Opportunity Information: Apply for W81XWH 12 NFRP CTA
Apply for W81XWH 12 NFRP CTA
- The Dept. of the Army USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "DOD FY12 Neurofibromatosis Clinical Trial 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 Mar 22, 2012 and posted on Mar 22, 2012.
- Applicants must submit their applications by May 31, 2012. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The funding agency has allocated a total of $2,880,000.00 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 DOD FY12 Neurofibromatosis Clinical Trial Award (Funding Opportunity Number W81XWH 12 NFRP CTA) was a U.S. Department of Defense Neurofibromatosis Research Program funding opportunity administered through the Department of the Army, U.S. Army Medical Research Acquisition Activity (USAMRAA). It was designed specifically to move neurofibromatosis (NF) research into patient-focused testing by supporting clinical trials that could meaningfully improve how NF is treated or managed. The intent of the mechanism was translational and impact-driven: applicants were expected to propose studies that could change clinical practice or substantially advance the evidence base for NF care, rather than exploratory laboratory work.
The award mechanism supported pilot trials as well as Phase 0, Phase I, or Phase II clinical trials. In practical terms, that scope covers early human studies that examine things like feasibility, safety, dosing, pharmacokinetics/pharmacodynamics, initial signals of efficacy, and early-stage comparative outcomes depending on the design. A key restriction was that funds had to be used to conduct a clinical trial; the announcement explicitly stated that the award could not be used for preclinical research studies. That makes this opportunity distinct from many biomedical grants that allow a mix of lab, animal, and human work. Here, the expectation was that the project would be trial-ready and focused on activities directly tied to executing the clinical study in humans.
From an administrative standpoint, the opportunity fell under the “Discretionary” category and supported awards through a Cooperative Agreement and/or Grant instrument type, within the Science and Technology / Research and Development activity area. The CFDA listing associated with the program was 12.420 (Military Medical Research and Development). The program anticipated making about two awards, with an estimated total funding amount of $2,880,000 across all awards. There was no cost sharing or matching requirement stated, meaning applicants were not required to contribute non-federal funds as a condition of receiving the award.
Eligibility was described as “Unrestricted,” indicating it was broadly open to any type of entity, subject to any additional eligibility clarifications that would have appeared in the full text of the announcement. The posting date and creation date were both March 22, 2012. The original and current closing date were May 31, 2012, and the opportunity was later archived on June 30, 2012. For applicant support, the announcement directed anyone having trouble accessing the full announcement to contact the CDMRP help resources (PA HELP and eReceipt HELP) via phone at 301-682-5507 or email at help@cdmrp.org.
Overall, this grant opportunity can be summarized as an early-phase NF clinical trial funding mechanism from the DoD intended to accelerate tangible patient impact by paying for the execution of pilot through Phase II clinical trials, while explicitly excluding preclinical research from allowable use of funds.
FAQs: DOD FY12 Neurofibromatosis Clinical Trial Award (W81XWH 12 NFRP CTA)
What is the DOD FY12 Neurofibromatosis Clinical Trial Award?
The DOD FY12 Neurofibromatosis Clinical Trial Award (Funding Opportunity Number W81XWH 12 NFRP CTA) was a U.S. Department of Defense funding opportunity under the Neurofibromatosis Research Program. It was administered through the Department of the Army, U.S. Army Medical Research Acquisition Activity (USAMRAA), and focused on supporting clinical trials in neurofibromatosis (NF).
What was the main purpose of this award?
The mechanism was designed to move NF research into patient-focused testing by funding clinical trials intended to meaningfully improve how NF is treated or managed. The emphasis was translational and impact-driven, with the expectation that funded studies could influence clinical practice or substantially strengthen the evidence base for NF care.
What kinds of studies were expected to be proposed?
Applicants were expected to propose clinical trials that were ready for human execution and focused on patient impact. The program intent favored studies positioned to change care or advance clinical evidence, rather than exploratory laboratory efforts.
Which clinical trial phases were supported?
The award supported pilot clinical trials as well as Phase 0, Phase I, and Phase II clinical trials.
What does it mean that the award supported early-phase trials?
Early-phase trial support generally includes human studies that assess feasibility, safety, dosing, pharmacokinetics/pharmacodynamics (PK/PD), early signals of efficacy, and other early comparative outcomes depending on study design.
Could the funds be used for preclinical research (lab or animal studies)?
No. A specific restriction of this opportunity was that funds had to be used to conduct a clinical trial in humans. The announcement explicitly stated that the award could not be used for preclinical research studies.
What was the required focus for use of the awarded funds?
The expectation was that the project would be trial-ready and that the budget would support activities directly tied to executing the clinical study in humans.
What funding category did this opportunity fall under?
The opportunity was listed under the “Discretionary” category.
What award instrument types were used?
The mechanism supported awards through a Cooperative Agreement and/or Grant instrument type.
What activity area did this opportunity support?
This opportunity was within the Science and Technology / Research and Development activity area.
What CFDA number was associated with this opportunity?
The CFDA listing associated with the program was 12.420 (Military Medical Research and Development).
How many awards were anticipated?
The program anticipated making about two awards.
What was the estimated total funding amount?
The estimated total funding amount across all awards was $2,880,000.
Was cost sharing or matching required?
No. There was no cost sharing or matching requirement stated for this opportunity.
Who was eligible to apply?
Eligibility was described as “Unrestricted,” meaning it was broadly open to any type of entity, subject to any additional eligibility clarifications that would have been included in the full announcement text.
When was the opportunity posted?
The posting date (and creation date) was March 22, 2012.
What was the application deadline?
The original and current closing date were both May 31, 2012.
When was the opportunity archived?
The opportunity was archived on June 30, 2012.
Who administered the award?
It was administered through the Department of the Army, U.S. Army Medical Research Acquisition Activity (USAMRAA), as part of the DoD Neurofibromatosis Research Program.
What should someone do if they cannot access the full announcement?
The announcement directed applicants having trouble accessing the full announcement to contact CDMRP help resources (PA HELP and eReceipt HELP) by phone at 301-682-5507 or by email at help@cdmrp.org.
What makes this opportunity different from many biomedical research grants?
This opportunity was distinct because it required funds to be used to conduct a clinical trial and explicitly excluded preclinical research. Many biomedical funding opportunities allow a mix of laboratory, animal, and human work; this one emphasized human clinical trial execution.
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