- Trials with a EudraCT protocol (133)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
133 result(s) found for: Epilepsy, Focal AND Seizures.
Displaying page 4 of 7.
| EudraCT Number: 2007-001458-22 | Sponsor Protocol Number: A0081157 | Start Date*: 2007-07-31 | |||||||||||
| Sponsor Name:PFIZER | |||||||||||||
| Full Title: "ESTUDIO ALEATORIZADO, DOBLE CIEGO, DE GRUPOS PARALELOS, MULTICÉNTRICO, CON DOSIS FLEXIBLES, COMPARATIVO DE PREGABALINA Y LEVETIRACETAM COMO TRATAMIENTO ADYUVANTE PARA REDUCIR LA FRECUENCIA DE LAS ... | |||||||||||||
| Medical condition: Tratamiento adyuvante de las crisis epilépticas parciales, con o sin generalización secundaria. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) GR (Completed) DE (Prematurely Ended) BE (Completed) FR (Completed) CZ (Completed) IT (Completed) LT (Completed) SI (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000490-13 | Sponsor Protocol Number: EstuEla2022 | Start Date*: 2023-01-09 |
| Sponsor Name:OILS4CURE S.L | ||
| Full Title: Treatment, with a full spectrum extract of cannabis, in refractory epilepsy associated with tuberous sclerosis complex (TSC) | ||
| Medical condition: Refractory epilepsy in tuberous sclerosis complex | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001549-96 | Sponsor Protocol Number: SP1042 | Start Date*: 2016-03-17 | |||||||||||
| Sponsor Name:UCB BioPharma SPRL | |||||||||||||
| Full Title: A MULTICENTER, OPEN-LABEL, FOLLOW-UP STUDY TO ASSESS THE LONG-TERM USE OF LACOSAMIDE (FLEXIBLE DOSE FROM 200 TO 600 MG/DAY) USED AS MONOTHERAPY IN SUBJECTS WHO COMPLETED SP0994 AND RECEIVED LACOSA... | |||||||||||||
| Medical condition: Epilepsy with partial-onset seizures or generalized tonic-clonic seizures | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Completed) DE (Completed) LV (Completed) BG (Completed) PL (Completed) FR (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002713-32 | Sponsor Protocol Number: N01367 | Start Date*: 2015-03-11 | |||||||||||
| Sponsor Name:Korea UCB Co. Ltd. | |||||||||||||
| Full Title: A Multi-Center, Open-label, Randomized Study to Evaluate the Long Term Effectiveness of Levetiracetam as Monotherapy in Comparison With Oxcarbazepine in Subjects With Newly or Recently Diagnosed Pa... | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002167-16 | Sponsor Protocol Number: E2007-G000-311 | Start Date*: 2017-01-30 | ||||||||||||||||
| Sponsor Name:Eisai Limited | ||||||||||||||||||
| Full Title: An Open-Label, Multicenter Study with an Extension Phase to Evaluate the Safety, Tolerability, and Exposure-Efficacy Relationship of Perampanel Oral Suspension when Administered as an Adjunctive Th... | ||||||||||||||||||
| Medical condition: Epilepsy : 1) Partial-Onset Seizures (POS) 2) Primary Generalized Tonic-Clonic Seizures (PGTC) | ||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) LV (Completed) ES (Completed) PL (Completed) BE (Completed) IT (Completed) Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-017744-14 | Sponsor Protocol Number: RGB113905 | Start Date*: 2010-07-28 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
| Full Title: An Open-Label, Flexible-Dose Study of Retigabine Immediate Release (IR) as Adjunctive Therapy to Specified Monotherapy Antiepileptic Treatments in Adults with Partial-Onset Seizures. | |||||||||||||
| Medical condition: Epilepsy - partial-onset seizures with or without secondary generalisation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) ES (Completed) FR (Completed) BE (Completed) DK (Completed) IT (Completed) BG (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001412-65 | Sponsor Protocol Number: A0081106 | Start Date*: 2012-01-25 | |||||||||||
| Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
| Full Title: A 12-MONTH OPEN-LABEL STUDY TO EVALUATE THE SAFETY AND TOLERABILITY OF PREGABALIN AS ADJUNCTIVE THERAPY IN PEDIATRIC SUBJECTS 1 MONTH TO 16 YEARS OF AGE WITH PARTIAL ONSET SEIZURES AND PEDIATRIC AN... | |||||||||||||
| Medical condition: Partial onset seizures and Primary Generalised Tonic Clonic Seizures | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) PL (Completed) EE (Completed) SE (Completed) BE (Completed) FR (Completed) IT (Completed) BG (Completed) GR (Completed) NL (Completed) LT (Completed) FI (Completed) AT (Completed) SK (Completed) ES (Completed) GB (Completed) DE (Completed) HR (Completed) PT (Not Authorised) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005439-27 | Sponsor Protocol Number: SP902 | Start Date*: 2009-02-16 | ||||||||||||||||
| Sponsor Name:UCB BIOSCIENCES, Inc. | ||||||||||||||||||
| Full Title: A Historical-controlled, Multicenter, Double-blind, Randomized Trial to Assess the Efficacy and Safety of Conversion to Lacosamide 400mg/day Monotherapy in Subjects with Partial-onset Seizures | ||||||||||||||||||
| Medical condition: Partial-onset seizures (with or without secondary generalization) | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) IE (Completed) ES (Completed) AT (Completed) DK (Completed) PT (Not Authorised) IT (Completed) FR (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-001664-38 | Sponsor Protocol Number: FFA-MAE | Start Date*: 2019-10-02 | |||||||||||
| Sponsor Name:University Hospital Schleswig-Holstein (UKSH) | |||||||||||||
| Full Title: A proof of concept and assessment of maximal effect study with low dose Fenfluramine as add-on therapy in Myoclonic Astatic Epilepsy (Doose-Syndrome) | |||||||||||||
| Medical condition: Childhood epilepsy: Myoclonic Astatic Epilepsy (Doose-Syndrome) | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002637-42 | Sponsor Protocol Number: EP0165 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:UCB Biopharma SRL | |||||||||||||
| Full Title: An Open-Label, Multicenter, Outpatient Extension Study to Evaluate the Safety and Tolerability of Staccato Alprazolam in Study Participants 12 Years of Age and Older With Stereotypical Prolonged Se... | |||||||||||||
| Medical condition: Treatment of stereotypical prolonged seizure | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) FR (Not Authorised) HU (Trial now transitioned) CZ (Trial now transitioned) PL (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004363-21 | Sponsor Protocol Number: 1042-0603 | Start Date*: 2015-03-11 | |||||||||||
| Sponsor Name:Marinus Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Multicenter, Double Blind, Randomized, Placebo-Controlled Trial to Determine the Efficacy and Safety of Ganaxolone as Adjunctive Therapy for Adults with Drug-Resistant Partial-Onset Seizures Foll... | |||||||||||||
| Medical condition: Drug-Resistant Epilepsy with Partial-Onset Seizures | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001433-98 | Sponsor Protocol Number: N01315 | Start Date*: 2008-08-11 | |||||||||||
| Sponsor Name:UCB BioSciences, Inc | |||||||||||||
| Full Title: An open-label, multinational, multicenter, follow-up study to evaluate the long-term safety and efficacy of brivaracetam, used at a flexible dose up to a maximum of 200 mg/day, in subjects aged 16 ... | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) SE (Completed) ES (Completed) FR (Completed) HU (Completed) FI (Prematurely Ended) IT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003324-19 | Sponsor Protocol Number: STEPONE05 | Start Date*: 2006-11-02 | |||||||||||
| Sponsor Name:University of Mainz | |||||||||||||
| Full Title: STEP ONE –trial (Study on the Treatment of Elderly Patients with Older and Newer antiepileptic drugs) - trial: A multicentre, double-blind, randomized, phase IV clinical trial comparing the safety... | |||||||||||||
| Medical condition: Patients with newly diagnosed focal epilepsy aged 60 years or older with at least 1 epileptic seizure and abnormalities on imaging or EEG or with two epileptic seizures within the last 6 month. Pat... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000869-11 | Sponsor Protocol Number: NC200601 | Start Date*: 2006-12-20 | |||||||||||
| Sponsor Name:Neuro-Consil GmbH | |||||||||||||
| Full Title: Comparison of efficacy and tolerability of rapid intravenous infusion of levetiracetam and sodium valproat. | |||||||||||||
| Medical condition: Focal epilepsy requiring rapid initiation of anticonvulsant protection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001243-36 | Sponsor Protocol Number: BIA-2093-311/EXT | Start Date*: 2015-11-06 | |||||||||||
| Sponsor Name:BIAL - Portela & Ca, S.A. | |||||||||||||
| Full Title: EFFICACY AND SAFETY OF ESLICARBAZEPINE ACETATE (BIA 2-093) AS MONOTHERAPY FOR PATIENTS WITH NEWLY DIAGNOSED PARTIAL-ONSET SEIZURES: A DOUBLE-BLIND, RANDOMIZED, ACTIVE-CONTROLLED, PARALLEL-GROUP, MU... | |||||||||||||
| Medical condition: Adult patients with recently diagnosed partial-onset seizures | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) HU (Completed) LT (Completed) CZ (Completed) LV (Completed) PT (Completed) BE (Completed) FR (Completed) ES (Completed) SE (Completed) EE (Completed) AT (Completed) BG (Completed) SK (Completed) FI (Completed) HR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006169-33 | Sponsor Protocol Number: E2007-G000-306 | Start Date*: 2008-07-17 |
| Sponsor Name:Eisai Ltd | ||
| Full Title: Estudio doble ciego, controlado con placebo, con aumento gradual de dosis, en grupos paralelos para evaluar la eficacia y la seguridad de E2007 (perampanel) administrado como terapia adyuvante en p... | ||
| Medical condition: Epilepsia: crisis parciales refractarias con o sin crisis secundarias generalizadas Epilepsy - refractory partial seizures with or without secondary generalisation | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) CZ (Completed) PT (Completed) HU (Completed) EE (Completed) LT (Completed) PL (Completed) LV (Completed) IT (Completed) BG (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-001887-55 | Sponsor Protocol Number: SCO/BIA-2093-305 | Start Date*: 2007-10-12 | |||||||||||
| Sponsor Name:BIAL - Portela & Ca, S.A. | |||||||||||||
| Full Title: Efficacy and safety of eslicarbazepine acetate (BIA 2-093) as adjunctive therapy for refractory partial seizures in children: a double-blind, randomised, placebo-controlled, parallel-group, multice... | |||||||||||||
| Medical condition: children and adolescents with refractory partial epileptic seizures | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Completed) HU (Completed) CZ (Completed) AT (Completed) FR (Completed) SK (Completed) IT (Completed) ES (Completed) GB (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001959-13 | Sponsor Protocol Number: EPICDKL5 | Start Date*: 2021-12-02 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: Adjunctive cannabidiol therapy in patients with CDKL5 deficiency disorder. Interventional drug study on efficacy and safety with focus on seizure effects | |||||||||||||
| Medical condition: patients with CDKL5 | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-003664-29 | Sponsor Protocol Number: EP0156 | Start Date*: 2021-04-30 | |||||||||||
| Sponsor Name:UCB Biopharma SRL | |||||||||||||
| Full Title: Open-Label, Single-Arm, Multicenter Study to Evaluate Long-Term Safety and Tolerability of Brivaracetam Used as Adjunctive Treatment in Pediatric Study Participants With Epilepsy | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) IE (Completed) HU (Completed) PL (Completed) CZ (Completed) BE (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006344-59 | Sponsor Protocol Number: N01252 | Start Date*: 2007-06-07 | |||||||||||
| Sponsor Name:UCB Pharma S.A. | |||||||||||||
| Full Title: A multi-center, double-blind, parallel-group, placebo-controlled, randomized study: evaluation of the efficacy and safety of brivaracetam in subjects (>= 16 to 70 years old) with Partial Onset Seiz... | |||||||||||||
| Medical condition: Partial Onset Seizures | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) FR (Completed) GB (Completed) HU (Completed) FI (Completed) IT (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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