Opportunity Information: Apply for W81XWH 12 PCRP CEA

  • 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 Clinical Exploration 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 $2,200,000.00 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.
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Opportunity Summary:

The DoD Prostate Cancer Clinical Exploration Award (Funding Opportunity Number W81XWH-12-PCRP-CEA) is a Department of Defense funding opportunity administered through the U.S. Army Medical Research Acquisition Activity (USAMRAA) under CFDA 12.420 (Military Medical Research and Development). It is designed to move quickly on promising, hypothesis-driven ideas by supporting early phase clinical trials and clinical studies that are directly tied to patient care, including correlative studies connected to ongoing or existing clinical trials. The central aim is to test innovative and largely unproven concepts that could meaningfully change how prostate cancer is managed in the clinic, generating the scientific rationale and early proof-of-principle data needed to justify larger, definitive trials.

The program emphasizes speed and practical clinical relevance. Projects are expected to be ready to launch soon after award, with clinical trials anticipated to begin within 12 months of the award date. In keeping with that fast-start expectation, any required regulatory clearances must already be secured prior to submitting an application. Specifically, if the proposed intervention requires an Investigational New Drug (IND) application or an Investigational Device Exemption (IDE), those approvals must be in place before the proposal is submitted, not after selection. This requirement signals that the award is meant for teams that have already completed key preparatory work and are positioned to execute without long regulatory delays.

A wide range of intervention types is considered responsive, reflecting an interest in both medical and non-medical approaches that could improve outcomes for patients with prostate cancer. Interventions may include pharmaceuticals, devices, biologics, surgical techniques or procedures, and behavior modification strategies, as well as other clinically relevant approaches. In addition to trials that directly test an intervention, the opportunity also supports studies that are correlative to existing trials, such as research that leverages patient samples, biomarkers, imaging, or other clinical data streams to clarify mechanisms, identify predictors of response, or refine patient selection strategies. The common thread across these options is an expectation that the work will provide actionable clinical insight and a credible early signal of benefit or feasibility that can guide next-stage development.

In terms of award mechanics, the opportunity uses grant and cooperative agreement funding instruments and falls under the broad category of science, technology, and other research and development. The total estimated funding for this cycle is $2.2 million, with an expected three awards. There is no cost sharing or matching requirement, which reduces the need for applicants to bring non-federal funds to the table. Eligibility is listed as unrestricted, meaning it is broadly open to organizations and entity types, subject to any additional eligibility details that may have been provided in the full announcement.

Key dates for this archived 2012 competition include a posted date of March 20, 2012, and an application deadline of August 23, 2012, with the archive date listed as September 22, 2012. For assistance accessing the full announcement (as referenced in the original posting), the contact listed is the CDMRP Help Desk at 301-682-5507. Overall, this award is geared toward teams ready to rapidly execute a well-justified, early clinical test of a novel prostate cancer intervention or a tightly linked correlative clinical study, with the explicit goal of producing the kind of early clinical evidence that can propel larger trials and, ultimately, influence patient management.

FAQs: DoD Prostate Cancer Clinical Exploration Award (W81XWH-12-PCRP-CEA)

What is the DoD Prostate Cancer Clinical Exploration Award?

The DoD Prostate Cancer Clinical Exploration Award (Funding Opportunity Number W81XWH-12-PCRP-CEA) is a Department of Defense funding opportunity intended to rapidly test promising, hypothesis-driven clinical ideas in prostate cancer. It supports early phase clinical trials and other clinical studies that are directly tied to patient care, with the goal of generating early proof-of-principle evidence that can justify larger, definitive trials.

Which agency administers this funding opportunity?

The opportunity is administered through the U.S. Army Medical Research Acquisition Activity (USAMRAA) under the Department of Defense.

What is the CFDA number associated with this opportunity?

The CFDA listing provided is 12.420, titled Military Medical Research and Development.

What is the main purpose of this award?

The central aim is to move quickly on innovative and largely unproven concepts by funding early clinical testing that could meaningfully change how prostate cancer is managed in the clinic. The expected outcome is a strong scientific rationale and early clinical evidence to support next-stage (larger) trials.

What types of projects does the award support?

The award supports early phase clinical trials and clinical studies directly tied to patient care. It also supports correlative studies that connect to ongoing or existing clinical trials, including work using patient samples, biomarkers, imaging, or other clinical data to clarify mechanisms, identify predictors of response, or refine patient selection.

Does this opportunity support studies tied to existing clinical trials?

Yes. Correlative studies connected to ongoing or existing clinical trials are specifically described as responsive, as long as they are clinically relevant and designed to produce actionable insight.

What kinds of interventions are considered responsive?

A wide range of intervention types may be considered, including pharmaceuticals, devices, biologics, surgical techniques or procedures, and behavior modification strategies, as well as other clinically relevant approaches.

Is the program focused on speed?

Yes. The program emphasizes rapid execution and practical clinical relevance, with an expectation that funded projects are ready to launch soon after award.

How soon are clinical trials expected to begin after an award is made?

Clinical trials are anticipated to begin within 12 months of the award date.

Are regulatory clearances required before applying?

Yes. Any required regulatory clearances must already be secured prior to submitting an application.

If an IND or IDE is needed, can it be obtained after submitting the application?

No. If the proposed intervention requires an Investigational New Drug (IND) application or an Investigational Device Exemption (IDE), those approvals must be in place before the proposal is submitted.

What funding instruments are used for this opportunity?

The opportunity uses grant and cooperative agreement funding instruments.

What is the broad funding category for this opportunity?

It falls under the broad category of science, technology, and other research and development.

How much total funding was estimated for this cycle?

The total estimated funding for this cycle is $2.2 million.

How many awards were expected?

The opportunity anticipated making approximately three awards.

Is cost sharing or matching required?

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

Who is eligible to apply?

Eligibility is listed as unrestricted, meaning it is broadly open to organizations and entity types, subject to any additional eligibility details that may have been provided in the full announcement.

When was this opportunity posted and when was the application deadline?

The posted date is March 20, 2012, and the application deadline is August 23, 2012.

Is this an active funding opportunity?

The information provided describes an archived 2012 competition, with an archive date of September 22, 2012.

Who should be contacted for help accessing the full announcement?

The contact listed for assistance is the CDMRP Help Desk at 301-682-5507.

What kind of results is the program trying to generate?

The program is designed to produce early clinical evidence of benefit or feasibility and actionable clinical insight, supporting a credible early signal that can guide next-stage development and larger trials.

What is the overall theme or expectation for applicants?

The opportunity is geared toward teams that have already completed key preparatory steps (including required regulatory approvals where applicable) and are positioned to execute quickly on a well-justified early clinical test of a novel prostate cancer intervention or a closely tied correlative clinical study.

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Funding Number: W81XWH 12 PCRP HDRA
Agency: Dept. of the Army USAMRAA
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Agency: Dept. of the Army USAMRAA
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