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| Name | Class |
|---|---|
| Wake Forest University Health Sciences | OTHER |
| Novartis Pharmaceuticals | INDUSTRY |
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The purpose of this study is to find out how vaccine-induced antibodies change the way the body processes nicotine from cigarettes. These antibodies absorb nicotine and can reduce nicotine levels in the brain. In this way, the vaccination may help to quit smoking. The central hypothesis is that anti-nicotine antibodies change kinetics of brain nicotine accumulation and distribution of nicotine between the brain and other body tissues. This vaccine is investigational which means that it is still being tested in research studies and is not approved by the U.S. Food and Drug Administration (FDA) to help people quit smoking.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NIC002 Vaccine in Aluminum hydroxide | Experimental | 4 subcutaneous vaccinations were performed over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 100 μg of NIC002 and 0.46 mg aluminum hydroxide. |
|
| Placebo Vaccine - Aluminum hydroxide | Placebo Comparator | 4 placebo injections were administered subcutaneously over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 0.46 mg aluminum hydroxide. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| NIC002 in Aluminum hydroxide (Alum) | Biological | Fifty-five subjects will receive 4 subcutaneous injections of 0.1 mg Nicotine-QB (NIC002) in Alum vaccine with a 4-week interval between injections. |
| Measure | Description | Time Frame |
|---|---|---|
| Vaccine-Induced Percent Change in Brain Nicotine Area Under Curve (AUC) After Single or Multiple (7) Puffs | There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments. | measured at week 1 and week 16 |
| Vaccine-Induced Percent Change in Brain Nicotine Maximum Concentration After Single or Multiple (7) Puffs | There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments. | measured at week 1 and week 16 |
| Vaccination-Induced Percent Change in T1/2 of Brain Nicotine Accumulation After Single or Multiple (7) Puffs | There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments. | measured at week 1 and week 16 |
| Vaccination-Induced Percent Change in Initial Slope of Brain Nicotine Accumulation After a Single Puff | measured at week 1 and week 16 |
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Inclusion Criteria:
18-55 years old
Smoked an average of at least 10 cigarettes per day for the past year
Have an expired air Carbon Monoxide (CO) reading of at least 15 ppm
Express a desire to quit smoking in the next three to four months.
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:
participation in any other nicotine-related modification strategy outside of this protocol
use of tobacco products other than cigarettes, including pipe tobacco, cigars, snuff, and chewing tobacco
Exclusion Criteria:
Hypertension (systolic >140 mm Hg, diastolic >100 mm Hg, coupled with a history of hypertension); subjects with no previous diagnosis of hypertension may have a screening blood pressure up to 160/100.
Hypotension with symptoms (systolic <90 mm Hg, diastolic <60 mm Hg).
Participants with a history of hypertension may, however, be allowed to participate in the study if the study physician or physician assistant determines that the condition is stable, controlled by medication, and in no way jeopardizes the individual's safety.
Coronary heart disease or other cardiovascular disorder;
Lifetime history of heart attack;
Cardiac rhythm disorder (irregular heart rhythm);
Chest pains (unless history, exam, and Electrocardiogram (ECG) clearly indicate a non-cardiac source);
Cardiac (heart) disorder (including but not limited to valvular heart disease, heart murmur, heart failure);
Liver or kidney disorder (except kidney stones, gallstones);
Gastrointestinal problems or disease other than gastroesophageal reflux or heartburn;
Active ulcers in the past 30 days;
Lung disorder (including but not limited to chronic obstructive pulmonary disease (COPD), emphysema, and asthma);
Brain abnormality or other neurological disorder (including but not limited to stroke, brain tumor, and seizure disorder);
Recent, unexplained fainting spells;
Problems giving blood samples;
Diabetes treated with insulin; non-insulin treated diabetes (unless glucose is less than 180mg/dcl and HbA1c is less than 7%);
Current cancer or treatment for cancer in the past six months (except basal or squamous cell skin cancer);
Skin disorder;
Autoimmune disease;
Human immunodeficiency virus (HIV) or HIV risk behavior;
Severe allergies;
Other major medical condition;
Current psychiatric disease including major depressive episode, panic attack, psychosis, bipolar disorder or eating disorder;
Pregnant or nursing mothers;
Use (within the past 30 days) of:
Alcohol abuse - The AUDIT (Alcohol Use Disorders Identification Test) questionnaire will be used to assess alcohol abuse.
Previous history of negative experiences with "flu" vaccine or any other vaccine.
High chronic exposure to aluminum (occupational or medical);
Pulmonary function test results < 60% of predicted value for FEV1 and FVC;
Body Mass Index > 38kg/m2;
History of psychosis or bipolar disorder;
Prior exposure to CTY002- NicQ or any other nicotine vaccine.
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| Name | Affiliation | Role |
|---|---|---|
| Alexey G Mukhin, M.D., Ph.D. | Duke University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Duke Center for Nicotine & Smoking Cessation Research | Durham | North Carolina | 27705 | United States | ||
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| ID | Title | Description |
|---|---|---|
| FG000 | NIC002 Vaccine in Aluminum Hydroxide | 4 subcutaneous vaccinations were performed over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 100 μg of NIC002 and 0.46 mg aluminum hydroxide. |
| FG001 | Placebo Vaccine - Aluminum Hydroxide | 4 placebo injections were administered subcutaneously over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 0.46 mg aluminum hydroxide. |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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|
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| ID | Title | Description |
|---|---|---|
| BG000 | NIC002 Vaccine in Aluminum Hydroxide | 4 subcutaneous vaccinations were performed over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 100 μg of NIC002 and 0.46 mg aluminum hydroxide. |
| BG001 | Placebo Vaccine - Aluminum Hydroxide |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Customized | One participant reported that she was 54 at the screening, but after she was consented, it was discovered that she was actually 56. However, the subject was discontinued after the first study visit because she could not use the smoking delivery device; therefore, she received no vaccinations. Safety Event #14 was submitted to Duke IRB to account for this Protocol Deviation in which the subject was out of the age range. |
| 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 | Vaccine-Induced Percent Change in Brain Nicotine Area Under Curve (AUC) After Single or Multiple (7) Puffs | There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments. | Posted | Mean | Standard Error | percentage of change | measured at week 1 and week 16 |
|
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The number of participants at risk is different from the number of enrolled participants because not all participants who were randomized to a vaccine or placebo received treatment. Of the 52 participants who were assigned to a treatment group, only 41 received at least one vaccination. Therefore, 41 participants were at risk.
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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 | NIC002 Vaccine in Aluminum Hydroxide | 4 subcutaneous vaccinations were performed over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 100 μg of NIC002 and 0.46 mg aluminum hydroxide. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Headache | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Alexey G Mukhin, M.D., Ph.D. | Duke University Medical Center | Telephone: 919-668-5055 | amukhin@duke.edu |
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| ID | Term |
|---|---|
| D014029 | Tobacco Use Disorder |
| ID | Term |
|---|---|
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D000536 | Aluminum Hydroxide |
| C041524 | aluminum sulfate |
| C519280 | nicotine Qbeta vaccine |
| ID | Term |
|---|---|
| D006878 | Hydroxides |
| D000468 | Alkalies |
| D007287 | Inorganic Chemicals |
| D017607 | Aluminum Compounds |
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| Placebo Vaccine - Aluminum hydroxide | Biological | Ten subjects will receive 4 subcutaneous injections of indistinguishable placebo (Alum alone) with a 4-week interval between injections. |
|
| Wake Forest University Health Sciences |
| Winston-Salem |
| North Carolina |
| 27157 |
| United States |
| Commuting Problems |
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| Anxiety |
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| Adverse Event |
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| Scheduling Conflicts |
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| Pre-existing Neurological Condition |
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| Unable to Smoke in Supine Position |
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4 placebo injections were administered subcutaneously over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 0.46 mg aluminum hydroxide. |
| BG002 | Total | Total of all reporting groups |
| Mean |
| Full Range |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Cigarettes Per Day | average number of cigarettes participant smokes each day | Mean | Full Range | cigarettes per day |
|
| Pack-Years | pack-years that each participant has smoked, calculated by multiplying the number of packs of cigarettes participant smokes each day by number of years participant has smoked | Mean | Full Range | pack-years |
|
| Placebo Vaccine - Aluminum Hydroxide |
4 placebo injections were administered subcutaneously over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 0.46 mg aluminum hydroxide. |
|
|
| Primary | Vaccine-Induced Percent Change in Brain Nicotine Maximum Concentration After Single or Multiple (7) Puffs | There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments. | Posted | Mean | Standard Error | percentage of change | measured at week 1 and week 16 |
|
|
|
| Primary | Vaccination-Induced Percent Change in T1/2 of Brain Nicotine Accumulation After Single or Multiple (7) Puffs | There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments. | Posted | Mean | Standard Error | percentage of change | measured at week 1 and week 16 |
|
|
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| Primary | Vaccination-Induced Percent Change in Initial Slope of Brain Nicotine Accumulation After a Single Puff | Posted | Mean | Standard Error | percentage of change | measured at week 1 and week 16 |
|
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|
| 0 |
| 36 |
| 13 |
| 36 |
| EG001 | Placebo Vaccine - Aluminum Hydroxide | 4 placebo injections were administered subcutaneously over the course of 3 months, with 4 weeks between each vaccination. The administered volume of 0.65 mL of sterile water contained 0.46 mg aluminum hydroxide. | 0 | 5 | 3 | 5 |
|
| Weight Changes | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
|
| Back Pain | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
|
| Feeling Cold | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Feeling Hot | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Nasal Congestion | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Runny Nose | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Sore Throat | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Fatigue | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| Tenderness at Injection Site | General disorders | Systematic Assessment | At each of 8 visits following first vaccination visit, participants filled out Side Effects Questionnaire and rated severity of side effect from 1 (not at all) to 7 (extremely). Adverse events represent side effects rated as 5 (a lot) or higher. |
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| D000838 |
| Anions |
| D007477 | Ions |
| D004573 | Electrolytes |
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