Opportunity Information: Apply for W81XWH 15 ALSRP TIA

  • 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 Amyotrophic Lateral Sclerosis Therapeutic Idea 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 30, 2015 and posted on Mar 18, 2015.
  • Applicants must submit their applications by Aug 20, 2015. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $3,200,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 4 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.
Apply for W81XWH 15 ALSRP TIA

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Opportunity Summary:

The DoD Amyotrophic Lateral Sclerosis (ALS) Therapeutic Idea Award (Funding Opportunity Number W81XWH-15-ALSRP-TIA) is a U.S. Army Medical Research Acquisition Activity (USAMRAA) funding program under CFDA 12.420 (Military Medical Research and Development) that supports early-stage, high-impact concepts aimed at improving treatment options for ALS. The program is structured to push forward new therapeutic directions, especially those that could realistically translate into better patient outcomes, rather than supporting broad basic science efforts that primarily explain how ALS works. In other words, the emphasis is on practical therapeutic discovery and enabling tools that move the field toward treatments, not on pathophysiology-focused studies that stop short of treatment relevance.

At the core of this opportunity is the expectation that projects will be hypothesis-driven. Applicants are expected to present a well-formulated, testable hypothesis backed by strong scientific rationale and a clear line of sight to translational value. The award is meant for ideas that are still early in development, including drug discovery concepts, treatment discovery approaches, and target discovery strategies. Importantly, the solicitation makes it clear that projects mainly aimed at investigating ALS disease mechanisms, without a direct therapeutic discovery angle, fall outside the intent and scope of the mechanism.

A key update highlighted for FY15 is that this Therapeutic Idea Award also welcomes certain topic areas that were previously placed under the ALSRP Therapeutic Development Award. Specifically, it supports the development, validation, and application of high-throughput screening platforms that can either define new therapeutic targets or identify lead candidate agents for ALS treatment. It also supports the development, modification, or validation of preclinical model systems that can be used to assess lead compounds and potential therapeutics, including pharmacological and pharmacokinetic testing. These models are framed not only as project-specific tools, but as improvements that could benefit the wider ALS research community by strengthening the preclinical toolkit used to evaluate potential therapies.

The program draws a clear boundary between early therapeutic discovery and later-stage product development. Applicants whose work goes beyond discovery and into more advanced preclinical development activities are directed toward the ALSRP Therapeutic Development Award instead. This positioning reflects the program's role in seeding novel, potentially transformative ideas before they are mature enough for late-stage development mechanisms.

Innovation and potential impact are explicitly described as the top priorities for this award. The solicitation states that even applications with excellent scientific merit can miss the mark if they are not sufficiently innovative or if they do not offer a strong potential for meaningful impact on ALS treatment. Another distinctive feature is its stance on preliminary data: the mechanism is not designed to reward proposals built around extensive preliminary results. While preliminary data may be included, the application is expected to stand on the strength of the concept, its rationale, and the magnitude of potential payoff, rather than on already-established findings. This is meant to encourage applicants to propose bolder, earlier ideas that could open new therapeutic directions.

From an administrative standpoint, the opportunity was posted on March 18, 2015, with a closing date of August 20, 2015, and an archive date of September 19, 2015. The total estimated funding was $3.2 million, with an expectation of making about four awards. The funding instrument types listed include cooperative agreement and grant, and there is no cost sharing or matching requirement. Eligibility is described as unrestricted, meaning it is open to any type of entity as long as it meets any additional criteria or clarifications provided in the full announcement. For technical access issues related to the full announcement, the CDMRP Help Desk is listed as the support contact at 301-682-5507.

FAQs: DoD ALS Therapeutic Idea Award (W81XWH-15-ALSRP-TIA)

What is this funding opportunity?

The DoD Amyotrophic Lateral Sclerosis (ALS) Therapeutic Idea Award (Funding Opportunity Number W81XWH-15-ALSRP-TIA) is a U.S. Army Medical Research Acquisition Activity (USAMRAA) program under CFDA 12.420 (Military Medical Research and Development). It supports early-stage, high-impact therapeutic concepts intended to improve ALS treatment options.

What is the main goal of the Therapeutic Idea Award?

The main goal is to push forward new therapeutic directions that can realistically translate into better outcomes for ALS patients. The emphasis is on practical therapeutic discovery and enabling tools that move the field toward treatments.

What kinds of projects does this award prioritize?

This mechanism prioritizes hypothesis-driven, early-stage therapeutic discovery projects, including drug discovery concepts, treatment discovery approaches, and target discovery strategies, as long as they maintain a clear line of sight to translational value.

Does the program require a hypothesis-driven approach?

Yes. Applications are expected to present a well-formulated, testable hypothesis supported by strong scientific rationale and a clear connection to translational relevance for ALS treatment.

Are basic science or disease mechanism studies allowed?

The opportunity is not intended to support broad basic science efforts that primarily explain how ALS works. Projects mainly aimed at investigating ALS pathophysiology or disease mechanisms, without a direct therapeutic discovery angle, are described as outside the intent and scope of this mechanism.

What is the program's stance on innovation and impact?

Innovation and potential impact are described as the top priorities. The solicitation indicates that even applications with strong scientific merit may not be considered a good fit if they are not sufficiently innovative or if they lack strong potential for meaningful impact on ALS treatment.

Is preliminary data required?

No. The mechanism is not designed to reward proposals built around extensive preliminary data. Preliminary data may be included, but the application is expected to stand primarily on the strength of the concept, rationale, and potential payoff.

What types of screening platform projects are supported?

A highlighted FY15 update is that the award welcomes development, validation, and application of high-throughput screening platforms that can define new therapeutic targets or identify lead candidate agents for ALS treatment.

Are preclinical model system projects supported?

Yes. The opportunity supports development, modification, or validation of preclinical model systems used to assess lead compounds and potential therapeutics, including pharmacological and pharmacokinetic testing. These models are framed as improvements that can also benefit the broader ALS research community.

What is the boundary between this award and later-stage development funding?

This award is positioned for early therapeutic discovery rather than later-stage product development. Applicants whose work goes beyond discovery into more advanced preclinical development activities are directed to the ALSRP Therapeutic Development Award.

What is the estimated total funding and number of awards?

The total estimated funding is $3.2 million, with an expectation of making about four awards.

What funding instrument types are used?

The listed funding instrument types include a cooperative agreement and a grant.

Is cost sharing or matching required?

No. The opportunity states there is no cost sharing or matching requirement.

Who is eligible to apply?

Eligibility is described as unrestricted, meaning it is open to any type of entity as long as it meets any additional criteria or clarifications provided in the full announcement.

When was the opportunity posted and when did it close?

The opportunity was posted on March 18, 2015. The closing date was August 20, 2015, and the archive date was September 19, 2015.

What is the CFDA number associated with this program?

The program is listed under CFDA 12.420, Military Medical Research and Development.

What should applicants do if they need technical help accessing the full announcement?

For technical access issues related to the full announcement, the listed support contact is the CDMRP Help Desk at 301-682-5507.

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