News February 2007
Study Eyes Generic Drug Savings
Patients and health insurance providers could save at least $71
billion over 10 years if there was a regulatory mechanism that allowed
for the marketing of generic biotech medicines, according to a study
being released today.
Currently there is no legal pathway that allows generic
drug makers to produce biotech medicines, so the pricey treatments,
which are derived from a living source such as proteins, have never
had to compete with copycat products that drive pharmaceutical costs
lower.
Most drug makers, such as Eli Lilly and Co., increasingly are
focusing on such medicines.
Controlling the cost of biotech medicines has become a top priority
for those providing health insurance because the cost of such treatments
is dramatically increasing.
Biotech treatments now account for 25 percent to 30 percent of
a company's overall drug costs, according to pharmacy benefit manager
Express Scripts Inc., which conducted the study.
Express Scripts said that the average biotech drug costs $71,600
a year, compared with the annual average for a traditional drug
of $1,200. It said that escalating biotech drug costs, which reached
$40 billion in 2005, are expected to more than double in four years
to a total of $90 billion in 2009, a rate three times faster than
traditional drug costs. But on Wednesday, a bill was introduced
by a group of bipartisan lawmakers in Washington, D.C., that would
give the Drug Administration the authority to approve copies of
biotech drugs. Similar legislation was introduced last year.
Express Scripts conducted the study by taking a 25 percent discount
off brand-name medicines in four classes of drugs that would already
have generic competition because of patent expirations if copycat
biologics were allowed. Express Scripts decided on that discount
because it said that the generic version of human growth hormone
sells at a 25 percent discount to its brand name counterparts in
Europe.
The four categories of drugs were: insulin for diabetes, erythropoietins
for anemia, growth hormones and treatments for multiple sclerosis.
Jim Greenwood, president and CEO of the Biotechnology Industry
Organization, cautioned against forecasting any savings from generic
biotech drugs without knowing how much testing regulators would
require. BIO maintains the drugs won't be true generics because
a product made from a living source can never be exactly copied.
Source http://www.indystar.com/
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