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Integrating Health Disparities into Immuno-Oncology (HDIO) (P20 Clinical Trial Not Allowed)

List of required information for application:

1. Project title: 

2. Project summary: A brief overview of the proposed research project, including the significance of integrating health disparities into immuno-oncology research.

3. Project objectives: Clearly state the scientific objectives and goals of the project.

4. Research plan: Provide a detailed description of the research plan, including the methodology, data collection methods, and analysis techniques.

5. Team composition: Describe the complementary, multi-disciplinary research team that will be involved in the project. Include relevant expertise and qualifications of team members.

6. Justification for integration: Explain why it is important to integrate cancer health disparities into immuno-oncology research studies.

7. Feasibility assessment: Provide an assessment of the feasibility of the proposed research, including potential challenges and how they will be addressed.

8. Novelty or high-risk research hypotheses: Describe any novel or high-risk research hypotheses that will be explored through the feasibility or pilot studies.

9. Anticipated outcomes: Describe the potential outcomes of the project and how they will contribute to advancing knowledge in the field of immuno-oncology and health disparities.

10. Budget: Provide a detailed budget for the project, including personnel, equipment, supplies, and any other associated costs.

11. Timeline: Outline the anticipated timeline for the project, including key milestones and deliverables.

12. Institutional support: Provide evidence of institutional support for the project, such as letters of collaboration or commitment from partnering organizations or institutions.

13. Relevant previous work: Describe any relevant previous work or research experience that supports the feasibility and potential success of the proposed project.

14. Ethical considerations: Discuss any ethical considerations associated with the research, such as data privacy, informed consent, and potential risks to study participants.

15. Regulatory approvals: Outline any necessary regulatory approvals that will be obtained for the project, such as Institutional Review Board (IRB) approval.

16. Dissemination plan: Describe how the findings and outcomes of the research will be disseminated to the scientific community and relevant stakeholders.

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88%

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93%

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