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NIDDK High Risk Multi-Center Clinical Study Cooperative Agreement (U01 Clinical Trial Required)

Required Information for Application:

1. Investigator name and contact information

2. Clinical trial title

3. Description of the high-risk multi-center clinical trial

4. Hypothesis driving the trial

5. Potential impact on clinical practice and/or public health

6. Relevance of the disease to the mission of NIDDK

7. Timeline and milestones for the trial

8. Budget information for the trial

9. Collaborating clinical centers and their qualifications

10. Plans for data collection and analysis

11. Plans for participant recruitment and retention

12. Previous experience and qualifications of the investigator and research team

13. Plan for ethical considerations and informed consent procedures

14. Plan for dissemination of trial results

15. Any additional supporting documents or letters of recommendation.

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Funding Amount

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Eligible Applicants

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Eligible Activities

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Deadline to Apply

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88%

Approval rating across all Canadian funding programs

93%

Average time savings to our clients, compared to
businesses that apply for funding in-house
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