Opportunity Information: Apply for W81XWH 10 NFRP NIA

  • 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 New Investigator 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 $1,800,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 3 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 10 NFRP NIA

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Opportunity Summary:

The DoD Neurofibromatosis New Investigator Award (NIA) is a funding opportunity under the Department of Defense Neurofibromatosis Research Program (NFRP) designed to help promising early-stage, independent researchers build or strengthen their careers in neurofibromatosis (NF) research. First introduced in FY1999, the program has a track record that shows it is competitive but established: 179 applications had been received over time, with 38 recommended for funding. The central goal is career transition and continued development, meaning it is aimed at investigators who are ready to lead their own NF-focused projects and establish themselves as independent contributors to the field.

A key feature of this award is that prior NF experience is allowed but not required. That makes it accessible to strong investigators coming from related disciplines who want to pivot into NF research. At the same time, the program signals that applicants without deep NF background should partner with a collaborator who has demonstrated NF expertise, which helps ensure the project is grounded in the realities of NF biology, clinical care, and the needs of the patient community. Another non-negotiable requirement is that applications must include preliminary data that relate to NF and to the proposed work. That preliminary evidence can come from the principal investigator, the research team, or a collaborator, but it needs to show that the approach is feasible and connected to NF in a concrete way.

For FY2010, the opportunity specifically encourages proposals that target urgent and practical needs in the NF community. One priority area is complications associated with high mortality, including cancers or tumor-related disease (neoplasms) and cerebrovascular abnormalities. A second priority area focuses on complications that may not be as immediately life-threatening but cause major long-term disability or reduced functioning (high morbidity). Examples listed include skeletal problems, learning deficits, hormone-associated effects, and pain, all of which can significantly impact daily life and long-term outcomes for people living with NF. A third encouraged area is the refinement and standardization of tools needed to make future clinical trials stronger and more comparable across sites, such as imaging techniques, molecular and cellular markers, and quality-of-life metrics. A fourth area emphasizes translational research, particularly the development of therapeutic candidates or preclinical testing of potential treatments, reflecting an interest in moving discoveries toward real-world interventions even if the work is not yet at the stage of testing in patients.

Human subjects research is permitted under this mechanism, but clinical trials are explicitly not allowed. The announcement uses a standard definition of a clinical trial as a prospective study in which an intervention (such as a drug, device, behavioral program, surgery, or similar) is tested in human subjects to measure an outcome. Applicants who want to run a clinical trial are directed instead to the FY2010 NFRP Clinical Trial Award mechanism. The notice also points applicants to the program’s general application instructions for rules and expectations related to human subjects, human data, or human anatomical substances, which suggests that compliance, ethical review, and proper handling of human-derived materials are taken seriously even when a project stops short of an interventional trial.

Administratively, this opportunity was posted March 2, 2010, with a closing date of May 20, 2010, and it was run by the Department of the Army through USAMRAA. The funding instrument types listed include cooperative agreement and grant, and the activity category is science and technology and other research and development. The program anticipated making about three awards, with an estimated total funding pool of $1.8 million, and it did not require cost sharing or matching funds. Eligibility was described as unrestricted, meaning a wide range of applicant organizations could apply, subject to any additional clarifications in the full announcement. The opportunity is associated with CFDA 12.420 (Military Medical Research and Development) and carried the funding opportunity number W81XWH-10-NFRP-NIA. Contact resources were provided through CDMRP support channels for technical issues accessing the announcement or using the electronic submission systems.

DoD Neurofibromatosis New Investigator Award (NIA) FAQ

What is the DoD Neurofibromatosis New Investigator Award (NIA)?

The Neurofibromatosis New Investigator Award (NIA) is a funding opportunity under the Department of Defense Neurofibromatosis Research Program (NFRP). It is designed to help promising early-stage, independent researchers build or strengthen their careers in neurofibromatosis (NF) research by leading NF-focused projects as independent contributors.

What is the main purpose of this award?

The central goal is career transition and continued development. The award targets investigators who are ready to lead their own NF-focused research and establish themselves as independent researchers in the field.

When was the NIA first introduced?

The NIA mechanism was first introduced in FY1999.

How competitive is this opportunity based on the program track record described?

The program is described as competitive but established. Over time, 179 applications were received, and 38 were recommended for funding.

Is prior neurofibromatosis (NF) research experience required to apply?

No. Prior NF experience is allowed but not required, which makes the award accessible to strong investigators from related disciplines who want to pivot into NF research.

If an applicant does not have deep NF experience, is collaboration expected?

Yes. The program indicates that applicants without a deep NF background should partner with a collaborator who has demonstrated NF expertise. This is intended to ensure the project is grounded in NF biology, clinical care, and patient community needs.

Is preliminary data required for an application?

Yes. Applications must include preliminary data related to NF and to the proposed work. This is described as a non-negotiable requirement.

Whose preliminary data can be used to meet the requirement?

The preliminary evidence can come from the principal investigator, the research team, or a collaborator, as long as it relates to NF and supports the feasibility and NF relevance of the proposed approach.

What research areas were specifically encouraged for FY2010?

For FY2010, proposals were encouraged to address urgent and practical needs in the NF community, including: (1) high-mortality complications such as cancers or tumor-related disease (neoplasms) and cerebrovascular abnormalities; (2) high-morbidity complications that drive long-term disability or reduced functioning, including skeletal problems, learning deficits, hormone-associated effects, and pain; (3) refinement and standardization of tools that strengthen future clinical trials (for example, imaging techniques, molecular and cellular markers, and quality-of-life metrics); and (4) translational research, including development of therapeutic candidates or preclinical testing of potential treatments.

Does the opportunity allow research involving human subjects?

Yes. Human subjects research is permitted under this mechanism.

Are clinical trials allowed under the NIA mechanism?

No. Clinical trials are explicitly not allowed under this award mechanism.

How does the announcement define a clinical trial in this context?

A clinical trial is described as a prospective study in which an intervention (such as a drug, device, behavioral program, surgery, or similar) is tested in human subjects to measure an outcome.

If an applicant wants to run a clinical trial, where should they apply instead?

Applicants who want to run a clinical trial are directed to the FY2010 NFRP Clinical Trial Award mechanism rather than the NIA.

Are there additional rules for projects involving human data or human anatomical substances?

Yes. The notice points applicants to the program's general application instructions for rules and expectations related to human subjects, human data, or human anatomical substances, indicating compliance and proper handling requirements apply even when the work is not a clinical trial.

Who administered this opportunity?

The opportunity was run by the Department of the Army through USAMRAA.

What were the posting and closing dates for the FY2010 opportunity?

The opportunity was posted on March 2, 2010, and the closing date was May 20, 2010.

What types of funding instruments were listed?

The listed funding instrument types included a cooperative agreement and a grant.

What was the activity category for this opportunity?

The activity category was listed as science and technology and other research and development.

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

The program anticipated making about three awards, with an estimated total funding pool of $1.8 million.

Was cost sharing or matching funds required?

No. The opportunity did not require cost sharing or matching funds.

Who was eligible to apply?

Eligibility was described as unrestricted, meaning a wide range of applicant organizations could apply, subject to any additional clarifications in the full announcement.

What is the CFDA number associated with this opportunity?

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

What is the funding opportunity number for the FY2010 NIA?

The funding opportunity number is W81XWH-10-NFRP-NIA.

Where could applicants get help with technical issues related to the announcement or electronic submission?

Contact resources were provided through CDMRP support channels for technical issues accessing the announcement or using the electronic submission systems.

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