October 23rd 2026
A commentary on Irish oncology spending finds hospital drug costs rose more than 3100% in under a decade, while biosimilar uptake remained low.
October 8th 2026
Teva's Robert Cook, PhD, explains the clinical data, interchangeability, and supply strategy behind its Degevma and Ponlimsi biosimilars.
September 29th 2026
The FDA approved Teva's Degevma, a denosumab biosimilar to Xgeva for cancer-related bone disease, rounding out its Xgeva/Prolia portfolio.
August 31st 2026
Bevacizumab-to-biosimilar-to-branded transitions delayed nAMD care and cost more than direct switches.
August 6th 2026
Analytical characterization supports monoclonal antibody biosimilar approvals and may reduce clinical testing needs, researchers found.
News Briefs: Samsung Bioepis, Cipla, Biocon Report Progress
Biocon and Viatris edge closer to EU marketing authorization for a bevacizumab biosimilar, among other biosimilar business developments.
Opinion: A Short History of Biosimilars
Biosimilars have come a long way, and their path has mirrored that of generics—fraught with obstacles. Still, a stronger embrace is needed from physicians and payers.
Study: Trastuzumab Biosimilar IV Offers Better Value Than Reference SC
In a review of trastuzumab treatment options, reviewers concluded subcutaneous (SC) vs intravenous (IV) options may be more costly and sometimes less practical.
Coherus BioSciences Squares Off Against Neulasta Onpro
Sales of the pegfilgrastim oncology support biosimilar Udenyca fell off in late 2020, but Coherus doesn't see orginator company Amgen's advantage lasting much longer.
Fresenius Kabi Maps Out Biosimilar Strategy
The Germany-based company with global operations plans to ramp up its biosimilars portfolio through 2025.
Rituximab Biosimilar Regimen Fails Cost-Effectiveness Test in FL
Although a more costly medicine, obinutuzumab proved more cost-effective over the long run than rituximab biosimilars in follicular lymphoma.
Filling in the Blanks: The Patient-Provider Conversation About Biosimilars
Gary H. Lyman, MD, PhD, provides an expert overview on overcoming the challenges of discussing biosimilars with patients.
Study: Gender, Internet Habits Influence Biosimilar Acceptance
Patient characteristics are predictive of whether a switch to a biosimilar is likely to be accepted, investigators found.
Roche's 2020 Losses to Biosimilars Were "Worst It Can Get"
Biosimilar competition took a big chunk of revenue from Roche's aging blockbusters in 2020, and the company is banking on its newer medicines to drive fresh revenue growth.
Study: Biosimilar Use Varies by Type of Institution and Physician Characteristics
Physician specialty and practice setting each play a significant role in whether biosimilars are administered vs originators, according to a large, cross-sectional study.
Amgen Profits Get a Ride on Biosimilar Growth
Amgen described how a double-edged biosimilars sword has worked for and against the company's profit margin.
Pfizer Biosimilar Revenues Top $525 Million in Fourth Quarter 2020
Pfizer's investment in biosimilars is starting to pay off, as it now ranks these agents among its top revenue drivers.
Oncology Biosimilar Roundup for January 2021
Findings from biosimilar studies of Kanjinti (trastuzumab) and Mvasi and Zirabev (bevacizumab) rounded out our oncology biosimilar coverage in January.
Magellan Rx Reports Step Therapy Is Workhorse in Biosimilar Utilization
The pharmacy benefit manager reported 90% biosimilar uptake among its health plans that adopted clinical management policies that included step therapy or parity usage.
Study: Bevacizumab Biosimilar Finds Acceptance in First-Line Treatment of mCRC
Investigators noted comparable use of bevacizumab biosimilar and reference products among patients treated for metastatic colorectal cancer (mCRC).
FDA Accepts Bio-Thera's BLA for Bevacizumab Biosimilar
Guangzhou, China-based Bio-Thera has filed a biologics license application (BLA) with the FDA for the approval of bevacizumab biosimilar candidate BAT1706.
Vizient Predicts 7.5% Humira Price Increase Before Biosimilars Arrive
In its annual drug price guide, Vizient predicts that US annual adalimumab (Humira) revenues could reach $24 billion before biosimilars enter the marketplace.
Nurses Can Counter Nocebo Effect in Biosimilar Switching
The study of originator infliximab and SB2 used nurses as the first point of contact when educating patients, relying partly on patient trust in these health care professionals.
Charles Bennett, MD, PhD, Discusses Hurdles for Biosimilar Adoption
Charles Bennett, MD, PhD, a hematologist, oncologist, and professor at the University of South Carolina, explained the many sticking points that prevent biosimilar savings.
China Pulls Out Stops for Biosimilar Development
It took Henlius years to get a rituximab biosimilar approved in China. Now, that process could be cut in half, owing to significant regulatory reforms.
Coherus CEO Discusses Post–COVID-19 Growth Prospects
Coherus BioSciences CEO Dennis M. Lanfear discusses the company's biosimilar marketing prospects in 2021.
Prestige Biopharma Plots Biosimilar Growth Strategy
Biosimilars will be the cornerstone for a leap into biologics development and commercialization, according to the CEO of Prestige Biopharma. Also, Innovent Biologics reaches a marketing agreement.
Investigators Study Risks of Hypertension, Proteinuria With Bevacizumab
The study was designed to elucidate incidence of hypertension and proteinuria in patients treated with bevacizumab reference vs biosimilar products.
Swift Uptake for Mvasi Suggests Provider Comfort With Use
Investigators looked at the first 9 months of use following the launch of the bevacizumab biosimilar Mvasi to gauge physician comfort with this agent across tumor types.
IGBA, Celltrion, Others Mark Biosimilar Advances
The Center for Biosimilars® reports on developments at the International Generic and Biosimilar Medicines Association (IGBA), Celltrion, Innovent Biologics, and Kamada.
With New Policy, CMS Promises to Exit "Stone Age" of Health Information
CMS looks to speed up health information transfer by putting faxes in the past. It also aims to set deadlines for payers to respond to prior authorization requests.
Hill Describes Supercharged Biologics Market in China
Lawrence A. Hill, PharmD, MBA, RPH, BCPS, provided an insider's view of the rapidly changing biologics and biosimilars market and regulatory structure in China.
Not So Different: Charles Bennett, MD, PhD, Discusses Why the FTC Needs to Join the Effort to Improve the Biosimilar Market
We spoke to Charles Bennett, MD, PhD, a clinical pharmacy specialist, about his recent oncology biosimilars study and how pay-for-delay schemes have somewhat stalled the biosimilar market.
Data From HERITAGE Confirm PK Biosimilarity for Ogivri
Pharmacokinetic (PK) parameters matched up with those of reference trastuzumab in an extended analysis of data from the HERITAGE trial.
Economists Probe Cost-Effectiveness of Biosimilars
Authors of a review found that biosimilar uptake and market share are not in themselves sufficient to establish whether these agents will lead to savings.