- Trials with a EudraCT protocol (205)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
205 result(s) found for: DSM-IV Schizophrenia.
Displaying page 2 of 11.
| EudraCT Number: 2016-003529-41 | Sponsor Protocol Number: ABR58805 | Start Date*: 2017-02-22 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: CANGLIA: Endocannabinoid control of microglia activation as a new therapeutic target in the treatment of schizophrenia | ||
| Medical condition: Schizophrenia patients | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NL (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: 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: 2013-005451-32 | Sponsor Protocol Number: F17464GE201 | Start Date*: 2014-07-09 | |||||||||||
| Sponsor Name:Pierre Fabre Médicament represented by the Institut de Recherche Pierre Fabre (IRPF) | |||||||||||||
| Full Title: Effects of F17464 in acute exacerbation of schizophrenia. | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) LV (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002538-38 | Sponsor Protocol Number: 331-10-231 | Start Date*: 2011-10-14 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial of Three Fixed Doses of OPC-34712 in the Treatment of Adults With Acute Schizophrenia | |||||||||||||
| Medical condition: Acute Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002513-11 | Sponsor Protocol Number: 331-10-230 | Start Date*: 2012-01-09 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial of Fixed dose OPC-34712 (4, 2, and 1 mg/day) in the Treatment of Adults With Acute Schizophrenia | |||||||||||||
| Medical condition: Acute Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002713-35 | Sponsor Protocol Number: AXCT01-01-03-2013 | Start Date*: 2014-07-29 | |||||||||||
| Sponsor Name:MediPsych SA | |||||||||||||
| Full Title: Randomized, controlled trial of the effectiveness of add-on tolcapone to usual antipsychotic therapy on cognitive and negative symptoms of patients with schizophrenia genotyped for COMT polymorphisms | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-003156-35 | Sponsor Protocol Number: EXPSY 0105 | Start Date*: 2005-12-01 |
| Sponsor Name:Department of Psychiatry and Psychotherapy (Cologne) | ||
| Full Title: Efficacy and tolerability of Ziprasidone vs. Clozapine in the treatment of dually diagnosed (DD-) patients with schizophrenia and cannabis use disorder: A randomised study | ||
| Medical condition: Patients with schizophrenia and cannabis abuse/dependency will be randomized to ziprasidone or clozapine treatment. Dose of medication and frequency of administration will be flexible and adjustab... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| 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: 2010-018416-33 | Sponsor Protocol Number: 2009_37/1001 | Start Date*: 2010-07-13 | |||||||||||
| Sponsor Name:Centre Hospitalier Régional et Universitaire de Lille | |||||||||||||
| Full Title: Effets du Fénofibrate durant la première année de schizophrénie (effects of Fenofibrate® in first year of schizophrenia) | |||||||||||||
| Medical condition: schizophrénia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000520-14 | Sponsor Protocol Number: NL46653 | Start Date*: 2014-07-31 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Prednisolone addition for atients with recent onset psychotic disorder: the role of immune-modulating strategies in the treatment of psychosis. | ||
| Medical condition: Schizophrenia, schizophreniphorm disorder, schizoaffective disorder, psychosis NOS. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022181-28 | Sponsor Protocol Number: 13639A | Start Date*: 2011-02-07 | ||||||||||||||||||||||||||
| Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||||||||||||
| Full Title: A 6-month, randomised, double-blind, parallel-group, risperidone-controlled, fixed-dose study evaluating the safety and efficacy of zicronapine in patients with schizophrenia | ||||||||||||||||||||||||||||
| Medical condition: Schizophrenia | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FI (Completed) EE (Completed) CZ (Completed) PL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2005-001845-40 | Sponsor Protocol Number: R092670-PSY-3005 | Start Date*: 2005-08-24 |
| Sponsor Name:Janssen-Cilag International N.V. | ||
| Full Title: A Randomized, Crossover Study to Evaluate the Overall Safety and Tolerability of Paliperidone Palmitate Injected in the Deltoid or Gluteus Muscle in Subjects With Schizophrenia | ||
| Medical condition: Schizophrenia according to DSM-IV-TM [disorganized type (295.10), catatonic type (295.20), paranoid type (295.30), residual type (295.60) or undifferentiated type (295.90)] | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) SK (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-001711-31 | Sponsor Protocol Number: D1050238 | Start Date*: 2012-02-29 | |||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
| Full Title: A double-blind, placebo-controlled, randomized withdrawal study of lurasidone for the maintenance treatment of subjects with schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-003519-33 | Sponsor Protocol Number: D1443L00003 | Start Date*: 2007-01-25 |
| Sponsor Name:AstraZeneca UK Limited | ||
| Full Title: RAPID - An Open-Label, Randomised, Multicentre Phase IIIb Study to Evaluate the Efficacy and Tolerability of Quetiapine IR (Immedicate Release), over 14 days, in Acute Schizophrenia / Schizoaffecti... | ||
| Medical condition: Acute Schizophrenia and Schizoaffective Disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-001523-39 | Sponsor Protocol Number: D1050300 | Start Date*: 2013-11-08 | |||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
| Full Title: A PHASE 1 OPEN-LABEL, MULTICENTER, SINGLE AND MULTIPLE ASCENDING DOSE STUDY TO EVALUATE PHARMACOKINETICS, SAFETY, AND TOLERABILITY OF LURASIDONE IN SUBJECTS 6 TO 17 YEARS OLD WITH SCHIZOPHRENIA SPE... | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000060-42 | Sponsor Protocol Number: D1001066 | Start Date*: 2017-03-15 | |||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
| Full Title: A 6-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Lurasidone (SM-13496) in Acutely Psychotic Subjects with Schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002048-29 | Sponsor Protocol Number: RGH-MD-06 | Start Date*: 2012-03-29 | |||||||||||
| Sponsor Name:Forest Research Institute, Inc | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, parallel-group study of cariprazine (RGH-188) in the prevention of relapse in patients with schizophrenia | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019897-33 | Sponsor Protocol Number: 2522518514 | Start Date*: 2011-04-14 |
| Sponsor Name:erasmus mc | ||
| Full Title: Selective D1 activation by addition of L-Dopa to antipsychotic treatment in patients with schizophrenia | ||
| Medical condition: patients with psychotic symptoms, diagnosed with schizophrenia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-017852-28 | Sponsor Protocol Number: H8Y-MC-HBBM(a) | Start Date*: 2010-05-04 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 2, Multicenter, Double-Blind, Placebo-Controlled Comparator Study of 2 Doses of LY2140023 versus Placebo in Patients with DSM-IVTR Schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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