovative Elecsys PRO-C3 test to improve precision in evaluating liver fibrosis severity
- Announcement of new collaboration with Broad Clinical Labs to accelerate adoption of cutting-edge SBX sequencing technology
- US approval for VENTANA MET (SP44) RxDx Assay as the first companion diagnostic to identify a form of lung cancer in patients eligible for targeted treatment
- US Breakthrough Device Designation for first AI-driven companion diagnostic for non-small cell lung cancer
Outlook for 2025 confirmed
Roche (SIX: RO, ROG; OTCQX: RHHBY) expects an increase in Group sales in the mid single digit range (CER). Core earnings per share are targeted to develop in the high single digit range (CER). Roche expects to further increase its dividend in Swiss francs.
Key figures | CHF millions | % change | ||
Գܲ–JܲԱ | 2025 | 2024 | At CER1 | In CHF |
Group sales | 30,944 | 29,848 | 7 | 4 |
Pharmaceuticals Division | 23,985 | 22,637 | 10 | 6 |
Diagnostics Division | 6,959 | 7,211 | 0 | -3 |
Core operating profit | 12,010 | 11,293 | 11 | 6 |
Core EPS � diluted (CHF) | 11.08 | 10.23 | 12 | 8 |
IFRS net income | 7,832 | 6,697 | 23 | 17 |
Roche CEO Thomas Schinecker: “Roche’s strong growth momentum continued in the second quarter, driven by the strong growth of
We received numerous important approvals and reported positive data in disease areas with high unmet medical need.
Over the past six months, we have made significant progress in our pipeline and advanced four potentially practice-changing therapies into the final phase of clinical development, based on encouraging data: NXT007 in haemophilia A, trontinemab in Alzheimer’s disease, prasinezumab in early-stage Parkinson’s disease, and zosurabalpin, a novel antibiotic that could become the first in over 50 years to tackle a type of bacteria that has become resistant to most other treatments.
We are confident in our continued strong momentum and resilience of our business due to our innovative on-market portfolio and pipeline.
Based on these strong results, we confirm our full-year outlook.�
Group results
In the first half of 2025, Roche achieved sales growth of
Core operating profit increased by
The appreciation of the Swiss franc against most currencies, notably the US dollar, had an adverse impact on the results when reported in Swiss francs compared to constant exchange rates.
Core earnings per share increased by
IFRS net income increased by
Sales in the Pharmaceuticals Division increased by
The top five growth drivers � Phesgo, Xolair, Hemlibra, Vabysmo and Ocrevus � achieved total sales of CHF 10.6 billion. This represents an increase of CHF 1.7 billion at CER compared to the first half of 2024.
This more than compensated for the total decrease of CHF 0.3 billion (CER) in sales of the ‘loss of exclusivity (LOE)� products � the decline in sales of Avastin (various types of cancer), Herceptin (breast and gastric cancer), MabThera/Rituxan (blood cancer, rheumatoid arthritis), Lucentis (severe eye diseases) and Esbriet (lung disease) was partially offset by an increase in sales of Actemra/RoActemra (rheumatoid arthritis).
In the United States, sales rose by
Sales in Europe grew
In Japan, sales increased by
Sales in the International region grew by
The Diagnostics Division’s sales remained stable (-
Sales in the Europe, Middle East and Africa (EMEA) region increased by
Pharmaceuticals: key developments
Compound | Milestone |
Regulatory | |
Itovebi Breast cancer | European Commission approves Itovebi for people with ER-positive, HER2-negative, advanced breast cancer with a PIK3CA mutation
More information: , 23 July 2025 |
Evrysdi Spinal muscular atrophy | Evrysdi tablet approved by European Commission as first and only tablet for spinal muscular atrophy (SMA)
More information: , 4 June 2025 |
Susvimo Severe eye diseases | FDA approves Susvimo for diabetic retinopathy
More information: , 22 May 2025 |
Columvi Blood cancer | Update on FDA Advisory Committee meeting on Columvi combination for people with relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL)
More information: , 20 May 2025 |
Pharmaceuticals sales
Sales | CHF millions | As % of sales | % change | |||
Գܲ–JܲԱ | 2025 | 2024 | 2025 | 2024 | At CER | In CHF |
Pharmaceuticals Division | 23,985 | 22,637 | 100.0 | 100.0 | 10 | 6 |
United States | 12,670 | 11,882 | 52.8 | 52.5 | 10 | 7 |
Europe | 4,566 | 4,425 | 19.0 | 19.5 | 5 | 3 |
Japan | 1,425 | 1,366 | 5.9 | 6.0 | 5 | 4 |
International | 5,324 | 4,964 | 22.3 | 22.0 | 14 | 7 |
International: Asia-Pacific, CEETRIS (Central Eastern Europe, Türkiye, Russia and Indian subcontinent), Latin America, Middle East, Africa, Canada, others
Top 20 best-selling pharmaceuticals | Total | United States | Europe | Japan | International | |||||
CHF m | % | CHF m | % | CHF m | % | CHF m | % | CHF m | % | |
Ocrevus Multiple sclerosis | 3,506 | 8 | 2,462 | 5 | 706 | 12 | - | - | 338 | 19 |
Hemlibra Haemophilia A | 2,421 | 17 | 1,324 | 11 | 493 | 7 | 183 | 8 | 421 | 66 |
Vabysmo Eye diseases (nAMD, DME, RVO) | 2,067 | 18 | 1,450 | 9 | 378 | 33 | 70 | 31 | 169 | 118 |
Tecentriq Cancer immunotherapy | 1,733 | -1 | 819 | -6 | 434 | 3 | 174 | -4 | 306 | 13 |
Perjeta2 Breast cancer | 1,613 | -12 | 677 | 1 | 282 | -16 | 37 | -44 | 617 | -18 |
Xolair2 Asthma, food allergies | 1,445 | 34 | 1,445 | 34 | - | - | - | - | - | - |
Actemra/RoActemra2 RA, COVID-19 | 1,279 | 4 | 619 | 7 | 308 | -14 | 152 | 5 | 200 | 26 |
Phesgo Breast cancer | 1,197 | 55 | 348 | 39 | 401 | 15 | 90 | 80 | 358 | 182 |
Kadcyla2 Breast cancer | 1,037 | 9 | 396 | 7 | 266 | -6 | 45 | -2 | 330 | 28 |
Evrysdi Spinal muscular atrophy | 869 | 7 | 309 | 12 | 292 | 4 | 46 | 5 | 222 | 5 |
Alecensa Lung cancer | 802 | 8 | 276 | 20 | 133 | -7 | 100 | 5 | 293 | 7 |
Polivy Blood cancer | 730 | 46 | 327 | 32 | 160 | 90 | 99 | 8 | 144 | 88 |
MabThera/Rituxan2 Blood cancer, RA | 630 | -8 | 387 | -6 | 70 | -8 | 7 | -14 | 166 | -11 |
Herceptin2 Breast and gastric cancer | 560 | -21 | 121 | -10 | 150 | -1 | 4 | -51 | 285 | -32 |
Activase/TNKase2 Cardiac diseases | 550 | -4 | 527 | -3 | - | - | - | - | 23 | -25 |
Avastin2 Various cancer types | 522 | -17 | 156 | -20 | 26 | -40 | 76 | -25 | 264 | -9 |
Gazyva/Gazyvaro2 Blood cancer | 490 | 14 | 253 | 20 | 121 | 1 | 17 | 20 | 99 | 14 |
Pulmozyme2 Cystic fibrosis | 239 | 11 | 167 | 22 | 34 | -12 | - | -18 | 38 | -3 |
CellCept2 Immunosuppressant | 196 | 2 | 9 | -17 | 65 | 12 | 24 | 35 | 98 | -6 |
Madopar2 Parkinson’s disease | 193 | 1 | - | - | 46 | -5 | - | - | 147 | 4 |
DME: diabetic macular edema / nAMD: neovascular or ‘wet� age-related macular degeneration / RVO: retinal vein occlusion / RA: rheumatoid arthritis
Diagnostics: key developments
Product | Milestone |
SBX sequencing technology Genetic disorders | Roche announces new collaboration with Broad Clinical Labs to accelerate adoption of cutting-edge SBX sequencing technology
More information: , 23 May 2025 |
VENTANA MET (SP44) RxDx Assay Lung cancer | FDA approves VENTANA MET (SP44) RxDx Assay as the first companion diagnostic to identify non-squamous non-small cell lung cancer patients eligible for targeted treatment
More information: , 14 May 2025 |
Elecsys PRO-C3 test Liver fibrosis | Roche introduces the innovative Elecsys PRO-C3 test to improve precision in evaluating liver fibrosis severity
More information: , 6 May 2025 |
VENTANA TROP2 (EPR20043) RxDx device Lung cancer | FDA grants Roche Breakthrough Device Designation for the first AI-driven companion diagnostic for non-small cell lung cancer
More information: , 29 April 2025 |
Chest pain triage algorithm Acute coronary syndrome | Roche receives CE mark for its chest pain triage algorithm to enhance detection of acute coronary syndrome
More information: , 23 April 2025 |
Phesgo Breast cancer | CHMP recommends EU label update for Phesgo to allow administration outside clinical settings
More information: , 30 April 2025 |
Phase III, pivotal and other key read-outs | |
Astegolimab Chronic obstructive pulmonary disease (COPD) | Roche provides update on astegolimab in chronic obstructive pulmonary disease
More information: , 21 July 2025 |
NXT007 Haemophilia A | Early data suggest NXT007 may have the potential to provide haemostatic normalisation in people with haemophilia A
More information: , 23 June 2025 |
Lunsumio and Polivy Blood cancer | Lunsumio and Polivy combination significantly prolongs remission for people with relapsed or refractory large B-cell lymphoma
More information: , 20 June 2025 |
Prasinezumab Parkinson’s disease | Roche to advance prasinezumab into phase III development for early-stage Parkinson’s disease
More information: , 16 June 2025 |
Tecentriq Lung cancer | Tecentriq combined with lurbinectedin shows significant survival benefit in extensive-stage small cell lung cancer (ES-SCLC)
More information: , 3 June 2025 |
Itovebi Breast cancer | New data show Itovebi significantly extended survival in a certain type of HR-positive advanced breast cancer
More information: , 31 May 2025 |
Fenebrutinib Multiple sclerosis | Fenebrutinib maintains near-complete suppression of disease activity and disability progression for up to two years in people with relapsing multiple sclerosis
More information: , 30 May 2025 |
Columvi Blood cancer | New two-year follow-up data show Columvi extends overall survival in relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL) patients
More information: , 23 May 2025 |
Perjeta Breast cancer | Ten-year APHINITY data show regimen based on Perjeta reduced the risk of death by
More information: , 13 May 2025 |
Other | |
Executive changes | Changes to the Roche Enlarged Corporate Executive Committee
More information: , 30 June 2025 |
Elevidys Duchenne muscular dystrophy | Roche provides safety update on Elevidys gene therapy for Duchenne muscular dystrophy in non-ambulatory patients
More information: , 15 June 2025 |
Xofluza Influenza | The New England Journal of Medicine publishes phase III data showing single-dose Xofluza significantly reduces influenza virus transmission
More information: , 25 April 2025 |
Diagnostics sales
Sales | CHF millions | As % of sales | % change | |||
Գܲ–JܲԱ | 2025 | 2024 | 2025 | 2024 | At CER | In CHF |
Diagnostics Division | 6,959 | 7,211 | 100.0 | 100.0 | 0 | -3 |
Customer areas3 | ||||||
Core Lab | 3,839 | 4,072 | 55.2 | 56.5 | -2 | -6 |
Molecular Lab | 1,250 | 1,257 | 18.0 | 17.4 | 3 | -1 |
Near Patient Care | 1,018 | 1,094 | 14.6 | 15.2 | -3 | -7 |
Pathology Lab | 852 | 788 | 12.2 | 10.9 | 12 | 8 |
Regions | ||||||
Europe, Middle East, Africa | 2,485 | 2,431 | 35.7 | 33.7 | 5 | 2 |
North America | 2,235 | 2,163 | 32.1 | 30.0 | 6 | 3 |
Asia-Pacific | 1,729 | 2,102 | 24.9 | 29.2 | -15 | -18 |
Latin America | 510 | 515 | 7.3 | 7.1 | 14 | -1 |
More information on Roche performance in the first half of 2025:
About Roche
Founded in 1896 in Basel, Switzerland, as one of the first industrial manufacturers of branded medicines, Roche has grown into the world’s largest biotechnology company and the global leader in in-vitro diagnostics. The company pursues scientific excellence to discover and develop medicines and diagnostics for improving and saving the lives of people around the world. We are a pioneer in personalised healthcare and want to further transform how healthcare is delivered to have an even greater impact. To provide the best care for each person we partner with many stakeholders and combine our strengths in Diagnostics and Pharma with data insights from the clinical practice.
For over 125 years, sustainability has been an integral part of Roche’s business. As a science-driven company, our greatest contribution to society is developing innovative medicines and diagnostics that help people live healthier lives. Roche is committed to the Science Based Targets initiative and the Sustainable Markets Initiative to achieve net zero by 2045.
Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan.
For more information, please visit .
All trademarks used or mentioned in this release are protected by law.
References
[1] Unless otherwise stated, all growth rates and comparisons to the previous year in this document are at constant exchange rates (CER: average rates 2024) and all total figures quoted are reported in CHF.
[2] Products launched before 2015.
[3] Core Lab: diagnostics solutions in the areas of immunoassays, clinical chemistry and CustomBiotech.
Molecular Lab: diagnostics solutions for pathogen detection and monitoring, donor screening, sexual health and genomics, genomic tumour profiling.
Near Patient Care: diagnostics solutions in emergency rooms, medical practices and directly with patients, including integrated personalised diabetes management.
Pathology Lab: diagnostics solutions for tissue biopsies and companion diagnostics.
In 2025, sales in the Pathology Lab customer area include sales previously reported in the Molecular Lab customer area to foster business transparency and harmonisation in the use of solutions in the area of cervical intraepithelial neoplasia technology (CINtec). The comparative information for 2024 has been restated accordingly.
In 2025, sales in the Core Lab customer area include sales previously reported in the Near Patient Care customer area to centralise digital healthcare solutions within Roche Information Solutions. The comparative information for 2024 has been restated accordingly
Cautionary statement regarding forward-looking statements
This document contains certain forward-looking statements. These forward-looking statements may be identified by words such as ‘believes�, ‘expects�, ‘anticipates�, ‘projects�, ‘intends�, ‘should�, ‘seeks�, ‘estimates�, ‘future� or similar expressions or by discussion of, among other things, strategy, goals, plans or intentions. Various factors may cause actual results to differ materially in the future from those reflected in forward-looking statements contained in this document, such as: (1) pricing and product initiatives of competitors; (2) legislative and regulatory developments and economic conditions; (3) delay or inability in obtaining regulatory approvals or bringing products to market; (4) fluctuations in currency exchange rates and general financial market conditions; (5) uncertainties in the discovery, development or marketing of new products or new uses of existing products, including without limitation negative results of clinical trials or research projects, unexpected side effects of pipeline or marketed products; (6) increased government pricing pressures; (7) interruptions in production; (8) loss of or inability to obtain adequate protection for intellectual property rights; (9) litigation; (10) loss of key executives or other employees; and (11) adverse publicity and news coverage. The statement regarding earnings per share growth is not a profit forecast and should not be interpreted to mean that Roche’s earnings or earnings per share for this or any subsequent period will necessarily match or exceed the historical published earnings or earnings per share of Roche.
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