HT942526PRCRPIPA_GG.pdf
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FY26 Peer Reviewed Cancer Research Program Impact Award Program Announcement
This is a program announcement for the Defense Health Agency's Fiscal Year 2026 Peer Reviewed Cancer Research Program (PRCRP) Impact Award, managed by the Congressionally Directed Medical Research Programs (CDMRP). The announcement solicits applications for mature, high-impact translational and clinical cancer research projects expected to achieve near-term clinical applicability. The funding opportunity number is HT942526PRCRPIPA, with a pre-application deadline of June 26, 2026 (5:00 p.m. ET) and a full application deadline of October 5, 2026 (11:59 p.m. ET). The CDMRP expects to allot approximately $45.0 million to fund roughly 30 Impact Award applications with total cost caps of $1.5 million per award for single-PI submissions, and $28.0 million to fund approximately 14 Impact Award-Partnering PI Option applications with total cost caps of $2.0 million. The maximum period of performance is three years, with awards anticipated by September 30, 2027, using FY26 funds that expire September 30, 2032. Peer review is scheduled for December 2026 and programmatic review for February 2027.
Research must address one of 20 congressionally directed FY26 PRCRP Topic Areas (including blood cancers, gastrointestinal cancers, neurological cancers, pediatric/adolescent/young adult cancers, solid tumors, and metastatic cancers) and cannot include melanoma or cancers originating in the breast, kidney, lung, pancreas, prostate, or ovary. Applications must demonstrate relevance to military health by addressing environmental exposure risk factors associated with military activities or filling gaps in mission readiness related to cancer prevention, detection, diagnosis, treatment, quality of life, or survivorship. Eligible applicants include extramural and intramural U.S. Department of Defense organizations, foreign and domestic organizations, and for-profit and nonprofit entities. Independent investigators at all career levels are eligible as principal investigators. The application process uses a two-step submission: pre-applications submitted through eBRAP and full applications through either Grants.gov (extramural organizations) or eBRAP (intramural DOW organizations). Key application components include a 10-page project narrative with preliminary data demonstrating feasibility, technical and lay abstracts, statement of work, statistical plan and data analysis, clinical strategy statement (if applicable), animal research plan (if applicable), post-award transition plan, relevance to military health statement, and impact statement. Applications must include preliminary data from the PI's or collaborators' laboratories, rigorous study design aligned with STROBE, CONSORT, SPIRIT, and ARRIVE 2.0 guidelines, and sex as a biological variable considerations. Clinical trials are permitted and must begin within 12 months of award, with IND/IDE applications submitted within 60 days of award. The funding mechanism is grants under 31 USC 6304, with direct cost restrictions limiting travel to two scientific/technical meetings per investigator annually.
FY26 PRCRP IPA Program Announcement
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This program announcement must be read in conjunction with the General Application Instructions, version CD26_01.
Program Announcement for the Defense Health Agency
Peer Reviewed Cancer Research Program
Impact Award
Funding Opportunity Number: HT942526PRCRPIPA
Pre-Application Due: June 26, 2026
Application Due: October 5, 2026 https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01
FY26 Peer Reviewed Cancer Impact Award 2
Content
Before You Begin 3
Basic Information Summarizes the funding opportunity, funding details, submission deadlines and review dates
Eligibility Details eligibility factors for the applicant organization and Principal Investigator
Program Description Describes the program mission and intent of the Impact Award; provides key award information and considerations; and outlines funding details
Application Contents Presents the two-step application process and instructions for preparing a pre-application and full application
Submission Requirements Provides locations for application packages, instructions for submitting pre-applications and full applications, and describes application verification
Application Review Information Outlines the processes for application compliance review, pre-application and full application selection/notification, and risk assessment. Also, details the review criteria for pre-application screening and both tiers of the CDMRP application review process – Peer Review and Programmatic Review
Federal Award Notices Outlines what a successful applicant can expect if recommended for funding
Post-Award Requirements References policy requirements for funded research; outlines reporting requirements and restrictions related to Principal Investigator changes and institutional award transfers
Other Information Outlines criteria for administrative actions including application rejection, modification, withdrawal and withhold
Appendix 1 Includes a checklist for all full application components to facilitate application submission
Appendix 2 Acronym List
FY26 Peer Reviewed Cancer Impact Award 3
Before You Begin
• Active SAM.gov, eBRAP.org and Grants.gov registrations are required for application submission. User registration for each of these websites can take several weeks or longer.
Each applicant must ensure their registrations are active and up to date prior to application preparation.
• Read this funding opportunity announcement in the order it is written before beginning to prepare application materials. It is the responsibility of the applicant to determine whether the proposed research meets the intent of this funding opportunity and that all parties meet eligibility requirements.
• To support application preparation, additional resources are available including an application process FAQ, a Guide for Intragovernmental & Intramural Applicants and a CDMRP Video Series detailing the application process.
Who to Contact for Support
This document uses internal links; you can go back to where you were by pressing the Alt + left arrow keys (Windows) or command + left arrow keys (Macintosh) on your keyboard.
Click to be taken to additional guidance and instructions within the General Application Instructions (GAI).
eBRAP Help Desk
301-682-5507 help@eBRAP.org
Questions regarding funding opportunity submission requirements, as well as technical assistance related to pre-application or intramural application submission.
Grants.gov Support Center
800-518-4726 International: 1-606-545-5035 support@grants.gov
Questions regarding Grants.gov registration and Workspace.
https://sam.gov/ https://ebrap.org/eBRAP/public/index.htm https://grants.gov/register https://cdmrp.health.mil/#:~:text=Frequently%20Asked%20Questions%20%C2%BB https://cdmrp.health.mil/#:~:text=Guide%20for%20Intragovernmental%20%26%20Intramural%20Applicants https://ebrap.org/eBRAP/public/Program.htm#:~:text=Journey%20of%20an,Tier%20Review%20Process mailto:help@eBRAP.org mailto:support@grants.gov https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01
Section Shortcuts Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 4
1. Basic Information About the Funding Opportunity
Summary: The fiscal year 2026 (FY26) Peer Reviewed Cancer Research Program (PRCRP) Impact Award supports mature research that will have a near-term impact on clinical cancer care in one of the congressionally directed FY26 PRCRP Topic Areas. Applicants must consider how the research project will lead to the advancement of knowledge in cancer research, patient care and/or treatment options in the Military Health System (MHS).
Distinctive Features:
• Applications must include preliminary data to support feasibility of the study.
• Projects must have strong potential to result in a near-term impact in cancer.
• The funding mechanism allows clinical trials.
• This funding mechanism allows for a single Principal Investigator (PI), or two partnering PIs referred to as the Initiating PI and the Partnering PI. Only the Initiating PI will submit a pre-application, but both PIs will need to submit full applications. The Partnering PI’s application is an abbreviated package specific to their distinct portion of the research project. Be advised, both applications for a research project may be withdrawn if the initiating or partnering application is rejected or administratively withdrawn.
Funding Details: The Congressionally Directed Medical Research Programs (CDMRP) expects to allot roughly $45.0M to fund approximately 30 Impact Award applications with total cost caps of $1.5M per award and $28.0M to fund approximately 14 Impact Award-Partnering PI Option applications with total cost caps of $2.0M. The maximum period of performance is 3 years. It is anticipated that awards made from this fiscal year 2026 (FY26) funding opportunity will be funded with FY26 funds, which will expire for use on September 30, 2032. Awards supported with FY26 funds will be made no later than September 30, 2027.
Submission and Review Dates and Times
• Pre-Application (Preproposal) Submission Deadline: 5:00 p.m. Eastern Time (ET), June 26, 2026
• Invitation to Submit an Application: August 10, 2026
• Application Submission Deadline: 11:59 p.m. ET, October 5, 2026
• End of Application Verification Period: 5:00 p.m. ET, October 8, 2026
• Peer Review: December 2026
• Programmatic Review: February 2027
Announcement Type: Initial
Funding Opportunity Number: HT942526PRCRPIPA
Assistance Listing Number: 12.420
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 5
2. Eligibility Information
2.1. Eligible Applicants
2.1.1. Organization
Extramural and intramural U.S. Department of Defense (DOW) organizations are eligible to apply, including foreign and domestic organizations, for-profit and nonprofit organizations, and public or private entities.
2.1.2. Principal Investigator
Independent investigators at all career levels are eligible to be named as the PI or partnering PI on the application.
Independent Investigators at all career levels affiliated with an eligible organization are eligible to be named PI on the application, regardless of ethnicity, nationality or citizenship status.
2.2. Cost Sharing
Cost sharing is not an eligibility requirement.
2.3. Other
Awards are made to eligible organizations, not to individuals. Refer to the GAI for additional recipient qualification requirements.
https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Content_Form_Full_App_Submission:~:text=pre%2Dapplication%20submission.-,Extramural%20Organization%3A,-A%20foreign%20or https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Definition_List:~:text=Intramural%20DOW%20Organization%3A%20A%20subset%20of%20intragovernmental%20organizations%3B%20refers%20specifically%20to%20DOW%20organizations%2C%20including%20DOW%20laboratories%2C%20DOW%20military%20treatment%20facilities%2C%20and/or%20DOW%20activities%20embedded%20within%20a%20civilian%20medical%20center https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=APPENDIX%201.%0ARECIPIENT%20QUALIFICATION%20AND%20RESTRICTION%20INFORMATION
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 6
3. Program Description
The Defense Health Agency Contracting Activity (DHACA) is soliciting applications to this funding opportunity using delegated authority provided by United States Code, Title 10, Section 4001 (10 USC 4001). The CDMRP is the program office managing this FY26 funding opportunity as part of the Peer Reviewed Cancer Research Program (PRCRP). The CDMRP is located within the Defense Health Agency Research and Development (DHA R&D), which is a part of the Department of Defense, DOD, herein referred to using the secondary title Department of War, DOW. Congress initiated the PRCRP in 2009 to provide support for research of high potential impact and exceptional scientific merit. Appropriations for the PRCRP from FY09 through FY25 totaled $1.17 billion. The FY26 appropriation is $165 million (M).
Congressional language stipulates the FY26 PRCRP must be relevant to Service Members, and address at least one of the congressionally directed FY26 PRCRP Topic Areas listed below.
• Bladder cancer
• Blood cancers
• Brain cancer
• Colorectal cancer
• Endometrial cancer
• Esophageal cancer
• Germ cell cancers
• Glioblastoma
• Liver cancer
• Lymphoma
• Mesothelioma
• Metastatic cancers
• Myeloma
• Neuroblastoma
• Neuroendocrine Tumors
• Pediatric, adolescent, and young adult cancers1
• Pediatric brain tumors
• Sarcoma
• Stomach cancer
• Thyroid cancer
Research proposed to the PRCRP must not address research in melanoma, or cancers originating in the breast, kidney, lung, pancreas, prostate or ovary. In addition, FY26 PRCRP funds must not be used to study rare cancers except FY26 PRCRP Topic Area cancer types that are rare by definition.
FY26 PRCRP Portfolios and Strategic Goals
To meet the intent of the funding opportunity, all applications for FY26 PRCRP funding must specifically address one of the FY26 PRCRP Topic Areas as directed by the U.S.
Congress and have direct relevance to military health. Additionally, the PRCRP implements a portfolio-driven approach by grouping related topic areas with strategic goals as a framework within which to address critical gaps in cancer research and patient care. All applications must address one of the FY26 PRCRP strategic goals as it relates to the portfolio-assigned FY26 PRCRP Topic Area. Some topic areas are present in more than one portfolio.
Applications must align to the strategic goal of the portfolio in which a topic area is included. If the proposed research does not specifically address one FY26 PRCRP Topic Area and one FY26 PRCRP strategic goal from a single portfolio, then the government reserves the right to administratively withdraw the application. The government reserves the right to reassign
1 The definition of adolescents and young adults is derived from the National Cancer Institute (https://www.cancer.gov/types/aya). Research should be targeted toward pediatric (ages 0-14 years), adolescents (ages 15-24 years), and/or young adults (ages 25-39 years).
https://www.cancer.gov/types/aya
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 7 the application’s topic area if submitted to an incorrect topic area. The table below lists the FY26 PRCRP Topic Areas and strategic goals in each PRCRP portfolio category.
Portfolio: Blood Cancers
All applications under this portfolio must address one topic area and one strategic goal listed below.
Topic Areas: Blood, Lymphoma, Myeloma
Knowledge Areas:
Strategic Goals:
Prevention and Etiology
• Improve risk assessment of precancerous conditions
• Develop early intervention strategies to prevent initiation and/or progression
• Investigate autoimmune disorders as risk factors for lymphoma to inform surveillance strategies
• Understand the role of cancer stem cells and the tumor microenvironment in the development of blood cancers
Diagnosis and Prognosis
• Improve methods for early detection, prognostic evaluation and/or therapeutic stratification
• Develop more cost-effective molecular diagnostics
• Identify biomarkers to predict progression from indolent disease
• Identify unique prognostic factors in pediatric, adolescent and young adult malignancies
Treatment • Develop new, less toxic therapies
• Develop methods to predict therapeutic vulnerabilities
• Develop therapies that don’t require hospitalization
• Develop therapies employing gene editing technologies and cell therapies
• Identify contribution of immune niche to initial treatment response and relapse
• Develop therapeutic options for patients who fail last line therapies
Survivorship • Develop strategies to minimize and mitigate treatment toxicities
• Improve quality of life for survivors and/or caregivers
• Identify long-term effects of gene editing and cell therapies and develop risk-based standards for surveillance of treated patients
• Improve understanding of the effects of long-term immunosuppression
Epidemiology • Design population-based studies to identify and characterize risk factors related to malignancy
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 8
Portfolio: Gastroenterological Cancers
All applications under this portfolio must address one topic area and one strategic goal listed below.
Topic Areas: Colorectal cancer, Esophageal cancer, Liver cancer, Stomach cancer
Knowledge Areas:
Strategic Goals:
Prevention and Etiology
• Identify modifiable and non-modifiable risk factors to inform prevention strategies
• Identify factors driving the increasing rates of early-age onset disease
• Identify environmental and genetic factors associated with an increased cancer risk
• Identify key drivers of conversion from precancerous lesions into cancer
• Explore the interplay between the microbiome and infectious agents in cancer initiation and progression
• Conduct integrative studies that analyze stool, blood and the microbiome as they impact disease onset and patient outcomes
Diagnosis and Prognosis
• Improve methods for early detection, prognostic evaluation and/or therapeutic stratification
• Develop cost-effective and minimally invasive tools for early detection
• Develop preclinical models to study disease development
Treatment • Develop new, less toxic therapies
• Develop effective treatments for advanced disease
• Develop immunotherapies and novel targeting therapies
• Identify combination therapies to improve patient outcomes
• Identify predictive biomarkers to determine treatment response
• Develop integrated treatment plans to address short and long-term impacts of cancer
Survivorship • Develop strategies to minimize and mitigate treatment toxicities
• Improve quality of life for survivors and/or caregivers
• Improve post treatment surveillance guidelines
• Develop validated tools to measure patient quality of life
Epidemiology • Design population-based studies to identify and characterize risk factors related to malignancy
• Implement systems to analyze disease patterns and track patient outcomes to inform best practices
• Examine the influence of familial genetics and geographic location on disease onset and treatment outcome
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 9
Portfolio: Neurological Cancers
All applications under this portfolio must address one topic area and one strategic goal listed below.
Topic Areas: Brain cancer, Glioblastoma, Pediatric Brain Tumors
Knowledge Areas:
Strategic Goals:
Prevention and Etiology
• Identify biological and environmental exposures, including maternal exposures during pregnancy, that increase risk
Diagnosis and Prognosis
• Develop early detection methods that avoid diagnostic uncertainties
• Develop effective monitoring for recurrence/refractory disease
• Develop less invasive diagnostic procedures
Treatment • Develop new, less toxic therapies
• Prevent or overcome treatment resistance
• Develop personalized oncological care and synergistic multi-modal therapies
• Identify protective therapies to be used in conjunction with toxic therapies to reduce treatment-related damage
• Develop less invasive treatment options
• Develop therapies that cross the blood-brain-barrier
Survivorship • Develop strategies to minimize and mitigate treatment toxicities
• Improve quality of life for survivors and/or caregivers
• Develop effective screening, monitoring, and provision of psychosocial support/care for the patient and family
• Develop care for patients as they transition from pediatric to adult survivors
Epidemiology • Analyze and assess the incidence/prevalence of brain tumors over time to identify changes in trends
Technology Development
• Advance the development or adoption of technologies in areas including artificial intelligence and machine learning, human microbiota, genomics, nanoparticles and robotics
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 10
Portfolio: Pediatric Adolescent and Young Adult Cancers (PAYAC)
All applications under this portfolio must address one topic area and one strategic goal listed below.
Topic Areas: PAYAC, Germ cell cancers, Neuroblastoma, Sarcoma, Thyroid cancer
Knowledge Areas:
Strategic Goals:
Prevention and Etiology
• Determine the molecular basis of cancer predisposition syndromes
• Determine the extent to which development of disease is attributable to genetic versus environmental differences
• Increase understanding of epigenetic influences on cancer development and progression
• Identify biological and environmental exposures, including maternal exposures during pregnancy, that increase risk
• Investigate the role of microbiome composition in cancer risk and outcomes
Diagnosis and Prognosis
• Improve methods for early detection, prognostic evaluation and/or therapeutic stratification
• Develop noninvasive techniques for monitoring progression and recurrence
• Identify biomarkers present in early-stage disease
• Develop preclinical models that accurately mimic disease
• Improve accurate and rapid diagnosis of sub-types of disease
Treatment • Develop new, less toxic therapies
• Develop treatments for relapse/recurrence, metastatic and advanced disease
• Increase the number of clinical trials, including ones that may not be curative but may improve the quality of life for terminal patients
• Generate evidence-based treatment and surveillance strategies to preserve fertility
• Reduce secondary cancers arising from treatment regimen
Survivorship • Develop strategies to minimize and mitigate treatment toxicities
• Improve quality of life for survivors and/or caregivers
• Develop strategies to improve the full implementation of survivorship guidelines
• Develop survivorship guidelines based on current/modern therapeutic agents
Epidemiology • Design population-based studies to identify and characterize risk factors related to malignancy
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 11
Portfolio: Solid Tumors
All applications under this portfolio must address one topic area and one strategic goal listed below.
Topic Areas: Bladder cancer, Endometrial cancer, Mesothelioma, Sarcoma, Germ cell cancers, Thyroid cancer, Neuroendocrine tumors
Knowledge Areas:
Strategic Goals:
Prevention and Etiology
• Develop methods that mitigate or identify risk
• Develop prevention strategies
• Explore the mechanistic relationship between novel and known risk factors and oncogenesis
• Identify convergent etiologies underlining the development of malignancies
Diagnosis and Prognosis
• Improve methods for early detection, prognostic evaluation and/or therapeutic stratification
• Investigate the interactions of pre-existing autoimmune disease and cancer
Treatment • Develop new, less toxic therapies
• Develop feasible precision medicine approaches
• Identify ways to tailor therapeutic strategies to minimize toxicity
Survivorship • Develop strategies to minimize and mitigate treatment toxicities
• Improve quality of life for survivors and/or caregivers
Epidemiology • Design population-based studies to identify and characterize risk factors related to malignancy
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 12
Portfolio: Metastatic Disease
All applications under this portfolio must address one topic area and one strategic goal listed below.
Topic Area: Metastatic Cancers, limited to PRCRP topic area cancers
Knowledge Areas:
Strategic Goals:
Prevention and Etiology
• Identify biomarkers in primary disease that could predict metastatic potential
• Prevent immune evasion by circulating tumor cells
• Identify how dormant, disseminated tumor cells (DTCs) persist
• Identify drivers that initiate DTCs progression to metastatic colonies
• Prevent metastatic colonization by maintaining dormancy of DTCs
• Investigate clonal divergence of primary tumor cells between metastatic sites to immunological disease
Diagnosis and Prognosis
• Improve early detection of metastasis and dormant residual disease
• Develop biomarkers that predict and monitor treatment efficacy
Treatment • Develop new, less toxic therapies
• Revert metastatic cells to a dormant state
• Identify strategies to prevent or overcome treatment resistance
• Investigate abscopal effects of primary disease treatment
• Determine optimal sequencing of treatments
• Eliminate chemotherapy-induced metastasis
Survivorship • Develop strategies to alleviate treatment toxicities
• Improve quality of life for survivors and/or caregivers
Metastatic cancer is cancer that has spread from its original location to another place in the body, representing what are known as stage III and stage IV cancer diagnoses. While recent research has revealed that there is a genetic basis for susceptibility or resistance to metastasis, more research is needed to develop a comprehensive understanding of this complex process.
Applications submitted under any PRCRP topic area, including the Metastatic Cancers topic area, may not address or include research focused on melanoma or cancers that originate in the breast, kidney, lung, pancreas, prostate, or ovaries, or rare cancers (excluding relevant subtypes of the FY26 PRCRP Topic Areas) as part of the research study; such applications will be administratively withdrawn.
FY26 PRCRP Military Health Focus Areas
It is central to the Vision and Mission of the PRCRP that applications are related to military health and mission readiness, and investigators must demonstrate how the proposed research will decrease the burden of cancer on Service Members, their dependents, Veterans and other military beneficiaries (i.e., Retirees and their Family members).
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 13
In addition to addressing at least one of the required FY26 PRCRP Topic Areas and FY26 Strategic Goals, applications for the FY26 Impact Award must define how the research is relevant to Service Members and their Families by addressing at least one of the FY26 PRCRP Military Health Focus Areas listed below.
FY26 PRCRP Military Health Focus Areas:
• Environmental exposure risk factors associated with cancer
○ Environmental and/or occupational risk factors should be relevant to activities specific to the military, such as assigned duties or deployments that may lead to exposures to potential carcinogens (ionizing radiation, chemicals, infectious agents, etc.). For more information on military-related exposures and risk factors for cancer, applicants should refer to Exposure-Related Health Concerns at https://www.publichealth.va.gov/exposures/health-concerns.asp or to the PRCRP website (https://cdmrp.health.mil/prcrp/default).
• Mission Readiness and Gaps in Cancer Research
○ Gaps in cancer prevention, early detection/diagnosis, prognosis, and/or treatment that may impact mission readiness and the health and well-being of military members, Veterans, their beneficiaries and the general public.
○ Gaps in quality of life and/or survivorship that may impact mission readiness and the health and well-being of military members, Veterans, their beneficiaries, and the general public.
Mission readiness under the FY26 PRCRP Military Health Focus Areas refers to the impact of cancer on the Service Member. Decreasing the impact of cancer on Service Members and/or their Families protects the overall military missions. Some examples of relevant research to decrease the impact on mission readiness may include, but are not limited to:
• Studies on the improvement in survival while minimizing effects that would allow a Service Member to return to full duty;
• Treatments to minimize a cancer patient’s (either a Service Member’s or their Family member’s) time in the hospital, thus maximizing the time the Service Member is on duty;
• Effective ways to minimize cancer relapse for Service Members or their Families; and
• Research into improvements in cancer detection that would lead to earlier diagnosis, thus allowing for improved treatment of the Service Member and early return to duty.
For more information on military health and cancer:
• PRCRP (https://cdmrp.health.mil/prcrp/default)
• MHS (https://www.health.mil)
• U.S. Department of Veterans Affairs (VA) (https://www.va.gov/)
The PRCRP strongly encourages investigators to collaborate, integrate, and/or align their research projects with DOW and/or VA research laboratories and programs (Refer to GAI Appendix 10).
3.1. Intent of the Impact Award
The FY26 PRCRP Impact Award supports high-impact and translational research that can accelerate promising findings toward clinical applicability. The intent of the Impact Award https://www.publichealth.va.gov/exposures/health-concerns.asp https://cdmrp.health.mil/prcrp/default https://cdmrp.health.mil/prcrp/default https://www.health.mil/ https://www.va.gov/ https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#DOW_AND_VA_WEBSITES:~:text=APPENDIX%2010.%0ADOW%20AND%20VA%20WEBSITES
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 14 mechanism is to fund mature research projects that specifically focus on critical scientific or clinical cancer issues, which have the potential to make a major near-term impact on at least one of the FY26 PRCRP Topic Areas and in at least one of the FY26 PRCRP Strategic Goals as outlined in the FY26 PRCRP portfolio categories.
The Impact Award is not intended for basic research. Applicants performing basic research in innovative, high-risk/high-gain studies should apply to the FY26PRCRP Idea Award (HT942526PRCRPIA).
3.1.1. Key Elements for the IPA
• Impact: Research supported by the Impact Award (IPA) will demonstrate the potential to accelerate promising findings and have a major impact in the near term on an area of paramount importance in cancer. The proposed study should demonstrate potential to improve patient outcomes in at least one of the FY26 PRCRP Topic Areas and in at least one of the FY26 PRCRP Strategic Goals as outlined in the FY26 PRCRP portfolio categories. Proposed projects may include translational or clinical research, including clinical trials. The potential impact of the proposed research must be near-term, and while it fundamentally may include the next step in research, it must be significant and go beyond an incremental advance. The applicant must articulate the potential impact the proposed work will have on cancer research and/or patient outcomes.
• Preliminary Data: The Impact Award is intended to support transformative investigations that leapfrog the cancer research field forward by utilizing previous research findings.
Applications must include preliminary data to support feasibility of the study. Any unpublished, preliminary data provided should originate from the laboratory of the PI or a member of the research team.
• Continuity of Research: The Impact Award is intended to support established projects that have moved beyond the realm of basic research.
• Data Evaluation: The proposed research should be rigorously designed to include a statistical plan and data analysis plan. The Impact Award is intended to have near-term relevance to patients; therefore, the statistical plan and data analysis plan should represent how significant the results and/or outcomes may be on patient outcomes.
• Military Relevance: Relevance to the health care needs of Service Members, Veterans and their Families is a key feature of this award. Investigators are encouraged to consider the following characteristics as examples of how a project may demonstrate relevance to military health:
○ Explanation of how the project addresses an aspect of the target disease that has direct relevance to the health of Service Members, Veterans and their Families.
○ Description of how the knowledge, information, products or technologies gained from the proposed research could be implemented in a dual-use capacity to benefit the civilian population and also address a military need.
○ Use of military or Veteran populations, samples or datasets in the proposed research, if appropriate.
○ Collaboration with DOW or VA investigators or consultants. A list of websites that may be useful in identifying additional information about ongoing DOW and VA areas of research interest or potential opportunities for collaboration within the FY26 PRCRP Topic Areas can be found in Appendix 10 of the GAI.
https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#DOW_AND_VA_WEBSITES:~:text=APPENDIX%2010.%0ADOW%20AND%20VA%20WEBSITES
Basic Information | Eligibility | Program Description | Application Contents and Format | Submission Requirements
Application Review Information | Federal Award Notices | Post-Award Requirements | Other Information
FY26 Peer Reviewed Cancer Impact Award 15
• Clinical Trial, if applicable: The proposed clinical trial should begin no later than 12 months after the award date. Investigational New Drug/Investigational Device Exemption application submission plans must be submitted to the program office within 60 days of the award. The application should demonstrate the documented availability of and access to the drug/compound, device and/or other materials needed, as appropriate, for the proposed duration of the study.
• Partnering PI Option: The Impact Award includes an option for more than one PI. One PI will be identified as the Initiating PI and will be responsible for the majority of the administrative tasks associated with application submission. The other PI will be identified as a Partnering PI. Both PIs should contribute significantly to the development and execution of the proposed research project. If recommended for funding, each PI will be named on separate awards to the recipient organization(s). Each award will be subject to separate reporting, regulatory and administrative requirements. For individual submission requirements for the Initiating and Partnering PI, refer to Section 5.3, Submission Instructions.
3.1.2. Other Important Considerations for the IPA
All projects should adhere to a core set of standards for rigorous study design and reporting to maximize the reproducibility and translational potential of clinical and preclinical research, such as those described in the STROBE, CONSORT, SPIRIT and ARRIVE 2.0 guidelines.
Applications from investigators within the DOW and applications involving multidisciplinary collaborations among academia, industry, the DOW, the VA and other federal government agencies are highly encouraged. These relationships can leverage knowledge, infrastructure and access to unique clinical populations that the collaborators bring to the research effort, ultimately advancing research that is of significance to Service Members, Veterans, their Families and the American Public. If the proposed research relies on access to unique resources or databases, the application must describe the access at the time of submission and include a plan for maintaining access as needed throughout the proposed research.
In accordance with the National Defense Authorization Act for Fiscal Year 2026, Section 732, CDMRP does not support the conduct of painful research (U.S. Department of Agriculture pain category D or E) involving domestic cats or dogs, except for studies relating to military or service animals.
Clinical trials are allowed within this funding opportunity.
For the purposes of this funding opportunity, research that meets the definition of a clinical trial is distinct from clinical research.
A congressionally mandated Metastatic Cancer Task Force was formed with the purpose of identifying ways to help accelerate clinical and translational research aimed at extending the lives of advanced state and recurrent patients. As a member of the Metastatic Cancer Task Force, CDMRP encourages applicants to review the recommendations and submit research ideas to address these recommendations provided they are within the limitations of this funding opportunity and fit within the FY26 PRCRP priorities.
3.2. Funding Instrument
The funding instrument for awards made under the program announcement will be grants (31
USC 6304).
https://www.strobe-statement.org/ https://www.nature.com/articles/s41591-025-03635-5#:~:text=SPIRIT%20and%20CONSORT%20are%20evidence,relevant%20empirical%20evidence%20where%20possible https://www.nature.com/articles/s41591-025-03668-w?fromPaywallRec=false https://arriveguidelines.org/arrive-guidelines https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Definition_List:~:text=or%20hardware%20procurement.-,Clinical%20Trial%3A,-As%20defined%20in https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Definition_List:~:text=considered%20clinical%20trials.-,Clinical%20Research%3A,-For%20the%20purposes https://health.mil/Reference-Center/Congressional-Testimonies/2018/05/03/Metastatic-Cancer-Research
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3.3. Funding Details
Period of Performance: The maximum period of performance is 3 years.
Application Submissions with a Single PI:
Cost Cap: The application’s total costs budgeted for the entire period of performance should not exceed $1.5M. If indirect cost rates have been negotiated, indirect costs are to be budgeted in accordance with the organization’s negotiated rate. Collaborating organizations should budget associated indirect costs in accordance with each organization’s negotiated rate.
Application Submissions with the Partnering PI Option:
Cost Cap: The combined total costs budgeted for the entire period of performance in the applications of the Initiating PI and the Partnering PI should not exceed $2.0M. If indirect cost rates have been negotiated, indirect costs are to be budgeted in accordance with the organization’s negotiated rate. Collaborating organizations should budget associated indirect costs in accordance with each organization’s negotiated rate.
A separate award will be made to each PI’s organization.
The PIs are expected to be partners in the research, and direct cost funding should be divided accordingly unless otherwise warranted and clearly justified.
For Both Options Within this Award Mechanism:
All direct and indirect costs of any subaward or contract must be included in the direct costs of the primary award.
The applicant may request the entire maximum funding amount for a project that may have a period of performance less than the maximum 3 years.
The appropriateness of the budget for the proposed research will be assessed during peer review.
Direct Cost Restrictions: For this award mechanism, direct costs:
May be requested for (not all-inclusive):
• Costs for one investigator to travel to two scientific/technical meeting per year. The intent of travel to scientific/technical meetings should be to present project information or disseminate project results from the PRCRP Impact Award.
• Travel in support of multi-institutional collaborations.
Must not be requested for:
• Costs for travel to scientific/technical meetings beyond the limits stated above.
https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=Period%20of%20Performance%3A%20The%20time%20interval%20between%20the%20start%20of%20a%20federal%20award%20and%20the%20planned%20end%20date.
https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=in%20project%20activities.-,Cost%20Cap%3A,-The%20maximum%20cost https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=in%20project%20activities.-,Cost%20Cap%3A,-The%20maximum%20cost
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4. Application Contents and Format
4.1. Application Overview
Application submission is a two-step process requiring both a pre-application submitted via the Electronic Biomedical Research Application Portal (eBRAP) and a full application submitted through eBRAP or Grants.gov. Depending on the submission portal, certain aspects of the application will differ.
Intramural DOW organizations submitting a full application should follow instructions for submission through eBRAP.
Extramural organizations submitting a full application must follow instructions for submission through Grants.gov.
4.2. Pre-Application Components
The Initiating PI must submit the following pre-application components.
Upload documents as individual PDF files unless otherwise noted. Files must comply with the formatting guidelines listed in the GAI.
• Preproposal Narrative (two-page limit):
The Preproposal Narrative should include the following:
○ Research Idea: State the FY26 PRCRP Topic Area(s) and FY26 PRCRP Strategic Goal the application will address. Describe the rationale and hypothesis and how these support the study’s objectives and specific aims. Demonstrate how the research is based on strong preliminary data.
○ Research Strategy: Describe the methodology and experimental design and explain how they support the project’s goals. If the application proposes a clinical trial, briefly describe the study including the intervention, study population, primary endpoints and phase of the trial. Describe the strategy to initiate the clinical study within the first year of the award. (Refer to the definition of a clinical trial in Section 3.1.2.).
○ Impact: Describe the potential near-term impact of the proposed research on at least one of the FY26 PRCRP Topic Areas.
○ Military Relevance: Explain how the proposed research will lead to promising outcomes for one or more of the selected FY26 PRCRP Military Health Focus Area(s).
• Pre-Application Supporting Documentation: The items to be included as supporting documentation for the pre-application must be uploaded as individual files and are limited to the following:
○ References Cited (one-page limit): List the references cited (including URLs if available) in the Preproposal Narrative using a standard reference format that includes the full citation (i.e., author[s], year published, reference title, and reference source, including volume, chapter, page numbers, and publisher, as appropriate).
○ List of Abbreviations, Acronyms and Symbols: Provide a list of abbreviations, acronyms and symbols used in the Preproposal Narrative.
https://ebrap.org/eBRAP/public/index.htm https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#Appendix2:~:text=APPENDIX%202.%0AFORMATTING%20GUIDELINES https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Full_App_Submission_Grants:~:text=IV.%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%20FULL%20APPLICATION%20SUBMISSION%20THROUGH%20GRANTS.GOV https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Full_App_Submission_eBRAP:~:text=V.%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%20FULL%20APPLICATION%20SUBMISSION%20THROUGH%20eBRAP
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○ Key Personnel Biographical Sketches: All biographical sketches should be uploaded as a single combined file. Biographical sketches should be used to demonstrate background and expertise through education, positions, publications, and previous work accomplished.
4.3. Full Application Components
Applicants must receive an invitation to submit a full application. Uninvited full application submissions will be rejected.
Partnering PI Option: The CDMRP requires separate full application package submissions for the Initiating PI and each Partnering PI, even if the PIs are located within the same organization.
The application submission process for the Partnering PI uses an abbreviated full application package.
4.3.1. Full Application Components for the PI or Initiating PI
Each application submission must include the completed full application package for this program announcement. See Appendix 1 for a checklist of the full application components.
(a) SF424 Research & Related Application for Federal Assistance Form (Grants.gov submissions only):
IMPORTANT: When completing the SF424 R&R, enter the eBRAP log number assigned during pre-application submission into Block 4a – Federal Identifier.
(b) Attachments:
Each attachment of the full application components must be uploaded as an individual file in the format specified and in accordance with the formatting guidelines in the GAI.
○ Attachment 1: Project Narrative (10-page limit): Upload as “ProjectNarrative.pdf”.
Describe the proposed project in detail using the outline below. Inclusion of preliminary data is required.
− Background: Describe how the proposed project addresses a FY26 PRCRP Topic Area and corresponding FY26 PRCRP Strategic Goal. Briefly state how the project addresses an FY26 PRCRP Military Health Focus Area(s). Applicants must provide additional detail about the Military Health focus area in Attachment 6.
– Hypothesis or Objective: State the hypothesis or the objective.
– Specific Aims: State the specific aims of the study.
– Research Strategy:
▪ Describe the proposed study in sufficient detail to evaluate its appropriateness and feasibility to test the hypothesis and reach the final objective.
▪ Include preliminary data and reconcile it with objectives of the research proposed. Demonstrate how the research is based on strong preliminary data and/or previous clinical and/or translational research outcomes. The application must include preliminary data such as published or unpublished results from the laboratory and/or clinic of the PI(s) or named collaborators.
https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=APPENDIX%202.%0AFORMATTING%20GUIDELINES https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=(a)%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%C2%A0%20SF424%20(R%26R)%20%E2%80%93%20Application%20for%20Federal%20Assistance%20Form https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=%C2%B7-,Project%20Narrative%3A,-Attach%20as%20%E2%80%9CProjectNarrative https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Content_Form_Full_App_Submission:~:text=eBRAP%20User%20Name-,Biographical%20Sketch,-%3A%20This%20file
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▪ Provide a well-developed, well-integrated and detailed research plan that supports the translational feasibility and promise of the approach. The application must outline details regarding translation feasibility for clinical studies in Attachment 8.
▪ Describe how the application designs all proposed animal studies to achieve the objectives, including the choice of model and endpoints or outcome measures, if applicable. Application must describe additional details on animal studies in Attachment 9.
▪ Demonstrate the availability of tissue, data or human subjects for the collection of samples, if applicable. If the proposed research will use human subjects or anatomical samples, include a plan for the recruitment of subjects or the acquisition of samples and document the experience of the PI(s) and/or key collaborators in recruiting human subjects for similar projects.
▪ If the application proposes a clinical trial, briefly describe the study including the intervention, study population, primary endpoints and phase of the trial. Describe the strategy to initiate the clinical study within the first year of the award. (Refer to the definition of a clinical trial in Section 3.1.2.) The application must outline additional details regarding the Clinical Trial Strategy in Attachment 8.
▪ Describe potential problems and potential pitfalls and address alternative approaches.
▪ Describe how data will be reported and how it will be assured that the documentation will support a regulatory filing with the U.S. Food and Drug Administration (FDA), if applicable.
▪ Statistical Plan and Data Analysis for all applications must be submitted in Attachment 10.
▪ Consult appropriate guidelines to ensure relevant aspects of rigorous and reproducible research are adequately planned for and, ultimately, reported.
○ Attachment 2: Supporting Documentation: Combine and upload as a single file named “Support.pdf”.
There are no page limits for these components unless otherwise noted. Include only components described below; inclusion of items not requested or viewed as an extension of the Project Narrative will result in the removal of those items or may result in administrative withdrawal of the application.
References Cited: List the references cited in the Project Narrative using a standard reference format (include URLs, if available).
List of Abbreviations, Acronyms and Symbols: Provide a list of abbreviations, acronyms and symbols.
Facilities, Existing Equipment and Other Resources: Describe the facilities and equipment available for performance of the proposed project; include any additional facilities or equipment proposed for acquisition at no cost to the award. Indicate whether government-furnished facilities or equipment are proposed for use. If so, reference the original or present government award under which the facilities or equipment items are now accountable. There is not a standardized form for this information.
https://ebrap.org/eBRAP/public/gai.htm?version=CD26_01#_Recipient_Qualification_Restriction_Info:~:text=%C2%B7-,Supporting%20Documentation%3A,-Combine%20and%20attach
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Publications and/or Patents: Include a list of relevant publication URLs and/or patent abstracts. If articles are not publicly available, then copies of up to five published manuscripts may be included in Attachment 2. Extra items will not be reviewed.
Letters of Support: Provide individual letters signed by collaborating individuals and/or organizational officials demonstrating that the PI has the support and resources necessary for the proposed work. Letters from the PI’s Department Chair, or appropriate organization official, should also confirm that the PI(s) meet eligibility criteria. If applicable, provide a letter of support, signed by the lowest-ranking person with approval authority, confirming participation of intramural DOW collaborator(s) and/or access to military populations, databases or DOW resources.
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