Maintaining Investments in New Innovation Act
This bill requires drug products with genetically targeted technology to have had market approval for at least 11 years in order to qualify for the Medicare Drug Price Negotiation Program. (The program requires the Centers for Medicare & Medicaid Services to negotiate the prices of certain prescription drugs under Medicare beginning in 2026. Among other requirements, drugs must have had market approval for at least 7 years (for drug products) or 11 years (for biologics) to qualify for negotiation.)
[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[H.R. 5547 Introduced in House (IH)]
<DOC>
118th CONGRESS
1st Session
H. R. 5547
To amend title XI of the Social Security Act to protect access to
genetically targeted technologies.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
September 18, 2023
Mr. Nickel (for himself, Mr. Joyce of Pennsylvania, and Mr. Davis of
North Carolina) introduced the following bill; which was referred to
the Committee on Energy and Commerce, and in addition to the Committee
on Ways and Means, 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
_______________________________________________________________________
A BILL
To amend title XI of the Social Security Act to protect access to
genetically targeted technologies.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Maintaining Investments in New
Innovation Act''.
SEC. 2. AMENDMENT TO DEFINITION OF QUALIFYING SINGLE SOURCE DRUG.
Section 1192(e) of the Social Security Act (42 U.S.C. 1320f-1(e))
is amended--
(1) in paragraph (1)(A)(ii), by inserting ``(or, in the
case of an advanced drug product (as defined in paragraph (4)),
11 years)'' after ``7 years''; and
(2) by adding at the end the following new paragraph:
``(4) Advanced drug product defined.--For purposes of
paragraph (1)(A)(ii), the term `advanced drug product' means a
drug that incorporates or utilizes a genetically targeted
technology (as defined in section 529A(c)(2) of the Federal
Food, Drug, and Cosmetic Act) that may result in the modulation
(including suppression, up-regulation, or activation) of the
function of a gene or its associated gene product.''.
<all>
Introduced in House
Introduced in House
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, 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.
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, 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.
Referred to the Subcommittee on Health.
Referred to the Subcommittee on Health.
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