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Preserve Access to Affordable Generics and Biosimilars Act

S. 142 Sen. Amy Klobuchar (D-MN) In committee
  1. Introduced Jan 30
  2. Committee Jan 30
  3. Passed Senate Next
  4. Passed House Not yet
  5. To President Not yet
  6. Law Not yet
Where it stands
In committee, Jan 30, 2023Next: Senate vote
1337d ago Mar 1, 2023: Placed on Senate Legislative Calendar under General Orders. Calendar No. 20.
Final votes
No roll callsNo recorded vote on this bill yet
Lobbying
6companies, 7 filings
Member trades
13trades in the last 90 days
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Companies lobbying on this bill

6 companies
Companies by sector
Biotech & Pharma 5Financials 1
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Summary

Preserve Access to Affordable Generics and Biosimilars Act

Full summary4 paragraphs

This bill authorizes the Federal Trade Commission (FTC) to initiate proceedings against parties to any agreement resolving or settling a patent infringement claim in connection with the sale of a drug or biological product. Such an agreement is presumed to have anticompetitive effects and is a violation of this bill if the filer of the 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 exempted 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 patent. An agreement is also exempt if the agreement's pro-competitive benefits outweigh the anticompetitive effects.

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 concerning the agreement contains the complete agreement and any agreements related to that main agreement, including descriptions of any oral agreements or representations.

The bill imposes penalties for violations of this bill, including the forfeiture of the 180-day marketing exclusivity period for a generic drug.

Library of Congress summary, Mar 1, 2023

Summary versions
  • Reported to SenateMar 1, 2023
  • Introduced in SenateJan 30, 2023

Official record from Congress.gov, the House Clerk and the Senate; lobbying from Lobbying Disclosure Act filings. Updated Oct 28, 2026.