This grant is designed to help researchers plan clinical trials focused on cancer prevention and control. It's about making sure these trials are well thought out and address any gaps in information before they start. This can help save time and money by reducing the need for changes once the trial is underway. The grant supports studies that prepare for trials by testing new designs and understanding the feasibility of the trial, which can improve outcomes for cancer prevention and care.
Who it's for: This grant is for a wide range of organizations, including public and private institutions of higher education, nonprofits with or without 501(c)(3) status, small businesses, for-profit organizations, and various government entities such as state, county, and city governments. Tribal organizations and federally recognized Indian tribal governments are also eligible.
More details
Likely Disqualifiers
- Individuals applying as sole proprietors
- Organizations not involved in healthcare or cancer research
- Entities without the capacity to conduct clinical trials
- Applications submitted after the deadline
- Incomplete applications lacking necessary documentation
What You May Need
- Detailed project proposal
- Preliminary data or scientific literature supporting the trial
- Information on study population and intervention
- Plan for addressing data/statistical challenges
- Budget and justification
- Organizational documents proving eligibility
- Letters of support or collaboration
- Timeline for trial planning and execution
- Ethical approval or plans for obtaining it
Cautions
- Ensure all eligibility criteria are met before applying.
- Be aware of the application deadline and submit well in advance.
- Prepare a comprehensive plan addressing all potential information gaps.
- Consult official resources or a grant advisor for detailed guidance.
Generated from official source details for readability
Eligibility
Eligible Applicant Types
Use of Funds
Funds from this grant can be used to conduct preparatory studies that address gaps in information needed to plan a clinical trial. This includes testing new trial designs, understanding the feasibility of the trial, and planning for the management of treatment-related symptoms and supportive care. The goal is to improve trial design and ensure the trial can be completed efficiently.
Cost Sharing
Not Required
Important Dates
- Posted
- Nov 5, 2024
- Deadline
- Oct 25, 2027(591 days)
- Archive Date
- Nov 30, 2027
- Last Updated
- Nov 5, 2024
Application Checklist
- Review the full grant announcement on the official source
- Confirm your organization's eligibility
- Check if registration on SAM.gov/Grants.gov is required
- Gather required documents (budgets, financials, etc.)
- Identify matching funds if cost-sharing is required
- Draft project narrative and work plan
- Get required internal approvals and signatures
- Submit application before the deadline