The high cost of healthcare is putting a strain on employers who provide health insurance coverage to their employees, and prescription drug prices are now front and center in the push to make coverage more affordable to provide to American workers.
The high cost of healthcare is putting a strain on employers who provide health insurance coverage to their employees, and prescription drug prices are now front and center in the push to make coverage more affordable to provide to American workers.
According to The Commonwealth Fund, about half of Americans are employed by small businesses, and as a result of rising insurance costs that are putting added pressure on these small employers’ budgets, more than 19% of these employees lack health coverage altogether, and one-fourth of small business owners say that the cost of prescription drugs is the biggest hurdle they face in providing coverage to their employees.
A number of policy proposals have been advanced in Congress with an eye toward bringing down drug costs, most notably HR 3, the Lower Drug Costs Now Act put forward by House Speaker Nancy Pelosi, D-California.
While the bill, which notably gives HHS the ability to negotiate drug prices, may not be likely to pass given a lack of Republican support (and the president has signaled that he will instead support bipartisan legislation in the form of the Prescription Drug Pricing Reduction Act, or S 2543), it does have some features that have appealed to parties on both sides of the aisle. Among the provisions shared by HR 3 and S 2543 are limits on out-of-pocket spending for Medicare beneficiaries in Part D, reduced federal reinsurance for some drugs in Part D, and mandatory rebates to Medicare when drug makers raise prices above the rate of inflation. Most of these provisions target Medicare, not the commercial market, but the hope is that the commercial marketplace will follow CMS’ lead.
Amid the ongoing debate over these policy proposals, the Employers’ Prescription for Affordable Drugs, a group comprising The Pacific Business Group on Health, the ERISA Industry Committee, and the National Alliance of Healthcare Purchaser Coalitions, said in a statement that “Our current system is unsustainable at all levels, and Congressional action is necessary to help address this pressing problem. Policymakers across the political spectrum want to lower drug costs, so the time to act is now.”
According to the group, where markets fail, government intervention is warranted, and HR 3 puts forward several proposals that would help balance the marketplace. The group says that targeted policies to allow for meaningful negotiations with drug makers and the ability of payers and purchasers to take advantage of negotiated prices are promising, but, with both HR 3 and S 2543, Congress should include “robust safeguards” to keep costs from shifting to consumers.
The group also called on law makers to adopt measures put forward by the Senate Health, Education, Labor and Pensions; Finance; and Judiciary Committees, as well as the House Ways and Means and Energy and Commerce Committees, including eliminating patent evergreening, prohibiting spread pricing, requiring drug makers to report and justify price hikes, curbing the abuse of citizen petitions, allowing generic and biosimilar developers to counteract wrongful delays of their products, and other proposals.
AAM Report: Generics and Biosimilars Savings Reach $445 Billion in 2023, Part 1
September 18th 2024Savings from generic and biosimilar drugs totaled $445 billion in 2023, showing promise for the growth of both markets and highlighting the success of expansion policies for these products, according to a new report from the Association for Accessible Medicines (AAM).
Expanding Biosimilar Adoption: Insights and Strategies With Dr Sophia Humphreys
September 16th 2024Sophia Humphreys, PharmD, MHA, BCBBS, director of system formulary management at Sutter Health, discusses the challenges of expanding biosimilars into new therapeutic areas and highlights the role of education, competitive pricing, and integrated delivery networks in improving adoption and market growth.
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.
BioRationality: FDA Clarification Provides New Indications and Process Change for Biosimilars
September 9th 2024Sarfaraz K. Niazi, PhD, explains the FDA's new guidelines on post-approval changes for biosimilars, emphasizing the processes for reporting modifications, comparability assessments, and the potential for biosimilars to introduce new indications or formulation changes, which could significantly impact their market competitiveness and accessibility.
The Role of Coverage Strategies in Biosimilar Market Impact and Cost Savings
September 4th 2024A recent study highlights that although biosimilars have led to significant price reductions, originator products with sole preferred coverage strategies have maintained market share, suggesting that increased biosimilar uptake alone may not fully leverage the market's competitive and cost-saving potential.