Overview

Study in Healthy Recreational Polydrug Users to Measure the Abuse Potential of TC-5214

Status:
Withdrawn
Trial end date:
2012-04-01
Target enrollment:
0
Participant gender:
All
Summary
This is a single dose, crossover study to assess the abuse potential of TC-5214 compared to placebo, ketamine, and phentermine in healthy recreational polydrug users.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
AstraZeneca
Treatments:
Ketamine
Phentermine
Criteria
Inclusion Criteria:

- Current recreational polydrug users with experience with at least 2 drug classes of
abuse.

- At least 10 lifetime uses of stimulants drugs (eg, amphetamine, cocaine,
methamphetamine) and 10 lifetime occasions of recreational use of psychedelic drugs
(eg, cannabis, ketamine, dextromethorphan, PCP, MDMA [ecstasy], LSD, mesacline, or
psilocybin).

- Recreational use of other classes of drugs is permitted, including opioids (eg,
codeine, morphine, or heroin), minor tranquilizers, or sedatives (eg, benzodiazepines
or barbiturates).

- Male or female volunteers aged 18 to 55, inclusive with a body mass index (BMI) within
the range of 19.0 to 33.0 kg/m2, inclusive, and a minimum weight of 50.0 kg at
screening.

- Must pass qualification phase eligibility criteria.

Exclusion Criteria:

- Self-reported history of drug or alcohol dependence (except caffeine) in the past 12
months, including subjects who have ever been in a drug rehabilitation program (other
than treatment for smoking cessation).

- Unwillingness or inability to abstain from recreational drug use for the duration of
the study from screening until follow-up.

- Positive for hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) at
screening.

- Any significant unstable hepatic, renal, pulmonary, cardiovascular, ophthalmologic,
neurologic, or any other medical conditions that might confound the study or put the
volunteer at greater risk during study participation.

- Currently smoking more than 20 cigarettes (or 2 cigars) per day, and/or unwillingness
to abstain from smoking for durations of at least 12 hours.

- Use of tobacco cessation product within 1 month (eg, nicotine substitution products,
bupropion, etc).