AI Article Synopsis

  • Cocaine use is increasingly leading to overdose deaths, and there are currently no proven medications to effectively treat cocaine use disorder (CUD).
  • GLP-1 receptor agonists (GLP-1RAs), typically used for diabetes and weight management, show promise in reducing cocaine use but lack human study validation.
  • A case study involving 3 patients showed that the GLP-1RA exenatide was well-tolerated and resulted in good patient attendance and satisfaction, indicating potential for future research on its effectiveness for CUD.

Article Abstract

Cocaine use remains a serious public health problem associated with a marked increase in overdose deaths in the past decade. No medications have yet been proven to be effective for the treatment of cocaine use disorder (CUD). Among the highly promising medications have been glucagon-like peptide 1 receptor agonists (GLP-1RA) that are currently used for the treatment of type 2 diabetes mellitus and weight management. Preclinically, GLP-1RAs have been shown to attenuate cocaine self-administration, however, this has not yet been demonstrated in a human laboratory study. The GLP-1RA extended-release exenatide is given as a once-weekly injection, which may be clinically advantageous for addressing medication nonadherence among individuals with CUD. Here, we assess feasibility and safety by reporting on 3 cases of patients with CUD who received 6 weeks of exenatide 2 mg subcutaneously once-weekly in an open-label fashion, along with standard individual drug counseling. We observed excellent attendance and compliance, along with positive end-of-study satisfaction ratings. The medication was well tolerated and without unexpected or severe adverse events. Results for cocaine use and related clinical effects were more mixed, yet encouraging. Future empirical testing of exenatide for treating CUD should utilize a randomized controlled trial design and longer treatment duration.

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http://dx.doi.org/10.1097/ADM.0000000000001147DOI Listing

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