Status:
COMPLETED
Quetiapine Extended Release (XR) in Bipolar Patients With Comorbid Generalized Anxiety Disorder (GAD)
Lead Sponsor:
University Hospitals Cleveland Medical Center
Collaborating Sponsors:
National Alliance for Research on Schizophrenia and Depression
AstraZeneca
Conditions:
Bipolar Disorder
Anxiety
Eligibility:
All Genders
18-65 years
Phase:
PHASE3
Brief Summary
The primary objective is to test the hypothesis that Quetiapine XR (Extended Release) monotherapy and adjunctive therapy is effective in the acute treatment of bipolar depression and comorbid generali...
Detailed Description
120 subjects aged 18 and up with Diagnostic and Statistical Manual -IV Generalized Anxiety Disorder and Bipolar Disorder type I or II as identified by extensive clinical interview and the Mini-Interna...
Eligibility Criteria
Inclusion
- Diagnostic and Statistical Manual-IV diagnosis of bipolar I or II disorder, and currently depressed as confirmed by the MINI-Plus at Screening.
- Diagnostic and Statistical Manual-IV diagnosis of lifetime GAD;
- Hamilton Depression Rating Scale -17 items total score ≥ 18;
- Hamilton Anxiety Rating Scale total score ≥ 18;
- Be male or female at least 18 year old and not older than 65.
Exclusion
- Pregnancy or breast feeding.
- Severe medical or neurological problems.
- Severe personality disorder.
- Currently suicidal risk judged by physician.
- Known history of intolerance or hypersensitivity to any of the medications involved in the study.
- Treatment with quetiapine at any dose in the 6 months prior to randomization.
- Known lack of response to quetiapine in a dosage of at least 50 mg for 4 weeks at any time, as judged by the investigator.
- Dependence on opiate, phencyclidine (PCP), and/or barbiturate.
- Acute mania as determined by a score \> 12 on the Young Mania Rating Scale at baseline.
- Concurrent obsessive compulsive disorder.
- Use of any of the following cytochrome P450 3A4 inhibitors in the 14 days preceding enrolment including but not limited to: ketoconazole, itraconazole, fluconazole, erythromycin, clarithromycin, troleandomycin, indinavir, nelfinavir, ritonavir, fluvoxamine and saquinavir
- Use of any of the following cytochrome P450 inducers in the 14 days preceding enrollment including but not limited to: phenytoin, carbamazepine, barbiturates, rifampin, St. John's Wort, and glucocorticoids
- Administration of a depot antipsychotic injection within one dosing interval (for the depot) before randomisation
- Medical conditions that would affect absorption, distribution, metabolism, or excretion of study treatment
- Unstable or inadequately treated medical illness (e.g. diabetes, angina pectoris, hypertension) as judged by the investigator
- Involvement in the planning and conduct of the study
- Previous enrolment or randomisation of treatment in the present study.
- Participation in another drug trial within 4 weeks prior enrolment into this study or longer in accordance with local requirements
- A patient with diabetes mellitus (DM) fulfilling one of the following criteria: a. Unstable DM defined as enrollment glycosylated hemoglobin (HbA1c) .8.5% b. Admitted to hospital for treatment of DM or DM related illness within the past 12 weeks c. Not under physician care for DM d. Physician responsible for patient's DM care has not indicated that the patient's DM is controlled f. Physician responsible for patient's DM care has not approved the patient's participation in the study g. Has not been on the same dose of oral hypoglycemic drug(s) and/or diet for the 4 weeks before randomization. For thiazolidinediones (glitazones) this period should not be less than 8 weeks before randomization h. Taking insulin whose daily dose on one occasion in the past 4 weeks has been more than 10% above or below their mean dose in the preceding 4 weeks Note: If a patient with DM meets one of these criteria, the patient is to be excluded even if the treating physician believes that the patient is stable and can participate in the study.
Key Trial Info
Start Date :
April 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2011
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT00671853
Start Date
April 1 2008
End Date
March 1 2011
Last Update
December 29 2016
Active Locations (1)
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1
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States, 44106