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Extends ALS Research Funding to 2031
Recent Bills/Extends ALS Research Funding to 2031

Extends ALS Research Funding to 2031

IntroducedApril 30, 2026
Passed Senate1 month ago
Intro
Senate
House
Pres
Waiting for a House floor vote.
It was held at the desk rather than sent to a committee, so it can be taken up directly.
HealthDepartment of Health and Human ServicesDrug therapyFood and Drug Administration (FDA)Government information and archivesHealth programs administration and fundingInternet, web applications, social mediaMedical researchNational Institutes of Health (NIH)Neurological disordersPublic-private cooperationResearch administration and funding
More:Bills That Passed the SenateHealthcareSenate Bills
Why This Matters

This bill extends funding for ALS research and improves the review process for clinical trials related to ALS therapies.

If you are involved in ALS research, this bill secures funding for your work through 2031.
Who this affects
Patients with ALS · ALS researchers
What changes is this bill making?
  1. 1This bill extends funding for the Accelerating Access to Critical Therapies for ALS Act until 2031.
  2. 2It requires the Food and Drug Administration to publish a report on actions taken regarding ALS therapies within one year.
  3. 3The bill improves the review process for clinical trial grants by requiring manufacturers to share interim data.
  4. 4It clarifies the definition of clinical trials to include combined phase 2/3 trials and planned phase 3 trials.
Read the detailed summary

Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026This 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 reauthorizesgrants 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, anda 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.

Read full document
Bill Progress3 of 4
Bills must pass the House, Senate, and be signed by the President to become law.
Intro
Senate
House
Pres
IntroducedApr 30
Sponsors
See all 16 sponsors
SenateAug 4
HouseCurrent

Waiting for a House floor vote.

It was held at the desk rather than sent to a committee, so it can be taken up directly.

President

The President

Donald Trump
President
Awaiting Vote
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