Growing use of innovator biologics, including those with biosimilar competition, has led to increased Medicare Part B drug expenditures, with the trend unlikely to stop.
Medicare Part B drug expenditures have grown in recent years, which is likely to endure due to the growing use and availability of innovator biologics, according to JAMA Health Forum.
Researchers aimed to evaluate the extent to which Medicare Part B spending growth was linked with changes in price vs quantity, and how these trends intermingled with marketplace entry of new drugs.
Almost 4 million beneficiaries of traditional Medicare used Part B-covered drugs in 2020, where total payments reached $38.5 billion. Even though total Part B spending was almost one-fifth of Medicare’s outpatient prescription drug benefit (Part D) in the same year. Part B has seen sustained increases, and beneficiaries of traditional Medicare encounter 20% cost sharing for most Part B drugs.
Cloud Pricing Stock Vector Illustration | © 123RF Stock Photos
The cross-sectional study quantified the degree of spending concentration and the link between price and use of Part B drugs among fee-for-service Medicare beneficiaries. Use and spending data for separately payable Part B drugs were included in this study, and source data were aggregated to the drug-year level and reported from 2016 to 2020.
Descriptive decomposition and index analyses quantified the relative association, separately, of price and use changes for present single-source drugs, existing drugs that met competition, and new drugs that came onto the market. Data analysis was undertaken from June to December 2022.
The main outcomes consisted of Part B spending by the fee-for-service Medicare program and beneficiaries, and use, defined as dosage units and beneficiary drug use.
A total of 535 unique Part B drug products were included in the study. During the period of 2016 to 2020, 15 or fewer products made up half of all Part B drug expenditures. The 7 drugs that made up the top 25% of spending was extremely consistent over time and were all biologics. Part B drug products that cost $1.85 or less per administration made up over 505 of the doses administered in 2020. Part B drug spending grew by $15 billion from 2016 to 2020.
The emergence of new, nonbiosimilar drugs during this time accounted for $12 billion of the increased spending (80%), while use shifts and price increases among present single-source brand drugs accounted for the leftover increase in spending. Part B spending lowered among the subset of existing drugs encountering generic or biosimilar competition. Among single-source drugs on the market in 2016, the index that varied dosage units surpassed the index that varied price in all years, confirming that changes in use were linked with more with spending growth for those drugs.
Three of the 7 drugs making up the top quarter of Medicare Part B spending every year have biosimilars on the US Market:
Related analyses had shown that most biologic drugs don’t have biosimilar competitors in the current market and the pipeline. High-spending, single-source drugs that have been on the market for years will probably be subject to price negotiations under the Inflation Reduction Act of 2022.
“Negotiations may curb future increases in the Medicare payment limit,” the researchers emphasized.
Compared with existing products, drugs more recently brought to market were linked with Part B spending increases in the past few years. Almost all increases in Part B drug spending over the last 10 years were associated with biologics.
“Although CMS cannot negotiate prices of newly marketed drugs, prices are subject to the inflation rebate,” continued the researchers.
Additionally, the researchers also found that the price of single-source drugs made up a fairly small share of the overall spending increase and suggests that the association of the rebate previsions with spending might be muted.
Analyses also suggest that policies targeting the highest-selling drugs have the most potential to reduce spending, while those targeting price jumps will have a smaller influence.
One notable limitation of this study is that drug spending and use for Medicare Advantage, which makes up over 40% of total Medicare enrollment in 2020, was not taken into consideration by these data.
“The findings [of this study] suggest that policies targeting top-selling drugs may have greater potential to curb Part B drug spending than those targeting price increases,” concluded the researchers.
Reference
Hyland MF, Sachs RM, Robillard L, Hayford TB, Bai G. Spending on and use of clinician-administered drugs in medicare. JAMA Health Forum. Published online September 8, 2023. doi:10.1001/jamahealthforum.2023.2941
Eye on Pharma: Sandoz Files Antitrust Suit; Yuflyma Interchangeability; Costco’s Ustekinumab Pick
April 22nd 2025Sandoz's antitrust suit against Amgen, the FDA’s interchangeability designation for Celltrion’s adalimumab biosimilar, and the inclusion of an ustekinumab biosimilar in Costco’s prescription program highlight growing momentum to expand biosimilar access and affordability for patients with chronic inflammatory diseases.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
President Trump Signs Executive Order to Bring Down Drug Prices
April 16th 2025To help bring down sky-high drug prices, President Donald Trump signed an executive order pushing for faster biosimilar development, more transparency, and tougher rules on pharmacy benefit managers—aiming to save billions and make meds more affordable for everyone.
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.
Latest Biosimilar Deals Signal Growth Across Immunology, Oncology Markets
April 14th 2025During Q1 2025, pharmaceutical companies accelerated biosimilar expansion through strategic acquisitions and partnerships in hopes of boosting patient access to lower-cost treatments in immunology and oncology.
Experts Pressure Congress to Remove Roadblocks for Biosimilars
April 12th 2025Lawmakers and expert witnesses emphasized the potential of biosimilars to lower health care costs by overcoming barriers like pharmacy benefit manager practices, limited awareness, and regulatory delays to improve access and competition in chronic disease management during a recent congressional hearing.