MHE Staff September
17, 2019
Medicare and its
beneficiaries could have saved an estimated $17.7 billion over a seven-year
period on generic versions of older medicines instead of paying for newer,
chemically similar but more expensive brand-name drugs, according to a study published in the Annals of
Internal Medicine last month.
The study was
conducted as part of the Collaboration for Research Integrity
and Transparency at Yale Law School, funded by the Laura and John
Arnold Foundation. The intent was to estimate the potential savings associated
with using racemic precursors instead of their single-enantiomer versions to
the Medicare Part D drug benefit program and its beneficiaries.
Between 2011 and
2017, Medicare and beneficiaries could have saved the $17.7 billion through
substitution of 12 single-enantiomer drugs with their racemic precursors.
Substitution of armodafinil for modafinil would have actually increased
Medicare spending, but substitution of esomeprazole for omeprazole accounted
for more than three quarters of the total estimated savings, and approval of
generic esomeprazole in January 2015 contributed to an approximate 20% decline
in total savings from 2015 to 2017 when compared with 2012 to 2014.
The study analysis
was limited to the seven-year period, which is only a partial amount of the
time that these drugs have been available, and does not take spending by
Medicare Advantage plans into consideration.
Researchers could not
account for actual rebates, which for some branded drugs (including
esomeprazole), may be substantially higher than 26.3%, the highest rebate
reported by Medicare for any therapeutic class in 2014.
The authors, led by
Alexander C. Egilman, BA, assumed that there was complete substitution of
racemic precursors, although patient-specific risk–benefit considerations will
influence drug choice, and not all substitutions would be clinically
appropriate.
Finally, savings vary
depending on several factors, such as beneficiary income status and Part D plan
benefit structure, as well as future market entry of generic single-enantiomer
drugs. Nevertheless, while $17.7 billion is only 2.1% of total Medicare Part D
spending from 2011 to 2017, the study findings suggest that racemic
substitution for single-enantiomer drugs offers an opportunity for Medicare
drug savings.
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