Opportunity Information: Apply for RFA AI 16 028

  • The HHS-NIH11 in the health sector is offering a public funding opportunity titled "Understanding HIV Rebound (P01)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.242, 93.855, 93.856,.
  • This funding opportunity was created on Apr 19, 2016 and posted on Apr 19, 2016.
  • Applicants must submit their applications by Jul 29, 2016. (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 $1,000,000.00 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 (see text field entitled Additional Information on Eligibility for clarification).
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Opportunity Summary:

The Understanding HIV Rebound (P01) funding opportunity (RFA AI 16 028) is a National Institutes of Health (NIH) grant announcement from the U.S. Department of Health and Human Services (HHS), designed to fund coordinated, multi-disciplinary Program Project (P01) research efforts focused on why HIV returns in the blood after being suppressed. The central scientific goal is to identify and explain the mechanisms, biomarkers, and biological pathways that are linked to HIV viremia rebound, meaning the reappearance or rapid rise of detectable virus after a period in which antiretroviral therapy (ART) had kept viral levels fully suppressed. This FOA is positioned to support team-based projects where multiple related subprojects and shared cores work together around a unified theme, rather than isolated single-investigator studies.

The research scope is specifically anchored in situations where rebound can be observed and analyzed in a structured way, and it highlights three main study contexts. First, it encourages studies in HIV- or SIV-positive hosts who started ART very early after infection, maintained long-term full viral suppression, and then later stopped therapy, creating an opportunity to examine what predicts or drives rebound once drug pressure is removed. Second, it supports work in HIV- or SIV-positive hosts who are receiving an intervention intended to control or delay rebound, which can include strategies that aim to extend the time to rebound or blunt the magnitude of returning viremia. Third, it includes hosts receiving interventions aimed at diminishing or eradicating viral reservoirs, reflecting cure-oriented approaches where the key question is whether reservoir-targeting strategies measurably change rebound dynamics and what biological signals correspond to those changes. By including both human HIV and animal SIV models, the announcement implicitly supports translational work that can combine controlled experimental systems with clinically relevant observations.

From a practical funding perspective, the opportunity is offered as a discretionary grant with an activity category in health, and it is associated with CFDA numbers 93.242, 93.855, and 93.856. The award ceiling is listed as $1,000,000, indicating the maximum funding level expected per award under the announcement. The FOA was created and posted on April 19, 2016, with an original and current closing date of July 29, 2016. While the listing shows an “ExpectedAwards” field without a specified number, the structure and wording indicate competitive funding for a limited set of program projects that best address the FOA’s targeted scientific questions.

Eligibility is broad and includes many organization types that commonly apply to NIH research programs. Eligible applicants include state, county, and city or township governments; special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments and other tribal organizations; public housing authorities/Indian housing authorities; nonprofit organizations with or without 501(c)(3) status (excluding institutions of higher education in those nonprofit categories); for-profit organizations other than small businesses; small businesses; and other applicants as clarified in the full eligibility text. This wide eligibility range signals an intent to attract strong, cross-sector teams, including academic, nonprofit, government, and industry-linked groups, as long as they can assemble the scientific breadth needed for a P01.

In essence, this FOA is aimed at accelerating progress toward HIV remission and cure strategies by funding integrated research programs that can explain the biology of rebound, discover measurable indicators that predict or track rebound, and map the pathways that interventions might alter. The emphasis on early-treated, long-suppressed individuals and on intervention studies reflects a practical focus on scenarios that are most informative for understanding reservoirs, immune control, viral persistence, and the triggers that allow virus to re-emerge when ART is interrupted or when cure-directed therapies are tested.

Frequently Asked Questions (FAQs): Understanding HIV Rebound (P01) - RFA AI 16 028

What is the Understanding HIV Rebound (P01) funding opportunity?

This is an NIH grant announcement from the U.S. Department of Health and Human Services (HHS) designed to support coordinated, multi-disciplinary Program Project (P01) research focused on understanding why HIV returns in the blood after having been suppressed by antiretroviral therapy (ART).

What is the FOA number for this opportunity?

The funding opportunity is titled "Understanding HIV Rebound (P01)" and is identified as RFA AI 16 028.

Which agency is offering this grant?

The opportunity is offered through the National Institutes of Health (NIH), within the U.S. Department of Health and Human Services (HHS).

What type of grant mechanism does this announcement support?

This FOA supports a Program Project (P01) mechanism. It is intended for team-based, coordinated research programs built around a unified theme, typically involving multiple related subprojects and shared cores working together.

What is the central scientific goal of the FOA?

The central goal is to identify and explain mechanisms, biomarkers, and biological pathways linked to HIV viremia rebound, meaning the reappearance or rapid rise of detectable virus after a period of full suppression on ART.

What does "HIV viremia rebound" mean in this context?

In this FOA, HIV viremia rebound refers to HIV returning to detectable levels in the blood (or rising rapidly) after ART had previously kept viral levels fully suppressed.

What kinds of studies does the FOA emphasize?

The FOA emphasizes research where rebound can be observed and analyzed in structured, informative contexts. It highlights three main study situations: (1) early ART initiation followed by long-term suppression and later ART interruption, (2) intervention studies intended to control or delay rebound, and (3) interventions aimed at diminishing or eradicating viral reservoirs.

What is the first main study context described in the FOA?

The first context involves HIV- or SIV-positive hosts who started ART very early after infection, maintained long-term full viral suppression, and then later stopped therapy. This setup creates an opportunity to study what predicts or drives rebound once drug pressure is removed.

What is the second main study context described in the FOA?

The second context involves HIV- or SIV-positive hosts receiving an intervention intended to control or delay rebound. This includes strategies aiming to extend the time to rebound or reduce the magnitude of returning viremia.

What is the third main study context described in the FOA?

The third context involves hosts receiving interventions aimed at diminishing or eradicating viral reservoirs. These are cure-oriented approaches that assess whether reservoir-targeting strategies change rebound dynamics and what biological signals correspond to those changes.

Does the FOA allow research in both humans and animals?

Yes. The FOA includes both human HIV and animal SIV models, supporting translational research that can combine controlled experimental systems with clinically relevant observations.

Why does the FOA include SIV models?

SIV models can provide controlled experimental settings that complement human observations, helping teams investigate mechanisms and pathways related to rebound in ways that may be difficult to study solely in clinical settings.

Is this FOA meant for single-investigator projects?

No. The FOA is positioned to support coordinated, multi-disciplinary P01 program projects with multiple related subprojects and shared cores, rather than isolated single-investigator studies.

What is the award ceiling for this opportunity?

The award ceiling is listed as $1,000,000, indicating the maximum funding level expected per award under this announcement.

How is this opportunity categorized from a funding perspective?

It is listed as a discretionary grant with an activity category in health.

What CFDA numbers are associated with this FOA?

The FOA is associated with CFDA numbers 93.242, 93.855, and 93.856.

When was this FOA posted?

The FOA was created and posted on April 19, 2016.

What is the closing date for applications?

The original and current closing date listed is July 29, 2016.

How many awards are expected under this FOA?

The listing shows an "ExpectedAwards" field without a specified number, suggesting competitive funding for a limited set of program projects that best address the FOA's targeted scientific questions.

Who is eligible to apply for this opportunity?

Eligibility is broad and includes many organization types, including government entities, higher education institutions, tribal governments and organizations, nonprofits, for-profits, small businesses, and other applicants as clarified in the full eligibility text.

Are state, county, and local governments eligible?

Yes. Eligible applicants include state governments, county governments, and city or township governments, as well as special district governments.

Are educational institutions eligible to apply?

Yes. Eligible applicants include independent school districts, public and state-controlled institutions of higher education, and private institutions of higher education.

Are tribal governments and tribal organizations eligible?

Yes. Eligibility includes federally recognized Native American tribal governments and other tribal organizations.

Are public housing authorities eligible?

Yes. Public housing authorities and Indian housing authorities are listed as eligible applicants.

Are nonprofit organizations eligible?

Yes. Nonprofit organizations with or without 501(c)(3) status are included as eligible (excluding institutions of higher education within those nonprofit categories as stated in the eligibility description).

Are for-profit organizations eligible?

Yes. For-profit organizations other than small businesses are eligible, and small businesses are also explicitly listed as eligible.

What is the intended impact or purpose of funding research under this FOA?

The FOA aims to accelerate progress toward HIV remission and cure strategies by funding integrated research programs that explain the biology of rebound, discover measurable indicators that predict or track rebound, and map the pathways that interventions may alter.

Why does the FOA emphasize early-treated, long-suppressed individuals?

The FOA emphasizes these populations because they offer especially informative scenarios for understanding viral reservoirs, immune control, viral persistence, and the triggers that allow virus to re-emerge when ART is interrupted.

What kinds of research outputs does the FOA highlight?

Based on the description, the FOA highlights identifying mechanisms, discovering biomarkers, and mapping biological pathways associated with HIV rebound, particularly in intervention and treatment interruption settings where rebound dynamics can be measured.

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