Bill Sponsor
House Bill 2375
116th Congress(2019-2020)
Preserve Access to Affordable Generics and Biosimilars Act
Introduced
Introduced
Introduced in House on Apr 29, 2019
Overview
Text
Introduced
Apr 29, 2019
Latest Action
Dec 24, 2020
Origin Chamber
House
Type
Bill
Bill
The primary form of legislative measure used to propose law. Depending on the chamber of origin, bills begin with a designation of either H.R. or S. Joint resolution is another form of legislative measure used to propose law.
Bill Number
2375
Congress
116
Policy Area
Health
Health
Primary focus of measure is science or practice of the diagnosis, treatment, and prevention of disease; health services administration and funding, including such programs as Medicare and Medicaid; health personnel and medical education; drug use and safety; health care coverage and insurance; health facilities. Measures concerning controlled substances and drug trafficking may fall under Crime and Law Enforcement policy area.
Sponsorship by Party
Democrat
New York
Republican
North Carolina
Democrat
Rhode Island
Democrat
Tennessee
House Votes (0)
Senate Votes (0)
No House votes have been held for this bill.
Summary

Preserve Access to Affordable Generics and Biosimilars Act

This bill 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.

Text (2)
December 24, 2020
April 29, 2019
Actions (8)
12/24/2020
Placed on the Union Calendar, Calendar No. 576.
12/24/2020
Committee on Energy and Commerce discharged.
12/24/2020
Reported by the Committee on Judiciary. H. Rept. 116-693, Part I.
04/30/2019
Ordered to be Reported by Voice Vote.
04/30/2019
Committee Consideration and Mark-up Session Held.
04/30/2019
Referred to the Subcommittee on Health.
04/29/2019
Referred to the Committee on the Judiciary, and in addition to the Committee on Energy and Commerce, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
04/29/2019
Introduced in House
Public Record
Record Updated
Jan 11, 2023 1:44:08 PM