Opportunity Information: Apply for W81XWH 12 PCRP TIA

  • 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 Transformative 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 Mar 20, 2012 and posted on Mar 20, 2012.
  • Applicants must submit their applications by Aug 23, 2012. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $19,200,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 2 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 12 PCRP TIA

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Opportunity Summary:

The DoD Prostate Cancer Transformative Impact Award (Funding Opportunity Number W81XWH-12-PCRP-TIA) is a U.S. Army Medical Research Acquisition Activity (USAMRAA) funding opportunity under the Congressionally Directed Medical Research Programs (CDMRP) that is designed to accelerate prostate cancer research with a clear, near-term and transformative benefit for patients. The program emphasizes work that can meaningfully change patient outcomes in the foreseeable future, rather than early-stage discovery projects that may take many years to reach clinical use. It is positioned within the Military Medical Research and Development CFDA listing (12.420) and falls under the broader category of science, technology, and research and development.

A key feature of this award is that it uses a two-step, invitation-only application process. Applicants must first submit a preproposal, and only those selected will be invited to submit a full application. This structure signals that the sponsor intends to be selective early, focusing full proposal review resources on the most promising, high-impact concepts. The funding instrument is listed as a cooperative agreement and/or grant, which typically indicates the government may have a more active partnership role than in a standard grant (for example, through substantial programmatic involvement, milestones, or coordination expectations), though the exact degree of involvement would be spelled out in the full announcement.

The award is built around a team-science approach. Competitive submissions are expected to be driven by a coordinated research team rather than a single-investigator effort, and the Principal Investigator is expected to have a demonstrated track record of successfully leading large, focused projects. In practice, this usually means the PI should be able to show prior experience managing complex, multidisciplinary programs with clear deliverables, such as multi-site clinical studies, translational pipelines, large consortia, or integrated research programs that move from mechanistic work into patient-facing evaluation. The emphasis is not just on assembling a group of collaborators, but on presenting an integrated plan where each component is aligned to an overarching clinical goal and the team structure supports fast execution.

Because the intent is near-term patient benefit, the required scope must include translational studies, clinical research, and/or clinical trials. This requirement draws a firm line around the kind of work the sponsor wants to fund: research that is already close enough to the clinic to be translated, tested in people, or otherwise directly inform clinical decision-making. Translational studies might include biomarker validation, development of clinically deployable diagnostics, preclinical packages that directly support human testing, or bridging work that moves a therapy or intervention toward clinical readiness. Clinical research could include prospective studies, observational cohorts with actionable endpoints, or comparative effectiveness components, while clinical trials indicate readiness to evaluate an intervention in patients under a formal protocol. The underlying expectation is that the work will not stop at generating scientific insight, but will produce outcomes that can influence patient care, clinical practice, or the therapeutic development pathway on a short timeline.

Another defining requirement is operational readiness: applicants must show they are prepared to initiate the study immediately upon receiving the award, meaning as of the award date. This is a strong signal that the sponsor is looking for projects with critical dependencies already in place, such as established collaborations, clinical and laboratory infrastructure, access to patient populations, trial-ready protocols, preliminary regulatory and ethics planning, and an execution plan that does not rely on long start-up periods. For clinical studies, this may imply that sites and investigators are identified, recruitment pathways are established, and major feasibility risks are already addressed. For translational programs, it suggests that key assays, models, manufacturing plans, or data systems are ready to run without extensive build-out after funding.

From a funding and administrative standpoint, the opportunity was posted March 20, 2012, with an original and current closing date of August 23, 2012, and an archive date of September 22, 2012. The estimated total funding was $19.2 million, with an expected two awards, implying a large, high-investment structure aimed at supporting a small number of ambitious programs. No cost sharing or matching was required. Eligibility is listed as unrestricted, meaning it is broadly open to different types of entities (such as universities, nonprofits, companies, and other organizations), subject to any additional eligibility clarifications that may appear in the full text of the announcement.

For support accessing the full announcement, the listed contact is the CDMRP Help Desk at 301-682-5507.

Frequently Asked Questions (FAQs)

What is the DoD Prostate Cancer Transformative Impact Award?

The DoD Prostate Cancer Transformative Impact Award is a funding opportunity administered by the U.S. Army Medical Research Acquisition Activity (USAMRAA) under the Congressionally Directed Medical Research Programs (CDMRP). It is intended to accelerate prostate cancer research that offers a clear, near-term, and transformative benefit for patients.

What is the funding opportunity number for this award?

The Funding Opportunity Number is W81XWH-12-PCRP-TIA.

What is the main goal of this award program?

The main goal is to support prostate cancer research that can meaningfully change patient outcomes in the foreseeable future. The emphasis is on projects that are close enough to clinical impact to benefit patients on a near-term timeline, rather than early-stage discovery efforts that may take many years to reach clinical use.

What types of research are expected to be included in the scope?

The required scope must include translational studies, clinical research, and/or clinical trials. The opportunity is oriented toward work that is already positioned to be translated to the clinic, evaluated in patient populations, or used to directly inform clinical decision-making.

Are early-stage discovery projects a fit for this opportunity?

Based on the program emphasis, this award is positioned away from early-stage discovery projects that may take many years to reach clinical use. The focus is on near-term, patient-relevant outcomes and transformative impact in the foreseeable future.

What does "transformative impact" mean in the context of this award?

In this context, transformative impact refers to work that can lead to meaningful changes in patient outcomes on a near-term timeline. The expectation is that the project will produce results that can influence patient care, clinical practice, or the therapeutic development pathway relatively quickly.

Does the program require a team-based approach?

Yes. The award is built around a team-science approach. Competitive submissions are expected to be driven by a coordinated research team rather than a single-investigator effort, with an integrated plan aligned to an overarching clinical goal.

What kind of experience is expected of the Principal Investigator (PI)?

The PI is expected to have a demonstrated track record of successfully leading large, focused projects. This generally implies experience managing complex, multidisciplinary programs with clear deliverables, such as multi-site clinical studies, translational pipelines, large consortia, or integrated programs that move toward patient-facing evaluation.

How does the application process work?

The award uses a two-step, invitation-only application process. Applicants must first submit a preproposal, and only applicants selected from the preproposal stage will be invited to submit a full application.

What does "invitation-only" mean for the full application?

It means you cannot submit a full application unless you are invited to do so after submitting a preproposal and being selected to move forward. The structure indicates the sponsor intends to be selective early and focus full proposal review on the most promising, high-impact concepts.

What is the funding instrument for this opportunity?

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

What does it imply if an award is a cooperative agreement and/or grant?

This typically suggests that the government may have a more active partnership role than with a standard grant, potentially involving substantial programmatic involvement, milestones, or coordination expectations. The exact degree of involvement would be specified in the full announcement.

What is meant by "operational readiness" for this award?

Operational readiness means applicants must show they are prepared to initiate the study immediately upon receiving the award (as of the award date). This indicates an expectation that key dependencies are already in place and the project does not rely on long start-up periods after funding.

What kinds of readiness elements are implied for clinical studies?

For clinical studies, readiness may include having sites and investigators identified, recruitment pathways established, and major feasibility risks addressed. It also implies preliminary regulatory and ethics planning and a trial-ready approach that can start immediately upon award.

What kinds of readiness elements are implied for translational programs?

For translational programs, readiness suggests that key assays, models, manufacturing plans, or data systems are already prepared to run without extensive build-out after funding.

How much total funding was estimated for this opportunity?

The estimated total funding was $19.2 million.

How many awards were expected to be made?

The opportunity anticipated approximately two awards.

Does this opportunity require cost sharing or matching funds?

No. No cost sharing or matching was required.

Who is eligible to apply?

Eligibility is listed as unrestricted, meaning it is broadly open to different types of entities (such as universities, nonprofits, companies, and other organizations), subject to any additional eligibility clarifications that may appear in the full announcement.

Which federal listing or program category is associated with this award?

The opportunity is positioned within the Military Medical Research and Development CFDA listing (12.420) and falls under the broader category of science, technology, and research and development.

When was this funding opportunity posted and when did it close?

The opportunity was posted on March 20, 2012. The original and current closing date was August 23, 2012.

When was the opportunity archived?

The archive date was September 22, 2012.

Who can be contacted for help accessing the full announcement?

For support accessing the full announcement, the listed contact is the CDMRP Help Desk at 301-682-5507.

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