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Stopping Pharma’s Ripoffs and Drug Savings For All Act

H.R. 890 Rep. Patrick Ryan (D-NY-18) In committee
  1. Introduced Jan 31
  2. Committee Jan 31
  3. Passed House Next
  4. Passed Senate Not yet
  5. To President Not yet
  6. Law Not yet
Where it stands
In committee, Jan 31, 2025Next: House vote
635d ago Jan 31, 2025: Referred to the House Committee on the Judiciary.
Final votes
No roll callsNo recorded vote on this bill yet
Lobbying
1company, 6 filings
Member trades
0trades in the last 90 days
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Companies lobbying on this bill

1 company
Companies by sector
Biotech & Pharma 1
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Summary

Stopping Pharma’s Ripoffs and Drug Savings For All Act

Full summary3 paragraphs

This bill addresses double patenting with respect to drug-related patents. Specifically, the bill requires an owner of drug-related patents, if the owner lists more than one patent as covering a particular drug, to prove in certain proceedings that each patent covers a distinct invention. If the patent owner fails to do so, then the owner shall have disclaimed patent protection from all the listed patents after the first patent expires.

This requirement shall apply to various proceedings challenging the validity of drug-related patents, as well as to infringement lawsuits filed by the patent owner against companies seeking Food and Drug Administration approval for generic or biosimilar versions of patented drugs.

The bill also directs the U.S. Patent and Trademark Office (USPTO) to review its examination procedures to prevent granting multiple patents for the same drug or biological product, unless the patents cover distinct inventions. The USPTO shall report to Congress its findings and recommendations from the review.

Library of Congress summary, Jan 31, 2025

Summary versions
  • Introduced in HouseJan 31, 2025

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