On April 24, Roche released its Q1 2024 performance.Total revenue of 14.399 billion Swiss francs(Approximately 15.695 billion USD), calculated at constant exchange rates (CER),Growth of 2%Excluding COVID-19 related products, sales increased by 7%.(This article's exchange rate calculation is based on 1 Swiss Franc =$1.09)
Looking ahead,Roche Reports Decline in Sales of COVID-19 ProductsNo.Further impact on the company's performance,Sales growth in the mid-single digits (CER) is expected for 2024.

From the perspective of specific department operations,First QuarterPharmaceutical business revenue of 10.921 billion Swiss francs (approximately 11.9 billion US dollars),Excluding products related to the epidemic,Increased by 7%, thisMainly benefited from the strong sales of the following drugs:Vabysmo(Ophthalmology|Dual Antibody):Sales847 million Swiss francs,An increase of 108% year-on-year
Phesgo (Breast Cancer | Trastuzumab + Pertuzumab):Sales 3.88100 million Swiss francs, Growth70%
Ocrevus (New Drug for Multiple Sclerosis):Sales16.58Million Swiss Francs,Increase by 8%
Polivy (Blood Cancer |CD79b ADC): Sales Revenue2.5Million Swiss Francs,Growth81%
- Hemlibra(Hemophilia A): Sales Revenue10.4Million Swiss Francs,GrowthIncrease by 8%

The combined sales of the above five strongly growing drugs reached 4.2 billion Swiss francs, increasing by 900 million Swiss francs compared to the first quarter of 2023 (at CER).Vabysmo Eye Drops Are the Largest Growth Driver,Sales reached 8.47 billionSwiss Franc(Approximately USD 923 million),An increase of 108% year-on-year.The best-performing asset in sales is Ocrevus., it gained in the first quarter1.658 billion Swiss francs (About18.07Billion US dollars), an increase of 8% compared to the same period in 2023.
Ophthalmology Bispecific Antibody Vabysmo
Vabysmo is the first and only bispecific antibody approved for ocular use., uniquely designed to restore vascular stability by neutralizing angiopoietin-2 (Ang-2) and vascular endothelial growth factor-A (VEGF-A), targeting and inhibiting two signaling pathways associated with many vision-threatening retinal diseases.VabysmoCurrentlyObtainedThree Indications Approved:First approved in February 2022Approved for treatment in more than 90 countries worldwideNeovascular or "Wet" Age-Related Macular Degeneration (nAMD)AndPatients with Diabetic Macular Edema (DME),AndOctober 2023Approved in the United States for the treatment of retinal vein occlusion (RVO)。Moreover, more than 1 million doses of the vaccine have been globally distributed with public reimbursement in over 25 markets and more than 2.5 countries.In the first quarter, Roche announced detailed results from two global Phase III studies of Vabysmo for the treatment of retinal vein occlusion (RVO): up to 60% of patients receiving Vabysmo were able to extend treatment intervals to three or four months. Additionally, patients in the studies maintained vision gains and robust retinal drying for over a year, continuing through the first 24 weeks. In both studies, Vabysmo was well-tolerated with a safety profile consistent with previous studies.
For its product pipeline, Roche announced that it has halted the development of five early-stage assets:
1. RG6185 Belvarafenib:Is an oral RAF kinase inhibitor, currentlyCorrectConducting two clinical studies targeting various cancers.Roche's Genentech acquired the license from Hanmi Pharmaceutical in 2016 with an $80 million upfront payment. At that time, the drug was in Phase I. In 2017, Hanmi initiated a Phase 1b study to test belvarafenib in combination with cobimetinib or cetuximab. Hanmi retained the rights to its assets in Korea, published data from the Phase 1 trial and extension study in 2019, and continued to follow patients in the Phase 1b study to evaluate the effects of belvarafenib in combination with MEK or EGFR inhibitors.
2. RG6526 camonsertinib:A potential first-in-class oral small-molecule ataxia telangiectasia and Rad3-related protein kinase (ATR) inhibitor. Phase I study results showed that Camonsertib monotherapy had a modest therapeutic effect on solid tumors, with a clinical benefit rate (CBR) of 13% and a molecular response rate of 43% in 99 treated patients, where ovarian cancer patients exhibited a relatively better response, achieving a CBR of 75%. On February 12, Repare announced that Roche decided to terminate the collaboration agreement for Camonsertib (RP-3500), effective May 7, 2024, due to pipeline adjustments and external factors.
3. RG6286: It is a bispecific antibody that can bind to the colorectal cancer antigen LY6G6D and CD3 on T cells. Roche initiated testing of this candidate drug (also known as BLYG8824A) in colorectal cancer patients in 2020. The estimated primary completion date for the Phase 1 clinical trial is early 2026.
4. RG6163: New candidate molecular drugs for psychiatric disorders, not publicly disclosed.
5. RG6319:LepB inhibitor, used for complicated urinary tract infections. Roche abandoned this drug and shifted focus to another molecule targeting the same site, RG6436.In addition,Due to the IL-6 monoclonal antibody Phase 3 clinical trial not meeting expectations,Roche alsoTerminatedRG6168Satralizumab(Product name Enspryng)Phase 3 Clinical Study for the Treatment of Myasthenia Gravis(LUMINESCE)。LUMINESCE Achieves Statistically Significant Data for Primary Endpoint, butThe degree of clinical benefit did not meet expectations.Enspryng was well-tolerated, with a safety profile consistent with its indication for Neuromyelitis Optica Spectrum Disorder (NMOSD). Chugai Pharmaceutical, a subsidiary of Roche, stated that these study results do not affect the use of Enspryng in NMOSD patients. The company is also developing Enspryng for the treatment of other neuro-autoimmune and inflammatory conditions.Since the third quarter of last year, Roche has removed 20% of new molecules from its pipeline.The Termination of Some Pipelines This TimeIs part of a broad realignment.AndIndicates,The focus of the removal is on those assets with "lower chances of success."Schinecker stated that Roche needs to terminate some projects to free up cash for investing in and accelerating "projects that are highly likely to succeed and have a significant impact on patients."
Looking ahead to the remainder of 2024,Roche Expects Mid-Single-Digit (CER) Sales Growth。
"Our CEO, Thomas Schinecker, stated: 'We had a strong start to the year, with both divisions showing high single-digit growth in underlying business – excluding COVID-19 sales.'"After this quarter, the sales impact related to COVID-19 has basically passed.Compared with the same period last year,The appreciation of the Swiss franc against most currencies affected sales reported in Swiss francs.. The use of our eye drug Vabysmo continues to gain momentum.We are confident2024The group's sales can achieve mid-single-digit growth (at constant exchange rates)."

Cell Line Product Inquiry
Submission | Business Cooperation
Repost | Join the Communication Group
Click "Pharmaceutical Research Network" below to follow more exciting content.