Opportunity Information: Apply for RFA CA 22 020
Cancer Prevention, Detection, Diagnosis, and Treatment Technologies for Global Health (RFA-CA-22-020) is a National Institutes of Health funding opportunity that uses a U01 cooperative agreement to support practical, cancer-focused technology development aimed specifically at low- and middle-income countries (LMICs). The core goal is to move promising technologies closer to real-world use by adapting and validating them so they can function reliably in resource-constrained settings. Rather than funding basic discovery, the announcement focuses on turning an existing or emerging assay, device, or treatment-related technology into a user-friendly, low-cost solution that can meaningfully improve cancer prevention, early detection, diagnosis, or treatment where infrastructure, trained personnel, and budgets are limited.
A key requirement is that applicants must already have a working prototype or assay in hand at the time of application. The prototype does not have to be originally designed for cancer, but it must be far enough along that the project can credibly pursue adaptation for cancer use and then demonstrate performance. The expected work includes (1) tailoring the technology to the target cancer use-case and LMIC context, (2) showing technical functionality, and (3) generating evidence of clinical performance in the intended setting. The FOA emphasizes objective, milestone-driven progress: teams are expected to hit measurable performance targets, then iterate on the design based on results, and finally conduct improvements and validation activities within LMIC environments. Clinical trials are optional, meaning projects may include clinical studies if they are appropriate for demonstrating clinical performance, but the mechanism does not require a clinical trial for every award.
Because success depends on more than just engineering, the FOA makes multidisciplinary collaboration non-negotiable. Applicant teams must include expertise spanning engineering or assay/treatment development, oncology, global health care delivery, and business development. This reflects the reality that technologies fail in global health not only due to weak technical performance, but also because they are too expensive, too hard to use, too dependent on fragile supply chains, or poorly aligned with local clinical workflows. As a result, applicants are expected to treat affordability, cost-effectiveness, and point-of-need usability as core design constraints, not as afterthoughts. In practice, that means designing for the realities of LMIC settings such as limited lab capacity, intermittent electricity, shortages of specialized staff, challenging maintenance conditions, and the need for clear, actionable results that fit local clinical decision-making.
This FOA sits within the National Cancer Institute (NCI) Affordable Cancer Technologies (ACTs) Program, which is oriented toward scalable, accessible cancer technology solutions. Consistent with that mission, the announcement supports projects that can be deployed and sustained, not just demonstrated in ideal conditions. The cooperative agreement structure also signals that NIH/NCI expects an active partnership role, typically involving programmatic involvement in shaping milestones, monitoring progress, and ensuring the project remains aligned with the program goals of affordability and deployability in LMICs.
Eligibility is broad and includes many types of organizations: public and private institutions of higher education, nonprofits (with or without 501(c)(3) status), for-profit organizations (other than small businesses) and small businesses, and multiple levels of government (state, county, city/township, special districts), as well as independent school districts and public housing authorities/Indian housing authorities. The FOA also explicitly welcomes a wide range of additional applicant categories and partners, including non-U.S. (foreign) organizations and regional organizations, as well as institutions serving historically underrepresented communities (for example, HBCUs, Hispanic-serving institutions, AANAPISIs, Tribal colleges and universities, and Alaska Native/Native Hawaiian serving institutions). Tribal governments and tribal organizations are included as well. This broad eligibility aligns with the FOA's emphasis on multidisciplinary and cross-sector teams that can combine technical innovation with on-the-ground implementation capability.
From the provided opportunity details, the awarding agency is NIH, the opportunity category is discretionary, and the activity category is listed under education and health. The CFDA numbers associated with the opportunity include 93.313, 93.394, and 93.395. The opportunity was created on 2022-04-05 and had an original closing date of 2022-06-17. The listed award ceiling is $475,000, indicating an upper bound on budget per award under this announcement as provided in the source data. Overall, the program is designed for teams that are ready to translate a prototype into a field-ready cancer technology by proving it works, proving it performs clinically in context, and shaping it into something affordable and usable where the need is greatest.Apply for RFA CA 22 020
- The National Institutes of Health in the education, health sector is offering a public funding opportunity titled "Cancer Prevention, Detection, Diagnosis, and Treatment Technologies for Global Health (U01 Clinical Trial Optional)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.313, 93.394, 93.395.
- This funding opportunity was created on 2022-04-05.
- Applicants must submit their applications by 2022-06-17. (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 $475,000.00 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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Frequently Asked Questions (FAQs)
What is RFA-CA-22-020?
RFA-CA-22-020 is a National Institutes of Health (NIH) funding opportunity titled "Cancer Prevention, Detection, Diagnosis, and Treatment Technologies for Global Health." It supports practical, cancer-focused technology development intended specifically for low- and middle-income countries (LMICs).
What funding mechanism does this opportunity use?
This opportunity uses a U01 cooperative agreement mechanism, which typically involves active partnership and programmatic involvement from NIH/NCI in shaping milestones and monitoring progress.
Which NIH institute/program is this associated with?
The opportunity sits within the National Cancer Institute (NCI) Affordable Cancer Technologies (ACTs) Program, which emphasizes scalable, accessible, and sustainable cancer technology solutions.
What is the core goal of this funding opportunity?
The core goal is to move promising cancer-related technologies closer to real-world use in LMIC settings by adapting and validating them so they function reliably in resource-constrained environments.
Is this FOA meant to fund basic research or discovery?
No. The focus is not on basic discovery. The announcement emphasizes translating an existing or emerging assay, device, or treatment-related technology into a user-friendly, low-cost solution suitable for LMIC conditions.
What kinds of technologies are in scope?
Projects can involve an assay, device, or treatment-related technology aimed at improving cancer prevention, early detection, diagnosis, or treatment, as long as the work centers on adaptation and validation for LMIC use.
Do applicants need to already have a prototype or assay?
Yes. A key requirement is that applicants must already have a working prototype or assay in hand at the time of application.
Does the prototype have to be originally designed for cancer?
No. The prototype does not need to have been originally designed for cancer, but it must be advanced enough to credibly support adaptation for a cancer use-case and subsequent performance demonstration.
What types of work are applicants expected to carry out?
The expected work includes: (1) tailoring the technology to the target cancer use-case and LMIC context, (2) demonstrating technical functionality, and (3) generating evidence of clinical performance in the intended setting.
Is the program milestone-driven?
Yes. The FOA emphasizes objective, milestone-driven progress, including measurable performance targets, iterative improvements based on results, and validation activities within LMIC environments.
Are clinical trials required?
No. Clinical trials are optional. Projects may include clinical studies if appropriate for demonstrating clinical performance, but a clinical trial is not required for every award.
What does "LMIC context" mean for technology design in this FOA?
It means designing for resource-constrained realities, such as limited laboratory capacity, intermittent electricity, shortages of specialized staff, difficult maintenance conditions, and the need for clear, actionable results that fit local clinical decision-making.
Why does the FOA stress multidisciplinary collaboration?
Because successful deployment depends on more than engineering. Teams must address technical performance as well as affordability, usability, supply chain constraints, and fit with local clinical workflows.
What expertise is required on the applicant team?
Teams must include expertise spanning engineering or assay/treatment development, oncology, global health care delivery, and business development.
What role do affordability and usability play in project expectations?
Affordability, cost-effectiveness, and point-of-need usability are treated as core design constraints. The FOA expects teams to plan for deployment and sustainability, not just demonstration in ideal conditions.
How does the cooperative agreement structure affect the project?
The cooperative agreement structure signals that NIH/NCI expects an active partnership role, which commonly includes involvement in shaping milestones, monitoring progress, and keeping the project aligned with affordability and deployability goals for LMICs.
Who is eligible to apply?
Eligibility is broad and includes: public and private institutions of higher education; nonprofits (with or without 501(c)(3) status); for-profit organizations (other than small businesses) and small businesses; and various government entities (state, county, city/township, special districts), as well as independent school districts and public housing authorities/Indian housing authorities.
Are non-U.S. (foreign) organizations allowed to apply or participate?
Yes. The FOA explicitly welcomes non-U.S. (foreign) organizations and regional organizations, aligning with its global health and LMIC focus.
Are organizations serving historically underrepresented communities encouraged or included?
Yes. The FOA explicitly welcomes institutions serving historically underrepresented communities, including HBCUs, Hispanic-serving institutions, AANAPISIs, Tribal colleges and universities, and Alaska Native/Native Hawaiian serving institutions.
Are Tribal governments and Tribal organizations eligible?
Yes. Tribal governments and Tribal organizations are included within the eligible applicant categories described.
What is the awarding agency and opportunity category?
The awarding agency is NIH. The opportunity category is discretionary, and the activity category is listed under education and health.
Which CFDA numbers are associated with this opportunity?
The CFDA numbers listed are 93.313, 93.394, and 93.395.
What is the award ceiling listed for this opportunity?
The listed award ceiling is $475,000, indicating the upper bound on budget per award as provided in the source information.
When was the opportunity created and what was the original closing date?
The opportunity was created on 2022-04-05, and the original closing date was 2022-06-17.
What types of outcomes is the program designed to support?
The program is designed to help teams translate a prototype into a field-ready cancer technology by proving technical function, demonstrating clinical performance in context, and shaping the solution to be affordable and usable in LMIC settings.
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