NIH-funded research R01 grant

Integrated medication approaches for people with both opioid and alcohol use disorders

Official title: Advancing Integrated Treatment for Co-Occurring Opioid and Alcohol Use Disorders: A Comprehensive Analysis of GLP-1 Receptor Agonists and Traditional Pharmacotherapies in Real-World Settings

Funded at Loyola University Chicago · NIH-11196080 · Data updated 2026-11-12

This project looks at how combining common addiction medicines and GLP-1 receptor agonists works for people who have both opioid and alcohol use problems using large-scale medical records.

More Alcohol Use research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionLoyola University Chicago
NIH-funded
Lab location1 site (Maywood, United States)
Project startSeptember 25, 2024
Project endAugust 31, 2027
Funding year2025
Award (this year)$385,000
NIH project number5R01AA031890-02
Project IDNIH-11196080 on NIH RePORTER

Who could benefit from this research

Could help

Adults diagnosed with both opioid use disorder and alcohol use disorder who receive care within participating US health systems are the patients whose records are included.

Less likely to help

People without both opioid and alcohol disorders, those not treated with medications, or those not seen in the included health systems would not be represented or directly helped by this analysis.

What this research studies

If you have both opioid and alcohol use disorders, the team will use anonymized electronic health records from a large US database to see which medication combinations people received and how they fared. They will compare standard OUD and AUD medications (like buprenorphine and first-line alcohol treatments) with regimens that include GLP-1 receptor agonists, and track outcomes over time. The study will look at substance use events, liver and other physical health measures, mental health, hospitalizations, detox use, and drug testing results. Researchers will also analyze patterns and patient factors that predict better or worse outcomes to help guide future care choices.

Why it matters

Potential benefit: If successful, the findings could help clinicians choose medication combinations that lower overdoses and heavy drinking and improve overall health for people with both conditions.

How similar studies have gone: Early lab and small clinical studies suggest GLP-1 receptor agonists may reduce substance use, but using large real-world EHR data to compare them alongside standard OUD/AUD medicines is a newer approach.

Where this research is happening

  • Loyola University Chicago
    Maywood, United States
    Active

Researchers

  • Principal investigator: Qeadan, Fares — Loyola University Chicago
  • Study coordinator: Qeadan, Fares

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.