The 2022 US law that for the first time lets Medicare negotiate prices for top-selling drugs, capped what older patients pay for prescriptions at 2,000 dollars a year, and exempted drugs approved only for rare diseases, an exemption widened in 2025.
United States, federal statute. The Inflation Reduction Act was signed on 16 August 2022 (Public Law 117-169). Its prescription drug title created the Medicare Drug Price Negotiation Program (Social Security Act sections 1191 to 1198), inflation rebates, and a redesign of Part D. Primary text: the Congress.gov record of H.R.5376; the Centers for Medicare and Medicaid Services publish the programme pages and negotiated prices.
What it changed: Medicare selects high-spending drugs that have been on the market without generic or biosimilar competition for at least seven years (small molecules) or eleven years (biologics) and negotiates a 'maximum fair price' that takes effect two years later. The first ten drugs, including the BTK inhibitor ibrutinib, had negotiated prices from 1 January 2026; the second list of fifteen, with prices from 2027, included the cancer drugs palbociclib, enzalutamide, pomalidomide and acalabrutinib. Part D out-of-pocket spending was capped at 2,000 dollars a year from 2025, which for patients on oral cancer drugs replaced bills of ten thousand dollars or more. Drugs with a single orphan designation and no other approved use were excluded; the One Big Beautiful Bill Act of July 2025 (Public Law 119-21) broadened that exclusion to drugs with multiple orphan-only indications and restarted the clock at the first non-orphan approval.
The arguments: manufacturers sued (unsuccessfully so far) and warned of fewer small-molecule cancer drugs, the 'pill penalty' of nine versus thirteen years; supporters point to the caps and the first negotiated savings. Oncology is disproportionately affected because cancer drugs dominate the highest-spending lists, and the orphan exclusion shapes which indications companies pursue first.
Showing the molecule this term concerns: Ibrutinib.
Shares Orphan drug designation, Orphan Drug Act 1983, US regulatory exclusivity periods, Hatch-Waxman Act 1984 and the tags law, us.
Shares Medicare coverage with evidence development, Health technology assessment (HTA), reimbursement and QALYs, Financial toxicity and the tags law, us.
Shares Incentives reward me-too drugs and marginal gains and the tags law, us.
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