In an ISS, the Investigator assumes responsibility for all aspects of the investigation, including:
- Trial design
- Ensuring appropriate institutional and regulatory approval
- Study conduct, including responsibility for ensuring appropriate medical safeguards, medical monitoring, and medical supervision
- Analysis and interpretation of the results
- Communication of the results (e.g., publications)
If you would like to request support for an ISS, please click the link below. Following our initial review, if we’re interested in learning more about your study concept, we will ask you to submit a full study protocol and budget for further evaluation to make a final determination on your proposal. You may also submit a copy of a full study protocol and budget, if available, for our initial review, but this is not required.
Submit a new clinical or preclinical proposal or access a previously submitted proposal.