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Completed

NCT Number: NCT00662571

Acamprosate: Genes Associated With Response

In 2004, acamprosate was approved in the U.S. for abstinence maintenance, by decreasing craving, in alcoholic patients who have undergone detoxification. while a new anti-craving drug was encouraging, only 36.1% of the subjects treated with acamprosate remained abstinent for 6 months. Having the ability to identify treatment responsive individuals would have a major impact on the use of acamprosate.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Mayo Clinic

Rochester, Minnesota, 55905, United States

About this study

The primary objective of this pharmacogenomic probe study of acamprosate is to identify genetic variations that predict response. Our hypothesis is that effective acamprosate response in alcohol dependent subjects may be influenced by genetically controlled variation in the functionality of the N-methyl-D-aspartate receptor (NMDA) and/or the type 5 metabotropic glutamate receptor (mGluR5). Hypothesis confirmation could lead to development of effective individualized treatment recommendations for alcohol dependent patients based on pharmacogenomically relevant genetic variations.

The general goal is to identify genetic polymorphic variants that differentiate subjects continuously abstinent for six months while taking acamprosate from relapsed subjects. The initial analysis will determine whether any of ten polymorphisms in four target genes (GRIN1, GRIN2A and GRIN2B that code for the NMDA receptor and GRM5 that codes for the type mGluR5 receptor) are associated with successful abstinence. Subsequent analyses will examine whether variation in a comprehensive set of 383 linkage disequilibrium haplotype tagged single nucleotide polymorphisms of these four genes predicts successfully abstinent subjects.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or females, Age 18-80.
  • 2. Primary diagnosis of alcohol dependence based on DSM-IV-TR criteria and determined by the Psychiatric Research Interview for Substance and Mental Disorders (PRISM) (stable mood and anxiety disorders will not be exclusionary).
  • Prior enrollment in the IRB approved protocol "Developing a DNA Repository for Genomic Studies of Addiction: A Pilot Study".

Exclusion criteria

  • Inability to provide informed consent.
  • Inability to speak English.
  • History of hypersensitivity or allergic reaction to acamprosate.
  • Moderate to severe renal impairment, as determined by a creatinine level > 1.5 mg/dL.
  • Diagnosis of primary biliary cirrhosis, chronic active hepatitis, and drug-induced hepatic insufficiency, as noted in the medical record.
  • Women who are pregnant, lactating, or are planning to become pregnant during the next year.
  • Any unstable active medical or additional psychiatric condition as determined by the investigator.
  • Active suicidal ideation as determined by responses provided during PRISM or as determined by the investigator.

Treatment and study plan

acamprosate

Drug

acamprosate 333mg tabs, 2tabs 3times per day = 1998mg/day

Other names: Campral is the brand name of acamprosate.

Primary outcomes

  1. Aim 1: To determine the relationship between genetically determined variation in the NMDA receptor and treatment response to acamprosate.

    Time frame: 6 months

Secondary outcomes

  1. Aim 2: To determine the relationship between genetically determined variation in the mGluR5 receptor and treatment response to acamprosate.

    Time frame: 6months

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • Samuel C. Johnson Foundation

Registry information

Official study title

A Probe Study of Acamprosate: Genes Associated With Response

Acronym: ACAM

Important dates

Study start
2008
Primary completion
2013
Study completion
2013
First posted
Apr 21, 2008
Registry last updated
Mar 22, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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