Opportunity Information: Apply for RFA CA 12 006

  • The National Institutes of Health in the education health sector is offering a public funding opportunity titled "Cancer Target Discovery and Development (CTDD) Network (U01)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.393 Cancer Cause and Prevention Research 93.394 Cancer Detection and Diagnosis Research 93.395 Cancer Treatment Research 93.396 Cancer Biology Research.
  • This funding opportunity was created on Mar 30, 2012 and posted on Mar 30, 2012.
  • Applicants must submit their applications by Jun 21, 2012. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Eligible applicants include: Public and State controlled institutions of higher education Others (see text field entitled Additional Information on Eligibility for clarification) Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education State governments Private institutions of higher education Small businesses Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education For profit organizations other than small businesses.
  • Other Eligible Applicants include the following Alaska Native and Native Hawaiian Serving Institutions Hispanic serving Institutions Historically Black Colleges and Universities (HBCUs) Tribally Controlled Colleges and Universities (TCCUs) U.S. Territory or Possession Non domestic (non U.S.) Entities (Foreign Institutions) are eligible to apply. Non domestic (non U.S.) components of U.S. Organizations are eligible to apply. Foreign components, as defined in the NIH Grants Policy Statement, are allowed.
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Opportunity Summary:

The Cancer Target Discovery and Development (CTDD) Network (U01) funding opportunity (RFA-CA-12-006) is a National Institutes of Health (NIH) cooperative agreement program designed to speed up the discovery, validation, and early characterization of new therapeutic targets in cancer, along with the discovery of molecules that can modulate those targets. At its core, the FOA is trying to solve a well-known bottleneck in modern cancer research: large consortia and tumor profiling efforts generate massive amounts of genomic and molecular data across many cancer subtypes, but converting those data into actionable drug targets, tractable assays, and credible response markers is much harder. CTDD is aimed at bridging that translation gap by supporting projects that can take high-volume molecular information and turn it into prioritized targets and modulators that are more ready for therapeutic development.

The scientific emphasis is on high-throughput approaches. Applicants are expected to propose projects that use scalable strategies to identify and/or characterize candidate cancer targets, or that identify small molecules capable of modulating already-validated cancer targets. In practice, this means the research should not be limited to one-off, low-throughput experiments; instead, it should leverage methods that can systematically evaluate many genes, pathways, or compounds. The FOA highlights combining in-depth mining of large-scale genomic datasets (for example, tumor sequencing and related multi-omics resources) with systems biology analyses and/or experimental platforms. The expectation is that projects will move beyond purely computational predictions by providing initial functional evidence that a target matters in cancer biology, such as demonstrating effects on tumor-relevant phenotypes, pathway activity, vulnerabilities, or drug response patterns.

Because this is a U01 cooperative agreement, the program is structured as a network-style effort where NIH typically plays an active partnership role compared with standard investigator-initiated grants. While the summary provided does not list operational details, U01 mechanisms generally imply substantial programmatic involvement, coordination, and milestone-driven progress, aligning well with the goal of producing broadly useful targets, chemical probes, and early response markers that can feed downstream therapeutic development.

Administratively, the opportunity was posted March 30, 2012, with an original and final application due date of June 21, 2012, and it was later archived on July 22, 2012. There is no cost sharing or matching requirement listed. The activity falls under NIH cancer research CFDA areas spanning cause and prevention, detection and diagnosis, treatment, and cancer biology (93.393, 93.394, 93.395, 93.396), reflecting that target discovery and validation can impact many parts of the cancer research pipeline.

Eligibility is broad and includes public and private institutions of higher education, state governments, small businesses, nonprofits (including both 501(c)(3) and certain non-501(c)(3) entities), and for-profit organizations other than small businesses. The FOA explicitly includes eligibility for several institution types such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving Institutions, Tribally Controlled Colleges and Universities, and Alaska Native and Native Hawaiian Serving Institutions, as well as U.S. territories or possessions. Foreign institutions may apply, and foreign components of U.S. organizations are allowed, consistent with NIH policy definitions for foreign involvement.

Overall, CTDD (U01) is best understood as a targeted NIH effort to fund teams that can systematically convert cancer genomics and systems-level data into experimentally supported targets and candidate modulators, generating the kind of early, high-confidence evidence needed to spark therapeutic programs and to identify markers that may predict or explain treatment response.

Frequently Asked Questions (FAQs)

What is the Cancer Target Discovery and Development (CTDD) Network (U01) funding opportunity?

The Cancer Target Discovery and Development (CTDD) Network (U01) is an NIH cooperative agreement program (RFA-CA-12-006) intended to speed the discovery, validation, and early characterization of new therapeutic targets in cancer, along with the discovery of molecules that can modulate those targets.

What problem is this program trying to address in cancer research?

The program targets a common bottleneck: large consortia and tumor profiling efforts produce massive genomic and molecular datasets across many cancer subtypes, but turning those data into actionable drug targets, tractable assays, and credible response markers is much harder. CTDD aims to bridge that translation gap.

What types of research projects does CTDD (U01) support?

CTDD supports projects that systematically identify and/or characterize candidate cancer targets and projects that identify small molecules capable of modulating already-validated cancer targets. The intent is to generate prioritized targets, candidate modulators, and early evidence that enables downstream therapeutic development.

Is the scientific emphasis on high-throughput or low-throughput research?

The emphasis is on high-throughput, scalable approaches rather than one-off, low-throughput experiments. Projects are expected to use methods that can evaluate many genes, pathways, or compounds in a systematic way.

Does CTDD encourage using large-scale genomic and multi-omics datasets?

Yes. The opportunity highlights in-depth mining of large-scale genomic datasets (such as tumor sequencing and related multi-omics resources), often combined with systems biology analyses and/or experimental platforms.

Are purely computational target predictions sufficient for this opportunity?

No. While computational analyses and systems-level mining are emphasized, projects are expected to move beyond purely computational predictions by providing initial functional evidence that a target matters in cancer biology.

What kind of functional evidence is expected to support a candidate target?

The description indicates that functional evidence could include demonstrating effects on tumor-relevant phenotypes, pathway activity, vulnerabilities, or drug response patterns. The goal is to show early, credible biological relevance.

Does the program support discovery of molecules in addition to targets?

Yes. In addition to discovering and validating targets, CTDD includes the discovery of molecules that can modulate those targets, helping make targets more ready for therapeutic development.

What is the funding mechanism, and why does it matter?

The mechanism is a U01 cooperative agreement. In general, U01 mechanisms imply that NIH typically plays an active partnership role compared with standard investigator-initiated grants, and projects often involve coordination and milestone-driven progress consistent with network-style efforts.

Is CTDD structured as a network program?

Yes. CTDD is described as a network-style effort where coordination and programmatic involvement align with producing broadly useful targets, chemical probes, and early response markers.

What kinds of outputs is CTDD aiming to produce?

The program is oriented toward producing prioritized cancer targets, molecules (including candidate modulators/chemical probes), and early response markers that can feed downstream therapeutic development.

When was this funding opportunity posted and when were applications due?

The opportunity was posted on March 30, 2012. The original and final application due date was June 21, 2012.

Is this funding opportunity still active?

No. The opportunity was archived on July 22, 2012.

Is there a cost sharing or matching requirement?

No cost sharing or matching requirement is listed in the provided information.

Which NIH/CFDA program areas are associated with this opportunity?

The activity falls under NIH cancer research CFDA areas spanning cause and prevention, detection and diagnosis, treatment, and cancer biology: 93.393, 93.394, 93.395, and 93.396.

What types of organizations are eligible to apply?

Eligibility is broad and includes public and private institutions of higher education, state governments, small businesses, nonprofits (including 501(c)(3) and certain non-501(c)(3) entities), and for-profit organizations other than small businesses.

Are specific institution categories explicitly included?

Yes. The opportunity explicitly includes eligibility for Historically Black Colleges and Universities (HBCUs), Hispanic-serving Institutions, Tribally Controlled Colleges and Universities, Alaska Native and Native Hawaiian Serving Institutions, as well as U.S. territories or possessions.

Can foreign institutions apply?

Yes. Foreign institutions may apply, and foreign components of U.S. organizations are allowed, consistent with NIH policy definitions for foreign involvement.

Does CTDD focus on a single cancer subtype or multiple cancer subtypes?

The description emphasizes leveraging large-scale data generated across many cancer subtypes and converting those data into actionable targets and modulators, suggesting applicability across multiple cancer contexts rather than a single subtype focus.

How does CTDD relate to downstream therapeutic development?

CTDD is positioned to create early, high-confidence evidence around targets and modulators (and related response markers) that can spark or accelerate therapeutic programs by making targets more tractable and better validated for later-stage development.

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