Bill · H.R. 8205· House(119-HR-8205)
Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026
- Introduced
- 4/6/2026
- Last activity
- 9/28/2026 — Passed Senate without amendment by Voice Vote. (consideration: CR S5120)
- Sponsored by
- Mike Quigley
- Cosponsors
- - 64 - 39
- Introduced
- Passed House
- Passed Senate
What this bill would do
This bill is known as the Accelerating Access to Critical Therapies for ALS Reauthorization Act of 2026. It extends the provisions and grants for ALS research found in the original Act through fiscal year 2031. It also makes improvements to the program for grants by requiring the assessment of enrollment, safety, and efficacy data when reviewing grant renewals. Additionally, entities seeking grants must promptly report unexpected new and serious adverse events and safety information to the grant-making institution. Finally, the bill requires the Food and Drug Administration to publish an action plan regarding rare neurodegenerative diseases and a later report describing the actions taken.
Yes
Does this put more money into medical research?+7
The bill extends the authorization of grants for ALS research through fiscal year 2031.
Would people with disabilities be better off under this?+6
The bill promotes research into therapies for ALS, a debilitating neurodegenerative disease.
Does this make health care easier to get in general?+5
The bill extends research grants and enhances FDA oversight to accelerate access to treatments for ALS.
The opposite
No question was scored the opposite.
Who it would affect, and how
Potential Positive Impacts for People
-
Section 2 extends the provisions and grants for ALS research through fiscal year 2031, which continues support for finding therapies.
-
Section 3 improves the grant program by requiring the Secretary to request and assess enrollment, safety, and available efficacy data when reviewing grant renewals under section 2(b).
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Section 3 requires entities seeking grants to promptly report any new and serious adverse events and safety information that is considered unexpected with respect to the phase 3 trial to the grant-making institution under section 3(b).
-
Section 4 requires the Commissioner of Food and Drugs to publish an action plan on the FDA website detailing actions the agency intends to take during a 5-year period regarding program enhancements, policy development, and regulatory science initiatives, and later publish a report describing the actions taken under section 4.
Potential Negative Impacts for People
Based on the provided text, there are no specific provisions identified that create negative consequences or burdens for individuals or groups of people in the United States.
Groups and Interests Ranking
Every group the model scored this bill for, from -10 to +10. Hover a score for the reason it gave.
- Healthcare
- Increases Research Funding+7Improves Healthcare Access+5
- Demographic And Interest Groups
- Good For People With Disabilities+6
- Enrolled Bill
The final version, on its way to the President
What changed from Placed on Calendar Senate: No change to the wording. Only the printed details that record the bill’s progress, such as the heading and dates, are different.
- 9/28/2026
- Passed/agreed to in Senate: Passed Senate without amendment by Voice Vote. (consideration: CR S5120)
- Passed Senate without amendment by Voice Vote. (consideration: CR S5120)
- 7/23/2026
- Received in the Senate. Read twice. Placed on Senate Legislative Calendar under General Orders. Calendar No. 466.
- 7/22/2026
- Motion to reconsider laid on the table Agreed to without objection.
- Passed/agreed to in House: On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote.
- On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote.
- Considered as unfinished business. (consideration: CR H5159)
- 7/20/2026
- At the conclusion of debate, the chair put the question on the motion to suspend the rules. Mr. Guthrie objected to the vote on the grounds that a quorum was not present. Further proceedings on the motion were postponed. The point of no quorum was considered as withdrawn.
- DEBATE - The House proceeded with forty minutes of debate on H.R. 8205.
- Considered under suspension of the rules. (consideration: CR H4652-4654; text: CR H4653)
- Mr. Guthrie moved to suspend the rules and pass the bill, as amended.
- 7/9/2026
- Reported (Amended) by the Committee on Energy and Commerce. H. Rept. 119-733.
- Placed on the Union Calendar, Calendar No. 637.
- 28 Cosponsors added.
- 6/11/2026
- 2 Cosponsors added.
- 6/10/2026
- 2 Cosponsors added.
- 6/2/2026
- 3 Cosponsors added.
- 5/29/2026
- 1 Cosponsor added.
- 5/26/2026
- 2 Cosponsors added.
- 5/21/2026
- Committee Consideration and Mark-up Session Held
- Ordered to be Reported (Amended) by the Yeas and Nays: 46 - 0.
- 2 Cosponsors added.
- 5/19/2026
- 2 Cosponsors added.
- 5/15/2026
- 2 Cosponsors added.
- 5/14/2026
- 4 Cosponsors added.
- 5/13/2026
- Subcommittee Consideration and Mark-up Session Held
- Forwarded by Subcommittee to Full Committee by Voice Vote.
- 2 Cosponsors added.
- 5/12/2026
- 6 Cosponsors added.
- 5/11/2026
- 4 Cosponsors added.
- 5/7/2026
- 4 Cosponsors added.
- 5/4/2026
- 2 Cosponsors added.
- 4/30/2026
- 2 Cosponsors added.
- 4/23/2026
- 2 Cosponsors added.
- 4/22/2026
- 2 Cosponsors added.
- 4/21/2026
- 2 Cosponsors added.
- 4/20/2026
- 8 Cosponsors added.
- 4/16/2026
- 4 Cosponsors added.
- 4/15/2026
- 4 Cosponsors added.
- 4/14/2026
- 6 Cosponsors added.
- 4/9/2026
- 6 Cosponsors added.
- 4/6/2026
- Referred to the House Committee on Energy and Commerce.
- Referred to the Subcommittee on Health.
- 1 Cosponsor added.
- Introduced in House
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