Blog
Article
Nicole M. Boschi, PhD, the director of regulatory affairs at the National MS Society, talked about the impact of the upcoming Medicare Part D and Medicare Advantage changes for the multiple sclerosis community.
On August 16, 2022, President Biden signed the Inflation Reduction Act (IRA) into law. This landmark legislation aims to address several issues related to healthcare, particularly high prescription drug prices. In addition to giving Medicare the authority to negotiate the price of certain prescription drugs, the IRA established out-of-pocket Medicare Part D cost-sharing limits. Additionally, the IRA gives Part D beneficiaries the option to spread out the cost of their drugs over the course of the calendar year.
The National Multiple Sclerosis Society (Society) continually works to increase access to the treatments that those living with MS rely on, including advocating for the passage of the IRA. These new provisions represent the most significant changes in Medicare Part D since the program was established in 2006, and the Society is committed to educating healthcare providers on how to assist individuals affected by multiple sclerosis (MS) to navigate these changes to more affordably access medications that allow them to live their best lives. Here’s what you need to know:
No MS therapies were among the ten drugs chosen for the first negotiation cycle, which will become effective in 2026. Like the first 10 drugs, these additional 15 drugs will be limited to Part D drugs. Medicare drug pricing negotiation will expand to Part B in addition to Part D drugs in 2026, with the negotiated prices taking effect in 2028.
In 2024, Medicare Part D enrollees' out-of-pocket costs were capped at about $3,300 - $3,800 - when they reached the catastrophic coverage phase. Beginning January 1, 2025, the IRA caps annual out-of-pocket costs for Part D beneficiaries at $2,000. Once an individual reaches this limit, they will pay nothing out-of-pocket for the rest of the year. Please remember that this cap only applies to Part D drugs (oral and self-administered therapies) and not Part B drugs (infused drugs administered by a medical facility). This new out-of-pocket cap could provide a huge relief for many living with MS!
One of the provisions of the IRA aimed at reducing the burden of high prescription drug prices on Medicare beneficiaries is the option to spread the cost of their Part D prescription drugs over a calendar year. Enrollment in this program, known as the Medicare Prescription Payment Plan (M3P), is voluntary and may benefit individuals with high out-of-pocket prescription drug costs early in the plan year. Part D beneficiaries need to understand that the M3P is not a discount program, and it will not lower the cost of their drugs, but it will allow them to divide up their costs over a longer period.
The Society will work with providers and individuals living with MS to help them navigate these changes. Be on the lookout for additional learning opportunities.
800-344-4867, 7 a.m. to 5 p.m. MT (M-F)
More Resources