- Trials with a EudraCT protocol (201)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
201 result(s) found for: Schizophrenia AND Schizophrenias.
Displaying page 2 of 11.
EudraCT Number: 2010-020370-42 | Sponsor Protocol Number: NN25310 | Start Date*: 2011-01-06 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A Phase III, multi-center, randomized, 24 week, double-blind, parallel-group, placebo-controlled study to evaluate efficacy and safety of RO4917838 in stable patients with persistent, predominant n... | |||||||||||||
Medical condition: Treatment of negative symptoms for patients with schizophrenia treated with antipsychotics. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) HU (Prematurely Ended) FI (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
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: 2009-011307-22 | Sponsor Protocol Number: 0911885 | Start Date*: 2009-05-18 | ||||||||||||||||
Sponsor Name:Niuvanniemen sairaala | ||||||||||||||||||
Full Title: Klotsapiiniresistentin skitsofrenian polyfarmasiatutkimus: satunnaistettu kaksoissokkotutkimus | ||||||||||||||||||
Medical condition: Potilaat, joilla on hoitoresistentti skitsofrenia. | ||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012568-14 | Sponsor Protocol Number: 331-08-210 | Start Date*: 2009-11-18 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization | |||||||||||||
Full Title: A Phase 2, Multicenter, Open-label Study to Assess the Safety and Tolerability of Oral OPC-34712 as Monotherapy in Adult Patients with Schizophrenia | |||||||||||||
Medical condition: schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BG (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: 2009-013020-23 | Sponsor Protocol Number: RAA09-002 | Start Date*: 2010-03-23 | |||||||||||
Sponsor Name:King's College London | |||||||||||||
Full Title: A Pilot study of cognitive enhancer and cognitive training combination – Testing a therapeutic paradigm for cognitive impairment in schizophrenia | |||||||||||||
Medical condition: Cognitive impairment associated with schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002740-82 | Sponsor Protocol Number: 1346-0038 | Start Date*: 2019-03-07 | |||||||||||
Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||
Full Title: A phase II randomized, double-blinded, placebo-controlled parallel group trial to examine the efficacy and safety of BI 425809 once daily with adjunctive Computerized Cognitive Training over 12 wee... | |||||||||||||
Medical condition: schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003239-47 | Sponsor Protocol Number: 14724B | Start Date*: 2013-11-12 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, open-label, flexible-dose extension study of aripiprazole once-monthly in patients with schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) ES (Completed) IT (Completed) EE (Completed) SE (Completed) FR (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 |
EudraCT Number: 2014-002176-83 | Sponsor Protocol Number: SNP-S-01 | Start Date*: 2015-04-01 | |||||||||||
Sponsor Name:Clinirx Tangent Research | |||||||||||||
Full Title: A randomized trial administering Sodium Nitroprusside vs. placebo as add-on to antipsychotics in patients with schizophrenia | |||||||||||||
Medical condition: schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000757-36 | Sponsor Protocol Number: ASA-CRP-01 | Start Date*: 2014-10-07 | ||||||||||||||||
Sponsor Name:Clinirx Tangent Research | ||||||||||||||||||
Full Title: A randomized trial administering aspirin vs. placebo as add-on to antipsychotics in patients with schizophrenia or schizoaffective disorder with high CRP levels | ||||||||||||||||||
Medical condition: schizophrenia and schizoaffective disorder. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: RO (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000350-26 | Sponsor Protocol Number: CL09-ORY-2001 | Start Date*: 2021-07-06 | |||||||||||
Sponsor Name:Oryzon Genomics, S.A. | |||||||||||||
Full Title: A double blind, randomized, placebo-controlled, adaptive 24-week Phase IIb trial to evaluate the efficacy of vafidemstat in negative symptoms and cognitive impairment associated with schizophrenia.... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002705-21 | Sponsor Protocol Number: 14644B | Start Date*: 2013-04-04 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, open-label, flexible-dose extension study of brexpiprazole in patients with schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) EE (Completed) SK (Completed) PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005661-13 | Sponsor Protocol Number: M13-765 | Start Date*: 2013-09-25 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: Long-Term Safety and Efficacy of ABT-126 in Subjects with Schizophrenia: A Double-Blind Extension Study for Subjects Completing Study M10-855 | |||||||||||||
Medical condition: Cognitive deficits in schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
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: 2019-002259-40 | Sponsor Protocol Number: SEP361-304 | Start Date*: 2021-06-03 | |||||||||||
Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Active Comparator-Controlled Study to Evaluate the Long-term Safety and Tolerability of SEP-363856 in Subjects with Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014469-19 | Sponsor Protocol Number: RECOVERY[OCTUMI-4] | Start Date*: 2010-08-17 | |||||||||||
Sponsor Name:University of Oxford [...] | |||||||||||||
Full Title: OCTUMI-4: Evaluation of Mirtazapine and Folic Acid for Schizophrenia: A randomised, double-blind, 2x2 factorial trial | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004265-34 | Sponsor Protocol Number: R076477SCH3017 | Start Date*: 2007-06-07 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: An Open-label Prospective Trial to Explore the Tolerability, Safety and Efficacy of Flexibly Dosed Paliperidone ER in Subjects With Schizophrenia | |||||||||||||
Medical condition: schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) DE (Completed) FR (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006434-17 | Sponsor Protocol Number: R092670PSY3007 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose Response Study to Evaluate the Efficacy and Safety of 3 Fixed Doses (25 mg eq., 100 mg eq., and 150 mg eq.) of Paliperidone Palm... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011594-33 | Sponsor Protocol Number: SMRI-07TGF-1152 | Start Date*: 2009-11-02 | |||||||||||
Sponsor Name:LWL University Hospital Bochum, Ruhr-University Bochum | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study of tetrabenazine as adjunctive therapy to risperidone in first-episode schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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