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Methamphetamine and Troriluzole

Advancing Troiluzole as a Treatment for Methamphetamine Use Disorder: A Human Laboratory Study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06989853
Acronym
BED IN 46
Enrollment
40
Registered
2025-05-25
Start date
2025-08-25
Completion date
2029-02-28
Last updated
2025-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Methamphetamine Use Disorder

Brief summary

This will be a human laboratory study evaluating the influence of troriluzole treatment on the effects of methamphetamine. Supported by and included in the Helping to End Addiction Long-term® (HEAL) Initiative.

Interventions

DRUGPlacebo

The effects of placebo will be determined.

Placebo and methamphetamine will be administered intravenously during experimental sessions.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
William Stoops
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

1. able to speak/read English, 2. not seeking treatment for drug use at the time of the study, 3. female or male between the ages of 18 and 55 years, 4. recent methamphetamine use verified by methamphetamine positive urine, as well as fulfillment of DSM-5 diagnostic criteria for MUD, 5. judged to be medically and psychiatrically healthy by study physicians other than the diagnosis for MUD (and OUD for the co-morbid MUD and OUD group, see below) at the time of screening, 6. ECG, read by a cardiologist, within normal limits, 7. females using an effective form of birth control and not pregnant or breastfeeding, 8. no known contraindications (e.g., hepatic disease \[save for asymptomatic HCV status as cleared by study physician\]) or allergies to troriluzole. Individuals in the MUD and OUD group must also report recent opioid use, verified by opioid positive urine, as well as fulfillment of DSM-5 diagnostic criteria for OUD with physiologic dependence (determined to not be physically dependent if a participant arrives with a urine sample for drug screening that is negative for a short-acting opioid and does not have a score of 5 or greater on the clinical opioid withdrawal scale \[COWS\]).

Exclusion criteria

1. unable to speak/read English, 2. seeking treatment for drug use, 3. under 18 years or over 55 years, 4. no recent methamphetamine use as indicated by methamphetamine negative urine and no DSM-5 diagnosis of MUD, 5. judged to be medically and psychiatrically unhealthy by study physicians at the time of screening, 6. ECG, read by a cardiologist, outside normal limits, 7. females not using an effective form of birth control or pregnant or breastfeeding, 8. blood pressure readings indicative of hypertension (i.e., blood pressure \> 140/90 mmHg) on 2 consecutive screening visits, 9. BMI \< 18 or \> 30; weight \< 50 kg, 10. taking any medications prescribed by a physician for a chronic condition, 11. any laboratory chemistry values (e.g., LFTs) \> 3 times normal at screening or during admission, 12. history of serious physical disease or diagnosis of any disorder (e.g., current hepatic disease \[save for asymptomatic HCV status; as noted above\], histories of seizure, diabetes, asthma or CNS tumors) or current or past histories of psychiatric disorder, including current or recent suicidal ideation that would limit compliance in the study, other than MUD or tobacco use disorder (and OUD for the co-morbid MUD/OUD group only) that in the opinion of the study physicians would interfere with participation and 13. contraindications (e.g., hepatic disease) or allergies to troriluzole.

Design outcomes

Primary

MeasureTime frameDescription
Reinforcing Effects of Methamphetamine9 times over approximately 1 month inpatient admissionNumber of Times Subjects Hypothetically Choose Methamphetamine Over Money between $0 and $140

Countries

United States

Contacts

Primary ContactWilliam W Stoops, PhD
william.stoops@uky.edu859-257-5388

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026