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SENATE 1096119th CongressPlaced on Senate Legislative Calendar under General Orders. Calendar No. 46.

Preserve Access to Affordable Generics and Biosimilars Act

Last Action
4/10/2025

Actions

  • 2025-04-10Placed on Senate Legislative Calendar under General Orders. Calendar No. 46.
  • 2025-04-10Committee on the Judiciary. Reported by Senator Grassley with an amendment in the nature of a substitute. Without written report.
  • 2025-04-10Committee on the Judiciary. Reported by Senator Grassley with an amendment in the nature of a substitute. Without written report.
  • 2025-04-03Committee on the Judiciary. Ordered to be reported with an amendment in the nature of a substitute favorably.
  • 2025-03-24Read twice and referred to the Committee on the Judiciary.
  • 2025-03-24Introduced in Senate

CRS Summary

As of 2025-03-24 (00)

Preserve Access to Affordable Generics and Biosimilars Act

This bill prohibits parties from entering into any agreement that resolves or settles a patent claim related to the sale of a drug or biological product and that has anticompetitive effects. Such an agreement is presumed to have anticompetitive effects if the filer of a generic drug or biosimilar application receives anything of value and agrees to limit or forego research, development, manufacturing, marketing, or sales of the generic drug or biosimilar.

An agreement is exempt if the only consideration granted to the generic manufacturer is (1) the right to market and secure final approval for its product prior to the expiration of any statutory exclusivity, (2) a payment for reasonable litigation expenses, or (3) a covenant not to sue on any claim that the generic drug or biosimilar infringes a U.S. patent. An agreement is also exempt if the agreement's pro-competitive benefits outweigh the anticompetitive effects.

The bill provides for enforcement by the Federal Trade Commission (FTC). Violators are subject to penalties including the forfeiture of the 180-day marketing exclusivity period for a generic drug.

Additionally, when a generic or biosimilar drug manufacturer enters into an agreement with another drug manufacturer related to the manufacturing, marketing, or sale of a drug, the manufacturers must certify that the material they have given the FTC and the Department of Justice concerning the agreement contains the complete agreement and any related agreements, including descriptions of any oral agreements or representations.

Cosponsors (8)

  • Chuck Grassley (R-IA)
  • Richard Durbin (D-IL)
  • Kevin Cramer (R-ND)
  • Richard Blumenthal (D-CT)
  • Joni Ernst (R-IA)
  • Peter Welch (D-VT)
  • Mark Kelly (D-AZ)
  • Cory Booker (D-NJ)

Subjects

  • Administrative law and regulatory procedures
  • Civil actions and liability
  • Competition and antitrust
  • Contracts and agency
  • Federal Trade Commission (FTC)
  • Intellectual property
  • Judicial review and appeals
  • Licensing and registrations
  • Manufacturing
  • Marketing and advertising
  • Prescription drugs
Read on Congress.gov

Sourced from Congress.gov (public domain).

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.