The Associated Press reports(below) that the total cost of the drug during a pregnancy could be as much as $30,000.
The cost of developing the drug, Makena, was not even borne by KV Pharmaceuticals. It was brought to market in the 1950s, and when the original manufacturer stopped making the drug, compounding pharmacies sold their own formulations for $20 a shot–apparently with no complaints about quality.
Using taxpayer funding–from NIH–KV conducted clinical trials to demonstrate the efficacy of an old drug. It then applied to the FDA for accelerated approval.
Even-though the FDA knew that the drug was available from compounding pharmacies, the FDA not only granted accelerated approval, it gave the company market exclusivity for an old drug with a known track record which had been available to pregnant women at $20 a shot. By granting market exclusivity to KV the FDA prevented women at risk of preterm labor from obtaining the drug at a reasonable price.
Dr. Roger Snow, deputy medical director of Massachusetts Medicaid program said, “For crying out loud this is about making money.”
As Merril Goozner points out, “This appears to be another case of [FDA granted] market exclusivity incentives gone awry.”
The FDA bears total responsibility for granting market exclusivity without regard for the public interest–its decisions appear to serve commercial interest only.
Unlike other industries, the pharmaceutical industry’s exceedingly high profit margins are contingent on non-competitive, government policies that favor this industry: not only are drug manufacturers protected from competitors by patents that run 20-years, there are added “incentives” that help pharmaceutical companies cash in on “me-too” drugs of minor clinical value–or even no value–by allowing additional extensions on market exclusivity beyond the end of life of the patent.
An additional seven years of market exclusivity is given for developing drugs for rare diseases; priority reviews–reducing the time to market by six months– are given for developing drugs for neglected diseases of the developing world; and six months patent extensions are awarded for testing a drug in children–whether the drug proves helpful or harmful.
The National Women’s Health Network is asking everyone to protest KV Pharmaceuticals’ price gouging for an old drug to prevent premature labor. “As if life weren’t hard enough for pregnant women at risk for preterm labor, KV Pharmaceuticals is making things even worse with a greedy grab for huge, new profits.”
Questions: Why are there are no government incentives to develop improved, clinically valuable, safe drugs?
Why are ALL the incentives formulated to encourage the drug industry to profiteer at the taxpayer’s expense?
Vera Hassner Sharav
The Associated Press
ATLANTA March 9, 2011
The price of preventing preterm labor is about to go through the roof.
A drug for high-risk pregnant women has cost about $10 to $20 per injection. Next week, the price shoots up to $1,500 a dose, meaning the total cost during a pregnancy could be as much as $30,000.
That’s because the drug, a form of progesterone given as a weekly shot, has been made cheaply for years, mixed in special pharmacies that custom-compound treatments that are not federally approved.
But recently, KV Pharmaceutical of suburban St.Louis won government approval to exclusively sell the drug, known as Makena (Mah-KEE’-Nah). The March of Dimes and many obstetricians supported that because it means quality will be more consistent and it will be easier to get.
None of them anticipated the dramatic price hike, though — especially since most of the cost for development and research was shouldered by others in the past.
“That’s a huge increase for something that can’t be costing them that much to make. For crying out loud, this is about making money,” said Dr. Roger Snow, deputy medical director for Massachusetts’ Medicaid program.
“I’ve never seen anything as outrageous as this,” said Dr. Arnold Cohen, an obstetrician at Albert Einstein Medical Center in Philadelphia.
“I’m breathless,” said Dr. Joanne Armstrong, the head of women’s health for Aetna, the Hartford-based national health insurer.
Doctors say the price hike may deter low-income women from getting the drug, leading to more premature births. And it will certainly be a huge financial burden for health insurance companies and government programs that have been paying for it.
The cost is justified to avoid the mental and physical disabilities that can come with very premature births, said KV Pharmaceutical chief executive Gregory J. Divis Jr. The cost of care for a preemie is estimated at $51,000 in the first year alone.
“Makena can help offset some of those costs,” Divis told The Associated Press. “These moms deserve the opportunity to have the benefits of an FDA-approved Makena.”
The U.S. Food and Drug Administration is not involved in setting the price for the drugs it approves.
A KV subsidiary, Ther-Rx Corp., will market the drug. On Tuesday, Ther-RX announced a patient assistance program designed to help uninsured and low-income women get the drug at little or no cost.
But Snow and others said someone is going to have to pay the higher price. Some of the burden will fall on health insurance companies, which will have to raise premiums or other costs to their other customers. And some will fall on cash-strapped state Medicaid programs, which may be forced to stop paying for the drug or enroll fewer people.
“There’s no question they can’t afford this,” said Matt Salo, executive director of the National Association of Medicaid Directors.
Salo and Snow said they do not know how many state Medicaid programs currently pay for Makena, which as a generic was recommended by the American College of Obstetricians and Gynecologists.
Aetna will continue to pay for the drug, Armstrong said, but it will be an expensive pill to swallow. Aetna currently covers it for about 1,000 women a year, so the new federal endorsement is likely to cost an estimated $30 million more each year.
Makena is a synthetic form of the hormone progesterone that first came on the market more than 50 years ago to treat other problems. Hormone drugs came under fire in the 1970s, following reports they might damage fetuses in early pregnancy. In the 1990s, the early incarnation of Makena was withdrawn from the market.
But the drug got a new life in 2003, with publication of a study that reported it helped prevent early births to women who had a history of spontaneous preterm deliveries.
These very early births produce children who — if they survive — need months of intensive care and often suffer disabilities. The cause of sudden preterm delivery is not understood, but it occurs in black mothers at much higher rates than whites or Hispanics.
The study of women at risk for this condition found that only about 36 percent of those given the progesterone drug had preterm births, compared with 55 percent among those not on the drug. It’s believed the treatment calms the muscles of the uterus, experts said.
There is no good alternative in most cases and in the years following the study, more obstetricians, Medicaid programs and others began prescribing it. By some estimates, about 130,000 women a year might benefit from the drug. Only a fraction of them get it, but the number has been growing steadily.
One success story is Beatrice Diaz, 33, of Chapel Hill, N.C.
During her first pregnancy nine years ago, Diaz unexpectedly went into labor at about 24 weeks. She delivered a son, Garrison, who was so fragile she was not allowed to hold him for a month. Today he is in a wheelchair and has the mental capacity of a 9-month-old.
It was a shock, said Diaz, who at the time was a legal assistant in a prosecutor’s office. “Honestly I thought the only people who had 1-pound babies were crackheads,” she said.
When she became pregnant again, her doctor prescribed the progesterone drug, a weekly injection that starts as early as the 16th week and may be given for as much as 20 weeks. She has since had two healthy, full-term baby girls, Hailyn and Alexa.
Diaz said she’s not planning to have any more children — and that’s a good thing. “That’s an insane amount of money. I don’t know what I would do to get the money to afford it.”
The Ther-Rx patient assistance program promises free injections or much reduced prices based on income. Uninsured households making less than $100,000 are eligible for a copay of $20 or less.
Ther-Rx and its parent company became involved about three years ago and acquired rights to the drug from a Massachusetts company named Hologic Inc., said Divis, who is also Ther-Rx’s president.
To get FDA approval, the company is spending hundreds of millions of dollars in additional research, including an international study involving 1,700 women, Divis said. The FDA last month signed off and gave Makena orphan drug status. That designation ensures Ther-Rx will be the sole source of the drug for seven years.
The March of Dimes, which gets hundreds of thousands of dollars in funding from Ther-Rx, celebrated the approval in a press release, saying if all women eligible for the shots receive them, nearly 10,000 spontaneous premature births could be prevented each year.
“For the first time, we have an FDA-approved treatment to offer women who have delivered a baby too soon, giving them hope that their next child will have a better chance at a healthy start in life,” said Dr. Alan Fleischman, the organization’s medical director.
As for the cost, he said the drug maker’s financial assistance program will ensure no eligible woman is denied the drug due to inability to pay.
Some doctors said they were happy getting the cheaper version from compounding pharmacies, and Aetna’s Armstrong said she was unaware of any quality concerns. Still, doctors will use the Ther-Rx brand, in part because of legal worries.
Not that they have a choice: Last month, KV sent cease-and-desist letters to compounding pharmacies, telling them they could face FDA enforcement actions if they kept making the drug.
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