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CompletedNCT01151813Updated Aug 18, 2020Results posted

Human Behavioral Pharmacology Laboratory (HBPL) Study of Varenicline's Impact on Cocaine and Alcohol Craving

A Phase 2 interventional study of Varenicline and Placebo in Alcohol Dependence and Cocaine Dependence, sponsored by University of Pennsylvania. Completed at 1 site in United States. Open to participants aged 21 Years to 65 Years. Per ClinicalTrials.gov, last updated 2020-08-18.

Sponsored by University of Pennsylvania · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
21 Years to 65 Years
Sex
All
01

Study summary

This is a Phase II within-subjects double-blind placebo-controlled human laboratory study. The purpose of the study is to determine the efficacy of varenicline (Chantix) for reducing cue-induced cocaine and alcohol craving.

02

Conditions studied

  • Alcohol Dependence
  • Cocaine Dependence
03

In context

Alcoholism

1,606 studies on the registry are indexed under Alcoholism; 329 are open to participants now.

This study's enrollment of 15 is below the median of 87 across 1,371 interventional studies indexed under Alcoholism.

Browse Alcoholism studies →

Lead sponsor

University of Pennsylvania is the lead sponsor of 1,635 studies on the registry; 239 are open to participants now.

Of its 154 completed or terminated interventional studies of FDA-regulated products, 104 (68%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Subject is male or female and is between 21 and 65 years of age.
  2. The subject has used cocaine, alcohol, or cocaine and alcohol at least once per month for at least the past year, and has used cocaine, alcohol, or cocaine and alcohol within the past 30 days.
  3. Live within a commutable distance of the Treatment Research Center (TRC) at the Penn/VA Center for Studies of Addiction, University of Pennsylvania. We define this to be a distance within the service area of Septa, within an hour drive, or a distance that both the patient and Principal Investigator (PI) find acceptable.
  4. Understands and signs the informed consent.

Exclusion criteria

Exclusion Criteria:

  1. Meets DSM-IV criteria for current dependence on any substance other than nicotine, cocaine, alcohol or marijuana.
  2. Subjects who are currently taking anti-depressant medications (e.g., SSRIs such as citalopram)
  3. Patients who are diagnosed during screening with clinical depression using the HAM-D rating scale and present with a score >10.
  4. Subjects who are diagnosed with anxiety as diagnosed using the HAM-A anxiety scale with a score >17
  5. Subjects who meet current- or lifetime DSM-IV criteria for a psychotic disorder (e.g., schizophrenia)
  6. Requires treatment with any psychotropic medication (e.g., antidepressant, antipsychotic, benzodiazepine, or mood stabilizing medication).
  7. Subjects who test positive on the urine drug screen for any illicit drugs other than cocaine and marijuana during screening will be allowed a single retest. Those individuals who test positive for amphetamine during screening, given that they provide a copy of a prescription, will only be included if they can safely discontinue amphetamine use for the duration of the study. Subjects will need to provide a urine free of all illicit drugs other than cocaine and marijuana at study onset to be randomized. Subjects who test positive for any drugs other than marijuana prior to a study session will be allowed a single retest and a chance to reschedule their session. If the subject tests positive for any drug other than marijuana at the retest, their participation in the study will be terminated.
  8. Use of any investigational medication within the past 30 days.
  9. Concomitant use of any one of the following drugs or classes of drugs:

    Anti-depressant drugs such as citalopram, fluoxetine; antipsychotic drugs such as haloperidol; benzodiazepines or other anxiolytic medications; Antihypertensive drugs such as Reserpine, Verapamil; Blood thinners Medications used to treat respiratory diseases such as theophylline; Trimethoprim; Cimetidine; Antiepileptic drugs (AEDs) such as phenytoin or valproic acid.

  10. Patients with a known hypersensitivity to varenicline.
  11. Patients with severe unstable or serious medical illness such as a seizure disorder, unstable cerebrovascular disease, bronchospastic disease, hyperthyroidism, or diabetes mellitus.
  12. Patients with known AIDS or other serious illnesses that may require hospitalization during the study.
  13. Female subjects who are pregnant, plan to become pregnant, are currently lactating, or are of child-bearing potential and are not using acceptable methods of birth control; acceptable methods of birth control would include:

    1. Barrier method (diaphragm or condom)
    2. Intrauterine progesterone contraceptive system
    3. Levonorgesterel implant
    4. Medroxyprogesterone acetate contraceptive injection, or
    5. Oral contraceptives.
  14. Patients with impaired renal function, as indicated by corrected creatinine clearance below 60 ml/min as determined by the modified Cockcroft equation (CDC, 1986).
  15. An unacceptable liver panel (liver function tests; LFTs) that may be indicative of hepatic dysfunction.
  16. Clinical laboratory tests (e.g., CBC, blood chemistries, urinalysis) outside normal limits, as determined by PI.
  17. History of significant heart disease or dysfunction (e.g., an arrhythmia which required medication, Wolff Parkinson -White Syndrome, angina pectoris, documented history of myocardial infarction, heart failure).
  18. Electrocardiography (EKG) indicative of 1st degree heart block, sinus tachycardia, left-axis deviation, non-specific ST or T-wave changes.
  19. History of chest pain associated with cocaine use that prompted a visit to a physician.
  20. Any medical or psychological condition that could jeopardize the subject's safe participation in the trial as determined by the PI.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
15 participants (actual)

Study arms

  • Active comparator
    Varenicline

    Varenicline, oral administration for 1 week

    Drug: Varenicline

  • Placebo comparator
    Placebo

    Placebo, oral administration for 1 week

    Drug: Placebo

Interventions

  • DrugVarenicline

    Varenicline, oral target dose of 1.0 mg BID, one week titration.

    Also known as: Chantix

  • DrugPlacebo

    Placebo

06

What researchers measure

Primary outcomes

  1. Visual Analog Scale Alcohol Craving

    Visual Analog Scale specific to alcohol craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for alcohol. 0 indicates no craving 100 indicates strongest possible craving.

    Time frame: average value over one week

  2. Visual Analog Scale Cocaine Craving

    Visual Analog Scale specific to cocaine craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for cocaine. 0 indicated no craving, 100 represents the worst craving imaginable. The subject draws a hatch mark line along the line closer to where there current craving is rated.

    Time frame: average value over one week

  3. Visual Analog Scale Alcohol Craving 2

    Visual Analog Scale specific to alcohol craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for alcohol. 0 indicated no craving, 100 represents the worst craving imaginable. The subject draws a hatch mark line along the line closer to where there current craving is rated. Closer to the 0 means less craving, closer to the 100 means more craving

    Time frame: average over one week

  4. Visual Analog Scale Cocaine Craving 2

    Visual Analog Scale specific to cocaine craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for cocaine. 0 indicated no craving, 100 represents the worst craving imaginable. The subject draws a hatch mark line along the line closer to where there current craving is rated. Closer to the 0 means less craving, closer to the 100 means more craving

    Time frame: average over one week

07

Results

Posted Aug 18, 2020

Participant flow

Period 1
Participant flow — Period 1
MilestoneVarenicline First, Then PlaceboPlacebo First, Then Varenicline
Started87
Completed87
Not completed00
Period 2
Participant flow — Period 2
MilestoneVarenicline First, Then PlaceboPlacebo First, Then Varenicline
Started87
Completed87
Not completed00

Outcome measures

PrimaryVisual Analog Scale Alcohol Craving

Visual Analog Scale specific to alcohol craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for alcohol. 0 indicates no craving 100 indicates strongest possible craving.

Time frame:
average value over one week
Reported as:
Mean · units on a scale
Visual Analog Scale Alcohol Craving
units on a scaleVarenicline First, Then PlaceboPlacebo First, Then Varenicline
Visual Analog Scale Alcohol Craving20 (0 to 100)35 (0 to 100)
Statistical analysis
  • Varenicline First, Then Placebo vs Placebo First, Then Varenicline · t-test, 2 sided · p = .02
PrimaryVisual Analog Scale Cocaine Craving

Visual Analog Scale specific to cocaine craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for cocaine. 0 indicated no craving, 100 represents the worst craving imaginable. The subject draws a hatch mark line along the line closer to where there current craving is rated.

Time frame:
average value over one week
Reported as:
Mean · units on a scale
Visual Analog Scale Cocaine Craving
units on a scaleVarenicline First, Then PlaceboPlacebo First, Then Varenicline
Visual Analog Scale Cocaine Craving25 (0 to 100)65 (0 to 100)
Statistical analysis
  • Varenicline First, Then Placebo vs Placebo First, Then Varenicline · t-test, 2 sided · p = 0.03
PrimaryVisual Analog Scale Alcohol Craving 2

Visual Analog Scale specific to alcohol craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for alcohol. 0 indicated no craving, 100 represents the worst craving imaginable. The subject draws a hatch mark line along the line closer to where there current craving is rated. Closer to the 0 means less craving, closer to the 100 means more craving

Time frame:
average over one week
Reported as:
Mean · units on a scale
Visual Analog Scale Alcohol Craving 2
units on a scaleVarenicline First, Then PlaceboPlacebo First, Then Varenicline
Visual Analog Scale Alcohol Craving 235 (0 to 100)55 (0 to 100)
Statistical analysis
  • Varenicline First, Then Placebo vs Placebo First, Then Varenicline · t-test, 2 sided · p = 0.03
PrimaryVisual Analog Scale Cocaine Craving 2

Visual Analog Scale specific to cocaine craving. The VAS has a 100 mm line anchored by 0 and 100. Participants mark the line to indicate how strong their craving is for cocaine. 0 indicated no craving, 100 represents the worst craving imaginable. The subject draws a hatch mark line along the line closer to where there current craving is rated. Closer to the 0 means less craving, closer to the 100 means more craving

Time frame:
average over one week
Reported as:
Mean · units on a scale
Visual Analog Scale Cocaine Craving 2
units on a scaleVarenicline First, Then PlaceboPlacebo First, Then Varenicline
Visual Analog Scale Cocaine Craving 265 (0 to 100)80 (0 to 100)
Statistical analysis
  • Varenicline First, Then Placebo vs Placebo First, Then Varenicline · t-test, 2 sided · p = 0.04

Adverse events

Collected over through study completion, two weeks. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Varenicline0/15 (0%)0/15 (0%)3/15 (20%)
Placebo0/15 (0%)0/15 (0%)1/15 (6.7%)
Most frequent other events
Most frequent other events
EventVareniclinePlacebo
FlatulenceGastrointestinal disorders3/151/15

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Within-subjects Design
<=18 years0
Between 18 and 65 years15
>=65 years0
Sex: Female, Male
Sex: Female, Male(Participants)Within-subjects Design
Female3
Male12
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Within-subjects Design
Hispanic or Latino1
Not Hispanic or Latino14
Unknown or Not Reported0
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Within-subjects Design
American Indian or Alaska Native0
Asian0
Native Hawaiian or Other Pacific Islander0
Black or African American12
White3
More than one race0
Unknown or Not Reported0
Region of Enrollment
Region of Enrollment(participants)Within-subjects Design
United States15
08

Study locations

1 site
  • University of Pennsylvania, Treatment Research Center
    Philadelphia, Pennsylvania 19104, United States
09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 18, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT01151813
Lead sponsor
University of Pennsylvania
Collaborators
National Institute on Drug Abuse (NIDA)
Responsible party
Sponsor
First posted
Jun 28, 2010
Start date
Jul 2010
Primary completion
Aug 2013
Completion
Dec 2013
Results posted
Aug 18, 2020
Last update
Aug 18, 2020

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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