S 771 — Improving Access To Affordable Prescription Drugs Act
Last action — Read twice and referred to the Committee on Finance.
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✓Introduced
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2In Committee
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3Passed Senate
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4Passed House
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5To Executive
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6Enacted
This bill died with 115th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
This bill is no longer active — its legislative session has ended, so there are no live odds of enactment. It would have to be reintroduced in the current session to move again.
Summary
This bill amends provisions of various laws relating to prescription-drug pricing and affordability. Specifically, the bill: expands reporting requirements for drug manufacturers and establishes corresponding civil penalties for noncompliance; adds reporting requirements for certain nonprofit patient-assistance programs; requires the Government Accountability Office (GAO) to report to Congress on the impact of patient-assistance programs on prescription-drug pricing and expenditures; requires the Centers for Medicare & Medicaid Services (CMS) to negotiate prices for certain prescription drugs under the Medicare program; requires the GAO to report to Congress on such negotiations conducted by the CMS; requires the Centers for Medicare and Medicaid Innovation within the CMS to test specified models for negotiating drug prices; establishes reporting requirements, and corresponding civil penalties for noncompliance, for pharmaceutical companies with respect to spikes in prescription-drug prices; establishes an excise tax on prescription drugs subject to price spikes; lessens prescription-drug cost-sharing requirements under qualified health plans, group health plans, and the Medicare program; modifies provisions related to the importation of prescription drugs; requires drug manufacturers to provide drug rebates for drugs dispensed to certain low-income individuals under the Medicare program; establishes a prize fund for new and more effective treatments of bacterial infections; establishes a Center for Clinical Research within the National Institutes of Health; modifies provisions related to drug exclusivity; allows the Federal Trade Commission to initiate enforcement proceedings against parties to an agreement resolving or settling a patent-infringement claim in connection with the sale of a drug product; requires the Food and Drug Administration to establish a database of generic drugs; and modifies other provisions related to generic drugs, prescription-drug advertising, and product hopping.
Bill Text
- Introduced Introduced in Senate Current html March 29, 2017
Action History
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Introduced in Senate
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Read twice and referred to the Committee on Finance.
Sponsors
- Al Franken · Primary
- Bernard Sanders · Cosponsor
- Sheldon Whitehouse · Cosponsor
- Sherrod Brown · Cosponsor
- Amy Klobuchar · Cosponsor
- Elizabeth Warren · Cosponsor
- Tammy Baldwin · Cosponsor
- Jack Reed · Cosponsor
- Kirsten E. Gillibrand · Cosponsor
- Margaret Wood Hassan · Cosponsor
- Richard J. Durbin · Cosponsor
- Chris Van Hollen · Cosponsor
- Jeff Merkley · Cosponsor
- Tom Udall · Cosponsor
- Richard Blumenthal · Cosponsor
- Cory A. Booker · Cosponsor
Sponsorship breakdown
Export CSV (upgrade) →1 sponsors · 15 co-sponsors · 531 not signed on
Sponsors (1)
- Franken, Al Democratic
Co-sponsors (15)
- Sanders, Bernard Independent
- Whitehouse, Sheldon Democratic
- Brown, Sherrod Democratic
- Klobuchar, Amy Democratic
- Warren, Elizabeth Democratic
- Baldwin, Tammy Democratic
- Reed, Jack Democratic
- Gillibrand, Kirsten E. Democratic
- Hassan, Margaret Wood Democratic
- Durbin, Richard J. Democratic
- Van Hollen, Chris Democratic
- Merkley, Jeff Democratic
- Udall, Tom Democratic
- Blumenthal, Richard Democratic
- Booker, Cory A. Democratic
Not signed on (531)
531 members have not signed on to this bill.
Show all 531 →"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.
Subjects
Frequently asked questions
- What does S 771 do?
- This bill amends provisions of various laws relating to prescription-drug pricing and affordability. Specifically, the bill: expands reporting requirements for drug manufacturers and establishes corresponding civil penalties for noncompliance; adds reporting requirements for certain nonprofit patient-assistance programs; requires the Government Accountability Office (GAO) to report to Congress on the impact of patient-assistance programs on prescription-drug pricing and expenditures; requires the Centers for Medicare & Medicaid Services (CMS) to negotiate prices for certain prescription drugs under the Medicare program; requires the GAO to report to Congress on such negotiations conducted by the CMS; requires the Centers for Medicare and Medicaid Innovation within the CMS to test specified models for negotiating drug prices; establishes reporting requirements, and corresponding civil penalties for noncompliance, for pharmaceutical companies with respect to spikes in prescription-drug prices; establishes an excise tax on prescription drugs subject to price spikes; lessens prescription-drug cost-sharing requirements under qualified health plans, group health plans, and the Medicare program; modifies provisions related to the importation of prescription drugs; requires drug manufacturers to provide drug rebates for drugs dispensed to certain low-income individuals under the Medicare program; establishes a prize fund for new and more effective treatments of bacterial infections; establishes a Center for Clinical Research within the National Institutes of Health; modifies provisions related to drug exclusivity; allows the Federal Trade Commission to initiate enforcement proceedings against parties to an agreement resolving or settling a patent-infringement claim in connection with the sale of a drug product; requires the Food and Drug Administration to establish a database of generic drugs; and modifies other provisions related to generic drugs, prescription-drug advertising, and product hopping.
- Who sponsors S 771?
- S 771 is sponsored by Franken, Al (Democratic), Sanders, Bernard (Independent), Whitehouse, Sheldon (Democratic), Brown, Sherrod (Democratic), Klobuchar, Amy (Democratic), Warren, Elizabeth (Democratic), Baldwin, Tammy (Democratic), Reed, Jack (Democratic), Gillibrand, Kirsten E. (Democratic), Hassan, Margaret Wood (Democratic), Durbin, Richard J. (Democratic), Van Hollen, Chris (Democratic), Merkley, Jeff (Democratic), Udall, Tom (Democratic), Blumenthal, Richard (Democratic), and Booker, Cory A. (Democratic).
- What is the current status of S 771?
- This bill died with 115th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
- Where can I track S 771?
- Track S 771 free on One Click Politics — get push/email alerts when it moves.
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