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| ID | Type | Description | Link |
|---|---|---|---|
| R01DA052203 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
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Cocaine potently inhibits the reuptake of serotonin (5-HT). Increased synaptic 5-HT resulting from this reuptake inhibition activates multiple 5-HT receptor subtypes. Some of these receptor subtypes have been implicated in the abuse-related effects of cocaine, including its primary reinforcing effects (i.e., cocaine taking behavior). 5-HT1b receptors, which are autoreceptors on 5-HT nerve endings that regulate 5-HT release and heteroreceptors that also mediate other neurotransmitter release, play a particularly important role in cocaine effects, likely because they are highly expressed in the mesocorticolimbic system. The 5-HT1b system displays profound dysregulation during both active cocaine use and abstinence. Initial preclinical research showed that selective 5-HT1b agonists enhanced the reinforcing and locomotor effects of cocaine during ongoing cocaine administration, but subsequent research showed that these agents robustly attenuated reinstatement of cocaine- and cue-primed cocaine seeking behavior. These findings have been replicated in rigorously conducted studies using multiple schedules of reinforcement and negative sucrose reinforcement controls across laboratories. Notably, though, these preclinical studies used compounds not approved for use in humans, hindering translation. Recently published data show that zolmitriptan, a commercially available selective 5-HT1b agonist migraine medication, also selectively attenuates the reinforcing and other abuse-related effects of cocaine, regardless of stage of use (i.e., ongoing or extinguished cocaine self-administration).
Although a robust preclinical literature supports the premise that 5-HT1b activation reduces a number of cocaine-associated behaviors (e.g., self-administration, cocaine seeking), this area remains unstudied in humans. The overarching goal of this project is to advance these promising preclinical findings, specifically those with zolmitriptan, to a clinical population, thereby demonstrating that the 5-HT1b system plays a key role in the effects of cocaine in humans
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | Subjects will be maintained on oral placebo. Cocaine will be administered acutely during placebo maintenance. Placebo will be administered acutely during placebo maintenance. |
|
| Zolmitriptan Dose 1 | Experimental | Subjects will be maintained on oral zolmitriptan dose 1. Cocaine will be administered acutely during zolmitriptan dose 1 maintenance. Placebo will be administered acutely during zolmitriptan dose 1 maintenance. |
|
| Zolmitriptan Dose 2 | Experimental | Subjects will be maintained on oral zolmitriptan dose 2. Cocaine will be administered acutely during zolmitriptan dose 2 maintenance. Placebo will be administered acutely during zolmitriptan dose 2 maintenance. |
|
| Zolmitriptan Dose 3 | Experimental | Subjects will be maintained on oral zolmitriptan dose 3. Cocaine will be administered acutely during zolmitriptan dose 3 maintenance. Placebo will be administered acutely during zolmitriptan dose 3 maintenance. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cocaine | Drug | The pharmacodynamic effects of cocaine will be determined during maintenance on placebo and zolmitriptan. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Reinforcing Effects of Cocaine | Number of Times Subjects Choose Cocaine (Maximum of 5 Choices) Over Money | Over approximately four hours on each experimental session day, which generally occurred on Days 5-7, 13-15, 21-23 and 29-31 of inpatient admission. |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Kentucky | Lexington | Kentucky | 40507 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Overall Study | This study used a within subjects design (i.e., all subjects were to receive all oral zolmitriptan maintenance conditions [0, 2.5, 5 and 10 mg] and intravenous cocaine doses [0, 10 and 30 mg/70 kg]). Nine subjects completed the full study. Three additional subjects were enrolled but discharged prior to completing the full study. Data from completed sessions for those subjects are included here. Dose Condition 1: 0 mg zolmitriptan, 0 mg cocaine Dose Condition 2: 0 mg zolmitriptan, 10 mg cocaine Dose Condition 3: 0 mg zolmitriptan, 30 mg cocaine Dose Condition 4: 2.5 mg zolmitriptan, 0 mg cocaine Dose Condition 5: 2.5 mg zolmitriptan, 10 mg cocaine Dose Condition 6: 2.5 mg zolmitriptan, 30 mg cocaine Dose Condition 7: 5 mg zolmitriptan, 0 mg cocaine Dose Condition 8: 5 mg zolmitriptan, 10 mg cocaine Dose Condition 9: 5 mg zolmitriptan, 30 mg cocaine Dose Condition 10: 10 mg zolmitriptan, 0 mg cocaine Dose Condition 11: 10 mg zolmitriptan, 10 mg cocaine Dose Condition 12: 10 mg zolmitriptan, 30 mg cocaine |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Overall Study | This study used a within subjects design (i.e., all subjects were to receive all oral zolmitriptan maintenance conditions [0, 2.5, 5 and 10 mg] and intravenous cocaine doses [0, 10 and 30 mg/70 kg]). Ten subjects completed the full study. Two additional subjects were enrolled but discharged prior to completing the full study. Data from completed sessions for those subjects are included here. |
| 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 | Reinforcing Effects of Cocaine | Number of Times Subjects Choose Cocaine (Maximum of 5 Choices) Over Money | Subjects completing the dose condition | Posted | Mean | Standard Deviation | number of times subjects chose cocaine | Over approximately four hours on each experimental session day, which generally occurred on Days 5-7, 13-15, 21-23 and 29-31 of inpatient admission. |
|
Approximately 1 month of inpatient admission.
Definitions for adverse events/serious adverse events follow clinicaltrials.gov guidelines.
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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 | Zolmitriptan (0 mg/Day) | Maintenance on 0 mg Zolmitriptan/day | 0 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Blood clot | Blood and lymphatic system disorders | MedDRA (Unspecified) | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Tachycardia | Cardiac disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| William W. Stoops | University of Kentucky | 8592575388 | william.stoops@uky.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 20, 2024 | Jun 5, 2025 | Prot_SAP_001.pdf |
| ICF | No | No | Yes | Informed Consent Form | Feb 20, 2024 | Feb 20, 2025 | ICF_000.pdf |
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| ID | Term |
|---|---|
| D003042 | Cocaine |
| C089750 | zolmitriptan |
| ID | Term |
|---|---|
| D014326 | Tropanes |
| D053961 | Azabicyclo Compounds |
| D001372 | Aza Compounds |
| D009930 | Organic Chemicals |
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| Placebo oral capsule | Drug | The pharmacodynamic effects of placebo will be determined. |
|
| Zolmitriptan | Drug | The pharmacodynamic effects of zolmitriptan maintenance will be determined. |
|
| years |
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| Sex: Female, Male | Count of Participants | Participants | No |
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| Race (NIH/OMB) | Count of Participants | Participants | No |
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| Ethnicity (NIH/OMB) | Count of Participants | Participants | No |
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| Region of Enrollment | Number | Participants |
|
| OG002 |
| Dose Condition 3 |
30 mg/70 kg IV Cocaine and 0 mg/day Oral Zolmitriptan |
| OG003 | Dose Condition 4 | 0 mg/70 kg IV Cocaine and 2.5 mg/day Oral Zolmitriptan |
| OG004 | Dose Condition 5 | 10 mg/70 kg IV Cocaine and 2.5 mg/day Oral Zolmitriptan |
| OG005 | Dose Condition 6 | 30 mg/70 kg IV Cocaine and 2.5 mg/day Oral Zolmitriptan |
| OG006 | Dose Condition 7 | 0 mg/70 kg IV Cocaine and 5 mg/day Oral Zolmitriptan |
| OG007 | Dose Condition 8 | 10 mg/70 kg IV Cocaine and 5 mg/day Oral Zolmitriptan |
| OG008 | Dose Condition 9 | 30 mg/70 kg IV Cocaine and 5 mg/day Oral Zolmitriptan |
| OG009 | Dose Condition 10 | 0 mg/70 kg IV Cocaine and 10 mg/day Oral Zolmitriptan |
| OG010 | Dose Condition 11 | 10 mg/70 kg IV Cocaine and 10 mg/day Oral Zolmitriptan |
| OG011 | Dose Condition 12 | 30 mg/70 kg IV Cocaine and 10 mg/day Oral Zolmitriptan |
|
|
| 10 |
| 1 |
| 10 |
| 10 |
| 10 |
| EG001 | Zolmitriptan (2.5 mg/Day) | Maintenance on 2.5 mg Zolmitriptan/day | 0 | 10 | 0 | 10 | 10 | 10 |
| EG002 | Zolmitriptan (5 mg/Day) | Maintenance on 5 mg Zolmitriptan/day | 0 | 11 | 0 | 11 | 11 | 11 |
| EG003 | Zolmitriptan (10 mg/Day) | Maintenance on 5 mg Zolmitriptan/day | 0 | 11 | 0 | 11 | 11 | 11 |
| Hypertension | Cardiac disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Deviated Midline Catheter | Surgical and medical procedures | MedDRA (Unspecified) | Systematic Assessment |
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| ST Elevation More Peaked | Cardiac disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Tasting Saline | Gastrointestinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Heartburn | Gastrointestinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Nausea | Gastrointestinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Dyspepsia | Gastrointestinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Diarrhea | Gastrointestinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Fever | Immune system disorders | MedDRA (Unspecified) | Systematic Assessment |
|
| Fluid Leak (from Midline) | Skin and subcutaneous tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
|
| Pain at Midline Site | Skin and subcutaneous tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
|
| Redness | Skin and subcutaneous tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
|
| Swelling | Skin and subcutaneous tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
|
| Skin Irritation from Adhesive | Skin and subcutaneous tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Itching at Midline Site | Skin and subcutaneous tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Headache | Nervous system disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Sleepiness | Nervous system disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Sinus Headache | Nervous system disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Insomnia | Nervous system disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Vivid dreams | Nervous system disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Hoarseness | Respiratory, thoracic and mediastinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Wheezing | Respiratory, thoracic and mediastinal disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Diffuse body pain | Musculoskeletal and connective tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| foot pain | Musculoskeletal and connective tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Jaw pain | Musculoskeletal and connective tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Neck pain | Musculoskeletal and connective tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Back pain | Musculoskeletal and connective tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
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| Shoulder pain | Musculoskeletal and connective tissue disorders | MedDRA (Unspecified) | Systematic Assessment |
|
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| D000470 |
| Alkaloids |
| D006571 | Heterocyclic Compounds |
| D019086 | Bridged Bicyclo Compounds, Heterocyclic |
| D006572 | Heterocyclic Compounds, Bridged-Ring |