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Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026

Introduced: April 30, 2026 Introduced by: Murkowski, Lisa Republican · Alaska See on congress.gov
 Everywhere this bill has been 10 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Aug 10, 2026
Held at the desk.
Aug 10, 2026
Received in the House.
Aug 10, 2026
Message on Senate action sent to the House.
Aug 4, 2026
Passed Senate with an amendment by Voice Vote. (consideration: CR S4425-4426; text: CR S4425-4426)
Aug 4, 2026
Passed/agreed to in Senate: Passed Senate with an amendment by Voice Vote.
Jul 16, 2026
Committee on Health, Education, Labor, and Pensions. Reported by Senator Cassidy with an amendment in the nature of a substitute. Without written report.
Jul 16, 2026
Placed on Senate Legislative Calendar under General Orders. Calendar No. 461.
Jun 17, 2026
Committee on Health, Education, Labor, and Pensions. Ordered to be reported with an amendment in the nature of a substitute favorably.
Apr 30, 2026
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Apr 30, 2026
Introduced in Senate
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 Plain-English summary Congressional Research Service

Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026

This bill reauthorizes through FY2031 and revises programs that support research and development of drugs and other therapies to address amyotrophic lateral sclerosis (also known as ALS or Lou Gehrig's disease) and other neurodegenerative diseases.

The bill reauthorizes

  • grants from the National Institutes of Health (NIH) for scientific research on investigational drugs to prevent or treat ALS for individuals not otherwise eligible for clinical trials,
  • grants from the Food and Drug Administration (FDA) for research and development of therapies to prevent and treat ALS and other neurodegenerative diseases, and
  • a Public-Private Partnership including the FDA and NIH that supports development and regulatory review of treatments for neurodegenerative diseases. 

Also, the bill revises the NIH grants to require (1) the NIH, in considering grant renewal, to assess available information on the safety and efficacy of the investigational drugs; (2) grantees to promptly report available safety data from ongoing clinical trials; and (3) the NIH to determine the timeframe for enrollment in clinical trials for the investigational drugs.

Additionally, every five years, the FDA must publish a plan describing actions it will take over a five-year period to foster development of safe and effective drugs, and facilitate access to investigational drugs, for ALS and other rare neurodegenerative diseases. Each plan must include the FDA's previous actions and recommendations for improvements.

Finally, the Government Accountability Office and the Department of Health and Human Services must report on the impacts of these grants. 

What's happening now August 10, 2026

Held at the desk.

 Hearings & markups 1
 Related & companion bills 1
 Bill text 3 versions

Source documents hosted by congress.gov.

 Committees of jurisdiction 1
 Lobbying activity 3

Registered lobbyists who named this bill in their disclosure filings. Source: federal Lobbying Disclosure Act filings.

Cite this page click to expand
APA
U.S. Congress. (2026). S. 4472: Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026. 119th Congress. Open America. https://openamerica.io/bill/119-S-4472/
MLA
"S. 4472: Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026." 119th Congress, 2026, Open America, https://openamerica.io/bill/119-S-4472/.
Bluebook (legal)
S. 4472, 119th Cong. (2026), https://openamerica.io/bill/119-S-4472/.
Markdown link
[S. 4472: Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026](https://openamerica.io/bill/119-S-4472/)
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