Opportunity Information: Apply for RFA DK 27 108

The NIH is soliciting applications to continue the Cardiovascular Repository for Type 1 Diabetes (CaRe-T1D) Consortium through a U01 cooperative agreement mechanism. The central goal is to sustain and expand a collaborative, interdisciplinary research effort that uses a shared cardiovascular-focused repository to deepen understanding of why people with type 1 diabetes (T1D) face such high rates of cardiovascular disease (CVD), and how CVD in T1D may differ in its biology, trajectory, and clinical presentation from CVD in other populations. This opportunity is explicitly research-focused and does not allow clinical trials, meaning the work should center on observational, mechanistic, translational, analytic, and repository-driven studies rather than testing interventions in a trial framework.

The scientific rationale behind the funding is the persistent and outsized burden of cardiovascular complications in T1D. CVD remains the leading cause of death for individuals with T1D and substantially reduces life expectancy. Despite progress in managing traditional risk factors such as hyperglycemia, hypertension, and dyslipidemia, many patients still experience a significant residual cardiovascular risk even under what would be considered optimal control. The NOFO highlights that key disease mechanisms in T1D remain incompletely understood across multiple domains, including atherosclerosis, diabetic cardiomyopathy (both diastolic and systolic dysfunction), endothelial dysfunction, and cardiac autonomic neuropathy. These gaps matter because there are currently no therapies specifically approved to prevent or treat several of these common, severe cardiovascular complications in T1D, particularly cardiomyopathy-related pathways that contribute heavily to morbidity and mortality alongside atherosclerotic disease.

Programmatically, the opportunity is intended to keep the CaRe-T1D consortium operating as a coordinated national resource rather than a collection of disconnected projects. Applicants should expect the cooperative agreement structure to involve substantial NIH programmatic involvement and coordination expectations typical of U01 awards, with an emphasis on team science, harmonized methods, shared governance, and data or biospecimen resource stewardship. The underlying idea is that a continuing repository and consortium model can accelerate discovery by enabling larger, well-characterized datasets, standardized phenotyping, reproducible analyses, and cross-study comparisons that would be difficult for any single lab or center to achieve alone.

This NOFO is supported through the Special Diabetes Program, a congressionally supported initiative that funds research aimed at preventing, treating, and ultimately curing T1D and its complications. In that context, CaRe-T1D is positioned as a specialized consortium resource focused on cardiovascular outcomes and mechanisms, aligning with the program's emphasis on unique, innovative, and collaborative consortia and networked research efforts. While the notice does not list specific required aims in the provided excerpt, the described priorities point toward projects that can leverage and enrich the existing CaRe-T1D infrastructure to clarify pathophysiology, identify novel risk markers or mechanistic pathways, and explain why standard risk-factor modification does not fully eliminate cardiovascular risk in T1D.

Key administrative details are as follows. The funding opportunity title is "Continuation of the Cardiovascular Repository for Type 1 Diabetes (CARE-T1D) Consortium U01 (Open Competition) - Research (U01, Clinical Trial Not Allowed)." The funding opportunity number is RFA-DK-27-108. The sponsor is the National Institutes of Health (NIH), and the instrument is a cooperative agreement (U01). The activity category is Health, and the CFDA/Assistance Listing numbers include 93.233, 93.837, 93.838, 93.839, 93.840, and 93.847. The application closing date listed is 2027-03-10. The expected number of awards is 8, and the award ceiling is $500,000 (as stated in the source data).

Eligibility is broad across many U.S.-based organization types, including state, county, and local governments; special district governments; independent school districts; public and private institutions of higher education; federally recognized Native American tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofits with or without 501(c)(3) status (excluding higher education institutions in those categories as specified); for-profit organizations other than small businesses; and small businesses. However, foreign eligibility is restricted: non-U.S. entities are not eligible to apply, and non-U.S. components of U.S. organizations are not eligible. At the same time, foreign components as defined by NIH policy are allowed, which typically means a U.S. applicant may include certain foreign elements in the project when well-justified and compliant with NIH Grants Policy Statement definitions, even though the applicant organization and primary components must remain domestic.

Overall, the opportunity is aimed at sustaining a national collaborative platform to tackle a stubborn clinical problem: cardiovascular disease that continues to claim lives in T1D even when conventional risk factors are addressed. The emphasis is on advancing mechanistic understanding and improving the research ecosystem (data, specimens, standardized measures, and interdisciplinary collaboration) necessary to develop future preventive and therapeutic strategies, while staying firmly in the non-clinical-trial research lane required by the NOFO.

  • The National Institutes of Health in the health sector is offering a public funding opportunity titled "Continuation of the Cardiovascular Repository for-Type 1 Diabetes (CARE-T1D) Consortium U01 (Open Competition)- Research (U01, Clinical Trial Not Allowed)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.233, 93.837, 93.838, 93.839, 93.840, 93.847.
  • This funding opportunity was created on 2026-06-04.
  • Applicants must submit their applications by 2027-03-10.
  • Each selected applicant is eligible to receive up to $500,000.00 in funding.
  • The number of recipients for this funding is limited to 8 candidate(s).
  • Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
Apply for RFA DK 27 108

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Frequently Asked Questions (FAQs)

What is the funding opportunity?

The NIH is soliciting applications to continue the Cardiovascular Repository for Type 1 Diabetes (CaRe-T1D) Consortium through a U01 cooperative agreement. The funding opportunity title is "Continuation of the Cardiovascular Repository for Type 1 Diabetes (CARE-T1D) Consortium U01 (Open Competition) - Research (U01, Clinical Trial Not Allowed)."

What is the funding opportunity number (NOFO/RFA number)?

The funding opportunity number is RFA-DK-27-108.

Who is the sponsor of this opportunity?

The sponsor is the National Institutes of Health (NIH).

What type of award mechanism is being used?

This opportunity uses a U01 cooperative agreement mechanism, which typically involves substantial NIH programmatic involvement and coordination expectations.

Are clinical trials allowed under this NOFO?

No. This is a research opportunity where clinical trials are not allowed. The work is expected to focus on observational, mechanistic, translational, analytic, and repository-driven studies rather than testing interventions in a clinical trial framework.

What is the overall goal of continuing the CaRe-T1D Consortium?

The central goal is to sustain and expand a collaborative, interdisciplinary research effort that uses a shared cardiovascular-focused repository to better understand why people with type 1 diabetes (T1D) experience high rates of cardiovascular disease (CVD), and how CVD in T1D may differ from CVD in other populations in terms of biology, trajectory, and clinical presentation.

Why is NIH prioritizing cardiovascular disease research in type 1 diabetes?

The scientific rationale is the persistent and outsized cardiovascular burden in T1D. CVD remains the leading cause of death for individuals with T1D and reduces life expectancy. Even with progress in managing traditional risk factors (such as hyperglycemia, hypertension, and dyslipidemia), many people with T1D still have substantial residual cardiovascular risk under what would be considered optimal control.

What types of cardiovascular complications and mechanisms are highlighted as gaps in knowledge?

The NOFO highlights that key disease mechanisms in T1D remain incompletely understood across multiple domains, including atherosclerosis, diabetic cardiomyopathy (both diastolic and systolic dysfunction), endothelial dysfunction, and cardiac autonomic neuropathy.

What is meant by a "repository" in this consortium context?

Based on the description provided, the repository is a shared cardiovascular-focused resource intended to support research by enabling larger, well-characterized datasets, standardized phenotyping, reproducible analyses, and cross-study comparisons. It is positioned as a coordinated national resource rather than separate, disconnected projects.

What research approach does NIH expect from applicants?

The opportunity emphasizes team science and coordinated consortium operations, including harmonized methods, shared governance, and stewardship of data and/or biospecimen resources. The intent is to support collaborative, interdisciplinary research that leverages and enriches the existing CaRe-T1D infrastructure.

What kinds of studies are a good fit, given that clinical trials are not allowed?

The notice frames the work as observational, mechanistic, translational, analytic, and repository-driven research. The described priorities point toward studies that clarify pathophysiology, identify novel risk markers or mechanistic pathways, and help explain why standard risk-factor modification does not fully eliminate cardiovascular risk in T1D.

How is this opportunity positioned programmatically within NIH?

This NOFO is supported through the Special Diabetes Program, a congressionally supported initiative that funds research aimed at preventing, treating, and ultimately curing type 1 diabetes and its complications. CaRe-T1D is positioned as a specialized consortium resource focused on cardiovascular outcomes and mechanisms.

What is the activity category for this opportunity?

The activity category is Health.

What are the CFDA/Assistance Listing numbers associated with this opportunity?

The CFDA/Assistance Listing numbers include 93.233, 93.837, 93.838, 93.839, 93.840, and 93.847.

When is the application closing date?

The application closing date listed is 2027-03-10.

How many awards does NIH expect to make?

The expected number of awards is 8.

What is the award ceiling?

The award ceiling is $500,000 (as stated in the source data provided).

Who is eligible to apply?

Eligibility is broad across many U.S.-based organization types, including state, county, and local governments; special district governments; independent school districts; public and private institutions of higher education; federally recognized Native American tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofits with or without 501(c)(3) status (excluding higher education institutions in those categories as specified); for-profit organizations other than small businesses; and small businesses.

Are non-U.S. (foreign) organizations eligible to apply as the main applicant?

No. Non-U.S. entities are not eligible to apply.

Can a U.S. applicant include non-U.S. components in the project?

Non-U.S. components of U.S. organizations are not eligible. However, foreign components (as defined by NIH policy) are allowed, which generally means certain foreign elements may be included when well-justified and consistent with NIH Grants Policy definitions, even though the applicant organization and primary components must remain domestic.

What does the cooperative agreement structure imply for awardees?

The cooperative agreement structure implies substantial NIH programmatic involvement and coordination expectations typical of U01 awards, with an emphasis on coordinated consortium operations, team science, harmonized methods, shared governance, and resource stewardship.

Is this opportunity focused on building a coordinated national resource or on independent projects?

It is intended to keep CaRe-T1D operating as a coordinated national resource rather than a collection of disconnected projects.

What problem is this consortium trying to address in practical terms?

The consortium is aimed at advancing understanding of why cardiovascular disease continues to claim lives in type 1 diabetes even when conventional risk factors are addressed. The emphasis is on improving the research ecosystem (data, specimens, standardized measures, and interdisciplinary collaboration) needed to support future preventive and therapeutic strategies, while staying within the non-clinical-trial scope.

Are there existing therapies specifically approved for several cardiovascular complications in T1D?

The provided description notes that there are currently no therapies specifically approved to prevent or treat several common, severe cardiovascular complications in T1D, particularly cardiomyopathy-related pathways that contribute to morbidity and mortality alongside atherosclerotic disease.

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