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DoW Amyotrophic Lateral Sclerosis Research Program, Pilot Clinical Trial Award

Federal funding opportunity HT942526ALSRPPCTA from Defense Health Agency Contracting Activity - DHACA (Department of Defense).

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

Posted
May 4, 2026
Closes
September 30, 2026
Program funding
$5,600,000
Expected awards
2
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
$329.9M
Awards in window
5,781

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, University of Pittsburgh - of the Commonwealth System of Higher Education

Source: USAspending.gov · refreshed July 2026

Synopsis

Summary: The fiscal year 2026 (FY26) Amyotrophic Lateral Sclerosis Research Program (ALSRP) Pilot Clinical Trial Award (PCTA) supports the rapid implementation of clinical trials with the potential to have a significant impact on the treatment or management of amyotrophic lateral sclerosis (ALS). Projects may range from phase 1 to small-scale phase 2 trials.


Applications must address one of the following focus areas:


·        Biomarker-Driven Interventions: Disease-modifying interventions, with mechanism-specific biomarkers to predict which clinical trial participants are likely to respond, demonstrate target engagement, and effects on the intended biological pathway.

·        Clinical Care: Improving aspects of clinical care and symptom management for ALS.


Distinctive Features: Funding from this award mechanism must support a clinical trial. The clinical trial should begin no later than 12 months after the award date or 18 months for U.S. Food and Drug Administration (FDA)-regulated studies.


Projects proposing a therapeutic intervention (drug, biologic, and/or device) must incorporate biomarkers specific to the intervention into the trial design.


All pre-applications and applications are required to incorporate community collaboration, as described in Section 3.2.2, to optimize research impact.


Applications must include a detailed Regulatory Strategy plan that outlines the approach for obtaining regulatory approvals, if required, specifically for the funded portion of the study. In addition, applications must provide a separate Transition Plan that describes how the outcomes of the study will be advanced to the next phase of development, beyond the scope of the funded work.

Who can apply

How to apply

Applications go through the official government listing. Grants Radar links you straight to the source.

View on Grants.gov

Agency contact: Jamie Shortall Grant Officer · help@eBRAP.org · 301-619-2393

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