Opportunity Information: Apply for W81XWH 15 NFRP IIRA

  • 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 Investigator Initiated Research 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 May 6, 2015 and posted on May 6, 2015.
  • Applicants must submit their applications by Jul 27, 2015. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $6,004,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 7 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.
Apply for W81XWH 15 NFRP IIRA

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Opportunity Summary:

The DoD Neurofibromatosis Investigator Initiated Research Award (IIRA) is a Department of Defense funding opportunity under the Neurofibromatosis Research Program (NFRP) designed to back investigator-driven projects that are both highly rigorous and likely to have a meaningful impact on neurofibromatosis (NF) research and, ultimately, patient care. The central goal is to support studies that can significantly advance understanding of NF biology, improve approaches to diagnosis or management, or help move promising concepts closer to real-world clinical benefit, while keeping the scientific bar high in terms of study design, execution, and reporting.

This award is intentionally broad in the kinds of research it will consider, as long as the work is clearly relevant to NF and positioned to make an important contribution. Projects can span essentially any stage of research (for example, basic mechanistic work, translational studies, or other non-trial human or population-based research), but clinical trials are explicitly excluded. The program also recognizes that strong research ideas can emerge from many sources, including laboratory discoveries, population-based observations, insights grounded in day-to-day clinical care, or even well-supported anecdotal observations that point to a testable hypothesis. A key requirement, however, is that applications must include preliminary and/or published data that directly ties into NF and supports the feasibility and rationale of the proposed project. In practice, this means applicants need to demonstrate that the idea is not purely speculative and that there is a credible foundation suggesting the approach can work and is worth pursuing.

A major theme of the opportunity is reproducibility and transparent research practices, especially for preclinical work. Applicants are expected to adhere to established standards for rigorous study design and reporting that increase the reliability and translational value of results. The announcement specifically points to the principles described by Landis et al. (Nature, 2012) emphasizing elements such as randomization, blinding, appropriate sample size estimation, and clear data handling procedures. Even though these standards are often discussed in the context of animal or other preclinical studies, the underlying logic applies widely: reduce bias, pre-plan analyses where possible, ensure adequate statistical power, and document methods and outcomes in a way that other researchers can evaluate and reproduce.

For projects that involve animal models, the requirements become more concrete. Applicants must include an Animal Research Plan (listed as Attachment 8 in the application package) explaining how the study will meet these rigor standards. They are also encouraged to use the ARRIVE guidelines (Animal Research Reporting of In Vivo Experiments) when planning and later reporting animal research, to help ensure that essential methodological details are included and that the study is set up to yield interpretable, reproducible results. This emphasis signals that the program is not just funding interesting ideas, but is also prioritizing work that is designed from the start to withstand scrutiny and to better predict what may eventually translate to human benefit.

Administratively, this opportunity was posted May 6, 2015, by the Department of the Army through USAMRAA (U.S. Army Medical Research Acquisition Activity), under Funding Opportunity Number W81XWH-15-NFRP-IIRA. The funding instrument is listed as a cooperative agreement and/or grant, and it falls under the Science and Technology and other Research and Development category, with CFDA 12.420 (Military Medical Research and Development). The program anticipated making about 7 awards, with an estimated total funding level of $6,004,000, and it did not require cost sharing or matching funds. Eligibility is described as unrestricted, meaning it is open to any type of entity, subject to any additional eligibility language contained in the full announcement. The original and current closing date listed for this cycle was July 27, 2015, and the opportunity was archived August 26, 2015. For applicants who had trouble accessing the announcement, the contact listed was the CDMRP Help Desk at 301-682-5507.

DoD Neurofibromatosis Investigator Initiated Research Award (IIRA) - FAQs

What is the DoD Neurofibromatosis Investigator Initiated Research Award (IIRA)?

The IIRA is a Department of Defense funding opportunity under the Neurofibromatosis Research Program (NFRP) that supports investigator-driven neurofibromatosis (NF) research projects. It is designed to fund studies that are rigorous and positioned to make a meaningful impact on NF research and, ultimately, patient care.

What is the main goal of this award?

The central goal is to support studies that can significantly advance understanding of NF biology, improve approaches to diagnosis or management, or move promising concepts closer to real-world clinical benefit, while maintaining high standards for study design, execution, and reporting.

What types of research projects are considered responsive to this opportunity?

The award is intentionally broad and can support projects at essentially any stage of research, as long as the work is clearly relevant to NF and positioned to make an important contribution. Examples mentioned include basic mechanistic work, translational studies, and other non-trial human or population-based research.

Are clinical trials allowed under this award?

No. Clinical trials are explicitly excluded from this funding opportunity.

Does the program require the research idea to come from a specific source (lab, clinic, etc.)?

No. The opportunity notes that strong research ideas can arise from many sources, including laboratory discoveries, population-based observations, insights grounded in day-to-day clinical care, and even well-supported anecdotal observations that point to a testable hypothesis.

Is preliminary data required to apply?

Yes. Applications must include preliminary and/or published data that directly ties into NF and supports the feasibility and rationale of the proposed project.

Can an application be purely hypothesis-generating or speculative?

The opportunity emphasizes that applicants must show the idea is not purely speculative by providing NF-relevant preliminary and/or published data that supports feasibility and rationale.

What does the opportunity emphasize about rigor and reproducibility?

A major theme is reproducibility and transparent research practices, especially for preclinical work. Applicants are expected to follow established standards for rigorous study design and reporting to increase the reliability and translational value of results.

Which rigor and reporting principles are specifically referenced?

The announcement points to principles described by Landis et al. (Nature, 2012), highlighting elements such as randomization, blinding, appropriate sample size estimation, and clear data handling procedures.

Are rigor expectations limited only to animal studies?

No. While the standards are often discussed for animal or other preclinical studies, the opportunity notes that the underlying logic applies widely (reducing bias, planning analyses where possible, ensuring adequate statistical power, and documenting methods and outcomes so others can evaluate and reproduce the work).

What additional requirements apply if my project uses animal models?

If animal models are involved, applicants must include an Animal Research Plan (Attachment 8 in the application package) that explains how the study will meet the rigor standards described in the announcement.

Are there specific guidelines encouraged for animal research?

Yes. Applicants are encouraged to use the ARRIVE guidelines (Animal Research Reporting of In Vivo Experiments) when planning and later reporting animal research to ensure essential methodological details are included and to improve interpretability and reproducibility.

Who posted this opportunity and under what program?

This opportunity was posted by the Department of the Army through USAMRAA (U.S. Army Medical Research Acquisition Activity) under the DoD Neurofibromatosis Research Program (NFRP).

What is the Funding Opportunity Number (FON)?

The Funding Opportunity Number is W81XWH-15-NFRP-IIRA.

What funding instrument is used for this opportunity?

The funding instrument is listed as a cooperative agreement and/or grant.

What category does this opportunity fall under?

It is listed under the Science and Technology and other Research and Development category.

What is the CFDA number associated with this opportunity?

The CFDA is 12.420 (Military Medical Research and Development).

How many awards were anticipated, and what was the estimated total funding?

The program anticipated making about 7 awards, with an estimated total funding level of $6,004,000.

Is cost sharing or matching required?

No. The opportunity states that cost sharing or matching is not required.

Who is eligible to apply?

Eligibility is described as unrestricted, meaning it is open to any type of entity, subject to any additional eligibility language contained in the full announcement.

When was this opportunity posted and when did it close?

The opportunity was posted on May 6, 2015. The original and current closing date listed for that cycle was July 27, 2015.

Is this opportunity still active?

No. The opportunity was archived on August 26, 2015.

Who should applicants contact if they have trouble accessing the announcement?

The listed contact for access issues was the CDMRP Help Desk at 301-682-5507.

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