A Study To Evaluate PRX-00023 In Patients With Generalized Anxiety Disorder (GAD)

Completed · Phase 3

Conditions studied: Anxiety Disorders

In brief

This is a randomized, double-blind, placebo controlled, multi-center outpatient study, in adults with GAD. Patients 18-65 years of age, with the diagnosis of GAD according to DSM-IV criteria, who fulfill the inclusion/exclusion criteria, will be enrolled in this study.

Key facts

Study ID

NCT00248183

Run by

Epix Pharmaceuticals, Inc.

People needed

310

Starts

2005-08-01

Expected to finish

2006-06-01

Last updated by the study team

2008-04-03

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be male or female, 18-65 years of age
• Meet DSM-IV diagnostic criteria for Generalized Anxiety Disorder (GAD)
• Have a total score of ≥ 20 on the HAM-A and a score of ≥ 2 on Items 1 and 2 (anxious mood and tension) of the HAM-A
• Have no more than a 20% decrease in total HAM-A score during the period from the screening visit to the randomization visit
• Have a negative serum (β-HCG) pregnancy test at screening and a negative urine pregnancy test at baseline (for all women)
• Female subjects must meet one of the following criteria: (a) Be surgically sterile (i.e., have had bilateral tubal ligation, hysterectomy, or bilateral oophorectomy at least six months prior to first dose of PRX-00023; appropriate documentation will be required) OR (b) Agree that, if sexually active, they and all male partners will use two (2) acceptable barrier forms of contraception (e.g., condoms and diaphragm) from screening until one month after the final dose of study drug
• Male subjects must agree that they and any female partners will use two(2) acceptable forms of contraception (e.g., condoms and hormonal contraceptives) from screening until one month following the final dose of study drug
• Be in generally good physical health as determined by the Investigator on the basis of medical history, physical examination, and screening laboratory results
• Have the ability to communicate with the investigative site staff in a manner sufficient to carry out all protocol procedures as described
• Be able to understand procedures and provide written informed consent prior to admission

You may not qualify if…

• A history of an inability to tolerate, or a failure to respond to, two or more anxiolytic or anti-depressant drugs given in adequate doses and duration for the treatment of symptoms present in the current illness
• Prior intolerance to buspirone, gepirone, tandospirone or other 5HT1A agonist
• A current or past history of mania, bipolar disorder, schizophrenia, or other psychotic disorder
• A current history (or within the six months prior to screening) of panic disorder, post traumatic stress disorder, major depression, obsessive-compulsive disorder, social phobia, acute stress disorder, adjustment disorder with anxious mood, performance anxiety, somatization disorder, or other principle psychiatric diagnosis (DSM-IV) which could interfere with the efficacy assessments
• A history of a major life event (e.g. divorce, death of family member) which in the opinion of the Investigator is likely to alter the efficacy ratings during the course of the study
• Clinically significant abnormalities on laboratory tests or ECG (includes QTc value >450 msec in males or > 470 msec in females)
• The presence of a serious or clinically unstable neurologic, cardiovascular, hepatic, renal, endocrinologic, pulmonary, hematologic or other medical illness or psychiatric condition that would, in the opinion of the Investigator, compromise participation in the study, confound study results, or likely lead to the need for early termination of study participation or hospitalization during the course of the study
• A history of allergic reactions to two or more medications of different chemical classes
• Use of any non-prescription drug with psychotropic effects within seven (7) days prior to initiation of the placebo lead in
• Chronic use of analgesics with opiates (e.g., codeine, hydrocodone, oxycodone) for >6 months or use of opiates within two weeks prior to screening
• Introduction or change in cognitive behavioral therapy, interpersonal therapy, or other psychotherapy within three months of screening
• Use of St. John's Wort, kava kava, ephedra, or other psychoactive herbal medications within the last two weeks before screening
• Known or suspected substance abuse or dependence, including alcohol, within one year of screening
• A positive urine drug screen (e.g., amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, methadone, methaqualone, opiates, and propoxyphene) at screening. The urine drug screen may be repeated once if after discussion with the patient there is a plausible reason for the positive test other than substance abuse
• A history of suicide attempts in the last two years, or current suicide risk in the judgment of the Investigator
• Women who are breast feeding, have been lactating within three months prior to screening, pregnant, expect to become pregnant during the course of the study, or are sexually active and are not using a medically acceptable double barrier method of birth control. Women relying solely on oral contraceptives for - The use of any investigational drug within 30 days prior to enrollment
• The concomitant use of any other antidepressants, anxiolytics, or any other psychoactive drugs
• Treatment with any potent inhibitor of CYP3A4, including ketoconazole, itraconazole, HIV protease inhibitors, clarithromycin, erythromycin, cyclosporine
• Treatment with CYP3A4 inducers such as carbamazepine, barbiturates, phenytoin, rifampin, or oral glucocorticoids
• Treatment with any of the psychoactive drugs listed in the table below within the interval specified below before enrollment
• Psychoactive drug - Interval (weeks)
• MAO Inhibitors - 4
• Fluoxetine - 4
• Fluvoxamine - 2
• Citalopram - 2

Where it is running

• Vista Medical Research — Mesa, Arizona, United States
• Pivotal Research Center — Mesa, Arizona, United States
• Anaheim Research Center — Anaheim, California, United States
• Pacific Clinical Research Group — Upland, California, United States
• Connecticut Clinical Research — Cromwell, Connecticut, United States
• The George Washington University — Washington D.C., District of Columbia, United States
• Gulf Coast Clinical Research Center — Fort Myers, Florida, United States
• Atlanta Institute of Research and Medicine — Atlanta, Georgia, United States
• Northwest Behavioral Research — Marietta, Georgia, United States
• Louisiana Research Associates — New Orleans, Louisiana, United States
• Pivotal Research Center — Royal Oak, Michigan, United States
• Comprehensive Neurosciences — Kenilworth, New Jersey, United States
• Mount Sinai School of Medicine — New York, New York, United States
• Oregon Center for Clinical Investigations — Portland, Oregon, United States
• Oregon Center for Clinical Investigations — Salem, Oregon, United States
• Unversity of Pennsylvania — Philadelphia, Pennsylvania, United States
• Future Search Trials — Austin, Texas, United States
• UT Southwestern Medical Center — Dallas, Texas, United States
• Comprehensive Neurosciences — Falls Church, Virginia, United States
• Sidney Lerfald, MD — Charleston, West Virginia, United States

Full record on ClinicalTrials.gov

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