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Contact Congress about H.R. 3269: ETHIC Act

Brand-name drug companies often use clusters of related patents to block generic competitors in court. This bill caps how many related patents can be used in a single lawsuit and bars repeat suits on the same patent group against the same company.

Modern Action explains legislation in plain English, helps you choose whether to support, oppose, or ask for changes, and drafts a message tied to the bill, your stance, and the elected officials who can act on it.

ETHIC Act is a House bill in committee. The latest recorded action: Referred to the House Committee on the Judiciary.

Latest action on H.R. 3269: Referred to the House Committee on the Judiciary.

Who this affects: This bill primarily affects brand-name drug and biologic companies that hold multiple related patents, as well as generic and biosimilar manufacturers that face patent infringement lawsuits. Consumers could be indirectly affected if changes in patent litigation lead to faster market entry for cheaper drug alternatives.

Why this matters: Drug patent thickets are a major barrier to affordable medications. When brand-name companies can pile on related patents in court, generic manufacturers face enormous legal costs and delays that keep cheaper alternatives off the market. This bill directly addresses that barrier by limiting how patents can be used in these specific lawsuits.

Key provisions in H.R. 3269

  • Changes a section of U.S. patent law (section 271(e) of title 35) that governs patent infringement lawsuits related to drugs and biologics.
  • Caps the number of patents that can be used in a single lawsuit at one patent per 'Patent Group.'
  • Defines a 'Patent Group' as two or more commonly owned patents or applications linked through statutory disclaimers (formal legal connections under patent law).
  • All patents or applications connected through the same disclaimer are treated as one Patent Group.
  • Once a patent owner sues a company using a patent from a specific group, they cannot file additional lawsuits against that same company using other patents from the same group.

How Modern Action helps you take action on H.R. 3269

You do not have to start with a blank letter. Modern Action turns the bill, your position, and the relevant congressional context into a message you can edit and send. The goal is to make contacting Congress clear, specific, and useful without forcing you to parse bill text or figure out the right office on your own.

Questions people ask about H.R. 3269

What is H.R. 3269?
Brand-name drug companies often use clusters of related patents to block generic competitors in court. This bill caps how many related patents can be used in a single lawsuit and bars repeat suits on the same patent group against the same company.
How do I support or oppose H.R. 3269?
Choose support, oppose, or ask for changes on Modern Action. The action flow drafts the message for you and keeps the wording tied to this bill.
Who should I contact about H.R. 3269?
Modern Action uses your location to route the action to the congressional offices relevant to the bill and your representation.
Can Modern Action explain H.R. 3269 before I act?
Yes. Modern Action gives you a plain-English summary, current status, and action context before you send anything.

Keep acting on Modern Action

More ways to act on this issue

Compare the broader issue and related bills without leaving Modern Action.

Related issues

  • Contact your reps on Generic Drug Competition and FDA TransparencyFDA would give generic applicants clearer information about ingredient matching, protect reliance on FDA answers, limit patent or petition tactics that delay generics and biosimilars, and study competition barriers.

Related bills

  • Take action on H.R. 1843: To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.
  • Take action on S. 113: Prescription Pricing for the People Act of 2023
  • Take action on S. 1095: Stop STALLING Act
  • Take action on S. 2276: ETHIC Act
  • Take action on S. 1114: Expanding Access to Low-Cost Generics Act of 2023
  • Take action on H.R. 3839: To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications
  • Take action on S. 1302: Increasing Transparency in Generic Drug Applications Act