Senate Finance Committee PBM Reform Results In ‘Decimal Dust’ Of Savings

A focus on transparency, impacts of vertical integration and concerns about increasing government costs shows in the Congressional Budget Office score of the Senate pharmacy benefits manager reform bill.

gold swirl of dust on black background
CBO projects relatively small savings from the Senate Finance PBM reform bill. • Source: Shutterstock

The Senate Finance Committee’s pharmacy benefits manager reform bill is anticipated to save the federal government $1.73bn over a decade, a relatively small sum given the cost of the Medicare and Medicaid programs they would modify, which illustrates the challenges of taking on drug prices by going after supply chain “middlemen.”

Key Takeaways
  • The CBO projects $1.73bn in savings from the Senate Finance Committee’s PBM reform effort.

  • The federal government spent about half a trillion on Medicare in fiscal year 2021 and $98bn on Medicare Part D that year.

  • The low score is in part a win as previous PBM reform ideas were expected to cost the government hundreds millions of dollars

The Congressional Budget Office released a preliminary score of the Modernizing and Ensuring PBM Accountability Act on 24 July ahead of a 26 July committee markup of the legislation. (Also see "Senate Finance Dives Deeper Into PBM Weeds, Including Brand Over Generic Preferences" - Pink Sheet, 17 July, 2023

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Legislation

EU Pharma Reform: Exclusivity Vouchers Alone Are Insufficient Incentive For Antimicrobials, Industry Says

 

European pharma trade associations EFPIA and EUCOPE outline their respective views on how the EU’s pharma legislation overhaul should tackle antimicrobial resistance, and why transferable exclusivity vouchers alone will not suffice as incentives.

Switzerland Simplifies Imports Of Unauthorized Drugs To Tackle Drug Shortages

 

Swiss authorities have introduced temporary measures that will make it easier for health care professionals to import medicines that are either not authorized or not available in Switzerland, which will particularly benefit pediatric drugs, in light of ongoing shortages.

EU ‘Can’t Expect Industry To Give Up Proprietary Insights’ Under Health Data & Clinical Trials Regulations

 

Both the EU Clinical Trials Regulation and the European Health Data Space Regulation have the potential to improve harmonization and be highly valuable for industry – but the importance of protecting company data will be paramount, a life sciences consultant says.

340B Not Designed To Pass Savings Directly To Patients, Hospitals Tell Senate Committee

 
• By 

Respondents to a Senate investigation that could re-energize 340B reform efforts said hospitals offer patient assistance programs and use 340B revenue for “capital improvement projects” and “community benefit programs,” though they do not account for specific program revenue allocations.

More from Pink Sheet

EU Pharma Reform: Exclusivity Vouchers Alone Are Insufficient Incentive For Antimicrobials, Industry Says

 

European pharma trade associations EFPIA and EUCOPE outline their respective views on how the EU’s pharma legislation overhaul should tackle antimicrobial resistance, and why transferable exclusivity vouchers alone will not suffice as incentives.

Trump Administration Push For Dismissal, Transfer Of Mifepristone Case Leaves Overhang For Pharma

 

The Trump Administration requested a dismissal or transfer of a lawsuit seeking to tighten the safety requirements for the abortion pill mifepristone on procedural grounds, which still leaves the administration's position on the case's merits unclear.

Opioid Safety: US FDA Hears Mixed Messages On Adding Posmarketing Studies To Labeling

 
• By 

Some advisory committee members said adding quantitative data on misuse, abuse, opioid use disorder and overdose to labeling would be helpful, but others worried the two epidemiological studies were not sufficiently generalizable to a broader population.