Skip to main content
HR 4712 116th Congress House Health Competition and antitrust Drug safety, medical device, and laboratory regulation Licensing and registrations Marketing and advertising Prescription drugs

Fairness in Orphan Drug Exclusivity Act

Introduced: October 17, 2019 Introduced by: Dean, Madeleine Democratic · Pennsylvania See on congress.gov
 Everywhere this bill has been 16 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Nov 18, 2020
Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Nov 17, 2020
Motion to reconsider laid on the table Agreed to without objection.
Nov 17, 2020
On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote. (text: CR H5807)
Nov 17, 2020
Passed/agreed to in House: On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote.(text: CR H5807)
Nov 17, 2020
DEBATE - The House proceeded with forty minutes of debate on H.R. 4712.
Nov 17, 2020
Considered under suspension of the rules. (consideration: CR H5807-5809)
Nov 17, 2020
Mr. Pallone moved to suspend the rules and pass the bill, as amended.
Nov 16, 2020
Placed on the Union Calendar, Calendar No. 470.
Nov 16, 2020
Reported (Amended) by the Committee on Energy and Commerce. H. Rept. 116-572.
Jul 15, 2020
Ordered to be Reported (Amended) by Voice Vote.
Jul 15, 2020
Committee Consideration and Mark-up Session Held.
Mar 11, 2020
Forwarded by Subcommittee to Full Committee (Amended) by Voice Vote .
Mar 11, 2020
Subcommittee Consideration and Mark-up Session Held.
Oct 18, 2019
Referred to the Subcommittee on Health.
Oct 17, 2019
Referred to the House Committee on Energy and Commerce.
Oct 17, 2019
Introduced in House
 Plain-English summary Congressional Research Service

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 specifically within its first 12 years of U.S. sales of the drug. This requirement shall also apply retroactively to an orphan drug that was granted such an exclusivity period before this bill's enactment.

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.

What's happening now November 18, 2020

Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

 Committees of jurisdiction 3