• Source : Press Release
  • Date : 2022-02-03
  • Companies : Roche

[Ad Hoc Announcement Pursuant to Art. 53 LR] Roche Reports Good Results in 2021

Basel, 3 February 2022

  • Group sales increase 9%1 at constant exchange rates (CER); 8% in Swiss francs
  • Pharmaceuticals Division sales increase 3%; continued strong demand for newly launched medicines more than offsets impact of biosimilars
  • Diagnostics Division sales grow 29%; strong momentum in base business and continued high demand for COVID-19 tests
  • Major approvals for medicines since the last quarter:
    United States: Susvimo and Vabysmo (age-related blindness)
    Europe: Gavreto (specific type of advanced lung cancer); Actemra/RoActemra (severe COVID-19); Ronapreve (non-hospitalised COVID-19 patients and prophylaxis)
  • Major approvals for diagnostics since the last quarter:
    cobas 5800 (molecular laboratory system); Avenio Edge (sequencing sample preparation system); cobas pulse and cobas infinity edge (digital ecosystem for clinical decision support); additional SARS-CoV-2 tests
  • Promising pipeline: 16 phase III trials initiated, 14 new compounds in phase III trials or filed for approval
  • Repurchase of Roche shares from Novartis completed
  • Core earnings per share (EPS) grow 6% ( 3% in CHF)
  • IFRS net income totals CHF 14.9 billion ( 2%; -1% in CHF)
  • Board proposes dividend increase to CHF 9.30. If approved by shareholders, this would be the 35th consecutive dividend increase

Outlook for 2022: Sales are expected to be stable or grow in the low-single digits (at constant exchange rates). Core earnings per share are targeted to grow in the low- to mid-single digit range (at constant exchange rates), including the accretive effect of the recent share repurchase. Roche expects to increase its dividend in Swiss francs further.

Roche anticipates sales of COVID-19 medicines and diagnostics to decrease by approximately CHF 2 billion to around CHF 5 billion, and sales losses to biosimilars in the current year to be roughly CHF 2.5 billion. Excluding those effects, Group sales are expected to grow in the high-single digit range.

Key figures CHF millions % change
January - December 2021 2021 2020 At CER1 In CHF
Group sales 62,801 58,323 9 8
Pharmaceuticals Division 45,041 44,532 3 1
Diagnostics Division 17,760 13,791 29 29
Core operating profit 21,897 21,536 4 2
Core EPS - diluted (CHF) 19.81 19.16 6 3
IFRS net income 14,935 15,068 2 -1

CEO Severin Schwan on the full-year results: “We achieved good results in 2021. The demand for our new medicines and diagnostics remains very high. I am particularly pleased with the progress of our product pipeline across several areas, including oncology, vision loss and neurological diseases. Based on our strong product portfolio in both divisions and the promising product pipeline, we are well positioned for future growth.”

Group results
In 2021, Group sales rose 9% (8% in CHF) to CHF 62.8 billion. Core operating profit increased 4% (2% in CHF), reflecting the strong underlying business performance, and core EPS grew 6% (3% in CHF). The Swiss franc’s appreciation against almost all currencies affected the results expressed in Swiss francs compared to constant exchange rates.

IFRS net income was CHF 14.9 billion. This represents an increase of 2% (-1% in CHF), driven by the operating results.

In December, Roche completed the CHF 19.0 billion repurchase of Roche shares held by Novartis. This restores Roche’s full strategic flexibility while retaining its operational scope of action.

Pharmaceuticals Division sales increased by 3% to CHF 45.0 billion. Strong demand for newly launched medicines to treat severe diseases, namely Hemlibra (haemophilia), Ocrevus (multiple sclerosis), Tecentriq (cancer), Evrysdi (spinal muscular atrophy), and Phesgo (cancer) drove this growth; medicines for the treatment of COVID-19 also contributed to sales growth (Ronapreve for high-risk COVID-19 patients and Actemra/RoActemra for severe COVID-19 pneumonia).

Overall, the medicines launched in the last ten years2 contributed an additional CHF 5.7 billion in new sales.

The impact of competition from biosimilars for the cancer medicines Avastin, Herceptin and MabThera/Rituxan has slowed down as expected (combined CHF 4.5 billion of sales reduction); and the second half of the year saw signs of recovery from the COVID-19 pandemic.

In the United States, sales decreased by 2%. While sales of Actemra/RoActemra, Hemlibra, Ocrevus, Evrysdi and Tecentriq increased, the impact of biosimilars and the COVID-19 pandemic affected total growth as expected.

In Europe, sales grew 7%. Growth of recently launched medicines more than compensated for the impact of biosimilars and the COVID-19 pandemic.

In Japan, sales increased by 26%, driven by strong demand for new medicines. This more than compensated for competition from biosimilars and government price cuts.

Sales in the International region grew by 4%. In China, sales were stable: Growth of Perjeta, Alecensa and Heceptin was offset by the impact from biosimilars. Excluding China, sales increased by 6%, mainly driven by new product sales, partially offset by the biosimilars competition.

The Diagnostics Division reported strong sales growth of 29% to CHF 17.8 billion. The division’s base business showed strong momentum throughout 2021 (overall 16%).

With sales totalling CHF 4.7 billion, Roche's leading portfolio of COVID-19 tests contributed significantly to the division’s overall sales.

Sales grew strongly across the world: Europe, Middle East and Africa (EMEA) 37%, Asia-Pacific 29%, North America 16%, and Latin America 48%.

In December, Roche completed its share purchase agreement with long-term partner TIB Molbiol to expand their PCR-test portfolio in the fight against new infectious diseases. TIB Molbiol will continue to operate as a subsidiary within the Diagnostics Division.

Pharmaceuticals: promising pipeline
Oncology remained the primary area of research and development, with the cancer immunotherapy portfolio being a key driver. Ophthalmology, neuroscience and immunology represent other significant areas of late-stage investments. Roche now has 14 new compounds in late-stage development or registration.

Regulatory milestones in the fourth quarter 2021 (incl. January 2022)

Neovascular or “wet” age-related macular degeneration (nAMD) affects about 20 million people worldwide and is a leading cause of blindness in people over 60. In October, Roche launched Susvimo in the United States, a first-in-kind therapeutic approach for nAMD. Susvimo is the first and only eye implant with continuous drug delivery – an alternative to frequent eye injections that makes life much easier for people with the condition.

Diabetic macular edema (DME) is a vision-threatening complication of diabetic retinopathy. In January 2022, the FDA approved Vabysmo for the treatment of nAMD and DME - the first in a new class of eye medicines targeting two key pathways that drive retinal disorders. Vabysmo potentially offers durable vision outcomes with fewer eye injections than the current standard of care.

RET gene alterations are key disease drivers in many types of cancer, including non-small cell lung cancer (NSCLC). Treatment options for people with RET fusion-positive advanced NSCLC have been limited to date. In November, the European Commission approved Gavreto for the treatment of adults with RET fusion-positive advanced NSCLC. Gavreto is the first and only precision medicine approved in the EU for first-line treatment of people with this specific form of cancer.

Roche is investigating more than a dozen medicines for neurological disorders, including Alzheimer's, multiple sclerosis and rare diseases, such as spinal muscular atrophy (SMA). SMA is the leading genetic cause of death in babies. In January 2022, Roche announced that the FDA has granted priority review of a supplemental new drug application for the use of Evrysdi to treat pre-symptomatic babies under two months of age with SMA. Interim data showed that the majority of pre-symptomatic babies treated with Evrysdi for at least one year were able to sit, stand and walk within timeframes typical of healthy babies, as well as maintain swallowing.

The COVID-19 pandemic has led to more than 5.6 million deaths so far, mostly involving hospitalised patients. While vaccines are mostly effective in preventing hospitalisation, there has been a high medical need for all those who have not been vaccinated or do not respond adequately to vaccines.

In November, Ronapreve was approved in Europe to treat non-hospitalised COVID-19 patients and for prophylaxis of the disease. Data showed that the antibody combination reduces the risk of hospitalisation in certain patients with mild to moderate disease and the risk of symptomatic COVID-19 infections in people exposed to the virus. While analyses have shown that Ronapreve does not retain neutralising activity against the Omicron variant, Ronapreve retains its activity against all other main variants of concern, including Delta. Activity of Ronapreve against potential future variants will be continually assessed.

In December, the European Commission extended the marketing authorisation for Actemra/RoActemra to include the treatment of COVID-19 in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation.

Key development milestones in the fourth quarter 2021

Diffuse large B-cell lymphoma (DLBCL) is an aggressive blood cancer. In 40% of people with DLBCL, the cancer returns after initial treatment, at which point treatment options are limited and survival is short. At the American Society of Hematology (ASH) congress in December, Roche showed that its Polivy combination therapy is the first in more than 20 years to significantly improve outcomes in previously untreated DLBCL compared to standard of care. Polivy reduces the risk of disease worsening or death by 27%.

Follicular lymphoma (FL) accounts for 20% of all blood cancer cases and can spread unnoticed in the body. Many people with FL do not respond to available therapies and there is currently no cure for this devastating disease. Roche also presented pivotal data for the novel cancer immunotherapy mosunetuzumab at ASH. Mosunetuzumab is a potential first-in-class treatment, showing high response rates in people with FL who have received two or more prior therapies. Roche recently submitted the marketing authorisation application for mosunetuzumab to the European Medicines Agency.

Latest data for glofitamab and cevostamab also underline the potential of this novel approach (T-cell engaging bispecific antibody immunotherapies) in the treatment of different types of blood cancers.

Lung cancer is one of the leading causes of cancer deaths worldwide; non-small cell lung cancer (NSCLC) accounts for around 85% of all cases. In December, Roche announced new data from the first randomised phase II trial of an anti-TIGIT therapy. The data showed encouraging results for tiragolumab plus Tecentriq for people with PD-L1-positive metastatic NSCLC. The data suggest that combining anti-TIGIT and anti-PD-L1 cancer immunotherapies such as tiragolumab and Tecentriq could potentially represent a novel approach to addressing unmet needs in cancer.

Haemophilia A
Haemophilia A is an inherited, serious disorder that affects the blood’s ability to clot, leading to uncontrolled bleeding. In December, Roche presented interim results from a phase III study of Hemlibra. The medicine demonstrated a favourable safety profile and effective bleed control in people with moderate or mild haemophilia A without factor VIII inhibitors. Hemlibra thus continues to show benefit in additional haemophilia A populations, regardless of severity.

The phase II study on AT-527 did not meet its primary endpoint. After a thorough analysis of the evolving COVID-19 treatment landscape, Roche announced in November that it would be ending its partnership with Atea on the AT-527 programme as of February 2022.

Pharma: Key development milestones 2021 (incl. January 2022)

  Compound Indication Milestone











Xofluza Influenza: healthy people; high-risk people; post exposure prophylaxis EU approval
Evrysdi Spinal muscular atrophy (SMA) type 1/2/3 EU approval
Vabysmo* Neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME)

US approval; EU filing
Tecentriq Adjuvant non-small cell lung cancer (NSCLC) US approval; EU filing
Tecentriq First-line PD-L1-positive NSCLC EU approval
Enspryng Neuromyelitis optica spectrum disorder (NMOSD) EU approval
Venclexta/Venclyxto azacitidine Acute myeloid leukaemia EU approval
Ronapreve* SARS-CoV-2 EU approval
Susvimo* nAMD (continuous delivery) US approval; EU filing
Actemra/RoActemra* COVID-19 pneumonia EU approval
Gavreto* RET-positive NSCLC EU approval
mosunetuzumab* Relapsed or refractory follicular lymphoma (FL) EU filing
Phase III / pivotal and other key readouts





Ronapreve SARS-CoV-2 outpatient Phase III study 2067
Ronapreve SARS-CoV-2 post-exposure prophylaxis Phase III study 2069
Phase II/III study 2066
Evrysdi SMA type 1/2/3 switching study Phase II RAINBOWFISH
tiragolumab Tecentriq* PD-L1-positive metastatic NSCLC (PD-L1-high) Phase II CITYSCAPE
Polivy R-CHP* First-line diffuse large B-cell lymphoma (DLBCL) Phase III POLARIX**
Hemlibra* Moderate to mild haemophilia A Phase III HAVEN 6**

* Fourth quarter 2021 (incl. January 2022)
** EU application for approval recently submitted

Diagnostics: key launches in the fourth quarter (incl. January 2022)
Diagnostic solutions are the backbone of treatment decisions: Whether it’s cancer, infectious diseases or other serious illnesses, the quest for better solutions to healthcare’s greatest challenges depends on diagnostics.

Diagnostics instruments
Access to reliable and accurate testing solutions is essential. In November, Roche launched the cobas 5800. This compact, fully automated molecular system provides efficiency, simplicity and timely results to laboratories of all sizes so clinicians can quickly determine the best treatment strategies for their patients.

In December, Roche launched the cobas pulse system, the first professional (point of care) blood glucose meter with digital capabilities similar to that of a smartphone. Its Android-based operating system is loaded with industry-leading medical apps that can perform a range of clinically valuable functions – from clinical decision support to the measurement of vital signs and digital biomarkers.

One of the major challenges in using next generation sequencing for diagnosis is the preparation of the samples. DNA is especially complex to prepare for sequencing and this process can be prone to human error. In December, Roche launched the AVENIO Edge System: it helps to simplify and automate next-generation sequencing sample preparation, thus reducing human error. 

Digital solutions
Healthcare professionals often face incomplete patient records and data silos across multiple IT systems. In December, Roche launched the NAVIFY Oncology Hub, a new digital solution that securely aggregates and organises patient data from disparate sources. It provides a central workspace where clinicians can quickly and easily access holistic, longitudinal patient data to inform more timely, personalised decisions across the cancer care continuum.

In addition, Roche introduced cobas infinity edge in January 2022. This cloud-based platform brings multiple capabilities together to create an open digital health ecosystem for “point of care” professionals. It enables the sharing of patients' data - from multiple sources - at the right time and place to the right caregivers. The platform connects an array of health status sources such as patients' electronic medical records (EMRs), third-party apps and point-of-care devices (e.g. Roche's new cobas pulse).

Oncology testing
To treat cancer effectively, we must understand what drives it at a molecular level. In October, Roche launched the AVENIO Tumor Tissue CGP Kit to expand access to personalised cancer research. This is the first product developed jointly by Roche and Foundation Medicine (FMI), and the first example of oncology research where scientists have used FMI’s comprehensive genomic profiling in their own laboratories.

Each year, around 340,000 women die from cervical cancer. This preventable cancer is caused by infection with high-risk types of the human papillomavirus (HPV). In October, Roche announced the IMPACT clinical trial data showing a clear benefit of the CINtec Plus Cytology test for women at higher risk of developing cervical cancer.

Early detection of lung cancer allows for more treatment options. In October, the VENTANA PD-L1 Assay received FDA approval as a companion diagnostic to identify people with non-small cell lung cancer who are eligible for Roche’s cancer immunotherapy Tecentriq.

COVID-19 testing
The pandemic has profoundly raised awareness of the role diagnostics play in disease prevention and management. The spread of the virus, and particularly the emergence of new variants, has heightened the need for reliable, high-quality testing.

In December, Roche’s newly acquired subsidiary TIB Molbiol rapidly developed six new test kits. They help researchers detect mutations in the new Omicron variant and study its spread versus other variants.

Later in December, the FDA granted Emergency Use Authorization (EUA) for the COVID-19 At-Home Rapid Antigen Test, which delivers fast, reliable results for infections with SARS-CoV-2 and all known variants, including Omicron.

In January 2022, Roche launched the SARS-CoV-2 & Flu A/B Rapid Antigen Test in markets accepting the CE mark. The test (with results in 15-30 minutes) is intended for use by healthcare professionals to rapidly differentiate between SARS-CoV-2 and influenza virus A and B infections in people with COVID-19 or influenza symptoms.

Roche has analysed the publicly available sequences of Omicron and concluded that all of Roche PCR tests correctly identify SARS-CoV-2, including the Omicron variant.

Pharmaceuticals sales

Sales CHF millions As % of sales % change    
January - December 2021 2021 2020 2021 2020 At CER In CHF    
Pharmaceuticals Division 45,041 44,532 100.0 100.0 3 1    
United States 22,505 23,647 50.0 53.1 -2 -5    
Europe 8,876 8,198 19.7 18.4 7 8    
Japan 4,506 3,765 10.0 8.5 26 20    
International* 9,154 8,922 20.3 20.0 4 3    
*Asia–Pacific, EEMEA (Eastern Europe, Middle East and Africa), Latin America, Canada, others
Top-selling pharmaceuticals

Total United States Europe Japan International*
CHFm % CHFm % CHFm % CHFm % CHFm %
Ocrevus 5,055 19 3,777 14 916 34 - - 362 50
Perjeta 3,955 4 1,416 -1 1,112 -4 268 -4 1,159 24
Actemra/RoActemra 3,562 27 1,761 49 915 15 382 10 504 5
Tecentriq 3,315 24 1,688 11 713 22 518 66 396 53
Avastin 3,056 -37 922 -47 430 -66 674 -1 1,030 -15
Hemlibra 3,022 41 1,815 34 609 61 365 23 233 102
Herceptin 2,694 -28 636 -52 544 -19 82 -38 1,432 -9
MabThera/Rituxan 2,565 -38 1,552 -44 268 -30 42 -30 703 -24
Kadcyla 1,982 16 813 4 687 21 130 53 352 29
Xolair 1,942 5 1,942 5 - - - - -  
Ronapreve 1,630 - - - 727 - 645 - 258 -
Alecensa 1,356 18 366 10 297 11 247 8 446 40
Lucentis 1,353 -4 1,353 -4 - - - - - -
Activase/TNKase 1,312 2 1,255 2 - - - - 57 5
Esbriet 1,039 -5 732 -4 269 0 - - 38 -28
* Asia–Pacific, EEMEA (Eastern Europe, Middle East and Africa), Latin America, Canada, others      

Pharmaceuticals: established products

Actemra/RoActemra (CHF 3.6 billion, 27%). Rheumatoid arthritis, forms of juvenile idiopathic arthritis and giant cell arteritis, CAR T cell-induced severe or life-threatening cytokine release syndrome and COVID-19 pneumonia. The inclusion of this medicine in treatment guidelines for severe COVID-19-associated pneumonia by a number of countries drove sales growth, with the United States and Europe as major contributors.

Avastin (CHF 3.1 billion, -37%). Advanced colorectal, breast, lung, kidney, cervical and ovarian cancer, relapsed glioblastoma (a type of brain tumour) and liver cancer in combination with Tecentriq. Sales were strongly impacted by the uptake of biosimilars, mainly in the United States and Europe.

Herceptin (CHF 2.7 billion, -28%). HER2-positive breast cancer and HER2-positive metastatic gastric cancer. The sales decrease was mainly due to biosimilar uptake in the United States and Europe.

MabThera/Rituxan (CHF 2.6 billion, -38%). Forms of blood cancer, rheumatoid arthritis and certain types of vasculitis. Sales further decreased due to the biosimilar erosion as well as COVID-19 pandemic restrictions.

Xolair (CHF 1.9 billion, 5%, United States only). Chronic idiopathic urticaria and allergic asthma. Sales growth in the chronic idiopathic urticaria indication was partly offset by competition in the allergic asthma indication. Xolair remains the market leader in the larger allergic asthma indication.

Pharmaceuticals: medicines launched since 2012

Ocrevus (first approved in 2017; CHF 5.1 billion, 19%). Relapsing and primary progressive forms of multiple sclerosis; 2-hour only infusion. The demand for this treatment in both indications remained strong, mainly in the United States, while the pandemic still had a certain negative impact. New and returning patients both boosted growth, the latter group generating stronger sales.

Perjeta (first approved in 2012; CHF 4.0 billion, 4%). HER2-positive breast cancer. Sales increased mostly due to high demand in China in both early and metastatic breast cancer settings. In the United States, sales of Perjeta declined by 1% due to certain patients being switched to Kadcyla and due to the launch of Phesgo in 2020.

Tecentriq (first approved in 2016; CHF 3.3 billion, 24%). Cancer immunotherapy (either alone or in combinations) for various types of cancer, e.g. lung, bladder, breast and liver cancer. Sales increased in all regions, most notably in Japan, primarily due to the demand for treatment of hepatocellular carcinoma (HCC). US sales were higher, driven by the new indications for HCC and first-line non-small cell lung cancer (NSCLC).

Hemlibra (first approved in 2017; CHF 3.0 billion, 41%). Haemophilia A with and without factor VIII inhibitors; only prophylactic treatment that can be administered subcutaneously once weekly, every two or every four weeks. Sales continued to show a strong uptake, especially in the United States and Europe.

Kadcyla (first approved in 2013; CHF 2.0 billion, 16%). HER2-positive breast cancer. Sales growth was driven by the usage of Kadcyla in the early breast cancer setting. Sales benefited from patients switching to this new standard of treatment.

Ronapreve (first approved in 2021; CHF 1.6 billion3). Antibody combination for the treatment of recently diagnosed high-risk patients with mild to moderate COVID-19. Roche is responsible for distribution in Europe and other countries outside the United States, its partner Regeneron for the United States. The uptake has been strong, mainly in Japan and Europe.

Alecensa (first approved in 2015; CHF 1.4 billion, 18%). ALK-positive non-small-cell lung cancer. The global uptake continued with sales growth across all regions.

Esbriet (first approved in 2014; CHF 1.0 billion, -5%). Idiopathic pulmonary fibrosis (IPF).

Gazyva/Gazyvaro (first approved in 2013; CHF 678 million, 9%). Chronic lymphocytic leukaemia, rituximab-refractory follicular lymphoma and previously untreated advanced follicular lymphoma.

Evrysdi (first approved in 2020; CHF 602 million, >500%). Spinal muscular atrophy (SMA) in adults and children two months of age and older. Evrysdi helps infants to survive without permanent ventilation. It is the first and only medicine for SMA that can be administered at home. Evrysdi continued to show a strong uptake across all regions.

Phesgo (first approved in 2020; CHF 340 million, >500%). Early and metastatic HER2-positive breast cancer (fixed-dose combination of Perjeta and Herceptin for subcutaneous injection). Offers faster administration in just minutes, compared to hours with standard intravenous administration.

Erivedge (first approved in 2012; CHF 269 million, -1%). Advanced basal cell carcinoma.

Polivy (first approved in 2019; CHF 247 million, 48%). Relapsed or refractory diffuse large B-cell lymphoma; part of combination therapy; a fixed-duration treatment option for people with this aggressive form of blood cancer.

Enspryng (first approved in 2020; CHF 107 million, >500%). Rare autoimmune disease of the central nervous system (neuromyelitis optica spectrum disorder; NMOSD); first subcutaneous NMOSD treatment that can be self- or carer-administered at home. Enspryng has continued to show a very good uptake, with over 1,000 people with this rare disease treated with Enspryng to date (including newly diagnosed and previously treated patients).

Rozlytrek (first approved in 2019; CHF 49 million, 109%). Specific form of non-small cell lung cancer (NSCLC); solid tumours expressing a specific gene fusion; ROS1-positive, advanced NSCLC.

Susvimo (first approved in 2021; CHF 1.0 million3). Eye implant with continuous drug delivery for nAMD treatment.

Diagnostics sales

Sales CHF millions As % of sales % change
January - December 2021 2021 2020 2021 2020 At CER In CHF
Diagnostics Division 17,760 13,791 100.0 100.0 29 29
Customer Areas            
Core Lab 7,473 6,194 42.1 44.9 21 21
Molecular Lab 4,812 3,760 27.1 27.3 29 28
Point of Care 2,583 1,079 14.5 7.8 138 139
Diabetes Care 1,690 1,670 9.5 12.1 3 1
Pathology Lab 1,202 1,088 6.8 7.9 12 10
Europe, Middle East, Africa 7,537 5,491 42.4 39.5 37 37
North America 4,369 3,867 24.6 28.4 16 13
Asia–Pacific 4,756 3,645 26.8 26.4 29 30
Latin America 1,098 788 6.2 5.7 48 39

Core Lab. Focuses on central labs; provides diagnostics solutions in the areas of immunoassays, clinical chemistry and custom biotech. Sales increased by 21% due to its immunodiagnostics business, with infectious and cardiac tests as main contributors. Sales grew across all regions, most strongly in EMEA and Asia-Pacific.

Molecular Lab. Focuses on molecular labs; provides diagnostics solutions for pathogen detection and monitoring, donor screening, sexual health and genomics. Sales grew 29%, led by the virology business. The Delta variant continued to push growth in COVID-19 testing such as high-throughput PCR tests. Sales increased in all regions, led by the North America and Asia-Pacific regions.

Point of Care. Focuses on diagnostics solutions in emergency rooms, medical practices or directly with patients; includes SARS-CoV-2 rapid tests, blood gas and electrolyte tests. Continued significant sales growth of 138%. The SARS-CoV-2 Rapid Antigen test was the main growth driver, especially in the EMEA region.

Diabetes Care. Focuses on integrated personalised diabetes management for people with diabetes and healthcare professionals. Sales increased 3%, driven by the blood glucose monitoring business (such as the Accu-Chek Guide system).

Pathology Lab. Focuses on pathology labs; provides diagnostics solutions for tissue biopsies and companion diagnostics. These targeted diagnostics support the specific therapy decisions for each patient. Sales increased 12%. This was mainly due to growth in the advanced staining business.

About Roche
Founded in1896 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.

In recognising our endeavor to pursue a long-term perspective in all we do, Roche has been named one of the most sustainable companies in the pharmaceuticals industry by the Dow Jones Sustainability Indices for the thirteenth consecutive year. This distinction also reflects our efforts to improve access to healthcare together with local partners in every country we work.

Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan.

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[1] Unless otherwise stated, all growth rates and comparisons to the previous year in this document are at constant exchange rates (CER: average 2020) and all total figures quoted are reported in CHF.
[2] Launches since 2012: Erivedge, Perjeta, Kadcyla, Gazyva/Gazyvaro, Esbriet, Cotellic, Alecensa, Tecentriq, Ocrevus, Hemlibra, Xofluza, Polivy, Rozlytrek, Phesgo, Enspryng, Evrysdi, Gavreto, Ronapreve, Susvimo
[3] recently approved; no growth figures available