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The objective of this study is to demonstrate that a larger proportion of vigabatrin-treated subjects than placebo-treated subjects will be cocaine-free in the last 2 weeks of treatment.
Cocaine addiction, a serious public health concern associated with significant medical, social, and economic consequences, is difficult to treat using traditional psychosocial and behavioral therapies. Despite testing of a number of different agents for cocaine dependency, there remains no proven pharmacologic treatment for cocaine addiction.
The addictive properties of cocaine have been associated with its actions on mesotelencephalic dopamine reward pathways in the central nervous system (CNS). Cocaine administration increases the levels of dopamine, a neurotransmitter associated with sensations of pleasure and reward. Therefore, blocking cocaine-induced increases in dopamine levels represents a valid pharmaceutical approach to the treatment of cocaine addiction.
Another neurotransmitter, gamma-aminobutyric acid (GABA), suppresses striatal dopamine release, and attenuates cocaine-induced increases in extracellular and synaptic dopamine levels in the striatum and nucleus accumbens in animal models of drug dependence. Significant elevation of brain GABA levels may reduce cocaine-stimulated dopamine release and dampen the sensations of pleasure and reward. Thus, drugs that potentiate or enhance GABA-ergic transmission are candidates for the treatment of cocaine addiction.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | 3 Vigabatrin Tablets, 500 mg, bid, for 9 weeks |
|
| 2 | Placebo Comparator | 3 Placebo Tablets, bid, for 9 weeks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| vigabatrin | Drug | Tablets twice a day for 9 weeks |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of Subjects in Each Treatment Group Abstinent During the Last 2 Weeks of Treatment. | Number of subjects in the CPP-109 Vigabatrin Group vs. Number in Placebo Group abstinent from using cocaine during Weeks 11 and 12 of the Treatment Phase. | Week 13 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Eugene Somoza, MD, PhD | University of Cincinnati | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Addiction Treatment Clinic | Little Rock | Arkansas | United States | |||
| St. Luke's Hospital Addiction Pharmacology Research Laboratory |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 23575810 | Derived | Somoza EC, Winship D, Gorodetzky CW, Lewis D, Ciraulo DA, Galloway GP, Segal SD, Sheehan M, Roache JD, Bickel WK, Jasinski D, Watson DW, Miller SR, Somoza P, Winhusen T. A multisite, double-blind, placebo-controlled clinical trial to evaluate the safety and efficacy of vigabatrin for treating cocaine dependence. JAMA Psychiatry. 2013 Jun;70(6):630-7. doi: 10.1001/jamapsychiatry.2013.872. | |
| 22704138 |
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After Informed Consent obtained, subjects entered a 2-4 week Screening/Baseline Phase to determine whether all Inclusion/Exclusion Criteria were met. Randomization strata included gender, primary method of cocaine administration (snort or intravenous/smoke) & use in last 30 days (≤18 days or >18 days)
01/08-01/09 at 11 US research trial sites.
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| ID | Title | Description |
|---|---|---|
| FG000 | CPP-109 Vigabatrin | CPP-109 tablets, 500 mg. 3 Tablets bid. |
| FG001 | Placebo | Matching Placebo Tablets. 3 tablets bid. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | CPP-109 Vigabatrin | CPP-109 tablets, 500 mg. 3 Tablets bid. |
| BG001 | Placebo | Matching Placebo Tablets. 3 tablets bid. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Proportion of Subjects in Each Treatment Group Abstinent During the Last 2 Weeks of Treatment. | Number of subjects in the CPP-109 Vigabatrin Group vs. Number in Placebo Group abstinent from using cocaine during Weeks 11 and 12 of the Treatment Phase. | intent-to-treat | Posted | Apr 2010 | Number | participants | Week 13 |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | CPP-109 Vigabatrin Tablets, 500 mg | Vigabatrin Tablets, 1.5 g bid po, 12 weeks. Subjects proceeded to a 12 week Treatment Phase, including a 2 week dose escalation period, a 9 week maintenance period (3.0 gm/day of vigabatrin), and a 1 week medication taper period. Finally, subjects then proceeded to a 12 week follow-up period. Subjects were scheduled for clinic visits 3 times per week (typically on Monday, Wednesday, and Friday) during the Screening/Baseline Phase and the 12 week Treatment Phase. Subjects returned for follow up visits at Weeks 13, 16, 20 and 24. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Drug Abuse & Major Depression | Psychiatric disorders |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Photopsia | Eye disorders |
|
Lack of subject medication compliance, site-to-site variability in medication compliance possibly indicative of differing site capabilities to attract subjects sufficiently motivated to stop using cocaine.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| M Douglas Winship | Catalyst Pharmaceutical Partners, Inc. | 305-529-2522 | 12 | dwinship@catalystpharma.com |
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| ID | Term |
|---|---|
| D019970 | Cocaine-Related Disorders |
| D016739 | Behavior, Addictive |
| ID | Term |
|---|---|
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
| D003192 | Compulsive Behavior |
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| ID | Term |
|---|---|
| D020888 | Vigabatrin |
| ID | Term |
|---|---|
| D005680 | gamma-Aminobutyric Acid |
| D000613 | Aminobutyrates |
| D002087 | Butyrates |
| D000144 | Acids, Acyclic |
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| placebo | Drug | tablets twice daily for 9 weeks |
|
| San Francisco |
| California |
| 94110 |
| United States |
| Friends Research Institute | Torrance | California | United States |
| Operation PAR | Largo | Florida | United States |
| Segal Institute for Clinical Research | North Miami | Florida | 33161 | United States |
| Johns Hopkins Bayview Medical Center Center for Chemical Dependence | Baltimore | Maryland | United States |
| Boston University School of Medicine | Boston | Massachusetts | United States |
| New York University Mental Health and Addictive Disorders Research Program | New York | New York | United States |
| Cincinnati Addiction Research Center (CinARC) | Cincinnati | Ohio | United States |
| Dayton Veterans Affairs Medical Center | Dayton | Ohio | United States |
| University of Texas Health Science Center at San Antonio | San Antonio | Texas | United States |
| Derived |
| Berezina TL, Khouri AS, Winship MD, Fechtner RD. Visual field and ocular safety during short-term vigabatrin treatment in cocaine abusers. Am J Ophthalmol. 2012 Aug;154(2):326-332.e2. doi: 10.1016/j.ajo.2012.02.026. Epub 2012 Jun 15. |
| Withdrawal by Subject |
|
| Other |
|
| Incarceration |
|
| Administrative |
|
| Adverse Event |
|
| Death |
|
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| OG001 | Matching Placebo Tablets | Subjects proceeded to a 12 week Treatment Phase,receiving 3 tablets bid po Finally, subjects then proceeded to a 12 week follow-up period. Subjects attended clinic visits 3 times per week (typically on Monday, Wednesday, and Friday) during the Screening/Baseline Phase and the 12 week Treatment Phase. Subjects returned for follow up visits at Weeks 13, 16, 20 and 24. |
|
|
| Post-Hoc | Medication Compliance | Using retained urine samples and prior to unblinding, up to 12 specimens/ subject were analyzed for vigabatrin levels. Compliance assessment based on > or = 70% of urines in subjects assigned to vigabatrin having quantitative levels of vigabatrin indicaticative of taking drug within the last 24 hours of clinic visit. | Completers were defined as those who attended the scheduled Week 13 visit or the third visit of Week 12 and who also had provided urines during Weeks 11 & 12. | Posted | Number | participants | Week 2, 4, 6 & 9-11 |
|
|
|
| 6 |
| 92 |
| 73 |
| 92 |
| EG001 | Matching Placebo Tablet | Subjects proceeded to a 12 week Treatment Phase,receiving 3 tablets bid po Finally, subjects then proceeded to a 12 week follow-up period. Subjects were scheduled for clinic visits 3 times per week (typically on Monday, Wednesday, and Friday) during the Screening/Baseline Phase and the 12 week Treatment Phase. Subjects returned for follow up visits at Weeks 13, 16, 20 and 24. | 0 | 94 | 81 | 94 |
| Gun shot wound, road traffic accident & tibia fracture | Injury, poisoning and procedural complications |
|
| Hepatitis, acute | Hepatobiliary disorders |
|
| Meningitis & Pneumonia | Infections and infestations |
|
| Tachycardia | Cardiac disorders | Systematic Assessment |
|
| Blurred vision | Eye disorders |
|
| Visual disturbance | Eye disorders |
|
| Constipation | Gastrointestinal disorders |
|
| Diarrhea | Gastrointestinal disorders |
|
| Nausea | Gastrointestinal disorders |
|
| Stomach discomfort | Gastrointestinal disorders |
|
| Toothache | Gastrointestinal disorders |
|
| Vomiting | Gastrointestinal disorders |
|
| Fatigue | General disorders |
|
| Nasopharyngitis | Infections and infestations |
|
| ALT decreased | Investigations |
|
| CPK increased | Investigations |
|
| Weight increased | Investigations |
|
| Arthralgia | Musculoskeletal and connective tissue disorders |
|
| Back pain | Musculoskeletal and connective tissue disorders |
|
| Pain in extremity | Musculoskeletal and connective tissue disorders |
|
| Headache | Nervous system disorders |
|
| Somnolence | Nervous system disorders |
|
| Dizziness | Nervous system disorders |
|
| Anxiety | Psychiatric disorders |
|
| Insomnia | Psychiatric disorders |
|
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| D007175 | Impulsive Behavior |
| D001519 | Behavior |
| D002264 |
| Carboxylic Acids |
| D009930 | Organic Chemicals |
| D000596 | Amino Acids |
| D000602 | Amino Acids, Peptides, and Proteins |