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This bill reauthorizes the Accelerating Access to Critical Therapies for ALS Act through fiscal year 2031, extending its grant programs and regulatory initiatives for amyotrophic lateral sclerosis (ALS) research and therapy development. It adds requirements for the FDA to review clinical trial enrollment status during grant renewals and clarifies the definition of phase 3 clinical trials to include combined phase 2/3 trials. The bill also requires the FDA to publish an updated action plan within one year describing its five-year strategy for ALS and rare neurodegenerative disease initiatives, and mandates a Government Accountability Office report on the program's effectiveness.
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