Mifepristone Treatment of Alcohol Use Disorder



Status:Recruiting
Conditions:Psychiatric, Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 65
Updated:10/27/2018
Start Date:September 2014
End Date:June 2020
Contact:Susan Quello, B.A. B.S
Email:squello@scripps.edu
Phone:858-784-7327

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Glucocorticoid Antagonist Treatment of Alcohol Use Disorder

This is an 8-week, randomized, double-blind, placebo-controlled, 3 arm, parallel groups,
dose-ranging study of 1-week of treatment with mifepristone (0, 600, 1200 mg/d) given in
conjunction with 8 weeks of manual-guided counseling, and a follow-up visit at Week 12.


Inclusion Criteria:

- Male or female volunteers, 18-65 years of age

- Meets Diagnostic and Statistical Manual (DSM)-V criteria for current alcohol use
disorder of moderate or greater severity, defined by DSM-V as ≥ 4 symptoms

- Abstinent a minimum of 3 days (but not more than 30 days) prior to randomization

- In acceptable health in the judgment of the study physician, on the basis of
interview, medical history, physical exam, ECG, urine test and lab tests

- Females with childbearing potential must have a negative serum pregnancy test on the
screening visit and a negative urine pregnancy test at randomization and agree to use
non-hormonal effective birth control for the study duration and one month thereafter

Exclusion Criteria:

- A medical condition or chronic use of a medication that contraindicates the
administration of mifepristone

- Significant medical disorders or clinically significant findings on ECG (e.g.,
prolongation of the corrected QT interval,urine or blood tests that increase potential
risk or interfere with study participation as determined by the Study Physician. Note:
serum potassium below the normal range must be replaced to normal prior to
randomization; individuals with serum potassium outside the range of normal will not
be randomized

- Liver function tests more than 3 times the upper limit of normal or elevated bilirubin

- Female subjects with childbearing potential who are pregnant, nursing, or refuse to
use effective non hormonal birth control for the 1-week of medication administration
and one month thereafter

- Meets Diagnostic and Statistical Manual -V criteria for a major Axis I disorder
including mood or anxiety disorders or substance use disorders other than alcohol or
nicotine use disorders
We found this trial at
1
site
La Jolla, California 92037
Principal Investigator: Barbara J. Mason, Ph.D
Phone: 858-784-7327
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mi
from
La Jolla, CA
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