CCRP Initiative: Countermeasures Against Chemical Threats (CounterACT) Therapeutics Discovery and Early-Stage Development (UG3/UH3 Clinical Trial Not Allowed)
ID: 341905Type: Posted
Overview

Buyer

National Institutes of Health (HHS-NIH11)

Award Range

$0 - $350K

Eligible Applicants

Others

Funding Category

Health

Funding Instrument

Cooperative Agreement

Opportunity Category

Discretionary

Cost Sharing or Matching Requirement

Yes
Timeline
    Description

    The National Institutes of Health (NIH) has announced a funding opportunity under the Countermeasures Against Chemical Threats (CounterACT) initiative, aimed at supporting the early-stage development of therapeutics to mitigate the adverse health effects of toxic chemical exposure. This initiative seeks applications for projects that validate therapeutic targets and characterize lead compounds, ultimately delivering a well-characterized therapeutic candidate that improves upon existing standards of care for chemical exposure treatment. The funding is particularly relevant in the context of potential mass casualty situations involving chemical threats, as identified by the Department of Homeland Security. Interested applicants can apply for a cooperative agreement with an award ceiling of $350,000, and the application deadline is set for October 17, 2024. For further inquiries, applicants may contact the NIH OER Webmaster at OERWebmaster03@od.nih.gov.

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    Title
    Posted
    The Department of Health and Human Services has issued a Funding Opportunity Announcement (FOA) under the Countermeasures Against Chemical Threats (CounterACT) initiative, focusing on the early-stage development of therapeutics to address toxic chemical exposure effects. The NIH's National Institute of Neurological Disorders and Stroke (NINDS) and other affiliated institutes will support projects that aim to develop medical countermeasures (MCMs) applicable in mass casualty situations involving chemical threats identified by the Department of Homeland Security. The UG3/UH3 cooperative agreement mechanism allows research teams to validate therapeutic targets, optimize candidate compounds, and demonstrate efficacy, all while adhering to regulatory and biosafety guidelines. Applications must demonstrate strong preliminary data supporting their approaches, detail annual milestones for project progress, and ensure safety compliance while working with hazardous chemicals. The total project period can extend up to five years, with specific budgetary limits for each phase, necessitating careful planning for scientific rigor and institutional collaboration. Successful projects are expected to deliver a characterized therapeutic candidate that improves upon existing standards of care for chemical exposure treatment.
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