Evidence map›Paper›PMID 41779519›Full record

Trial reportJournal of clinical psychopharmacology

Safety of Intravenous Methamphetamine in Patients Taking Mirtazapine: A Two-Site Phase 1b Randomized Controlled Trial.

Finn Black, Glenn-Milo Santos, Vanessa M McMahan, Annie Fraser, Jesse Clark, Lizette Sturgeon, John Walker, Marta Kochanska, Steve Shoptaw, Phillip O Coffin

Abstract readRandomized Controlled TrialClinical Trial, Phase IMulticenter Study
In one paragraph

Trial report in Journal of clinical psychopharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Finn BlackSan Francisco Department of Public Health, Center on Substance Use and Health.ORCID 0009-0002-5797-2604
Glenn-Milo SantosSan Francisco Department of Public Health, Center on Substance Use and Health.ORCID 0000-0003-1009-5317
Vanessa M McMahanSan Francisco Department of Public Health, Center on Substance Use and Health.ORCID 0000-0003-2331-7206
Annie FraserSan Francisco Department of Public Health, Center on Substance Use and Health.ORCID 0009-0004-2161-7170
Jesse ClarkDepartment of Family Medicine, University of California, Los Angeles, CA.ORCID 0000-0001-5862-6530
Lizette SturgeonDepartment of Family Medicine, University of California, Los Angeles, CA.
John WalkerSan Francisco Department of Public Health, Center on Substance Use and Health.
Marta KochanskaDepartment of Community Health Systems (Santos), Division of HIV, Infectious Disease, and Global Medicine (Coffin, Kochanska), University of California, San Francisco, CA.
Steve ShoptawDepartment of Family Medicine, University of California, Los Angeles, CA.
Phillip O CoffinSan Francisco Department of Public Health, Center on Substance Use and Health.ORCID 0000-0002-3891-6570

Funding

Mirtazapine for methamphetamine use disorder: drug-drug interaction studyU01DA051080 · NIDA · PUBLIC HEALTH FOUNDATION ENTERPRISES · PI COFFIN, PHILLIP O · 2020 to 2021
$4.4M
Midcareer K24 Award for Mentoring and Patient-Oriented ResearchK24DA042720 · NIDA · SAN FRANCISCO DEPARTMENT OF PUBLIC HEALTH · PI PHILLIP O COFFIN · 2016 to 2026
$1.6M
NIDA NIH HHS K24 DA042720NIDA NIH HHS U01 DA051080
6 · The paper itself

Abstract

backgroundThere are no approved medications to treat methamphetamine use disorder. We conducted a phase 1b, inpatient,randomized, double-blind, placebo-controlled, within-subject crossover study to evaluate the safety of mirtazapine, a potential treatment for methamphetamine use disorder with positive phase 2 trial findings, in people receiving intravenous methamphetamine.

methodsParticipants received mirtazapine 30 mg or placebo daily for 5 days, underwent an intravenous methamphetamine 30 mg challenge on day 5, followed by 2 days of washout, and then switched to the other study arm and received a second methamphetamine infusion at day 12. We monitored participants for adverse events, cardiovascular effects, and pharmacokinetics.

resultsParticipants (N = 15; 12 with no opioid use and 3 on methadone maintenance treatment) reached steady state mirtazapine levels before methamphetamine infusions. During the mirtazapine phase, participants reached methamphetamine peak plasma concentration 0.26 hours earlier than the placebo phase ( P = 0.02); no other impacts on methamphetamine pharmacokinetics were observed. Mirtazapine neither attenuated nor enhanced the expected cardiovascular effects of methamphetamine, including in participants receiving methadone maintenance therapy. Adverse events were similar between mirtazapine 30 mg and placebo.

conclusionsMirtazapine 30 mg was safe and well-tolerated in people receiving a clinically relevant intravenous methamphetamine challenge, supporting further development of this medication for the treatment of methamphetamine use disorder.

Indexed as

Amphetamine-Related DisordersCentral Nervous System StimulantsMethamphetamineMianserinMirtazapineAdultCross-Over StudiesDouble-Blind MethodFemaleHumansInfusions, IntravenousMaleMethadoneMiddle AgedYoung AdultCentral Nervous System StimulantsMethadoneMethamphetamineMianserinMirtazapinedrug-drug interactionmethamphetaminemirtazapinepharmacokinetics

Identifiers

PMID41779519
PMCPMC13229006

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.