Addiction Science & Substance Use
Could GLP-1 and naltrexone combination therapy make addiction craving suppression a clinical reality by 2028

The Ashley Addiction Treatment Center in Havre de Grace, Maryland, has launched a specialized research facility to investigate the efficacy of GLP-1 receptor agonists in treating substance use disorders. Researchers are conducting a clinical trial in partnership with Johns Hopkins to evaluate whether pairing GLP-1 medications with naltrexone can more effectively reduce alcohol cravings than existing monotherapies. This approach is based on the observation that the brain's control centers for food and drug cravings overlap, with patients reporting reduced substance use while taking GLP-1s for weight management.
The Neurobiological Convergence of Craving
The recent expansion of research at the Ashley Addiction Treatment Center in Havre de Grace, Maryland, marks a significant shift in how addiction is being approached clinically (WBAL, 2026). By establishing a dedicated research facility, the center is focusing on the intersection of metabolic health and substance use disorders. The core hypothesis driving this research is that the brain's control centers for food and drug cravings share common neural pathways (WBAL, 2026). This conceptual framework suggests that medications originally developed for metabolic regulation, specifically GLP-1 receptor agonists, may have cross-utility in suppressing the neurobiological drivers of addiction (WBAL, 2026).
This approach is supported by observations that patients prescribed GLP-1s for weight management often report secondary reductions in alcohol consumption and cigarette smoking (WBAL, 2026). The research team, led by experts in clinical research, is now moving beyond anecdotal evidence to conduct a formal clinical trial in partnership with Johns Hopkins (WBAL, 2026). This trial specifically pairs GLP-1s with naltrexone, an established treatment for alcohol use disorder, to determine if the combination provides a synergistic effect in reducing cravings (WBAL, 2026). The study aims to provide the empirical data necessary to validate this pharmacological strategy as a viable treatment option for a broader range of substance use disorders (WBAL, 2026).
Methodological Innovation in Addiction Neuroscience
The broader field of addiction neuroscience is currently experiencing a period of rapid methodological innovation, which is providing the tools necessary to test these new pharmacological hypotheses (Bioengineer.org, 2026). A collection of studies published in Frontiers in Behavioral Neuroscience highlights how technological advances and mechanistic insights are reshaping the understanding of addiction as a clinical condition (Bioengineer.org, 2026). This shift is characterized by a move away from viewing addiction solely as a behavioral issue toward a more nuanced understanding of the neurobiological and physiological dynamics involved (Bioengineer.org, 2026).
Researchers are increasingly using longitudinal tracking of physiological and mental health functioning to tailor therapeutic interventions (Bioengineer.org, 2026). This data-driven approach allows for a more personalized treatment model, where interventions can be adjusted based on real-time patient outcomes (Bioengineer.org, 2026). The integration of these new tools into clinical practice is essential for addressing the chronic nature of addiction, which requires consistent care over extended periods rather than short-term interventions (Tenovi, 2026). The convergence of animal and human research, along with experimental and clinical investigations, is creating a robust foundation for these new treatment strategies (Bioengineer.org, 2026).
Challenges in Clinical Retention and Care
Despite these promising pharmacological developments, the field faces significant challenges regarding patient retention in treatment programs (Drugfree.org, 2026). A study by Scott Hadland and colleagues, analyzing Medicaid claims from 2016 to 2023, found that retention rates for medications for opioid use disorder (MOUD) among young people remain low (Drugfree.org, 2026). This highlights a critical barrier to the success of any new treatment: the ability to keep patients engaged in care long enough to achieve meaningful outcomes (Drugfree.org, 2026). The study underscores the need for treatments that are not only effective but also accessible and acceptable to younger populations who may be apprehensive about long-term medication commitments (Drugfree.org, 2026).
Telemedicine has emerged as a vital tool for improving access to care, particularly for those who face geographic or logistical barriers to traditional clinic visits (Tenovi, 2026). Research from the University at Buffalo, studying referrals through the Medication for Addiction Treatment and Electronic Referrals (MATTERS) Network, demonstrates the potential of telemedicine to bridge the gap between patients and providers (Tenovi, 2026). By allowing patients to connect with licensed practitioners remotely, telemedicine can help overcome the stigma and logistical hurdles that often prevent individuals from seeking help (Tenovi, 2026). The continued renewal of regulatory flexibility for prescribing controlled substances via telemedicine through December 31, 2026, is a crucial component of this strategy (Tenovi, 2026).
Evidence and Limitations of Current Research
The evidence supporting the use of GLP-1s for addiction is currently in the early stages of clinical validation (WBAL, 2026). While the initial observations are promising, the transition from laboratory and observational findings to standardized clinical practice requires rigorous, large-scale randomized controlled trials (WBAL, 2026). The ongoing study at the Ashley Addiction Treatment Center is a critical step in this process, but it is only one piece of a larger puzzle (WBAL, 2026). The field must also address the potential for side effects and the long-term safety profile of combining GLP-1s with other medications like naltrexone (WBAL, 2026).
Furthermore, the heterogeneity of substance use disorders means that a single pharmacological solution is unlikely to be effective for all patients (Bioengineer.org, 2026). Future research must focus on identifying biomarkers that can predict which patients are most likely to respond to GLP-1-based therapies (Bioengineer.org, 2026). This precision medicine approach will be essential for maximizing the impact of these new treatments and ensuring that resources are directed toward the most effective interventions (Bioengineer.org, 2026). The integration of behavioral therapies, such as Mindfulness-Oriented Recovery Enhancement (MORE), alongside pharmacological treatments also shows promise in reshaping brain responses to drug cues, suggesting that a multimodal approach may be the most effective path forward (Medical Xpress, 2026).
What It Will Take to Advance This
Large-scale, multi-site randomized controlled trials are required to definitively prove the efficacy and safety of GLP-1 and naltrexone combinations. These trials must include diverse patient populations to ensure the findings are generalizable across different demographics and substance use profiles. Researchers must identify the specific neurobiological mechanisms by which GLP-1s modulate craving to optimize dosing and patient selection. Understanding these mechanisms is crucial for developing personalized treatment plans that minimize side effects and maximize efficacy. Sustained federal and private funding is necessary to support the transition from pilot studies to Phase III clinical trials. This includes investment in the infrastructure required to conduct high-quality, longitudinal addiction research. The FDA must establish a clear regulatory pathway for the approval of GLP-1 agonists for addiction treatment. This involves reviewing comprehensive safety and efficacy data to support potential label expansion. Pharmaceutical manufacturers must scale production to meet the potential demand for addiction treatment applications while ensuring supply chain stability. This is essential for making these therapies accessible to a broad patient population.
Future Possibilities
The integration of GLP-1 agonists into addiction treatment could revolutionize the standard of care for alcohol and opioid use disorders. If clinical trials confirm efficacy, clinicians could prescribe these medications to suppress cravings, potentially reducing relapse rates by a significant margin. This would shift the treatment paradigm from purely behavioral or opioid-agonist-based models to a more comprehensive approach that addresses the metabolic and neurobiological drivers of addiction. Success depends on the successful completion of ongoing trials and the development of clear clinical guidelines for safe administration.
- •Near term (0-2 years)
- •Moderate confidence
Reference: The Ashley Addiction Treatment Center is currently conducting a clinical trial in partnership with Johns Hopkins to test the combination of GLP-1s and naltrexone (WBAL, 2026).
Addressing the addiction crisis more effectively could have profound implications for national security by reducing the societal and economic burden of substance use disorders. A healthier, more stable population is less susceptible to the destabilizing effects of widespread addiction, which can impact workforce participation and social cohesion. By providing more effective treatment tools, the U.S. can mitigate the long-term costs associated with the opioid epidemic and other substance-related crises. This requires sustained investment in research and the successful scaling of effective treatment programs.
- •Mid term (2-5 years)
- •Moderate confidence
Reference: Opioid use disorder diagnoses rose nearly 33% between 2022 and 2025, highlighting the urgent need for more effective interventions (Addiction Center, 2026).
Effective addiction treatments could lead to significant economic gains by increasing workforce productivity and reducing healthcare expenditures. Substance use disorders are a major driver of lost productivity and high medical costs, and successful interventions could help individuals return to the workforce and lead more stable lives. The widespread adoption of cost-effective pharmacological treatments could alleviate the financial strain on public health systems and insurance providers. This outcome is contingent on the affordability and accessibility of these new therapies.
- •Mid term (2-5 years)
- •High confidence
Reference: Addiction is a chronic condition that works best when care stays consistent, and improving treatment outcomes can reduce the long-term economic burden (Tenovi, 2026).
While the direct environmental impact of this advancement is minimal, the broader shift toward more effective, evidence-based healthcare could lead to more efficient use of medical resources. By reducing the need for repeated emergency department visits and long-term inpatient stays, the healthcare system could lower its overall carbon footprint. This would require a systemic shift toward outpatient and telemedicine-based care models that are less resource-intensive. The long-term sustainability of this approach depends on the continued development of digital health infrastructure.
- •Long term (5+ years)
- •Low confidence
Reference: Telemedicine for addiction treatment is already maturing as a way to provide consistent care outside of traditional emergency departments (Tenovi, 2026).
For individuals struggling with addiction, the availability of effective craving-suppression medications could significantly improve quality of life and social functioning. By reducing the intensity of cravings, these treatments could help individuals maintain employment, rebuild relationships, and participate more fully in their communities. This would represent a major step forward in destigmatizing addiction and treating it as a manageable medical condition rather than a moral failing. The success of this shift depends on public awareness and the destigmatization of pharmacological interventions for addiction.
- •Long term (5+ years)
- •Moderate confidence
Reference: Mindfulness-based therapies and new pharmacological tools are being explored to help people with opioid use disorder respond better to treatment (Medical Xpress, 2026).
The National Institutes of Health (NIH) should prioritize grant allocations for multi-site clinical trials investigating GLP-1 and naltrexone combinations to establish standardized dosing protocols. By leveraging the existing HEAL Initiative infrastructure, the NIH can accelerate the transition from pilot studies to large-scale Phase III trials. This funding would enable the recruitment of diverse patient cohorts, ensuring the treatment's efficacy is validated across different demographics and substance use profiles. The goal is to secure sufficient data to support FDA label expansion for addiction treatment within the next 36 months.
- •The Ashley Addiction Treatment Center has already established a dedicated research hub for this specific study (WBAL, 2026).
- •Prior research indicates that GLP-1s show promise in reducing alcohol-related problems and cravings (Neuroscience News, 2026).
Reference: NIH HEAL Initiative
Medical boards and professional societies should develop clinical practice guidelines that integrate GLP-1 agonists into standard-of-care protocols for alcohol and opioid use disorders. This involves creating training modules for addiction specialists to safely manage the side-effect profiles of these medications in combination with naltrexone. By establishing these standards, healthcare providers can move beyond anecdotal off-label use to a structured, evidence-based treatment model. This transition would be supported by the publication of peer-reviewed results from the ongoing Johns Hopkins partnership study.
- •The Ashley Addiction Treatment Center is currently partnering with Johns Hopkins to conduct this clinical trial (WBAL, 2026).
- •Addiction is a chronic condition requiring consistent, long-term care strategies (Tenovi, 2026).
Reference: Journal of Substance Use and Addiction Treatment
Pharmaceutical manufacturers should scale production of GLP-1 agonists to meet the projected surge in demand for addiction treatment applications. This requires coordinating with the FDA to ensure supply chain stability, preventing shortages that could disrupt ongoing addiction recovery programs. By optimizing manufacturing processes, companies can reduce the per-dose cost, making these therapies more accessible to Medicaid and private insurance beneficiaries. This scale-up is essential for transitioning from specialized research settings to widespread clinical availability.
- •GLP-1s are already widely used for weight loss, providing a foundation for manufacturing capacity (WBAL, 2026).
- •Consistent care is critical for the success of addiction treatment programs (Tenovi, 2026).
Reference: FDA Drug Shortage Program
The FDA should establish a clear regulatory pathway for the approval of GLP-1 agonists as a treatment for substance use disorders, potentially through a supplemental New Drug Application (sNDA). This process would require the submission of comprehensive data from randomized controlled trials demonstrating both safety and efficacy in reducing relapse rates. By providing a clear regulatory roadmap, the FDA can encourage further investment in addiction-focused pharmaceutical research. This would ultimately provide clinicians with the legal and regulatory confidence to prescribe these medications for addiction.
- •Regulatory bodies have previously shown flexibility in renewing telemedicine and medication access for addiction (Tenovi, 2026).
- •The current research at Ashley Addiction Treatment Center aims to provide the necessary data for such clinical advancements (WBAL, 2026).
Reference: FDA Center for Drug Evaluation and Research
Academic medical centers should incorporate neurobiology of addiction and the role of metabolic-modulating drugs into residency and fellowship curricula. This ensures that the next generation of addiction medicine specialists is equipped to utilize emerging pharmacological tools like GLP-1s. By standardizing this training, the medical community can ensure that the implementation of new treatments is consistent and safe across all clinical settings. This workforce development is a prerequisite for the widespread adoption of these therapies in community-based treatment centers.
- •Addiction neuroscience is undergoing a conceptual overhaul driven by methodological innovation (Bioengineer.org, 2026).
- •The integration of new research into clinical practice is essential for improving patient outcomes (WBAL, 2026).
Reference: American Society of Addiction Medicine
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