Grant Details

General Overview

Grant Information

Grant name: Clinical Coordinating Center for NCCIH Multi-Site Investigator-Initiated Clinical Trials of Natural Products

Funding organization: National Institutes of Health (NIH)

Total funding amount: Not specified

Duration: UG3 phase up to 1 year, UH3 phase expected 4 years (up to 6 years with justification)

Primary objective: To study the effects of natural products in NCCIH designated areas of high research priority.

Key stakeholders: NIH, NCCIH, participating organizations, and research participants.

Funding source: Federal government.

Funding type: Cooperative agreement.

Significance: Addresses gaps in knowledge regarding the efficacy of natural products.

Grant frequency: One-time application for each cycle.

Organizational Aspects

Eligible Organization Types

Higher Education Institutions (Public/State Controlled, Private)

Nonprofits (with and without 501(c)(3) status)

For-Profit Organizations (including Small Businesses)

Local, State, and Federal Governments

Indian/Native American Tribal Governments

Other (e.g., Independent School Districts, Public Housing Authorities)

Ineligibility

Foreign organizations are not eligible to apply.

Scope and Focus

Primary Focus Areas

Natural products including botanicals, probiotics, and dietary supplements.

High research priority areas such as pain management, gastrointestinal disorders, and mental health.

Expected Outcomes

Contribute to the evidence base for the efficacy of natural products.

Enhance understanding of the mechanisms of action of natural products.

Technical Details

Technical Expertise Requirements

Experience in conducting multi-site clinical trials.

Expertise in clinical trial design and data management.

Financial Structure

Budget Information

Application budgets are not limited but must reflect actual project needs.

Combined budgets of CCC and DCC will determine direct costs policy.

Timeline and Implementation

Key Dates

Posted Date: February 02, 2024

Open Date: February 04, 2024

Application Due Dates: Various deadlines from March 2024 to July 2026.

Compliance and Requirements

Regulatory Compliance

Must adhere to FDA regulations for clinical research.

Investigators must determine if an Investigational New Drug (IND) application is necessary.

Application Process

Required Documentation

Plan for Enhancing Diverse Perspectives (PEDP).

Clinical trial project management plan.

Grant Details

clinical trials natural products healthcare research botanicals dietary supplements mental health pain management NCCIH NIH
Clinical Coordinating Center for NCCIH Multi-Site Investigator-Initiated Clinical Trials of Natural Products
PAR-24-123
NIH Grants
EDU NGO PUBLIC ENTERPRISE OTHER
US
HEALTHCARE RESEARCH
DEVELOPMENT OTHER
0-10 11-50 51-250 251-500 500+
SDG3
FUNDING RESEARCH_DEVELOPMENT
True
None
None
None
USD
None
July 14, 2026, 10 p.m.
March 2024 - July 2026