H.R. 3, The Lower Drug Costs Now Act, passed 2 committees in the House of Representatives Thursday, with a bipartisan amendment intended to boost uptake of biosimilars tucked inside.
H.R. 3, The Lower Drug Costs Now Act, passed 2 committees in the House of Representatives Thursday, with a bipartisan amendment intended to boost uptake of biosimilars tucked inside.
At the hearing in the House Energy and Commerce Committee, legislators amended the bill to include a proposal from Representatives Kurt Schrader, D-Oregon, and Greg Gianforte, R-Montana. The change would increase reimbursement for biosimilar drugs in Medicare Part B to the average sales price (ASP) plus 8%, up from the current 6% plus ASP, for 5 years. The idea was introduced last month as a separate bill, the BIOSIM Act.
The bill, which was also passed in the Education and Labor Committee, aims to lower prescription drug costs by giving the federal government the ability to negotiate price based on an international pricing index and sets a $2000 out-of-pocket limit in Medicare Part D.
Another amendment increased the minimum number of drugs that the administration could negotiate from the top 25 most costly drugs to the top 35. And it raised the threshold for drugs that could be subject to HHS negotiations from those with 1 generic competitor to those with 2 generic competitors.
House Speaker Nancy Pelosi, D-California, is moving ahead with the bill despite the communication breakdown with President Donald Trump, who campaigned on lowering drug prices, but is now the subject of an impeachment inquiry, making the bill’s future in the Republican-controlled Senate uncertain.
Pelosi’s bill would force companies to negotiate by imposing strict taxes on the medications if the firms refused. The Congressional Budget Office has estimated the legislation would cut industry revenues by $500 billion to $1 trillion over 10 years, but also save Medicare $345 billion over 7 years, partly because beneficiaries would no longer have to engage in drug rationing, and thus staying healthier.
A separate estimate from HHS found that households would save $158 billion over 10 years.
The House Ways and Means Committee is expected to mark up and vote on the measure next week, setting the bill up for a full House vote during the last week of October, according to reports.
The AARP was one of the organizations testifying in favor of the bill in Ways and Means, which had a hearing Thursday. Last month, the organization released a report saying drug prices have been rising for 12 straight years.
“Simply put, current prescription drug price trends are not sustainable. There is no reason Americans should continue to have to pay the highest brand-name drug prices in the world. No one should be forced to choose between buying groceries and buying the prescription drugs they need. It is long past time for Congress to take action to lower prescription drug prices,” said AARP National Volunteer President Catherine Alicia Georges, EdD, RN, in remarks prepared for testimony.
FTC Releases Second Report on PBMs Meddling in Generic Drug Markets
January 19th 2025The 3 largest pharmacy benefit managers (PBMs) increased many specialty generic drugs prices by hundreds of percent, with some drugs seeing thousands of percent markups, according to the Federal Trade Commission (FTC)’s second interim report on PBM practices.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Eye on Pharma: Korean Drugmakers’ Impact in Europe; New Denosumab, Eculizumab Deals
January 11th 2025Korean drugmakers hold over 50% market share in the 6 best-selling biosimilar markets, 2 companies sign exclusive licensing partnership for a denosumab biosimilar, and 2 others join forces for an eculizumab biosimilar.
Senators Introduce Bipartisan Legislation to Protect Skinny Labeling
January 2nd 2025To close out the year, 4 senators came together to introduce a new bipartisan bill to protect biosimilar and generic drug manufacturers from patent litigation when obtaining “skinny label” approvals for their products.