Roche has begun another year of biosimilar sales erosion, although the company has said this year will not be as bad as 2020.
Biosimilars took a $1.74 billion bite out of revenues for Roche, the company said in its first-quarter financial report, contributing to an overall sales decline of 1% from January to March 2021. This stiff competition from biosimilars was not unanticipated, Roche said. However, the company hit milestones with new product sales and sees a rebound as pandemic effects are mitigated.
“The uptake of our recently introduced diagnostic tests and medicines remains strong, while we continue to see the expected impact from biosimilars on sales of our established medicines,” Roche said in a statement. Sales for the first 3 months of 2021 were $16.26 billion, down from $16.49 billion in the comparable year-ago quarter.
Roche produces the blockbuster biologic originator products rituxmab (Rituxan), bevacizumab (Avastin), and trastuzumab (Herceptin). These are now facing significant biosimilar competition, “especially in the United States,” the company reported.
Whereas in the first quarter of 2020 Rituxan, Avastin, and Herceptin accounted for 33% of the pharma sales mix at Roche, that percentage dropped to 22% in the first quarter of this year, the company reported. Sales of Avastin were down 40% in the just-ended quarter vs the year-ago period. Among hematology products, which include Rituxan, sales were down 37%. Herceptin is sold among a basket of Roche products for treatment of human epidermal growth factor receptor 2–positive cancer, and this portfolio saw an 11% sales decline.
Conversely, sales of new products represented 50% of the total revenue mix, as opposed to 37% this time last year. Products identified as new included pertuzumab (Perjeta), trastuzumab emtansine (Kadcycla), introduced in 2012 and 2013, respectively; atezolizumab (Teqcentriq) and ocrelizumab (Ocrevus), introduced in 2016 and 2017, respectively; and satralizumab (Enspryng) and subcutaneous pertuzumab/trastuzumab (Phesgo), introduced in 2020, among many others.
The pandemic continues to have a downward effect on patient volume at hospitals and health practices, where infusions have declined, Roche said. However, the Switzerland-based pharmaceutical giant has benefited from the sale of medicines used to treat COVID-19.
For a while now, Roche has battled the effects of biosimilar competition. In its 2020 year-end report, the company predicted that losses to biosimilars that year would be the worst and that the hemorrhaging would start to lessen. Full-year 2020 revenue declines from biosimilars amounted to $6.34 billion. “I think we’ve seen the worst that it can get,” said Bill Anderson, CEO of Roche Pharmaceuticals, in a report. At that time, Anderson predicted a negative $5.1 billion biosimilar sales impact in 2021.
Biosimilars Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.
Insights from Festival of Biologics: Dracey Poore Discusses Cardinal Health’s 2024 Biosimilar Report
May 19th 2024The discussion highlights key emerging trends from the Festival of Biologics conference and the annual Cardinal Health Biosimilars Report, including the importance of sustainability in the health care landscape and the challenges and successes in biosimilar adoption and affordability.
Switching to Rituximab Biosimilars Is Safe, Effective for Patients With Oncohematological Diseases
December 5th 2024Patients with oncohematological diseases switching to rituximab biosimilars experienced similar safety and efficacy, highlighting biosimilars' potential for cost-effective treatment across various medical conditions.
Cost and Efficacy Insights on Infliximab Biosimilars in Pediatric Uveitis
December 3rd 2024The study highlights the safety, efficacy, and cost benefits of infliximab biosimilars in managing pediatric noninfectious uveitis, showing fewer disease flares and reduced costs compared with reference infliximab, as well as the influence of insurance mandates on treatment decisions.