Are any Glucagon-like peptide-1 (GLP-1) or Glucagon-like peptide-2 (GLP-2) agonists approved for the treatment of alcohol cravings or dependence?

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Last updated: July 3, 2025View editorial policy

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From the Guidelines

No, currently there are no GLP-1 or GLP-2 agonists approved by regulatory agencies for the treatment of alcohol cravings or alcohol dependence. Medications that are FDA-approved specifically for alcohol use disorder include naltrexone, acamprosate, and disulfiram 1. While there is emerging research suggesting that GLP-1 agonists like semaglutide (Ozempic, Wegovy) and liraglutide (Saxenda, Victoza) might reduce alcohol consumption and cravings through their effects on reward pathways in the brain, these findings are preliminary and based on limited clinical studies 1. GLP-1 receptors are present in brain regions associated with reward processing, which explains the scientific interest in these medications for addiction treatment. However, prescribing GLP-1 agonists for alcohol use disorder would currently be considered off-label use, and patients seeking treatment for alcohol dependence should discuss established, evidence-based options with their healthcare provider rather than pursuing unapproved applications of these medications. Some key points to consider in the treatment of alcohol dependence include:

  • The importance of abstinence or reduced consumption in preventing liver disease progression and improving quality of life 1
  • The use of pharmacological aids, such as naltrexone, acamprosate, and disulfiram, to help maintain long-term low or zero consumption targets 1
  • The potential for other medications, such as topiramate and gabapentin, to be used off-label for the treatment of alcohol use disorder, although their tolerance profile is not considered harmless 1
  • The need for careful assessment of the benefit-risk ratio when prescribing any medication for alcohol dependence 1.

From the Research

GLP-1 and GLP-2 Agonists for Alcohol Cravings or Dependence

  • There are no FDA-approved GLP-1 or GLP-2 agonists for the treatment of alcohol cravings or dependence 2, 3, 4, 5.
  • However, a clinical trial is being conducted to investigate the effect of the GLP-1 receptor agonist exenatide on alcohol intake in patients with alcohol dependence 6.
  • The trial aims to determine if exenatide can reduce the number of heavy drinking days and total alcohol consumption in patients with alcohol dependence 6.
  • Preclinical experiments have shown that GLP-1 receptor stimulation can reduce alcohol consumption, but the effect of GLP-1 receptor agonists in humans has not been fully investigated 6.

Current Treatments for Alcohol Dependence

  • Currently, several medications are approved for the treatment of alcohol dependence, including disulfiram, naltrexone, acamprosate, and nalmefene 2, 3, 4, 5.
  • Other medications, such as baclofen, gabapentin, and topiramate, have also shown promise in reducing alcohol consumption, but their efficacy and safety profiles vary 2, 3, 4.
  • The choice of medication for alcohol dependence treatment depends on various factors, including the patient's medical history, comorbidities, and personal preferences 2, 3, 5.

Future Directions

  • Further research is needed to fully understand the potential of GLP-1 and GLP-2 agonists in the treatment of alcohol cravings or dependence 6.
  • The development of new medications and therapies for alcohol dependence is crucial to improve treatment outcomes and reduce the burden of this condition on individuals and society 2, 3, 5.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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