In its announcement, the drug maker said that its Udenyca sales are expected to be in the range of $36 million to $38 million.
Coherus BioSciences, maker of the pegfilgrastim biosimilar Udenyca, has announced its preliminary unaudited sales for the first quarter of 2019. In its announcement, the drug maker said that its Udenyca sales are expected to be in the range of $36 million to $38 million.
The company says that it will discuss its sales in further detail after the data are reported in its Form 10-Q for the quarter, and it will provide additional financial updates on May 9, 2019.
The biosimilar developer brought its pegfilgrastim biosimilar to the US market on January 3, 2019, with a comprehensive launch that included 340B hospitals and non-340B hospitals and clinics. The company launched the product at a list price of $4175 per unit, or a 33% discount to the reference pegfilgrastim, Neulasta. Udenyca’s list price matches that of Mylan’s Fulphila, the first pegfilgrastim biosimilar to launch in the United States, although these list prices do not reflect any rebates that may be provided by the respective drug makers.
The early sales numbers for the biosimilar pegfilgrastim reflect the success of what Coherus’ president and chief executive officer, Dennis M. Lanfear, has called the company’s “branded approach” to the product’s launch.
During the recent 37th Annual J.P. Morgan Healthcare Conference, Lanfear said that “Our approach is that of a branded launch…this has never been done before with a biosimilar.” This strategy involves a focus on payers, integrated delivery networks, and group purchasing organizations that consolidate purchasing for clinics and hospitals, as well as provider segments comprising community oncology clinics, 340B hospitals, and non-340B hospitals, he explained.
In addition to Udenyca, Coherus is currently advancing 2 additional late-stage biosimilar programs: an adalimumab biosimilar referencing Humira and an etanercept biosimilar referencing Enbrel. It is also developing ophthalmology biosimilars, including ranibizumab, referencing Lucentis, and aflibercept, referencing Eylea. It is also developing CHS-131, a novel small-molecule agent that is intended to treat both nonalcoholic steatohepatitis and multiple sclerosis.
From Amjevita to Zarxio: A Decade of US Biosimilar Approvals
March 6th 2025Since the FDA’s groundbreaking approval of Zarxio in 2015, the US biosimilars market has surged to 67 approvals across 18 originators—though the journey has been anything but smooth, with adoption facing hurdles along the way.
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.
The Banking of Biosimilars: Insights From a Leading Health Economist
February 4th 2025Biosimilars have the potential to reduce health care costs and expand patient access, but economic and policy barriers affect adoption, explored James D. Chambers, PhD, MPharm, MSc, associate professor at the Tufts Medical Center Institute for Clinical Research and Health Policy Studies, in an interview.