A Phase 3 interventional study of ziprasidone versus olanzapine , risperidone or quetiapine and Panss , CGI-C, UKU-SERS-Pa in Schizophrenia, Schizoaffective Disorder and Psychotic Disorders, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris Inc.. Completed at 43 sites in 4 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-02-21.
Sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris Inc. (part of Viatris Inc.) · Phase 3, Interventional, and Treatment
Evaluation of the antipsychotic efficacy and safety of ziprasidone versus olanzapine, risperidone or quetiapine in patients with schizophrenia, schizoaffective and schizophreniform disorders under naturalistic conditions of clinical practice
3,539 studies on the registry are indexed under Schizophrenia; 473 are open to participants now.
This study's enrollment of 290 is above the median of 70 across 2,924 interventional studies indexed under Schizophrenia.
Browse Schizophrenia studies →Pfizer's Upjohn has merged with Mylan to form Viatris Inc. is the lead sponsor of 434 studies on the registry; none are open to participants now.
Of its 9 completed or terminated interventional studies of FDA-regulated products, 8 (89%) have results posted.
First submitted before Pfizer's Upjohn has merged with Mylan to form Viatris Inc. became part of Viatris Inc..
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Exclusion Criteria:
PANSS (The Positive And Negative Syndrome Scale) in a 12 week period
CGI-C score (Clinical Global Impression of Change), UKU-SERS-Pa (Patient self rating version). Safety and tolerability: ECG, serum cholesterol, triglycerides, prolactin, glucose and body weight
This study is completed, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.
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Pfizer's Upjohn has merged with Mylan to form Viatris Inc. →