Corticotropin-Releasing Hormone Receptor 1 (CRH1) Antagonism in Anxious Alcoholics^

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Institute on Alcohol Abuse and Alcoholism (NIAAA) )
ClinicalTrials.gov Identifier:
NCT01227980
First received: October 22, 2010
Last updated: July 11, 2014
Last verified: June 2014
  Purpose

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 ^.

Condition Intervention Phase
Alcohol-Related Disorders
Alcohol Dependence
Alcoholism
Anxiety Disorder
Drug: Pexacerfont
Drug: Placebo
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacodynamics Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Corticotropin-Releasing Hormone Receptor 1 (CRH1) Antagonism in Anxious Alcoholics

Resource links provided by NLM:


Further study details as provided by National Institutes of Health Clinical Center (CC):

Primary Outcome Measures:
  • Cravings for alcohol on the combined social stress-alcohol cue challenge session, brain responses to emotional alcohol-assocaiated and motivational stimuli on the fMRI session. [ Time Frame: 3 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Spontaneous psychopathology and craving ratings over time. [ Time Frame: Outcome measured biweekly over 3 week period (6 total assessments) ] [ Designated as safety issue: No ]

Enrollment: 70
Study Start Date: October 2010
Study Completion Date: July 2014
Primary Completion Date: July 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Pexacerfont Drug: Pexacerfont
300 mg, orally, once/day during week 1, 100 mg, orally, once/day during weeks 2 and 3.
Placebo Comparator: Placebo Drug: Placebo
300 mg, orally, once/day during week 1, 100 mg, orally, once/day during weeks 2 and 3.

Detailed Description:

OBJECTIVE :

To evaluate pexacerfont, an orally available, brain penetrant selective CRH1 antagonist for its ability to modulate emotional and motivational processes in anxious, recently detoxified alcohol dependent patients.

STUDY POPULATION:

Up to 70 anxious, alcohol dependent subjects, aged 21-65 years will be enrolled to complete the study in 50 patients.

DESIGN

Subjects will be inpatients and enter the present protocol once withdrawal treatment, if needed, is completed. They will undergo interviews for construction of guided imagery scripts during a 3 day pre-treatment phase, after which they will receive randomized double blind treatment with active medication or placebo for 23 days, followed by a 3 day post-treatment inpatient monitoring phase, and two follow-up outpatient visits. While hospitalized, repeated measures of spontaneous craving for alcohol, ratings of psychopathology, and blood chemistry including cortisol will be obtained over this time. During the second week of treatment, craving responses will be assessed in a challenge session that combines a social stressor and exposure to physical alcohol cues. During the final week, three sessions of guided imagery will be carried out, on separate days and in a counter-balanced order, exposing the subject to personalized stress-, alcohol- or neutral condition associated stimuli. The final week will also include an fMRI session with emotional and motivational tasks, on a day separate from any guided imagery session. Subjects will remain hospitalized throughout the study, will remain on the unit for a 3 day post-medication monitoring period, and will return for follow up app. 1 and 4 weeks following completion of randomized treatment.

OUTCOME MEASURES

The primary outcome will be craving for alcohol on guided imagery challenge sessions. Secondary outcomes will include craving as measured in the combined social stress alcohol cue challenge session, spontaneous craving and psychopathology ratings repeatedly measured on the inpatient unit over time. Exploratory blood biomarkers and brain responses to positive and negative affective stimuli on the fMRI session will also be obtained.

  Eligibility

Ages Eligible for Study:   21 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria
  • 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 eqaul to 9g/dL
    4. Neutrophils, Absolute less than or eqaul 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 eqaul 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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01227980

Locations
United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States, 20892
Sponsors and Collaborators
Investigators
Principal Investigator: Markus A Heilig, M.D. National Institute on Alcohol Abuse and Alcoholism (NIAAA)
  More Information

Additional Information:
Publications:
Responsible Party: National Institutes of Health Clinical Center (CC) ( National Institute on Alcohol Abuse and Alcoholism (NIAAA) )
ClinicalTrials.gov Identifier: NCT01227980     History of Changes
Other Study ID Numbers: 110010, 11-AA-0010
Study First Received: October 22, 2010
Last Updated: July 11, 2014
Health Authority: United States: Federal Government

Keywords provided by National Institutes of Health Clinical Center (CC):
Addiction
Alcohol
Alcohol Treatment
Alcoholics
Alcohol Dependence
Anxiety Disorder
Alcoholism

Additional relevant MeSH terms:
Alcoholism
Anxiety Disorders
Alcohol-Related Disorders
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders
Adrenocorticotropic Hormone
Corticotropin-Releasing Hormone
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on August 21, 2014