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Published on: January 22, 2016
Mirtazapine for Methamphetamine Use Disorder: A Randomized Clinical Trial
Rebecca McKetin1, Steven Shoptaw2, Lucy Saunders1
1National Drug and Alcohol Research Centre, University of New South Wales, Sydney, New South Wales, Australia.
Mirtazapine reduced methamphetamine use in adults with moderate to severe disorder. While effective, it caused more drowsiness and weight gain than placebo, with higher discontinuation rates due to adverse events.
Area of Science:
- Pharmacology
- Psychiatry
- Clinical Trials
Background:
- Methamphetamine use disorder (MUD) is a global health concern lacking approved pharmacotherapies.
- Mirtazapine shows promise for MUD, but its safety and effectiveness in routine practice require evaluation.
Purpose of the Study:
- To assess the safety and effectiveness of mirtazapine as a pharmacotherapy for MUD in a real-world clinical setting.
Main Methods:
- A phase 3, double-blind, placebo-controlled randomized trial involving 339 adults with moderate to severe MUD across 6 Australian outpatient clinics.
- Participants received either mirtazapine (30 mg daily) or placebo for 12 weeks.
- The primary outcome was the change in days of methamphetamine use over 28 days from baseline to week 12.
Main Results:
- Mirtazapine significantly reduced methamphetamine use by a mean of 7.0 days compared to 4.8 days in the placebo group (mean difference: 2.2 days; P=.02).
- Increased drowsiness (47% vs 33%) and weight gain (10% vs 3%) were more common with mirtazapine.
- Adverse events led to discontinuation in 23% of the mirtazapine group versus 15% of the placebo group.
Conclusions:
- Mirtazapine effectively reduced methamphetamine use in adults with MUD within a routine clinical practice setting.
- No unexpected safety concerns were identified, offering a potential treatment option in the absence of approved pharmacotherapies.
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