Opportunity Information: Apply for W81XWH 10 NFRP EHDA
Apply for W81XWH 10 NFRP EHDA
- The Dept. of the Army USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "DoD Neurofibromatosis Exploration Hypothesis Development Award" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 12.420 Military Medical Research and Development.
- This funding opportunity was created on Mar 2, 2010 and posted on Mar 2, 2010.
- Applicants must submit their applications by May 20, 2010. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The funding agency has allocated a total of $750,000.00 to eligible and selected applicants.
- The number of recipients for this funding is limited to 5 candidate(s).
- Eligible applicants include: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled Additional Information on Eligibility.
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Opportunity Summary:
The DoD Neurofibromatosis Exploration - Hypothesis Development Award (EHDA) is a Department of Defense funding opportunity run through the Neurofibromatosis Research Program (NFRP) under the U.S. Army Medical Research and Acquisition Activity (USAMRAA). It is designed to help researchers take early, exploratory steps on new ideas in neurofibromatosis and/or schwannomatosis, especially ideas that are innovative, high-risk, and potentially high-reward. The award is meant to generate the kind of initial findings that either justify building a brand-new hypothesis or establish early guiding principles for an unconventional hypothesis. A core theme of the mechanism is giving investigators room to follow promising, even unexpected, observations rather than requiring a fully mature research plan backed by extensive preliminary results.
A key expectation is that the Principal Investigator clearly explains what makes the proposed work novel and why it represents a genuinely innovative direction for the field. Preliminary data can be included and may strengthen an application, but it is not required, which signals that the program is intentionally set up to support early-stage concept testing rather than later-stage validation. Historically, the program had received 46 applications since it began in FY08, with 13 recommended for funding, underscoring that it is competitive and selective.
Because this mechanism is intended for preliminary investigations, it places strict limits on human subjects research. Projects involving human subjects or human specimens are generally not supported unless they qualify as exempt under 32 CFR 219.101(b) or are eligible for expedited review under 32 CFR 219.110 or 21 CFR 56.110. Applications that propose human research that does not meet exempt or expedited criteria are not simply scored poorly; they are administratively withdrawn. Researchers who want to run a clinical trial are directed to use a separate Clinical Trial Award mechanism instead, meaning the EHDA is not the right vehicle for trial-based clinical studies.
For FY10, the program explicitly encouraged proposals aligned with pressing needs in the NF community. Priority themes included complications associated with high mortality, such as tumors (neoplasms) and cerebrovascular abnormalities, as well as high-morbidity complications like skeletal problems, learning deficits, hormone-related effects, and pain. The program also encouraged work that improves the tools needed for future clinical trials, including refining and standardizing imaging methods, molecular and cellular markers, and quality-of-life measures. Another emphasized area was translational research, particularly development or preclinical testing of therapeutic agents aimed at treating NF.
Administratively, this opportunity was posted March 2, 2010, and closed May 20, 2010 (archived June 19, 2010). It used grant and cooperative agreement instruments under a science and technology research and development category, with an estimated total funding level of $750,000 and an expectation of about five awards. There was no cost-sharing requirement, and eligibility was described as unrestricted (open to any entity type, subject to any clarifications in the full announcement). The funding opportunity number was W81XWH-10-NFRP-EHDA and the CFDA number listed was 12.420 (Military Medical Research and Development). Contact points were provided through the CDMRP help resources for assistance with accessing the announcement and with electronic submission.
FAQs: DoD Neurofibromatosis Exploration - Hypothesis Development Award (EHDA)
What is the DoD Neurofibromatosis Exploration - Hypothesis Development Award (EHDA)?
The EHDA is a Department of Defense funding opportunity offered through the Neurofibromatosis Research Program (NFRP) and managed under the U.S. Army Medical Research and Acquisition Activity (USAMRAA). It is intended to support early, exploratory research in neurofibromatosis and/or schwannomatosis.
What is the main purpose of the EHDA mechanism?
The EHDA is designed to help researchers take initial steps on new, innovative ideas, particularly those that are high-risk and potentially high-reward. The goal is to generate early findings that either justify forming a brand-new hypothesis or provide early guiding principles for an unconventional hypothesis.
What types of projects are a good fit for this award?
Projects that test early-stage concepts, explore promising new directions, and allow investigators to follow unexpected or emerging observations are a good fit. The mechanism is built for concept testing rather than mature, later-stage validation efforts.
How important is innovation and novelty in the application?
A key expectation is that the Principal Investigator clearly explains what makes the work novel and why it represents a genuinely innovative direction for the neurofibromatosis and/or schwannomatosis field.
Is preliminary data required to apply?
No. Preliminary data may be included and could strengthen an application, but it is not required. This reflects the program intent to support early-stage exploration rather than proposals that already have extensive supporting results.
How competitive is the EHDA?
Historically, since the mechanism began in FY08, 46 applications were received and 13 were recommended for funding. This indicates the award has been competitive and selective.
Are human subjects studies allowed under the EHDA?
Human subjects research and research involving human specimens are generally not supported unless the work qualifies as exempt under 32 CFR 219.101(b) or is eligible for expedited review under 32 CFR 219.110 or 21 CFR 56.110.
What happens if an application proposes human subjects research that is not exempt or eligible for expedited review?
Applications proposing human research that does not meet the exempt or expedited criteria are administratively withdrawn (not merely scored poorly).
Can EHDA funds be used to run a clinical trial?
No. Researchers intending to conduct a clinical trial are directed to use a separate Clinical Trial Award mechanism. The EHDA is not intended for trial-based clinical studies.
What research priorities or themes were encouraged for FY10?
For FY10, the program encouraged proposals addressing pressing needs in the NF community, including complications associated with high mortality (such as tumors/neoplasms and cerebrovascular abnormalities) and high-morbidity complications (such as skeletal problems, learning deficits, hormone-related effects, and pain).
Did the program encourage development of tools for future clinical trials?
Yes. The program encouraged work to improve tools needed for future clinical trials, including refining and standardizing imaging methods, molecular and cellular markers, and quality-of-life measures.
Was translational research encouraged?
Yes. Translational research was emphasized, including the development or preclinical testing of therapeutic agents aimed at treating neurofibromatosis.
Who runs or manages this funding opportunity?
The opportunity is part of the DoD Neurofibromatosis Research Program (NFRP) and is administered through USAMRAA.
What was the posting and closing timeline for this opportunity?
The opportunity was posted on March 2, 2010, and closed on May 20, 2010. It was archived on June 19, 2010.
What kind of funding instruments were used?
The opportunity used grant and cooperative agreement instruments under a science and technology research and development category.
What was the estimated total funding amount and the expected number of awards?
The estimated total funding level was $750,000, with an expectation of about five awards.
Was cost sharing required?
No cost-sharing requirement was listed for this opportunity.
Who was eligible to apply?
Eligibility was described as unrestricted (open to any entity type), subject to any clarifications included in the full announcement.
What is the funding opportunity number for the EHDA?
The funding opportunity number was W81XWH-10-NFRP-EHDA.
What CFDA number was associated with this opportunity?
The CFDA number listed was 12.420, Military Medical Research and Development.
Where could applicants get help with the announcement or electronic submission?
Contact points were provided through CDMRP help resources for assistance with accessing the announcement and with electronic submission.
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