HR 7506 · 117th Congress 2021–2023, ended

New Era of Preventing End-Stage Kidney Disease Act

Fact sheet

Latest action · Apr 15, 2022 Referred to the Subcommittee on Health.

Progress

Where this bill reached, and when. A stage with no date was not reached; one that failed a vote and later carried shows the date it carried.

  1. IntroducedApr 14, 2022
  2. Passed HouseNot reached
  3. Passed SenateNot reached
  4. To the PresidentNot reached
  5. Became lawNot reached

Summary

New Era of Preventing End-Stage Kidney Disease Act

This bill addresses rare kidney diseases through research, training for health professionals, and other means. It also modifies requirements for Medicare drug plan formularies that include drugs for rare diseases or conditions.

The Department of Health and Human Services (HHS) must

  • convene a conference focused on diagnosis and treatment of rare kidney diseases;
  • study risk factors, access to care (including to genetic and genomic testing), and other matters related to rare kidney diseases; and
  • establish grants for supporting kidney disease education and referrals in communities of color.

HHS may award grants to educate and train health professionals about kidney disease and nephrology. Additionally, health professional schools that receive certain HHS funding for educating underrepresented minority individuals must support postgraduate nephrology training.

The National Institutes of Health (NIH) must report on diversity in its kidney disease research. The NIH may also (1) support research on rare kidney diseases that, among other requirements, includes persons of color in study populations; and (2) establish regional centers of excellence for rare kidney diseases.

The Centers for Medicare & Medicaid Services must evaluate methods for (1) treating rare kidney diseases, with a focus on delaying dialysis and transplant; and (2) raising awareness about rare kidney diseases, including in communities of color.

Furthermore, if a Medicare drug plan formulary includes a drug to treat a rare disease or condition, at least two members of the committee that develops or reviews the formulary must have expertise in the field of medicine related to that drug.

Cosponsors 13

Members who signed on, in the order they did. Signatures ran from Apr 14, 2022 to Dec 15, 2022, with 1 there on the day it was introduced.

SeatCosponsorSigned on
R-FLGus M. BilirakisOriginalApr 14, 2022
D-GASanford D. Bishop, Jr.Jun 7, 2022
D-CAMike LevinJul 1, 2022
D-NCDeborah K. RossJul 21, 2022
D-PASusan WildJul 21, 2022
D-CAZoe LofgrenAug 5, 2022
D-MNDean PhillipsAug 12, 2022
R-FLBill PoseySep 22, 2022
D-ORKurt SchraderOct 28, 2022
R-TXMichael C. BurgessOct 28, 2022
D-CAScott H. PetersNov 10, 2022
R-TXDan CrenshawDec 15, 2022
D-ILDanny K. DavisDec 15, 2022

Actions 3

Everything that happened, newest first.

  1. Apr 15, 2022Referred to the Subcommittee on Health.
  2. Apr 14, 2022Introduced in House
  3. Apr 14, 2022Referred 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.

Subjects

Assigned by the Library of Congress. Policy area: Health.

Text 1

Each version as it was printed, newest first.

  1. Apr 14, 2022Introduced in House

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Everything here is as published by Congress: the summary is the Congressional Research Service's, the action wording is the clerks', and the subjects are the Library of Congress's. How far it got is read from the actions themselves, taking the most recent one of each kind, so a bill that failed a vote and later passed is shown as having passed. Records come from this bill on Congress.gov and govinfo.gov.