In its latest earnings report, Sandoz championed 7% growth overall throughout 2023, including a 15% spike in biosimilar revenues.
Sandoz revenues increased 7% overall last year, including a 15% spike in biosimilar sales, according to the company’s earnings report for the fourth quarter (Q4) and full year (FY) 2023.
Additionally, the company’s overall revenue for Q4 2023 was up 10% from the same quarter in 2022, with net sales reaching $2.5 billion. Net sales for FY 2023 reached $9.6 billion, including $2.2 billion from biosimilars and $7.1 billion from generics.
“2023 was a year of many achievements for Sandoz, thanks to the passion and tireless efforts of our employees worldwide”, said Richard Saynor, CEO of Sandoz. “We launched Hyrimoz (biosimilar adalimumab) in the US, expanded our biosimilar pipeline through a commercialization agreement with Samsung on biosimilar ustekinumab (reference medicine Stelara) and enhanced our generic portfolio with the acquisition of Mycamine (an anti-fungal agent), while becoming an independent public company.”
By region, sales were up 20% in North America and 10% in Europe during Q4 2023. Net sales in Europe reached $1.3 billion, which was primarily driven by solid generic volume growth and strong performance of Omnitrope, a somatropin biosimilar in Europe. The growth in North American sales, which reached $2.1 billion, was driven by Omnitrope and the launch of Hyrimoz, 1 of 9 adalimumab biosimilars to enter the US market in 2023. Sandoz noted that Omnitrope is the current somatropin market leader with 34% market share globally.
Hyrimoz (adalimumab-adaz) received FDA approval in October 2018 and is 1 of 2 adalimumab biosimilars that is available in high-concentration and low-concentration versions. Although the high-concentration version is citrate-free, the low-concentration version is not.
For biosimilars, European sales of biosimilars reached $1.2 billion for Q4 and $5.0 billion for the year. In North America, biosimilars brought in $615 million and $2.1 billion for Q4 and FY, respectively.
The report comes after Sandoz received FDA approval for the first denosumab biosimilars (Wyost and Jubbonti; denosumab-bddz) for the treatment of musculoskeletal conditions. Sandoz also recently acquired the rights to Coherus Biosciences’ Cimerli (ranibizumab-eqrn), a biosimilar referencing Lucentis (ranibizumab) used to treat retinal conditions, such as neovascular age-related macular degeneration. In August 2023, Sandoz received approval for Tyruko (natalizumab-sztn), which was the first biosimilar approved to treat multiple sclerosis.
Coherus Biosciences also reported growth for Q4 and FY 2023, citing biosimilars as main drivers for the increases. Q4 earnings more than doubled from the same quarter in 2022, and FY earnings were 12 times higher in 2023 compared with 2022.
Overcoming Challenges to Improve Access and Reduce Costs
November 12th 2024Biosimilars hold the potential to dramatically lower health care costs and improve access to life-changing treatments, but realizing this potential will require urgent policy reforms, market competition, and better education for both providers and patients.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Skyrizi Overtakes Humira: “Product Hopping” Leaves Biosimilar Market in Limbo
November 7th 2024For the first time, Skyrizi (risankizumab-rzaa) has replaced Humira (reference adalimumab) as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.
Exploring the Biosimilar Horizon: Julie Reed's Predictions for 2024
February 18th 2024On this episode of Not So Different, Julie Reed, executive director of the Biosimilars Forum, returns to discuss her predictions for the biosimilar industry for 2024 and beyond as well as the impact that the Forum's 4 new members will have on the organization's mission.
Panelists Stress Stakeholder Education to Build Confidence in Biosimilars
October 31st 2024By expanding educational initiatives to clarify biosimilar safety, efficacy, and interchangeability, stakeholders can foster trust, improve access, and ensure that biosimilars are widely accepted as high-quality, cost-effective alternatives to originator biologics.