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Effects of GTS-21 on Smoking Behavior and Neurocognitive Functions

Effects of GTS-21 on Smoking Behavior and Neurocognitive Functions

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02432066
Enrollment
0
Registered
2015-05-01
Start date
2018-09-29
Completion date
2020-12-29
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Use Disorder

Keywords

Smoking, Smoking Cessation

Brief summary

Attempts to quit cigarette smoking are often accompanied by negative mood and problems in attention and memory. These effects, in turn, may contribute to smoking relapse. This exploratory/developmental project examines the effects of a novel medication, GTS-21, on individuals interested in smoking cessation. It is hypothesized that GTS-21 will reduce negative affect, improve cognition and/or reduce smoking relapse in healthy adult men and women who are chronic cigarette smokers.

Detailed description

The project is a clinical trial assessing the effects of GTS-21 (an α7 nicotinic receptor partial agonist) on smoking, mood, neurocognition, and neurophysiology, in a small sample of chronic smokers who are currently healthy and interested in smoking cessation. Using a double-blind, placebo controlled, parallel group design, 54 (27 women) community smokers who have demonstrated a readiness to quit will participate over a 7 week active trial. Subjects will be randomly assigned to active drug or placebo groups. Across the study period, participants will undergo repeated neurobehavioral testing, laboratory assessments of cardiovascular and liver function, and provide weekly updates regarding smoking behavior, mood state and side-effects.

Interventions

DRUGGTS-21

GTS-21 is a partial alpha7 nicotinic agonist. GTS-21 will be compounded by the UF investigational pharmacy, and administered orally.

DRUGPlacebo

Oral placebo pills, compounded by the UF investigational pharmacy

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Minimum of 12 years of education * Must report typical daily smoking of \> 10 cigarettes/day over the previous year * Must report a history of at least 3 years of regular smoking * Must provide carbon monoxide measures of at least 6.5 ppm * Must report a willingness to quit smoking

Exclusion criteria

* Participants engaged in behavioral and/or nicotine replacement therapies, or assisted quit efforts, within previous 6 months. * Must not meet criteria for other substance dependence or major psychiatric disorders. * Must be absent chronic medical conditions that might jeopardize health and safety, confound data interpretation or that contraindicate the administration of compounds acting at nAChR sites. This list includes disorders with direct effects on neurologic function (e.g., seizure disorders, transient ischemic events, chronic or active hepatic disease), metabolic disorders (e.g., uncontrolled Type 2 diabetes), or cardiovascular disease (e.g., hypertension, mitral valve compromise, tachycardia, or irregular heart rates). * Must not smoke only cigars, pipes or hookahs or use nicotine products but not cigarettes * Must not report current use of nicotine replacement therapies (i.e., occasions of \> 4 h/week during a typical week, even if not used as a cessation aid) * Must not have used bupropion within the previous year * Must not report any past use (regardless of year) of varenicline * Women may not be breastfeeding, pregnant or intending to become pregnant during the study period

Design outcomes

Primary

MeasureTime frameDescription
Change in Reported Nicotine Use from baseline at weeks 1, 2, 3, 4, 5, 6, 7, 8Change in baseline at Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8Nicotine use will be assessed using Timeline Followback procedures. Nicotine use will be reported to a trained interviewer using a Timeline Followback calendar, facilitated by calendars distributed to participants.
Change in Carbon Monoxide (CO) from baseline at weeks 5, 8Change in baseline at Week 5, Week 8Expired Carbon Monoxide levels will be quantified in parts per million.
Change in Urine Cotinine (COT) from baseline at weeks 5, 8Change in baseline at Week 5, Week 8Cotinine excreted in urine will be quantified in ng/mL

Secondary

MeasureTime frameDescription
Pill Count - Week 1Week 1Medication compliance will be assessed with pill counts.
Pill Count - Week 5Week 5Medication compliance will be assessed with pill counts.
Pill Count - Week 8Week 8Medication compliance will be assessed with pill counts.
Change in Minnesota Withdrawal Scale from baseline at weeks 1, 2, 3, 4, 5, 6, 7, 8Change in baseline at Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8The Minnesota Withdrawal Scale measures self-reported severity of nicotine withdrawal. The measure has 15 items, with five possible responses (0-5), thus scores on the scale range from 0 to 60.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 1Week 1The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 2Week 2The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 3Week 3The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 4Week 4The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 5Week 5The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 6Week 6The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 7Week 7The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Systematic Assessment for Treatment Emergent Events (SAFTEE) - Week 8Week 8The SAFTEE assesses potential side effects across a broad range of potential somatic effects. The measure includes 132 potential areas in which participants might report effects, including opportunities for the participant to describe otherwise unlisted option. Each area is scored on a 5-point scale.
Change in Profile of Mood States 2-A from Baseline at Week 1, 2, 3, 4, 5, 6, 7, 8Change in baseline at Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8The Profile of Mood States-2 (short-form for adults) The POMS 2 is a multi-dimensional, assessment of transient moods, and states of affect. The measure includes 35 items, each rated on a 5-point scale (0-4).
Rapid Visual Information Processing task (Behavior) - BaselineBaselineThe Rapid Visual Information Processing task is an attention task. Subjects are instructed to detect and respond as quickly, yet as accurately, as possible when a target of three consecutive odd or even digits are presented. Digits are presented at the rate of approximately 100 per minute. Hits are separated by a varying number of stimuli (e.g., between 5 and 30 digits). Dependent variables will include accuracy and reaction time.
Rapid Visual Information Processing task - (Behavior) - Week 8Week 8The Rapid Visual Information Processing task is an attention task. Subjects are instructed to detect and respond as quickly, yet as accurately, as possible when a target of three consecutive odd or even digits are presented. Digits are presented at the rate of approximately 100 per minute. Hits are separated by a varying number of stimuli (e.g., between 5 and 30 digits). Dependent variables will include accuracy and reaction time.
Rapid Visual Information Processing task - (EEG) - BaselineBaselineThe Rapid Visual Information Processing task is an attention task. Subjects are instructed to detect and respond as quickly, yet as accurately, as possible when a target of three consecutive odd or even digits are presented. Digits are presented at the rate of approximately 100 per minute. Hits are separated by a varying number of stimuli (e.g., between 5 and 30 digits). Dependent variables will include electrophysiological measures gathered during task participation, including the peak and latency of the P3, P2, and N1 components.
Rapid Visual Information Processing task - (EEG) - Week 8Week 8The Rapid Visual Information Processing task is an attention task. Subjects are instructed to detect and respond as quickly, yet as accurately, as possible when a target of three consecutive odd or even digits are presented. Digits are presented at the rate of approximately 100 per minute. Hits are separated by a varying number of stimuli (e.g., between 5 and 30 digits). Dependent variables will include electrophysiological measures gathered during task participation, including the peak and latency of the P3, P2, and N1 components.
Measurement of GTS-21 Concentration in Blood - Week 5Week 5Blood samples will be collected and analyzed for their concentration of GTS-21.
Measurement of GTS-21 Concentration in Blood - Week 8Week 8Blood samples will be collected and analyzed for their concentration of GTS-21.
Trail Making Test A (TMT-A) - BaselineBaselineThe Trail Making Test A consists of numbered 25 circles distributed over a sheet of paper. Participants draw a line between consecutive circles as quickly and accurately as possible. The dependent variable is time to completion of the task.
Trail Making Test A (TMT-A) - Week 5Week 5The Trail Making Test A consists of numbered 25 circles distributed over a sheet of paper. Participants draw a line between consecutive circles as quickly and accurately as possible. The dependent variable is time to completion of the task.
Trail Making Test A (TMT-A) - Week 8Week 8The Trail Making Test A consists of numbered 25 circles distributed over a sheet of paper. Participants draw a line between consecutive circles as quickly and accurately as possible. The dependent variable is time to completion of the task.
Trail Making Test B (TMT-B) - BaselineBaselineThe Trail Making Test B consists of 25 circles distributed over a sheet of paper, labeled with numbers (1-13) and letters (A-L). Participants draw a line between circles, alternating between consecutive numbers and letters (i.e., 1 to A, A to 2, 2 to B, etc.) as quickly and accurately as possible. The dependent variable is time to completion of the task.
Trail Making Test B (TMT-B) - Week 5Week 5The Trail Making Test B consists of 25 circles distributed over a sheet of paper, labeled with numbers (1-13) and letters (A-L). Participants draw a line between circles, alternating between consecutive numbers and letters (i.e., 1 to A, A to 2, 2 to B, etc.) as quickly and accurately as possible. The dependent variable is time to completion of the task.
Trail Making Test B (TMT-B) - Week 8Week 8The Trail Making Test B consists of 25 circles distributed over a sheet of paper, labeled with numbers (1-13) and letters (A-L). Participants draw a line between circles, alternating between consecutive numbers and letters (i.e., 1 to A, A to 2, 2 to B, etc.) as quickly and accurately as possible. The dependent variable is time to completion of the task.
N-Back Working Memory Task (Behavior) - BaselineBaselineThe 'n-back' test is a measure of working memory entailing the presentation of a stream of numbers, presented singly, and separated by neutral stimuli (i.e., +). Ss press a button when the presented stimulus is the same as the one that occurred 'n-back', i.e., some specific number back. The 'n-back' will vary across blocks (i.e., 1 or 2 back). A control condition, requiring Ss to press the button when a blank slide appears, will also be employed. Dependent variables will include accuracy and reaction time.
Digit Symbol Substitution Task - Week 8Week 8The Digit Symbol Substitution Task requires attention and set-switching. Subjects must translate between numbers and symbols, using a key provided. The dependent measure is number of correct responses completed.
N-Back Working Memory Task (Behavior) - Week 8Week 8The 'n-back' test is a measure of working memory entailing the presentation of a stream of numbers, presented singly, and separated by neutral stimuli (i.e., +). Ss press a button when the presented stimulus is the same as the one that occurred 'n-back', i.e., some specific number back. The 'n-back' will vary across blocks (i.e., 1 or 2 back). A control condition, requiring Ss to press the button when a blank slide appears, will also be employed. Dependent variables will include accuracy and reaction time.
N-Back Working Memory Task (EEG) - BaselineBaselineThe 'n-back' test is a measure of working memory entailing the presentation of a stream of numbers, presented singly, and separated by neutral stimuli (i.e., +). Ss press a button when the presented stimulus is the same as the one that occurred 'n-back', i.e., some specific number back. The 'n-back' will vary across blocks (i.e., 1 or 2 back). A control condition, requiring Ss to press the button when a blank slide appears, will also be employed. Dependent variables will include electrophysiological measures gathered during task participation, including the peak and latency of the P3, P2, and N1 components.
N-Back Working Memory Task (EEG) - Week 8Week 8The 'n-back' test is a measure of working memory entailing the presentation of a stream of numbers, presented singly, and separated by neutral stimuli (i.e., +). Ss press a button when the presented stimulus is the same as the one that occurred 'n-back', i.e., some specific number back. The 'n-back' will vary across blocks (i.e., 1 or 2 back). A control condition, requiring Ss to press the button when a blank slide appears, will also be employed. Dependent variables will include electrophysiological measures gathered during task participation, including the peak and latency of the P3, P2, and N1 components.
Simple Reaction Time Test - BaselineBaselineIn this computerized task, subjects must press a button as quickly as possible each time a designed symbol appears on the screen. This test serves as a perceptual-motor control. The dependent measure is reaction time.
Simple Reaction Time Test - Week 5Week 5In this computerized task, subjects must press a button as quickly as possible each time a designed symbol appears on the screen. This test serves as a perceptual-motor control. The dependent measure is reaction time.
Simple Reaction Time Test - Week 8Week 8In this computerized task, subjects must press a button as quickly as possible each time a designed symbol appears on the screen. This test serves as a perceptual-motor control. The dependent measure is reaction time.
Little Man Test - BaselineBaselineIn this computerized mental rotation test, subjects must indicate the hand in which a simulated figure holds an object. The dependent measures are accuracy and reaction time.
Little Man Test - Week 8Week 8In this computerized mental rotation test, subjects must indicate the hand in which a simulated figure holds an object. The dependent measures are accuracy and reaction time.
Visual-Perceptual Analysis Test - BaselineBaselineIn this computerized task, subjects must distinguish which of three similar shapes differs from the other two. Dependent measures include accuracy and reaction time.
Visual-Perceptual Analysis Test - Week 5Week 5In this computerized task, subjects must distinguish which of three similar shapes differs from the other two. Dependent measures include accuracy and reaction time.
Visual-Perceptual Analysis Test - Week 8Week 8In this computerized task, subjects must distinguish which of three similar shapes differs from the other two. Dependent measures include accuracy and reaction time.
Wisconsin Card Sorting Test - BaselineBaselineThe Wisconsin Card Sort Test is a computerized task which requires subjects to match cards based on shifting matching rules which include color, shape, and number of symbols. The dependent measures for this task include accuracy and response time.
Wisconsin Card Sorting Test - Week 8Week 8The Wisconsin Card Sort Test is a computerized task which requires subjects to match cards based on shifting matching rules which include color, shape, and number of symbols. The dependent measures for this task include accuracy and response time.
Sternberg Short-Term Memory Test - BaselineBaselineThe Sternberg Short-Term Memory Test is a computerized task in which participants are shown four digits, presented one at a time, followed by a probe digit. They must determine if the probe digit was in the original set of digits, and recall the digits. The dependent variables are probe accuracy, number of correct recalls, and time to completion.
Sternberg Short-Term Memory Test - Week 8Week 8The Sternberg Short-Term Memory Test is a computerized task in which participants are shown four digits, presented one at a time, followed by a probe digit. They must determine if the probe digit was in the original set of digits, and recall the digits. The dependent variables are probe accuracy, number of correct recalls, and time to completion.
Stroop Color Word Task - BaselineBaselineThe Stroop Task is a measure of inhibitory control. Subjects are directed to name the colors words are printed in (i.e., blue), while ignoring the incongruent meaning of the words. The dependent measures include number correct and number completed.
Stroop Color Word Task - Week 8Week 8The Stroop Task is a measure of inhibitory control. Subjects are directed to name the colors words are printed in (i.e., blue), while ignoring the incongruent meaning of the words. The dependent measures include number correct and number completed.
Digit Symbol Substitution Task - BaselineBaselineThe Digit Symbol Substitution Task requires attention and set-switching. Subjects must translate between numbers and symbols, using a key provided. The dependent measure is number of correct responses completed.
Digit Symbol Substitution Task - Week 5Week 5The Digit Symbol Substitution Task requires attention and set-switching. Subjects must translate between numbers and symbols, using a key provided. The dependent measure is number of correct responses completed.
Metabolic Panel - BaselineBaselineLiver Function Test will measure a standard array of blood chemistries, including electrolytes, blood glucose, protein, liver enzymes (aminotransferase/alanine aminotransferase), bilirubin, creatinine, and blood urea nitrogen.
Metabolic Panel - Week 2Week 2Liver Function Test will measure a standard array of blood chemistries, including electrolytes, blood glucose, protein, liver enzymes (aminotransferase/alanine aminotransferase), bilirubin, creatinine, and blood urea nitrogen.
Metabolic Panel - Week 5Week 5Liver Function Test will measure a standard array of blood chemistries, including electrolytes, blood glucose, protein, liver enzymes (aminotransferase/alanine aminotransferase), bilirubin, creatinine, and blood urea nitrogen.
Metabolic Panel - Week 8Week 8Liver Function Test will measure a standard array of blood chemistries, including electrolytes, blood glucose, protein, liver enzymes (aminotransferase/alanine aminotransferase), bilirubin, creatinine, and blood urea nitrogen.
Metabolic Panel - Week 9 (Followup)Week 9Liver Function Test will measure a standard array of blood chemistries, including electrolytes, blood glucose, protein, liver enzymes (aminotransferase/alanine aminotransferase), bilirubin, creatinine, and blood urea nitrogen.
Urinalysis - BaselineBaselineStandard urinalysis will be conducted, including urine pH, red cell count, white cell count, specific gravity, and bacteria content.
Urinalysis - Week 2Week 2Standard urinalysis will be conducted, including urine pH, red cell count, white cell count, specific gravity, and bacteria content.
Urinalysis - Week 5Week 5Standard urinalysis will be conducted, including urine pH, red cell count, white cell count, specific gravity, and bacteria content.
Change in Beck Depression Inventory - II (BDI-II) from baseline at weeks 5, 8Change in baseline at Week 5, Week 8The Beck Depression Inventory will be used to quantify depressive symptomatology. The measure is a 21-item, self-report, multiple-choice inventory, with scores ranging from 0-63.
Urinalysis - Week 9 (Followup)Week 9Standard urinalysis will be conducted, including urine pH, red cell count, white cell count, specific gravity, and bacteria content.
Electrocardiogram - BaselineBaselineStandard electrocardiographic data will be collected, including heart rate (BPM) and time between start of the Q wave and end of the T wave (QT interval).
Electrocardiogram - Week 1Week 1Standard electrocardiographic data will be collected, including heart rate (BPM) and time between start of the Q wave and end of the T wave (QT interval).
Change in Reported Drug and Alcohol Use from baseline at weeks 1, 2, 3, 4, 5, 6, 7, 8Change in baseline at Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8Drug and alcohol use will be assessed using Timeline Followback procedures. Drug and alcohol use will be reported to a trained interviewer using a Timeline Followback calendar, facilitated by calendars distributed to participants.
Change in Blood Pressure from baseline at weeks 2, 5, 8, 9Change in baseline at Week 2, Week 5, Week 8, Week 9Systolic and Diastolic pressures will be collected.
Urinalysis - Week 8Week 8Standard urinalysis will be conducted, including urine pH, red cell count, white cell count, specific gravity, and bacteria content.
Change in State Anxiety Inventory (AI) from baseline at weeks 5, 8Change in baseline at Week 5, Week 8The State Anxiety Inventory will be used to quantify anxiety symptomatology. The measure is a 20-item, self-report, multiple-choice inventory, with scores ranging from 20-80.
Change in State Anger (ANG-S) from baseline at weeks 5, 8Change in baseline at Week 5, Week 8The Spielberger State Anger Inventory will be used to assess state anger. The measure is a 20-item, self-report, multiple-choice inventory, with scores ranging from 20-80.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026