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The NIAID Investigator-Initiated Clinical Trials program from the National Institute of Allergy and Infectious Diseases provides funding for clinical research on infectious diseases, allergic diseases, and immunological conditions.
NIAID supports a wide range of clinical trial designs, from early-phase feasibility studies to large pivotal trials, enabling investigators to test novel treatments, vaccines, diagnostics, and prevention strategies. Eligible applicants include nonprofits, for-profit organizations, and other entities conducting biomedical research in areas aligned with NIAID's mission.
Award amounts vary by the scope and phase of the proposed clinical trial.
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Investigator-Initiated Clinical Trial Resources | NIAID: National Institute of Allergy and Infectious Diseases Resources for Researchers Division of Intramural Research Labs Research at Vaccine Research Center Intramural Scientist & Clinician Directory Research Rules & Policies Allergy, Immunology & Transplantation Resources for Researchers Antimicrobial (Drug) Resistance Antimicrobial Resistance Threats Information for Researchers Risk Factors & Prevention Research Immune Tolerance Processes Disease-Specific Research Information for Researchers Autoimmune Lymphoproliferative Syndrome (ALPS) Basic & Preclinical Research Information for Researchers Information for Researchers Shiga Toxin-Producing E.
coli (STEC) Researching Ebola in Africa Information for Researchers Information for Researchers Why Food Allergy is a Priority for NIAID Characterizing Food Allergy & Addressing Related Disorders Information for Researchers Diagnosis & Management Guidelines Disease-Specific Research Information for Researchers Genomics & Advanced Technologies Pathogen-Based Initiatives Information for Researchers Information for Researchers Group A Streptococcal Infections Disease-Specific Research Information for Researchers Overview of the Immune System Features of an Immune Response Information for Researchers Information for Researchers Leprosy (Hansen's Disease) How NIAID is Addressing Lyme Disease Information for Researchers Parasite, Mosquito & Human Host Prevention, Treatment & Control Strategies Strategic Partnerships & Research Capacity Information for Researchers Information for Researchers Neglected Tropical Diseases Information for Researchers Translational & Clinical Research Cross-cutting Preparedness Molecular & Genetic Research Primary Immune Deficiency Diseases (PIDDs) Information for Researchers Animal Prion Diseases and Humans Information for Researchers Respiratory Syncytial Virus (RSV) Schistosomiasis (Bilharzia) Research in Endemic Regions Sexually Transmitted Infections (STIs) NIAID's Research Approach Information for Researchers Disease-Specific Research Information for Researchers Information for Researchers Disease-Specific Vaccines Information for Researchers Translational & Clinical Research Information for Researchers Biology, Genetics & Clinical Research NIAID's Approach to Women's Health Research Sex-Specific Health Challenges Facing Women Biennial Report (FY 2019-2020) Information for Researchers Why NIAID Is Researching Zika Virus Information for Researchers Find a Funding Opportunity NIAID Research Priorities Plan Your Budget & Personnel Additional Application Elements Research with Special Considerations After You Submit an Application Understand the Review Process Respond to Pre-Award Requests Negotiation & Initial Award Become a Healthy Volunteer Participant's Guide to Clinical Trials HIV and Emerging Infectious Diseases Laboratory of Infectious Diseases Primary Immune Deficiency Clinic Vaccine Research Center Clinical Studies Fill Out the Volunteer Form Q&A: Vaccine Clinical Studies Vaccine Clinical Studies Safeguards Clinical Trial Publications NIAID-Funded Research News Division of Allergy, Immunology, and Transplantation Division of Microbiology and Infectious Diseases Division of Extramural Activities Division of Clinical Research Division of Intramural Research Dr. Joseph J.
Kinyoun: Father of the NIH Dr. Joseph Kinyoun The Indispensable Forgotten Man Dr. Joseph Kinyoun: Selected Bibliography NIAID 60th Anniversary Timeline Research Training at NIAID Campuses Grant Programs that NIAID Funds AIDS Research Advisory Committee AIDS Vaccine Research Subcommittee Board of Scientific Counselors Members Advisory and Peer Review Committees Autoimmune Diseases Committee Website Policies and Notices External Link Icon and Disclaimers Freedom of Information Act (FOIA) Voluntarily Submitted Information Investigator-Initiated Clinical Trial Resources Due to current HHS and NIH restructuring, some content on niaid.
nih. gov is not being updated regularly. Please refer to clinicaltrials.
gov and nih. gov for the most up-to-date information on NIH research. 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). Follow the NIAID IICT Process What To Do If You Need an Extension After Award IICT Resources for Staff and Applicants 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’s Special About Clinical Trial Applications? Four Tips for Investigator-Initiated Clinical Trial Applications 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: Investigator-Initiated Clinical Trial Administrative Extension SOP Extension of Investigator-Initiated Clinical Trials Questions and Answers 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 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 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.
Content last reviewed on July 16, 2025
Based on current listing details, eligibility includes: Nonprofits, for-profit organizations, and other entities conducting biomedical research. Applicants should confirm final requirements in the official notice before submission.
Current published award information indicates Varies Always verify allowable costs, matching requirements, and funding caps directly in the sponsor documentation.
The current target date is rolling deadlines or periodic funding windows. Build your timeline backwards from this date to cover registrations, approvals, attachments, and final submission checks.
Federal grant success rates typically range from 10-30%, varying by agency and program. Build a strong proposal with clear objectives, measurable outcomes, and a well-justified budget to improve your chances.
Requirements vary by sponsor, but typically include a project narrative, budget justification, organizational capability statement, and key personnel CVs. Check the official notice for the complete list of required attachments.
Yes — AI tools like Granted can help research funders, draft proposal sections, and check compliance. However, always review and customize AI-generated content to reflect your organization's unique strengths and the specific requirements of the solicitation.
Review timelines vary by funder. Federal agencies typically take 3-6 months from submission to award notification. Foundation grants may be faster, often 1-3 months. Check the program's timeline in the official solicitation for specific dates.
Many federal programs offer multi-year funding or allow competitive renewals. Check the official solicitation for continuation and renewal policies. Non-competing continuation applications are common for multi-year awards.
Research Project Grant (Parent R01 Clinical Trial Not Allowed) is a flagship NIH grant administered by the National Institute of Allergy and Infectious Diseases that funds investigator-initiated biomedical and behavioral research projects not involving clinical trials. The R01 supports hypothesis-driven research across a wide range of health topics including infectious diseases, immune disorders, and allergy-related conditions. Eligible applicants include higher education institutions such as public and private universities. Award amounts range from $250,000 to $2,500,000 with a deadline of June 5, 2026.
Tuberculosis Research Advancement Centers (TRACs) (P30 Clinical Trial Not Allowed) is sponsored by National Institute of Allergy and Infectious Diseases (NIAID). This program supports the establishment of Tuberculosis (TB) Research Advancement Centers (TRACs) to develop the next generation of TB researchers and catalyze multidisciplinary and innovative TB science by providing expertise and resources to facilitate basic and clinical TB re…