Opportunity Information: Apply for W81XWH 15 PRARP MRFA

  • 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 FY15 Peer Reviewed Alzheimer s Military Risk Factors 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 Jul 20, 2015 and posted on Jul 20, 2015.
  • Applicants must submit their applications by Nov 25, 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 $5,000,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 1 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 PRARP MRFA

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Opportunity Summary:

The DoD FY15 Peer Reviewed Alzheimer s Research Program (PRARP) Military Risk Factors Research Award (MRFA) is a funding opportunity from the Department of the Army (USAMRAA) designed to support high impact, systematic, population based research on how traumatic brain injury (TBI) may be linked to the later development of Alzheimer s disease (AD). The central goal is to generate evidence that clarifies whether, how, and in whom TBI contributes to progression toward AD, with results intended to benefit not only military Service members and Veterans, but also the broader civilian community. Projects are expected to go beyond general associations and clearly lay out how the research team will characterize the relationship between a history of TBI and subsequent AD outcomes, including careful description of cognitive and behavioral symptoms that translate into real world functional impairment in the study population.

A key expectation of this award is that applicants already have expedited access to a well defined, already identified cohort, and that they can provide data showing how that cohort will be used to test the proposed hypothesis or hypotheses. In other words, this mechanism is not meant for teams that are still trying to locate participants or build a cohort from scratch; the application must convincingly demonstrate that the cohort exists, is accessible quickly, and is appropriate for the planned analyses. While preliminary data is not strictly required, it is encouraged, and the program emphasizes that supporting data should strongly align with and substantiate the proposed research direction.

The MRFA encourages comprehensive study designs that use multiple, complementary measurement approaches to capture neurological change and clinical progression. Competitive applications are expected to think in an integrated way about assessment, for example combining neuropsychological testing with imaging approaches, genomics, and cerebrospinal fluid biomarkers, rather than relying on a single data stream. The program also explicitly encourages the formation of interdisciplinary teams or consortia, reflecting the idea that understanding TBI to AD trajectories often requires expertise spanning neurology, neuropsychology, epidemiology, imaging science, molecular biology, bioinformatics, and related fields.

In terms of the scientific problems the DoD is trying to push forward, applications must address one or more overarching challenges identified for FY15. These include the limited availability of research resources specifically suited to examining TBI and later AD in military and Veteran populations, the shortage of strong clinical or epidemiological studies focused on this interrelationship, and the need for diagnostic technologies, tests, or devices that can detect or track progression toward AD following TBI. Applicants are also encouraged to align with at least one of the listed FY15 focus areas, although work outside these areas can still be considered if the applicant makes a strong case for why it is relevant and necessary. The named focus areas include genomics, proteomics, and bioinformatics strategies to characterize neurological changes tied to TBI and subsequent AD; research into Tau pathology mechanisms that may connect TBI to AD; studies of non neuronal cells such as astrocytes and their roles in AD type neurodegeneration following TBI; and the development or application of anatomic or molecular imaging methods to capture TBI related changes and later AD associated progression.

The opportunity is open broadly with unrestricted eligibility in terms of entity type, but it sets clear expectations for leadership and expertise. The Principal Investigator must be at or above the Assistant Professor level (or equivalent), and while investigators may come from any discipline, the application must demonstrate that the study team has credible experience across both TBI and AD research. The funding instrument type listed includes cooperative agreement and grant, and the activity category is research and development (science and technology). The total estimated funding amount is $5,000,000 with an expectation of a single award, and there is no cost sharing or matching requirement.

One major boundary is that pharmacologic interventions are specifically discouraged under this program announcement. That includes clinical or basic research that requires investigational drugs or even FDA approved medicines as part of the proposed work. In practice, this steers applicants toward observational, epidemiological, biomarker, imaging, and mechanistic or diagnostic tool development studies rather than drug based trials.

Administrative details from the announcement include the funding opportunity number W81XWH 15 PRARP MRFA, CFDA 12.420 (Military Medical Research and Development), a posted and created date of July 20, 2015, and an original/current closing date of November 25, 2015 (archived December 25, 2015). For help accessing the full announcement, the listed contact is the CDMRP Help Desk (301 682 5507, help@eBRAP.org).

Frequently Asked Questions (FAQs)

What is the DoD FY15 PRARP Military Risk Factors Research Award (MRFA)?

The Military Risk Factors Research Award (MRFA) is a funding opportunity under the DoD FY15 Peer Reviewed Alzheimer's Research Program (PRARP), managed by the U.S. Army Medical Research Acquisition Activity (USAMRAA). It supports high-impact, systematic, population-based research focused on how traumatic brain injury (TBI) may be linked to later development of Alzheimer's disease (AD).

What is the main goal of this award?

The central goal is to generate evidence that clarifies whether, how, and in whom TBI contributes to progression toward Alzheimer's disease. The intent is that findings benefit military Service members and Veterans, and also translate to the broader civilian community.

What kind of research approach is expected?

Projects are expected to go beyond showing general associations between TBI and AD. Applications should clearly explain how the team will characterize the relationship between a history of TBI and later AD outcomes, including careful description of cognitive and behavioral symptoms that translate into real-world functional impairment in the study population.

Does the program require applicants to already have a study cohort?

Yes. A key expectation is expedited access to a well-defined, already identified cohort. This mechanism is not intended for teams that still need to locate participants or build a cohort from scratch. The application must convincingly demonstrate that the cohort exists, can be accessed quickly, and is appropriate for the proposed analyses.

Is preliminary data required?

Preliminary data is not strictly required, but it is encouraged. Supporting data should strongly align with and substantiate the proposed research direction, especially in showing how the existing cohort will be used to test the proposed hypothesis or hypotheses.

What kinds of measurements or data sources are encouraged in study design?

The MRFA encourages comprehensive, integrated study designs that use multiple complementary measurement approaches to capture neurological change and clinical progression. Competitive applications are expected to integrate assessments such as neuropsychological testing, imaging approaches, genomics, and cerebrospinal fluid biomarkers rather than relying on a single data stream.

Are interdisciplinary teams or consortia encouraged?

Yes. The program explicitly encourages interdisciplinary teams or consortia, reflecting that understanding TBI-to-AD trajectories often requires expertise across areas such as neurology, neuropsychology, epidemiology, imaging science, molecular biology, and bioinformatics.

What overarching scientific challenges must an application address?

Applications must address one or more FY15 overarching challenges, which include: (1) limited availability of research resources suited to examining TBI and later AD in military and Veteran populations, (2) a shortage of strong clinical or epidemiological studies focused on the TBI-AD interrelationship, and/or (3) the need for diagnostic technologies, tests, or devices that can detect or track progression toward AD following TBI.

Are there specific FY15 focus areas applicants are encouraged to align with?

Yes. Applicants are encouraged to align with at least one FY15 focus area, although work outside these areas may still be considered if the applicant makes a strong relevance case. The named focus areas include genomics/proteomics/bioinformatics approaches, Tau pathology mechanisms linking TBI to AD, roles of non-neuronal cells (such as astrocytes) in AD-type neurodegeneration following TBI, and anatomic or molecular imaging methods to capture TBI-related changes and later AD-associated progression.

Is eligibility restricted by organization type?

No. Eligibility is described as unrestricted in terms of entity type (open broadly). However, the program sets expectations for leadership, qualifications, and team expertise.

What are the Principal Investigator (PI) requirements?

The Principal Investigator must be at or above the Assistant Professor level (or equivalent). The application should also demonstrate that the study team has credible experience across both TBI and Alzheimer's disease research.

What funding instrument types are associated with this opportunity?

The listed funding instrument types include a cooperative agreement and a grant, under the research and development (science and technology) activity category.

How much funding is available and how many awards are expected?

The total estimated funding amount is $5,000,000, with an expectation of a single award.

Is cost sharing or matching required?

No. There is no cost sharing or matching requirement stated for this opportunity.

Are drug or pharmacologic intervention studies allowed?

Pharmacologic interventions are specifically discouraged. This includes clinical or basic research that requires investigational drugs or even FDA-approved medicines as part of the proposed work. The announcement therefore steers applicants toward observational, epidemiological, biomarker, imaging, mechanistic, and diagnostic tool development studies rather than drug-based trials.

Who is the sponsoring/issuing agency?

The opportunity is from the Department of the Army (USAMRAA) under the DoD PRARP framework.

What is the funding opportunity number and CFDA number?

The funding opportunity number is W81XWH-15-PRARP-MRFA. The CFDA number is 12.420 (Military Medical Research and Development).

When was this opportunity posted and when did it close?

The posted/created date is July 20, 2015. The original/current closing date is November 25, 2015, and it is noted as archived on December 25, 2015.

Who should applicants contact for help accessing the full announcement?

The listed contact is the CDMRP Help Desk at 301-682-5507 or help@eBRAP.org.

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