Opportunity Information: Apply for HT942524TERPTRA
The Toxic Exposures Translational Research Award (TERP TRA), funding opportunity number HT942524TERPTRA, is a discretionary federal grant program offered by the Department of the Army through the U.S. Army Medical Research Acquisition Activity (USAMRAA). It falls under the Science and Technology and other Research and Development funding activity category (CFDA 12.420). The program was created on June 26, 2024, and the original application closing date is November 7, 2024. Eligibility is listed as unrestricted, meaning the opportunity is broadly open to applicants rather than being limited to a narrow set of institution types.
The core purpose of the FY24 TERP TRA is to fund translational research focused on military-related toxic exposures, specifically work that moves strong scientific ideas closer to real-world clinical use. The emphasis is not on basic discovery for its own sake, but on accelerating the path from promising research findings to practical outcomes that can be used in health care settings. The notice makes clear that desired end products can include health care products (for example, diagnostics or therapeutic approaches), interventions (such as prevention or treatment strategies), technologies (tools or platforms that enable better detection, monitoring, or care), and/or clinical practice guidelines (evidence-backed recommendations that clinicians can apply in practice).
In this program, translational research is framed as an intentional integration of basic science and clinical observations. In other words, projects should connect mechanistic or laboratory insights with patient-centered or clinically relevant data, and they should be designed in a way that makes the eventual clinical application credible and achievable. A key expectation is bidirectional, or reciprocal, flow of information between the basic and clinical sides of the work. That could look like clinical observations shaping the laboratory experiments and target selection, while laboratory findings inform clinical hypotheses, biomarker development, patient stratification approaches, or the design of future clinical studies. The application is expected to demonstrate this back-and-forth connection as a concrete part of the research plan, rather than treating basic and clinical components as separate, loosely related activities.
The announcement also notes that New Approach Methodologies (NAMs) may be used. While the opportunity text does not list specific NAM examples, the intent is generally to support modern approaches that can improve relevance, reduce uncertainty, or speed translation, such as advanced in vitro human-relevant systems, computational and modeling approaches, or other innovative methods that strengthen the link between exposure science, biological effect, and clinical decision-making. The practical takeaway is that applicants can incorporate these methods when they help bridge the gap between early-stage findings and clinical implementation.
Finally, the opportunity anticipates making approximately six awards. The public summary does not specify an award ceiling amount, so prospective applicants would need to consult the full funding announcement or related guidance for budget constraints, allowable costs, and other requirements. Overall, the TERP TRA is positioned as a translational pipeline accelerator: it is meant to take military toxic exposure research that is already promising and push it toward deliverables that can realistically influence clinical care, tools, or guidelines.Apply for HT942524TERPTRA
- The Dept. of the Army -- USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "Toxic Exposures Translational 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 2024-06-26.
- Applicants must submit their applications by 2024-11-07. (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 6 candidate(s).
- Eligible applicants include: Unrestricted.
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Frequently Asked Questions (FAQs)
What is the Toxic Exposures Translational Research Award (TERP TRA)?
The Toxic Exposures Translational Research Award (TERP TRA) is a discretionary federal grant program focused on translational research related to military-relevant toxic exposures. Its goal is to move strong scientific ideas closer to practical, real-world clinical use rather than supporting basic discovery alone.
What is the funding opportunity number for this grant?
The funding opportunity number (FON) is HT942524TERPTRA.
Which federal agency is offering this opportunity?
This opportunity is offered by the Department of the Army through the U.S. Army Medical Research Acquisition Activity (USAMRAA).
What funding activity category does this opportunity fall under?
It falls under the Science and Technology and other Research and Development funding activity category.
What is the CFDA number associated with this program?
The opportunity is associated with CFDA 12.420.
When was the TERP TRA program created?
The program was created on June 26, 2024.
What is the original application closing date?
The original application closing date is November 7, 2024.
Who is eligible to apply?
Eligibility is listed as unrestricted. That means the opportunity is broadly open to applicants and is not limited to a narrow set of institution types based on the information provided.
What is the core purpose of the FY24 TERP TRA?
The core purpose is to fund translational research focused on military-related toxic exposures, with an emphasis on accelerating the movement of promising research findings toward practical outcomes that can be used in health care settings.
Is this program intended to fund basic research?
The emphasis is not on basic discovery for its own sake. Projects should be designed to accelerate translation to practical clinical outcomes, connecting scientific findings to credible and achievable clinical applications.
What kinds of end products are expected or encouraged?
The notice indicates that desired end products can include health care products (such as diagnostics or therapeutic approaches), interventions (such as prevention or treatment strategies), technologies (tools or platforms that enable better detection, monitoring, or care), and/or clinical practice guidelines (evidence-backed recommendations for clinicians).
What does "translational research" mean in this opportunity?
Translational research is described as an intentional integration of basic science and clinical observations. Projects should connect mechanistic or laboratory insights with patient-centered or clinically relevant data, and they should be designed so that eventual clinical application is credible and achievable.
What does the opportunity mean by "bidirectional" or "reciprocal" flow?
A key expectation is back-and-forth information flow between basic and clinical components. Clinical observations should help shape laboratory experiments and target selection, while laboratory findings should inform clinical hypotheses, biomarker development, patient stratification approaches, or the design of future clinical studies.
Can an application include both basic science and clinical elements?
Yes. In fact, the opportunity expects an integrated approach that ties mechanistic/basic insights to clinically relevant observations or data and shows how they inform each other as part of the research plan.
Can an application treat basic and clinical work as separate tracks?
The program expects the basic and clinical components to be connected through concrete, demonstrated back-and-forth interaction. The information provided indicates applicants should avoid presenting basic and clinical activities as loosely related or isolated components.
What topic area must the research address?
Projects must focus on military-related toxic exposures, with the translational intent of moving findings toward clinical use.
Are New Approach Methodologies (NAMs) allowed?
Yes. The announcement notes that New Approach Methodologies (NAMs) may be used.
Does the opportunity list specific NAM examples?
No specific examples are listed in the information provided. The general intent described is to support modern approaches that improve relevance, reduce uncertainty, or speed translation, such as advanced in vitro human-relevant systems, computational approaches, or modeling methods, when they strengthen the link between exposure science, biological effects, and clinical decision-making.
How many awards does the program expect to make?
The opportunity anticipates making approximately six awards.
Is the maximum award amount (ceiling) provided in the summary?
No. The public summary described here does not specify an award ceiling amount.
Where can applicants find information on budget constraints and allowable costs?
Based on the information provided, applicants would need to consult the full funding announcement or related guidance to identify budget constraints, allowable costs, and other requirements.
What is the overall positioning of the TERP TRA program?
It is positioned as a translational pipeline accelerator: it is intended to take promising military toxic exposure research and push it toward deliverables that can realistically influence clinical care, tools/technologies, interventions, and/or clinical practice guidelines.
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