Natural History of Disorders Screenable in the Newborn Period (R01 Clinical Trial Optional)
ID: 331379Type: Posted
Overview

Buyer

National Institutes of Health (HHS-NIH11)

Eligible Applicants

Others

Funding Category

Income Security and Social Services

Funding Instrument

Grant

Opportunity Category

Discretionary

Cost Sharing or Matching Requirement

Yes

Original Source

https://grants.gov/search-results-detail/331379

Additional Information

http://grants.nih.gov/grants/guide/pa-files/PAR-21-115.html
Timeline
    Description

    The National Institutes of Health (NIH) is offering a funding opportunity titled "Natural History of Disorders Screenable in the Newborn Period (R01 Clinical Trial Optional)" aimed at advancing research on disorders identifiable through newborn screening. This initiative encourages applications that propose comprehensive studies to enhance understanding of these disorders, which is crucial for timely interventions for affected infants. The funding seeks to bridge knowledge gaps in newborn screening practices, ultimately improving diagnosis, treatment, and support for families, with no budget limits but a maximum project duration of five years. Interested applicants, including a diverse range of organizations such as higher education institutions and nonprofit entities, must submit their proposals by January 7, 2025, and can find additional information at NIH Grants.

    Point(s) of Contact
    FBOWebmaster@OD.NIH.GOV
    Files
    Title
    Posted
    PAR-21-115-Full-Announcement.html
    PAR-21-115.html
    The Department of Health and Human Services (HHS), through the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), announces the funding opportunity for research projects that explore the natural history of disorders identifiable through newborn screening. The goal is to develop comprehensive studies leading to improved understanding of these disorders, which will facilitate timely interventions for affected infants. The announcement invites applications that either enhance existing knowledge of currently screened disorders or investigate new conditions that could benefit from screening, emphasizing partnerships across multiple states for broader data collection. Eligible applicants include a wide array of organizations, from higher education institutions to nonprofit organizations and government entities. There are no budget limits, but proposals should reflect actual project needs, with a maximum project duration of five years. The initiative aligns with legislative goals to improve newborn screening practices and public health outcomes. Applications are subject to rigorous peer review based on significance, innovation, approach, and investigator qualifications. This funding opportunity aims to bridge knowledge gaps in newborn screening, ultimately improving diagnosis, treatment, and support for affected families.
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