Opportunity Information: Apply for RFA AI 20 007
The Asthma and Allergic Diseases Cooperative Research Centers (AADCRC) opportunity (RFA-AI-20-007) is a National Institutes of Health (NIH) cooperative agreement (U19) focused on building and supporting multi-project research centers that combine clinical and translational science to tackle major asthma and allergy-related diseases. The intent is to fund centers based at a single institution or formed as consortia across multiple institutions, with the expectation that teams will work in an integrated way rather than as isolated projects. Because this is a cooperative agreement, the NIH role is typically more collaborative than in a standard research grant, with substantial scientific involvement from the funding institute in coordinating, guiding, and aligning the center activities with program goals.
Scientifically, the program is aimed at understanding the mechanisms that drive the onset and progression of a set of closely related, high-burden inflammatory and hypersensitivity conditions. The diseases explicitly highlighted include asthma; rhinitis (both allergic and non-allergic); chronic rhinosinusitis; atopic dermatitis; food allergy; and drug allergy. The unifying theme is pathogenesis: applicants are expected to propose research that clarifies the biological and clinical processes that cause these conditions to begin, worsen, or persist, and to translate those insights into a rational basis for better treatments and prevention strategies. In practical terms, a competitive application would typically connect mechanistic studies (for example, immune pathways, epithelial barrier biology, host-microbe interactions, environmental triggers, genetics, or biomarkers) to clinically relevant questions, such as why certain patients progress to more severe disease, why some respond to specific therapies while others do not, or what early changes predict later development of asthma or allergy.
The FOA is “Clinical Trial Optional,” meaning applicants may include clinical trials if they are justified by the proposed aims, but a trial is not required. This gives flexibility to design a center around observational clinical studies, mechanistic studies using human samples, translational experiments that bridge lab findings to patient phenotypes, and, where appropriate, interventional trials that test prevention or treatment approaches grounded in the mechanistic framework developed by the center. The overall expectation is that the center structure enables coordinated projects and shared resources that accelerate progress beyond what separate R01-type projects would accomplish on their own.
Eligibility is broad across U.S.-based research and community organizations that can support the scope of a center-level program. Eligible applicants include a wide range of government entities (state, county, city or township, special district governments), independent school districts, public housing authorities/Indian housing authorities, public and state-controlled institutions of higher education, private institutions of higher education, nonprofit organizations (with or without 501(c)(3) status), for-profit organizations (other than small businesses), and small businesses. The FOA also explicitly welcomes applications from institutions and organizations that often serve underrepresented communities, including Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, regional organizations, eligible federal agencies, U.S. territories or possessions, and Indian/Native American tribal governments that are not federally recognized (in addition to federally recognized tribal governments listed in the general eligibility set). This framing signals an interest in broad participation and, potentially, research approaches that are relevant to diverse populations and real-world clinical settings.
Foreign participation is limited in a specific way. Non-domestic (non-U.S.) entities and non-domestic components of U.S. organizations are not eligible to apply as the main applicant organization. However, “foreign components” as defined by the NIH Grants Policy Statement are allowed, which generally means a U.S. applicant can include certain types of scientifically necessary work conducted abroad under NIH rules and oversight, even though a foreign institution cannot serve as the primary awardee.
From the administrative details provided, the opportunity falls under the NIH health research activity area and is associated with CFDA number 93.855. The original closing date listed is August 28, 2020, indicating this specific solicitation was time-bound to that cycle. The listed award ceiling is $900,000 (as presented in the source data), which can be read as an upper bound on the budget level anticipated by the announcement, although actual allowable budgets in NIH center programs can depend on the FOA’s detailed budget instructions and the final NIH award negotiations. The expected number of awards is not stated in the provided excerpt.
In essence, this FOA was designed to create coordinated research centers that can connect patient-oriented investigation with mechanistic discovery across asthma and a spectrum of allergic diseases, with the explicit purpose of turning improved understanding of disease biology into better, more targeted therapies and prevention approaches. The center model is meant to foster shared infrastructure, harmonized clinical and laboratory methods, and cross-project synergy so that advances in one area (for example, biomarker discovery in asthma) can quickly inform related areas (such as food allergy or atopic dermatitis) when the underlying biology overlaps.Apply for RFA AI 20 007
- The National Institutes of Health in the health sector is offering a public funding opportunity titled "Asthma and Allergic Diseases Cooperative Research Centers (U19 Clinical Trial Optional)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.855.
- This funding opportunity was created on 2020-03-23.
- Applicants must submit their applications by 2020-08-28. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Each selected applicant is eligible to receive up to $900,000.00 in funding.
- Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
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Frequently Asked Questions (FAQs)
What is the Asthma and Allergic Diseases Cooperative Research Centers (AADCRC) opportunity?
The Asthma and Allergic Diseases Cooperative Research Centers (AADCRC) opportunity (RFA-AI-20-007) is an NIH cooperative agreement (U19) intended to build and support multi-project research centers focused on asthma and allergic diseases. The emphasis is on integrated, center-based programs that combine clinical and translational science rather than standalone, isolated projects.
What does the U19 cooperative agreement structure mean for applicants and awardees?
This opportunity uses a cooperative agreement mechanism (U19), which typically involves more collaborative NIH participation than a standard research grant. The funding institute is expected to have substantial scientific involvement in coordinating, guiding, and aligning center activities with the program goals.
What is the overall goal of this program?
The program aims to improve understanding of the mechanisms driving the onset and progression of major, closely related inflammatory and hypersensitivity conditions (asthma and multiple allergic diseases). The intent is to translate mechanistic insights into a rational basis for better treatments and prevention strategies.
Which diseases are specifically highlighted by this opportunity?
The opportunity explicitly highlights the following diseases and conditions:
- Asthma
- Rhinitis (allergic and non-allergic)
- Chronic rhinosinusitis
- Atopic dermatitis
- Food allergy
- Drug allergy
What kinds of scientific questions is the FOA trying to address?
The unifying theme is pathogenesis, meaning applicants are expected to propose research that clarifies the biological and clinical processes that cause these conditions to begin, worsen, or persist. The FOA also encourages connecting mechanistic findings to clinically relevant questions, such as why some patients progress to severe disease, why treatment responses differ among patients, or which early changes predict later development of asthma or allergy.
What types of research approaches are likely to fit this FOA?
Based on the description provided, a competitive center would typically connect mechanistic studies to clinically relevant questions. Examples of mechanistic areas mentioned include immune pathways, epithelial barrier biology, host-microbe interactions, environmental triggers, genetics, and biomarkers, paired with patient-oriented or clinically grounded investigation.
Is a clinical trial required under this FOA?
No. The FOA is described as "Clinical Trial Optional," meaning clinical trials may be included if they are justified by the aims, but a clinical trial is not required.
If clinical trials are optional, what other study types are allowed or expected?
The FOA allows flexibility to build a center around approaches such as observational clinical studies, mechanistic studies using human samples, and translational experiments that bridge lab findings to patient phenotypes. Interventional trials may be included when appropriate and when grounded in the center's mechanistic framework.
What makes this a "center" opportunity rather than a set of independent projects?
The intent is to fund multi-project research centers that work in an integrated way. The center model is meant to foster shared infrastructure, harmonized clinical and laboratory methods, and cross-project synergy, helping the overall program progress faster than separate R01-type projects would on their own.
Can a center be based at a single institution, or does it have to be a consortium?
Centers may be based at a single institution or formed as consortia across multiple institutions. In either case, the expectation is that teams will operate as an integrated center rather than as isolated projects.
Who is eligible to apply?
Eligibility is broad across U.S.-based research and community organizations that can support a center-level program. Eligible applicants include government entities (state, county, city or township, special district governments), independent school districts, public housing authorities/Indian housing authorities, public and state-controlled institutions of higher education, private institutions of higher education, nonprofit organizations (with or without 501(c)(3) status), for-profit organizations (other than small businesses), and small businesses.
Does the FOA encourage applications from institutions serving underrepresented communities?
Yes. The FOA explicitly welcomes applications from organizations such as Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, regional organizations, eligible federal agencies, U.S. territories or possessions, and Indian/Native American tribal governments (including those that are not federally recognized, in addition to federally recognized tribal governments).
Can a non-U.S. institution apply as the main applicant?
No. Non-domestic (non-U.S.) entities and non-domestic components of U.S. organizations are not eligible to apply as the primary applicant organization.
Are any international activities allowed at all?
Yes. While foreign institutions cannot be the primary awardee, "foreign components" (as defined by the NIH Grants Policy Statement) are allowed. This generally means a U.S. applicant may include certain scientifically necessary work conducted abroad under NIH rules and oversight.
What NIH activity area and identifier information is provided for this opportunity?
The opportunity is under the NIH health research activity area and is associated with CFDA number 93.855.
What is the closing date listed for this solicitation?
The original closing date listed is August 28, 2020, indicating the solicitation was time-bound to that cycle.
What is the award ceiling mentioned in the provided information?
The listed award ceiling is $900,000 (as presented in the source data). The description notes that actual allowable budgets in NIH center programs can depend on the FOA's detailed budget instructions and final NIH award negotiations.
How many awards are expected under this FOA?
The expected number of awards is not stated in the provided excerpt.
What is the practical advantage of the AADCRC center model?
The center structure is meant to enable coordinated projects and shared resources that accelerate progress beyond what separate R01-type projects would accomplish. It is designed so that advances in one area (for example, biomarker discovery in asthma) can quickly inform related areas (such as food allergy or atopic dermatitis) when underlying biology overlaps.
What is the core theme that ties the targeted diseases together?
The diseases are presented as closely related, high-burden inflammatory and hypersensitivity conditions, with a shared focus on understanding pathogenesis and translating that understanding into improved therapies and prevention approaches.
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