Investigator-Initiated Trials
At Harrow, we believe in the need to support independent research conducted by qualified individuals that address important unanswered questions and improve patient care. Submission of a proposal does not guarantee funding. The committee will evaluate proposals for scientific merit, alignment with our medical strategy, and available funding.
Please fill out all fields with as much detail as possible so we may better evaluate your proposal. You will need to attach a formal study synopsis, itemized budget proposal, your CV, and GCP certificate. Incomplete submissions may not be reviewed.
If your proposal is accepted, you will be responsible for study design, initiation, management, data analysis, monitoring, reporting, writing, and publishing.
- Study title
- Study type (e.g. retrospective chart review, prospective clinical trial, survey, basic science, etc.)
- Background rationale, including relevant medical literature
- Primary study objective and secondary objectives, if applicable
- Primary and secondary endpoints, if applicable
- Key inclusion/exclusion criteria
- Statistical analysis plan (power analysis, sample size calculation, proposed statistical tests)
- Study duration
- Publication plan
- IRB/Ethics Committee fees
- Biostatistics/data management
- Study coordinator costs
- Procedure costs/patient care costs
- Medical writing
- Open access publication fee
- Amount of product needed, strength, and dosage form
- Note: Third-party payers should be billed for standard of care costs. Only research-related costs should be included in the budget.