Pilot study of the effects of lisdexamfetamine on cocaine use: A randomized, double-blind, placebo-controlled trial

Marc E. Mooney, David V. Herin, Sheila Specker, David Babb, Frances R. Levin, John Grabowski

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Background: Amphetamine analogs have been demonstrated to have some efficacy in reducing use in cocaine dependent individuals. However, these agents also have potential for abuse. Lisdexamfetamine (LDX), a lysine + dextroamphetamine formulation, has been approved for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) and as a prodrug, has less abuse potential. Objective: This pilot study sought to evaluate the safety, tolerability, and efficacy of LDX as a candidate treatment for cocaine dependence. Methods: A randomized, double-blind, placebo-controlled parallel group study served to evaluate LDX in 43 cocaine-dependent individuals: (1) placebo (PBO; 0 mg, n= 21), (2) LDX (70 mg, n= 22). Participants received medication for 14 weeks. Cocaine use was determined based on urine analysis for benzoylecgonine (BE; a cocaine metabolite). Results: Retention rates were higher though not significantly different in the PBO (71.4%) than the LDX condition (57.1%). Compared to those in the PBO condition, those receiving LDX were more likely to report experiencing (ps < 0.05) diarrhea (45.5% vs. 14.3%), headaches (45.5% vs. 9.5%), and anxiety (31.8% vs. 4.8%). No differences in medication conditions were observed for blood pressure, heart rate, or body weight. In the randomized sample, no differences in cocaine use were seen. Those receiving LDX reported significantly less craving for cocaine than participants receiving PBO. Conclusions: LDX did not significantly reduce cocaine use compared to PBO in the randomized sample.

Original languageEnglish (US)
Pages (from-to)94-103
Number of pages10
JournalDrug and alcohol dependence
Volume153
DOIs
StatePublished - Aug 1 2015

Bibliographical note

Funding Information:
All authors were supported by funding from the National Institute on Drug Abuse of the National Institutes of Health. Initially, Dr. Herin was supported by NIDA K99R00-DA-023548 . Grabowski, Mooney and Specker were supported in part by DA RO1 23561 . Dr Mooney was supported in part by National, Institute of Drug Abuse (NIDA) grant K01-DA-019446 and NIDA K99-DA-023548 .

Keywords

  • Agonist-like treatment
  • Amphetamine analogs
  • Cocaine
  • Dextroamphetamine
  • Lisdexamfetamine dimesylate
  • l-Lysine-dextroamphetamine

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