An 8 Week Open-Label Study to Evaluate the Efficacy and Safety of Acamprosate Calcium (Campral) as Augmentation Therapy in Patients With Anxiety Symptoms Who Are Only Partial Responders to SSRI or SNRI Antidepressants

NCT00591565 | Completed Results

• 1 other identifier: CMP-MD-15
• Study Type: interventional
• Target: 13
• Locations: 1 country
• Sites: 1

Brief Summary

This study is designed to evaluate anxious patients who are only partially responsive to typical SSRI or SNRI anti-anxiety medication therapy. Patients who are less than 50% anxiety-alleviated on their SSRI medication will be asked to join the study and be placed on Acamprosate as well. This type of add-on therapy is common in outpatient psychiatric care. This is a rater-blinded, patient open-label, non-placebo prospective study, where all subjects will receive Acamprosate for 8 weeks. This study would be the first to date in this treatment-resistant patient population, as the investigators will utilize the a comprehensive set of rating scales in order to best categorize patient responses in regards to anxiety, co-occurring depression, sleep disorders, alcohol use, and social functioning with this drug. This study may be pivotal to the initiation of future double-blind, placebo-controlled studies for this agent

Conditions

Anxiety

Keywords

Anxiety; SSRI; SNRI; Acamprosate

Outcome Measures

Primary Outcomes (1)

• Change From Baseline at 8 Weeks in the HAM-A Scale

  this is a validated clinician administered scale that can range from 0-44 (mild to severe illness).

  baseline and 8wk

Study Arms (1)

1

EXPERIMENTAL

acamprosate tablets

Drug: Acamprosate

Interventions

Acamprosate DRUG

acamprosate 333mg tab, 3 by mouth 3 times a day

1

Eligibility Criteria

• Age: 18 Years - 64 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Written informed consent is obtained.
• The patient is English-speaking and 18 through 64 years of age inclusive.
• The patient meets the DSM-IV criteria for anxiety disorder as determined by the MINI and psychiatric evaluation. These include: Post-Traumatic Stress Disorder (PTSD), General Anxiety Disorder (GAD), Social Anxiety, and Panic Disorder.
• The patient is currently taking a monotherapy SSRI for ≥ 6 weeks and on a stable, adequate therapeutic for ≥ 4 weeks and remains anxiety symptomatic
• The patient has a total score of at least 16 on the HAM-A scale
• The patient has a score of at least 7 on the HADS anxiety subscale score at the screening and baseline visits.
• The patient has a CGI-S rating of 4 or higher at screening
• The patient is in good health as determined by a medical and psychiatric history, medical examination, and cannot have major medical illness that would jeopardize patient health during the study.
• Women must be of nonchildbearing potential \[i.e., postmenopausal, be surgically sterile (hysterectomy or tubal ligation)\] or must meet all of the following conditions: using a reliable, medically accepted form of contraception for at least 60 days before the baseline visit, and agree to continue such use throughout the duration of the study and for 30 days after the final dose of study drug. Reliable forms of contraception include oral, implanted, or injected contraceptives; intrauterine devices in place for at least 3 months; and adequate barrier methods in conjunction with spermicide (abstinence is considered an acceptable contraceptive regimen). Women must be given a pregnancy test (ßHCG), unless they are at least 2 years postmenopausal or surgically sterile, and the results of the test must be negative.
• The patient must be willing and able to comply with study restrictions and to remain at the clinic for the required duration during the study period, and willing to return to the clinic for the follow-up evaluation as specified in this protocol.

You may not qualify if:

• Patients are excluded from participating in this study if 1 or more of the following criteria are met:
• The patient is on more than one antidepressant or takes a standing sedative anxiolytic
• The patient has a substance misuse disorder (including alcohol, caffeine, but not nicotine)
• The patient is a significant risk of suicide
• The patient has recently started psychotherapy or counseling (within last 6 weeks)
• The patient has other psychiatric Axis-I disorders as a principal diagnosis (except anxiety) within 6 months of screening and baseline visits; any history of OCD, psychotic disorder, bipolar disorder, or eating disorder, mental retardation, or clear personality disorder. Patient may have a co-morbid substance misuse, depressive or anxiety disorder if it has been in remission for at least 6 months prior to screening visit.
• The patient has previously participated in any clinical study with acamprosate or treated with acamprosate.
• The patient has used an investigational drug within 1 month before the screening visit or is participating in a concurrent clinical trial.
• The patient has any disorder that may interfere with drug absorption, distribution, metabolism, or excretion (including gastrointestinal surgery).
• The patient is unlikely to comply with the study protocol, be unreliable in providing ratings, or is unsuitable for any reason, as judged by the investigator.

Sponsors & Collaborators

• State University of New York - Upstate Medical University: lead
• Forest Laboratories: collaborator

Study Sites (1)

SUNY Upstate Medical University Psychiatry Dept.

Syracuse, New York, 13210, United States

Location

MeSH Terms

Conditions

Anxiety Disorders

Interventions

Acamprosate

Condition Hierarchy (Ancestors)

Mental Disorders

Intervention Hierarchy (Ancestors)

Taurine; Alkanesulfonic Acids; Alkanes; Hydrocarbons, Acyclic; Hydrocarbons; Organic Chemicals; Sulfonic Acids; Sulfur Acids; Sulfur Compounds

Limitations and Caveats

open label design without placebo control

Results Point of Contact

• Title: Thomas Schwartz
• Organization: SUNY Upstate

schwartt@upstate.edu

3154643166

Study Officials

• Thomas L. Schwartz, MD

  State University of New York - Upstate Medical University

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assoc Professor

Study Record Dates

• First Submitted: December 26, 2007
• First Posted: January 11, 2008
• Study Start: June 1, 2006
• Primary Completion: December 1, 2009
• Study Completion: December 1, 2009
• Last Updated: December 18, 2014
• Results First Posted: December 18, 2014

Record last verified: 2014-12

Locations

US (1)