Opportunity Information: Apply for RFA RM 27 016
The Cellular Senescence Network (SenNet): Discovery, Validation Centers (UM1 Clinical Trials Not Allowed) funding opportunity (RFA-RM-27-016) is a National Institutes of Health (NIH) Common Fund program that will support a set of cooperative agreement research centers as part of SenNet Stage 2. The overall focus is to move beyond initial resource-building and push toward clearer, validated definitions of what cellular senescence looks like in different human tissues and disease contexts, and what it means functionally for health and disease. The award mechanism is a UM1 cooperative agreement, which typically means funded teams will not operate as fully independent projects; instead, they will work closely with NIH and other awardees in a coordinated consortium structure with shared expectations for collaboration, data standards, and deliverables. As stated in the title and terms, clinical trials are not allowed under this NOFO.
At the scientific level, these Discovery and Validation Centers (DVCs) are expected to define, refine, and validate tissue- and disease-relevant senescence signatures, described here as "senotypes." In practical terms, this means identifying molecular and cellular patterns that reliably indicate senescent states in specific biological settings, then testing and confirming that those patterns hold up across samples, conditions, and measurement approaches. Alongside signature development, the NOFO emphasizes biomarkers associated with senotypes, suggesting a strong interest in markers that are measurable and useful across studies, potentially enabling comparison across tissues, diseases, and experimental systems. The intent is not only to label cells as senescent, but to build a more rigorous framework for distinguishing different flavors or subtypes of senescence that may matter for pathology, aging, regeneration, inflammation, fibrosis, cancer biology, and other domains where senescence has been implicated.
A central requirement of the program is the generation and contribution of high-quality datasets. The NOFO specifically calls out molecular, cellular, and spatial datasets, along with relevant metadata and documentation. This signals that SenNet is aiming for resources that are broadly reusable by the community, not just results reported in papers. "Spatial" implies approaches that preserve tissue context (for example, spatial transcriptomics, multiplex imaging, or other methods that map senescence-associated signals within intact tissue architecture). The explicit emphasis on metadata and documentation is important because it points to expectations around standardization, provenance, and interoperability: datasets should be accompanied by enough contextual information (sample attributes, experimental conditions, processing pipelines, quality metrics, and other descriptors) to make them interpretable and comparable within the consortium and to external users later.
Beyond data generation, the DVCs are expected to use complementary experimental systems to validate senotypes and biomarkers and to characterize responses to perturbations. This includes studying how senescent cells or senotype-associated biomarkers change when senescence is induced, modulated, or challenged, and how they respond to senescence-associated perturbations or senotherapeutic approaches. While human clinical trials are not allowed, the NOFO language leaves room for non-trial experimental work that tests senescence mechanisms and interventions in appropriate model systems or experimental platforms, as long as it fits within the non-clinical-trial boundaries. The functional consequences component is a key part of the program's purpose: the network is not only cataloging senescence signatures, but also trying to link those signatures to downstream biological effects that matter for disease processes and health outcomes.
Another distinctive feature is that applicants are asked to propose goals and aims that support consortium-wide organizational and outreach activities, referred to as SenNet OOC functions. This indicates that each DVC is expected to contribute not just to its own science, but also to the broader SenNet infrastructure and community engagement. In practice, this could include participating in working groups, helping shape shared protocols and standards, contributing to cross-center coordination, and supporting outreach that makes SenNet resources more accessible and useful to the wider research community. The inclusion of these consortium responsibilities in the application suggests they will be part of how applications are judged and how centers will be held accountable after award.
From an administrative standpoint, the opportunity is listed as discretionary funding and uses a cooperative agreement instrument, under the health activity category (CFDA 93.310). The NIH is the funding agency. The NOFO anticipates up to 25 awards, indicating a fairly large network intended to cover multiple tissues, disease areas, and technical approaches. The original closing date is 2026-11-23. An award ceiling is not provided in the posted summary, which often means applicants need to rely on the full NOFO text for budget guidance, or that budgets may vary by center scope within programmatic constraints.
Eligibility is broad and includes many U.S.-based organization types such as state, county, and local governments; public and state-controlled institutions of higher education; private institutions of higher education; nonprofit organizations with or without 501(c)(3) status; for-profit organizations (including those other than small businesses); small businesses; and certain housing authorities. It also explicitly includes Native American tribal governments (federally recognized) and Native American tribal organizations (other than federally recognized tribal governments). The eligibility list further notes additional eligible applicants such as Indian/Native American tribal governments that are not federally recognized, eligible federal agencies, U.S. territories or possessions, faith-based or community-based organizations, regional organizations, and non-domestic (non-U.S.) entities (foreign institutions). Taken together, this suggests NIH is aiming to attract a wide range of capable teams, including international partners, provided they can meet consortium expectations for data sharing, standards, and coordinated participation.
In plain terms, this NOFO is designed to fund centers that can do three things well at the same time: generate rigorous, high-dimensional datasets that describe senescence across tissues and diseases; validate and stress-test senescence signatures and biomarkers using multiple experimental angles; and operate as reliable consortium partners who help build shared infrastructure and outreach for a network meant to serve the broader biomedical community.Apply for RFA RM 27 016
- The National Institutes of Health in the health sector is offering a public funding opportunity titled "Cellular Senescence Network (SenNet): Discovery, Validation Centers (UM1 Clinical Trials Not Allowed)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.310.
- This funding opportunity was created on 2026-10-09.
- Applicants must submit their applications by 2026-11-23. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The number of recipients for this funding is limited to 25 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.
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FAQs: The Cellular Senescence Network (SenNet) - Discovery, Validation Centers (UM1 Clinical Trials Not Allowed) (RFA-RM-27-016)
1) What is this funding opportunity?
This opportunity (RFA-RM-27-016) is a National Institutes of Health (NIH) Common Fund program to support Cellular Senescence Network (SenNet) Stage 2 through a set of Discovery, Validation Centers (DVCs) funded as UM1 cooperative agreement research centers.
2) What is the overall goal of SenNet Stage 2 for these centers?
The overall focus is to move beyond initial resource-building and push toward clearer, validated definitions of what cellular senescence looks like in different human tissues and disease contexts, and what it means functionally for health and disease.
3) What does "Discovery, Validation Center (DVC)" mean in this NOFO?
DVCs are expected to define, refine, and validate tissue- and disease-relevant senescence signatures (called "senotypes") and associated biomarkers, and to generate high-quality datasets that can be contributed to the broader SenNet effort.
4) What award mechanism is used?
The award mechanism is a UM1 cooperative agreement.
5) What does it mean that this is a "cooperative agreement" (UM1)?
A cooperative agreement typically means funded teams will not operate as fully independent projects. Instead, they will work closely with NIH and other awardees in a coordinated consortium structure with shared expectations for collaboration, data standards, and deliverables.
6) Are clinical trials allowed under this opportunity?
No. As stated in the title and terms, clinical trials are not allowed under this NOFO.
7) If clinical trials are not allowed, what kinds of studies are emphasized?
The NOFO emphasizes discovery and validation work to define senotypes and biomarkers, generation of molecular/cellular/spatial datasets with metadata and documentation, and use of complementary experimental systems to validate signatures and characterize responses to perturbations (within non-clinical-trial boundaries).
8) What are "senotypes" in the context of this NOFO?
9) What is the importance of validating senotypes?
The program intent is not only to label cells as senescent, but to build a more rigorous framework for distinguishing different flavors or subtypes of senescence that may matter for pathology, aging, regeneration, inflammation, fibrosis, cancer biology, and other domains where senescence has been implicated.
10) Does the NOFO emphasize biomarkers?
Yes. Alongside senotype signature development, the NOFO emphasizes biomarkers associated with senotypes, indicating a strong interest in markers that are measurable and useful across studies and may enable comparisons across tissues, diseases, and experimental systems.
11) What kinds of data are DVCs expected to generate?
The NOFO calls for generation and contribution of high-quality datasets, specifically including molecular, cellular, and spatial datasets, along with relevant metadata and documentation.
12) What does "spatial datasets" imply for this program?
"Spatial" implies approaches that preserve tissue context, such as methods that map senescence-associated signals within intact tissue architecture (for example, spatial transcriptomics or multiplex imaging, as referenced in the description).
13) Why does the NOFO stress metadata and documentation?
The explicit emphasis on metadata and documentation points to expectations around standardization, provenance, and interoperability. Datasets should include enough contextual information (such as sample attributes, experimental conditions, processing pipelines, and quality metrics) to make them interpretable and comparable within the consortium and to external users later.
14) What does the NOFO expect regarding validation approaches?
DVCs are expected to use complementary experimental systems to validate senotypes and biomarkers and to characterize responses to perturbations, including studying how senescent cells or senotype-associated biomarkers change when senescence is induced, modulated, or challenged.
15) Does the NOFO involve testing senescence-related interventions?
The description indicates DVCs may characterize responses to senescence-associated perturbations or senotherapeutic approaches in appropriate experimental systems, as long as the work stays within the non-clinical-trial boundaries stated by the NOFO.
16) Is linking senescence signatures to function part of the scope?
Yes. A key purpose is to link senescence signatures to downstream biological effects that matter for disease processes and health outcomes, rather than only cataloging signatures.
17) What are "SenNet OOC functions" mentioned in the description?
Applicants are asked to propose goals and aims that support consortium-wide organizational and outreach activities, referred to as SenNet OOC functions. This indicates each DVC is expected to contribute to broader SenNet infrastructure and community engagement in addition to its own scientific work.
18) What kinds of consortium-wide responsibilities might DVCs have?
Based on the description, these responsibilities may include participating in working groups, helping shape shared protocols and standards, contributing to cross-center coordination, and supporting outreach that makes SenNet resources more accessible and useful to the wider research community.
19) How will consortium responsibilities affect applications?
The inclusion of consortium responsibilities in the application suggests they will be part of how applications are judged and how centers will be held accountable after award.
20) Who is the funding agency?
The funding agency is the National Institutes of Health (NIH), and the program is part of the NIH Common Fund.
21) How many awards does the NOFO anticipate making?
The NOFO anticipates up to 25 awards.
22) What is the application closing date listed in the summary?
The original closing date is 2026-11-23.
23) Is there an award ceiling listed?
An award ceiling is not provided in the posted summary. The description notes that applicants may need to rely on the full NOFO text for budget guidance, or budgets may vary by center scope within programmatic constraints.
24) What is the funding type/category described?
The opportunity is listed as discretionary funding and uses a cooperative agreement instrument under the health activity category (CFDA 93.310).
25) What organizations are eligible to apply?
Eligibility is broad and includes many organization types such as state, county, and local governments; public and state-controlled institutions of higher education; private institutions of higher education; nonprofit organizations with or without 501(c)(3) status; for-profit organizations (including those other than small businesses); and small businesses.
26) Are tribal entities eligible?
Yes. The eligibility list explicitly includes Native American tribal governments (federally recognized) and Native American tribal organizations (other than federally recognized tribal governments). It also notes Indian/Native American tribal governments that are not federally recognized as additional eligible applicants.
27) Are U.S. territories and federal agencies eligible?
Yes. The eligibility list notes additional eligible applicants such as eligible federal agencies and U.S. territories or possessions.
28) Are faith-based or community-based organizations eligible?
Yes. Faith-based or community-based organizations are included in the additional eligible applicants list.
29) Are regional organizations eligible?
Yes. Regional organizations are included in the additional eligible applicants list.
30) Are non-U.S. (foreign) institutions eligible?
Yes. The eligibility list includes non-domestic (non-U.S.) entities (foreign institutions).
31) What does NIH appear to be looking for in funded centers, in practical terms?
In plain terms, the NOFO is designed to fund centers that can (1) generate rigorous, high-dimensional datasets describing senescence across tissues and diseases, (2) validate and stress-test senescence signatures and biomarkers using multiple experimental angles, and (3) operate as reliable consortium partners who help build shared infrastructure and outreach for a network meant to serve the broader biomedical community.
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