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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.


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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

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Email

terrin.brown@fda.hhs.gov

terrin.brown@fda.hhs.gov

Phone

2404027610

Link to additional information

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Forecasted

Application process

This site is a work in progress. Go to www.grants.gov to apply, track application status, and subscribe to updates.

Award

$--

Program Funding

2

Expected awards

$--

Award Ceiling

$--

Award Floor

Funding opportunity number:

FOR-FD-25-015

Cost sharing or matching requirement:

No

Funding instrument type:

Cooperative agreement

Opportunity Category:

Discretionary

Opportunity Category Explanation:

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Category of Funding Activity:

Agriculture

Consumer protection

Food and nutrition

Category Explanation:

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History

Version:

1

Posted date:

November 20, 2024

Archive date:

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