A new study shows the average annual
cost for orphan drugs — $123,543 – is 25x more expensive than traditional drugs
WASHINGTON, D.C. – Out-of-control drug prices mean too many patients
are forced to choose between paying for their prescription or paying their
mortgage. The prices for drugs to treat rare medical conditions are 25
times more expensive than traditional drugs. That is a 26-fold
increase in two decades, according to a new report by America’s Health
Insurance Plans (AHIP). The study shows that orphan drugs are now entering the
market at higher prices than ever before, ranging from tens-of-thousands to
hundreds-of-thousands of dollars per patient.
The Orphan Drug Act was passed in 1983 to
encourage pharmaceutical manufacturers to invest in treatments for rare
diseases and conditions – so-called “orphan diseases” – that had been ignored
because their small patient populations (fewer than 200,000 Americans) made
them unprofitable. The intent was to create incentives to encourage drug makers
to develop treatments for rare diseases by enabling them to realize a modest
profit. Unfortunately, drug makers have responded by building lucrative
business models that empower them to achieve a gross profit margin of more than 80% – compared to an average
gross profit margin of 16% for the rest of the pharmaceutical industry.
Here are the takeaways from the AHIP study:
·
From 1998 to
2017, the average per-patient annual cost for orphan drugs increased
26-fold, while the cost for specialty and traditional drugs merely doubled
·
The average annual
orphan drug cost rose from $7,136 in 1997 to $186,758 in 2017
·
Orphan drugs are 25x
more expensive than non-orphan drugs
·
Today, 88% of
orphan drugs cost more than $10,000 per year per patient
·
In 2017, 7 out
of 10 best-selling drugs had orphan indications
·
Among
newly launched drugs, the share of orphan drugs increased more than 4-fold, from 10% to 44%, over a 20-year period
“Every patient deserves to get the medications
they need at a cost they can afford, but drug makers are gaming
well-intentioned legislation to generate outsized profits from drugs intended
to treat a small population of patients with rare diseases,” said Matt Eyles,
president and CEO of AHIP. “Now more than ever we need lawmakers to revisit the
Orphan Drug Act. We must balance the incentives to develop new treatments for
rare diseases while preventing drug makers from exploiting the system with
launch prices that defy gravity, blocking competition, and increasing their
prices on the same products year after year.”
The detailed issue brief can be found
here and the full website can be found at https://orphandrug.ahip.org/.
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