Los Angeles Times

Scrutiny for high drug prices

-

Having a child who suffers from Duchenne muscular dystrophy, a rare and fatal musclewast­ing disease that affects about 12,000 boys in the United States, is tragic enough. But watching drugmaker Marathon Pharmaceut­icals seek a 70-fold increase in the price of a drug that can extend those patients’ lives — that’s beyond the pale. In fact, it should persuade California lawmakers finally to shine a light on how drug companies set their prices.

Illinois-based Marathon won the Food and Drug Administra­tion’s approval this month to sell its version of deflazacor­t, an anti-inflammato­ry drug that can help (but not cure) Duchenne muscular dystrophy patients. The drug has long been available in Canada and Europe, and some U.S. patients have been able to mail-order it for about $1,200 per year. Those imports will become unlawful now that Marathon has a seven-year monopoly on deflazacor­t sales in the U.S. The price tag for Marathon’s version, dubbed Emflaza: $89,000 per year.

Most patients won’t pay that much, thanks to coupons and other assistance Marathon will offer. The FDA approval may also result in more patients being able to get reimbursed for the drug by their insurer. But gouging patients has never been the drug industry’s business model: Its goal has been to extract as much as possible from insurers and taxpayers. Hence the common practice of helping patients minimize their co-pays, while public and private insurers continue to pay the bulk of the price.

A top Marathon executive told the Wall Street Journal that, after accounting for discounts and rebates, he expects to collect about $54,000 per year per patient. Meanwhile, the discounts for patients help boost demand for the drug, sustaining a price that market forces, public outrage and political pressure might otherwise beat down.

Patients may end up getting the drugs they need, but the costs get passed on to everyone who buys health insurance or pays income taxes. The Kaiser Family Foundation estimates that prescripti­ons accounted for more than 19% of the cost of employee health coverage. An estimated $11 billion in state tax dollars will be spent in the coming fiscal year just on pharmacy benefits for Medi-Cal enrollees.

Drugmakers insist that their products and prices are being unfairly singled out for criticism. Neverthele­ss, spending on drugs is growing faster than any other part of the healthcare industry. Manufactur­ers sought fewer double-digit increases in January than they have in recent years, yet half of the increases were 8.9% or greater — more than four times the rate of inflation.

The question is what to do about it. Manufactur­ers argue that artificial price caps can reduce the supply of vital medicines and discourage investment in new drugs, particular­ly for medical conditions that afflict a limited number of people. It’s hugely expensive to bring a new drug to the market, and manufactur­ers have to set prices high enough to recover the costs of the drugs that don’t get approved as well as the ones that do. But more than a third of the R&D dollars for new drugs comes from taxpayers and private donors, not from the industry itself. And much of the money spent by pharmaceut­ical companies these days is for marketing drugs, not developing them.

Still, it would be self-defeating if the government’s efforts to hold down drug costs resulted in fewer drugs being available. That’s why policymake­rs need a much clearer view into what it actually costs to keep the pipeline of new and innovative medicines open. A number of states have adopted or are considerin­g measures that would require drug makers to reveal to state officials more about what they spend on materials, research, clinical trials and advertisin­g. Sen. Ed Hernandez (D-West Covina) pushed a transparen­cy bill through the California Senate last year, only to have it die in the Assembly in the face of all-out opposition by pharmaceut­ical companies.

Hernandez is trying again with a new transparen­cy bill, SB 17. Meanwhile, Marathon has put the introducti­on of Emflaza on hold as it deals with the backlash against its proposed pricing. The company argues that even though it didn’t discover or develop the drug, it still spent a considerab­le amount of money analyzing patient data and conducting new trials to win approval in the United States, which will make it more readily available here. But we shouldn’t have to simply accept Marathon’s word that it’s not pricegougi­ng. And if lawmakers require more transparen­cy, we won't.

Newspapers in English

Newspapers from United States