Opportunity Information: Apply for RFA CA 21 007

This NIH/National Cancer Institute funding opportunity (RFA-CA-21-007) supports revision applications to active NCI-funded R01 projects, with the goal of speeding up or expanding the parent study by adding a new technology that was developed with NCI Innovative Molecular Analysis Technologies (IMAT) program support. In practice, it is designed for research teams who already have an ongoing R01 and want to incorporate an IMAT-supported instrument, platform, or technical approach to either broaden the original aims or accelerate the pace and impact of the existing work. A key idea behind the announcement is that promising IMAT technologies often need rigorous, independent validation in real-world research settings before they are widely adopted, and these revision awards are meant to help bridge that gap by placing emerging tools into appropriate cancer research communities.

The main scientific purpose is twofold: first, to incentivize independent testing and validation of novel IMAT-supported technologies within the context of a currently funded cancer research project; and second, to promote faster adoption of those technologies by demonstrating their value for answering important cancer biology, prevention, diagnosis, treatment, or related research questions. The FOA emphasizes that the revision should clearly build on the parent grant by either expanding the scope of the original research questions or materially accelerating progress toward the original objectives. The technology component is not meant to be a generic methods upgrade; it is specifically tied to incorporating a technical approach or instrument that originated from NCI IMAT funding, aligning the revision with IMATs broader mission of enabling innovative molecular and analytical methods for cancer research.

The award mechanism is an R01 revision (formerly known as a competing revision), meaning applicants are not proposing a brand-new standalone project. Instead, they submit a request to modify and add to an existing R01 in a way that remains anchored to the funded parent award. The announcement is labeled "Clinical Trial Optional," which signals that applicants may propose a clinical trial component if it is appropriate and justified for the revision, but a clinical trial is not required. The overall activity category is listed under Education and Health, and the program is associated with CFDA number 93.394.

Funding details in the provided source indicate an award ceiling of $150,000. The expected number of awards is not specified in the excerpt. The original closing date listed is 2021-09-29, and the FOA record creation date is 2020-11-24, indicating this was a time-bound opportunity tied to a specific receipt window.

Eligibility is broad and includes many typical NIH-eligible applicant organizations, spanning public and private institutions of higher education, nonprofits (including 501(c)(3) and non-501(c)(3)), for-profit organizations (other than small businesses), small businesses, and multiple levels of government (state, county, city/township, special district), as well as independent school districts and public housing authorities/Indian housing authorities. It also includes federally recognized Native American tribal governments and Native American tribal organizations that are not federally recognized tribal governments. The FOA also explicitly highlights additional eligible applicant types such as Alaska Native and Native Hawaiian Serving Institutions, AANAPISIS institutions, Hispanic-serving institutions, Historically Black Colleges and Universities, Tribally Controlled Colleges and Universities, faith-based or community-based organizations, eligible federal agencies, regional organizations, U.S. territories or possessions, and even non-domestic (non-U.S.) entities/foreign organizations. This breadth reflects an intent to encourage participation from a wide range of research settings and communities, including institutions that serve historically underrepresented populations and organizations outside the United States when appropriate.

At its core, the opportunity is about accelerating cancer research by pairing active, question-driven R01 projects with cutting-edge IMAT-derived technologies in a way that produces clear, publishable evidence that the new technology improves capability, speed, rigor, or reach. Successful revision applications under this FOA would be expected to make a strong case that the added IMAT-supported approach is both technically and scientifically compelling for the parent projects goals, and that the revision work will meaningfully advance cancer research by validating and demonstrating the technologys utility in an independent, mission-relevant context.

  • The National Institutes of Health in the education, health sector is offering a public funding opportunity titled "Revision Applications for Incorporation of Novel NCI-Supported Technology to Accelerate Cancer Research (R01 Clinical Trial Optional)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.394.
  • This funding opportunity was created on 2020-11-24.
  • Applicants must submit their applications by 2021-09-29. (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 $150,000.00 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.
Apply for RFA CA 21 007

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Frequently Asked Questions (FAQs)

What is this funding opportunity?

This is an NIH/National Cancer Institute (NCI) funding opportunity announcement (FOA) identified as RFA-CA-21-007. It supports revision applications to active NCI-funded R01 projects to speed up or expand the parent study by adding a new technology developed with NCI Innovative Molecular Analysis Technologies (IMAT) program support.

What is the main goal of the FOA?

The goal is to accelerate or broaden ongoing NCI-funded R01 research by incorporating an IMAT-supported instrument, platform, or technical approach. A central idea is to help promising IMAT technologies gain rigorous, independent validation in real research settings, which can support wider adoption in cancer research communities.

Who is this opportunity intended for?

It is designed for research teams that already have an ongoing, active NCI-funded R01 and want to incorporate an IMAT-supported technology to either (1) expand the scope of the existing work or (2) materially accelerate progress toward the original objectives of the parent award.

What type of application is required (new project vs. modification)?

This is an R01 revision application (formerly called a competing revision). It is not for proposing a brand-new standalone project. The application requests modifications and additions that remain anchored to the currently funded parent R01.

What kinds of changes should the revision propose?

The FOA emphasizes that the revision should clearly build on the parent grant by doing at least one of the following:

  • Expanding the scope of the original research questions/aims, or
  • Accelerating progress toward the original objectives in a meaningful way.

What is the role of IMAT-supported technology in the revision?

The technology addition is central to the FOA. The revision is meant to incorporate a technical approach or instrument that originated from NCI IMAT funding. It is not described as a general or generic methods upgrade; it should align with the IMAT mission of enabling innovative molecular and analytical methods for cancer research.

Why does the FOA emphasize independent validation of IMAT technologies?

The FOA is based on the idea that even promising IMAT technologies often need rigorous, independent testing and validation in real-world settings before broad adoption. These revision awards are intended to help bridge that gap by placing emerging IMAT tools into appropriate cancer research projects where their performance and value can be demonstrated.

What scientific areas can the revision support?

The FOA frames the technology validation and adoption goal around cancer research questions such as cancer biology, prevention, diagnosis, treatment, or related areas, as long as the work is grounded in the active NCI-funded R01 and the revision meaningfully advances the parent project.

Is a clinical trial required?

No. The FOA is labeled Clinical Trial Optional. That means a clinical trial component may be included if appropriate and well-justified for the revision, but it is not required.

What is the award ceiling (maximum amount)?

The provided information lists an award ceiling of $150,000.

How many awards will be made?

The expected number of awards is not specified in the provided excerpt.

What is the closing date for this opportunity?

The original closing date listed is 2021-09-29.

When was the FOA record created?

The FOA record creation date is listed as 2020-11-24.

What is the CFDA number associated with this program?

The program is associated with CFDA number 93.394.

What is the activity category?

The overall activity category is listed under Education and Health.

What types of organizations are eligible to apply?

Eligibility is broad and includes many NIH-eligible organization types, including:

  • Public and private institutions of higher education
  • Nonprofits (including 501(c)(3) and non-501(c)(3))
  • For-profit organizations (other than small businesses)
  • Small businesses
  • State, county, city/township governments, special districts
  • Independent school districts
  • Public housing authorities/Indian housing authorities
  • Federally recognized Native American tribal governments
  • Native American tribal organizations that are not federally recognized tribal governments

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

Yes. The FOA explicitly highlights additional eligible applicant types including (among others) Historically Black Colleges and Universities (HBCUs), Hispanic-serving institutions, Tribally Controlled Colleges and Universities, Alaska Native and Native Hawaiian Serving Institutions, AANAPISIS institutions, and faith-based or community-based organizations.

Are non-U.S. organizations eligible to apply?

Yes. The FOA’s eligibility list explicitly includes non-domestic (non-U.S.) entities/foreign organizations, as well as U.S. territories or possessions, and regional organizations.

What makes a strong revision application under this FOA?

Based on the provided description, a strong application would be expected to clearly argue that:

  • The added IMAT-supported approach is technically compelling and appropriate for the parent R01’s context.
  • The added technology is scientifically compelling for answering the parent project’s cancer research questions.
  • The revision will meaningfully expand scope or accelerate progress, rather than serving as a routine methods update.
  • The work will produce clear evidence (e.g., publishable validation/demonstration) that the technology improves capability, speed, rigor, or reach in an independent, mission-relevant setting.

Does the revision need to be directly tied to the parent R01’s aims?

Yes. The FOA emphasizes that the revision is not a standalone effort; it must remain anchored to the parent award and should either broaden the original aims or materially accelerate progress toward the original objectives.

What is the broader program rationale behind this FOA?

The broader rationale is to speed progress in cancer research by bridging the gap between promising IMAT-derived tools and widespread use. By supporting independent, real-world validation within active R01 projects, the FOA aims to demonstrate the value of emerging technologies and promote faster adoption by the cancer research community.

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