NINDS Efficacy Clinical Trials (UG3/UH3 Clinical Trial Required)
ID: 333695Type: Posted
Overview

Buyer

National Institutes of Health (HHS-NIH11)

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 titled "NINDS Efficacy Clinical Trials (UG3/UH3 Clinical Trial Required)" aimed at encouraging investigator-initiated efficacy clinical trials focused on neurological disorders. This initiative seeks to support trials that evaluate drugs, biologics, devices, and various therapies, with a particular emphasis on addressing unmet medical needs within the mission of the National Institute of Neurological Disorders and Stroke (NINDS). The funding mechanism consists of a two-phase cooperative agreement, with an initial planning phase (UG3) lasting up to one year, followed by a clinical trial phase (UH3) lasting a maximum of four years, totaling no more than five years for the entire project. Interested applicants, including educational institutions and nonprofits, must submit their proposals by January 9, 2025, and can reach out to the NIH OER Webmaster at grantsinfo@nih.gov for further assistance.

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    Title
    Posted
    The Department of Health and Human Services, through the National Institutes of Health (NIH), has announced a funding opportunity titled "NINDS Efficacy Clinical Trials (UG3/UH3 Clinical Trial Required)" aimed at encouraging investigator-initiated efficacy clinical trials, specifically for neurological disorders. The funding mechanism, a UG3/UH3 cooperative agreement, consists of two phases: an initial planning phase (UG3) lasting up to one year and a clinical trial phase (UH3) lasting a maximum of four years, with a total project duration not exceeding five years. The trials must fulfill specific scientific milestones in the UG3 phase to transition to UH3. Eligible applicants include educational institutions, nonprofits, and government entities, with no limit on the number of applications, provided they are scientifically distinct. A critical focus is on trials addressing unmet medical needs, with detailed requirements for study design and oversight. The application process involves compliance with rigorous standards for data management, safety monitoring, and patient recruitment. Key dates for application submission are outlined, and budget requests should reflect the actual needs of the proposed study. Applicants are encouraged to establish collaborations with patient advocacy groups and consult with NINDS staff to refine their proposals. This initiative emphasizes advancing public health interventions through well-designed clinical research within the NINDS mission.
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