JULY 24, 2024
Representative Mike Connolly joined his Cambridge and Somerville colleagues in the House today to pass H.4891, An Act promoting access and affordability of prescription drugs, which protects patients and independent pharmacists by regulating the pharmacy benefit manager (PBM) industry; by banning many of the industry’s worst business practices; by increasing transparency into PBMs and drug manufacturers through the Health Policy Commission (HPC) and the Center for Health Information and Analysis (CHIA); and by reducing or eliminating copays for certain chronic conditions.
"Patients are paying way too much for the lifesaving medicines they need, because of corporate greed," Representative Connolly said. "I was proud to vote to both reign in certain tactics deployed by PBMs to unscrupulously increase their profits and vote to cap the price of certain drugs to help patients save money."
Via an amendment cosponsored by Rep. Connolly and filed by Rep. Worrell, the Health Policy Commission will be tasked with surveying the Commonwealth for so called "pharmacy deserts" where constituents don't have good access to pharmacies based on where they live. This analysis will also include policy recommendations on how to address access inequities and was we can stop the creation of new deserts. Constituents may recall experiencing a temporary pharmacy desert when during a one week period in September 2022 three Walgreens Pharmacies were closed for a total of four days in Cambridge, Somerville, and Greater Boston, due to staffing and IT issues. At that time Rep. Connolly sounded the alarm in the press and made a formal complaint to the Department of Public Health. Rep. Connolly is hopeful that with the passage of this amendment, we can take proactive steps to protect pharmacy access across the state.
Regulation & Auditing of the PBM Industry
Following a Federal Trade Commission (FTC) report issued earlier this month which details the undue influence of PBMs on the prescription drug market, the bill passed today licenses PBMs operating in the Commonwealth, subjects them to the Massachusetts Division of Insurance (DOI) and health insurer audits, and curbs some of their most abusive practices.
As the FTC report details, the PBM industry has experienced significant horizontal consolidation and vertical integration, with five of the top six PBMs vertically integrated with insurers, pharmacies, and provider services.
Due to decades of mergers and acquisitions, the three largest PBMs now manage nearly 80 percent of all prescriptions filled in the United States, while six PBMs manage more than 90 percent of total U.S. prescription claims. A mostly unregulated industry, PBMs wield enormous power and influence over patients’ access to drugs and the prices they pay, negotiating the terms and conditions for access to prescription drugs for hundreds of millions of Americans.
The bill passed by the House today requires PBMs to be licensed with DOI every three years. PBMs will also be required to pay an application fee of $25,000. It also mandates that DOI audit PBMs once every three years and provides for periodic audits by health insurers who contract with PBMs.
Read on for a full list of provisions in the bill.
Consumer & Pharmacy Protections from PBM Abusive Practices
Spread pricing is a practice by which a PBM pays a pharmacy a lower price for a dispensed drug than the price a health insurer agrees to pay for the drug. This allows PBMs to use their significant market power to increase their own profits, rather than pass along savings to consumers.
To ensure protection of consumers and pharmacies, the bill passed today prohibits PBM spread pricing, as well as point of sale fees and retroactive fees, and imposes a 10 percent surcharge on PBMs that engage in these banned practices.
PBMs also use their market power to negotiate significant discounts, called “rebates,” from pharmaceutical manufacturing companies on the list price of prescription drugs. These savings are generally shared by PBMs and health insurers. Rebates retained by PBMs are another source of profits for PBMs, while health insurers claim their share of rebates is used to reduce premiums.
The bill passed today requires PBMs and health insurers to forward at least 80 percent of rebates received by carriers or PBMs to consumers at the point of sale.
Further, the bill passed by the House today:
- Requires pharmacies to charge consumers the lesser of their applicable cost-sharing amount or the pharmacy retail price, so that consumers no longer unknowingly pay more for their prescription drugs when using their health insurance benefits than they would if they paid the pharmacy retail price.
- Ensures that patients that get assistance paying for their prescription drugs are not penalized by their health insurers by requiring health insurers and PBMs to include any cost-sharing amounts paid by an enrollee or another third party on behalf of an enrollee when calculating an enrollee’s total cost-sharing contributions.
- Imposes a duty of good faith and fair dealing on PBMs when dealing with all parties with which they interact in the performance of PBM services.
- Requires PBMs to provide an adequate and accessible network for prescription drugs.
- Establishes that PBMs must maintain a Maximum Allowable Cost (MAC) list for generic prescription drugs and must reimburse an independent pharmacy for drugs at the same amount that the PBM reimburses PBM affiliates for providing the same pharmacist services.
- Makes permanent the ability of consumers to use drug manufacturer coupons to pay for prescription drugs.
- Requires any entity that intends to close a pharmacy or pharmacy department to notify the state in writing at least 60 days before the proposed closure date. If the state finds that the intended closing is likely to result in the creation of a pharmacy desert, the state must conduct a public hearing to present information on alternative sources of pharmacy services available to impacted consumers and allow interested parties the opportunity to share comments and concerns about the proposed closure.
Transparency into PBM & PMC Business Practices
Currently, there is limited transparency into PBMs’ operations and revenue. This bill increases transparency into the business practices of PBMs and pharmaceutical manufacturing companies by requiring PBMs and certain pharmaceutical manufacturing companies to submit data to CHIA for the HPC’s annual cost trends report, and mandatory participation in the HPC’s annual benchmark hearing process.
It also assesses PBMs and pharmaceutical manufacturing companies for the expenses of HPC and CHIA in a similar manner as current health care providers, while increasing the penalty for noncompliance with CHIA data reporting requirements from $1,000 per week to $25,000 per week. This applies to all entities required to report, which would now include PBMs and pharmaceutical manufacturing companies.
The bill also establishes an Office of Pharmaceutical Policy and Analysis within the HPC to better advise the Legislature and state agencies on matters related to pharmaceutical drug policy and tasks the new office with studying cost and access issues with groundbreaking cell and gene therapies that are due to be released by 2035.
Co-payment Caps on Medications for Certain Chronic Illnesses
This legislation passed today reduces or eliminates the price on medications for diabetes, asthma, and the most prevalent heart condition among a health plan’s enrollees.
Twenty-two percent of Massachusetts residents reported they did not fill a prescription, cut pills in half, or skipped a dose because they couldn’t afford it, according to a Alterum report. Limiting and reducing copays is a health equity issue – people of color are disproportionately impacted by chronic conditions such as diabetes, asthma, and hypertension. Black and Hispanic residents were more likely to cut pills in half, skip a dose, or not to fill a prescription due to cost.
To ensure that everyone, especially at-risk populations, are getting equitable access to the medication they need, the bill requires insurance carriers to identify one generic drug and one brand name drug used to treat diabetes, asthma, and the most prevalent heart condition among its enrollees.
Identified generic drugs are covered without any cost sharing and the co-pay for identified brand name drugs are capped at $25 per 30-day supply. It also provides for annual reporting by insurance carriers to DOI on the list of drugs with no or limited cost sharing.
Having been passed by both chambers, a conference committee will be appointed to reconcile differences in the House and Senate versions of the bill.