Rare Diseases Clinical Research Consortia (RDCRC) for the Rare Diseases Clinical Research Network (RDCRN) (U54 Clinical Trial Optional)
ID: 353330Type: Posted
Overview

Buyer

National Institutes of Health (HHS-NIH11)

Award Range

$0 - $1M

Eligible Applicants

Others

Funding Category

Income Security and Social Services

Funding Instrument

Cooperative Agreement

Opportunity Category

Discretionary

Cost Sharing or Matching Requirement

Yes
Timeline
    Description

    The National Institutes of Health (NIH) is inviting applications for the Rare Diseases Clinical Research Consortia (RDCRC) as part of the Rare Diseases Clinical Research Network (RDCRN), with a focus on advancing the diagnosis, management, and treatment of rare diseases affecting fewer than 200,000 individuals in the U.S. This funding opportunity, structured as a Cooperative Agreement, encourages both new and renewal applications that emphasize collaborative, patient-centered research and the importance of early diagnosis and clinical trial readiness. The RDCRCs will engage with patient advocacy groups and utilize innovative methodologies to enhance therapeutic development, with an award ceiling of $1 million available for successful applicants. Interested parties should submit their applications by August 19, 2024, and can direct inquiries to grantsinfo@nih.gov for further information.

    Point(s) of Contact
    Files
    Title
    Posted
    The Department of Health and Human Services is issuing a Notice of Funding Opportunity (NOFO) for the Rare Diseases Clinical Research Consortia (RDCRC) as part of the Rare Diseases Clinical Research Network (RDCRN). This initiative aims to foster collaborative, multi-site clinical research focused on advancing diagnosis and treatment for diverse rare diseases affecting fewer than 200,000 individuals in the U.S. The program encourages applications for both new and renewal projects, emphasizing patient-centered research and the need for early diagnosis and clinical trial readiness. Key components of the RDCRCs include forming partnerships with patient advocacy groups, conducting longitudinal studies, and leveraging technologies to enhance therapeutic development. The funding opportunity is structured around several cores, including Administrative, Clinical Research, and Data Management, ensuring coordinated efforts across the network. Applicants must engage actively with the Coalition of Patient Advocacy Groups and align research initiatives with specific NIH Institute priorities. The RDCRN has already supported numerous projects that have led to significant findings and FDA treatment approvals. This funding opportunity seeks to build upon those successes to improve health outcomes and enhance the understanding of rare diseases through innovative research methodologies and collaborative networks.
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