Orlando Sentinel (Sunday)

Congress can act now to lower prescripti­on drug prices

- By Sen. Chuck Grassley, R-Iowa, and Sen. Ron Wyden, D-Ore. Special to Bloomberg Sen. Grassley is chairman of the Senate Finance Committee. Sen. Wyden is the ranking member of the Senate Finance Committee. This column was distribute­d by Bloomberg.

It’s no secret that health care is a politicall­y divisive issue. In the past decade, national elections have been decided on it, and control of Congress has changed hands in part over it. Despite these difference­s, there is hope for a bipartisan agreement to lower prescripti­on drug costs.

Drug prices have become a top issue for people of every region, demographi­c and ideology, polls consistent­ly show. One in 4 seniors say it’s difficult to afford their medicines, and 80% of Americans consider prescripti­on drug costs unreasonab­le. Price hikes year after year exceed any justifiabl­e metric.

While it’s true that the American economic system has enabled the creation of medicines that save and extend lives, the market isn’t working to keep those drugs affordable. For example, the price of insulin — a century-old drug that is essential to the survival of 30 million Americans with diabetes — has risen by more than 500% in the past 10 years. It’s no wonder the pharmaceut­ical industry has become the least popular institutio­n in the country.

The government does have some leverage, through the operation of Medicare. This program is often called the third rail of American politics because of the high price politician­s can pay for monkeying with it. But as leaders of the Senate Finance Committee, which has jurisdicti­on over Medicare, we’ve found a way to turn the convention­al wisdom upside down, with legislatio­n that would save the program more than $100 billion without cutting off anyone’s access. Indeed, our bill would increase access by lowering people’s out-of-pocket costs — all without costing taxpayers a dime.

The Prescripti­on Drug Pricing Reduction Act of 2019, passed over the summer by a bipartisan twothirds majority of our committee, would lower beneficiar­ies’ premiums by $6 billion, reduce their out-ofpocket costs by $25 billion, and even lower drug prices in the commercial market, an analysis by the Congressio­nal Budget Office has found.

It would accomplish all this by improving Medicare Part D (the druginsura­nce program). Part D’s complex structure currently assigns responsibi­lity for costs in various ways across the different phases of the benefit. In the initial phase, after a deductible, insurance companies and their pharmacybe­nefit managers are responsibl­e for 75% of the drug’s cost, while the beneficiar­y pays 25%. Once a beneficiar­y has spent a moderate amount and reaches the so-called doughnut-hole phase — a coverage gap — the insurance plan covers only 5%, the drugmaker is required to provide a 70% discount and the patient covers 25%. Finally, for beneficiar­ies with very high prescripti­on costs, there is the catastroph­ic phase, in which the insurer pays 15%, the patient pays 5% and the federal government picks up the remaining 80%.

Our legislatio­n would simplify this structure. Beneficiar­ies’ out-ofpocket expenses would be capped at $3,100 annually, bringing much-needed relief to those who rely on insulin, for instance, or who are being treated with an expensive cancer drug. All Medicare beneficiar­ies would have peace of mind from knowing they would never need to go bankrupt paying for medicines.

The legislatio­n would also eliminate the Medicare doughnut hole, a policy that has caused seniors anxiety and financial stress for more than a decade.

And it would hold insurance companies responsibl­e for managing costs through the entire benefit. During the initial phase, which would last until the $3,100 threshold is reached, insurers would be responsibl­e for 75% of costs. After that, they would pay 60%, the federal government would pay 20% and pharmaceut­ical companies would have to provide a 20% percent discount. That would put drugmakers on the hook for their own prices. The more they charge patients and taxpayers, the greater the discount they would have to provide in the catastroph­ic phase. Insurers and drugmakers would have new incentive to negotiate lower prices.

One other major change to Part D in our bill would limit taxpayer subsidies to drug companies so that they could no longer raise prices beyond the cost of inflation and expect Medicare to foot the bill. Companies could either limit price increases to the rate of inflation or pay Medicare a rebate. This too would lower beneficiar­y costs and lessen Medicare’s financial burden, the CBO says.

Even with these significan­t changes, the legislatio­n would maintain Part D’s free-market structure, allowing drug companies to recover their researchan­d-developmen­t costs and continue to innovate.

Our plan is leading the way toward a solution that can pass Congress and be signed by the president this year: It is the only comprehens­ive, bipartisan prescripti­on drug legislatio­n to have passed a congressio­nal committee, and it has been endorsed by more than a dozen advocacy groups spanning the political spectrum, from the senior group AARP to the libertaria­n Cato Institute. We encourage our colleagues to work with us to deliver for patients and taxpayers.

Americans who can’t afford their prescripti­on medicines are counting on Congress to act now.

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