Opportunity Information: Apply for W81XWH 17 DMRDP MID ARA
Apply for W81XWH 17 DMRDP MID ARA
- The DOD-AMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "DoD Joint Program Committee-2/Military Infectious Diseases Applied 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.
- This funding opportunity was created on Dec 17, 2015 and posted on Dec 17, 2015.
- Applicants must submit their applications by May 09, 2016. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The number of recipients for this funding is limited to 10 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 Joint Program Committee-2/Military Infectious Diseases Applied Research Award (FY17 JPC-2/MIDRP ARA) is a Department of Defense funding opportunity aimed at reducing illness and death caused by combat-related or trauma-induced wound infections. The program is focused on applied research that can directly move potential medical solutions closer to use in people. In practical terms, the DoD is looking for projects that help determine which candidate products, technologies, or approaches are most ready to advance toward human testing, especially in the context of military-relevant wounds where infection can rapidly worsen outcomes.
This award is designed to support hypothesis-driven, proof-of-concept, and translational preclinical work rather than exploratory basic science. Proposed efforts can include hypothesis testing and proof-of-concept studies using in vitro and/or in vivo models, as well as refinement of early concepts into more defined solutions to demonstrate technical feasibility. It also supports the evaluation, maturation, and down-selection of candidate products, including drugs, biologics or vaccine constructs, and devices or systems, again using laboratory and animal model testing where appropriate. Another major emphasis is enabling studies needed to reach key regulatory milestones, such as preclinical safety and toxicity work sufficient to support Investigational New Drug (IND) or Investigational Device Exemption (IDE) applications. Taken together, the program is structured to help investigators cross the gap between promising research findings and a development-ready package that could realistically progress into regulated human testing.
While studies may include human subjects, the award cannot be used to run clinical trials. The opportunity uses a specific definition of a clinical trial: any prospective enrollment of human subjects where an intervention (such as a drug, device, biologic, procedure, rehabilitation method, behavioral intervention, or similar) is tested for a measurable outcome related to safety, effectiveness, efficacy, or exploratory endpoints in a way that directly affects the subject. Investigators who want to conduct a clinical trial are directed instead to apply to the separate FY17 JPC-2/MIDRP Clinical Studies Award (W81XWH-17-DMRDP-MID-CSA). This boundary makes it clear that ARA projects should stop short of interventional clinical testing, even though certain human-subject elements that are not clinical trials may be allowable.
Applications are expected to be grounded in strong preliminary or published data that directly supports the proposed work. Competitiveness depends on demonstrating a clear scientific rationale built from a critical analysis of existing literature, along with a well-formulated, testable hypothesis. The program explicitly excludes early-stage fundamental basic research, defined as work aimed primarily at expanding general knowledge without a specific product or process application in view. In other words, the DoD wants proposals that are already pointed toward a tangible solution for wound infection prevention, diagnosis, or treatment and that can credibly show a pathway toward eventual human use.
A notable feature of this mechanism is the Partnering PI Option, which is meant to encourage meaningful collaborations. Under this structure, up to three principal investigators can participate, with one designated as the Initiating PI and the others as Partnering PIs; each PI receives a separate award. The expectation is that the team jointly develops and submits a single, integrated research project, and that each investigator contributes substantial intellectual leadership with complementary expertise. Multidisciplinary and multi-organization partnerships are allowed, but participating organizations must be willing to address intellectual property and materials-related issues early and remove administrative barriers that could slow or prevent successful completion of the project.
From an administrative standpoint, this is a discretionary DoD opportunity administered by DOD-AMRAA under CFDA 12.420, using grant and cooperative agreement instruments. Eligibility is listed as unrestricted (open broadly to entity types, subject to any additional eligibility clarifications in the full announcement). The opportunity was posted December 17, 2015, with an application closing date of May 9, 2016, and it anticipated making around 10 awards. The listed award ceiling is shown as 0 in the provided data, which typically signals that applicants should rely on the full funding announcement for budget limits and program-specific caps rather than the summary field.
Frequently Asked Questions (FAQs)
What is the FY17 JPC-2/MIDRP Applied Research Award (ARA) trying to accomplish?
This Department of Defense (DoD) opportunity supports applied research intended to reduce illness and death from combat-related or trauma-induced wound infections. The emphasis is on work that can move a potential medical solution closer to use in people, especially for military-relevant wounds where infection can quickly worsen outcomes.
What kind of research does this award fund?
The ARA funds hypothesis-driven, proof-of-concept, and translational preclinical research. It supports studies that help determine which candidate products, technologies, or approaches are most ready to advance toward human testing, based on credible data and a clear development pathway.
Does the program support basic science or exploratory research?
No. The program explicitly excludes early-stage fundamental basic research aimed primarily at expanding general knowledge without a specific product or process application in view. Proposals need to be pointed toward a tangible solution for wound infection prevention, diagnosis, or treatment.
What types of studies are encouraged under this mechanism?
Encouraged efforts include hypothesis testing and proof-of-concept studies using in vitro and/or in vivo models, refining early concepts into more defined solutions to demonstrate technical feasibility, and evaluating/maturing/down-selecting candidate products through laboratory and animal model testing where appropriate.
What kinds of products or technologies can be supported?
The award can support work on candidate products and approaches such as drugs, biologics or vaccine constructs, and devices or systems, as long as the work is consistent with applied, translational preclinical development for wound infection-related needs.
Is the ARA intended to help with regulatory readiness (IND/IDE steps)?
Yes. A major emphasis is enabling studies needed to reach key regulatory milestones, including preclinical safety and toxicity work sufficient to support an Investigational New Drug (IND) or Investigational Device Exemption (IDE) application.
Can human subjects be included in an ARA project?
Studies may include human subjects, but the award cannot be used to run clinical trials. Any human-subject elements must stay within what is allowable while stopping short of interventional clinical testing as defined by the opportunity.
Are clinical trials allowed under this award?
No. The ARA cannot be used to run clinical trials.
How does this opportunity define a "clinical trial"?
It uses a specific definition: any prospective enrollment of human subjects where an intervention (for example, a drug, device, biologic, procedure, rehabilitation method, behavioral intervention, or similar) is tested for a measurable outcome related to safety, effectiveness, efficacy, or exploratory endpoints in a way that directly affects the subject.
If a project needs to run a clinical trial, where should the applicant apply instead?
Investigators intending to conduct a clinical trial are directed to the separate FY17 JPC-2/MIDRP Clinical Studies Award: W81XWH-17-DMRDP-MID-CSA.
What level of prior evidence is expected for a competitive application?
Applications are expected to be grounded in strong preliminary or published data that directly supports the proposed work. Competitiveness depends on showing a clear scientific rationale based on a critical analysis of existing literature and a well-formulated, testable hypothesis.
What is the overall development position expected for proposed work?
The program is structured to help investigators bridge the gap between promising findings and a development-ready package that could realistically progress into regulated human testing (without actually conducting clinical trials under this mechanism).
What is the Partnering PI Option?
The Partnering PI Option is designed to promote meaningful collaboration. Up to three principal investigators may participate: one Initiating PI and up to two Partnering PIs. The team jointly develops and submits one integrated research project, and each PI is expected to provide substantial intellectual leadership with complementary expertise.
How are awards handled when using the Partnering PI Option?
Each PI receives a separate award under the Partnering PI structure, while still operating as part of a single, integrated project.
Are multidisciplinary or multi-organization collaborations allowed?
Yes. Multidisciplinary and multi-organization partnerships are allowed under this opportunity.
What administrative or collaboration issues should partnering organizations address early?
Participating organizations are expected to address intellectual property and materials-related issues early and remove administrative barriers that could slow or prevent successful completion of the project.
Who administers this funding opportunity?
This is a discretionary DoD opportunity administered by DOD-AMRAA.
What CFDA number is associated with this opportunity?
The opportunity is listed under CFDA 12.420.
What type of funding instruments are used?
The opportunity uses grant and cooperative agreement instruments.
Who is eligible to apply?
Eligibility is listed as unrestricted (open broadly to entity types), subject to any additional eligibility clarifications in the full announcement.
When was this opportunity posted and when did it close?
It was posted on December 17, 2015, and the application closing date was May 9, 2016.
How many awards were anticipated?
The opportunity anticipated making around 10 awards.
What is the maximum award amount (ceiling)?
The provided summary data shows an award ceiling of 0. This typically indicates applicants should rely on the full funding announcement for actual budget limits and any program-specific caps rather than the summary field.
What is the main topic area or problem space for projects?
The focus is on military-relevant wound infections, including prevention, diagnosis, or treatment approaches that can be matured through applied and translational preclinical work toward eventual human use.
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