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Pharmacogenetic Response to Naltrexone For Alcohol Dependence

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
David Oslin, University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT00831272
First received: January 26, 2009
Last updated: June 30, 2014
Last verified: June 2014
  Purpose

The aims of the study are to test for treatment outcome differences in alcohol dependent subjects randomly assigned to 12 weeks of treatment with NTX (50mg/day) or placebo among those with one or two copies of the Asp40 allele of the mu-opioid receptor compared to those homozygous for the Asn40 allele. Thus, the design of the study is a 2X2 cell double-blind randomization to NTX or placebo stratified by genotype. To meet these aims, 150 alcohol dependent outpatients with one or two copies of the Asp40 variant of the mu-opioid receptor and 190 subjects homozygous for the Asn40 variant will be recruited across the four participating sites.


Condition Intervention Phase
Alcohol Dependence
Drug: naltrexone
Drug: Placebo
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Pharmacogenetic Response to Naltrexone for Alcohol Dependence

Resource links provided by NLM:


Further study details as provided by University of Pennsylvania:

Primary Outcome Measures:
  • Clinical response to naltrexone, as measured by a reduction in the number of heavy drinking days (as defined by >5 drinks/day for males; >4 for females) during the 12 weeks of the trial. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Experience of a "high" from alcohol consumption as measured on the Biphasic Alcohol Effects Scale, and levels of alcohol craving over time as measured on the Penn Alcohol Craving Scale. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Enrollment: 221
Study Start Date: January 2009
Study Completion Date: January 2014
Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
50mg/day of naltrexone
Drug: naltrexone
50mg/day
Other Name: ReVia
Placebo Comparator: 2
Placebo
Drug: Placebo
Placebo
Other Name: sugar pill

Detailed Description:

Despite the well established efficacy of naltrexone, there are significant variations in individual responses to naltrexone. A critical question remains: under what circumstances and for which patients will naltrexone (NTX) be most beneficial? Recent work at our center provides evidence that the mu-opioid receptor (OPRM1) gene polymorphism A118G (Asn40Asp) imparts a significant change in treatment response. We have shown that patients with 1-2 copies of the Asp40 variant have significantly better treatment responses than patients with Asn40 variant (absence of heavy drinking -73.9% v/s 49% response). To further consolidate our knowledge, we wish to test the relationship between A118G polymorphism and the response to treatment with naltrexone. This work is focused on subjects of European or Asian descent as the A118G polymorphism occurs in less than 1% of those of African descent.

The study consists of 12 weeks of outpatient treatment with 50mg/day of naltrexone or placebo. Up to 340 subjects will be recruited across four sites. The inclusion criteria include adult males and females of European or Asian descent with DSM-IV diagnosis of alcohol dependence and heavy drinking per TLFB criteria. Patients with major psychiatric disorders or on psychotropic medications, other substance dependence problems (except nicotine), severe cognitive impairment, active suicidal/homicidal thoughts and serious medical conditions (including liver disorders) will be excluded.

The ultimate aim of this line of investigation is to further establish a genetic link between alcohol dependence and treatment by defining an endophenotype associated with treatment response.

Based upon these very promising findings, the aim of this study is to examine prospectively the interaction between a functional polymorphism of the mu-opioid receptor (A+118G (Asn40Asp)) and response to treatment with naltrexone. A secondary aim of this study is to examine the role of the Asp40 allele in alternating the subjective effects from alcohol use in alcohol dependent individuals that have been demonstrated in human laboratory experiments.

We hypothesize that naltrexone - but not placebo - will produce a greater clinical response during the 12 weeks of the trial in subjects with one or two copies of the Asp40 variant ("Asp40 positives") than in subjects homozygous for the Asn40 allele. Response to naltrexone will be measured by a reduction in the number of heavy drinking days (as defined by >5 drinks/day for males; >4 for females) during the 12 weeks of the trial.

We also expect that there will be an interaction between medication and genotype such that, as compared to the groups on placebo or homozygous for Asn40, Asp40 positive subjects randomized to naltrexone will report less "high" from alcohol consumption (on the Biphasic Alcohol Effects Scale), and the lowest levels of alcohol craving over time (on the Penn Alcohol Craving Scale).

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Participant is male or female, 18 years of age or older, and of European or Asian descent.
  2. Participant has a current DSM-IV diagnosis of alcohol dependence using the SCID/MINI.
  3. The participant has signed a witnessed informed consent form.
  4. Participant meets the following drinking criteria as measured by the Timeline Follow Back (TLFB): a. Drinks at least an average of 21 drinks/wk in the 60-day period prior to intake and b. Has 2 or more days of heavy drinking (defined as 5 or more drinks per day in males, 4 or more in females) in this same pre-treatment period.
  5. Participant has at least 48 hours of abstinence, as determined by subject report and breathalyzer measure immediately prior to randomization.
  6. Participant scores below 8 on the Clinical Inventory of Withdrawal from Alcohol (CIWA) prior to starting Naltrexone.
  7. Participant has adequate vision, hearing and ability to communicate to allow study participation.
  8. Participant is able to speak, print and understand English.

Exclusion Criteria:

  1. Participant meets DSM-IV criteria for dependence on any substance other than alcohol or nicotine in the last 6 months.
  2. Participant has tested positive on the urine drug screen for opioids, benzodiazepines, or cocaine at the screening visit. Presence of THC is allowable.
  3. Participant has a current or lifetime DSM-IV diagnosis of bipolar affective disorder, schizophrenia, or any psychotic disorder.
  4. Participant has presence of unstable or serious medical illness such as a recent stroke, idiopathic seizure disorder, or cardiac disease.
  5. Participant has severe liver disease (SGPT (ALT) or SGOT (AST) of at least 3 times normal value at the time of randomization or an elevated Total Bilirubin level without evidence of Gilbert's Syndrome.
  6. Participant has taken any psychotropic medications (including disulfiram) regularly within the last seven days (14 for fluoxetine) prior to randomization or needs immediate treatment with a psychotropic medication (antidepressant, antipsychotic, benzodiazepine, or mood stabilizing medication). EXCEPTIONS: Zolpidem and ramelteon used sparingly if necessary for sleep; Oxazepam for alcohol detoxification; Seizure disorder medications.
  7. Participant is over the age of 64 and has evidence of severe cognitive impairment as evidenced by a Mini-mental status exam (MMSE) score < 24.
  8. Participant meets DSM-IV criteria for current major depression (non-substance induced), PTSD, or panic disorder.
  9. Participant has suicidal or homicidal ideation necessitating inpatient hospitalization.
  10. Participant is a pre-menopausal female who is pregnant, nursing, or not using a reliable method of contraception.
  11. Participant is over age 64 and has evidence of severe cognitive impairment as evidenced by a Mini-mental status exam (MMSE) score less than 20.12. Participant is of African descent.
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00831272

Locations
United States, Pennsylvania
Geisinger Medical Center
Danville, Pennsylvania, United States, 17822
Philadelphia VA Medical Center
Philadelphia, Pennsylvania, United States, 19104
University of Pennsylvania Treatment Research Center
Philadelphia, Pennsylvania, United States, 19104
VA Pittsburgh Healthcare System
Pittsburg, Pennsylvania, United States, 15206
Sponsors and Collaborators
David Oslin
Investigators
Principal Investigator: Adam J Gordon, MD, MPH VA Pittsburg Healthcare System
Principal Investigator: David Oslin, MD University of Pennsylvania/ Philadelphia VA Medical Center
  More Information

Additional Information:
No publications provided

Responsible Party: David Oslin, Sponsor-Investigator, University of Pennsylvania
ClinicalTrials.gov Identifier: NCT00831272     History of Changes
Other Study ID Numbers: 807991, RO1AA017164
Study First Received: January 26, 2009
Last Updated: June 30, 2014
Health Authority: United States: Food and Drug Administration
United States: Institutional Review Board

Additional relevant MeSH terms:
Alcoholism
Alcohol-Related Disorders
Chemically-Induced Disorders
Mental Disorders
Substance-Related Disorders
Naltrexone
Central Nervous System Agents
Narcotic Antagonists
Peripheral Nervous System Agents
Pharmacologic Actions
Physiological Effects of Drugs
Sensory System Agents
Therapeutic Uses

ClinicalTrials.gov processed this record on November 20, 2014