Approved? (Admin-only)
  • Approved
Opportunity TypePre-Release
Funding Opportunity Posted ByDOW
ComponentDHA - CDMRP
Funding Opportunity TitleDuchenne Muscular Dystrophy Research Program
Link to Funding Opportunityhealth.mil
Funding Opportunity Short DescriptionTo support innovative, high-impact research with clinical relevance that will preserve and improve the function and quality of life across the lifespan of all individuals with Duchenne muscular dystrophy.
Funding Opportunity CategoryHealth and Biomedical Technologies
Important Dates
Funding Details
Required Registrations
  • SAM
  • eBRAP
Funding Opportunity Full Description

Two Award Mechanisms (1) Idea Development Award (2) Clinical/Translational Research Award

The FY26 Defense Appropriations Act provides funding for the DMDRP to support innovative, high-impact research with clinical relevance that will preserve and improve the function and quality of life across the lifespan of all individuals with Duchenne muscular dystrophy. As part of the DHA R&D-MRDC, the CDMRP is the program office managing these anticipated FY26 funding opportunities.

The DMDRP provides the information in this pre-announcement to allow investigators time to plan and develop ideas for submission to the anticipated FY26 funding opportunities. Investigators should not construe this pre-announcement as an obligation or promise by the government. The CDMRP will post FY26 DMDRP funding opportunity announcements on the Grants.gov website. Once released, the funding opportunity announcements will include pre-application and application deadlines.

Applications submitted to the FY26 DMDRP Idea Development Award must address opportunities and challenges in the development of safe and effective macromolecular and cellular therapies that focus on the primary pathology of DMD. Therapies that will be efficacious across the lifespan, including infants, toddlers, and non-ambulatory individuals are strongly encouraged.

Applications submitted to the FY26 DMDRP Clinical/Translational Research Award must address at least one of the following focus areas:

For applications proposing preclinical translational research

Extension or expansion of existing preclinical data in support of Investigational New Drug (IND) application-enabling studies
For applications proposing clinical research

Prospective, real world data, or post-market studies for combination or sequential therapies and/or long-term safety and efficacy studies
Clinical studies designed to improve care and quality of life
Assessment of clinical trial tools and outcome measures across the lifespan
Natural history studies in understudied systems or understudied age groups with an aim toward clinical trial readiness

Type your search here