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Terminated Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT05034874

Public ClinicalTrials.gov record NCT05034874. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose Study to Evaluate the Safety and Efficacy of IXT-m200 in Treatment-Seeking Individuals With Methamphetamine Use Disorder

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT05034874
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
InterveXion Therapeutics, LLC
Industry
Enrollment
61 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 9, 2022 (Actual)
Primary completion
Sep 11, 2023 (Actual)
Completion
Nov 7, 2023 (Actual)
Last update posted
Oct 4, 2024

2022 – 2023

United States locations

U.S. sites
9
U.S. states
6
U.S. cities
9
Facility City State ZIP Site status
Pillar Clinical Research Bentonville Arkansas 72712 —
Woodlands International Research Group Little Rock Arkansas 72211 —
Artemis Institute for Clinical Research San Diego California 92103 —
Pillar Clinical Research Lincolnwood Illinois 60712 —
Midwest Clinical Research Center Dayton Ohio 45417 —
InSite Clinical Research DeSoto Texas 75115 —
HD Research Houston Texas 77008 —
Pillar Clinical Research Richardson Texas 75080 —
Alpine Research Clinton Utah 84015 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05034874, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 4, 2024 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05034874 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →