EVarQuit: Extended Pre-quit Varenicline to Assist in Quitting Smoking

Tobacco Smoking Clinical Trial

— EVarQuit  

Official title:

EVarQuit: Extended Pre-quit Varenicline to Assist in Quitting Smoking

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03262662
• Other study ID #: STUDY00000911
• Secondary ID: R01CA206193
• Status: Completed
• Phase: Phase 3
• Start date: October 1, 2017
• Est. completion date: July 8, 2021

Study information

• Verified date: July 2023
• Source: State University of New York at Buffalo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Varenicline is the most effective smoking cessation therapy available. Nevertheless, most smokers using varenicline relapse within the first few months after quitting. Varenicline is hypothesized to help smokers to quit in part by reducing the reinforcing effects of smoking during the standard 1-week pre-quitting treatment phase. Learning theory and previous human and animal research support the hypothesis that a longer period of varenicline treatment prior to the target quit date (TQD) will lead to greater reductions in smoking before quitting, and higher long-term cessation rates, compared to standard varenicline treatment. Building on promising preliminary clinical data, the study tests these hypotheses with a full-scale randomized clinical trial (RCT). 320 treatment-seeking smokers will be randomized to a standard run-in group (3 weeks of placebo, followed by the standard 1 week of pre-TQD varenicline) or an extended run-in group (4 weeks of pre-TQD varenicline). Both groups will receive brief individual cessation counseling and 11 weeks of post-TQD varenicline. The primary outcome measure will be bio-verified continuous abstinence at end-of-treatment (weeks 8-11 post-quit; cessation at 26-weeks post TQD will also be examined. Hypothesized mediating mechanisms (e.g., smoking reinforcement) will be evaluated by behavioral, physiological, and subjective measures assessed both in the lab and using real-world, real-time electronic momentary assessments (EMA). The investigators predict that long-term, bio-verified smoking cessation will be improved among the extended run-in group compared to the standard run-in group. The investigators further predict the improved clinical outcomes with extended run-in varenicline will be explained (or mediated) by greater pre-quit reductions in smoking reinforcement among the extended run-in group compared to the standard run-in group. The significance of this work is clear: The project aims to make best available treatment for smoking cessation even better, using a method that is ripe for dissemination and an approach that will elucidate critical mechanisms to target in the next generation of treatment enhancement.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 320
• Est. completion date: July 8, 2021
• Est. primary completion date: April 5, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Smoking at least 10 cigarettes per day (CPD) for the past 6 months and expired-air carbon monoxide (CO) >7 at intake. NOTE: To reduce exclusion of Black participants, the CPD criterion was reduced to 5 and the carbon monoxide criterion was eliminated in November, 2019.
• At least moderately motivated to quit smoking and intention to make a quit attempt with varenicline 1 month after treatment begins.
• Planning to remain in western New York (NY) during the study period
• Willing to use varenicline and to refrain from other cessation treatments and tobacco products during the study period.
• English speaker
• To be intent-to-treat (ITT), the participant must complete Lab Visit 1 and meet minimal completion rate for real-world (EMA) assessments.

Exclusion Criteria:

• Use of other tobacco products, including e-cigarettes, in past 7 days
• Use of smoking cessation medication, including nicotine replacement therapy, in the past 14 days
• Prior allergy/hypersensitivity to varenicline
• Pregnant or breast-feeding
• Substance use:
• Alcohol: AUDIT score > 15 at intake, suggestive of alcohol dependence and warranting treatment; for those with scores between 8 and 15, the investigators will advise reducing drinking).
• Medical treatment for substance use (SU) in past 3 months, including Suboxone (buprenorphine) and methadone (at phone screen)
• Using a combination of the National Institute on Drug Abuse (NIDA) modified ASSIST (4-26 = moderate risk; 27+ = high risk) and urine toxicology screen (both

at intake):

• Cannabis: ASSIST=27+ (tox screen not used)
• Cocaine: ASSIST=7+ OR positive tox screen
• Methamphetamine: ASSIST=7+ OR positive tox screen
• Inhalants, hallucinogens, sedatives, or sleeping pills: ASSIST score = 7+
• Prescription stimulants: With prescription, ASSIST 27+; Without prescription, ASSIST 7+
• Opioids: With prescription, ASSIST 27+ (note ineligible if prescription is for buprenorphine or methadone); Without prescription, ASSIST 7+ OR positive tox screen (Note: ASSIST 4+ modified to 7+ in 2018 to avoid excluding people with past SU problems. clinicaltrials.gov edited 12/18/18)
• Psychiatric:
• Antipsychotic medications
• Lifetime history of schizophrenia or bipolar disorder
• Evidence of current major depression (per Patient Health Questionnaire (PHQ-9) at intake
• Past 10 years suicidal ideation (SI) / behavior. At intake, all of the following are exclusionary on the baseline Columbia-Suicide Severity Rating Scale (Posner et al., 2008): SI without intent (C-SSRS #1, #2, or #3), if any intensity rating (Frequency, Duration, Controllability, Deterrents, or Reasons for Ideation) is > 2; SI with intent (C-SSRS #4, or #5), regardless of intensity ratings; Suicidal Behavior (any suicide attempt, interrupted attempt, aborted attempt, or suicide preparatory acts or behavior on the C-SSRS).
• Any medical condition, illness, disorder or concomitant medication that compromises participant safety or treatment, as determined by the Principal Investigator and/or Study Physician.
• Inability to provide informed consent or complete any of the study tasks as determined by the Principal Investigator and/or Study Physician.

Related Conditions & MeSH terms

• Tobacco Smoking

Intervention

Drug:
• Varenicline
oral varenicline tablets

Behavioral:
• Brief smoking cessation counseling
~10-minute individual counseling at each of 6 clinic visits

Locations

Country	Name	City	State
United States	State University of New York at Buffalo	Buffalo	New York

Sponsors (3)

Lead Sponsor	Collaborator
State University of New York at Buffalo	National Cancer Institute (NCI), Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Continuous Abstinence at End-of-Treatment (EOT) as Assessed by Self-Report and Bio-verification	Number of participants with bio-verified (cotinine level of 15 ng/mL or less) self-reported continuous abstinence from smoking (not even a puff) during the final four weeks of treatment	Self-report Treatment Weeks 12-15; bio-verification ~Week 16
Secondary	Pre-quit Change in Cigarettes Smoked Per Day	Percent change in smoking behavior (self-reported cigarettes per day; CPD) from timeline follow-back (TLFB) interviews during the pre-quit phase of the study.	Treatment Week 1 vs. Treatment Week 4 (final week before TQD)
Secondary	Number of Participants With Continuous Abstinence at 6-Month Follow-Up as Assessed by Self-Report and Bio-verification	Number of participants with continuous abstinence at the 6-month follow-up (no self-reported smoking during weeks 12-28 AND cotinine level 15 ng/mL or less at EOT and 6 month follow-up)	Self-report Treatment Weeks 12-28; bio-verification ~Week 16 and ~Week 29