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Applied regulatory science research to evaluate and treat cardiotoxicity of oncology therapeutics
Agency: Food and Drug Administration
Assistance Listings: 93.103 -- Food and Drug Administration Research
Last Updated: November 20, 2024
Funding opportunity
Summary
The goal of this funding opportunity announcement is to support applied regulatory science research to evaluate and treat cardiotoxicity of oncology therapeutics. The main outcomes of this work will be publications and presentations; however, FDA staff anticipate substantial involvement in study design and reviewing interim deliverables to ensure that the studies develop practical approaches and solutions that have the potential to inform regulatory decision making in the future. We anticipate organizing regular calls with funded investigators to support the collaboration with FDA - reviewing annual reports would be insufficient to ensure that direction of the research addresses FDA's needs.
OCE is interested in supporting research that improve the detection, monitoring and treatment of cardiotoxicity of oncology therapeutics.
Specific areas of interest include:
-Standardize Definitions: Develop clear definitions for different types and grades of cardiotoxicity
-Biomarkers and Imaging: Standardize the use of biomarkers and imaging techniques for assessing cardiotoxicity in oncology trials
-Functional Measures: Define consistent criteria for evaluating cardiac function
-Monitoring Plan: Develop a standardized cardiotoxicity monitoring plan that specifies the timing of cardiac assessments during the trial.
-Risk Stratification: Use a risk stratification model to identify patients at higher risk for cardiotoxicity based on pre-existing conditions and treatment regimens.
-Electronic Health Records and Real-World Data: Utilize electronic health records to standardize and systematically collect and store cardiotoxicity data, ensuring data accuracy and completeness.
-Patient-Reported Outcomes: Integrate patient-reported outcomes related to cardiovascular health (e.g., symptoms of heart failure, quality of life).
-Collaborative Networks: Engage in collaborative networks with other research institutions and industry partners to share data, best practices, and insights.
-Public Databases: Contribute to and utilize public databases of cardiotoxicity data to enhance the generalizability of findings and support broader research efforts.
-Treatment: Develop innovative approaches to treat cardiotoxicities with new oncology therapeutics.
-Natural history: Studies to investigate the natural history of various cardiotoxicities with new oncology therapeutics.
Eligibility
Eligible applicants
Private institutions of higher education
Public and state institutions of higher education
Special district governments
Small businesses
Independent school districts
Nonprofits non-higher education with 501(c)(3)
Nonprofits non-higher education without 501(c)(3)
Unrestricted
Other Native American tribal organizations
City or township governments
County governments
For-profit organizations other than small businesses
Federally recognized Native American tribal governments
Public and Indian housing authorities
State governments
Additional information
Grantor contact information
Description
terrin.brown@fda.hhs.gov
Phone
Link to additional information
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Forecasted
Award
$--
Program Funding
2
Expected awards
$--
Award Ceiling
$--
Award Floor
Funding opportunity number:
FOR-FD-25-015
Cost sharing or matching requirement:
Funding instrument type:
Cooperative agreement
Opportunity Category:
Discretionary
Opportunity Category Explanation:
Category of Funding Activity:
Agriculture
Consumer protection
Food and nutrition
Category Explanation:
History
Version:
1
Posted date:
November 20, 2024
Archive date:
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