Extends federal support for ALS research and requires FDA to plan for rare brain diseases.
This bill would continue federal support for research into Amyotrophic Lateral Sclerosis (ALS). It would extend the current research program and grants through the government's budget year 2031. It would also require the Food and Drug Administration (FDA) to create a public plan for how it will help develop therapies for rare brain conditions.
Today, federal support for ALS research and related grants is set to end in the government's budget year 2026, and the Food and Drug Administration (FDA) is not required to publish a specific action plan for rare brain diseases. If this bill becomes law, federal support for ALS research and grants would continue through the government's budget year 2031. The FDA would also be required to publish a 5-year action plan for rare brain diseases within 18 months and a report on its progress within 5 years.
HR 8205 · 119th Congress · April 6, 2026 · AI Summary by gemini-2.5-flash · 10/10
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