US SB64 | 2019-2020 | 116th Congress
Status
Spectrum: Bipartisan Bill
Status: Introduced on January 9 2019 - 25% progression, died in committee
Action: 2019-01-09 - Read twice and referred to the Committee on the Judiciary.
Pending: Senate Judiciary Committee
Text: Latest bill text (Introduced) [PDF]
Status: Introduced on January 9 2019 - 25% progression, died in committee
Action: 2019-01-09 - Read twice and referred to the Committee on the Judiciary.
Pending: Senate Judiciary Committee
Text: Latest bill text (Introduced) [PDF]
Summary
Authorizes the Federal Trade Commission (FTC) to initiate proceedings against parties to any agreement resolving or settling a patent infringement claim in connection with the sale of a drug or biological product. Such an agreement is presumed to have anticompetitive effects and is a violation of this bill if the filer of the generic drug or biosimilar application receives anything of value and agrees to limit or forego research, development, manufacturing, marketing, or sales of the generic drug or biosimilar. An agreement is exempted if the only consideration granted to the generic manufacturer is (1) the right to market its product prior to the expiration of any statutory exclusivity, (2) a payment for reasonable litigation expenses, or (3) a covenant not to sue on any claim that the generic drug or biosimilar infringes a patent. An agreement is also exempt if the agreement's pro-competitive benefits outweigh the anticompetitive effects. When a generic or biosimilar drug manufacturer enters into an agreement with another drug manufacturer related to the manufacturing, marketing, or sale of a drug, the manufacturers must certify that the material they have given the FTC concerning the agreement contains the complete agreement and any agreements related to that main agreement, including descriptions of any oral agreements or representations. The bill imposes penalties for violations of this bill, including the forfeiture of the 180-day marketing exclusivity period for a generic drug.
Title
Preserve Access to Affordable Generics and Biosimilars Act
Sponsors
Sen. Amy Klobuchar [D-MN] | Sen. Chuck Grassley [R-IA] | Sen. Patrick Leahy [D-VT] | Sen. Joni Ernst [R-IA] |
Sen. Kevin Cramer [R-ND] | Sen. Richard Durbin [D-IL] | Sen. Chris Van Hollen [D-MD] | Sen. Susan Collins [R-ME] |
History
Date | Chamber | Action |
---|---|---|
2019-01-09 | Senate | Read twice and referred to the Committee on the Judiciary. |
Same As/Similar To
HB2375 (Related) 2020-12-24 - Placed on the Union Calendar, Calendar No. 576.
SB3384 (Related) 2020-03-03 - Read twice and referred to the Committee on Finance.
SB1801 (Related) 2019-06-12 - Read twice and referred to the Committee on Finance.
HB1344 (Related) 2019-03-25 - Referred to the Subcommittee on Antitrust, Commercial, and Administrative Law.
SB3384 (Related) 2020-03-03 - Read twice and referred to the Committee on Finance.
SB1801 (Related) 2019-06-12 - Read twice and referred to the Committee on Finance.
HB1344 (Related) 2019-03-25 - Referred to the Subcommittee on Antitrust, Commercial, and Administrative Law.
Subjects
Administrative law and regulatory procedures
Civil actions and liability
Competition and antitrust
Contracts and agency
Federal Trade Commission (FTC)
Health
Intellectual property
Judicial review and appeals
Licensing and registrations
Marketing and advertising
Prescription drugs
Civil actions and liability
Competition and antitrust
Contracts and agency
Federal Trade Commission (FTC)
Health
Intellectual property
Judicial review and appeals
Licensing and registrations
Marketing and advertising
Prescription drugs
US Congress State Sources
Type | Source |
---|---|
Summary | https://www.congress.gov/bill/116th-congress/senate-bill/64/all-info |
Text | https://www.congress.gov/116/bills/s64/BILLS-116s64is.pdf |