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Clinical Trial Summary

This Phase 2 study will evaluate the safety and efficacy of monthly intravenous doses of IXT-m200 in treatment-seeking individuals with methamphetamine (METH) use disorder. The hypothesis are that following an initial relapse, IXT-m200 will reduce the occurrence of stimulant-positive saliva samples compared to placebo and improve the signs and symptoms of METH Use Disorder (MUD).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05034874
Study type Interventional
Source InterveXion Therapeutics, LLC
Contact
Status Terminated
Phase Phase 2
Start date June 9, 2022
Completion date November 7, 2023

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