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Last Updated: November 5, 2024

CLINICAL TRIALS PROFILE FOR FLUPHENAZINE HYDROCHLORIDE


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All Clinical Trials for FLUPHENAZINE HYDROCHLORIDE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00014001 ↗ CATIE- Schizophrenia Trial Completed National Institute of Mental Health (NIMH) Phase 4 2000-12-01 The CATIE Schizophrenia Trial is part of the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Project. The schizophrenia trial is being conducted to determine the long-term effects and usefulness of antipsychotic medications in persons with schizophrenia. It is designed for people with schizophrenia who may benefit from a medication change. The study involves the newer atypical antipsychotics (olanzapine, quetiapine, risperidone, clozapine, and ziprasidone)and the typical antipsychotics (perphenazine and fluphenazine decanoate). All participants will receive an initial comprehensive medical and psychiatric evaluation and will be closely followed throughout the study. For most participants the study will last up to 18 months. Everyone in the study will be offered an educational program about schizophrenia and family members will be encouraged to participate.
NCT00161018 ↗ New Antipsychotic Strategies: Quetiapine and Risperidone vs. Fluphenazine in Treatment Resistant Schizophrenia Completed University of Maryland Phase 3 2003-11-01 The purpose of this study is to: 1. Evaluate the efficacy and safety of the new antipsychotics, quetiapine (300-500mg/day) and risperidone (3-4mg/day) compared to each other and to fluphenazine (10-15mg/day), a high potency typical antipsychotic in patients who meet the DSM IV criteria for schizophrenia. 2. To evaluate the efficacy and safety of quetiapine (1200mg/day) in patients who have not responded to conventional and newer antipsychotics. 3. To evaluate the effectiveness of quetiapine (300-500mg/day), and risperidone (3-5mg/day) compared to each other and fluphenazine (10-15mg/day) in the treatment of hostility and aggression in treatment-resistant schizophrenic patients. 4. To evaluate the effectiveness of quetiapine (300-500mg/day) and risperidone (3-5mg/day) compared to each other and fluphenazine (10-15mg/day) on rates of discharge, quality of life, and independent living skills. 5. To assess prolactin levels and to evaluate any relationship with sexual dysfunction and menstrual irregularities. 6. To evaluate the possible differential impact of treatment conditions on cognitive functioning including measures of attention, motor speed, problem solving, verbal and visual memory, and verbal processing speed. 7. To measure changes in weight and health consequences associated with weight changes.
NCT00161018 ↗ New Antipsychotic Strategies: Quetiapine and Risperidone vs. Fluphenazine in Treatment Resistant Schizophrenia Completed University of Maryland, Baltimore Phase 3 2003-11-01 The purpose of this study is to: 1. Evaluate the efficacy and safety of the new antipsychotics, quetiapine (300-500mg/day) and risperidone (3-4mg/day) compared to each other and to fluphenazine (10-15mg/day), a high potency typical antipsychotic in patients who meet the DSM IV criteria for schizophrenia. 2. To evaluate the efficacy and safety of quetiapine (1200mg/day) in patients who have not responded to conventional and newer antipsychotics. 3. To evaluate the effectiveness of quetiapine (300-500mg/day), and risperidone (3-5mg/day) compared to each other and fluphenazine (10-15mg/day) in the treatment of hostility and aggression in treatment-resistant schizophrenic patients. 4. To evaluate the effectiveness of quetiapine (300-500mg/day) and risperidone (3-5mg/day) compared to each other and fluphenazine (10-15mg/day) on rates of discharge, quality of life, and independent living skills. 5. To assess prolactin levels and to evaluate any relationship with sexual dysfunction and menstrual irregularities. 6. To evaluate the possible differential impact of treatment conditions on cognitive functioning including measures of attention, motor speed, problem solving, verbal and visual memory, and verbal processing speed. 7. To measure changes in weight and health consequences associated with weight changes.
NCT00335647 ↗ Fluphenazine in Treating Patients With Refractory Advanced Multiple Myeloma Completed Immune Control Phase 1/Phase 2 2006-01-01 RATIONALE: Drugs used in chemotherapy, such as fluphenazine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase I/II trial is studying the side effects and best dose of fluphenazine and to see how well it works in treating patients with refractory advanced multiple myeloma.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for FLUPHENAZINE HYDROCHLORIDE

Condition Name

Condition Name for FLUPHENAZINE HYDROCHLORIDE
Intervention Trials
Schizophrenia 7
Psoriasis 2
Multiple Myeloma 1
Multiple Myeloma and Plasma Cell Neoplasm 1
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Condition MeSH

Condition MeSH for FLUPHENAZINE HYDROCHLORIDE
Intervention Trials
Schizophrenia 7
Disease 3
Multiple Myeloma 2
Psoriasis 2
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Clinical Trial Locations for FLUPHENAZINE HYDROCHLORIDE

Trials by Country

Trials by Country for FLUPHENAZINE HYDROCHLORIDE
Location Trials
United States 60
India 3
Canada 2
Germany 2
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Trials by US State

Trials by US State for FLUPHENAZINE HYDROCHLORIDE
Location Trials
Texas 4
Pennsylvania 4
New York 4
Massachusetts 3
Georgia 3
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Clinical Trial Progress for FLUPHENAZINE HYDROCHLORIDE

Clinical Trial Phase

Clinical Trial Phase for FLUPHENAZINE HYDROCHLORIDE
Clinical Trial Phase Trials
Phase 4 2
Phase 3 2
Phase 2 4
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Clinical Trial Status

Clinical Trial Status for FLUPHENAZINE HYDROCHLORIDE
Clinical Trial Phase Trials
Completed 9
Terminated 2
Unknown status 1
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Clinical Trial Sponsors for FLUPHENAZINE HYDROCHLORIDE

Sponsor Name

Sponsor Name for FLUPHENAZINE HYDROCHLORIDE
Sponsor Trials
Immune Control 4
Tufts Medical Center 2
Canadian Institutes of Health Research (CIHR) 2
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Sponsor Type

Sponsor Type for FLUPHENAZINE HYDROCHLORIDE
Sponsor Trials
Other 11
Industry 6
NIH 1
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