Varenicline in Combination With Nicotine Replacement Therapy for Smoking Cessation

NCT ID: NCT01444131

Last Updated: 2014-03-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 446 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-04-30
• Study Completion Date: 2013-06-30

Brief Summary

The purpose of this study is to test whether the addition of a nicotine patch to varenicline increases smoking cessation success rate and whether the combination is safe.

Detailed Description

This is a phase-II multicenter study involving 438 smokers, to be conducted at 7 sites in South Africa, over 6 months. In a randomized 1:1 allocation varenicline tartrate 1 mg twice daily, given in an incremental dosage for the first week before target quit date (TQD), will be compared to varenicline tartrate in the same dose combined with a 15mg nicotine patch. The nicotine patch (active and placebo) will be provided by McNeil. The patch will be given 2 weeks prior TQD. Treatment duration from TQD is 12 weeks with varenicline being tapered off during week 13.

A total of 12 clinic visits and 1 telephonic contact is planned for the 6-month study duration. The main efficacy outcome will be the 4-week continuous abstinence rate during the last four weeks of treatment, i.e. weeks 9 - 12. Efficacy assessments will be based on a Nicotine Use Inventory and measurements of end-expiratory exhaled carbon monoxide. Safety assessments will be based on adverse events evaluation, with special attention being given to the occurrence of nausea during the pretreatment period, as well as neuro-psychiatric symptoms such as depression or suicidal ideation. Participants will not be subjected to any invasive procedures.

This protocol is based on current evidence and two further abstracts presented at the European Respiratory Society Conference in Vienna, September 2009, that a combination of varenicline tartrate and nicotine replacement therapy indicate superior efficacy in cessation rate, but also an excellent good safety profile.

This study relates to the area of pharmacotherapy of smoking cessation, and will answer a frequently asked question. Importantly, several leading pulmonologists with experience in smoking cessation in South Africa have expressed their keen interest to participate in this study.

Conditions

Tobacco Dependence

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Varenicline and Placebo Patch

Varenicline and Nicotine Patch (placebo)

Group Type: PLACEBO_COMPARATOR

Varenicline and Placebo Patch

Intervention Type: DRUG

placebo nicotine patches added to varenicline.

Varenicline and Nicotine Patch

Varenicline and Nicotine Patch 15mg

Group Type: ACTIVE_COMPARATOR

Varenicline, Nicotine Patch

Intervention Type: DRUG

active nicotine patches added to varenicline.

Interventions

Varenicline, Nicotine Patch

active nicotine patches added to varenicline.

Intervention Type: DRUG

Varenicline and Placebo Patch

placebo nicotine patches added to varenicline.

Intervention Type: DRUG

Other Intervention Names

Champix; Nicorette

Eligibility Criteria

Inclusion Criteria

1. Current cigarette smokers, male and female, aged between 18-75 years (both limits inclusive), and who are motivated to stop smoking.

2. Have smoked on average at least 10 cigarettes per day during past year and during the month prior to screening, and no period of abstinence greater than 3 months in the past year.

3. Women of child-bearing potential (WCBP) may be included provided they are not pregnant, not nursing, and meet all of the following criteria:

• instructed and agree to avoid pregnancy through 30 days after the last dose of study medication
• negative screening test (beta-HCG) at screening
• agree to use at least one birth control method (oral contraceptive, IUD, implantable or injectable contraceptive for at least 1 month prior to entering the study and will continue its use through at least 30 days after the last dose of study medication, or use a barrier method of contraception (p.e.condom, diaphragm with spermicide) while participating in the study through at least 30 days after the last dose of study medication; or abstinence.

4. Patients must have no serious or unstable disease in the past 6 months.

5. Patients must be able to be outpatients, to be assessed in a clinical setting, and be able and willing to comply with all study visits during the treatment and non-treatment periods.

6. Only one subject per household may participate.

Exclusion Criteria

1. Patients currently suffering from depression or who have been diagnosed with depression or treated with anti-depressants within the past 12 months.

2. Patients with a past of present history of psychosis, panic disorder, or bipolar disorder.

3. Patients with severe chronic obstructive pulmonary disease (COPD).

4. Patients with clinically significant cardiovascular disease in the past 6 months. such as myocardial infarction, coronary artery bypass graft (CABG), percutaneous transluminal coronary angioplasty (PTCA), severe or unstable angina, serious arrhythmia, and clinically significant ECG conduction abnormalities.

5. Patients with uncontrolled hypertension or a systolic blood pressure greater than 150mmHg or as diastolic pressure greater than 95mmHg at screening or baseline.

6. Patients with clinically significant neurological disorders or cerebrovascular diseases (for example, stroke, transient ischemic attack, etc.) in the past 6 months.

7. Patients with a history of clinically significant endocrine disorders or gastrointestinal diseases, including insulin dependent diabetes mellitus, uncontrolled hyperthyroidism, and active peptic ulcer.

8. Patients with clinically significant hepatic or renal impairment or other clinically significant abnormal laboratory test values.

9. Patients with a history of cancer (cured basal cell or squamous cell carcinoma of the skin allowed).

10. Patients with a history of clinically significant allergic reactions to drugs (for example, severe cutaneous and/or systemic allergic reactions).

11. Patients with a history of drug (except nicotine) or alcohol abuse or dependence within the past 12 months.

12. Patients with a body mass index (BMI) less than 15 or greater than 38 when wearing indoor clothing without shoes. No subject will be enrolled with a weight less than 45.5kg (100 pounds).

13. Patients previously enrolled in a study that included varenicline.

14. Patients having used nicotine replacement therapy within the last 6 months.

15. Patients taking another investigational drug within 30 days or 5 half-lives (whichever is longer) before the Baseline visit or within 30 days of study completion.

16. Use of prohibited medications: any antidepressants, including bupropion; antipsychotic agents; mood stabilizers; naltrexone; steroids (inhaled and topical steroids are permitted); insulin.

17. Patients who do not agree to completely abstain from using non-cigarette tobacco products (including for example, pipe tobacco, cigars, snuff, chewing tobacco, etc.) or marijuana during study participation.

18. Patients who intend to donate blood or blood components while receiving study drug or within 1 month of the completion of the study treatment.

19. Patients unable/or unlikely to comprehend and follow the study protocol, including patients unable and/or unwilling to participate in the non-treatment follow-up. Patients who, in the investigator's opinion, will be unlikely to commit to a 6 month-long study.

20. Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

QuitSupport

UNKNOWN

Sponsor Role: collaborator

University of Stellenbosch

OTHER

Sponsor Role: lead

Responsible Party

Prof Elvis M Irusen

Clinical Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Elvis M Irusen, MBChB, FCP, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Stellenbosch

Locations

Respiratory Research Unit

Cape Town, Western Cape, South Africa

Synopsis Research

Cape Town, Western Cape, South Africa

UCT Lung Institute

Cape Town, Western Cape, South Africa

Dr JA O'Brien

Cape Town, Western Cape, South Africa

Dr AHH Brüning

Gatesville / Cape Town, Western Cape, South Africa

Dr MS Abdool-Gaffar

eManzimtoti, , South Africa

Dr C Smith

Sandton, , South Africa

Countries

South Africa

References

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Reference Type: BACKGROUND

PMID: 16820546 (View on PubMed)

Jorenby DE, Hays JT, Rigotti NA, Azoulay S, Watsky EJ, Williams KE, Billing CB, Gong J, Reeves KR; Varenicline Phase 3 Study Group. Efficacy of varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, vs placebo or sustained-release bupropion for smoking cessation: a randomized controlled trial. JAMA. 2006 Jul 5;296(1):56-63. doi: 10.1001/jama.296.1.56.

Reference Type: BACKGROUND

PMID: 16820547 (View on PubMed)

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Reference Type: BACKGROUND

PMID: 16820548 (View on PubMed)

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Koegelenberg CF, Noor F, Bateman ED, van Zyl-Smit RN, Bruning A, O'Brien JA, Smith C, Abdool-Gaffar MS, Emanuel S, Esterhuizen TM, Irusen EM. Efficacy of varenicline combined with nicotine replacement therapy vs varenicline alone for smoking cessation: a randomized clinical trial. JAMA. 2014 Jul;312(2):155-61. doi: 10.1001/jama.2014.7195.

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Other Identifiers

VarNic

Identifier Type: -

Identifier Source: org_study_id