science_technology_and_other_research_and_development · DOD-AMRAA
DoW Amyotrophic Lateral Sclerosis Research Program, Pilot Clinical Trial Award
Defense Health Agency Contracting Activity - DHACA · HT942526ALSRPPCTA
Total Program Funding
$5.6M
Expected Awards
2
Deadline
September 30, 2026
GRANTQUICK SUMMARYPlain-English Overview
DoW Amyotrophic Lateral Sclerosis Research Program, Pilot Clinical Trial Award. Defense Health Agency Contracting Activity - DHACA. 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... $5,600,000 total program funding; ~2 awards expected.
Who Should Apply
Unrestricted (any eligible entity)
Who Should NOT Apply
Few restrictions — most eligible entities can apply
Key Requirements (Plain English)
- •Deadline: 2026-09-30
💡 GrantQuick Tip
High-value award — invest significantly in proposal quality. Consider hiring a grant writer.
Competitiveness: Very high — extremely limited awards available
What This Grant Funds
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.
Attachments
Who Can Apply
Eligible Applicant Types
Funding Details
- Total Program Funding
- $5.6M
- Expected Number of Awards
- 2
- Cost Sharing Required?
- No
- Funding Instrument
- grant
Key Dates
Agency Contact
eBRAP Help Desk Phone: 301-682-5507 Email: help@eBRAP.org
help@eBRAP.orgReady to apply?
View the full NOFO and submit your application on Grants.gov