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临床试验/NCT01280968
NCT01280968已完成2 期

Improving the Efficacy of Anti-Nicotine Immunotherapy

Alexey Mukhin4 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2010年12月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
52
试验地点
4
主要终点
Vaccine-Induced Percent Change in Brain Nicotine Area Under Curve (AUC) After Single or Multiple (7) Puffs

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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
  • use of experimental (investigational) drugs or devices;
  • use of illegal drugs;
  • use of psychiatric medications;
  • use of opiate medications;
  • use of systemic steroids or other immunosuppressive agents.

排除标准

  • 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/
  • 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:
  • Illegal drugs (or if the urine drug screen is positive),
  • Experimental (investigational) drugs;
  • Psychiatric medications including antidepressants, anti-psychotics or any other medications that are known to affect smoking cessation (e.g. clonidine);
  • Opiate medications for pain or sleep (non-opiate medication for pain or sleep will be allowed)
  • Smokeless tobacco (chewing tobacco, snuff), cigars, pipes or e-cigarettes;
  • Nicotine replacement therapy or any other smoking cessation aid.
  • 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.

结局指标

主要结局

Vaccine-Induced Percent Change in Brain Nicotine Area Under Curve (AUC) After Single or Multiple (7) Puffs

时间窗: measured at week 1 and week 16

There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments.

Vaccine-Induced Percent Change in Brain Nicotine Maximum Concentration After Single or Multiple (7) Puffs

时间窗: measured at week 1 and week 16

There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments.

Vaccination-Induced Percent Change in T1/2 of Brain Nicotine Accumulation After Single or Multiple (7) Puffs

时间窗: measured at week 1 and week 16

There was a 2 hour washout period between the "single puff" and "multiple puffs" assessments.

Vaccination-Induced Percent Change in Initial Slope of Brain Nicotine Accumulation After a Single Puff

时间窗: measured at week 1 and week 16

次要结局

未报告次要终点

研究者

发起方
Alexey Mukhin
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Alexey Mukhin

Professor of Psychiatry and Behavioral Science

Duke University

研究点 (4)

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