A 10-week Study Evaluating the Efficacy and Safety of PD 0332334 in Patients With Generalized Anxiety Disorder (2)
Stopped early · Phase 3 · Has a placebo group
Conditions studied: Generalized Anxiety Disorder
In brief
This is a 10-week trial that evaluates the efficacy and safety of PD 0332334 in subjects, ages 18 to 65, with generalized anxiety disorder.
Key facts
- Study ID
- NCT00658372
- Run by
- Pfizer
- People needed
- 360
- Starts
- 2008-05-01
- Expected to finish
- 2009-03-01
- Last updated by the study team
- 2012-11-16
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of GAD (Diagnostic and Statistical Manual IV [DSM IV], 300.02) as established by the clinician (psychiatrist or licensed clinical psychologist) who has interviewed the subject using all sources of data including the Mini International Neuropsychiatric Interview (MINI) for DSM IV Axis I disorders and other clinical information. Subjects with specific phobia(s) (as defined in DSM IV) or dysthymic disorder will be allowed in the study.
- Subjects must have a HAM A total score ≥20 at the screening (V1) and randomization (V2) visits. Subjects must also have a Covi Anxiety Scale score of ≥9 and a Raskin Depression Scale score ≤7 at the Screening (V1) visit to ensure predominance of anxiety symptoms over depression symptoms.
You may not qualify if…
- Subjects with evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, pancreatic, neurologic, active infections, immunological, or allergic disease (including drug allergies).
- Any of the following current (within the past 6 months through the present) DSM-IV Axis I diagnosis: Major Depressive Disorder, Obsessive Compulsive Disorder, Panic Disorder, Agoraphobia, Posttraumatic Stress Disorder, Anorexia, Bulimia, Caffeine induced anxiety disorder, Alcohol or substance abuse or dependence unless in full remission for at least 6 months, Social anxiety disorder.
- Any of the following past or current DSM-IV Axis I diagnoses: Schizophrenia, Psychotic disorder, Delirium, dementia, amnestic, and other clinically significant cognitive disorders, Bipolar or schizoaffective disorder, Cyclothymic disorder, Dissociative disorders.
- Antisocial or borderline personality disorder.
- Serious suicidal risk per the clinical investigator's judgment.
Where it is running
- Pfizer Investigational Site — Arcadia, California, United States
- Pfizer Investigational Site — Costa Mesa, California, United States
- Pfizer Investigational Site — Escondido, California, United States
- Pfizer Investigational Site — Los Angeles, California, United States
- Pfizer Investigational Site — San Diego, California, United States
- Pfizer Investigational Site — Hamden, Connecticut, United States
- Pfizer Investigational Site — Boca Raton, Florida, United States
- Pfizer Investigational Site — Honolulu, Hawaii, United States
- Pfizer Investigational Site — Naperville, Illinois, United States
- Pfizer Investigational Site — Park Ridge, Illinois, United States
- Pfizer Investigational Site — Prairie Village, Kansas, United States
- Pfizer Investigational Site — New Orleans, Louisiana, United States
- Pfizer Investigational Site — Haverhill, Massachusetts, United States
- Pfizer Investigational Site — Pittsfield, Massachusetts, United States
- Pfizer Investigational Site — Flint, Michigan, United States
- Pfizer Investigational Site — Flint, Michigan, United States
- Pfizer Investigational Site — Minneapolis, Minnesota, United States
- Pfizer Investigational Site — Saint Paul, Minnesota, United States
- Pfizer Investigational Site — New York, New York, United States
- Pfizer Investigational Site — Olean, New York, United States
- Pfizer Investigational Site — Rochester, New York, United States
- Pfizer Investigational Site — Dayton, Ohio, United States
- Pfizer Investigational Site — Allentown, Pennsylvania, United States
- Pfizer Investigational Site — Bartlett, Tennessee, United States
- Pfizer Investigational Site — Memphis, Tennessee, United States
Full record on ClinicalTrials.gov
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