Alcoholism Clinical Trial
Official title:
Corticotropin-Releasing Hormone Receptor 1 (CRH1) Antagonism in Anxious Alcoholics
Background:
- Individuals who are dependent on alcohol often have feelings of anxiety, irritability,
anger, and depression. These feelings, as well as stress, may contribute to the risk of
relapse and continued drinking. Studies have shown that alcohol consumption increases the
activity of certain molecules in the brain known as CRH1 receptors, which are key to
producing the body s response to stress, and whose activation generates feelings of anxiety.
Researchers are interested in learning whether the experimental drug pexacerfont, which
blocks CRH1 receptors and has been studied in individuals with anxiety disorders and
depression, can lessen anxiety and craving for alcohol as part of alcohol-dependence
treatment.
Objectives:
- To determine the safety and effectiveness of pexacerfont as a treatment for
anxiety-related alcohol craving.
Eligibility:
- Individuals between 21 and 65 years of age who are alcohol-dependent and have problems
with anxiety.
Design:
- This study requires an inpatient admission to the NIH Clinical Center for approximately
1 month, with two additional study visits 1 week and 1 month after discharge from the
hospital.
- Participants will be screened with a medical history, physical examination, and blood
and urine tests.
- During the inpatient period, participants will have standard treatment for alcohol
dependence, including support and interventions from institute staff to address
cravings, anxiety, or other psychological problems. Participants will not receive
formal psychological treatment or psychiatric medications for anxiety, but will receive
training in relaxation techniques.
- Participants will be assigned to take either pexacerfont or placebo for 3 weeks. During
this time, participants will have the following procedures:
- Frequent blood tests.
- Rating scales and questionnaires about alcohol cravings and anxiety.
- Dexamethasone suppression test with frequent blood draws to study hormone response to
stress.
- Social stress test involving public speaking, followed by blood samples and
questionnaires on alcohol craving.
- Cue Reactivity (CR) session to study cravings and responses to alcohol-based cues.
- Functional magnetic resonance imaging scan to evaluate brain activity while taking the
medication or placebo.
- Participants will have two follow-up visits for additional blood tests and
questionnaires about the effects of the treatment ^.
Status | Completed |
Enrollment | 70 |
Est. completion date | July 2014 |
Est. primary completion date | July 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 21 Years to 65 Years |
Eligibility |
- INCLUSION CRITERIA: 1. Signed written informed consent: a. Patients must be competent to understand the nature of the study, sign the informed consent prior to any study-related procedures, agree to comply with the prescribed dosage regimens, agree to remain hospitalized at the NIH Clinical Center throughout the duration of the study and to return for follow-up visits as specified, and agree to communicate to study personnel about adverse events and concomitant medication use. 2. Target population: 1. DSM-IV diagnosis of alcohol dependence on SCID interview, 2. alcohol problems as primary complaint among substance use disorders, 3. alcohol use within the last month. 4. Spielberger trait anxiety inventory score > 39. 5. Right-handedness 3. Age and sex: 1. Men and women, ages 21 65 years. 2. Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) prior to enrollment, and agree to using an adequate method of contraception to avoid pregnancy for a period of 6 months beginning from first dose of randomized treatment. WOCBP include any female who has experienced menarche and who has not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or is not postmenopausal. Adequate methods of contraception are practicing complete abstinence from intercourse for two weeks prior to administration of study drug; having a male sexual partner(s) who is surgically sterilized (vasectomy with documentation of azoospermia) prior to inclusion; having a sexual partner(s) who is/are exclusively female; using oral contraceptives (either combined or progestogen only) with single-barrier method of contraception consisting of spermicide and condom or diaphragm; using double-barrier contraception, specifically, a condom plus spermicide and a female diaphragm or cervical cap; using an approved intrauterine device (IUD) with established efficacy. 3. Men, unless surgically sterilized (vasectomy with documentation of azoospermia), must agree to practicing abstinence or using barrier contraception, and not donate sperm, for a period of 6 months beginning from first dose of randomized treatment. EXCLUSION CRITERIA: 1. General: 1. Investigator site personnel directly affiliated with this study and/or their immediate families. Immediate family is defined as a spouse, parent, child or sibling, whether biological or legally adopted. 2. Employees of Bristol-Meyers Squibb (BMS) or immediate family of BMS employees. 3. Subjects with current participation in another clinical study in which the subject is or will be exposed to an investigational or non investigational drug or device; participation in a clinical study for an illness unrelated to alcohol use within the preceding month; or any previous participation in a trial involving pexacerfont or closely related compounds. 4. Inability or unwillingness to participate in an MR scan, including presence of ferromagnetic metallic objects in the body, or pronounced claustrophobia 5. Any medical or psychiatric condition or laboratory finding that, in the judgment of the investigator could adversely affect subject safety or study integrity. 6. Subjects who are unlikely or unable to complete this study because of impending or likely incarceration while on the protocol. 7. Subjects who are required to receive treatment by a court of law or involuntarily committed to treatment. 2. Sex and reproductive status: 1. Inability or unwillingness to practice contraception as described above 2. Women who are pregnant, breastfeeding, or planning to become pregnant within 6 months from the administration of first study drug dose. 3. Men who are planning to father a child within 6 months from the administration of the first study drug dose 3. Exclusionary psychiatric conditions: 1. Past or present diagnosis of schizophrenia, bipolar disease, or any psychotic disorder other than one determined to be substance induced; past or present diagnosis of dementia, or any other disorder which has led to a clinically significant cognitive impairment; any other psychiatric condition which at the present time requires, or in the past month has required pharmacological intervention other than standard withdrawal treatment as described in the NIAAA Assessment and Treatment Protocol (#05-AA-0121). 2. A personality disorder which, in the investigator s judgment could lead to non-compliance with study procedures. 3. Subjects, who in the investigator's judgment, pose a significant suicide risk. Evidence of serious suicide risk may include any history of suicidal behavior in the last 6 months and/or any suicidal ideation of type 4 or 5 on the Columbia Suicide Severity Rating Scale (C-SSRS) in the last 2 months. 4. Positive urine test for illegal drug use. 4. Exclusionary medical history and concurrent medical conditions: 1. Subjects with clinically significant thyroid pathology that would interfere with efficacy or safety evaluations, or who are undergoing treatment for their thyroid pathology (e.g., thyroid supplementation). 2. Subjects with adrenal or pituitary pathology as evidenced by medical history or suggested from abnormal screening laboratory tests. 3. Subjects with a significant history (as judged by the Investigator) of seizure disorder (e.g., epilepsy or withdrawal seizures), other significant neurological disorders (e.g., Parkinson s Disease, multiple sclerosis, stroke, neurodegenerative disease, cerebral palsy) or severe head trauma. 4. Subjects with active liver disease or a history of hepatic intolerance to medications that in the Investigator s judgment, is medically significant. 5. Subjects with a history of Diabetes Mellitus Type I and II or gastric bypass or reduction surgery. 6. Subjects with Human Immunodeficiency Virus (HIV) infection. 7. Subjects with difficulty swallowing tablets or capsules. 5. Exclusionary physical and laboratory test findings 1. QTc > 475 msec 2. Platelets less than or equal to 75,000/mm(3) 3. Hemoglobin less than or equal to 9g/dL 4. Neutrophils, Absolute less than or equal to 1000/mm(3) 5. SGOT (AST) > 3.0 times Upper Limit of Normal 6. SGPT (ALT) > 3.0 times Upper Limit of Normal 7. Bilirubin 2 times Upper Limit of Normal 8. Creatinine greater than or equal to 2mg/dL 9. Diastolic blood pressure > 105 mmHg 10. TSH > 1.6 times Upper Limit of Normal 11. Creatine kinase > 5 times Upper Limit of Normal 6. Prohibited treatments 1. Regular use of psychotropic medication (antidepressant, lithium, antipsychotic, anxiolytic, antiepileptic, opiates, or hypnotics), within one week prior to inclusion, with the exception of benzodiazepines administered within the NIAAA program as part of alcohol withdrawal treatment. Fluoxetine may not have been taken within 5 weeks, and depot antipsychotics may not have been taken within 12 weeks. 2. Any change in a non-excluded medication in the past 3 months. 3. Systemic intake of corticosteroids acutely within two weeks or chronically within the last 6 months (Topical hydrocortisone and inhaled corticosteroids are allowed). 4. Patients taking medications that are CYP3A4 inhibitors or inducers, should not be taking these medications for at least seven days prior to randomization and during the remainder of the study. |
Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | National Institutes of Health Clinical Center, 9000 Rockville Pike | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Institute on Alcohol Abuse and Alcoholism (NIAAA) |
United States,
Anton RF, Moak DH, Latham PK. The obsessive compulsive drinking scale: A new method of assessing outcome in alcoholism treatment studies. Arch Gen Psychiatry. 1996 Mar;53(3):225-31. Erratum in: Arch Gen Psychiatry 1996 Jul;53(7):576. — View Citation
Epstein DH, Preston KL, Stewart J, Shaham Y. Toward a model of drug relapse: an assessment of the validity of the reinstatement procedure. Psychopharmacology (Berl). 2006 Nov;189(1):1-16. Epub 2006 Sep 22. Review. — View Citation
Heilig M, Egli M. Pharmacological treatment of alcohol dependence: target symptoms and target mechanisms. Pharmacol Ther. 2006 Sep;111(3):855-76. Epub 2006 Mar 20. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 15 minutes prior to the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 5 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 15 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 30 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 45 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 60 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 75 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Alcohol Cue Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 90 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 15 minutes prior to the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 5 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 15 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 30 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 45 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 60 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 75 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
Primary | Alcohol Craving in Response to the Stress Script | Alcohol craving was measured using the Alcohol Urges Questionnaire (AUQ). The AUQ is an 8-item self-administered instrument that assesses craving for alcohol among alcohol users in the current context (i.e., right now). The score ranges from 8 (lowest craving value) to 56 (highest craving value). | 90 minutes after the beginning of script presentation, which occurred on Day 24, 25, or 26 of the treatment period | No |
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