The
high cost of cancer drugs recently prompted top oncologist Dr. Leonard
Saltz to publicly call for limits. "These drugs cost too much," he told thousands of his colleagues at the American Society of Clinical Oncology annual meeting. Many cancer drugs debut with a price tag of $10,000 a month according to an analysis from staff at Memorial Sloan Kettering Cancer Center.
The country’s largest pharmacy benefits manager, Express Scripts, estimates
576,000 Americans had prescription drug costs above $50,000 last year,
up 63% from the year before. The number of patients with costs of
$100,000 or more nearly tripled.
Express
Scripts put the impact of these costs on payers in the U.S. at $52
billion a year, a number they call unsustainable. They find
insurers foot most of the bill but say the costs pressure health
insurance premiums and taxpayer-funded government healthcare programs
like Medicaid.
Two-thirds
of spending for patients with six-figure drug bills went to medications
for cancer, hepatitis C and compounded therapies.
So
what exactly goes into determining a drug’s price, leading to a price
tag in the tens or even hundreds of thousands of dollars?
“First
you need to look at the time and cost it takes to develop a medicine,
test it, get it approved by regulators, and ultimately bring it to
patients," Robert Zirkelbach tells us. Zirkelbach is a senior vice president at the organization, PhRMA, which represents U.S. biotech companies. "You also have to look at the value these medicines provide to patients, the healthcare system and to society broadly."
Developing
and winning approval for a new prescription drug is estimated to take
more than a decade and cost nearly $2.6 billion dollars, according to Tufts Center for the Study of Drug Development. That
figure factors in the money and time spent on drug development. It also
factors in the failures: Data show only 12 percent of medicines that go
to clinical trials ever make it to patients.
No comments:
Post a Comment