Over the past 2 years, commercially insured patients enrolled in plans that had value-based contracts for certain high-cost drugs had lower copays for their medications than did patients enrolled in plans without such contracts. That finding comes from “Delivering Results for Patients: The Value of Value-Based Contracts,” a new report from the Pharmaceutical Research and Manufacturers of America (PhRMA).
Over the past 2 years, commercially insured patients enrolled in plans that had value-based contracts for certain high-cost drugs had lower copays for their medications than did patients enrolled in plans without such contracts. That finding comes from “Delivering Results for Patients: The Value of Value-Based Contracts,” a report released today by the Pharmaceutical Research and Manufacturers of America (PhRMA).
PhRMA’s report identifies the following types of value-based contracts:
According to PhRMA, value-based contracting has the potential benefit of allowing for broader access to innovative medicines by reducing the payers’ risk of suboptimal outcomes and encouraging the appropriate use of medicines. These agreements may also help to reduce medicine costs, says PhRMA, if manufacturers pay higher rebates for patients who do not meet their outcome targets. Patients could realize a savings if rebates are passed on to them.
As a result of these potential benefits, many health plans are warming to the idea of value-based arrangements, especially in the form of outcomes-based contracts, according the report. PhRMA says that, according to a 2017 Avalere Health report on payer perspectives on outcomes contracting, approximately 70% of commercial plans have a favorable view of this contract type, approximately 25% have implemented at least 1 such contract, and 30% report that they are negotiating a contract or contracts.
Among plans that have at least 1 outcomes-based contract, 55% report that they have entered into a contract that focuses on endocrine disorders—including diabetes—and another 33% are considering doing so. “If new value-based contracts are able to improve use of medicines for diabetes and reduce the burden of this disease in the United States by as little as [5%], these contracts could save nearly $9 billion annually in direct medical costs by preventing 365,000 emergency department visits, 390,000 hospital outpatient visits and 1.3 million hospital inpatient days,” according to the report.
Patients, too, could see a positive financial impact from such contracts. PhRMA says that it has worked with Avalere Health to analyze formulary coverage for existing outcomes-based contracts, including those for drugs that treat diabetes, high cholesterol, and HIV. Copays for patients enrolled in silver-level exchange plans with outcomes-based contracts were an average of 28% lower for these drugs than they were for patients enrolled in market average silver-level exchange plans.
However, barriers to value-based contracts—including concerns about how such arrangements might affect price reporting, issues with potentially implicating the federal anti-kickback statue, and uncertainty about the FDA’s rules regarding manufacturers’ communications with plans—make it difficult to accurately judge the potential that these contracts could have, says PhRMA.
“Small policy changes to modernize outdated regulations have the potential to lead to tremendous benefits for patients and the health care system,” the report concludes.
Empowering Vulnerable Populations: The Path to Equitable Biologic Therapy Access
December 22nd 2024Elie Bahou, PharmD, senior vice president and system chief pharmacy officer at Providence, discusses strategies to improve equitable access to biologic therapies, including tiered formularies, income-based cost sharing, patient assistance programs, and fostering payer partnerships.
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.
BioRationality: Withdrawal of Proposed Terminal Disclaimer Rule Spells Major Setback for Biosimilars
December 10th 2024The United States Patent and Trademark Office (USPTO)’s withdrawal of its proposed terminal disclaimer rule is seen as a setback for biosimilar developers, as it preserves patent prosecution practices that favor originator companies and increases costs for biosimilar competition, according to Sarfaraz K. Niazi, PhD.
Commercial Payer Coverage of Biosimilars: Market Share, Pricing, and Policy Shifts
December 4th 2024Researchers observe significant shifts in payer preferences for originator vs biosimilar products from 2017 to 2022, revealing growing payer interest in multiple product options, alongside the increasing market share of biosimilars, which contributed to notable reductions in both average sales prices and wholesale acquisition costs.
Perceptions of Biosimilar Switching Among Veterans With IBD
December 2nd 2024Veterans with inflammatory bowel disease (IBD) prioritize shared decision-making, transparency, and individualized care in biosimilar switching, favoring delayed switching for severe cases and greater patient control.