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Affordable Prescriptions for Patients Act of 2023

S. 150 Sen. John Cornyn (R-TX) Passed Senate
  1. Introduced Jan 30
  2. Committee Jan 30
  3. Passed Senate Jul 11
  4. Passed House Next
  5. To President Not yet
  6. Law Not yet
Where it stands
Passed Senate, Jul 11, 2024Next: House vote
835d ago Jul 15, 2024: Held at the desk.
Final votes
No roll callsNo recorded vote on this bill yet
Lobbying
8companies, 11 filings
Member trades
18trades in the last 90 days
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Companies lobbying on this bill

8 companies
Companies by sector
Biotech & Pharma 7Financials 1
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Summary

Affordable Prescriptions for Patients Act of 2023

Full summary2 paragraphs

This bill limits in certain instances the number of patents that a reference biological product manufacturer can assert in a patent infringement lawsuit against a company seeking to sell a biosimilar version.

Specifically, if the biosimilar manufacturer completes certain actions as part of an abbreviated pathway to get market approval, the bill limits, subject to exceptions and waivers, the number of certain types of patents that the reference product manufacturer may assert, such as patents filed more than four years after the reference product received market approval.

Library of Congress summary, Jul 11, 2024

Summary versions
  • Passed SenateJul 11, 2024
  • 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 27, 2026.