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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00656357
Other study ID # SYN117-CL01
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date June 2008
Est. completion date May 2009

Study information

Verified date August 2017
Source Biotie Therapies Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will assess the potential interaction and subjective effects between intravenous cocaine and SYN117 in non-treatment seeking cocaine dependant subjects


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date May 2009
Est. primary completion date May 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- non treatment seeking cocaine dependent

- English speaking

- meet DSM IV TR criteria for cocaine dependence

- pulse 50-90bpm

- systolic BP 85-140 mmHg

- diastolic BP 45-90 mmHg

- essentially normal liver and kidney function blood tests

- ECG normal

- sign informed consent

- negative urine pregnancy test at screening and admission

Exclusion Criteria:

- history or evidence of seizure disorder or brain injury

- previous medically adverse reaction to cocaine, including loss of consciousness, chest pain or epileptic seizure

- neurological disorders, organic brain disease, dementia

- psychiatric disorders such as psychosis, schizophrenia, bipolar disorder, major depression

- history of suicide attempts within past 3 months or suicidal ideation/plan

- history of clinically significant heart disease or hypertension

- family history in 1st degree relatives of early cardiovascular morbidity or mortality

- untreated or unstable medical conditions

- positive HIV test

- pregnant or nursing

- have asthma or are currently using alpha, beta agonists or theophylline or other sympathomimetics

- test positive for other drugs of abuse with the exception of cocaine, cocaine metabolites or marijuana

- any other illness, condition or use of psychotropic medications which preclude safe/successful completion of the study

- currently on parole

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
SYN117 Placebo
Placebo
SYN117 80 mg
SYN117 80 mg
SYN117 160 mg
SYN117 160 mg
Cocaine 10mg
IV Cocaine 10mg
Cocaine 20mg
IV Cocaine 20mg
Cocaine 40mg
IV Cocaine 40mg
Saline
IV Cocaine Placebo

Locations

Country Name City State
United States University of Texas Medical Branch (UTMB) Galveston Texas

Sponsors (2)

Lead Sponsor Collaborator
Biotie Therapies Inc. National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Determine the safety of treatment with SYN117 in cocaine-dependent volunteers by measuring hemodynamic and subjective effects of administration of ascending doses of cocaine(10mg, 20mg, 40mg)and placebo during treatment with ascending doses of SYN117. inpatient 14 days with 2 week outpatient follow-up
Secondary Determine tolerability by measuring adverse events inpatient 14 days, 2 weeks post followup visit
Secondary Determine subjective effects produced by self administration of cocaine or placebo Days 4, 8, 12 and 13
Secondary Determine the effect of SYN117 of the pharmacokinetics of IV cocaine Days 3 and 11
Secondary Determine if any baseline measures of impulsivity or drug use severity predict efficacy of SYN117 in reducing subjective effects of cocaine Days 4, 8 and 12
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