Bills/H.R. 890

Stopping Pharma’s Ripoffs and Drug Savings For All Act

Stopping Pharma’s Ripoffs and Drug Savings For All Act

In CommitteeEconomyHouseHouse Bill · 119th Congress
Bill Progress · House
Introduced
Committee
Passed House
Passed Senate
Passed Both
Signed

Plain Language Summary

# Summary of HR 890: Stopping Pharma's Ripoffs and Drug Savings For All Act **What the bill would do:** This bill tackles a practice called "double patenting," where pharmaceutical companies obtain multiple patents on the same drug. The bill would require drug companies to prove that each patent covers a genuinely different invention; if they can't prove this, all the extra patents would expire when the first patent does. The bill also directs the U.S. Patent and Trademark Office to tighten its review process to prevent granting multiple patents on identical drugs in the first place. **Who it affects:** Primarily pharmaceutical companies and the generic drug industry.

The bill aims to help generic and biosimilar drug makers bring cheaper alternatives to market faster by preventing companies from using multiple patents to extend monopoly control over a drug. Ultimately, patients could benefit through lower drug prices and faster access to more affordable medications. **Current status:** The bill is currently in committee (HR 890, 119th Congress), meaning it hasn't yet advanced for a full vote in the House. It was introduced by Representative Patrick Ryan, a Democrat from New York.

CRS Official Summary

Stopping Pharma’s Ripoffs and Drug Savings For All ActThis 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.

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Latest Action

January 31, 2025

Referred to the House Committee on the Judiciary.

Sponsor

Key Dates

Introduced
January 31, 2025
Last Updated
January 31, 2025
Read Full Text on Congress.gov →
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