Opportunity Information: Apply for RFA DK 27 301

The Kidney Precision Medicine Project Recruitment Sites (U01 Clinical Trial Not Allowed) funding opportunity (RFA DK-27-301) is a National Institutes of Health cooperative agreement aimed at expanding and strengthening the KPMP network of clinical recruitment sites. The core purpose is to enroll people with acute kidney injury (AKI) and/or chronic kidney disease (CKD) into a longitudinal cohort study that includes kidney biopsies and deep clinical characterization over time. These recruitment sites are expected to serve as the front door for participant identification, consent, clinical data collection, biospecimen acquisition (including biopsy tissue), and ongoing follow-up so the program can build a high-quality, well-annotated resource for precision medicine discovery in kidney disease.

A major emphasis of this round is improving enrollment where there have historically been gaps, with AKI specifically called out as under-enrolled and therefore a priority population. Beyond simply increasing participant numbers, the NOFO stresses comprehensive phenotyping, meaning applicants should be prepared to capture detailed clinical context and relevant physiologic and laboratory information that can help interpret tissue-level and molecular findings. The intent is to connect what is seen in the kidney tissue to what is happening in the patient clinically, enabling more precise disease subtyping, improved understanding of mechanisms, and identification of targets for future interventions.

The announcement also highlights several expanded or newer participation opportunities for recruitment sites. These include the ability to leverage clinically indicated biopsies where residual tissue can be used for research, which may broaden feasibility and increase the diversity of samples obtained in real-world care settings. It also includes enhanced physiologic phenotyping, suggesting an interest in richer functional assessments beyond standard clinical measurements. In addition, the NOFO allows or encourages repeat biopsies in appropriate circumstances, which can be valuable for studying disease progression, treatment response, or changes over time. Pediatric recruitment is explicitly mentioned, signaling a push to include children and adolescents where scientifically and ethically appropriate, and to fill knowledge gaps in pediatric kidney disease. Another notable expansion is the collection of healthy reference tissue, which can strengthen interpretation of disease-associated findings by providing well-characterized baseline comparators.

This mechanism is a cooperative agreement (U01), which typically means the NIH expects substantial scientific and programmatic involvement during the award. In practice, recruitment sites should anticipate close coordination with the broader KPMP consortium, adherence to common protocols and data standards, participation in network governance and working groups, and responsiveness to evolving consortium needs. The NOFO also makes clear that KPMP personnel are expected to actively participate in scientific discovery and to promote open science, reflecting a commitment to broad data sharing, transparency, and collaborative analysis so that the resulting datasets and biospecimens can accelerate kidney research for the wider community.

Eligibility is broad across U.S.-based domestic entities and includes many common applicant types such as state, county, and local governments; public and private institutions of higher education; independent school districts; special district governments; federally recognized tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofit organizations with or without 501(c)(3) status; for-profit organizations (including those other than small businesses); small businesses; and other domestic organizations that meet NIH requirements. At the same time, the geographic restriction is explicit: non-U.S. entities are not eligible to apply, non-U.S. components of U.S. organizations are not eligible, and foreign components (as defined by NIH policy) are not allowed. Applicants are directed to consult Section III of the NOFO for any additional eligibility conditions or clarifications beyond these high-level rules.

In terms of funding and scale, the opportunity lists an expected eight awards, with an award ceiling of $450,000. The original application closing date is July 10, 2026, and the program is categorized under Health with CFDA number 93.847. Overall, the opportunity is designed for clinical centers and partner organizations capable of recruiting and longitudinally following AKI and CKD participants, performing or coordinating kidney biopsy-based research activities, and operating within a highly collaborative, standardized, open-science consortium environment.

  • The National Institutes of Health in the health sector is offering a public funding opportunity titled "Kidney Precision Medicine Project Recruitment Sites (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): 93.847.
  • This funding opportunity was created on 2026-06-03.
  • Applicants must submit their applications by 2026-07-10. (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 $450,000.00 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 27 301

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Frequently Asked Questions (FAQs)

What is the funding opportunity called?

The opportunity is titled Kidney Precision Medicine Project Recruitment Sites (U01 Clinical Trial Not Allowed) and is associated with RFA DK-27-301.

Which agency is offering this opportunity?

This is a National Institutes of Health (NIH) funding opportunity.

What type of award mechanism is this?

This opportunity uses a cooperative agreement (U01) mechanism, which typically involves substantial NIH scientific and/or programmatic involvement during the project period.

Are clinical trials allowed under this opportunity?

No. The opportunity is labeled "Clinical Trial Not Allowed".

What is the main purpose of funding KPMP Recruitment Sites?

The core purpose is to expand and strengthen the KPMP network of clinical recruitment sites that enroll participants with acute kidney injury (AKI) and/or chronic kidney disease (CKD) into a longitudinal cohort study involving kidney biopsies and deep clinical characterization over time.

What is KPMP trying to build through these recruitment sites?

The program aims to build a high-quality, well-annotated resource to support precision medicine discovery in kidney disease, connecting tissue-level and molecular findings with detailed clinical context.

What participant populations are a priority for enrollment?

The announcement emphasizes improving enrollment in historically under-enrolled groups, with AKI specifically called out as under-enrolled and therefore a priority population.

What diseases or conditions should recruitment sites focus on?

Recruitment sites are expected to enroll participants with AKI and/or CKD into the KPMP longitudinal cohort.

What does "longitudinal cohort study" mean in this context?

In this opportunity, it refers to enrolling participants and then following them over time, including ongoing collection of clinical information and biospecimens (including biopsy tissue) to understand disease mechanisms and progression.

What roles are recruitment sites expected to play in KPMP?

Recruitment sites are described as the program's "front door" and are expected to support: participant identification, informed consent, clinical data collection, biospecimen acquisition (including biopsy tissue), and ongoing follow-up.

What kinds of data collection are emphasized in the NOFO?

The NOFO stresses comprehensive phenotyping, meaning the capture of detailed clinical context and relevant physiologic and laboratory information to help interpret kidney tissue and molecular findings.

Why is comprehensive phenotyping emphasized?

The intent is to connect what is seen in kidney tissue with what is happening clinically, enabling more precise disease subtyping, improved understanding of mechanisms, and identification of targets for future interventions.

Does the opportunity allow use of clinically indicated biopsies?

Yes. The announcement highlights the ability to leverage clinically indicated biopsies where residual tissue can be used for research, which may broaden feasibility and increase diversity of samples from real-world care settings.

Is enhanced physiologic phenotyping included in the scope?

Yes. The NOFO highlights enhanced physiologic phenotyping, indicating interest in richer functional assessments beyond standard clinical measurements.

Are repeat kidney biopsies permitted?

Yes. The NOFO allows or encourages repeat biopsies in appropriate circumstances, which can support studies of progression, treatment response, or changes over time.

Does the opportunity include pediatric recruitment?

Yes. Pediatric recruitment is explicitly mentioned, reflecting an intent to include children and adolescents when scientifically and ethically appropriate and to address knowledge gaps in pediatric kidney disease.

Is the collection of healthy reference tissue included?

Yes. The NOFO includes collection of healthy reference tissue to help interpret disease-associated findings by providing well-characterized baseline comparators.

What level of coordination with NIH and the KPMP consortium is expected?

As a U01 cooperative agreement, recruitment sites should anticipate close coordination with the broader KPMP consortium, including adherence to common protocols and data standards, participation in governance and working groups, and responsiveness to evolving consortium needs.

What does the opportunity say about open science and data sharing?

The announcement states that KPMP personnel are expected to actively participate in scientific discovery and to promote open science, reflecting a commitment to broad data sharing, transparency, and collaborative analysis to accelerate kidney research for the wider community.

Who is eligible to apply?

Eligibility is broad for U.S.-based domestic entities, including (as listed in the opportunity): state, county, and local governments; public and private institutions of higher education; independent school districts; special district governments; federally recognized tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofit organizations with or without 501(c)(3) status; for-profit organizations (including those other than small businesses); small businesses; and other domestic organizations that meet NIH requirements.

Are non-U.S. (foreign) organizations eligible to apply?

No. The geographic restriction is explicit: non-U.S. entities are not eligible to apply.

Can a U.S. organization include a non-U.S. component on the application?

No. The opportunity states that non-U.S. components of U.S. organizations are not eligible.

Are foreign components allowed under NIH policy for this opportunity?

No. The announcement states that foreign components (as defined by NIH policy) are not allowed.

Where should applicants look for additional eligibility conditions?

Applicants are directed to consult Section III of the NOFO for any additional eligibility conditions or clarifications.

How many awards are expected?

The opportunity lists an expectation of eight awards.

What is the award ceiling?

The opportunity lists an award ceiling of $450,000.

What is the application due date?

The original application closing date is July 10, 2026.

What is the CFDA number and program category?

The program is categorized under Health with CFDA number 93.847.

What types of organizations are this opportunity designed for?

It is designed for clinical centers and partner organizations capable of recruiting and longitudinally following AKI and CKD participants, performing or coordinating kidney biopsy-based research activities, and operating within a highly collaborative, standardized, open-science consortium environment.

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