Opportunity Information: Apply for RFA DK 15 019
The grant opportunity titled "Research Using Biosamples and Subjects from Type 1 Diabetes Clinical Studies Complications (DP3)" (Funding Opportunity Number RFA-DK-15-019) is a discretionary NIH research grant designed to support studies focused specifically on complications of type 1 diabetes. The central goal is to encourage investigators to take advantage of existing resources from prior or ongoing type 1 diabetes clinical studies, particularly by using already-enrolled human subjects and/or previously collected biospecimens. In practical terms, the program is aimed at accelerating new discoveries about why complications happen, how they progress, and what factors might predict or influence outcomes, by leveraging the value of well-characterized clinical study cohorts and sample collections rather than starting entirely new cohorts from scratch.
The opportunity sits in NIH's health-related funding portfolio (CFDA 93.847) and is categorized under Food and Nutrition, Health. It uses the grant funding instrument and is labeled with the DP3 mechanism, indicating a targeted program type intended to drive a particular research aim. The FOA was created on October 8, 2015, with an original closing date of March 3, 2016. The posted award ceiling is $1,000,000, which signals that projects were expected to be substantial in scope, potentially involving complex analyses of clinical data, deep phenotyping of complications, advanced laboratory assays on stored biosamples, or follow-on clinical evaluations of participants from legacy studies.
A defining feature of this announcement is the emphasis on "using subjects and/or samples from clinical studies on type 1 diabetes." That phrasing points toward research that is anchored in established clinical-study infrastructures: cohorts with known histories, standardized data collection, and existing consent frameworks, as well as biorepositories containing blood, urine, tissue, DNA, or other materials collected under rigorous protocols. By focusing on these already-developed assets, applicants would be expected to propose efficient, well-justified studies that extract new scientific value from prior investments in type 1 diabetes clinical research, especially around microvascular and macrovascular complications and other long-term outcomes that can be difficult and expensive to study prospectively.
Eligibility is broad and intentionally inclusive. Standard eligible applicants include a wide range of U.S. government entities (state, county, city/township, and special district governments), independent school districts, public housing authorities and Indian housing authorities, federally recognized Native American tribal governments, and Native American tribal organizations that are not federally recognized tribal governments. Academic eligibility includes public and state-controlled institutions of higher education as well as private institutions of higher education. The FOA also allows participation by nonprofit organizations both with and without IRS 501(c)(3) status (as long as they are not institutions of higher education in those categories), and it explicitly includes for-profit organizations (other than small businesses) and small businesses. In addition, the announcement highlights other eligible applicant types such as Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISI), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, eligible federal agencies, regional organizations, U.S. territories or possessions, tribal governments other than federally recognized ones, and even non-U.S. entities (foreign organizations). Taken together, that scope suggests NIH wanted to draw proposals from many kinds of institutions, including those serving underserved or underrepresented communities, and also to allow international expertise where it could strengthen the science.
In summary, this FOA is best understood as an NIH-funded push to deepen understanding of type 1 diabetes complications by reusing and reanalyzing high-value human subjects and biospecimen resources from existing clinical studies. It supports applicants across academia, government, nonprofit, and industry, including domestic and foreign organizations, with a relatively high maximum award level that could accommodate multidisciplinary projects. The intent is to generate new insights efficiently by building on established cohorts and sample repositories, rather than recreating them, ultimately helping clarify mechanisms, risk factors, biomarkers, and trajectories of complications in type 1 diabetes.Apply for RFA DK 15 019
- The National Institutes of Health in the food and nutrition, health sector is offering a public funding opportunity titled "Research Using Biosamples and Subjects from Type 1 Diabetes Clinical Studies Complications (DP3)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.847.
- This funding opportunity was created on 2015-10-08.
- Applicants must submit their applications by 2016-03-03. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Each selected applicant is eligible to receive up to $1,000,000.00 in funding.
- 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.
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Frequently Asked Questions (FAQs)
What is the title of this grant opportunity?
The opportunity is titled "Research Using Biosamples and Subjects from Type 1 Diabetes Clinical Studies Complications (DP3)."
What is the Funding Opportunity Number (FOA number)?
The Funding Opportunity Number is RFA-DK-15-019.
What type of grant is this?
This is a discretionary NIH research grant that uses the NIH grant funding instrument and is offered under the DP3 mechanism (a targeted program type intended to drive a specific research aim).
What is the main purpose of this FOA?
The central purpose is to support research focused specifically on complications of type 1 diabetes by encouraging investigators to use existing resources from prior or ongoing type 1 diabetes clinical studies, including already-enrolled human subjects and/or previously collected biospecimens.
What scientific topic does the FOA focus on?
The focus is on complications of type 1 diabetes, including long-term outcomes that may involve microvascular and macrovascular complications and other difficult-to-study complication trajectories.
What is the key research approach encouraged by this FOA?
The defining feature is reuse of established clinical study resources: leveraging well-characterized cohorts and existing biorepository samples rather than starting entirely new cohorts from scratch.
What kinds of resources are applicants expected to use?
Applicants are expected to take advantage of assets from prior or ongoing type 1 diabetes clinical studies, particularly (1) already-enrolled human subjects and/or (2) previously collected biospecimens stored in biorepositories.
Does the FOA require using human subjects, biospecimens, or both?
The FOA emphasizes using subjects and/or samples from clinical studies on type 1 diabetes, meaning proposals may be based on already-enrolled participants, previously collected biospecimens, or a combination of both.
Why does the FOA emphasize existing cohorts and biospecimens?
The intent is to accelerate discovery by building on prior investments in type 1 diabetes clinical research, using cohorts with known histories and standardized data collection and samples collected under rigorous protocols, which can make research on complications more efficient and well-justified.
What kinds of studies might fit within the scope described?
Based on the scope described, projects could include complex analyses of clinical data, deep phenotyping of complications, advanced laboratory assays on stored biosamples, or follow-on clinical evaluations of participants from legacy studies, all aimed at understanding why complications occur, how they progress, and what predicts outcomes.
What types of biospecimens are referenced as examples?
The FOA references biorepositories that may include blood, urine, tissue, DNA, or other materials collected under rigorous protocols.
What kinds of outcomes or insights is the program trying to generate?
The program aims to generate new insights into mechanisms, risk factors, biomarkers, and trajectories of type 1 diabetes complications, including factors that may predict or influence outcomes.
What is the CFDA number and category for this opportunity?
This opportunity is listed under CFDA 93.847 and categorized under Food and Nutrition, Health.
When was the FOA created?
The FOA was created on October 8, 2015.
What was the original closing date?
The original closing date was March 3, 2016.
What is the maximum (ceiling) award amount?
The posted award ceiling is $1,000,000.
What does the $1,000,000 award ceiling suggest about project scope?
The ceiling suggests projects were expected to be substantial in scope, potentially supporting multidisciplinary research and analyses that can involve complex clinical datasets, advanced assays, and/or follow-on evaluations within established cohorts.
Who is eligible to apply?
Eligibility is broad and includes many organization types across government, academia, nonprofit, and industry, as well as foreign (non-U.S.) entities.
Which U.S. government entities are eligible applicants?
Eligible U.S. government applicants include state governments, county governments, city or township governments, special district governments, independent school districts, public housing authorities, and Indian housing authorities.
Are federally recognized Native American tribal governments eligible?
Yes. Federally recognized Native American tribal governments are included as eligible applicants.
Are Native American tribal organizations that are not federally recognized eligible?
Yes. Native American tribal organizations (other than federally recognized tribal governments) are explicitly included.
Are colleges and universities eligible?
Yes. Eligible academic applicants include public and state-controlled institutions of higher education and private institutions of higher education.
Are nonprofit organizations eligible?
Yes. Nonprofit organizations are eligible both with and without IRS 501(c)(3) status (as long as they are not institutions of higher education in those categories).
Are for-profit organizations eligible?
Yes. For-profit organizations (other than small businesses) are explicitly included, and small businesses are also eligible.
Are faith-based or community-based organizations eligible?
Yes. The FOA explicitly includes faith-based or community-based organizations among eligible applicant types.
Are minority-serving institutions highlighted as eligible?
Yes. The FOA highlights multiple minority-serving institution categories as eligible, including HBCUs, Hispanic-serving Institutions, Tribally Controlled Colleges and Universities (TCCUs), Alaska Native and Native Hawaiian Serving Institutions, and Asian American Native American Pacific Islander Serving Institutions (AANAPISI).
Are U.S. territories or possessions eligible to apply?
Yes. U.S. territories or possessions are listed among eligible applicant types.
Are eligible federal agencies allowed to apply?
Yes. Eligible federal agencies are included in the eligible applicant types.
Are regional organizations eligible?
Yes. Regional organizations are included among eligible applicant types.
Are non-U.S. (foreign) organizations eligible?
Yes. The FOA indicates that non-U.S. entities (foreign organizations) are eligible.
What is the overall intent of funding this program?
The intent is to deepen understanding of type 1 diabetes complications efficiently by reusing and reanalyzing high-value human subject and biospecimen resources from existing clinical studies, rather than recreating cohorts, thereby accelerating discovery related to complication mechanisms and predictors.
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