If you haven’t done so already, check NIAID’s Clinical Trial Research page and confirm whether your planned research meets NIH’s definition of a clinical trial. Then read this page for NIAID’s unique requirements for investigator-initiated clinical trials (IICTs).
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Follow the NIAID IICT Process
To apply for your own clinical trial outside of NIAID’s Networks , you must follow NIAID’s rules and process for IICTs as described below. Otherwise, we will not accept your application.
Start with NIAID’s Investigator-Initiated Clinical Trial Planning and Implementation Awards SOP , then read the following:
- Investigator-Initiated Clinical Trials Questions and Answers
- Four Tips for Investigator-Initiated Clinical Trial Applications
Decide which notice of funding opportunity (NOFO) best suits your research:
- NIH Research Project Grant (Parent R01, Clinical Trial Required) —best for clinical trials that are not high-risk*
- NIH Exploratory/Developmental Research Grant Program (Parent R21, Clinical Trial Required) —best for mechanistic or investigative studies that are not high-risk*
- NIAID Clinical Trial Implementation Cooperative Agreement (U01, Clinical Trial Required) —best for clinical trials that are high-risk*
- NIAID SBIR Phase II Clinical Trial Implementation Cooperative Agreement (U44, Clinical Trial Required) —the only choice for small businesses
*For the NIAID definition of high risk, check How do I determine my level of risk? on IICT Awards – General Questions and Answers .
At least 10 weeks before your application’s due date (12 weeks for applications that request more than $1 million a year in direct costs), speak to the scientific/research contact listed in the NOFO to request a prior consultation.
The purpose of this consultation is four-fold:
- Assure you that your proposed clinical trial meets NIAID’s goals, fits within our mission, and addresses a high-priority research area.
- Determine the risk level of your proposed trial.
- Review the information and documents you’ll need to include in your application.
- Identify other mechanisms to support your clinical trial, e.g., through a different notice of funding opportunity or one of our clinical trial networks.
Prepare for that discussion using our guide, Requesting Prior Consultation—Clinical Trial Applications and Planning Grants .
Last, write your application and gather all documentation you’ll need when you apply. Learn more and get advice from NIAID:
What To Do If You Need an Extension After Award
If you can't complete a clinical trial by the end of the award, you may be able to apply for an extension. For NIAID policy on extending an IICT, read the following pages:
IICT Resources for Staff and Applicants
In addition to the websites noted above, we have the following resources to help you with your application:
- Requesting Prior Consultation—Clinical Trial Applications and Planning Grants
- Investigator-Initiated Clinical Trial Planning and Implementation Awards SOP
- Investigator-Initiated Clinical Trials Questions and Answers
- Types of Funding Opportunities
- Research Using Human Subjects . Includes IRB and assurance information
- Checklists for Planning and Writing a Human Subjects Grant Application
- Apply for a Grant . Advice on how to plan and write an application and manage a grant
- NIAID Clinical Terms of Award
- NIAID Clinical Terms of Award—Guidance for Compliance on using the Terms
- Rules and Policies for Clinical Research
- ClinRegs —an online database of country-specific clinical research regulatory information designed to assist in planning and implementing international clinical research
- Human Subjects Warning
- Sample Letter to Document Training in the Protection of Human Subjects
- Research Methods Resources
For more information, check NIAID Research Using Human Subjects , which includes SOPs. Also learn more about how to Apply for a Grant and First-Level Peer Review .
We also advise you to review NIAID’s clinical research policies Rules and Policies for Clinical Research . These policies may differ somewhat depending on your research and topic area.