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DoW Amyotrophic Lateral Sclerosis Research Program, Therapeutic Development Award

Apply on Grants.gov →Application closes September 30, 2026

Posted
May 4, 2026
Closes
September 30, 2026
Program funding
$12,000,000
Expected awards
6
Cost sharing
No
Instrument
Grant
Assistance listing
12.420
Category
Science and Technology and other Research and Development
Archives
October 30, 2026

Program funding history

Awards made under Assistance Listing 12.420 across FY2024–FY2026, from public federal spending records.

FY2024 obligated
$1.4B
FY2025 obligated
$1.3B
FY2026 (to date) obligated
$448.9M
Awards in window
5,933

Top recipients: The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., The Univeristy of Texas M.d. Anderson Cancer Center, Regents of the University of California, San Francisco, the, The Johns Hopkins University, Duke University

Source: USAspending.gov · refreshed August 2026

Synopsis

Summary: The fiscal year 2026 (FY26) Amyotrophic Lateral Sclerosis Research Program (ALSRP) Therapeutic Development Award (TDA) supports research ranging from preclinical validation of therapeutic leads through U.S. Food and Drug Administration (FDA) Investigational New Drug (IND)-enabling studies. The proposed studies are expected to be empirical in nature and product-driven. Applicants with limited amyotrophic lateral sclerosis (ALS) experience are strongly encouraged to include collaborators with substantial experience in the relevant ALS model systems, endpoints and pathophysiology.


Applications supported by this award must begin with lead compounds in hand and must already demonstrate proof-of-concept efficacy data in at least one appropriate preclinical model system of ALS, including whole-animal and cellular model systems.


Distinctive Features: Mechanism-specific, predictive/cohort-selective, target engagement and pharmacodynamic biomarker development, in parallel to the main therapeutic effort, is a critical component of the FY26 ALSRP Therapeutic Development Award. If appropriate mechanism-specific biomarkers are already available or currently in development, how the existing biomarkers will improve trial design, patient selection, and efficiency or interpretation of the proposed ALS therapeutic approach must be apparent in the application. Development of biomarkers for the purposes of diagnosis, prognosis, or measurement of general disease progression without consideration of the therapeutic development process will not be supported.


Therapeutic candidates which have already been granted an IND are not appropriate for this mechanism.

Who can apply

How to apply

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View on Grants.gov

Agency contact: Jamie Shortall Grant Officer · [email protected] · 301-619-2393

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