[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[H.R. 6807 Introduced in House (IH)]
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118th CONGRESS
1st Session
H. R. 6807
To increase funding for cancer research by the National Cancer
Institute to be more in proportion to the mortality rates of cancer.
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IN THE HOUSE OF REPRESENTATIVES
December 14, 2023
Mr. Fitzpatrick (for himself and Mrs. Dingell) introduced the following
bill; which was referred to the Committee on Appropriations, 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
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A BILL
To increase funding for cancer research by the National Cancer
Institute to be more in proportion to the mortality rates of cancer.
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 ``Knock Out Cancer Act'' or the ``KO
Cancer Act''.
SEC. 2. INCREASING NCI BUDGET FOR CANCER RESEARCH.
To conduct or support cancer research, there is hereby
appropriated, for each of fiscal years 2024 through 2028, to the
National Cancer Institute, out of amounts in the Treasury not otherwise
appropriated, an amount that is equal to 25 percent of the total amount
appropriated to the National Cancer Institute for fiscal year 2022, to
remain available until expended. Amounts appropriated pursuant to the
preceding sentence shall be in addition to amounts otherwise made
available to the National Cancer Institute.
SEC. 3. REPORT TO CONGRESS ON CANCER DRUG SHORTAGES.
(a) Study.--The Secretary of Health and Human Services, acting
through the Commissioner of Food and Drugs, in collaboration with such
other agencies as the Secretary deems necessary, shall study the
reasons for cancer drug shortages, including--
(1) economic reasons;
(2) supply chain failures;
(3) delays and other complications relating to--
(A) the development of cancer drugs; and
(B) the approval of such drugs by the Food and Drug
Administration; and
(4) insufficient generic drugs and biosimilar biological
products.
(b) Report.--
(1) In general.--Not later than 1 year after the date of
enactment of this Act, the Secretary of Health and Human
Services, acting through the Commissioner of Food and Drugs,
shall complete the study under subsection (a) and submit a
report to the appropriate committees of the Congress on the
results of such study.
(2) Recommendations.--The report under paragraph (1) shall
include recommendations for addressing the reasons for cancer
drug shortages.
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