In its earnings report for the fourth quarter and full year of 2023, Coherus Biosciences detailed its rising revenue growth, which it partly attributed to increased sales for its pegfilgrastim and ranibizumab biosimilars.
Coherus Biosciences reported a significant increase in net revenue during 2023, which was largely attributed to increased sales for its pegfilgrastim and ranibizumab biosimilars (Udenyca and Cimerli, respectively), according to the company’s fourth quarter and full year earnings report for 2023.
During the final quarter of 2023 (Q4 2023), revenue reached $91.5 million, a meaningful jump from $45.4 million from the same quarter in 2023. For the entire year, Coherus achieved $257.2 million in revenues, up from $21.0 million in 2022.
Image credit: utah51 - stock.adobe.com
In Q4 2023, intravenous Udenyca net product sales saw a 10% increase, reaching $36.2 million, compared to $33.0 million in the third quarter. Total unit demand also experienced growth, rising by 7% quarter over quarter. Additionally, the Udenyca autoinjector presentation unit demand soared by 129% during the same period. Since its commercial launch in May 2023, the autoinjector presentation has garnered orders from more than 727 accounts, highlighting its growing popularity and acceptance in the market.
For Cimerli, sales reached $52.4 million for the quarter and $125.4 million for all of 2023. Cimerli launched on the US market in September 2023 after receiving approval from the FDA in August 2022.
However, the year was not without its challenges, including a net loss of $79.7 million in Q4 2023 and $237.9 million for the whole year. The losses were primarily caused by increased cost of goods sold, which included a $47.0 million charge for writing down of Yusimry (adalimumab-aqvh) inventory after experiencing slow uptake. Yusimry launched on the US market in July 2023 as 1 of 9 biosimilars referencing Humira (adalimumab) to become available to Americans in 2023.
Coherus reported that it hopes the recent launches of its onbody injector for Udenyca (Udenyca Onpro), the first biosimilar competitor to Neulasta Onpro (onbody reference pegfilgrastim), and Loqtorzi (toripalimab-tpzi), a novel melanoma medication, will help offset these challenges. Additionally, it issued a “workforce reduction of 30%” to aid in operation streamlining and cost reductions.
“Throughout 2023, Coherus demonstrated significant progress in transforming the Companys business model and product portfolio for long-term sustainable growth,” Denny Lanfear, chairman and CEO of Coherus, said in a statement. “With a robust portfolio of FDA-approved products and a promising immuno-oncology pipeline, we are now better positioned than ever to execute on our mission of extending the lives of cancer patients.”
Research and development expenditures decreased from $29.0 million in Q4 2022 to $26.4 million in Q4 2023. For the full year, these expenses dropped from $199.4 million in 2022 to $109.4 million in 2023. With a total of $117.7 million in cash, cash equivalents, and investments in marketable securities, Coherus said that it is well positioned to weather challenges and pursue strategic opportunities.
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
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.
Similar Survival, Safety for Bevacizumab Biosimilar vs Originator in Colorectal Cancer
February 8th 2025A retrospective observational study found no significant differences in progression-free survival or safety in patients with colorectal cancers in Japan treated with ABP 215, Amgen’s bevacizumab biosimilar, or reference bevacizumab (Avastin), and estimated cost savings of 800,000 Japanese yen (approximately $5100) per patient with the biosimilar.