Opportunity Information: Apply for RFA CA 19 027
Revisions for Incorporation of Novel NCI-Supported Technology to Accelerate Cancer Research (P50 Clinical Trial Optional) (RFA-CA-19-027) is a National Cancer Institute (NCI) grant opportunity designed specifically for currently funded NCI P50 Specialized Center programs that want to submit a revision application (previously referred to as a competing revision). The central idea is to help established cancer research centers move faster or broaden the impact of their existing, peer-reviewed center research by adding a new technical approach or instrument that was developed with support from the NCI Innovative Molecular Analysis Technologies (IMAT) program. Rather than funding an entirely new center or a brand-new standalone project, this FOA focuses on targeted expansions to the active parent award that meaningfully enhance what the center is already doing.
The purpose of the program is twofold: first, to accelerate progress on the parent P50 study by incorporating an IMAT-developed technology that can deepen, refine, or extend the original research questions in one or more of the center's projects; and second, to promote independent validation of emerging technologies. In practice, this means the NCI is trying to bridge the gap between promising, innovative tools and their real-world usefulness in broader cancer research settings. By supporting independent testing and application within active P50 centers, the FOA aims to demonstrate reliability, suitability, and value for the larger research community, not just for the group that originally invented the technology.
A defining feature of the opportunity is its emphasis on interdisciplinary collaboration. Because IMAT technologies often sit at the intersection of engineering, computational science, molecular measurement, and cancer biology or clinical research, the FOA encourages teams to bring together diverse expertise to integrate a novel method into ongoing cancer research. The revisions are meant to be practical and additive: they should either expand the scope of specific projects under the P50 or remove bottlenecks and accelerate discovery by enabling measurements or analyses that were not previously feasible within the parent study.
The funding mechanism is a discretionary grant administered by the U.S. Department of Health and Human Services through the NIH (specifically NCI). The activity category is listed under Education and Health, with CFDA number 93.394. Clinical trials are optional under this FOA, meaning applicants may propose work that includes a clinical trial component if it fits the revision aims and the parent center structure, but a clinical trial is not required.
In terms of scale and competitiveness, the FOA anticipated a small number of awards (expected awards: 3), reflecting a targeted initiative rather than a broad-based funding program. The maximum award amount listed is $150,000, which reinforces that these are intended to be focused revision efforts that add a defined technological component to an existing, well-supported P50 program, rather than large multi-year expansions comparable to a new center award.
Eligibility is broad in the general NIH sense and includes many organization types (such as public and private institutions of higher education, nonprofits with or without 501(c)(3) status, for-profit organizations, small businesses, and various government and tribal entities). However, the practical eligibility constraint is that the applicant must already hold an active NCI P50 Specialized Center award that can serve as the parent grant for the revision, since the FOA is explicitly for revision applications tied to currently funded P50 centers.
Key administrative details include the FOA creation date of January 7, 2019, and an original closing date of September 27, 2019. Overall, the opportunity is best understood as a targeted NCI effort to speed adoption and rigorous testing of IMAT-enabled innovations inside established cancer research centers, with the near-term goal of accelerating progress on the parent center projects and the longer-term goal of moving novel technologies closer to routine use by appropriate cancer research communities.Apply for RFA CA 19 027
- The Department of Health and Human Services, National Institutes of Health in the education, health sector is offering a public funding opportunity titled "Revisions for Incorporation of Novel NCI-Supported Technology to Accelerate Cancer Research (P50 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 Jan 07, 2019.
- Applicants must submit their applications by Sep 27, 2019. (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.
- The number of recipients for this funding is limited to 3 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 (see text field entitled Additional Information on Eligibility for clarification).
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Frequently Asked Questions (FAQs)
What is the name of this grant opportunity?
The opportunity is titled Revisions for Incorporation of Novel NCI-Supported Technology to Accelerate Cancer Research (P50 Clinical Trial Optional) and is identified as RFA-CA-19-027.
Which agency is offering this funding?
This is a National Cancer Institute (NCI) funding opportunity administered through the National Institutes of Health (NIH) within the U.S. Department of Health and Human Services (HHS).
What type of application is this FOA requesting?
This FOA is for a revision application (previously referred to as a competing revision) to an existing parent award, not for a new standalone project or a brand-new center.
Who is this FOA designed for?
It is designed specifically for organizations that already have a currently funded NCI P50 Specialized Center award and want to revise that active parent grant by adding a qualifying technology component.
What is the practical eligibility requirement beyond general NIH eligibility?
Although many organization types may be eligible in general, the key practical constraint is that the applicant must have an active NCI P50 Specialized Center award that will serve as the parent grant for the revision.
What is the main goal of the program?
The program aims to help established P50 cancer research centers accelerate progress or broaden the impact of their existing peer-reviewed research by incorporating a new technology developed with support from the NCI Innovative Molecular Analysis Technologies (IMAT) program.
What kind of technology is the FOA focused on?
The FOA focuses on incorporating an IMAT-developed technology, meaning a new technical approach or instrument that was developed with support from the NCI IMAT program.
Does the FOA fund entirely new centers or brand-new standalone projects?
No. This FOA is focused on targeted expansions to an existing, currently funded P50 center award. It is intended to meaningfully enhance what the center is already doing rather than create a new center or a separate project unrelated to the parent award.
How should the revision relate to the parent P50 award?
The revision should be additive and practical, meaning it should enhance the active parent award by incorporating an IMAT technology that can deepen, refine, or extend the original research questions in one or more projects within the P50.
What does it mean that the FOA aims to "accelerate" the parent P50 study?
In this context, "accelerate" means using an IMAT-developed method or instrument to help remove bottlenecks, enable new measurements or analyses, and allow the center to move faster or further on the research goals already established under the parent P50.
What is the second major purpose of this FOA besides accelerating research?
A major additional purpose is to support independent validation of emerging IMAT-supported technologies by testing and applying them within active P50 centers.
Why is independent validation emphasized?
The FOA is intended to help bridge the gap between a promising tool and broader real-world usefulness by demonstrating the technology's reliability, suitability, and value in settings beyond the team that originally developed it.
Is interdisciplinary collaboration expected or encouraged?
Yes. The FOA emphasizes interdisciplinary collaboration, reflecting that IMAT technologies often span engineering, computational science, molecular measurement, and cancer biology and/or clinical research.
Are clinical trials required under this FOA?
No. Clinical trials are optional under this FOA. Applicants may include a clinical trial component if it fits the aims of the revision and the parent center structure, but a clinical trial is not required.
What is the funding mechanism and category listed for this opportunity?
The opportunity is described as a discretionary grant. The activity category is listed under Education and Health.
What is the CFDA number associated with this opportunity?
The CFDA number listed is 93.394.
How many awards were expected under this FOA?
The FOA anticipated a small number of awards, with expected awards: 3, indicating a targeted initiative rather than a broad funding program.
What is the maximum award amount?
The maximum award amount listed is $150,000, reinforcing that the revisions are intended to be focused additions to an existing P50 program rather than major multi-year expansions comparable to a new center award.
What types of organizations are generally eligible?
General eligibility includes a wide range of organization types, including public and private institutions of higher education, nonprofits (with or without 501(c)(3) status), for-profit organizations, small businesses, and various government, tribal, and related entities, subject to the key requirement of having an active NCI P50 parent award for the revision.
When was this FOA created?
The FOA creation date is listed as January 7, 2019.
What was the original closing date for this opportunity?
The original closing date is listed as September 27, 2019.
What is the simplest way to describe what this FOA is trying to do?
It is a targeted NCI effort to speed adoption and rigorous testing of IMAT-enabled innovations inside established NCI-funded P50 cancer research centers, with the near-term goal of accelerating parent center projects and the longer-term goal of moving validated technologies closer to routine use by appropriate cancer research communities.
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