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DoW Toxic Exposures Clinical Trial Award

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The fiscal year 2026 Toxic Exposures Research Program Clinical Trial Award (HT942526TERPCTA) is a grant mechanism administered by the Defense Health Agency to support clinical trials aimed at preventing, treating, or managing conditions resulting from military-related toxic exposures. The program focuses on three primary goals: predicting and preventing adverse effects, improving diagnostics, and minimizing disease progression. Eligible research must align with specific topic areas, including neurotoxin exposure, Gulf War Illness, airborne hazards and burn pits, and other general military toxic exposures. Projects may range from small proof-of-concept pilot studies to large-scale pragmatic trials, with the ultimate objective of advancing research toward FDA device or drug approval or the establishment of clinical practice guidelines. The award features a Partnering Principal Investigator Option (PPIO) to encourage interdisciplinary collaborations between clinicians and research scientists, allowing for separate awards to an initiating PI and a partnering PI. The combined cost cap for the entire period of performance is 4.5 million dollars, with a maximum performance period of four years. The application process is a two-step submission via eBRAP or Grants.gov, beginning with a pre-application deadline of August 19, 2026, followed by a full application deadline of November 19, 2026. Selection is based on a two-tier review process consisting of a peer review for technical merit and a programmatic review for strategic alignment. Evaluation criteria emphasize clinical impact and military relevance, as well as adherence to rigorous study design standards such as STROBE, CONSORT, SPIRIT, and ARRIVE guidelines.

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DHA grant for military toxic exposure clinical trials, capped at 4.5 million dollars.

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AgencyDepartment Of Defense → Department Of The Army -- Usamraa
Contacts1 person available
OfficeUSA

Full Description

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Summary: The fiscal year 2026 (FY26) Toxic Exposures Research Program (TERP) Clinical Trial Award (CTA) mechanism supports the advancement, execution, and analysis of clinical trials with the potential to have a significant impact on the prevention, treatment, or management of symptoms, diseases or conditions associated with or resulting from military-related toxic exposures. Proposed projects may range from small proof-of-concept clinical trials (e.g., pilot, first-in-human, phase 0) designed to demonstrate the feasibility or inform the design of more advanced trials, through large-scale trials (including pragmatic clinical trials) to determine efficacy in relevant patient populations. 


Distinctive Features: To encourage applications that include meaningful and productive collaborations, the FY26 TERP CTA includes a Partnering Principal Investigator Option (PPIO). One Principal Investigator (PI) is identified as the initiating PI, and an additional PI may be identified as a Partnering PI. If recommended for funding, each PI will be named on separate awards. The intent is to support interdisciplinary partnerships, such as those between clinicians and research scientists, that will accelerate the movement of promising interventions/​knowledge products into clinical applications. Partnering should significantly advance the research beyond what would be possible through independent efforts.


https://cdmrp.health.mil/pubs/press/2026/terppreann

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