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| ID | Type | Description | Link |
|---|---|---|---|
| 1P50DA027840-01A1 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
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The purpose of this research study is to evaluate whether the investigational drug ganaxolone can help smokers quit smoking. Ganaxolone is a drug that has been investigated (in other research studies) for the treatment of seizures and migraines. This drug is considered investigational in the US.
The purpose of this proof-of-concept study is to evaluate whether expired air carbon monoxide (CO) will be reduced and smoking cessation success rates enhanced for smokers who receive the neurosteroid analog ganaxolone. The trial will be seeking preliminary indications of efficacy and tolerability in the smoking population and allow us to estimate effect sizes for future controlled trials.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ganaxolone -- Nicotine Patch | Experimental | Pre-Quit Period: Ganaxolone -- 400mg daily for the first 3 days, 800mg daily for the next 3 days and 1200mg daily for the remainder of the first 2 wks. Nicotine Patches -- 21mg/24h nicotine patches applied daily during wks. 3 and 4. Post-Quit Period: Ganaxolone -- 1200mg daily for wk. 5, 800mg daily for 3 days, and 400mg daily for 3 days. Nicotine Patches -- 21mg/24h for 4 wks., 14mg/24h for 1 wk., and 7mg/24h for 1 wk. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ganaxolone | Drug | Pre-Quit Period: Beginning at Session P1, subjects will receive ganaxolone at a dose of 400mg total daily (200mg bid) for the first three days, 800mg total daily (400mg bid) for the next three days and 1200mg total daily (600mg bid) for the remainder of the first four weeks. Post-Quit Period: Following the quit-day, subjects will receive ganaxolone at a dose of (1200mg total daily) for the next week. Down-titration of ganaxolone will begin at post-quit week two. Subjects will receive ganaxolone at a dose of 800mg total daily (400mg bid) to take for three days and 400mg total daily (200mg bid) to take for three. |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Change in Expired Air Carbon Monoxide (CO) at End of Week 2 | To evaluate the effects of ganaxolone on ad lib smoking by looking at the percent change in expired air CO at the end of week two (relative to baseline). | Baseline and 2 Weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Change in Expired Air Carbon Monoxide (CO) at End of Week 4 | To evaluate the effects of ganaxolone as an augmentation treatment in conjunction with nicotine patch by looking at the percent change in expired air CO at the end of week four (relative to baseline). | Baseline and 4 Weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants Completing Continuous 2-week Abstinence From Smoking | Continuous two week abstinence from smoking at the first post-quit visit (approximately 2 weeks post quit date), based on self-reported abstinence confirmed by expired air CO. | 2 Weeks post quit |
| Number of Participants Completing Point Abstinence From Smoking Two Weeks After Quitting |
Inclusion Criteria:
Potential subjects must agree to use acceptable contraception during their participation in this study.
Potential subjects must agree to avoid the following during their participation in this study:
Exclusion Criteria:
Inability to attend all required experimental sessions;
Inability to take oral drugs or adhere to medication regimens;
Hypertension (systolic >140 mm Hg, diastolic >90 mm Hg);
Hypotension with symptoms (systolic <90 mm Hg, diastolic <60 mm Hg).
Coronary heart disease;
Lifetime history of heart attack;
Clinically significant cardiac rhythm disorder (irregular heart rhythm);
Chest pains;
Cardiac (heart) disorder;
Extensive active skin disorder;
Liver or kidney disorder;
Gastrointestinal disease other than gastroesophageal reflux or heartburn;
Active ulcers in the past 30 days;
Currently symptomatic lung disorder/disease;
Brain abnormality;
Migraine headaches that occur more frequently than once per week;
History of seizures;
Recent, unexplained fainting spells;
Problems giving blood samples;
Diabetes (unless treated with diet and exercise alone);
Current cancer or treatment for cancer in the past six months (except basal or squamous cell skin cancer);
Other major medical condition;
Current symptomatic psychiatric disease;
Current depression;
Current suicidal ideation or history of suicide attempt (in the past 5 years);
Pregnant or nursing mothers;
Use (within the past 30 days) of:
Use (within the past 14 days) of:
Use of more than one cigar a month;
Regular alcohol use;
Significant adverse reaction to nicotine patches in the past.
Significant past adverse reaction to ganaxolone in the past.
Current participation or recent participation (in the past 30 days) in another smoking study at our center or another research facility.
Current participation in another research study.
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| Name | Affiliation | Role |
|---|---|---|
| Jed E Rose, Ph.D. | Duke University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Duke Center for Smoking Cessation | Charlotte | North Carolina | 28210 | United States | ||
| Duke Center for Smoking Cessation |
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| ID | Title | Description |
|---|---|---|
| FG000 | Ganaxolone -- Nicotine Patch | Pre-Quit Period: Ganaxolone -- 400mg daily (200mg bid) for the first 3 days, 800mg daily (400mg bid) for the next 3 days and 1200mg daily (600mg bid) for the remainder of the first 2 wks. Nicotine Patches -- 21mg/24h nicotine patches applied daily during wks. 3 and 4. Post-Quit Period: Ganaxolone -- 1200mg daily for wk. 5, 800mg daily for 3 days, and 400mg daily for 3 days. Nicotine Patches -- 21mg/24h for 4 wks., 14mg/24h for 1 wk., and 7mg/24h for 1 wk. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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| ID | Title | Description |
|---|---|---|
| BG000 | Ganaxolone -- Nicotine Patch | Pre-Quit Period: Ganaxolone -- 400mg daily for the first 3 days, 800mg daily for the next 3 days and 1200mg daily for the remainder of the first 2 wks. Nicotine Patches -- 21mg/24h nicotine patches applied daily during wks. 3 and 4. Post-Quit Period: Ganaxolone -- 1200mg daily for wk. 5, 800mg daily for 3 days, and 400mg daily for 3 days. Nicotine Patches -- 21mg/24h for 4 wks., 14mg/24h for 1 wk., and 7mg/24h for 1 wk. |
| 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 | Percentage of Change in Expired Air Carbon Monoxide (CO) at End of Week 2 | To evaluate the effects of ganaxolone on ad lib smoking by looking at the percent change in expired air CO at the end of week two (relative to baseline). | Posted | Mean | Standard Error | percentage change | Baseline and 2 Weeks |
|
Subjects were receiving study drugs for ten weeks. At each study session during this period subjects completed a questionnaire about side effects. Subjects were also told to contact us between study sessions if side effects were bothersome.
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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 | Ganaxolone -- Nicotine Patch | Pre-Quit Period: Ganaxolone -- 400mg daily (200mg bid) for the first 3 days, 800mg daily (400mg bid) for the next 3 days and 1200mg daily (600mg bid) for the remainder of the first 2 wks. Nicotine Patches -- 21mg/24h nicotine patches applied daily during wks. 3 and 4. Post-Quit Period: Ganaxolone -- 1200mg daily for wk. 5, 800mg daily for 3 days, and 400mg daily for 3 days. Nicotine Patches -- 21mg/24h for 4 wks., 14mg/24h for 1 wk., and 7mg/24h for 1 wk. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Headache | Nervous system disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Jed E. Rose | Duke Center for Smoking Cessation | 919-668-5055 | jed.rose@duke.edu |
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| ID | Term |
|---|---|
| D016540 | Smoking Cessation |
| ID | Term |
|---|---|
| D015438 | Health Behavior |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| C105051 | ganaxolone |
| D061485 | Tobacco Use Cessation Devices |
| D009538 | Nicotine |
| ID | Term |
|---|---|
| D013812 | Therapeutics |
| D012991 | Solanaceous Alkaloids |
| D000470 | Alkaloids |
| D006571 | Heterocyclic Compounds |
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|
| Nicotine Patch | Drug | Pre-Quit Period: Beginning at Session P2, subjects will receive active 21mg/24h nicotine patches to apply daily for the next two weeks. Post-Quit Period: Following the quit-day, subjects will continue to apply active nicotine patches daily for the remainder of the study (21mg/24h for four weeks, 14mg/24h for one week, and 7mg/24h for one week). |
|
|
Point abstinence from smoking two weeks post quit, based on self-reported abstinence during last seven days confirmed by expired air CO at first post-quit visit. |
| 7 day point abstinence from smoking at 2 weeks post quit |
| Number of Participants Completing Continuous 6-week Abstinence From Smoking | Continuous six week abstinence from smoking at final study visit (approximately 6 weeks post quit date), based on self-reported abstinence confirmed by expired air CO | 6 Weeks post quit |
| Number of Participants Completing Abstinence From Smoking During the Last Four Weeks of Treatment | End of treatment abstinence from smoking during the last four weeks of treatment, based on self-reported abstinence during last four weeks confirmed by expired air CO | 4 Week abstinence from smoking at 6 weeks post quit |
| Durham |
| North Carolina |
| 27705 |
| United States |
| Duke Center for Smoking Cessation | Raleigh | North Carolina | 27609 | United States |
| Duke Center for Smoking Cessation | Winston-Salem | North Carolina | 27103 | United States |
| years |
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| Age, Categorical | Count of Participants | Participants |
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| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units | Counts |
|---|---|
| Participants |
|
|
| Secondary | Percentage of Change in Expired Air Carbon Monoxide (CO) at End of Week 4 | To evaluate the effects of ganaxolone as an augmentation treatment in conjunction with nicotine patch by looking at the percent change in expired air CO at the end of week four (relative to baseline). | Three of the original 16 subjects dropped out prior to week 4, so only 13 subjects had a week 4 CO reading and could be included in this analysis. | Posted | Mean | Standard Error | percentage change | Baseline and 4 Weeks |
|
|
|
| Other Pre-specified | Number of Participants Completing Continuous 2-week Abstinence From Smoking | Continuous two week abstinence from smoking at the first post-quit visit (approximately 2 weeks post quit date), based on self-reported abstinence confirmed by expired air CO. | Posted | Number | 95% Confidence Interval | participants | 2 Weeks post quit |
|
|
|
| Other Pre-specified | Number of Participants Completing Point Abstinence From Smoking Two Weeks After Quitting | Point abstinence from smoking two weeks post quit, based on self-reported abstinence during last seven days confirmed by expired air CO at first post-quit visit. | Posted | Number | 95% Confidence Interval | participants | 7 day point abstinence from smoking at 2 weeks post quit |
|
|
|
| Other Pre-specified | Number of Participants Completing Continuous 6-week Abstinence From Smoking | Continuous six week abstinence from smoking at final study visit (approximately 6 weeks post quit date), based on self-reported abstinence confirmed by expired air CO | Because 6-week abstinence is counted backward from the final study visit, one additional subject (n=4) qualified as abstinent than at 2-weeks post-quit (n=3) due to the fact that the day(s) that one of the subjects smoked did not fall into the range evaluated at 6 weeks. | Posted | Number | 95% Confidence Interval | participants | 6 Weeks post quit |
|
|
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| Other Pre-specified | Number of Participants Completing Abstinence From Smoking During the Last Four Weeks of Treatment | End of treatment abstinence from smoking during the last four weeks of treatment, based on self-reported abstinence during last four weeks confirmed by expired air CO | Posted | Number | 95% Confidence Interval | participants | 4 Week abstinence from smoking at 6 weeks post quit |
|
|
|
| 0 |
| 16 |
| 16 |
| 16 |
| Fatigue | Nervous system disorders | Systematic Assessment |
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| Dizziness | Nervous system disorders | Systematic Assessment |
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| Loss of balance | Nervous system disorders | Systematic Assessment |
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| Anxiety | Psychiatric disorders | Systematic Assessment |
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| Depression | Psychiatric disorders | Systematic Assessment |
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| Irritability | Nervous system disorders | Systematic Assessment |
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| Insomnia | Nervous system disorders | Systematic Assessment |
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| Nightmares | Nervous system disorders | Systematic Assessment |
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| Vivid dreams | Nervous system disorders | Systematic Assessment |
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| Muscle / joint pain | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Thirst | General disorders | Systematic Assessment |
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| Mouth irritation | General disorders | Systematic Assessment |
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| Dry mouth | General disorders | Systematic Assessment |
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| Itching at patch site | Skin and subcutaneous tissue disorders | Systematic Assessment |
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| Rash at patch site | Skin and subcutaneous tissue disorders | Systematic Assessment |
|
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| D011725 |
| Pyridines |
| D006573 | Heterocyclic Compounds, 1-Ring |