Opportunity Information: Apply for PAR 20 292

The NCI Clinical and Translational Exploratory/Developmental Studies (R21 Clinical Trial Optional) opportunity (PAR-20-292) is a National Institutes of Health grant program designed to jump-start early-stage, high-impact cancer research projects that are still in the exploratory or developmental phase. Its main purpose is to help investigators generate initial evidence, proof-of-concept data, or enabling tools that can move an idea forward toward larger-scale studies, including eventual clinical translation. The scope is intentionally broad within cancer research, covering work related to cancer diagnosis, treatment, imaging, symptom and toxicity management, and prevention, with an emphasis on projects that can meaningfully accelerate the development of new interventions or approaches.

A central theme of this FOA is supporting research that sits at the intersection of clinical and translational science. That includes correlative studies tied to clinical trials (for example, biomarker discovery/validation efforts, pharmacodynamic assays, immune monitoring, or imaging correlates that help explain why a treatment works or fails), as well as research that directly enables novel cancer therapeutic development, preventive agent development, symptom/toxicity interventions, and radiotherapy development. It also highlights mechanism-driven combinations, meaning combinations of therapies or modalities that are justified by biology and aimed at a clear mechanistic hypothesis rather than trial-and-error pairing. In addition, the announcement explicitly welcomes innovative preclinical studies, particularly those using newer clinically relevant models (such as improved patient-derived systems or other translationally faithful platforms) and advanced imaging technologies, when these efforts are geared toward producing knowledge or tools that could reasonably support first-in-human clinical trials.

Because this is an R21, it is structured for early, conceptual, and potentially higher-risk projects. The program is intended for studies that may not yet have the extensive preliminary data expected for larger NIH mechanisms, but that are scientifically compelling and could produce outsized impact if successful. In practical terms, the R21 format is meant to fund work like feasibility testing, development of a novel method or platform, early validation of a target or biomarker, initial testing of a therapeutic concept in a translational model, or foundational correlative work that strengthens or de-risks a clinical development path. The "clinical trial optional" designation means applications may propose a clinical trial if appropriate, but a clinical trial is not required, and many responsive projects will be preclinical or clinical-correlative rather than interventional.

Funding details in the source information indicate an award ceiling of $200,000. The opportunity is categorized as a discretionary grant within NIH health-related funding activity areas (CFDA numbers listed include 93.393, 93.394, 93.395, 93.396, and 93.399, which correspond to NIH/NCI-related programs). The listing shows an original closing date of 2022-07-20 and a creation date of 2020-08-24, which is useful context for timing, although applicants typically need to confirm current submission windows and any reissues or updates to the FOA on the NIH notice and funding pages.

Eligibility is broad and includes a wide range of U.S. and non-U.S. organizations. Eligible applicants include state, county, and local governments; special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofit organizations both with and without 501(c)(3) status (outside higher education); for-profit organizations (other than small businesses); and small businesses. The FOA also explicitly calls out additional eligible applicant categories such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving institutions, Tribally Controlled Colleges and Universities (TCCUs), Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), faith-based or community-based organizations, U.S. territories or possessions, regional organizations, eligible federal agencies, and non-domestic (foreign) entities.

Overall, this opportunity is aimed at researchers with bold, translationally grounded cancer ideas that need focused early funding to prove feasibility, develop a novel tool or model, generate key correlative insights connected to clinical trials, or produce the enabling evidence required to justify a next-step clinical effort. The expectation is not necessarily a finished product, but a strong, testable concept and a clear path to future impact in cancer research and, ultimately, patient care.

  • The National Institutes of Health in the education, health sector is offering a public funding opportunity titled "NCI Clinical and Translational Exploratory/Developmental Studies (R21 Clinical Trial Optional)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.393, 93.394, 93.395, 93.396, 93.399.
  • This funding opportunity was created on 2020-08-24.
  • Applicants must submit their applications by 2022-07-20. (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 $200,000.00 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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FAQs: NCI Clinical and Translational Exploratory/Developmental Studies (R21 Clinical Trial Optional) (PAR-20-292)

What is this grant opportunity?

This opportunity is the NCI Clinical and Translational Exploratory/Developmental Studies program (R21 Clinical Trial Optional), identified as PAR-20-292. It is an NIH/NCI grant mechanism intended to jump-start early-stage, high-impact cancer research projects that are still exploratory or developmental.

What is the main purpose of this R21 program?

The purpose is to support projects that can generate initial evidence, proof-of-concept data, or enabling tools that move an idea toward larger-scale studies and eventual clinical translation. The focus is on getting compelling concepts to the next decision point by producing actionable early results.

What kinds of research areas are within scope?

The scope is intentionally broad across cancer research. Examples mentioned include cancer diagnosis, treatment, imaging, symptom and toxicity management, and prevention, especially where the project can meaningfully accelerate development of new interventions or approaches.

How does this FOA define the clinical and translational focus?

The FOA emphasizes work at the intersection of clinical and translational science. That includes studies connected to clinical trials (correlative work) as well as research that directly enables development of new therapeutics, preventive agents, symptom/toxicity interventions, and radiotherapy approaches.

What are "correlative studies tied to clinical trials" in this context?

Correlative studies are research components linked to clinical trials that help explain mechanisms of action, response, or resistance. Examples provided include biomarker discovery/validation, pharmacodynamic assays, immune monitoring, and imaging correlates that clarify why a treatment works or fails.

Does an application have to include a clinical trial?

No. The opportunity is labeled "clinical trial optional," meaning a clinical trial may be proposed if appropriate, but it is not required. Many responsive projects may be preclinical or clinical-correlative rather than interventional.

What does "R21" imply about the project stage and risk?

As an R21, this program is structured for early, conceptual, and potentially higher-risk projects. It is intended for scientifically compelling studies that may not yet have extensive preliminary data but could have outsized impact if successful.

What types of projects are specifically well-suited to the R21 format described here?

Examples described include feasibility testing, development of a novel method or platform, early validation of a target or biomarker, initial testing of a therapeutic concept in a translational model, and foundational correlative work that strengthens or de-risks a clinical development pathway.

Are mechanism-driven therapy combinations encouraged?

Yes. The FOA highlights mechanism-driven combinations, meaning combinations of therapies or modalities justified by biology and aimed at testing a clear mechanistic hypothesis, rather than trial-and-error pairing.

Are innovative preclinical studies allowed or encouraged?

Yes. The announcement explicitly welcomes innovative preclinical studies, particularly those using newer clinically relevant models (such as improved patient-derived systems or other translationally faithful platforms) and advanced imaging technologies, when the work could support first-in-human clinical trials.

Does the FOA prioritize projects that can lead to first-in-human studies?

It supports efforts that produce knowledge or tools that could reasonably support first-in-human clinical trials, especially when the studies are translationally grounded and generate enabling evidence for next-step clinical efforts.

What is the stated funding ceiling for this opportunity?

The provided information indicates an award ceiling of $200,000.

What type of funding mechanism is this categorized under?

It is described as a discretionary grant within NIH health-related funding activity areas.

Which CFDA numbers are associated with this listing?

The listing includes CFDA numbers 93.393, 93.394, 93.395, 93.396, and 93.399, which correspond to NIH/NCI-related programs.

What are the dates mentioned for this opportunity?

The information provided notes a creation date of 2020-08-24 and an original closing date of 2022-07-20. These dates provide timing context, but applicants are advised (per the provided description) to confirm current submission windows and any reissues or updates through official NIH notices and funding pages.

Who is eligible to apply?

Eligibility is broad and includes U.S. and non-U.S. organizations. Eligible applicants listed include state, county, and local governments; special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofit organizations with or without 501(c)(3) status (outside higher education); for-profit organizations (other than small businesses); and small businesses.

Are non-U.S. (foreign) entities eligible?

Yes. The FOA explicitly includes non-domestic (foreign) entities among eligible applicant categories.

Are minority-serving institutions and community-based organizations included in eligibility?

Yes. The FOA explicitly calls out eligibility for categories such as HBCUs, Hispanic-serving institutions, TCCUs, Alaska Native and Native Hawaiian Serving Institutions, AANAPISIs, and faith-based or community-based organizations.

Are U.S. territories or regional organizations eligible?

Yes. The FOA lists U.S. territories or possessions and regional organizations among eligible applicant categories.

What is the overall goal for applicants under this opportunity?

The opportunity targets researchers with bold, translationally grounded cancer ideas that need focused early funding to prove feasibility, develop a novel tool or model, generate key clinical-trial-linked correlative insights, or produce enabling evidence required to justify a next-step clinical effort.

Is a fully finished intervention or product expected at the end of an R21 project?

The description emphasizes that the expectation is not necessarily a finished product. Instead, the emphasis is on a strong, testable concept and a clear path to future impact in cancer research and, ultimately, patient care.

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