- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
43 result(s) found for: Schizophrenia AND Dementia AND olanzapine.
Displaying page 1 of 3.
EudraCT Number: 2015-003373-15 | Sponsor Protocol Number: ALK3831-A305 | Start Date*: 2016-04-25 | |||||||||||
Sponsor Name:Alkermes Inc | |||||||||||||
Full Title: A Phase 3 Study to Determine the Antipsychotic Efficacy and Safety of ALKS 3831 in Adult Subjects with Acute Exacerbation of Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008366-13 | Sponsor Protocol Number: 3.0edition | Start Date*: 2009-03-17 | |||||||||||||||||||||||||||||||
Sponsor Name:Unit for Psychiatric Research | |||||||||||||||||||||||||||||||||
Full Title: Comparison of the effects of Sertindole and Olanzapine on Cognition | |||||||||||||||||||||||||||||||||
Medical condition: Cognitive deficits in patients with schizophrenia | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) SE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006967-22 | Sponsor Protocol Number: R076477-SCH-3020 | Start Date*: 2007-10-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: A Prospective Randomized Open-label 6-Month Head-To-Head Trial to Compare Metabolic Effects of Paliperidone ER and Olanzapine in Subjects with Schizophrenia | |||||||||||||
Medical condition: Subjects 18 – 65 years of age, who meets the DSM-IV criteria for schizophrenia with a PANSS total score at screening of 60-100 inclusive. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) SE (Prematurely Ended) GR (Completed) EE (Completed) FR (Completed) GB (Prematurely Ended) IT (Completed) SK (Completed) LV (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010966-47 | Sponsor Protocol Number: NeSSy_200901 | Start Date*: 2010-01-13 | |||||||||||
Sponsor Name:Universität Bremen | |||||||||||||
Full Title: Clinical Effectiveness Of The Newer Antipsychotic Compounds Olanzapine, Quetiapine And Aripiprazole In Comparison With Low Dose Conventional Antipsychotics (Haloperidol And Flupentixol) In Patients... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000497-11 | Sponsor Protocol Number: ALK3831-A307 | Start Date*: 2017-07-13 | |||||||||||||||||||||
Sponsor Name:Alkermes Inc | |||||||||||||||||||||||
Full Title: A Study to Evaluate the Effect of ALKS 3831 Compared to Olanzapine on Body Weight in Young Adults with Schizophrenia, Schizophreniform, or Bipolar I Disorder Who are Early in Their Illness | |||||||||||||||||||||||
Medical condition: Schizophrenia, schizophreniform disorder or bipolar I disorder | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) DE (Completed) ES (Ongoing) IT (Completed) RO (Ongoing) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002169-35 | Sponsor Protocol Number: 25544 | Start Date*: 2005-12-27 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A Multicenter, Double-Blind, Flexible-Dose, 6-Month Extension Trial Comparing the safety and Efficacy of Asenapine With Olanzapine in Subjects who Completed Protocol 25543 | |||||||||||||
Medical condition: Schizophrenia with predominant, persistent negative symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Completed) ES (Completed) CZ (Completed) DE (Completed) HU (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002560-17 | Sponsor Protocol Number: 25543 | Start Date*: 2005-04-14 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A Multicenter, Double-Blind, Flexible-Dose, 6-Month Trial Comparing the Efficacy and Safety of Asenapine With Olanzapine in Stable Subjects With Predominant, Persistent Negative Symptoms of Schizop... | |||||||||||||
Medical condition: Schizophrenia with predominant, persistent negative symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Prematurely Ended) SE (Completed) DE (Completed) CZ (Completed) GB (Completed) IT (Completed) ES (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003880-13 | Sponsor Protocol Number: ALK3831-A306 | Start Date*: 2016-04-25 | |||||||||||
Sponsor Name:Alkermes Inc | |||||||||||||
Full Title: A Phase 3, Multicenter Study to Assess the Long Term Safety and Tolerability of ALKS 3831 in Subjects with Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001865-11 | Sponsor Protocol Number: TV44749-CNS-30096 | Start Date*: 2023-03-08 | |||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
Full Title: A Multinational, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo Controlled Study with an Open-Label, Long-Term Safety Phase to Evaluate the Efficacy, Safety, and Tolerability of Ola... | |||||||||||||
Medical condition: Schizophrenia is a serious mental disorder in which people interpret reality abnormally. It is a severely debilitating psychotic disorder characterized by positive symptoms (eg, delusions, hallucin... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018407-28 | Sponsor Protocol Number: P05688 | Start Date*: 2013-05-10 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Fixed-Dose, 6-Week Trial of the Efficacy and Safety of Asenapine Compared With Placebo Using Olanzapine as an Active Control in Subjects With an Acute Ex... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000800-34 | Sponsor Protocol Number: H8Y-MC-HBBI | Start Date*: 2007-08-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Eli Lilly and Company Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Multi-center, Inpatient, Phase 2, Double-blind, Placebo-controlled Dose Ranging Study of LY2140023 in Patients with DSM-IV Schizophrenia. | |||||||||||||||||||||||||||||||||
Medical condition: Patients must have a diagnosis of Schizophrenia as defined in Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) (Disorganized, 295.10; Catatonic, 295.20; Paranoid, 295.... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) PT (Completed) AT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018408-96 | Sponsor Protocol Number: P05689 | Start Date*: 2013-06-12 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering | |||||||||||||
Full Title: A Multicenter, Double-Blind, Fixed-Dose, Long-Term Extension Trial of the Safety of Asenapine using Olanzapine as an Active Control in Subjects Diagnosed with Schizophrenia who Completed Protocol... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000479-11 | Sponsor Protocol Number: 12396A | Start Date*: 2008-07-21 | ||||||||||||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||||||||||||
Full Title: A randomised, double-blind, parallel-group, active-controlled, flexible dose study exploring the efficacy and safety of 12 weeks treatment with Lu 31-130 in patients with schizophrenia | ||||||||||||||||||||||||||||
Medical condition: Lu 31-130 is under development by H. Lundbeck A/S as an antipsychotic in the treatment of schizophrenia | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Completed) FR (Completed) ES (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-006062-36 | Sponsor Protocol Number: NW-3509/008A/II/2020 | Start Date*: 2021-06-30 | |||||||||||
Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
Full Title: A PHASE II/III, PROSPECTIVE, MULTI-CENTER, RANDOMIZED, 4-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY, DESIGNED TO DETERMINE THE SAFETY, TOLERABILITY, EEG EFFECTS AND EFFICACY OF ORAL DOSES OF 30 M... | |||||||||||||
Medical condition: Chronic schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) CZ (Completed) ES (Ongoing) RO (Ongoing) HU (Completed) PL (Completed) EE (Completed) LV (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006184-23 | Sponsor Protocol Number: CL2-33138-011 | Start Date*: 2008-01-11 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: A randomised, double-blind, placebo- and olanzapine- controlled, parallel-group study to evaluate the efficacy and safety of 3 fixed doses of S 33138 in treatment of patients with an acute episode ... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020185-19 | Sponsor Protocol Number: KP7242114 | Start Date*: 2011-05-30 | ||||||||||||||||
Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||
Full Title: Optimization of Treatment and Management of Schizophrenia in Europe | ||||||||||||||||||
Medical condition: Schizophrenia ICD-10 code F20 or schizophreniform disorder ICD-10 code F23.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Prematurely Ended) NL (Prematurely Ended) CZ (Completed) DK (Prematurely Ended) AT (Completed) BE (Completed) IT (Completed) BG (Completed) RO (Suspended by CA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001211-39 | Sponsor Protocol Number: ALK3831-401 | Start Date*: 2015-01-27 |
Sponsor Name:Alkermes, Inc. | ||
Full Title: A Phase 2, Efficacy, Safety, and Tolerability Study of ALKS 3831 in Schizophrenia with Alcohol Use Disorder | ||
Medical condition: Schizophrenia with alcohol use disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BG (Completed) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002960-85 | Sponsor Protocol Number: NN20372 | Start Date*: 2008-03-18 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled add-on trial of the safety and efficacy of RO4917838 in outpatients on select atypical antipsychotics with prominent negative or disorganized thought sy... | |||||||||||||
Medical condition: Schizophrenia - This study will be conducted to investigate whether or not administration of RO4917838 along with their current antipsychotic regimen to stable patients can lead to further improvem... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) FR (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000418-13 | Sponsor Protocol Number: M10-855 | Start Date*: 2012-12-21 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Dose-ranging, Parallel-group Study of the Safety and Efficacy of ABT-126 in the Treatment of Cognitive Deficits in Schizophrenia (CDS) | |||||||||||||
Medical condition: Cognitive Deficits in Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003080-31 | Sponsor Protocol Number: 172003 | Start Date*: 2006-12-12 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A multi-center, double-blind, flexible-dose efficacy trial with Org 25935 versus placebo as add-on therapy in subjects with predominant, persistent negative symptoms of schizophrenia treated with a... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FI (Completed) FR (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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