National Institutes of Health

Clinical Coordinating Center for NCCIH Multi-Site Investigator-Initiated Clinical Trials of Natural Products (Collaborative UG3/UH3 Clinical Trial Required)

This Notice of Funding Opportunity (NOFO) encourages cooperative agreement applications for investigator-initiated, multi-site, clinical trials (Phase III and beyond) to study…

Agency
National Institutes of Health
Deadline
Jul 14, 2026 (2 days left)
Opportunity #
PAR-24-312
CFDA
93.213
Cost sharing
Not required
HealthPublic and State controlled institutions of higher educationOthers (see text field entitled "Additional Information on Eligibility" for clarification)State governmentsNonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher educationNonprofits having a 501(c)(3) status with the IRS, other than institutions of higher educationCity or township governmentsNative American tribal governments (Federally recognized)Small businessesPublic housing authorities/Indian housing authoritiesFor profit organizations other than small businessesIndependent school districtsSpecial district governmentsPrivate institutions of higher educationNative American tribal organizations (other than Federally recognized tribal governments)County governments

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About this opportunity

This Notice of Funding Opportunity (NOFO) encourages cooperative agreement applications for investigator-initiated, multi-site, clinical trials (Phase III and beyond) to study the effects of natural products (i.e. botanicals, probiotics, and products marketed as dietary supplements) in NCCIH designated areas of high research priority.

For this NOFO, natural products include promising nutritional regimens that standardize the amount of a specific naturally occurring nutritional compound (e.g., omega-3 fatty acids, anthocyanidins, or polyphenols) and have compelling preliminary evidence.

Applicants should describe plans for a Clinical Coordinating Center to develop and implement the proposed multi-site clinical trial. The objective of the Clinical Coordinating Center application is to provide the scientific rationale and a comprehensive scientific and operational plan for the clinical trial.

Clinical Coordinating Center applications are expected to describe plans for project management, participant recruitment and retention strategies, performance milestones, scientific conduct, and dissemination of results.

Clinical Coordinating Center applications submitted under this NOFO will utilize a two-phase, milestone-driven, cooperative agreement (UG3/UH3) funding mechanism. In addition, an accompanying Data Coordinating Center application, submitted under PAR-24-125, proposing a data analysis and data management plan for the clinical project is required.

Both a Clinical Coordinating Center application and a corresponding Data Coordinating Center (DCC) application need to be submitted simultaneously for consideration by NCCIH. For additional information about the mission, strategic vision, and research priorities of the NCCIH, applicants are encouraged to consult the NCCIH website: (https://nccih.nih.gov/about/plans).

Who can apply

Other Eligible Applicants include the following: Alaska Native and Native Hawaiian Serving Institutions; Asian American Native American Pacific Islander Serving Institutions (AANAPISISs); Eligible Agencies of the Federal Government; Faith-based or Community-based Organizations; Hispanic-serving Institutions; Historically Black Colleges and Universities (HBCUs); Indian/Native American Tribal…

How to apply

Applications for federal grants are submitted through grants.gov under opportunity number PAR-24-312. Before you start, confirm your organization's eligibility, register in SAM.gov if you haven't already, and note the response deadline of Jul 14, 2026. AutoGrantHunter helps you decide whether this opportunity is worth pursuing before you invest in a full application.

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