{"database": "press", "table": "releases", "rows": [["https://www.crapo.senate.gov/media/newsreleases/finance-committee-republicans-new-medicaid-rule-risks-disrupting-patient-care", "Finance Committee Republicans: New Medicaid Rule Risks Disrupting Patient Care", "2023-11-01", "2023", "2023-11", "Republican", "Senate", "ID", "Mike Crapo", "C000880", "www.crapo.senate.gov", "crapo", "https://www.crapo.senate.gov/media/newsreleases", "scraper", "Washington, D.C.--In a concerning departure from precedent, the Centers for Medicare & Medicaid Services (CMS) proposed a new rule to change Medicaid Drug Rebate Program (MDRP) operations in ways that offer no material benefit for patients. In a letter to Administrator Chiquita Brooks-LaSure, Republican members of the U.S. Senate Finance Committee, led by Ranking Member Mike Crapo (R-Idaho), urged the Administration to withdraw problematic components of the proposed rule and work with Congress to develop improvements to the Medicaid program so patients have access to cutting-edge, life-saving prescription drugs.\n\nThe senators note:\n\nWhile we share some of the agency\u2019s objectives, including preventing certain problematic practices within the prescription drug supply chain, many of the [rule\u2019s] proposed changes defy longstanding statutory understanding and impose costly new mandates, creating fiscal uncertainty for states and risking patient access to the most innovative therapies and cures.\n\nThey identify several problems with the proposal, including \u201cstacking\u201d to compute the \u201cBest Price\u201d benchmark, which would create technical complications and risk undercutting the policy\u2019s core objectives by disincentivizing larger price concessions.\n\nThe senators also highlight the lack of a patient-oriented justification for the proposal\u2019s price verification survey, noting that the proposed rule seeks to establish a survey process for certain \u201chigh cost\u201d covered outpatient drugs, like cell and gene therapies, instead of addressing the access barriers identified by states, patients and providers.\n\nThey end the letter:\n\nWe urge CMS to preserve the MDRP\u2019s statutory balance consistent with Congress\u2019s intent by withdrawing the misguided proposals that risk disrupting patient care. We would welcome the opportunity to work with you to improve the Medicaid program so that patients have access to cutting-edge, live-changing prescription drugs.\n\nIn addition to Ranking Member Crapo, the letter is signed by Senators John Cornyn (R-Texas), John Thune (R-South Dakota), Tim Scott (R-South Carolina), James Lankford (R-Oklahoma), Steve Daines (R-Montana), Todd Young (R-Indiana), John Barrasso (R-Wyoming), Ron Johnson (R-Wisconsin), Thom Tillis (R-North Carolina) and Marsha Blackburn (R-Tennessee).\n\nRead the full letter here or below:\n\nDear Administrator Brooks-LaSure:\n\nWe write to express concerns with several policies included in the proposed rule \u201cMisclassification of Drugs, Program Administration and Program Integrity Updates Under the Medicaid Drug Rebate Program\u201d (NPRM). While we share some of the agency\u2019s objectives, including preventing certain problematic practices within the prescription drug supply chain, many of the NPRM\u2019s proposed changes defy longstanding statutory understanding and impose costly new mandates, creating fiscal uncertainty for states and risking patient access to the most innovative therapies and cures. Rather than establishing new reporting requirements or altering foundational definitions, we ask that you work with states, patients, providers and policymakers to implement reforms that promote adoption of value-based arrangements or other innovative purchasing models that improve health outcomes and reduce costs.\n\nAs enacted by Congress, the Medicaid Drug Rebate Program (MDRP) intends to ensure patients have widespread access to life-sustaining and lifesaving outpatient prescription drugs through a voluntary partnership with pharmaceutical manufacturers. The rebates required under this program, coupled with broad prescription drug coverage, aim to contain costs for states while serving the needs of Medicaid recipients and preserving incentives for medical breakthroughs.\n\nUnfortunately, the NPRM proposes to disrupt this approach dramatically, upending more than three decades of statutory understanding and practice by rewriting the rules of the road for MDRP rebate calculations. Specifically, the proposal would require the aggregation of all manufacturer rebates and discounts to all supply-chain participants for the computation of the \u201cBest Price\u201d benchmark used as the basis for Medicaid rebates for numerous drugs. The Centers for Medicare and Medicaid Services\u2019 (CMS\u2019s) proposed \u201cstacking\u201d policy reverses the plain language of the statute, along with previous regulations and relevant caselaw, replacing Medicaid Best Price\u2019s traditional definition, as the best price provided to an individual purchaser, with a hypothetical \u201cbest price\u201d merging any number of unrelated price concessions, offered to unaffiliated and wholly separate entities.\n\nThe operational complexities inherent in this sweeping shift could render the proposal entirely unworkable, even from a purely practical standpoint, as neither CMS nor supply-chain participants have systems in place to \u201cstack\u201d unrelated rebates and discounts stemming from a range of different transactions and contracts, often incorporating proprietary information, into a clear and verifiable figure. That said, even setting aside technical complications and potential legal headwinds, the substantive policy change at issue risks undercutting its own core objectives by disincentivizing, rather than encouraging, larger price concessions. Stacking rebates and discounts could result in withheld price concessions, smaller supplemental rebates for states, and a new set of hurdles for price reporting oversight. In the meantime, patients would receive no benefit from this novel departure from precedent.\n\nThe NPRM also fails to provide a patient-oriented justification for its proposed price verification survey. Gene and cell therapies have the potential to transform health care delivery, offering treatments and cures for previously incurable diseases. While the private sector has developed payment arrangements for these truly novel products, federal government programs have fallen short on providing a viable pathway to coverage for patients. Instead of addressing the access barriers identified by states, patients and providers, the NPRM seeks to establish a drug price verification survey process for certain \u201chigh cost\u201d covered outpatient drugs, including cell and gene therapies. The new price-based listing would require manufacturers to report information related to the costs of research, development and production or prices charged outside of the United States, which the agency proposes to publish. These new reporting requirements are irrelevant to the enforcement of the MDRP and risk disclosing proprietary information without remedying the underlying statutory and regulatory barriers to value-based coverage arrangements for gene and cell therapies under Medicaid.\n\nWe urge CMS to preserve the MDRP\u2019s statutory balance consistent with Congress\u2019s intent by withdrawing the misguided proposals that risk disrupting patient care. We would welcome the opportunity to work with you to improve the Medicaid program so that patients have access to cutting-edge, live-changing prescription drugs.\n\nSincerely,\n\n###", 1, "2026-03-30T01:40:41Z", "2026-04-08T01:01:09Z"]], "columns": ["url", "title", "date", "year", "month", "party", "chamber", "state", "member_name", "bioguide_id", "domain", "scraper", "source", "date_source", "text", "has_text", "collected_at", "updated_at"], "primary_keys": ["url"], "primary_key_values": ["https://www.crapo.senate.gov/media/newsreleases/finance-committee-republicans-new-medicaid-rule-risks-disrupting-patient-care"], "units": {}, "query_ms": 0.8198940195143223, "source": "dwillis/congress-press", "source_url": "https://github.com/dwillis/congress-press", "license": "MIT", "license_url": "https://github.com/dwillis/congress-press/blob/main/LICENSE"}