COST OF LIVING
Why hemophilia drugs, crucial for some people’s survival, are so expensive
YUBA CITY, Calif. — When Landon Morris was diagnosed with hemophilia shortly after birth, his mother, Jessica Morris, was devastated. “It was like having your dreams — all the dreams you imagined for your child — just kind of disappear,” she recalled.
Hemophilia, a rare bleeding disorder caused by a gene mutation that prevents blood from clotting properly, is typically passed from mother to son. ( Hemophilia Awareness Day is April 17). Morris’ grandfather had it, and she remembered hearing how painful it was. “It was almost like he was bubble- wrapped,” she said. “He was coddled, because his mom didn’t want him to get hurt.” But Landon’s life turned out much different than she expected. “He’s wild. He’s probably sometimes the roughest of them all,” she said, as she watched the 6- year- old race around a park. “He leads a totally normal life. He plays T- ball. He’ll start soccer in the fall. He runs and jumps and wrestles with his brothers.”
That’s due almost entirely to his medication — the kind that wasn’t available in his grandfather’s day. For the Morris family, this type of drug — broadly known as clotting factor — is a miracle, helping Landon’s blood clot normally. And its cost is almost entirely covered by his father’s federal employee health plan.
But for the health care system, such drugs are enormously expensive, among the priciest in the nation. Medications to treat hemophilia cost an average of more than $ 270,000 annually per patient, according to a 2015 Express Scripts report. If complications arise, that annual price tag can soar above $ 1 million. The U. S. hemophilia drug market, which serves about 20,000 patients, is worth $ 4.6 billion a year, according to the investment research firm AllianceBernstein.
Examining the stubbornly high cost of these medications opens a window into why some prescription drugs in the United States— especially those for rare diseases — have stratospheric prices. The short answer: Competition doesn’t do its traditional job of tamping down costs.
Vying for patients
The market for hemophilia medicines in the United States is flooded with 28 different drugs, with another 21 drugs in development. Because blood factor drugs are biological products— in this case, a protein— there are no
cheaper copies, called biosimilars, available. Not only do prices rise steadily as each new product comes on the market, demand is growing— and pushing costs upward— as more and more clotting factor is used to prevent bleeding episodes, not just to treat them.
Yet competition has not brought prices down in the way someone “operating at the level of undergrad Econ 101 would expect,” said Jerry Avorn, a professor at Harvard Medical School who studies prescription drug costs.
The problem is that companies have no incentive to lower prices. Patients generally don’t push back because insurers pay the bulk of the cost. And insurers tend not to object because the market for the drugs— expensive as they are— is small and the patients are especially vulnerable.
For drug companies, Avorn said, “it’s a magical formula: Lifesaving drug, child at risk of bleeding to death— it kind of casts anybody who looks at costs into the role of some evil Scroogelike person.
“The insurers don’t want to end up on the front page of the newspaper saying Little Timmy bled to death because his drug wasn’t covered,” he said.
Also, because prices are high across the hemophilia market, no drug company wants to be the one to blink first. “They don’t want to get a price war started and end up at a super low price point,” said Edmund Pezalla, a consultant to pharmaceutical companies and former executive at Aetna.
So, these drugmakers compete not on price but clinical benefits— such as how long the drugs’ effects last— and through intensive marketing. The pool of potential customers is so valuable that companies often vie directly for individual patients.
Manufacturers, as well as specialty pharmacies that sell the drugs, hire patients and parents as recruiters and advisers, hold dinners and holiday parties, offer scholarships to patients and even run summer camps for children with the disease. The Morris family regularly receives such invitations.
Dr. Jonathan Ducore, a pediatric hematologist- oncologist at the University of California- Davis Hemophilia Treatment Center in Sacramento, said some of his patients are persuaded by drug company presentations to switch medications. ” But the real differences between the drugs are limited,” he said.
Ducore said he tells patients if he thinks they are being misled by drugmakers about what a product will do. “But even though the tactics may seem a little smarmy, if it’s the patient’s choice, you have to go with it,” said Ducore, who has been Landon’s doctor since the boy was born.
The first clotting factor products, which came onto the market in the mid- 1960s, were derived from human blood plasma, with thousands of donations combined to create one batch. This proved disastrous in the 1980s, when donors unwittingly spread HIV into the blood supply. An estimated 4,000 people with hemophilia— about 40 percent of the patient population in the U. S.— died from AIDS as a result.
Pushing back on costs
In Europe, hemophilia drugs cost less than half what they cost in the U. S. That’s because payers — usually governments— request bids and pick products based on cost and quality.
Without pushback from insurers in the U. S., “the price of any drug in the U. S. is whatever the market will bear as seen by the manufacturer,” said Avorn of Harvard.
Recently, a few insurance companies have quietly started to push back on costs. Bayer’s O’Leary said several insurers have approached the company and demanded rebates in exchange for offering the drug to their customers. O’Leary would not discuss the details because he said the contracts are confidential.
State Medicaid programs, which provide health insurance to low- income Americans and cover about half of hemophilia patients, already receive significant rebates from hemophilia drug manufacturers.
Michelle Rice, a senior vice president at the National Hemophilia Foundation, said she has been working with several insurers to help them manage costs safely. “We understand the need to control costs, but they can’t impede access to the product a patient needs,” she said.
It is not yet clear whether such efforts will work, let alone spread.
Sitting at a picnic bench at a park, Jessica Morris pages through Landon’s insurance documents. Over the past year, his care cost over $ 120,000. She wonders sometimes what would happen if they lost their coverage.
“How much would you be willing to pay to have your child lead a normal life?” she said. “I don’t think that there’s anything we wouldn’t pay or sacrifice for him.”
It’s a problem she prays they’ll never have to face.
“HE LEADS A TOTALLY NORMAL LIFE. HE PLAYS T- BALL. HE’LL START SOCCER IN THE FALL. HE RUNS AND JUMPS AND WRESTLES WITH HIS BROTHERS.” Jessica Morris, who’s son Landon uses a drug broadly known as clotting factor to help his blood clot normally, since being diagnosed with hemophilia shorlty after birth