Opportunity Information: Apply for W81XWH 09 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 Jan 20, 2009 and posted on Jan 20, 2009.
  • Applicants must submit their applications by Apr 14, 2009. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $4,600,000.00 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.
Apply for W81XWH 09 NFRP IIRA

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Opportunity Summary:

The DOD Neurofibromatosis Investigator Initiated Research Award (IIRA) is a funding opportunity under the Department of Defense Neurofibromatosis Research Program (NFRP) that supports investigator-driven projects focused on neurofibromatosis (NF) and related conditions, including schwannomatosis. This award mechanism has been in place since FY96 and, as of the FY09 cycle described here, it has attracted substantial interest (293 applications received historically, with 86 recommended for funding). The program is geared toward both basic science and clinically oriented research, but with a clear emphasis on work that can meaningfully shift the field forward by improving understanding of disease development, advancing diagnosis and treatment approaches, and ultimately improving quality of life for people living with NF and schwannomatosis.

For FY09, the announcement highlights specific “areas of encouragement” that reflect major unmet needs in the NF community. One major priority is research on high-mortality complications, particularly tumors (neoplasms) and cerebrovascular abnormalities. A second priority is high-morbidity complications that can severely affect daily functioning and long-term outcomes, including skeletal problems, learning and cognitive deficits, hormone-related effects, and pain. A third priority focuses on the tools needed to run better studies and future trials, encouraging refinement and standardization of imaging methods, molecular and cellular markers, and quality-of-life metrics so that results can be compared across sites and used reliably in later-stage clinical research. A fourth priority is translational research, especially the development or preclinical testing of therapeutic agents intended to treat NF, which signals the program’s interest in bridging laboratory discoveries toward interventions that could eventually reach patients.

A key boundary of the IIRA mechanism is that clinical trials are not permitted. Investigators who want to run an actual clinical trial are directed to apply through a separate Clinical Trial Award mechanism instead. Even though clinical trials are excluded, the program still expects applications to be grounded in evidence: proposals must include preliminary data that is relevant to NF and to the proposed project, and that data must originate from the principal investigator, the research team, or a collaborator. This requirement signals that the program is looking for projects that are ready to move beyond purely speculative ideas and have a credible foundation suggesting feasibility and relevance.

Collaboration is strongly encouraged and is treated as a programmatic strength rather than an optional add-on. The announcement specifically supports partnerships between basic scientists and clinical researchers, and also collaborations spanning academia and biotechnology or pharmaceutical industry. The intent is to bring together complementary expertise, speed up translation, and introduce new perspectives or disciplines into NF research. The notice also states that certain collaborations that meet defined criteria can qualify for a higher level of funding, with details referenced in the full program announcement, indicating that the funder is willing to invest more when the team structure is likely to amplify impact.

Administratively, this opportunity was issued by the Department of the Army through USAMRAA under CFDA 12.420 (Military Medical Research and Development). The funding instrument type is listed as grant/cooperative agreement, with no cost sharing or matching requirement. For the FY09 cycle captured in the listing, the program anticipated about 5 awards from an estimated total funding pool of $4.6 million. Eligibility is described as unrestricted (open to any type of entity), subject to any additional eligibility clarifications in the full text. Key dates for that cycle include a posted date of January 20, 2009 and an application closing date of April 14, 2009 (archived May 14, 2009). Contact and help resources are provided through the CDMRP/USAMRAA support channels for assistance accessing the announcement and for electronic submission troubleshooting.

Frequently Asked Questions (FAQs)

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

The Investigator Initiated Research Award (IIRA) is a funding opportunity under the Department of Defense (DOD) Neurofibromatosis Research Program (NFRP) that supports investigator-driven research projects focused on neurofibromatosis (NF) and related conditions, including schwannomatosis.

Which program sponsors and issues this award?

This opportunity is part of the DOD Neurofibromatosis Research Program (NFRP) and was issued by the Department of the Army through USAMRAA.

What is the CFDA number for this grant program?

The listing identifies CFDA 12.420 (Military Medical Research and Development).

What types of research does the IIRA support?

The IIRA supports both basic science and clinically oriented research, with an emphasis on projects that can meaningfully advance the field by improving understanding of disease development, advancing diagnostic and treatment approaches, and improving quality of life for people living with NF and schwannomatosis.

What diseases and conditions are in scope for this funding opportunity?

The opportunity is focused on neurofibromatosis (NF) and related conditions, including schwannomatosis.

What are the FY09 "areas of encouragement" highlighted in the announcement?

For FY09, the announcement highlights four encouraged areas: (1) high-mortality complications such as tumors (neoplasms) and cerebrovascular abnormalities; (2) high-morbidity complications including skeletal problems, learning and cognitive deficits, hormone-related effects, and pain; (3) refinement and standardization of tools such as imaging methods, molecular and cellular markers, and quality-of-life metrics; and (4) translational research, including development or preclinical testing of therapeutic agents intended to treat NF.

Does the IIRA allow clinical trials?

No. Clinical trials are not permitted under the IIRA mechanism. Investigators who want to conduct a clinical trial are directed to apply through a separate Clinical Trial Award mechanism.

Are preliminary data required?

Yes. Proposals must include preliminary data relevant to NF and to the proposed project.

Where must the preliminary data come from?

The preliminary data must originate from the principal investigator, the research team, or a collaborator.

Is the program looking for speculative ideas or more established concepts?

Based on the stated requirement for relevant preliminary data, the program is looking for projects with a credible foundation demonstrating feasibility and relevance, rather than purely speculative concepts.

Is collaboration required or just encouraged?

Collaboration is strongly encouraged and is described as a programmatic strength. The announcement specifically supports partnerships between basic scientists and clinical researchers, as well as collaborations spanning academia and biotechnology or pharmaceutical industry.

What kinds of collaborations are specifically encouraged?

The opportunity encourages collaborations between basic and clinical researchers, and collaborations between academia and biotechnology or pharmaceutical industry partners, to combine complementary expertise and accelerate translation.

Can collaboration affect the funding level?

Yes. The announcement indicates that certain collaborations meeting defined criteria can qualify for a higher level of funding, with details referenced in the full program announcement.

What is the funding instrument type?

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

Is cost sharing or matching required?

No. The listing states there is no cost sharing or matching requirement.

Who is eligible to apply?

Eligibility is described as unrestricted (open to any type of entity), subject to any additional eligibility clarifications in the full announcement text.

How many awards were anticipated for the FY09 cycle?

For the FY09 cycle captured in the listing, the program anticipated approximately 5 awards.

What was the estimated total funding available for the FY09 cycle?

The estimated total funding pool for the FY09 cycle was $4.6 million.

When was the FY09 opportunity posted and when did it close?

The posted date was January 20, 2009 and the application closing date was April 14, 2009. The listing notes the opportunity was archived on May 14, 2009.

Where can applicants get help accessing the announcement or troubleshooting electronic submission?

Contact and help resources are provided through the CDMRP/USAMRAA support channels for assistance accessing the announcement and for electronic submission troubleshooting.

What is the program's overall goal for the research it funds?

The program emphasizes work that can shift the field forward by improving understanding of NF disease development, advancing diagnosis and treatment approaches, and ultimately improving quality of life for individuals living with NF and schwannomatosis.

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