HR 456 United States House · 118th Congress

Fairness in Orphan Drug Exclusivity Act

Summary
Fairness in Orphan Drug Exclusivity Act This bill limits which orphan drugs may be granted a market exclusivity period by the Food and Drug Administration (FDA). (Generally, an orphan drug is one that is not economically viable because of the rarity of the disease that it treats; the sponsor of an FDA-designated orphan drug may be granted various incentives, such as a seven-year period in which the FDA may not grant market approval to a different sponsor for the same drug to treat the same disease.) Under this bill, if a drug is designated as an orphan drug on the basis that there is no reasonable expectation that the sponsor will recover the costs of developing and distributing the drug from U.S. sales, the drug shall be granted the seven-year exclusivity period only if the sponsor demonstrates that there is no reasonable expectation that it will recover such costs within its first 12 years of U.S. sales of the drug. When deciding whether an orphan drug meets this requirement, the FDA shall consider the sales of all drugs from the sponsor that are covered by the same orphan drug designation.
Bill status in committee 1 of 4 stages cleared
Introduction
Jan 2023
Committee Review
Floor Vote
President
Introduced Jan 24, 2023 Last action Feb 3, 2023
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Full legislative history

Actions timeline

Total actions
3
Key actions
0
Committee
2
Feb 3, 2023
Committee
Referred to the Subcommittee on Health.
lower
Jan 24, 2023
Committee
Referred to the House Committee on Energy and Commerce.
lower
Jan 24, 2023
Introduced
Introduced in House
lower
1 primary · 0 co-sponsors

Sponsors

Role
Legislator
Party
State
District
P
Photo of Earl L. "Buddy" Carter
Earl L. "Buddy" Carter
RRepublican
GA
1