Opportunity Information: Apply for W81XWH 15 PCRP IA
Apply for W81XWH 15 PCRP IA
- 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 Prostate Cancer Impact 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 20, 2015 and posted on May 20, 2015.
- Applicants must submit their applications by Sep 24, 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 $11,200,000.00 to eligible and selected applicants.
- The number of recipients for this funding is limited to 6 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 Prostate Cancer Impact Award (FY15 PCRP Impact Award; Funding Opportunity Number W81XWH-15-PCRP-IA) is a U.S. Army Medical Research Acquisition Activity opportunity under the Congressionally Directed Medical Research Programs (CDMRP) Prostate Cancer Research Program (PCRP). It supports high-impact prostate cancer research projects across the full pipeline, from fundamental laboratory work through translational studies and clinical research, including clinical trials. The central expectation is that the proposed work, if successful, could meaningfully advance the field toward eliminating deaths from prostate cancer and improving quality of life for men affected by the disease. This mechanism has historically been highly selective; since its first offering in FY10, 42 applications were received and 5 were recommended for funding, signaling that applications must be unusually compelling in both significance and potential downstream influence.
The defining feature of this award is "impact." Applicants are expected to make a clear, explicit, and persuasive case that their project addresses an issue of paramount importance in prostate cancer and that the anticipated benefits are substantial rather than incremental. Proposals are strongly encouraged to take on one of the PCRP overarching challenges and must address at least one PCRP focus area. If a project does not align with an overarching challenge, the applicant must justify how it still meets a critical unmet need in prostate cancer research or patient care. Importantly, even when the work is basic science or early-stage, the application must spell out a credible pathway to clinical impact for people who have prostate cancer or are at risk for it. The time horizon can be near-term or long-term, but the program is looking for ideas that could change practice, understanding, or outcomes in a noticeable way, not simply extend existing lines of work.
From a scientific and technical standpoint, the announcement emphasizes study quality and translatability. Applicants are strongly encouraged, where relevant, to build in practices that strengthen reliability and clinical relevance, including authentication of proposed cell lines, strong statistical rigor for preclinical animal experiments, and experiments that directly test clinical relevance or support translation of findings. The program also points applicants toward major shared resources, particularly when human specimens or linked clinical data are important. Two highlighted resources are the PCRP-funded Prostate Cancer Biorepository Network (PCBN) and the North Carolina-Louisiana Prostate Cancer Project (PCaP). The opportunity additionally encourages the use of large patient datasets with long-term health records and biospecimen repositories, especially when paired with modern genomic/proteomic approaches and advanced analytics such as bioinformatics or mathematical modeling.
The scope of eligible research is intentionally broad and multidisciplinary. The PCRP invites applications from investigators spanning basic science, engineering, bioinformatics, population science, translational research, and clinical research. Population science-based approaches are singled out as particularly encouraged, reflecting the program's interest in studies that can explain real-world risk, outcomes, disparities, and intervention impact at scale. Regardless of the domain, applications must include preliminary data demonstrating feasibility, and any unpublished preliminary data must come from the Principal Investigator's laboratory or from a member of the research team, reinforcing that the project is grounded in demonstrated capability rather than purely speculative plans.
A notable requirement of this mechanism is a Data and Research Resource Sharing Plan. The PCRP states an explicit intent that data and research resources created through funded work be shared with the broader research community, including both scientific and consumer advocacy communities, and also with the general public. Applications are therefore expected to outline how unique and/or final datasets will be shared and how any resulting resources (for example, tools, reagents, or other research assets) will be made accessible. This aligns with the program's emphasis on accelerating progress beyond any single lab by enabling reuse, validation, and follow-on discovery.
FY15 also offers a Partnering PI Option designed to support larger, synergistic collaborations with a higher funding level. Under this structure, up to three Principal Investigators may participate: one Initiating PI who leads most of the administrative submission duties and one or two Partnering PIs. The proposal must clearly explain how the combined expertise of the PIs creates synergy that materially increases the likelihood, speed, or magnitude of outcomes compared to separate independent projects. If funded, each PI receives a separate award, which underscores that the collaboration must be genuine, well-integrated, and operationally planned. Multidisciplinary and multi-institutional projects are allowed and encouraged, but they must include explicit interaction plans covering communication, coordination of research progress and results, and data transfer. For multi-institution efforts, an intellectual property plan is required to proactively address potential IP or material ownership issues and to remove institutional barriers that could undermine cooperation.
Administratively, this opportunity is a discretionary award offered as a grant or cooperative agreement in the Science and Technology/Research and Development category, with no cost sharing requirement and eligibility listed as unrestricted (open to any entity type, subject to any additional clarifications in the announcement). For FY15, the estimated total funding is $11.2 million with an expected 6 awards. The opportunity was posted May 20, 2015, and the application closing date was September 24, 2015 (archived October 24, 2015). The CFDA number associated with the program is 12.420 (Military Medical Research and Development). For technical access issues, applicants were directed to the CDMRP Help Desk at 301-682-5507.
DoD Prostate Cancer Impact Award (FY15 PCRP Impact Award) FAQs
What is the FY15 PCRP Impact Award?
The FY15 Prostate Cancer Research Program (PCRP) Impact Award is a U.S. Department of Defense (DoD) funding opportunity administered by the U.S. Army Medical Research Acquisition Activity under the Congressionally Directed Medical Research Programs (CDMRP). It supports high-impact prostate cancer research projects across the full research pipeline, including fundamental laboratory work, translational studies, clinical research, and clinical trials.
What is the Funding Opportunity Number for this grant?
The Funding Opportunity Number is W81XWH-15-PCRP-IA.
What is the central goal or expectation of this award?
The central expectation is "impact." The proposed work, if successful, should meaningfully advance the field toward eliminating deaths from prostate cancer and improving quality of life for men affected by the disease. The program is looking for benefits that are substantial rather than incremental.
How competitive is this award mechanism?
This mechanism has historically been highly selective. Since it was first offered in FY10, 42 applications were received and 5 were recommended for funding, indicating that proposals must be unusually compelling in both significance and potential downstream influence.
What types of research are supported (basic, translational, clinical)?
The scope is intentionally broad. Supported research can range from basic/fundamental laboratory studies through translational research and clinical research, including clinical trials, as long as the work makes a persuasive case for meaningful impact on prostate cancer outcomes or quality of life.
Does basic science qualify, and what is expected for clinical relevance?
Yes. Even for basic science or early-stage work, the application is expected to spell out a credible pathway to clinical impact for people who have prostate cancer or are at risk for it. The pathway can be near-term or long-term, but it must be clear and credible.
What does the program mean by "impact"?
"Impact" means the project addresses an issue of paramount importance in prostate cancer and is likely to produce substantial benefits rather than small extensions of existing work. The program is seeking ideas that could noticeably change practice, understanding, or outcomes.
Do applications need to align with PCRP overarching challenges and focus areas?
Applications are strongly encouraged to take on one of the PCRP overarching challenges and must address at least one PCRP focus area. If a project does not align with an overarching challenge, the applicant must justify how it still meets a critical unmet need in prostate cancer research or patient care.
What scientific practices are encouraged to strengthen study quality and translatability?
Where relevant, the announcement encourages practices that strengthen reliability and clinical relevance, including authentication of proposed cell lines, strong statistical rigor for preclinical animal experiments, and experiments that directly test clinical relevance or support translation of findings.
Are specific shared resources recommended for human specimens or clinical data?
Yes. The opportunity points applicants toward major shared resources, particularly when human specimens or linked clinical data are important. Two highlighted resources are the PCRP-funded Prostate Cancer Biorepository Network (PCBN) and the North Carolina-Louisiana Prostate Cancer Project (PCaP).
Does the opportunity encourage use of large patient datasets and advanced analytics?
Yes. The opportunity encourages the use of large patient datasets with long-term health records and biospecimen repositories, especially when paired with modern genomic/proteomic approaches and advanced analytics such as bioinformatics or mathematical modeling.
Are population science approaches encouraged?
Yes. Population science-based approaches are singled out as particularly encouraged, reflecting interest in studies that can explain real-world risk, outcomes, disparities, and intervention impact at scale.
Is preliminary data required?
Yes. Applications must include preliminary data demonstrating feasibility. Any unpublished preliminary data must come from the Principal Investigator's laboratory or from a member of the research team.
What is the Data and Research Resource Sharing Plan requirement?
A Data and Research Resource Sharing Plan is a notable requirement. The PCRP states an explicit intent that data and research resources created through funded work be shared with the broader research community (including scientific and consumer advocacy communities) and with the general public. Applications are expected to describe how unique and/or final datasets will be shared and how resulting resources (such as tools, reagents, or other research assets) will be made accessible.
What is the Partnering PI Option?
FY15 offers a Partnering PI Option to support larger, synergistic collaborations with a higher funding level. Under this structure, up to three Principal Investigators may participate: one Initiating PI and one or two Partnering PIs.
What is the role of the Initiating PI versus Partnering PIs?
The Initiating PI leads most of the administrative submission duties. Partnering PIs contribute complementary expertise. The proposal must clearly explain how the combined expertise creates synergy that increases the likelihood, speed, or magnitude of outcomes compared to separate independent projects.
How are awards handled if the Partnering PI Option is used?
If funded under the Partnering PI Option, each PI receives a separate award. This underscores the expectation that the collaboration is genuine, well-integrated, and operationally planned.
Are multidisciplinary and multi-institutional projects allowed?
Yes. Multidisciplinary and multi-institutional projects are allowed and encouraged. However, they must include explicit interaction plans covering communication, coordination of research progress and results, and data transfer.
Is an intellectual property (IP) plan required?
For multi-institution efforts, an intellectual property plan is required to proactively address potential IP or material ownership issues and to remove institutional barriers that could undermine cooperation.
What type of award is this (grant or cooperative agreement)?
This opportunity is a discretionary award offered as either a grant or a cooperative agreement in the Science and Technology/Research and Development category.
Is cost sharing required?
No. The opportunity states there is no cost sharing requirement.
Who is eligible to apply?
Eligibility is listed as unrestricted (open to any entity type), subject to any additional clarifications in the announcement.
What is the estimated total funding and expected number of awards for FY15?
The estimated total funding for FY15 is $11.2 million, with an expected 6 awards.
When was this opportunity posted and when did it close?
The opportunity was posted on May 20, 2015. The application closing date was September 24, 2015, and it was archived on October 24, 2015.
What is the CFDA number associated with this program?
The CFDA number is 12.420 (Military Medical Research and Development).
Who should applicants contact for technical access issues?
For technical access issues, applicants were directed to the CDMRP Help Desk at 301-682-5507.
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