Overview

Multiple-Dose Study to Evaluate the Safety and Efficacy of IXT-m200

Status:
Not yet recruiting
Trial end date:
2023-12-20
Target enrollment:
Participant gender:
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 is that treatment with IXT-m200 will reduce the occurrence of stimulant-positive samples compared to placebo (following an initial grace period during which relapses may occur).
Phase:
Phase 2
Details
Lead Sponsor:
InterveXion Therapeutics, LLC
Collaborator:
National Institute on Drug Abuse (NIDA)