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OpenTrials
Completed

NCT Number: NCT00318383

Efficacy of NicVAX in Smokers Who Want to Quit Smoking

The purpose of this study is to determine whether vaccination with NicVAX will result in a higher continuous abstinence rate than vaccination with placebo in smokers who want to quit smoking. In addition, two different formulations and dosing schedules will be studied, to select the dose and dosing schedule which generates the highest level of anti-nicotine antibodies. The primary study period is 12 months, which was extended by amendment to include up to 2 years of observations.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

David Geffen School of Medicine at UCLA, Los Angeles, California, United States

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About this study

Cigarette smoking is responsible for over 400,000 (1 out of every 5) deaths in the United States each year. Most smokers are aware of the health consequences and want to quit, but have difficulty doing so. Only 3-5% of smokers who quit on their own are successful. Since the vast majority of those who attempt to quit will fail, the need for better approaches to smoking cessation is clear and urgent. A safe and effective means of blocking the effects of nicotine would be of considerable interest as a potential treatment for tobacco use. Vaccination to produce nicotine-specific antibodies may be viewed as an alternative method of blocking nicotine effects. Nicotine is a small molecule that does not elicit an immune response in animals of humans. In order for the immune system to respond to this hapten, nicotine can be combined or bound to a larger molecule in a unique manner so that an immune response is mounted against nicotine. Nabi Biopharmaceuticals has developed a conjugate vaccine (NicVAX) that consists of 3'-aminomethylnicotine bound to Pseudomonas aeruginosa exoprotein A, an exotoxin that has been made non-toxic by an amino acid deletion. Subjects will be randomized to one of four treatment groups.

Within each treatment group, 75 subjects will be randomized in a 2:1 ratio (NicVAX:Placebo), yielding a total of 50 active and 25 placebo subjects for each treatment group. There will be 12 subjects enrolled in a fifth open label arm to evaluate immunogenicity. A quit date will be set at the end of week 7 or at the end of week 5, depending on the dosing schedule. Continuous abstinence will be measured between the end of week 18 and the end of week 26.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Smokes at least 15 cigarettes per day
  • Wants to quit smoking
  • Good general health
  • Negative pregnancy test prior to study entry
  • Carbon monoxide level greater than 10 ppm

Exclusion criteria

  • Prior exposure to NicVAX or any other nicotine vaccine
  • Known allergic reaction to alum or any of the components of the vaccine
  • Use of steroids, immunosuppressive agents or other medication that might interfere with an immune response

Treatment and study plan

NicVAX conjugate vaccine

Biological

200 mcg or 400 mcg IM in 4 doses over 6 months; 200 mcg or 400 mcg IM in 5 doses over 6 months; 200 mcg (formulation 2) IM in 5 doses over 6 months; All are adsorbed onto Alhydrogel

Other names: 3'-aminomethylnicotine-rEPA conjugate vaccine

Placebo

Biological

Phosphate buffered saline and ALhydrogel of identical appearance to NicVAX; IM in 4 or 5 doses over 6 months

Primary outcomes

  1. Continuous smoking abstinence

    Time frame: 8 week interval (Weeks 19 to 26, inclusive, following the first vaccination)

Secondary outcomes

  1. Point prevalence abstinence

    Time frame: at 12 months, and other time points; extended up to 24 months

  2. Duration of smoking abstinence

    Time frame: at 6 and 12 months

  3. Safety

    Time frame: 0-12 months, and extended up to 24 months

  4. Numbers of cigarettes per day

    Time frame: Target quit day to 12 months

  5. Cumulative number of cigarettes smoked

    Time frame: during weeks 18-26

  6. Exhaled CO

    Time frame: at clinic visits

  7. Urine cotinine

    Time frame: at clinic visits

  8. Modified Minnesota Nicotine Withdrawal Questionnaire

    Time frame: weekly for 6 months, daily for 14 days after quit attempt

  9. Cigarette Evaluation Questionnaire (a.k.a. Nabi Questionnaire)

    Time frame: weekly for 6 motnhs

  10. Fagerstrom Test for Nicotine Dependence

    Time frame: baseline, weeks 26 and 52

  11. serum anti-nicotine antibody concentrations by Elisa

    Time frame: periodic from baseline to month 12, extended to month 24

Sponsors and collaborators

Lead sponsor

National Institute on Drug Abuse (NIDA)

Nih

Collaborators

  • Nabi Biopharmaceuticals

Registry information

Official study title

A Phase 2, Multi-center, Randomized, Double-blinded, Placebo-controlled Study to Assess Efficacy of 3'-Aminomethylnicotine-P.Aeruginosa r-Exoprotein A Conjugate Vaccine (NicVAX) in Smokers Who Want to Quit Smoking

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
Apr 26, 2006
Registry last updated
Jan 12, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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