RecruitingPhase 2NCT06617312
Examining the Effects of Cytisinicline on Neural Substrates of Cigarette Cue-reactivity
Examining the Effects of Cytisinicline on Neural Substrates of Cigarette Cue-Reactivity
Sponsor
University of California, Los Angeles
Enrollment
64 participants
Start Date
Dec 5, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
This study will randomize 64 non-treatment seeking individuals who smoke cigarettes daily in a double-blind, placebo-controlled laboratory study testing the effects of cytisinicline on the neural substrates of cigarette cue reactivity.
Eligibility
Min Age: 18 YearsMax Age: 65 Years
Inclusion Criteria3
- be between the ages of 18 and 65 and provide informed consent;
- smoke 5 or more combustible cigarettes per day;
- not seeking treatment for smoking;
Exclusion Criteria29
- current use of other smoking cessation aid (bupropion, varenicline, nortriptyline, NRT);
- more than 3 months of smoking abstinence in past year;
- use of non-cigarette tobacco product (pipe tobacco, cigars, smokeless tobacco, hookah) or electronic cigarettes more than 5 times in the 28-days prior to enrollment;
- current use of psychoactive drug (excluding cannabis), as determined by urine toxicology;
- current (past 12-month) DSM-5 diagnosis of substance use disorder for any substances other than tobacco and mild cannabis or mild-to-moderate alcohol use disorders;
- lifetime history of psychotic disorders, bipolar disorders, or major depression with suicidal ideation;
- current suicidal ideation or lifetime history of suicide attempt;
- serious medical illness within past 3 months, including recent history of acute myocardial infarction, unstable angina, stroke, cerebrovascular incident, or hospitalization for congestive heart failure;
- medical condition that may interfere with safe study participation;
- renal impairment defined as a creatinine clearance (CrCl) greater than 60 mL/min (estimated with the Cockroft-Gault equation);
- exceed Grade 2 laboratory abnormalities, based on FDA Guidance Document "Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials";
- uncontrolled hypertension (blood pressure ≥160/100 mmHg);
- abnormal electrocardiogram;
- non-removable ferromagnetic object in body;
- claustrophobia;
- serious head injury or period of unconsciousness (more than 30 minutes);
- more than 250lbs;
- Be pregnant, nursing, or planning to become pregnant while taking part in the study; and must agree to one of the following methods of birth control (if female), unless she or partner are surgically sterile:
- Oral contraceptives
- Contraceptive sponge
- Patch
- Double barrier
- Intrauterine contraceptive device
- Etonogestrel implant
- Medroxyprogesterone acetate contraceptive injection
- Hormonal vaginal contraceptive ring
- Complete abstinence from sexual intercourse;
- have experienced adverse effects to varenicline;
- have an intense fear of needles or have had an adverse reaction to needle puncture.
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Interventions
DRUGCytisinicline
Targets α4β2 nicotinic acetylcholine receptors
DRUGPlacebo Oral Capsule
Matched to active drug, cytisinicline
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06617312
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