Opportunity Information: Apply for HT9425 23 PRCRP TTSA
The DoD Peer Reviewed Cancer, Translational Team Science Award (TTSA) is a Department of Defense funding opportunity under the Peer Reviewed Cancer Research Program (PRCRP) that is designed to push promising cancer findings closer to real-world patient benefit. In practical terms, it supports hypothesis-driven translational research that is tightly connected to an ongoing or completed clinical trial. The expectation is that applicants are not starting from scratch: the proposed work should build directly on clinical investigation results and use trial-derived information to guide the next logical steps toward a next-phase clinical trial or a future clinical application. While the mechanism can include funding for clinical trial activities, the program is not meant to function as a simple clinical trial funding source. Instead, it emphasizes a broader, team-based translational effort where clinical observations and laboratory or mechanistic work inform each other in a way that clearly advances patient-relevant questions.
A central feature of the TTSA is its required team structure and true collaboration model. Each application must be led by a multi-investigator team with at least two and no more than three Principal Investigators working under one overarching research strategy within one or more of the required FY23 PRCRP Topic Areas. One PI serves as the Initiating PI and typically handles most submission and administrative coordination, while the other(s) serve as Partnering PI(s). Importantly, the program expects this to be more than a formality: all PIs should play major, substantive roles in shaping the science, including contributing meaningfully to the project narrative, the statement of work, and other core proposal components. If selected, each PI is named on an individual award within their organization, reinforcing the idea that this is a shared scientific responsibility rather than a single-lab project with minor collaborators.
The DoD also strongly encourages inclusion of at least one military or Department of Veterans Affairs (VA) investigator as an equal partner. This is not presented as a strict eligibility requirement, but it is clearly a priority within the program. The announcement defines qualifying military/VA investigators broadly, including active-duty or active-reserve personnel detailed to agencies outside DoD, civilian DoD investigators, and investigators at VA research facilities. Just as important is how they are expected to participate: the military/VA investigator should have a substantial intellectual and effort-based role in the research and should not be added simply to facilitate access to military or VA patient populations. The emphasis is on genuine scientific partnership that strengthens the project.
From a scientific scope standpoint, the TTSA targets advanced translational studies that address concrete clinical problems and near-term patient impact. Competitive projects are expected to tackle critical knowledge gaps tied to clinical outcomes, validate key results emerging from clinical research, expand on potentially game-changing signals, or pursue novel clinical findings that emerged from trial work. The award is intentionally focused on translation that moves both ways between bench and bedside, meaning proposals should show a clear plan for reciprocal flow of information between laboratory science and clinical science. For example, clinical trial observations might drive mechanistic lab studies to explain responders versus non-responders, or lab-derived hypotheses might be tested and refined using clinical trial biospecimens and outcome data, with the goal of informing treatment strategies, biomarkers, or future study design.
The program also draws lines around what it does not want to fund. High-throughput screening efforts or broad sequencing exercises that are not tightly justified as translational steps tied to a clinical trial context are explicitly discouraged. This reflects the program’s preference for focused, clinically anchored investigations rather than large exploratory discovery projects that may take longer to translate or may not be clearly linked to actionable clinical decisions.
Application readiness is another key theme. The TTSA requires preliminary clinical data relevant to the proposed studies, reinforcing that proposals should be grounded in real clinical evidence rather than early-stage concepts. In addition, the research plan is expected to be rigorously designed with a clear statistical plan and data analysis plan. The stated rationale for this requirement is the award’s emphasis on near-term patient relevance: reviewers want to see that the study design, endpoints, and analysis approach are capable of producing results that are interpretable, robust, and meaningful for clinical decision-making and patient outcomes.
Impact is treated as a primary review driver. Applicants are expected to articulate how the work could significantly influence cancer research and/or patient care and how it could accelerate the movement of promising ideas into clinical use. This can include prevention, detection, diagnosis, prognosis, treatment, and survivorship, but the work must align with at least one of the FY23 PRCRP Overarching Challenges referenced in the full announcement. The overall goal is to assemble a synergistic, multidisciplinary team whose combined expertise can solve a clinical problem in a way that would be difficult for any single investigator or single-discipline group to accomplish alone.
Administratively, this opportunity was released by the Department of Defense, Department of the Army, U.S. Army Medical Research Acquisition Activity (USAMRAA). It is listed under Funding Opportunity Number HT9425 23 PRCRP TTSA and uses grant and cooperative agreement funding instruments under the Science and Technology / Research and Development activity category (CFDA 12.420). Eligibility is described as unrestricted, meaning it is broadly open to many entity types, subject to any additional eligibility details in the full funding notice. The opportunity anticipated making around nine awards, and it listed an award ceiling of 0 in the source record, which typically indicates that applicants must rely on the full announcement for budget limits or that budgeting is handled through other stated constraints. The original closing date for FY23 was August 10, 2023, which is mainly useful as a reference point for the cycle described, since future years may reissue similar mechanisms with updated dates and requirements.Apply for HT9425 23 PRCRP TTSA
- The Department of Defense, Dept. of the Army -- USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "DoD Peer Reviewed Cancer, Translational Team Science 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 Apr 04, 2023.
- Applicants must submit their applications by Aug 10, 2023. (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 9 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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FAQs: DoD Peer Reviewed Cancer, Translational Team Science Award (TTSA)
What is the DoD Peer Reviewed Cancer, Translational Team Science Award (TTSA)?
The Translational Team Science Award (TTSA) is a funding opportunity under the Department of Defense (DoD) Peer Reviewed Cancer Research Program (PRCRP) intended to move promising cancer findings closer to real-world patient benefit. It supports hypothesis-driven translational research that is closely connected to an ongoing or completed clinical trial, with a clear path toward a next-phase clinical trial or a future clinical application.
What type of research does TTSA support?
TTSA supports advanced translational studies that address concrete clinical problems and aim for near-term patient impact. Proposed work is expected to build directly on clinical investigation results and use clinical trial-derived information (such as observations, biospecimens, and outcome data) to guide the next logical translational steps.
Does the proposed research need to be tied to a clinical trial?
Yes. The research is expected to be tightly connected to an ongoing or completed clinical trial. The intent is that applicants are not starting from scratch; the proposal should leverage clinical trial results and/or trial-derived information to drive the translational plan toward a future clinical application or next-phase trial.
Is this award intended to primarily fund a clinical trial?
No. While the mechanism can include funding for clinical trial activities, it is not intended to serve as a simple clinical trial funding source. The emphasis is on a broader, team-based translational effort where clinical observations and laboratory or mechanistic work inform each other to advance patient-relevant questions.
What is meant by "hypothesis-driven translational research" in this program?
Within the TTSA context, hypothesis-driven translational research means the project should test clear, specific hypotheses that are grounded in clinical evidence from a trial and designed to generate interpretable results that can inform clinical decision-making, biomarker strategies, treatment approaches, or the design of future studies.
What is the required team structure for a TTSA application?
Each application must be led by a multi-investigator team with at least two and no more than three Principal Investigators (PIs). The PIs work under one overarching research strategy and the project must be within one or more of the required FY23 PRCRP Topic Areas.
What is the difference between the Initiating PI and Partnering PI(s)?
One PI serves as the Initiating PI and typically manages most submission and administrative coordination. The other PI(s) serve as Partnering PI(s). The program expects all PIs to have major, substantive roles in shaping the science and contributing meaningfully to core proposal components such as the project narrative and statement of work.
Do all Principal Investigators need to contribute substantially, or can one PI lead while others play minor roles?
All PIs are expected to play major, substantive roles. The collaboration model is intended to be a true team science structure, not a single-lab project with minor collaborators.
How are awards handled if the application is selected for funding?
If selected, each PI is named on an individual award within their organization. This structure reinforces shared scientific responsibility across the team.
Is participation by a military or Department of Veterans Affairs (VA) investigator required?
No. The opportunity strongly encourages including at least one military or VA investigator as an equal partner, but it is described as a priority rather than a strict eligibility requirement.
Who qualifies as a military or VA investigator for this opportunity?
The announcement defines qualifying military/VA investigators broadly, including active-duty or active-reserve personnel detailed to agencies outside DoD, civilian DoD investigators, and investigators at VA research facilities.
What level of involvement is expected from a military or VA investigator if included?
The military/VA investigator is expected to have a substantial intellectual and effort-based role and should not be included simply to enable access to military or VA patient populations. The emphasis is on genuine scientific partnership that strengthens the project.
What makes a TTSA project competitive from a scientific standpoint?
Competitive projects are expected to address critical knowledge gaps tied to clinical outcomes, validate key results emerging from clinical research, expand on potentially game-changing signals, or pursue novel clinical findings arising from trial work. Strong proposals also show a clear plan for reciprocal flow of information between laboratory science and clinical science.
What does "reciprocal flow" between bench and bedside mean in this program?
It means clinical observations should inform laboratory or mechanistic studies, and laboratory insights should be tested or refined using clinical trial-derived materials and data, with the aim of producing findings that are directly relevant to patients and can inform future clinical application.
Are high-throughput screening or broad sequencing projects a good fit for TTSA?
Generally no. High-throughput screening efforts or broad sequencing exercises that are not tightly justified as translational steps linked to a clinical trial context are explicitly discouraged. The program prefers focused, clinically anchored investigations rather than broad exploratory discovery projects.
Is preliminary clinical data required?
Yes. The TTSA requires preliminary clinical data relevant to the proposed studies, reflecting the expectation that proposals are grounded in real clinical evidence rather than early-stage concepts.
What are the expectations for study design and analysis?
The research plan is expected to be rigorous and include a clear statistical plan and data analysis plan. Reviewers are looking for designs and analyses capable of producing robust, interpretable, clinically meaningful results.
What areas of cancer research or care can TTSA projects address?
The announcement notes potential relevance across prevention, detection, diagnosis, prognosis, treatment, and survivorship, provided the work aligns with at least one of the FY23 PRCRP Overarching Challenges referenced in the full announcement.
Does the project need to fit within specific PRCRP topics?
Yes. The team must pursue one overarching research strategy within one or more of the required FY23 PRCRP Topic Areas.
What is the main review emphasis for TTSA applications?
Impact is treated as a primary review driver. Applicants are expected to explain how the work could significantly influence cancer research and/or patient care and how it could accelerate translation of promising ideas into clinical use.
Who released this funding opportunity?
The opportunity was released by the Department of Defense, Department of the Army, U.S. Army Medical Research Acquisition Activity (USAMRAA).
What is the Funding Opportunity Number for this TTSA announcement?
The Funding Opportunity Number listed is HT9425 23 PRCRP TTSA.
What funding instrument and activity category does this opportunity use?
The opportunity uses grant and cooperative agreement funding instruments under the Science and Technology / Research and Development activity category. It is associated with CFDA 12.420.
Who is eligible to apply?
Eligibility is described as unrestricted, meaning it is broadly open to many entity types, subject to any additional eligibility details in the full funding notice.
How many awards were anticipated for this cycle?
The opportunity anticipated making around nine awards.
What is the award ceiling for TTSA?
The source record listed an award ceiling of 0, which typically indicates that applicants must rely on the full announcement for budget limits or that budgeting is handled through other stated constraints.
When was the original closing date for the FY23 TTSA opportunity?
The original closing date for FY23 was August 10, 2023. This is mainly a reference point for that cycle; future years may reissue similar mechanisms with updated dates and requirements.
What is the overall goal of the TTSA collaboration model?
The goal is to assemble a synergistic, multidisciplinary team whose combined expertise can solve a clinically relevant problem in a way that would be difficult for any single investigator or single-discipline group to accomplish alone.
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