Opportunity Information: Apply for RFA DC 11 002
Apply for RFA DC 11 002
- The National Institutes of Health in the health sector is offering a public funding opportunity titled "Identification of Immune Mediated Causes of Sensorineural Hearing Loss (R21/R33)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.173 Research Related to Deafness and Communication Disorders.
- This funding opportunity was created on Aug 18, 2010 and posted on Aug 18, 2010.
- Applicants must submit their applications by Jun 8, 2011. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Eligible applicants include: Small businesses For profit organizations other than small businesses Private institutions of higher education Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Public and State controlled institutions of higher education Others (see text field entitled Additional Information on Eligibility for clarification) State governments 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 Native American tribal governments (Federally recognized).
- Other Eligible Applicants include the following Alaska Native and Native Hawaiian Serving Institutions Eligible Agencies of the Federal Government Faith based or Community based Organizations Hispanic serving Institutions Historically Black Colleges and Universities (HBCUs) Indian/Native American Tribal Governments (Other than Federally Recognized) Non domestic (non U.S.) Entities (Foreign Organizations) Tribally Controlled Colleges and Universities (TCCUs) U.S. Territory or Possession.
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Opportunity Summary:
The grant opportunity titled "Identification of Immune Mediated Causes of Sensorineural Hearing Loss (R21/R33)" (Funding Opportunity Number RFA-DC-11-002) is a National Institutes of Health (NIH) program run through the National Institute on Deafness and Other Communication Disorders (NIDCD). It is designed to push forward research on immune mediated sensorineural hearing loss (IMSNHL), with a clear emphasis on understanding what causes it, how it develops, and what biological mechanisms drive the damage that ultimately affects hearing. The overall goal is practical and clinically focused: generate findings that can be translated into real-world tools such as biomarkers and diagnostic tests that perform well (high sensitivity, high specificity, and strong positive predictive value), and ultimately support the development of treatments that protect or preserve natural hearing.
The scientific scope is intentionally targeted at immune-related forms of sensorineural hearing loss. The announcement highlights three areas that are considered responsive. First are studies focused on ear organ-specific autoimmune sensorineural hearing loss, commonly referred to as autoimmune inner ear disease (AIED). Second are studies of sudden sensorineural hearing loss when it can be attributed to AIED, which speaks to rapid-onset cases where immune activity may be the trigger or driver. Third are studies looking at sensorineural hearing loss that occurs in connection with systemic autoimmune diseases, where the immune dysfunction is not limited to the ear but may involve broader inflammatory or autoimmune processes affecting multiple organs. In other words, the program is interested both in immune attacks that appear confined to the inner ear and in hearing loss that shows up as part of larger autoimmune conditions.
A central feature of the program is the priority it gives to human-centered research. Proposals that primarily involve human subjects or human tissues are stated to receive the highest priority. That emphasis signals that the institute wants studies that are close to clinical reality, such as work using patient samples, clinically characterized cohorts, or tissue-based investigations that can directly inform diagnostics and treatment strategies. While basic and mechanistic questions are still part of the mission, the framing makes it clear that the preferred path is one that can bridge the gap between laboratory insights and clinical use.
In terms of funding structure, this opportunity uses the NIH R21/R33 Exploratory/Developmental Phased Innovation mechanism. This is a milestone-driven, phased approach: the R21 phase typically supports early, exploratory, or developmental work, and the R33 phase supports a subsequent stage that builds on success in the first phase. The milestone-driven language matters because it implies applicants are expected to define concrete, measurable goals and decision points that justify moving from the initial exploratory phase into the more advanced phase. The intent is to support innovative, interdisciplinary projects while keeping them accountable to progress markers that show the work is on track and ready for expansion.
The funding levels and award expectations are spelled out in the announcement. NIDCD set aside approximately $700,000 for fiscal year 2011 and $1.3 million for fiscal year 2012. The institute anticipated making about 2 to 3 awards per application cycle, indicating a competitive program with a limited number of funded projects, likely focused on proposals with clear milestones and a strong translational line of sight toward diagnostics, biomarkers, and therapeutic development.
Administrative details further define who can apply and how the program is categorized. The opportunity is listed as a discretionary grant under the health activity category, associated with CFDA number 93.173 (Research Related to Deafness and Communication Disorders). There is no cost sharing or matching requirement, meaning applicants are not required to contribute non-federal funds as a condition of the award. The posting and creation date for the opportunity was August 18, 2010, with an original and final closing date of June 8, 2011, and an archive date of July 9, 2011, which indicates the opportunity is now historical rather than currently open.
Eligibility is broad and spans a wide range of organization types. Eligible applicants include small businesses, for-profit organizations (including those other than small businesses), public and private institutions of higher education, nonprofits (including 501(c)(3) and certain non-501(c)(3) entities), state governments, U.S. territory or possession entities, and a variety of tribal organizations (including federally recognized tribal governments and other tribal entities). The eligibility language also explicitly includes several institution categories and community-based organizations, such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving Institutions, Alaska Native and Native Hawaiian Serving Institutions, Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, and even non-U.S. entities (foreign organizations). Federal agencies are also listed among eligible applicants, reflecting NIH rules that sometimes allow intramural or federal participation depending on the specific terms.
Taken together, the opportunity is essentially a call for interdisciplinary, milestone-oriented projects that can explain immune-driven hearing loss in humans and move the field toward better clinical detection and intervention. It is not just about describing associations; it is about identifying mechanisms and measurable indicators that can become reliable clinical tools, and about laying the groundwork for therapies that can prevent hearing loss from progressing or preserve existing hearing in people affected by autoimmune or immune-mediated processes. For reference, the full announcement was hosted by NIH at: http://grants.nih.gov/grants/guide/rfa-files/RFA-DC-11-002.html.
FAQs: Identification of Immune Mediated Causes of Sensorineural Hearing Loss (R21/R33) (RFA-DC-11-002)
What is this grant opportunity?
"Identification of Immune Mediated Causes of Sensorineural Hearing Loss (R21/R33)" (Funding Opportunity Number RFA-DC-11-002) is an NIH grant opportunity administered by the National Institute on Deafness and Other Communication Disorders (NIDCD). It focuses on research to understand immune mediated sensorineural hearing loss (IMSNHL), including what causes it, how it develops, and which biological mechanisms drive damage that affects hearing.
Which NIH institute runs this program?
The program is run through the National Institute on Deafness and Other Communication Disorders (NIDCD), a component of the National Institutes of Health (NIH).
What is the main goal of the program?
The overall goal is clinically focused: generate findings that can be translated into real-world tools such as biomarkers and diagnostic tests with high sensitivity, high specificity, and strong positive predictive value. The program also aims to support the development of treatments that protect or preserve natural hearing.
What kinds of hearing loss are considered responsive to this announcement?
The scientific scope is intentionally targeted to immune-related forms of sensorineural hearing loss. The announcement highlights three responsive areas: (1) ear organ-specific autoimmune sensorineural hearing loss (autoimmune inner ear disease, or AIED); (2) sudden sensorineural hearing loss when it can be attributed to AIED; and (3) sensorineural hearing loss associated with systemic autoimmune diseases.
Does the program focus only on inner-ear-specific autoimmune disease (AIED)?
No. The program is interested both in immune attacks that appear confined to the inner ear (AIED) and in hearing loss that occurs as part of broader systemic autoimmune diseases.
How does sudden sensorineural hearing loss fit within the scope?
Sudden sensorineural hearing loss is considered responsive when it can be attributed to autoimmune inner ear disease (AIED), meaning rapid-onset cases where immune activity may be the trigger or driver.
Is there a preference for human-centered research?
Yes. Proposals that primarily involve human subjects or human tissues are stated to receive the highest priority. This reflects an emphasis on studies that are close to clinical reality, such as patient samples, clinically characterized cohorts, and tissue-based investigations that can directly inform diagnostics and treatment strategies.
What research outcomes does NIDCD appear to be looking for?
Based on the announcement description, NIDCD is looking for outcomes that move beyond association and toward practical clinical impact, including: (1) identification of causes and mechanisms of immune-mediated damage; (2) measurable indicators that can become biomarkers; (3) diagnostics that perform well (high sensitivity, specificity, and positive predictive value); and (4) groundwork that supports therapies designed to protect or preserve natural hearing.
What funding mechanism is used for this opportunity?
This opportunity uses the NIH R21/R33 Exploratory/Developmental Phased Innovation mechanism. It is a milestone-driven, phased approach in which the R21 phase supports early exploratory or developmental work and the R33 phase supports a subsequent stage that builds on success in the R21 phase.
What does "milestone-driven" mean in the context of the R21/R33 mechanism?
Milestone-driven means applicants are expected to define concrete, measurable goals and decision points that help determine whether the project should transition from the initial R21 exploratory phase to the R33 phase. The structure is intended to support innovation while requiring accountability to progress markers.
How much funding was set aside for this program?
NIDCD set aside approximately $700,000 for fiscal year 2011 and $1.3 million for fiscal year 2012 for this opportunity.
How many awards did NIDCD expect to make?
NIDCD anticipated making about 2 to 3 awards per application cycle, indicating a competitive program with a limited number of funded projects.
Is cost sharing or matching required?
No. The announcement specifies that there is no cost sharing or matching requirement.
What is the CFDA number and program area for this opportunity?
The opportunity is associated with CFDA number 93.173, "Research Related to Deafness and Communication Disorders," and is categorized as a discretionary grant under the health activity category.
Who is eligible to apply?
Eligibility is broad and includes small businesses; for-profit organizations (including those other than small businesses); public and private institutions of higher education; nonprofits (including 501(c)(3) and certain non-501(c)(3) entities); state governments; U.S. territory or possession entities; tribal organizations (including federally recognized tribal governments and other tribal entities); faith-based or community-based organizations; and foreign organizations (non-U.S. entities). Federal agencies are also listed among eligible applicants.
Are minority-serving institutions specifically included as eligible applicants?
Yes. The eligibility language explicitly includes categories such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving Institutions, Alaska Native and Native Hawaiian Serving Institutions, and Tribally Controlled Colleges and Universities (TCCUs).
Are community-based and faith-based organizations allowed to apply?
Yes. The eligibility language explicitly includes faith-based or community-based organizations.
Are foreign (non-U.S.) organizations eligible?
Yes. The eligibility language explicitly includes non-U.S. entities (foreign organizations).
Is this opportunity currently open?
No. The information provided indicates this opportunity is historical. The posting/creation date was August 18, 2010; the original and final closing date was June 8, 2011; and the archive date was July 9, 2011.
Where can the original NIH announcement be found?
The full announcement was hosted by NIH at: http://grants.nih.gov/grants/guide/rfa-files/RFA-DC-11-002.html
What is the program trying to advance in the long run?
The long-term intent is to enable better clinical detection and intervention for immune-mediated hearing loss by identifying mechanisms and measurable indicators that can become reliable clinical tools and by laying groundwork for therapies that prevent progression or preserve existing natural hearing.
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