Promoting research partnerships 

to improve veterans’ health

NAVREF News Center

  • 31 May 2018 12:30 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriation provides $125 million (M) to the Department of Defense Psychological Health/Traumatic Brain Injury Research Program (PH/TBIRP) to support critical PH- and TBI-related research and development efforts to benefit Service members, Veterans, and other beneficiaries of the military health system.  As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency, J9 Research and Development Directorate manages the Defense Health Program (DHP) Research, Development, Test, and Evaluation (RDT&E) appropriation.  The managing agent for the anticipated Program Announcement/Funding Opportunity is the Congressionally Directed Medical Research Programs (CDMRP) at the U.S. Army Medical Research and Materiel Command (USAMRMC).  The CDMRP provides PH/TBIRP execution management support for DHP core research program areas, including the Joint Program Committee 6/ Combat Casualty Care Research Program (JPC-6/CCCRP).  JPC-6/CCCRP provides strategic oversight for the PH/TBI funds associated with this funding Program Announcement.  The Defense Health Agency is working in collaboration with the U.S. Department of Veterans Affairs (VA) and other Federal agencies on research efforts to improve the lives of Service members and Veterans affected by traumatic brain injury, posttraumatic stress disorder, and other mental health conditions.

    The PH/TBIRP is providing the information in this pre-announcement to allow investigators time to plan and develop applications.  The FY18 PH/TBIRP Program Announcement and General Application Instructions for the following award mechanism is anticipated to be posted on the Grants.gov website in July 2018.  Pre-application and application deadlines will be available when the Program Announcement is released.  This pre-announcement should not be construed as an obligation by the Government.

    http://cdmrp.army.mil/pubs/press/2018/18phtbipreann_limbic

    FY18 PHTBIRP Joint DoD and VA Long-term Impact of Military-relevant Brain Injury Consortium (LIMBIC)

    • Independent investigators at all academic levels (or equivalent)
    • Preproposal is required; application submission is by invitation only.
    • The objective of this funding opportunity is to support a single consortium to study a large cohort of TBI subjects to include Service members and Veterans.

    Required Focus Areas (each must be addressed in application)

    • Identification of differences in long-term neurological outcomes from blast-related vs. impact only TBI.
    • Identification of pathophysiological and biomarker signatures that may be predictive of long-term outcomes and healthcare utilization.
    • Analysis of existing biorepositories and/or biospecimens from a longitudinal cohort to identify novel biomarkers for chronic TBI.
    • Stratification and characterization of TBI subgroups based on recovery and neurodegeneration.
    • Analysis of existing DoD and VA TBI databases for correlations and associations of TBI comorbidities.

    Secondary Focus Areas (in no particular order)

    • Understanding the economic burden of TBI. 
    • Identification of potential differences between single vs. multiple TBI history on outcomes.
    • Identification of potential differences in long-term neurological outcomes from blast-related vs. impact-only TBI.
    • Identification of potential differences between individuals with exposure to repetitive low-level blast and those without.
    • Identification and investigation of neurodegeneration and TBI-associated comorbidities.
    • Evaluation of chronic mTBI biomarker profile(s) over time and injury severity.
    • Identification of potential variations in long-term outcomes in deployment-related vs nondeployment-related TBI.
    • Determination of whether a history of TBI is associated with lower performance metrics.
    • Maximum allowable costs (direct and indirect) are $25M via the DoD.
    • Up to an additional $5M per year for 5 years will be provided by the VA to VA sites, depending on availability of funds.
      • To be eligible for VA funding at a specific research site, a participating investigator must have a VA-paid appointment of at least five-eighths at the time of pre-application submission, unless a previous eligibility waiver has been granted.
    • Maximum period of performance is 5 years.

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline. All applications must conform to the final Program Announcements and General Application Instructions that will be available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP and other USAMRMC extramural funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

    Submission deadlines are not available until the Program Announcements are released.  For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the PH/TBIRP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Public Affairs
    301-619-9783
    usarmy.detrick.medcom-cdmrp.mbx.cdmrp-public-affairs@mail.mil


  • 30 May 2018 1:11 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriation provides $30 million (M) to the Department of Defense Spinal Cord Injury Research Program (SCIRP) to support innovative, high-impact spinal cord injury research. As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency, J9 Research and Development Directorate manages the Defense Health Program (DHP) Research, Development, Test, and Evaluation (RDT&E) appropriation. The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP) at the U.S. Army Medical Research and Materiel Command (USAMRMC).

    FY18 SCIRP Program Announcements and General Application Instructions for the following award mechanisms are posted on the Grants.gov website.

     

    For FY18, SCIRP encourages applications that address the critical needs of SCI research and patient care in one or more of the following FY18 Focus Areas:

    *             Neuroprotection

    *             Biomarkers

    *             Bladder and bowel dysfunction and neuropathic pain

    *             Psychosocial issues relevant to SCI in individuals with SCI and their caregivers

    *             Rehabilitation and regeneration

    http://cdmrp.army.mil/funding/scirp

     

    Clinical Trial Award – Preproposal due July 9, 2018

    Independent investigators at all academic levels (or equivalent)

    *         Preproposal is required; application submission is by invitation only.

    *             Fund Phase 0, I, or II clinical trials with the potential to have a major impact on treatment or management of spinal cord injury (SCI) and its consequences.

    *             Preclinical data required for all clinical trial applications.

    *         Maximum funding of $3M for direct costs (plus indirect costs)

    *             Maximum period of performance is 4 years

    Investigator-Initiated Research Award – Preproposal due July 9, 2018

    Independent investigators at all academic levels (or equivalent)

    *         Preproposal is required; application submission is by invitation only.

    *         Fund SCI-related research that has the potential to make an important contribution to SCI research and/or patient care.

    *         Preliminary data required.

    *         Clinical trials not allowed.

    *         Maximum funding of $500,000 for direct costs (plus indirect costs)

    *         Maximum period of performance is 3 years.

    Qualitative Research Award – Preproposal due July 9, 2018

    Independent investigators at all academic levels (or equivalent)

    *         Preproposal is required; application submission is by invitation only.

    *         Fund qualitative research on military Service members and Veterans in the years following SCI.

    *         Qualitative research is defined as a form of social inquiry that focuses on understanding the way that people interpret and make sense of their experiences and the world in which they live (i.e., seek to understand the human experience).

    *         Preliminary data encouraged, but not required.

    *         Clinical trials not allowed.

    *         Maximum funding of $500,000 for direct costs (plus indirect costs)

    *         Maximum period of performance is 3 years

    Translational Research Award – Preproposal due July 9, 2018

    Independent investigators at all academic levels (or equivalent)

    *         Preproposal is required; application submission is by invitation only.

    *         Fund studies that accelerate the movement of promising ideas in SCI research into clinical applications.

    *         Preliminary data required

    *         The SCIRP TRA may include a pilot clinical trial as part of the proposed research where limited clinical testing of a novel intervention or device is necessary to inform the next step in the continuum of translational research.

    *         Maximum funding of $1.25M for direct costs (plus indirect costs)

    *         Maximum period of performance is 3 years

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline. All applications must conform to the final Program Announcements and General Application Instructions available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP and other USAMRMC extramural funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

    For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the SCIRP or other CDMRP-administered programs, please visit the CDMRP website   (http://cdmrp.army.mil <http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Help Desk

    301-682-5507

    help@eBrap.org


  • 30 May 2018 1:11 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriation provides $10 million (M) to the Department of Defense Orthotics and Prosthetics Outcomes Research Program (OPORP) to support research that evaluates the comparative effectiveness of orthotic and prosthetic clinical interventions using patient-centric outcomes for Service members and Veterans who have undergone limb amputation.  As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency J9, Research and Development Directorate, manages the Defense Health Program Research, Development, Test, and Evaluation appropriation.  The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP) at the U.S. Army Medical Research and Materiel Command (USAMRMC).

    The OPORP is providing the information in this pre-announcement to allow investigators time to plan and develop applications.  FY18 OPORP Program Announcements and General Application Instructions for the following award mechanisms are anticipated to be posted on the Grants.gov website in June 2018.  Pre-application and application deadlines will be available when the Program Announcements are released.  This pre-announcement should not be construed as an obligation by the government.

    OPORP awards are focused on outcomes-based best practices through analysis of the merits of prosthetic and orthotic device options currently available, not on the development of new or the improvement of existing technology.  The intent of the awards is to generate clinically useful evidence that will enhance and optimize patient outcomes.

    Focus Areas:  The OPORP will only consider applications that specifically address the critical needs of the Orthotics and Prosthetics Outcomes research community in one or more of the FY18 Focus Areas.  The OPORP will solicit research applications that address at least one of the following FY18 Focus Areas:

    • Orthotic or Prosthetic Device Form:  Understand patient outcomes through the analysis and characterization of variables related to the form of currently available clinical options such as device size, shape, material, and/or configurations.
    • Orthotic or Prosthetic Device Fit:  Understand patient outcomes related to human-device interface and component connection through the analysis of variables in currently available clinical options that facilitate fit-related metrics such as comfort and/or usability.
    • Orthotic or Prosthetic Device Function:  Understand patient outcomes through the analysis of variables related to currently available device function such as device control, sensors, and passive or active response with respect to activities of daily living and other real-world activities.

    http://cdmrp.army.mil/pubs/press/2018/18oporppreann

    Clinical Research Award

    • Independent investigators at all academic levels (or equivalent)
    • Funding Level 1 may support pilot research that has the potential to make significant advancement towards clinical translation. Preliminary data are allowed but not required.
    • Funding Level 2 is supported by preliminary data and has the potential to make significant impact towards clinical translation.
    • Animal studies are not allowed.
    • Clinical trials are not allowed.
    • Funding Level 1:
      • Maximum funding of $350,000 for total costs.
      • Maximum period of performance is years.
    • Funding Level 2:
      • Maximum funding of $1.5M for total costs.
      • Maximum period of performance is years.

    Clinical Trial Award

    Independent investigators at all academic levels (or equivalent

    • Funding Level 1 may support pilot clinical trials for exploratory studies involving limited human exposure with the potential to make significant advancement towards clinical translation. Preliminary data are allowed but not required.
    • Funding Level 2 supports rapid implementation of clinical trials with the potential to make significant impacts on improving the health and well-being of Service members, Veterans, and other individuals with limb deficit.
    • Preclinical research is not allowed.
    • Funding Level 1:
      • Maximum funding of $350,000 for total costs.
      • Maximum period of performance is years.
    • Funding Level 2:
      • Maximum funding of $2.5M for total costs.
      • Maximum period of performance is years.

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline.  All applications must conform to the final Program Announcements and General Application Instructions that will be available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP and other USAMRMC extramural funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

    Submission deadlines are not available until the Program Announcements are released.  For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the OPORP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Public Affairs
    301-619-9783
    usarmy.detrick.medcom-cdmrp.mbx.cdmrp-public-affairs@mail.mil


  • 30 May 2018 1:10 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriation provides $125 million (M) to the Department of Defense Psychological Health/Traumatic Brain Injury Research Program (PH/TBIRP) to support critical traumatic brain injury (TBI)- and psychological health (PH)-related research and development efforts to benefit Service members, Veterans, and other beneficiaries of the military health system.  As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency (DHA) J9, Research and Development Directorate, manages the Defense Health Program’s Research, Development, Test, and Evaluation appropriation.  The U.S. Army Medical Research and Materiel Command (USAMRMC) Congressionally Directed Medical Research Programs (CDMRP) provides execution management support for DHA research program areas, including the Joint Program Committee-8/Clinical and Rehabilitative Medicine Research Program (JPC-8/CRMRP).  The managing agent for this Program Announcement is the CDMRP with strategic oversight from the JPC-8/CRMRP.

    The PH/TBIRP is providing the information in this pre-announcement to allow investigators time to plan and develop applications.  FY18/19 PH/TBIRP Complex TBI Rehabilitation Research (CTRR) Program Announcements and General Application Instructions for the following award mechanisms are anticipated to be posted on the Grants.gov website in June 2018.  Pre-application and application deadlines will be available when the Program Announcements are released.  This pre-announcement should not be construed as an obligation by the government.

    The FY18/19 PH/TBIRP will solicit research applications for the following CTRR Focus Areas:

    • Mechanisms of Recovery following isolated or cumulative TBI(s) in Service member-relevant injuries:  Clinical research in human subjects that measures physiologic responses to cognitive rehabilitation with the intent to better understand how rehabilitation remediates cognitive or sensorimotor deficits, and ultimately to optimize rehabilitation prescription.

    Ecological Assessment:  Investigation of outcome measures focused on military-specific tasks that inform return-to-duty/participation decisions following rehabilitation in patients with TBI. 

    Cognitive Rehabilitation:  Evaluation of rehabilitation intervention effectiveness in remediating cognitive impairments and functional limitations after TBI. 

    http://cdmrp.army.mil/pubs/press/2018/18phtbipreann

    CTRR – Clinical Research Award (CTRR-CRA)

    Independent investigators at all academic levels (or equivalent)

    ·      Supports applied and translational research to advance the development of knowledge and materiel products for rehabilitation and restoration of function following TBI.

    ·      Supported research can include preclinical studies using human subjects or samples and observational or mechanistic clinical research studies.

    ·      Clinical trials are not allowed.

    ·      Preclinical research using animals is not allowed.

    ·      Must address one or more FY18/19 PH/TBIRP CTRR Focus Areas.

    Preproposal is required; application submission is by invitation only.

    ·      Maximum funding of $2.0M for total costs (direct plus indirect costs).

    • ·      Maximum period of performance is years.

    CTRR – Clinical Trial Award (CTRR-CTA)

    Independent investigators at all academic levels (or equivalent)

    ·      Supports small, single-site, Phase I clinical trials to advance the development of knowledge and materiel products for rehabilitation and restoration of function following TBI in Service members, Veterans, and other individuals.

    ·      Interventions should be limited, existing, and manualized.  Studies may include seeking to optimize dosing in existing interventions.

    ·      Preclinical studies are not allowed.

    ·      Must address one or more FY18/19 PH/TBIRP CTRR Focus Areas.

    Preproposal is required; application submission is by invitation only.

    ·      Maximum funding of $1.5M for total costs (direct plus indirect costs).

    • ·      Maximum period of performance is 2 years.

    CTRR – Clinical Trial Development Award (CTRR-CTDA)

    Independent investigators at all academic levels (or equivalent)

    ·      Supports design and development of the necessary research resources that will serve as a foundation for investigator-initiated clinical trials as described above under CTRR – Clinical Trial Award (CTRR-CTA)

    ·      Final supporting studies required for approval of Investigational New Drug Applications/Investigational Device Exemptions (IND/IDE-enabling) are allowed.  Other preclinical studies are not allowed. 

    ·      Clinical trials are not allowed within the period of performance of the CTRR-CTDA.

    ·      Must address one or more FY18/19 PH/TBIRP CTRR Focus Areas.

    Preproposal is required; application submission is by invitation only.

    ·     Maximum funding of $200,000 for total costs (direct plus indirect costs).

    • ·      Maximum period of performance is 1 year.

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline. All applications must conform to the final Program Announcements and General Application Instructions that will be available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP and other USAMRMC extramural funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

    Submission deadlines are not available until the Program Announcements are released.  For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the PH/TBIRP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Public Affairs
    301-619-9783
    usarmy.detrick.medcom-cdmrp.mbx.cdmrp-public-affairs@mail.mil


  • 22 May 2018 2:09 PM | Hawk Tran (Administrator)

    FY18 ARP Program Announcements and General Application Instructions for the following award mechanisms are posted on Grants.gov. 

    As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency (DHA) J9, Research and Development Directorate manages the Defense Health Program (DHP) Research, Development, Test, and Evaluation (RDT&E) appropriation.  The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP).

    http://cdmrp.army.mil/funding/arp

    Clinical Trial Award – Preapplication due July 5, 2018

    • Investigators at or above the level of Associate Professor (or equivalent), or
    • Early-Career Investigator Partnering PI Option: Investigators at or above the level of Associate Professor (or equivalent) may collaborate on a single application with a young investigator (at the level of postdoctoral fellow up to early-career independent faculty) who meets the following criteria at the application submission deadline date:
    • Must be in a current postdoctoral training position or have completed postdoctoral training by the  application deadline
    • Is no more than 7 years from the receipt of a terminal degree
    • Has the freedom to commit at least 50% time to the project
    • Supports research with the potential to have a major impact on the treatment and/or management of ASD.
    • Applications in the following areas are strongly encouraged:
      • Behavioral cognitive, and other non-pharmacological therapies.
      • Pharmacological, genetic, and other biological treatments in ASD.
      • Dissemination/Implementation of clinically validated interventions.
      • Therapies to alleviate conditions co-occurring with ASD (i.e., sleep disturbances, gastrointestinal issues, inflammation, aggression, depression, anxiety, attention deficit, seizures).
      • Interventions promoting success in key transitions to adulthood for individuals living with ASD.
      • Healthcare provider-focused training or tools to improve healthcare delivery for individuals with ASD across the lifespan and the continuum of care (i.e., primary care, urgent/emergent care, and disaster relief).
      • Improve diagnosis across the lifespan.
      • Cultural and socioeconomic factors in treatment efficacy, delivery, and access to services.
    • Preliminary data relevant to the proposed clinical trial are required.
    • Pre-application is required; application submission is by invitation only.
    • Early-Career Investigator Partnering PI Option: Supports the development of young investigators pursuing or wishing to clinical trial.
    • The maximum allowable funding for the entire period of performance is $1,000,000 in direct costs (plus indirect costs)
    • The maximum period of performance is years
    • Early-Career Investigator Partnering PI Option:
    • Maximum funding of $1,155,000 in direct costs (plus indirect costs)
    • Maximum period of performance is years

    Clinical Translational Award – Preapplication is due July 5, 2018

    • Investigators at or above the level of Assistant Professor (or equivalent)
    • Supports early-phase, proof-of-principle translational studies with the potential to have a major impact on the treatment and/or management of autism spectrum disorder (ASD).
    • Applications in the following areas are strongly encouraged:
      • Behavioral cognitive, and other non-pharmacological therapies.
      • Pharmacological, genetic, and other biological treatments in ASD.
      • Dissemination/Implementation of clinically validated interventions.
      • Therapies to alleviate conditions co-occurring with ASD (i.e., sleep disturbances, gastrointestinal issues, inflammation, aggression, depression, anxiety, attention deficit, seizures).
      • Interventions promoting success in key transitions to adulthood for individuals living with ASD.
      • Healthcare provider-focused training or tools to improve healthcare delivery for individuals with ASD across the lifespan and the continuum of care (i.e., primary care, urgent/emergent care, and disaster relief).
      • Improve diagnosis across the lifespan.
      • Cultural and socioeconomic factors in treatment efficacy, delivery, and access to services.
    • Preliminary data relevant to the proposed project are required.
    • Pre-application is required; application submission is by invitation only.
    • The maximum allowable funding for the entire period of performance is $500,000 in direct costs (plus indirect costs)
    • The maximum period of performance is 3 years

    Idea Development Award – Preapplication is due July 5, 2018

    • Investigators at or above the level of Assistant Professor (or equivalent) or
    • Multiple PI Option: 
      Up to two investigators may collaborate on a single application, each of whom will be recognized as a Principal Investigator and receive a separate award. 
    • Supports the development of innovative, high-impact ideas that advance the understanding of ASD and ultimately lead to improved outcomes.
    • Applications in the following areas are strongly encouraged:
    •  Preliminary Behavioral cognitive, and other non-pharmacological therapies.
    • Pharmacological, genetic, and other biological treatments in ASD.
    • Dissemination/Implementation of clinically validated interventions.
    • Therapies to alleviate conditions co-occurring with ASD (i.e., sleep disturbances, gastrointestinal issues, inflammation, aggression, depression, anxiety, attention deficit, seizures).
    • Interventions promoting success in key transitions to adulthood for individuals living with ASD.
    • Healthcare provider-focused training or tools to improve healthcare delivery for individuals with ASD across the lifespan and the continuum of care (i.e., primary care, urgent/emergent care, and disaster relief).
    • Improve diagnosis across the lifespan.
    • Cultural and socioeconomic factors in treatment efficacy, delivery, and access to services.
    • Preliminary data are required.
    • Pre-application is required; application submission is by invitation only.
    • Multiple Principal Investigator (PI) Option: Up to two investigators may collaborate on a single application, each of whom will be recognized as a PI and receive a separate award.
    • The maximum allowable funding for the entire period of performance is $500,000 in direct costs (plus indirect costs)
    • For multiple PIs, the combined funding for all PIs for the entire period of performance may not exceed $500,000 in direct costs (plus indirect costs)
    • The maximum period of performance is 3 years

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline.  All applications must conform to the final Program Announcements and General Application Instructions that are available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

    Applications must be submitted through the federal government’s single-entry portal, Grants.govFor email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org For more information about the ARP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Help Desk

    301-682-5507
    help@eBrap.org


  • 22 May 2018 2:08 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriations Act provides $100 million (M) to the Department of Defense Prostate Cancer Research Program (PCRP) to support innovative, high-impact prostate cancer research. As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency, Research, Development, and Acquisition (DHA RDA) Directorate manages the Defense Health Program (DHP) Research, Development, Test, and Evaluation (RDT&E) appropriation. The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP).

    FY18 PCRP Program Announcements and General Application Instructions for the following award mechanisms are posted on Grants.gov.

    The mission of the PCRP is to fund research that will lead to the elimination of death from prostate cancer and enhance the well-being of Service members, Veterans, and all men experiencing the impact of the disease.  Applications submitted to the FY18 PCRP must addresses one or more of the Overarching Challenges (revised for FY18):

    ·        Develop treatments that improve outcomes for men with lethal prostate cancer

    ·        Reduce lethal prostate cancer in African Americans, Veterans, and other high-risk populations

    ·        Define the biology of lethal prostate cancer to reduce death

    ·        Improve the quality of life for survivors of prostate cancer

    http://cdmrp.army.mil/funding/pcrp

    Impact Award – Preproposal due July 19, 2018

    • Independent investigators at or above the level of Assistant Professor (or equivalent)
    • Preproposal is required; application submission is by invitation only.
    • Supports research projects that have the strong potential to make a major impact on scientific and clinical prostate cancer issues.
    • Must address at least one of the FY18 PCRP Overarching Challenges.
    • The potential impact of the research is expected to be near-term, with the potential to transform the clinical management of prostate cancer within 5 years after the end of the award.
    • Proposed projects may include basic, translational, or clinical research, including small scale clinical trials.
    • Detailed transition plan to describe the pathway for moving the project’s findings to the next phase of development after the award is required.
    • Preliminary data to support feasibility are required.
    • Maximum funding of $750,000 for direct costs (plus indirect costs).
    • Maximum period of performance is years.

    Idea Development Award – Preproposal due July 6, 2018

    • Established Investigators:  Independent investigators at or above the level of Assistant Professor (or equivalent)
    • Or New Investigators:  Investigators that meet the following criteria at the application submission deadline date:
    • Have the freedom to pursue individual aims without formal mentorship
    • Have not previously received a PCRP Health Disparity Research Award and/or Idea Development Award
    • Have completed at least 3 years of postdoctoral training or fellowship and are within 10 years after completion of terminal degree (excluding residency or family medical leave)
    • Preproposal is required; application submission is by invitation only.
    • Supports new ideas that represent innovative, high-risk/high-gain approaches to prostate cancer research and have the potential to make an important contribution to eliminating death and enhancing the well-being of men with prostate cancer.
    • Emphasis is equally placed on Innovation and Impact.
    • Preliminary data are encouraged, but not required.
    • Clinical trials are not allowed.
    • New Investigator Option supports applicants early in their faculty appointments or in the process of developing independent research careers.
    • Maximum funding of $600K for direct costs (plus indirect costs).
    • Maximum period of performance is years.

    Physician Research Award – Letter of Intent due August 16, 2018

    • At the time of application submission, the PI must be either:
    • In the last year of an accredited graduate medical education program, either as a resident or fellow:
    • or
    • Within 3 years of having initiated an appointment as Instructor, Assistant Professor, or equivalent
    • Supports a mentored research experience to prepare physicians with clinical duties for careers in prostate cancer research.
    • PIs must demonstrate a commitment to a career at the forefront of prostate cancer research and clinical practice.
    • PIs must have a designated mentor with an established research program in prostate cancer.
    • Institutions must provide at least 40% protection of PI’s time for research.
    • Projects that focus on basic research are highly encouraged.
    • Must address at least one of the FY18 PCRP Overarching Challenges.
    • Maximum funding of $750,000 for direct costs (plus indirect costs).
    • Maximum period of performance is 4 years.

    Early Investigator Research Award- Letter of Intent due August 16, 2018

    By March 31, 2019

    Postdoctoral Ph.D. or M.D. PIs:

    • Must have successfully defended a doctoral thesis or possess an M.D. degree
    • Have 3 years or less of postdoctoral research experience
    • Supports research opportunities focused on prostate cancer for individuals in the early stages of their careers.
    • PIs must have a designated mentor who is an experienced prostate cancer researcher.
    • Must address at least one of the FY18 PCRP Overarching Challenges.
    • Maximum funding of $200,000 for direct costs (plus indirect costs).
    • Maximum period of performance is 2 years.

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline.  All applications must conform to the final Program Announcements and General Application Instructions that will be available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

    Applications must be submitted through the Federal Government’s single-entry portal, Grants.govFor email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the PCRP or other CDMRP-administered programs, please visit the CDMRP website.

    Point of Contact:

    CDMRP Help Desk

    301-682-5507
    help@eBrap.org


  • 16 May 2018 4:18 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriation provides $5 million (M) to the Department of Defense Lupus Research Program (LRP) to support innovative and impactful research that addresses fundamental issues in lupus.  As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency, J9 Research and Development Directorate manages the Defense Health Program (DHP) Research, Development, Test, and Evaluation (RDT&E) appropriation. The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP) at the U.S. Army Medical Research and Materiel Command (USAMRMC).

    The LRP is providing the information in this pre-announcement to allow investigators time to plan and develop applications.  FY18 LRP Program Announcements and General Application Instructions for the following award mechanisms are anticipated to be posted on the Grants.gov website in June 2018.  Pre-application (Letter of Intent) and application deadlines will be available when the Program Announcements are released.  This pre-announcement should not be construed as an obligation by the government.

    Applications submitted to the FY18 LRP must address at least one of the three Focus Areas listed below:

    •           Understand lupus disease heterogeneity including, but not limited to, progressive stages of lupus disease over time, strategies and technologies to subtype patients, lupus disease mechanisms, biopsychosocial studies, personalized medicine, variation in treatment and its effects on patient outcomes, socioeconomic studies, environmental studies, and epidemiological studies.

    •           Understand how the underlying genetic components and gene environment interactions of lupus disease relate to clinical disease characteristics using functional genomic studies.

    •           Determine the pathobiology of lupus in target human tissues including, but not limited to, imaging studies, genomics of lupus disease in particular tissues, and metabolomics and how understanding the underlying pathobiology will improve quality of life of patients.

    http://cdmrp.army.mil/pubs/press/2018/18lrppreann

    Concept Award

    Investigators at all academic levels

    ·         Submission of a pre-application (Letter of Intent) is required prior to full application submission.

    ·         Supports highly innovative, untested, potentially groundbreaking concepts in lupus research

    ·         Emphasis is on innovation

    ·         Clinical trials are not allowed

    • Preliminary data is not required

    ·         Maximum funding of $150,000 for total costs

    • Maximum period of performance is year

     

    Impact Award

    Investigators at or above Assistant Professor (or equivalent)

    ·         Submission of a pre-application (Letter of Intent) is required prior to full application submission.

    ·         Supports innovative, high-risk/high-reward research

    ·         Emphasis is on impact

    ·         Clinical trials are not allowed

    • Preliminary data is encouraged but not required

    ·         Maximum funding of $525,000 for total costs

    • Maximum period of performance is 3 years

    A pre-application (Letter of Intent) is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline. All applications must conform to the final Program Announcements and General Application Instructions that will be available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP and other USAMRMC extramural funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

     

    Submission deadlines are not available until the Program Announcements are released.  For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the LRP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Public Affairs
    301-619-9783
    usarmy.detrick.medcom-cdmrp.mbx.cdmrp-public-affairs@mail.mil


  • 16 May 2018 1:26 PM | Hawk Tran (Administrator)

    The FY18 Defense Appropriations Act provides $6 million (M) to the Department of Defense Tuberous Sclerosis Complex Research Program (TSCRP) to support innovative, high-impact TSC research.  As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency (DHA) J9, Research and Development Directorate manages the Defense Health Program (DHP) Research, Development, Test, and Evaluation (RDT&E) appropriation.  The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP).

    FY18 TSCRP Program Announcements and General Application Instructions for the following award mechanisms are posted on the Grants.gov website. 

    Focus Areas:  The goal of the FY18 TSCRP is to fund exploratory, pioneering and transformative science that promotes discoveries in TSC, from mechanistic insights to clinical application, by supporting new ideas and investigators for the benefit of Service members, their beneficiaries, and the American public.  Within this context, the FY18 TSCRP encourages applications that address the critical needs of the TSC community in one or more of the following FY18 Focus Areas:

    ·         Gaining a deeper knowledge of TSC signaling pathways and the cellular consequences of TSC deficiency

    ·         Improving TSC disease models

    ·         Examining the clinical aspects of TSC, including phenotypic heterogeneity

    ·         Facilitating therapeutics, biomarkers, and clinical trials research

     

    http://cdmrp.army.mil/funding/tscrp

     

    Exploration - Hypothesis Development Award – Letter of Intent due July 11, 2018

    • ·         Investigators at all academic levels (or equivalent), including postdoctoral fellows

    ·         Supports the initial exploration of innovative, high-risk, high gain, and potentially groundbreaking concepts in the TSC research field.

    ·         Projects involving human subjects or human biological substances must be exempt under 32 CFR 219.101(b)(4) or eligible for expedited review under 32 CFR 219.110 or 21 CFR 56.110.

    ·         Preliminary data are not required.

    • ·         Clinical trials are not allowed.

    ·         Maximum funding of $100,000 for direct costs

    ·         Indirect costs may be proposed in accordance with the institution’s negotiated rate agreement

    • ·         Maximum period of performance is year

     

    Idea Development Award – Letter of Intent due July 11, 2018

    • ·         Established Investigators:  Independent investigators at or above the level of Assistant Professor (or equivalent);
    • ·         or
    • ·         New Investigators:  Independent investigator at or below the level of Assistant Professor (or equivalent); or Established investigators in an area other than TSC at or above the level of Assistant Professor seeking to transition to a career in TSC.

    ·         Supports new ideas that have the potential to yield high-impact findings and new avenues of investigation.

    ·         Preliminary data are expected.

    ·         Clinical trials are not allowed.

    ·         New Investigator Option supports the continued development of promising independent investigators and/or the transition of established investigators from other research fields into a career in TSC research.

    • o   Applications from New Investigators and Established Investigators will be peer- and programmatically reviewed separately.

    ·         The maximum allowable funding for the entire period of performance is $450,000 in direct costs

    ·         Indirect costs may be proposed in accordance with the institution’s negotiated rate agreement

    • ·         Maximum period of performance is 3 years

     

    Clinical Translational Research Award – Letter of Intent due July 11, 2018

    • ·         Independent investigators at or above the level of Assistant Professor (or equivalent)

    ·         Supports forward or reverse clinical/translational research studies that have the potential to improve the diagnosis, prognosis, or treatment of TSC.

    ·         Preference will be given to studies that involve human samples, patients, or leverage existing clinical data and/or ongoing clinical studies. 

    ·         Preclinical studies may be appropriate but must include a clinical component.

    ·         Applications may include a small, pilot clinical trial intended to inform the next step in the continuum of translational research.

    ·         Should provide evidence for the reciprocal transfer of information between basic and clinical science.

    • ·         Preliminary data are required

    ·         The maximum allowable funding for the entire period of performance is $600,000 in direct costs.

    ·         Indirect costs may be proposed in accordance with the institution’s negotiated rate agreement.

    • ·         Maximum period of performance is 3 years

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline.  All applications must conform to the final Program Announcements and General Application Instructions available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

     

    Applications must be submitted through the federal government’s single-entry portal, Grants.gov.  For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the TSCRP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Help Desk

    301-682-5507
    help@eBrap.org


  • 16 May 2018 12:41 PM | Hawk Tran (Administrator)

    FY18 NFRP Program Announcements and General Application Instructions for the following award mechanisms are posted on the Grants.gov website.  The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP).

    Areas of Emphasis: The NFRP encourages applications that specifically address the critical needs of the NF community in one or more of the FY18 Areas of Emphasis.  Not all Areas of Emphasis are applicable to each award mechanism offered by the FY18 NFRP.  If the proposed research project does not address one of the FY18 Areas of Emphasis, justification that the proposed research project addresses an important problem related to NF research and/or patient care should be provided.

    ·         Health services research

                        Evidence-based best clinical practices

                        Implementation and access to NF-specific health care

                        Utilization of technology and informatics

    ·         Heterogeneity of neurofibromas and other NF-related tumors

    ·         Nontumor manifestations

                        Cognitive, behavior, sleep, pain, hypotonia, communication, etc., including quality of life measures, self-reported and underreported manifestations

    ·         Novel disease and treatment response markers using genomics, epigenetics, systems biology, metabolomics, or similar approaches

                        Transition from benign to malignant

    ·         Nutritional, environmental, and other modifiers of NF

    ·         Post-adolescent manifestations

    ·         Preclinical efficacy studies

    ·         Target identification, drug discovery, targeted and immunotherapies

    ·          

    http://cdmrp.army.mil/funding/nfrp

     

    Clinical Trial Award – Letter of Intent due 7/26/18

    • Independent investigators at or above the level of Assistant Professor (or equivalent)
    • Fund Phase 0, I, or II clinical trials relevant to NF and/or schwannomatosis; combinations of phases are permitted.
    • Funding must support a clinical trial and may not be used for preclinical studies.
    • Scientific rationale and preliminary data required for Phase I, II clinical trial applications.

    ·         Maximum funding of $800,000 for direct costs (plus indirect costs)

    ·         Maximum funding of $1,000,000 for direct costs (plus indirect costs) for applications including a Collaborator

    • Maximum period of performance is years

     

    Exploration – Hypothesis Development Award – Letter of Intent due 7/26/18

    • All academic levels (or equivalent)

    ·         Fund the initial exploration of innovative, high-risk, high-gain and potentially. groundbreaking concepts in NF research

    ·         Projects involving human subjects or human biological substances must be exempt under 32 CFR 219.101(b) or eligible for expedited review under 32 CFR 219.110 or 21 CFR 56.110.

    ·         Preliminary and/or published data is encouraged but not required.

    • Clinical trials not allowed

    ·         Maximum funding of $100,000 for direct costs (plus indirect costs)

    • Maximum period of performance is 2 years

     

    Investigator-Initiated Research Award – Letter of Intent due July 26, 2018

    • Independent investigators at or above the level of Assistant Professor (or equivalent) and must plan to commit at least a 10% level of effort for each budget period throughout the entirety of the award
    • Fund highly rigorous, high-impact research projects that have the potential to make an important contribution to NF research and/or patient care.
    • ·         Optional Feature:  Applications that include a Qualified Collaborator who meets criteria identified in the announcement may apply for a higher level of funding.

    ·         Preliminary and/or published data required.

    • Clinical trials not allowed.

    ·         Maximum funding of $525,000 for direct costs (plus indirect costs)

    ·         Maximum funding of $575,000 for direct costs (plus indirect costs) for applications including an Optional Qualified Collaborator

    • Maximum period of performance is 3 years

     

    New Investigator Award – Letter of Intent due July 26, 2018

    • Independent investigators at or below the level of Assistant Professor (or equivalent) or an established investigator at or above the level of Assistant Professor seeking to transition into a career in NF research

    ·         Support the continued development of promising independent investigators and/or the transition of established investigators into a career in the field of NF research

    ·         Experience in NF research is allowed, but not required

    ·         Preliminary and/or published data required

    • Clinical trials not allowed

    ·         Maximum funding of $450,000 for direct costs (plus indirect costs)

    • Maximum period of performance is 3 years

     

    Early Investigator Research Award – Letter of Intent due July 26, 2018

    ·         Postdoctoral Ph.D. or M.D. PIs:

    • Must have successfully defended a doctoral thesis or possess an M.D. degree and
    • Have at least 3 years and up to 6 years of consecutive postdoctoral fellowship

    ·         Supports research opportunities focused on NF for individuals in the early stages of their careers.

    • PIs must have a designated mentor who is an experienced NF researcher

    ·         Maximum funding of $200,000 for direct costs (plus indirect costs)

    • Maximum period of performance is 2 years

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline. All applications must conform to the final Program Announcements and General Application Instructions available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

     

    Applications must be submitted through the federal government’s single-entry portal, Grants.govFor email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the NFRP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Help Desk

    301-682-5507
    help@reBrap.org


  • 16 May 2018 10:07 AM | Hawk Tran (Administrator)

    The FY18 Defense Appropriations provides $3.2 million (M) to the Department of Defense Duchenne Muscular Dystrophy Research Program (DMDRP) to support innovative, high-impact Duchenne muscular dystrophy research.  As directed by the Office of the Assistant Secretary of Defense for Health Affairs, the Defense Health Agency, J9 Research and Development Directorate manages the Defense Health Program Research, Development, Test, and Evaluation appropriation.  The managing agent for the anticipated Program Announcements/Funding Opportunities is the Congressionally Directed Medical Research Programs (CDMRP) at the U.S. Army Medical Research and Materiel Command (USAMRMC).

     

    The DMDRP is providing the information in this pre-announcement to allow investigators time to plan and develop applications.  FY18 DMDRP Program Announcements and General Application Instructions for the following award mechanisms are anticipated to be posted on the Grants.gov website in June 2018. Pre-application and application deadlines will be available when the Program Announcements are released.  This pre-announcement should not be construed as an obligation by the government.

     

    All applications for the FY18 DMDRP funding opportunities are required to address at least one of the following Focus Areas:

    • ·         Bone, cardiac, central nervous system (CNS), and/or gastrointestinal tract studies, including identifying mechanisms of pathology and therapeutic interventions
    • ·         Translational and clinical studies, novel interventions, and drug and biologic delivery technologies designed to improve care and quality of life in areas such as:
    •         Cognitive function
    •         Endocrinology
    •         Gastrointestinal issues
    •         Immunology
    •         Orthopaedics
    •         Psychosocial issues
    •         Pulmonology (including sleep-focused studies)
    •         Skeletal muscle
    • ·         Assessment of clinical trial tools and outcome measures, such as:
    •         Discovery and qualification of pharmacodynamic, prognostic, and predictive biomarkers
    •         Novel clinical outcome assessment
    •         Patient-centered outcomes (e.g., quality of life, activities of daily living)
    •         Potential surrogate markers
    •         Secondary data analysis that helps to address clinical research tool validation and/or to understand natural history
    • ·         Extension or expansion of existing preclinical translational data in support of a specific therapeutic development path (such as optimizing delivery to target tissues, including drug exposure, independent replication, and comparative studies)
    •  
    •  
    • http://cdmrp.army.mil/pubs/press/2018/18dmdrppreann
    •  
    • Investigator-Initiated Research Award
    • Principal Investigator:  Must be an independent investigator at or above the level of Assistant Professor (or equivalent).

      Optional Nested Resident or Medical Student Trainee: Resident trainee must be enrolled in an accredited residency program.  Medical student trainee must be enrolled in a nationally accredited (or equivalent) medical school.  Trainees must be able to devote a minimum of 40% level of effort.
    • ·         Optional Interdisciplinary Collaborator:  Must be an independent investigator at or above the level of Assistant Professor (or equivalent), whose primary training, research, and experience is in a different field than the PI.  The collaborator is required to devote a minimum of 10% level of effort to this project.

    ·         Supports translational research that will have an impact on preserving and improving the function and quality of life, and extending the lifespan for all individuals with Duchenne.

    ·         Supports translational research that will accelerate the movement of promising new ideas in Duchenne research into clinical applications.

    ·         Optional Interdisciplinary Collaborator (OIC): Supports projects that include interdisciplinary collaborations that bring new perspectives from other disciplines and/or bring new investigators into the Duchenne field that through their collaboration the team can undertake conceptually and technically novel approaches that would be less likely to succeed if undertaken by a more narrowly focused group of investigators. Applications that include an OIC who meets criteria identified in the Program Announcement/Funding Opportunity may apply for a higher level of funding.

    ·         Clinical trials are allowed.

    • ·         Preliminary data are required.

    ·         Maximum funding of $600,000 for direct costs (plus indirect costs).

    ·         Maximum period of performance is years.

    ·         Nested traineeship: Additional maximum of $50,000 for residents or $30,000 for medical students in direct costs (plus indirect costs) over a one-year period of performance.

    • ·         Optional Interdisciplinary Collaborator:  Additional maximum of $150,000 in direct costs over the 3-year period of performance.
    •  

    Career Development Award

    Principal Investigator:  Must be research (Ph.D.) or physician (M.D.) scientists at an early stage of their research careers with a minimum of 2 years post terminal degree (excluding medical residency or family medical leave), working to become independent investigators who exhibit a strong desire to pursue careers in Duchenne research.
    Mentor:  Must hold a position at or above the level of an Associate Professor (or equivalent).

    ·         Supports early-career investigators to conduct impactful research under the mentorship of an experienced muscular dystrophy researcher.

    ·         Clinical trials are not allowed.

    • Preliminary data are required.

    ·         Maximum funding of $275,000 for direct costs (plus indirect costs).

    • Maximum period of performance is 2 years.

    A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline.  All applications must conform to the final Program Announcements and General Application Instructions that will be available for electronic downloading from the Grants.gov website.  The application package containing the required forms for each award mechanism will also be found on Grants.gov.  A listing of all CDMRP funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420. 

     

    Applications must be submitted through the Federal Government’s single-entry portal, Grants.gov.  Submission deadlines are not available until the Program Announcements are released.  For email notification when Program Announcements are released, subscribe to program-specific news and updates under “Email Subscriptions” on the eBRAP homepage at https://eBRAP.org.  For more information about the DMDRP or other CDMRP-administered programs, please visit the CDMRP website (http://cdmrp.army.mil).

    Point of Contact:

    CDMRP Public Affairs
    301-619-9783
    usarmy.detrick.medcom-cdmrp.mbx.cdmrp-public-affairs@mail.mil


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