Opportunity Information: Apply for PAR 15 075

  • The National Institutes of Health in the education health sector is offering a public funding opportunity titled "Academic Industrial Partnerships for Translation of Technologies for Cancer Diagnosis and Treatment (R01)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.394 Cancer Detection and Diagnosis Research 93.395 Cancer Treatment Research.
  • This funding opportunity was created on Dec 16, 2014 and posted on Dec 16, 2014.
  • Applicants must submit their applications by Jan 7, 2017. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Eligible applicants include: Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education State governments Small businesses Private institutions of higher education City or township governments Public housing authorities/Indian housing authorities Native American tribal organizations (other than Federally recognized tribal governments) Independent school districts For profit organizations other than small businesses County governments Others (see text field entitled Additional Information on Eligibility for clarification) Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Special district governments Native American tribal governments (Federally recognized) Public and State controlled institutions of higher education.
  • Other Eligible Applicants include the following Alaska Native and Native Hawaiian Serving Institutions Asian American Native American Pacific Islander Serving Institutions (AANAPISISs) Eligible Agencies of the Federal Government Faith based or Community based Organizations Hispanic serving Institutions Historically Black Colleges and Universities (HBCUs) Indian/Native American Tribal Governments (Other than Federally Recognized) Non domestic (non U.S.) Entities (Foreign Organizations) Regional Organizations Tribally Controlled Colleges and Universities (TCCUs) U.S. Territory or Possession.
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Opportunity Summary:

The Academic Industrial Partnerships for Translation of Technologies for Cancer Diagnosis and Treatment (R01) funding opportunity (PAR-15-075) is an NIH grant program meant to push cancer-related diagnostic and treatment-enabling technologies out of the lab and closer to real-world use. The core idea is that progress happens faster when academic groups and industry partners work together in a coordinated way, so the FOA is built around formal partnerships that combine academic scientific expertise with industrial development, engineering, manufacturing, regulatory, and productization know-how. Projects are expected to be problem-driven, meaning applicants should start with a clearly defined cancer need and then build a translational plan that uses or advances a specific technology, assay, device, method, or system to address that need.

This FOA focuses on translation for preclinical or clinical molecular diagnosis and in vitro imaging, along with molecular imaging and related research resources that directly support these goals. NIH is not asking for early-stage discovery science here; instead, the emphasis is on taking something that already has a credible foundation and doing the work required to make it perform reliably in realistic settings. That can include improving or adapting existing commercially supported platforms, developing next-generation versions of existing tools, and doing the practical development steps that often block adoption, such as optimization, robustness testing, workflow integration, and performance validation. The announcement explicitly highlights support for quality assurance and quality control activities, validation and correlation studies, and quantitative imaging work, all of which are typical prerequisites for clinical confidence and broader deployment.

A key point in the FOA is how it defines innovation. Innovation is not framed as purely novel biology or a brand-new invention; it is framed as a coherent translational plan that delivers new or emerging capabilities into preclinical or clinical use where they are not yet widely employed. In other words, a project can be considered innovative if it credibly moves a technology into the hands of end users or enables a capability that clinicians or researchers do not currently have in routine practice, even if the underlying concept is not brand new. This makes the program well-suited for efforts that bridge the common gap between a promising prototype and a validated, usable system.

The required partnership structure is also central. Applications are expected to bring together an interdisciplinary, multi-institutional team operating as a strategic alliance, with a unified strategy and clear roles across the academic and industrial sides. The intent is that the partnership is not superficial; it should be organized around a shared development and translation roadmap with milestones that move the system toward practical deployment for the targeted cancer problem. Because real translation often requires testing under real conditions, the FOA allows and supports clinical trials, specifically those designed to test functionality and to optimize and validate performance of the proposed technology as part of the translation process.

At the same time, the FOA draws boundaries around what it will not support. It is not intended to pay for commercial-scale production, and it is not meant for basic research projects that do not put translation front and center. Applicants should therefore be prepared to show why their work is positioned at the development/translation stage, what remains to be done to make it usable and trustworthy in preclinical or clinical contexts, and how the academic-industry team is uniquely positioned to complete those steps.

Administratively, this is an R01 discretionary grant opportunity under NIH, categorized under health and education-related activities, and tied to CFDA numbers 93.394 (Cancer Detection and Diagnosis Research) and 93.395 (Cancer Treatment Research). It does not require cost sharing or matching. The FOA was posted December 16, 2014, and the opportunity’s listed closing date was January 7, 2017, with an archive date of February 7, 2017, indicating it is no longer an active open solicitation in its original form, though it remains useful as a reference point for similar NIH translational partnership announcements. Eligibility is broad and includes many organization types across academia, nonprofit, for-profit (including but not limited to small businesses), and government entities, including U.S. and non-U.S. entities, minority-serving institutions, tribal organizations, and community-based or faith-based organizations, as long as the project structure fits the academic-industry partnership model and the work aligns with the translational scope described.

Frequently Asked Questions (FAQs)

What is the PAR-15-075 funding opportunity?

PAR-15-075, titled "Academic Industrial Partnerships for Translation of Technologies for Cancer Diagnosis and Treatment (R01)," is an NIH grant program designed to move cancer-related diagnostic and treatment-enabling technologies out of the lab and closer to real-world use through formal academic-industry partnerships.

What is the main goal of this program?

The goal is to accelerate translation by combining academic scientific expertise with industry capabilities such as development engineering, manufacturing know-how, regulatory experience, and productization so that promising technologies become reliable and usable in practical preclinical or clinical settings.

What types of technologies or research areas does the FOA emphasize?

The FOA emphasizes translation for preclinical or clinical molecular diagnosis and in vitro imaging, as well as molecular imaging and related research resources that directly support these goals.

Is this funding intended for basic discovery research?

No. The announcement is not aimed at early-stage discovery science. It prioritizes development and translation work that takes an already credible technology foundation and advances it toward reliable performance in realistic settings.

What does "problem-driven" mean in the context of this FOA?

Projects are expected to start with a clearly defined cancer need and then propose a translational plan that uses or advances a specific technology, assay, device, method, or system to address that need.

What kinds of development activities are encouraged?

Examples of supported activities include improving or adapting commercially supported platforms, developing next-generation versions of existing tools, and addressing practical barriers to adoption such as optimization, robustness testing, workflow integration, and performance validation.

Does the FOA support quality assurance and validation work?

Yes. The announcement explicitly highlights support for quality assurance (QA) and quality control (QC) activities, validation and correlation studies, and quantitative imaging work, which are often prerequisites for clinical confidence and broader deployment.

How does this FOA define "innovation"?

Innovation is defined as a coherent translational plan that delivers new or emerging capabilities into preclinical or clinical use where they are not yet widely employed. A project can be considered innovative if it credibly moves a technology into the hands of end users or enables a capability not available in routine practice, even if the underlying concept is not entirely new.

What kind of partnership structure is expected?

Applications are expected to include an interdisciplinary, multi-institutional academic-industry team operating as a strategic alliance. The partnership should be organized around a unified strategy with clear roles on both sides and a shared development and translation roadmap with milestones.

Does the partnership need to be more than a nominal collaboration?

Yes. The intent is that the partnership is not superficial. The FOA is built around formal partnerships that combine complementary strengths and execute a coordinated plan that moves the system toward practical deployment for a targeted cancer problem.

Are clinical trials allowed under this FOA?

Yes. The FOA allows and supports clinical trials when they are designed to test functionality and to optimize and validate performance of the proposed technology as part of the translation process.

What is the FOA not intended to support?

It is not intended to pay for commercial-scale production, and it is not meant for basic research projects that do not put translation front and center.

What should applicants be prepared to demonstrate in a proposal?

Applicants should be prepared to explain why the work is positioned at the development/translation stage, what remains to be done to make the technology usable and trustworthy in preclinical or clinical contexts, and why the academic-industry team is uniquely positioned to complete those steps.

What type of NIH award mechanism is this?

This opportunity is described as an NIH R01 discretionary grant.

What activity categories and CFDA numbers are associated with this opportunity?

It is categorized under health and education-related activities and tied to CFDA 93.394 (Cancer Detection and Diagnosis Research) and 93.395 (Cancer Treatment Research).

Is cost sharing or matching required?

No. The opportunity does not require cost sharing or matching.

When was the FOA posted, and is it still active?

The FOA was posted on December 16, 2014. The listed closing date was January 7, 2017, and the archive date was February 7, 2017, which indicates it is no longer an active open solicitation in its original form.

If it is archived, is the FOA still useful?

Yes. While it is not open in its original form, it can still be useful as a reference point for similar NIH translational partnership announcements focused on moving cancer technologies toward real-world deployment.

Who is eligible to apply?

Eligibility is described as broad and includes many organization types across academia, nonprofit organizations, for-profit entities (including but not limited to small businesses), and government entities.

Are non-U.S. organizations eligible?

Yes. The eligibility description includes U.S. and non-U.S. entities, provided the project structure fits the academic-industry partnership model and aligns with the translational scope described in the FOA.

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

Yes. The eligibility description explicitly includes minority-serving institutions, tribal organizations, and community-based or faith-based organizations, as long as the proposed work fits the partnership model and translational focus.

What is the overarching theme that reviewers would likely expect to see?

Based on the FOA description, reviewers would expect a credible, milestone-driven translation plan grounded in a real cancer need, executed by a genuine academic-industry strategic alliance, and focused on practical steps that make a technology reliable, validated, and ready for preclinical or clinical use.

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