Opportunity Information: Apply for PA 15 255

  • The National Institutes of Health in the health sector is offering a public funding opportunity titled "Human Studies to Evaluate Promising Medications to Treat Alcohol Use Disorder (R03)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.273 Alcohol Research Programs.
  • This funding opportunity was created on May 13, 2015 and posted on May 13, 2015.
  • Applicants must submit their applications by May 7, 2018. (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 $50,000.00 in funding.
  • Eligible applicants include: State governments For profit organizations other than small businesses Native American tribal governments (Federally recognized) Native American tribal organizations (other than Federally recognized tribal governments) County governments City or township governments Public and State controlled institutions of higher education Private institutions of higher education Independent school districts Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Small businesses Public housing authorities/Indian housing authorities Others (see text field entitled Additional Information on Eligibility for clarification) Special district governments.
  • Other Eligible Applicants include the following Alaska Native and Native Hawaiian Serving Institutions Asian American Native American Pacific Islander Serving Institutions (AANAPISISs) 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) Regional Organizations Tribally Controlled Colleges and Universities (TCCUs) U.S. Territory or Possession.
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Opportunity Summary:

The grant opportunity "Human Studies to Evaluate Promising Medications to Treat Alcohol Use Disorder (R03)" (Funding Opportunity Number PA-15-255) is a National Institutes of Health (NIH) discretionary grant program under CFDA 93.273 (Alcohol Research Programs). Its main goal is to spur early stage, human focused research that tests promising medication candidates for alcohol use disorder (AUD), including cases where AUD occurs alongside comorbid post-traumatic stress disorder (PTSD). The emphasis is on medications that are either genuinely novel or repurposed from other indications, but in both cases the compounds should act on new biological targets relevant to AUD and/or AUD plus PTSD. In practical terms, the FOA is designed to move beyond purely preclinical work and encourage studies that can generate initial human evidence about whether these compounds are safe, tolerable, and potentially effective.

This FOA specifically encourages the use of human laboratory paradigms and/or clinical trials. Human laboratory paradigms generally refer to controlled experimental approaches in people that can measure outcomes such as craving, stress reactivity, alcohol cue responses, alcohol self-administration behavior, or other mechanistic and behavioral signals that help predict clinical benefit. Clinical trials, in turn, are intended to provide more direct tests of safety and efficacy in individuals with AUD, including those with comorbid PTSD when relevant. The overarching idea is to support smaller, targeted human studies that can help decide whether a medication is ready for larger scale testing, while also providing meaningful information about how and why it might work.

The award structure reflects that early, exploratory intent. The listed award ceiling is $50,000, consistent with an R03 mechanism that typically supports smaller projects, pilot studies, or tightly focused proof-of-concept work. The opportunity does not require cost sharing or matching funds, which can lower the barrier for institutions that might otherwise struggle to assemble matching support.

Eligibility is broad and includes a wide range of domestic and non-domestic organizations. Eligible applicants include state, county, and city or township governments; public and state controlled institutions of higher education; private institutions of higher education; nonprofit organizations (including both 501(c)(3) and certain non-501(c)(3) nonprofits, excluding some higher education-related constraints as specified); small businesses and other for-profit organizations (other than small businesses); independent school districts; public housing authorities/Indian housing authorities; special district governments; and additional categories such as faith-based or community-based organizations. The FOA also lists various minority-serving and tribal-serving institutions and entities as eligible, including Historically Black Colleges and Universities (HBCUs), Hispanic-Serving Institutions, Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Tribally Controlled Colleges and Universities (TCCUs), Native American tribal governments and organizations (including those other than federally recognized), U.S. territories or possessions, regional organizations, foreign organizations (non-U.S. entities), and eligible federal agencies. This wide eligibility is intended to attract applications from many settings where clinical and translational AUD research is conducted.

Key administrative details indicate that the opportunity was posted and created on May 13, 2015, with an original and current closing date of May 7, 2018, and an archive date of June 7, 2018, meaning it is no longer open for new submissions under that announcement. The official full announcement was hosted by NIH at http://grants.nih.gov/grants/guide/pa-files/PA-15-255.html. For technical issues accessing or linking to the announcement, the listed contact point is the NIH Office of Extramural Research (OER) Webmaster at FBOWebmaster@OD.NIH.GOV.

Taken together, PA-15-255 was aimed at accelerating the early human evaluation of medication strategies for AUD (and AUD with PTSD), prioritizing compounds that hit new targets and using experimental human lab approaches and/or clinical trials to produce actionable safety and efficacy signals that can guide future, larger studies.

Frequently Asked Questions (FAQs)

What is the name of this grant opportunity?

The opportunity is titled "Human Studies to Evaluate Promising Medications to Treat Alcohol Use Disorder (R03)."

What is the Funding Opportunity Number (FON)?

The Funding Opportunity Number is PA-15-255.

Which agency offers this funding opportunity?

This is a National Institutes of Health (NIH) discretionary grant program.

What CFDA program is associated with this opportunity?

This opportunity is listed under CFDA 93.273, Alcohol Research Programs.

What is the main purpose of this FOA?

The main goal is to spur early-stage, human-focused research that tests promising medication candidates for alcohol use disorder (AUD), including situations where AUD occurs alongside comorbid post-traumatic stress disorder (PTSD).

What types of medications does the FOA prioritize?

The FOA emphasizes medications that are either genuinely novel or repurposed from other indications. In both cases, the compounds should act on new biological targets relevant to AUD and/or AUD plus PTSD.

Does the FOA support preclinical-only studies?

No. The FOA is designed to move beyond purely preclinical work and encourage studies that generate initial human evidence about whether compounds are safe, tolerable, and potentially effective.

What kinds of study designs are encouraged?

The FOA specifically encourages the use of human laboratory paradigms and/or clinical trials.

What is meant by "human laboratory paradigms" in this FOA?

Human laboratory paradigms refer to controlled experimental approaches in people that can measure outcomes such as craving, stress reactivity, alcohol cue responses, alcohol self-administration behavior, or other mechanistic and behavioral signals that help predict clinical benefit.

What is the role of clinical trials under this FOA?

Clinical trials are intended to provide more direct tests of safety and efficacy in individuals with AUD, including those with comorbid PTSD when relevant.

What is the overall research intent of the R03 structure here?

The intent is to support smaller, targeted human studies that help determine whether a medication is ready for larger-scale testing, while also providing meaningful information about how and why it might work.

What is the award ceiling for this opportunity?

The listed award ceiling is $50,000, consistent with the R03 mechanism supporting smaller projects, pilot studies, or tightly focused proof-of-concept work.

Is cost sharing or matching required?

No. The opportunity does not require cost sharing or matching funds.

Who is eligible to apply?

Eligibility is broad and includes a wide range of domestic and non-domestic organizations, including:

  • State, county, and city or township governments
  • Public and state controlled institutions of higher education
  • Private institutions of higher education
  • Nonprofit organizations (including 501(c)(3) and certain non-501(c)(3) nonprofits, with exclusions as specified)
  • Small businesses
  • Other for-profit organizations (other than small businesses)
  • Independent school districts
  • Public housing authorities/Indian housing authorities
  • Special district governments
  • Faith-based or community-based organizations
  • Minority-serving and tribal-serving institutions and entities (including HBCUs, Hispanic-Serving Institutions, Alaska Native and Native Hawaiian Serving Institutions, AANAPISIs, and TCCUs)
  • Native American tribal governments and organizations (including those other than federally recognized)
  • U.S. territories or possessions
  • Regional organizations
  • Foreign organizations (non-U.S. entities)
  • Eligible federal agencies

Are foreign (non-U.S.) organizations eligible?

Yes. Foreign organizations (non-U.S. entities) are listed as eligible applicants.

Are for-profit organizations eligible?

Yes. The FOA lists small businesses and other for-profit organizations (other than small businesses) as eligible applicants.

Does the FOA include eligibility for minority-serving and tribal-serving institutions?

Yes. The FOA lists multiple minority-serving and tribal-serving categories, including HBCUs, Hispanic-Serving Institutions, Alaska Native and Native Hawaiian Serving Institutions, AANAPISIs, TCCUs, and Native American tribal governments and organizations (including those other than federally recognized).

When was this opportunity posted and created?

It was posted and created on May 13, 2015.

What was the closing date for applications under this announcement?

The original and current closing date listed is May 7, 2018.

Is this funding opportunity still open?

No. The archive date is June 7, 2018, which indicates it is no longer open for new submissions under that announcement.

Where can the full official announcement be found?

The official full announcement was hosted by NIH at: http://grants.nih.gov/grants/guide/pa-files/PA-15-255.html

Who should be contacted for technical issues accessing or linking to the announcement?

For technical issues, the listed contact is the NIH Office of Extramural Research (OER) Webmaster at FBOWebmaster@OD.NIH.GOV.

Does this FOA explicitly include research on AUD with comorbid PTSD?

Yes. The FOA explicitly includes interest in AUD occurring alongside comorbid PTSD and supports studies relevant to AUD plus PTSD when appropriate.

What kinds of outcomes or signals are considered useful in the early human studies described?

The FOA highlights outcomes such as craving, stress reactivity, alcohol cue responses, alcohol self-administration behavior, and other mechanistic and behavioral signals that may help predict clinical benefit.

What is the practical "next step" this FOA is trying to enable?

It aims to generate actionable early human safety, tolerability, and potential efficacy signals that can guide decisions about whether a medication should advance to larger-scale testing.

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