Cocaine Dependence Clinical Trial
Official title:
A Human Laboratory Assessment of the Safety and Potential Efficacy of SYN117 (Nepicastat) in Cocaine-dependent Volunteers Receiving Cocaine
Verified date | August 2017 |
Source | Biotie Therapies Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will assess the potential interaction and subjective effects between intravenous cocaine and SYN117 in non-treatment seeking cocaine dependant subjects
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 |
Country | Name | City | State |
---|---|---|---|
United States | University of Texas Medical Branch (UTMB) | Galveston | Texas |
Lead Sponsor | Collaborator |
---|---|
Biotie Therapies Inc. | National Institute on Drug Abuse (NIDA) |
United States,
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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