The U.S. Federal Trade Commission has released a comment in support of the NIST’s guidelines concerning the exercise of march-in rights under the Bayh-Dole Act. The Press Release states:
Today the Federal Trade Commission issued
a comment in response to the National Institute of Standards and
Technology’s (NIST) request for information on its Draft Interagency Guidance
Framework for Considering the Exercise of March-In Rights under the Bayh-Dole
Act.
Under the Bayh-Dole Act, the federal government has the right
to “march in” on patents on inventions created using taxpayer funds—to require
the patent holder to license the federally funded patent to other applicants.
The draft interagency framework provides guidance outlining when the government
should exercise its march-in rights, which have never before been utilized. The
draft framework makes clear that high price is an appropriate basis for
exercising march-in rights.
In the comment, the FTC applauds NIST, which is part of the
U.S. Department of Commerce, and the Interagency Working Group for Bayh-Dole,
which includes the U.S. Department of Health and Human Services, for their
efforts to reactivate march-in rights as an important check on companies
charging Americans inflated prices for drugs developed with taxpayer-funded
research. In the comment, the FTC expressed support for an expansive and
flexible approach to march-in rights, including providing that agencies can march
in on the basis of high prices.
The FTC’s comment draws on its experience in promoting
competition and combatting anticompetitive practices in the pharmaceuticals
industry. Lack of competition in pharmaceutical markets can lead to inflated
pricing, rendering some lifesaving treatments out of reach for many Americans.
Nearly three in 10 Americans report rationing or skipping their medications due
to high costs. Contrary to industry claims that high drug prices are necessary
to fund research and development (R&D), drug prices often depend more on
whether the drug faces competition than the drug’s R&D costs. At the same
time, pharmaceutical firms enjoy hundreds of billions of dollars of taxpayer
investment in R&D. March-in rights are an essential check to ensure that
taxpayer-funded inventions are affordable and accessible to the public.
The FTC’s comment further explains that although march-in
rights can be a valuable tool to address potential harms in the pharmaceutical
industry, broader challenges requiring government-wide solutions remain. For
example, dense “patent thickets” result from pharmaceutical companies using
increasingly large patent portfolios to protect a single treatment. This may
weaken the utility of march-in rights to provide affordable public access to
drugs because some pharmaceuticals may be protected by patent thickets
that include privately funded blocking patents in addition to government-funded
patents subject to march-in rights. In its comment, the FTC urges
agencies to work collaboratively to also address such patent thickets.
The Commission voted 3-0 to approve filing of the comment.
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