Safety and Efficacy Study of Vigabatrin to Treat Methamphetamine Dependence

Stopped early · Phase 2 · Has a placebo group

Conditions studied: Methamphetamine Dependence

In brief

The objective of this study is to demonstrate that a larger proportion of vigabatrin-treated subjects than placebo-treated subjects will be methamphetamine-free in the last 2 weeks of the study's Treatment Phase (Weeks 11 and 12).

Key facts

Study ID

NCT00730522

Run by

Catalyst Pharmaceuticals, Inc.

People needed

55

Starts

2008-07-01

Expected to finish

2009-11-01

Last updated by the study team

2020-12-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Able to understand the study and provide written informed consent.
• Male or female at least 18 years of age.
• Meets DSM-IV (Diagnostic and Statistical Manual of Mental Disorders Fourth Edition) criteria for methamphetamine dependence as major diagnosis, as determined by the Substance Abuse module of SCID (Structured Clinical Interview for DSM-IV).
• Provides at least one urine specimen which is positive for methamphetamine according to a rapid screening test.
• Seeking treatment for methamphetamine dependence.
• Have normal visual fields.
• Be in generally good health based on history, physical examination and laboratory findings.
• If female of childbearing potential, use acceptable contraceptive methods

You may not qualify if…

• Has current dependence on any psychoactive substance other than methamphetamine, alcohol, nicotine, or cannabinoid or physiologic dependence on alcohol requiring medical detoxification.
• Has any serious medical or psychiatric illness and/or clinically significant abnormal laboratory values.
• Has history of serious cardiovascular reaction to methamphetamine.
• Has clinically significant cardiovascular impairment, abnormal ECG or uncontrolled hypertension.
• Be under court or other governmental agency (e.g. social services) mandate to obtain treatment or requiring outside urine monitoring.
• Be enrolled in an opiate substitution treatment program within 2 months of randomization.
• Has ever taken vigabatrin in the past.
• Is pregnant or lactating.
• Has clinically significant ophthalmologic disease, which would preclude safety monitoring, is undergoing treatment for ocular disease or intends to have any ocular surgery or procedure performed during the time of their participation in the trial.
• Has received a drug with known major organ toxicity, including retinotoxicity.
• Is currently participating in, or has been enrolled in another clinical trial within the last 30 days.
• Be anyone who, in the judgment of the investigator, would not be expected to attend regular study visits or to complete the study protocol.

Where it is running

• North County Clinical Research (NCCR) — Oceanside, California, United States
• South Bay Treatment Center — San Diego, California, United States
• Addiction Pharmacology Research Laboratory, St. Luke's Hospital — San Francisco, California, United States
• START Research and Treatment — Kansas City, Missouri, United States
• Creighton University Medical Center — Omaha, Nebraska, United States
• Behavioral Health Research Center of the Southwest — Albuquerque, New Mexico, United States
• Pahl Pharmaceutical Research — Oklahoma City, Oklahoma, United States
• Pillar Research — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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