Senate Judiciary Committee Revisits Drug Pricing Reform Bills – Life Sciences, Biotechnology & Nanotechnology

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The Senate Judiciary Committee is showing renewed Congressional
interest in oversight of the pharmaceutical industry, with five
bipartisan drug bills on the agenda for review and discussion on
February 9, 2023.

On February 9, 2023, the Senate Judiciary Committee will hold an
executive business meeting to review various drug-related bills on
the agenda. The proposed bipartisan legislation comes in the wake
of the Inflation Reduction Act of 2022, which was passed in August
2022 and included several sweeping provisions related to
prescription drug pricing and reform. Notably, the committee is
reassessing a package of bills largely focused on increasing
competition for brand drugs. The following bills are scheduled to
be discussed by the committee:

  • S. 79, Interagency Patent Coordination and Improvement
    Act of 2023 (Durbin, Tillis, Grassley, Coons).
    This bill
    would create a task force between the U.S. Patent and Trademark
    Office and the Food and Drug Administration (“FDA”)
    reportedly to improve communication and coordination in
    implementing each agency’s patent activities by encouraging the
    agencies to collaborate and share information on developments in
    science and technology.

  • S. 113, Prescription Pricing for the People Act of 2023
    (Grassley, Cantwell, Blumenthal, Blackburn, Tillis).
    This
    bill aims to increase transparency into pharmacy benefit manager
    (“PBM”) practices by directing the Federal Trade
    Commission (“FTC”) to issue a report addressing alleged
    anticompetitive PBM behaviors along with other trends,
    observations, or information on pharmaceutical pricing. As
    proposed, the FTC also would issue a supplemental report based on
    this review to highlight the agency’s recommendations for
    related policy or legislative recommendations.

  • S. 142, Preserve Access to Affordable Generics and
    Biosimilars Act (Klobuchar, Grassley, Durbin, Blumenthal, Booker,
    Ossoff).
    This bill would limit what the bill identifies as
    an anticompetitive practice, whereby manufacturers allegedly use
    pay-off agreements to delay the introduction of cheaper
    substitutes, ultimately, in the view of the bill, resulting in
    higher prescription drug costs.

  • S. 148, Stop STALLING Act (Klobuchar, Grassley, Durbin,
    Blumenthal, Cruz, Booker, Ossoff).
    This bill seeks to
    disincentivize branded pharmaceutical companies from filing what it
    claims is a “sham” petition with the FDA for the alleged
    intention of interfering with the regulatory approval process for
    generics and biosimilars that would compete with their own
    products. If passed, this bill also would provide additional
    enforcement authority to the FTC against companies who file such
    petitions.

  • S. 150, Affordable Prescriptions for Patients Act of
    2023 (Cornyn, Blumenthal, Grassley, Durbin, Cruz,
    Klobuchar).
    This bill seeks to lower drug prices by
    foreclosing what the bill alleges are anticompetitive practices
    related to patents being deployed by manufacturers to block generic
    and biosimilar competition from coming to market.

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