CDMRP: Duchenne Muscular Dystrophy Research Program (DMDRP)

Updated October 2026: This opportunity is closed. The FY26 application cycle for this program has closed. See our CDMRP guide for the next fiscal year’s announcements. Browse currently open opportunities in our funding database.

Below is a brief summary. Please check the full solicitation before applying (link in resources section).

Executive Summary:

The FY26 Duchenne Muscular Dystrophy Research Program (DMDRP), managed by the Congressionally Directed Medical Research Programs (CDMRP), will fund high-impact research to improve function and quality of life for individuals with Duchenne muscular dystrophy (DMD). This is a pre-announcement, meaning application deadlines are not yet specified. Founders and investigators should begin preparing now ahead of the official release on Grants.gov, where deadlines will be published.

Pre-applications are due on September 4th.

Full applications are due on September 18th.

How much funding would I receive?

Two award mechanisms are anticipated:

Idea Development Award

  • Maximum funding: $500,000 in total costs

  • Period of performance: 2 years

Clinical/Translational Research Award

Funding Level 1

  • Single PI: $910,000 in total costs

  • Partnering PI Option: $1 million in total costs

  • Period of performance: 3 years

Funding Level 2

  • Single PI: $1.75M in total costs

  • Partnering PI Option: $1.9M in total costs

  • Period of performance: 4 years

Total costs include direct and indirect costs.

What could I use the funding for?

Idea Development Award

  • High-risk/high-reward research advancing understanding of DMD

  • Development of macromolecular and cellular therapies targeting primary pathology

  • Research must include preliminary data

  • Cannot fund clinical trials or clinical trial aims

Clinical/Translational Research Award

  • Translational research with near-term clinical impact

  • Preclinical work supporting IND-enabling studies

  • Clinical research including:

    • Real-world data or post-market studies

    • Combination or sequential therapy studies

    • Long-term safety and efficacy studies

    • Studies to improve care and quality of life

    • Clinical trial tools and outcome measures

    • Natural history studies for trial readiness

  • Can include clinical trials, pilot trials, and readiness studies

  • Must include preliminary data

Are there any additional benefits I would receive?

  • Access to CDMRP-managed funding programs within the Defense Health Agency Research and Development ecosystem

  • Optional Partnering PI structure for Clinical/Translational Research Awards to support collaboration between investigators

What is the timeline to apply and when would I receive funding?

  • Pre-applications are due on September 4th.

  • Full applications are due on September 18th.

  • Deadlines will be released with the official funding opportunity announcements on Grants.gov

  • A pre-application submission through eBRAP is required prior to full application submission

Where does this funding come from?

  • FY26 Defense Appropriations Act

  • Managed by the Congressionally Directed Medical Research Programs (CDMRP)

  • Under the Defense Health Agency Research and Development – Medical Research and Development Command (DHA R&D-MRDC)

Who is eligible to apply?

Idea Development Award

  • Established independent investigators

  • Early-stage investigators:

    • Within 10 years of first faculty appointment

    • Must not have previously received this award

  • Transitioning investigators entering DMD from another field

  • Must:

    • Be pursuing an active line of DMD research

    • Commit at least 10% effort annually

Clinical/Translational Research Award

  • Independent investigators at all academic levels

  • Optional Partnering PI must be:

    • Early-career (within 10 years), or

    • Established investigator from another field entering DMD

What companies and projects are likely to win?

  • Projects focused on safe and effective macromolecular and cellular therapies addressing the primary pathology of DMD

  • Research with clinical relevance and translational potential

  • Studies that demonstrate impact across the lifespan, including:

    • Infants

    • Toddlers

    • Non-ambulatory individuals

  • Applications supported by strong preliminary data

  • High-risk/high-reward ideas (Idea Development Award) or near-term clinical impact (Clinical/Translational Award)

Are there any restrictions I should know about?

  • Idea Development Award:

    • Cannot fund clinical trials or clinical trial aims

  • All applications:

    • Must include preliminary data

    • Must align with specified focus areas

  • Pre-application submission via eBRAP is required

  • Applications must conform to final FOA requirements once released

How long will it take me to prepare an application?

  • Not specified in the pre-announcement

  • However, preparation should begin now given:

    • Required preliminary data

    • Mandatory pre-application step

    • Competitive, high-impact nature of the program

How can BW&CO help?

  • Evaluate fit across Idea Development vs. Clinical/Translational tracks

  • Shape your research into a CDMRP-aligned, reviewer-ready narrative

  • Support Partnering PI strategy and positioning

  • Develop compliant pre-applications and full submissions

  • Maximize competitiveness for high-risk/high-reward and translational proposals

How much would BW&CO Charge?

We have both fractional engagements ($250 an hour) and full engagements ($13,000 + 5%) available.

Additional Resources

Review the solicitation here.

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