Bill Sponsor
Senate Bill 1813
117th Congress(2021-2022)
Accelerating Access to Critical Therapies for ALS Act
Introduced
Introduced
Introduced in Senate on May 25, 2021
Overview
Text
Introduced
May 25, 2021
Latest Action
May 25, 2021
Origin Chamber
Senate
Type
Bill
Bill
The primary form of legislative measure used to propose law. Depending on the chamber of origin, bills begin with a designation of either H.R. or S. Joint resolution is another form of legislative measure used to propose law.
Bill Number
1813
Congress
117
Policy Area
Health
Health
Primary focus of measure is science or practice of the diagnosis, treatment, and prevention of disease; health services administration and funding, including such programs as Medicare and Medicaid; health personnel and medical education; drug use and safety; health care coverage and insurance; health facilities. Measures concerning controlled substances and drug trafficking may fall under Crime and Law Enforcement policy area.
Sponsorship by Party
Democrat
Delaware
Democrat
Arizona
Republican
Arkansas
Democrat
California
Democrat
Connecticut
Democrat
Delaware
Democrat
Georgia
Democrat
Illinois
Republican
Indiana
Republican
Louisiana
Republican
Louisiana
Democrat
Massachusetts
Democrat
Massachusetts
Democrat
Michigan
Democrat
Minnesota
Democrat
Minnesota
Republican
Missouri
Democrat
Montana
Republican
Nebraska
Democrat
New Hampshire
Democrat
New Hampshire
Democrat
New Jersey
Democrat
New Jersey
Democrat
New Mexico
Democrat
New Mexico
Republican
North Carolina
Republican
North Dakota
Republican
Oklahoma
Democrat
Pennsylvania
Democrat
Rhode Island
Democrat
Rhode Island
Republican
South Dakota
Republican
South Dakota
Republican
Tennessee
Democrat
Virginia
Democrat
West Virginia
Democrat
Wisconsin
Senate Votes (0)
House Votes (0)
No Senate votes have been held for this bill.
Summary

Accelerating Access to Critical Therapies for ALS Act

This bill establishes grant programs to address neurodegenerative diseases, such as amyotrophic lateral sclerosis (also known as ALS or Lou Gehrig's disease), and contains other related provisions.

The Department of Health and Human Services (HHS) shall award grants to eligible entities to facilitate patients' access to investigational drugs that diagnose or treat ALS. The Food and Drug Administration (FDA) shall award grants to public and private entities to cover the costs of research and development of drugs that diagnose or treat ALS and other severely debilitating neurodegenerative diseases.

HHS shall also establish the Public-Private Partnership for Neurodegenerative Diseases between the National Institutes of Health, the FDA, and at least one eligible entity (generally, an institution of higher education or a nonprofit organization). The partnership shall support the development and regulatory review of drugs that address ALS and other rare neurodegenerative diseases.

The FDA shall publish on its website a five-year action plan for fostering the development of drugs that improve or extend the lives of people living with rare neurodegenerative diseases.

Text (1)
Actions (2)
05/25/2021
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
05/25/2021
Introduced in Senate
Public Record
Record Updated
Jan 11, 2023 1:50:03 PM