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Human Behavioral Pharmacology Laboratory Study of Varenicline's Impact on Cocaine Reinforcement

Primary Purpose

Cocaine Dependence

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Varenicline
Sponsored by
Jennifer Plebani
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cocaine Dependence

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria

  1. Males and females, 18 to 60 years old.
  2. Recreational users of cocaine reporting at least six instances of cocaine use in the past 12 months and at least one use in 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:

  1. Current DSM-IV diagnosis of any psychoactive substance dependence other than nicotine dependence, as determined by the Structured Clinical Interview for the DSM (SCID).
  2. Current severe psychiatric symptoms (e.g., psychosis, dementia, suicidal or homicidal ideation, mania or depression requiring anti-depressant therapy) as diagnosed using the SCID, the Hamilton Anxiety Rating Scale (Ham A), and Hamilton Ration Scale for Depression (HAM-D).
  3. Individuals scoring > 10 on the Hamilton Rating Scale for Depression (HAM-D).
  4. Use of any investigational medication within the past 30 days.
  5. Concomitant treatment with psychotropic medications.
  6. Concomitant use of any one of the following drugs or classes of drugs:

    • Reserpine
    • Verapamil
    • theophylline,
    • trimethoprim,
    • cimetidine,
    • haloperidol,
    • benzodiazepines, or
    • antiepileptic drugs (AEDs).
  7. Patients with a known hypersensitivity to varenicline.
  8. Patients with severe concurrent illnesses such as bronchospastic disease, hyperthyroidism, diabetes mellitus.
  9. Patients with known AIDS or other serious illnesses that may require hospitalization during the study.
  10. Female subjects who are pregnant or lactating, or female subjects of child-bearing potential who are not using acceptable methods of birth control; acceptable methods of birth control include:

    • Barrier method (diaphragm or condom) with spermicide
    • Intrauterine progesterone contraceptive system
    • Levonorgesterel implant
    • Medroxyprogesterone acetate contraceptive injection, or
    • Oral contraceptives.
  11. Patients with impaired renal function, as indicated by corrected creatinine clearance below 60 ml/min/70 kg as determined by the modified Cockcroft equation (CDC, 1986).
  12. An unacceptable liver panel (liver function tests; LFTs) that may be indicative of hepatic dysfunction.
  13. Clinical laboratory tests (e.g., CBC, blood chemistries, urinalysis) outside normal limits.
  14. 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).
  15. Electrocardiography (EKG) indicative of 1st degree heart block, sinus tachycardia, left-axis deviation, non-specific ST or T-wave changes.
  16. History of chest pain associated with cocaine use that prompted a visit to a physician.

Sites / Locations

  • University of Pennsylvania, Treatment Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Varenicline

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Varenicline's impact on reinforcing effects of cocaine
The primary aim of this study is to examine what impact sub-chronic dosing with varenicline has on the subjective and reinforcing effects of cocaine and on cocaine self-administration in cocaine experienced individuals.

Secondary Outcome Measures

Full Information

First Posted
June 11, 2010
Last Updated
October 14, 2013
Sponsor
Jennifer Plebani
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01143857
Brief Title
Human Behavioral Pharmacology Laboratory Study of Varenicline's Impact on Cocaine Reinforcement
Official Title
Human Behavioral Pharmacology Laboratory Study of Varenicline's Impact on Cocaine Reinforcement
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Withdrawn
Study Start Date
June 2010 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jennifer Plebani
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cocaine use, abuse and dependence is a public health problem that is directly responsible for hundreds of billions of dollars in health care expenditures per year. Relapse rates to cocaine use are high, creating a pressing need to develop effective therapies for cocaine dependence. The proposed research will focus on investigating the determinants and consequences of cocaine dependence via measurement of physiological, behavioral and subjective effects of acute doses of cocaine in healthy non-drug dependent human volunteers in the laboratory, and through examination of the effects of pharmacotherapies on the above effects of cocaine. This study will examine cocaine-derived reinforcement under week-long sub-chronic varenicline (Chantix) dosing, and under placebo conditions. The study is a within-subjects crossover design using 24 subjects. Subjects will be screened and consented into the study at the Treatment Research Center (TRC). Study visits where behavioral and physiological outcome data will be obtained will be conducted at the Clinical and Translational Research Center (CTRC) of the Hospital of the University of Pennsylvania. Subjects will be outpatients for this trial, with CTRC sessions scheduled at least one week apart.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine Dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Varenicline
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Varenicline
Intervention Description
Varenicline 2.0 mg/day or Placebo
Primary Outcome Measure Information:
Title
Varenicline's impact on reinforcing effects of cocaine
Description
The primary aim of this study is to examine what impact sub-chronic dosing with varenicline has on the subjective and reinforcing effects of cocaine and on cocaine self-administration in cocaine experienced individuals.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria Males and females, 18 to 60 years old. Recreational users of cocaine reporting at least six instances of cocaine use in the past 12 months and at least one use in the past 30 days. 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. Understands and signs the informed consent. Exclusion Criteria: Current DSM-IV diagnosis of any psychoactive substance dependence other than nicotine dependence, as determined by the Structured Clinical Interview for the DSM (SCID). Current severe psychiatric symptoms (e.g., psychosis, dementia, suicidal or homicidal ideation, mania or depression requiring anti-depressant therapy) as diagnosed using the SCID, the Hamilton Anxiety Rating Scale (Ham A), and Hamilton Ration Scale for Depression (HAM-D). Individuals scoring > 10 on the Hamilton Rating Scale for Depression (HAM-D). Use of any investigational medication within the past 30 days. Concomitant treatment with psychotropic medications. Concomitant use of any one of the following drugs or classes of drugs: Reserpine Verapamil theophylline, trimethoprim, cimetidine, haloperidol, benzodiazepines, or antiepileptic drugs (AEDs). Patients with a known hypersensitivity to varenicline. Patients with severe concurrent illnesses such as bronchospastic disease, hyperthyroidism, diabetes mellitus. Patients with known AIDS or other serious illnesses that may require hospitalization during the study. Female subjects who are pregnant or lactating, or female subjects of child-bearing potential who are not using acceptable methods of birth control; acceptable methods of birth control include: Barrier method (diaphragm or condom) with spermicide Intrauterine progesterone contraceptive system Levonorgesterel implant Medroxyprogesterone acetate contraceptive injection, or Oral contraceptives. Patients with impaired renal function, as indicated by corrected creatinine clearance below 60 ml/min/70 kg as determined by the modified Cockcroft equation (CDC, 1986). An unacceptable liver panel (liver function tests; LFTs) that may be indicative of hepatic dysfunction. Clinical laboratory tests (e.g., CBC, blood chemistries, urinalysis) outside normal limits. 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). Electrocardiography (EKG) indicative of 1st degree heart block, sinus tachycardia, left-axis deviation, non-specific ST or T-wave changes. History of chest pain associated with cocaine use that prompted a visit to a physician.
Facility Information:
Facility Name
University of Pennsylvania, Treatment Research Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

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Human Behavioral Pharmacology Laboratory Study of Varenicline's Impact on Cocaine Reinforcement

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