Opportunity Information: Apply for W81XWH 09 LCRP CTRA
Apply for W81XWH 09 LCRP CTRA
- The Dept. of the Army USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "FY09 DOD Lung Cancer Research Program Collaborative Translational Research Award" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 12.420 Military Medical Research and Development.
- This funding opportunity was created on Aug 28, 2009 and posted on Aug 3, 2009.
- Applicants must submit their applications by Dec 3, 2009. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The funding agency has allocated a total of $10,500,000.00 to eligible and selected applicants.
- The number of recipients for this funding is limited to 2 candidate(s).
- Eligible applicants include: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled Additional Information on Eligibility.
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Opportunity Summary:
The FY09 Department of Defense Lung Cancer Research Program (LCRP) Collaborative Translational Research Award (CTRA) is a funding opportunity designed to push lung cancer discoveries out of the lab and closer to real clinical use. Its core goal is to support multi-institution, multi-disciplinary teams that combine clinical expertise (people who diagnose and treat patients) with laboratory and translational science expertise (people who study disease mechanisms, biomarkers, and intervention strategies). The emphasis is on collaboration that meaningfully accelerates the path from promising concepts to practical applications that can improve detection, prediction, prevention, or treatment of lung cancer.
A key requirement is that every application must address at least two of seven specific Areas of Emphasis. These focus areas are: (1) creating or validating non-invasive or minimally invasive approaches that improve detection of the earliest stages of lung cancer; (2) developing tools for screening or early detection, including approaches such as CT, X-ray or other imaging, biomarkers, genetics/genomics/proteomics, and risk-factor assessment; (3) understanding molecular mechanisms that drive clinically significant lung cancer; (4) identifying mechanisms that lead to the development of different lung cancer types; (5) developing innovative strategies for prevention and treatment specifically aimed at early lung cancer; (6) improving understanding of predictive and prognostic markers that distinguish responders from non-responders; and (7) studying how lung cancers develop acquired resistance to treatment. Proposals are expected to integrate at least two of these themes in a way that genuinely benefits from the combined skills of the team.
The award structure is built around a four-investigator partnership model. Each application must include one Initiating Principal Investigator (PI) and three Partnering PIs, for a total of four independent investigators referred to as partners. These partners must be based at a minimum of two distinct institutions, reinforcing the program’s intent to fund cross-institutional collaboration rather than a single-site project. Team composition is also constrained to ensure clinical relevance and demonstrated lung cancer competence: at least one partner must be a clinician, and at least two partners must have prior experience in lung cancer research and/or lung cancer patient care. Just as important, the program expects that all four partners contribute equally to the intellectual leadership of the project. Applications where one partner functions mainly as a passive contributor (for example, only providing tissue samples, data, or access to patients without substantial scientific leadership and design input) are explicitly described as not meeting the intent of the mechanism.
From an administrative and funding standpoint, this opportunity was offered by the Department of the Army through the U.S. Army Medical Research Acquisition Activity (USAMRAA) under the Military Medical Research and Development CFDA listing (12.420). The funding instrument type is listed as a cooperative agreement/grant, meaning recipients should expect active involvement or oversight consistent with cooperative agreement mechanisms. The program anticipated making two awards, with an estimated total funding level of $10.5 million. Cost sharing or matching was not required, and eligibility was described as unrestricted (open to any applicant type), subject to any additional eligibility details in the full announcement.
Key dates for the FY09 cycle included a posting date of August 3, 2009, and an application closing date of December 3, 2009, with the opportunity archived on January 2, 2010. The funding opportunity number is W81XWH-09-LCRP-CTRA. Applicants who needed assistance were directed to CDMRP/USAMRAA support contacts for access to the announcement and for electronic submission troubleshooting.
Frequently Asked Questions (FAQs)
What is the FY09 DoD Lung Cancer Research Program Collaborative Translational Research Award (CTRA)?
The Collaborative Translational Research Award (CTRA) is a FY09 funding opportunity under the Department of Defense Lung Cancer Research Program (LCRP) intended to move promising lung cancer discoveries from the laboratory toward real-world clinical use. It is designed to support collaborative, team-based translational research that accelerates practical applications that can improve lung cancer detection, prediction, prevention, or treatment.
What is the main goal of this award mechanism?
The core goal is to fund multi-institution, multi-disciplinary teams that combine clinical expertise (diagnosis and treatment of patients) with laboratory and translational science expertise (mechanisms, biomarkers, intervention strategies) in order to speed the path from concept to clinical impact.
What type of research is this opportunity trying to support?
This opportunity emphasizes collaborative translational research, meaning projects should meaningfully bridge laboratory findings and clinical application. The intent is for the collaboration itself to accelerate progress toward improving how lung cancer is detected, predicted, prevented, or treated.
Are there specific scientific focus areas applicants must address?
Yes. Every application must address at least two of the seven specified Areas of Emphasis. The application is expected to integrate those themes in a way that clearly benefits from the combined strengths of the team.
What are the seven Areas of Emphasis?
The seven Areas of Emphasis are:
- Creating or validating non-invasive or minimally invasive approaches that improve detection of the earliest stages of lung cancer.
- Developing tools for screening or early detection (including CT, X-ray, other imaging, biomarkers, genetics/genomics/proteomics, and risk-factor assessment).
- Understanding molecular mechanisms that drive clinically significant lung cancer.
- Identifying mechanisms that lead to the development of different lung cancer types.
- Developing innovative prevention and treatment strategies aimed specifically at early lung cancer.
- Improving understanding of predictive and prognostic markers that distinguish responders from non-responders.
- Studying how lung cancers develop acquired resistance to treatment.
How many Areas of Emphasis must a proposal include?
At least two of the seven Areas of Emphasis must be addressed in every application.
Does the program require that the chosen Areas of Emphasis be integrated?
Yes. Proposals are expected to integrate at least two Areas of Emphasis in a way that genuinely benefits from the team structure and the combined skills of the partners, rather than treating them as unrelated components.
What is the required team structure for an application?
Each application must use a four-investigator partnership model consisting of one Initiating Principal Investigator (PI) and three Partnering PIs, for a total of four independent investigators (partners).
How many institutions must be involved?
The four partners must be based at a minimum of two distinct institutions. This reflects the program intent to fund cross-institutional collaboration rather than a single-site project.
Are there clinical participation requirements?
Yes. At least one partner must be a clinician.
Is prior lung cancer experience required for the team?
Yes. At least two partners must have prior experience in lung cancer research and/or lung cancer patient care.
Do all four investigators need to contribute equally?
Yes. The program expects all four partners to contribute equally to the intellectual leadership of the project.
What kinds of partner roles are considered inconsistent with the intent of the award?
Applications where one partner functions mainly as a passive contributor are described as not meeting the intent of the mechanism. Examples given include a partner whose role is largely limited to providing tissue samples, data, or access to patients without substantial scientific leadership and design input.
Who is the sponsoring and administering organization for this opportunity?
The opportunity was offered by the Department of the Army through the U.S. Army Medical Research Acquisition Activity (USAMRAA), under the Military Medical Research and Development CFDA listing.
What is the CFDA listing for this opportunity?
The CFDA listing is 12.420 (Military Medical Research and Development).
What is the funding instrument type?
The funding instrument type is listed as a cooperative agreement/grant.
What does it mean that the instrument is a cooperative agreement/grant?
It indicates recipients should expect active involvement or oversight consistent with cooperative agreement mechanisms, rather than a purely hands-off grant arrangement.
How many awards were anticipated?
The program anticipated making two awards.
What was the estimated total funding level for this opportunity?
The estimated total funding level was $10.5 million.
Is cost sharing or matching required?
No. Cost sharing or matching was not required.
Who was eligible to apply?
Eligibility was described as unrestricted (open to any applicant type), subject to any additional eligibility details in the full announcement.
What is the funding opportunity number?
The funding opportunity number is W81XWH-09-LCRP-CTRA.
When was the opportunity posted?
The posting date was August 3, 2009.
What was the application closing date?
The application closing date was December 3, 2009.
When was the opportunity archived?
The opportunity was archived on January 2, 2010.
Where could applicants get help with the announcement or submission issues?
Applicants needing assistance were directed to CDMRP/USAMRAA support contacts for access to the announcement and for electronic submission troubleshooting.
Is this opportunity focused on early lung cancer specifically?
Several Areas of Emphasis explicitly focus on early detection and early lung cancer, including non-invasive/minimally invasive early-stage detection, screening tools, and prevention/treatment strategies aimed at early lung cancer.
Does the opportunity include biomarker or genomics-related research?
Yes. The Areas of Emphasis include screening and early detection tools such as biomarkers and genetics/genomics/proteomics, as well as predictive and prognostic markers distinguishing responders from non-responders.
Does the opportunity include research on treatment resistance?
Yes. One Area of Emphasis specifically focuses on studying how lung cancers develop acquired resistance to treatment.
Does the opportunity support imaging-based early detection research?
Yes. The Areas of Emphasis include development of screening or early detection tools, including approaches such as CT, X-ray, or other imaging.
Does the opportunity support research into mechanisms behind different lung cancer types?
Yes. One Area of Emphasis calls for identifying mechanisms that lead to the development of different lung cancer types.
Is the award designed for a single-lab or single-institution project?
No. The structure requires four independent investigators across at least two distinct institutions, reinforcing that the intent is cross-institutional collaboration.
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