- Trials with a EudraCT protocol (47)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
47 result(s) found for: Oxcarbazepine.
Displaying page 2 of 3.
| EudraCT Number: 2016-001072-29 | Sponsor Protocol Number: BIA-2093-211/EXT | Start Date*: 2017-06-29 | |||||||||||
| Sponsor Name:BIAL - Portela & Ca, S.A. | |||||||||||||
| Full Title: OPEN-LABEL, 2-DOSE LEVEL TRIAL TO EVALUATE PHARMACOKINETICS, SAFETY, AND TOLERABILITY OF ESLICARBAZEPINE ACETATE (ESL) AS ADJUNCTIVE THERAPY IN INFANTS WITH REFRACTORY EPILEPSY WITH PARTIAL-ONSET S... | |||||||||||||
| Medical condition: refractory epilepsy with partial-onset seizures in children aged from 1 month to < 2 years | |||||||||||||
|
|||||||||||||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) PT (Completed) IT (Completed) HR (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000374-60 | Sponsor Protocol Number: N01266 | Start Date*: 2011-07-05 | |||||||||||
| Sponsor Name:UCB Pharma SA | |||||||||||||
| Full Title: OPEN-LABEL, SINGLE-ARM, MULTICENTER, LONG-TERM STUDY TO EVALUATE SAFETY AND EFFICACY OF BRIVARACETAM USED AS ADJUNCTIVE TREATMENT IN PEDIATRIC SUBJECTS WITH EPILEPSY | |||||||||||||
| Medical condition: Localization-related, generalized or undetermined whether focal or generalized epileptic syndrome, according to ILAE classification | |||||||||||||
|
|||||||||||||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) ES (Completed) PL (Completed) Outside EU/EEA IE (Completed) GB (GB - no longer in EU/EEA) DE (Completed) HU (Completed) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001105-28 | Sponsor Protocol Number: E2007-G000-232 | Start Date*: 2016-06-27 |
| Sponsor Name:Eisai Inc. | ||
| Full Title: An Open-label Pilot Study With an Extension Phase to Evaluate the Pharmacokinetics, and to Generate Preliminary Safety, Tolerability, and Efficacy of Perampanel (E2007) Oral Suspension When Given a... | ||
| Medical condition: Epilepsy | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2008-005065-64 | Sponsor Protocol Number: CBGG492A2202 | Start Date*: 2009-03-12 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A multicenter, double-blind, randomized, placebo-controlled, two-arm parallel-group study of BGG492 as monotherapy in individuals with refractory partial seizures undergoing inpatient evaluation fo... | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004827-30 | Sponsor Protocol Number: RASLOW | Start Date*: 2017-03-21 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA "BIANCHI-MELACRINO-MORELLI" | |||||||||||||
| Full Title: RAPID VERSUS SLOW WITHDRAWAL OF ANTIEPILEPTIC MONOTHERAPY IN TWO-YEAR SEIZURE-FREE ADULTS PATIENTS WITH EPILEPSY (RASLOW) STUDY: A PRAGMATIC MULTICENTRE, PROSPECTIVE, RANDOMIZED, CONTROLLED STUDY. | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003049-13 | Sponsor Protocol Number: 7347 | Start Date*: 2022-08-24 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: EEG-MRI study of the effect of methylphenidate on neural mechanisms in adult patients with ADHD with or without mood disorders: A randomized controlled trial versus placebo. | ||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| 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 | |||||||||||||
|
|||||||||||||
| 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: 2011-000265-12 | Sponsor Protocol Number: E2007-G000-332 | Start Date*: 2011-08-31 | |||||||||||
| Sponsor Name:Eisai Limited | |||||||||||||
| Full Title: A Double-blind, Randomized, Placebo-controlled, Multicenter, Parallel-group Study with an Open-label Extension Phase to Evaluate the Efficacy and Safety of Adjunctive Perampanel in Primary Generali... | |||||||||||||
| Medical condition: Primary Generalized Tonic-Clonic Seizures | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) LV (Completed) GR (Completed) AT (Completed) CZ (Completed) NL (Completed) PL (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012587-14 | Sponsor Protocol Number: BIA-2093-401 | Start Date*: 2010-01-14 | |||||||||||
| Sponsor Name:BIAL - Portela & Ca, S.A. | |||||||||||||
| Full Title: SEGURIDAD Y EFICACIA DEL ACETATO DE ESLICARBAZEPINA (ESL) COMO TERAPIA ADYUVANTE PARA CRISIS PARCIALES EN PACIENTES MAYORES/ SAFETY AND EFFICACY OF ESLICARBAZEPINE ACETATE (ESL) AS ADJUNCTIVE THERA... | |||||||||||||
| Medical condition: Terapia adyuvante de crisis parciales en pacientes mayores / Adjunctive therapy of partial-onset seizures in elderly patients | |||||||||||||
|
|||||||||||||
| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) CZ (Completed) AT (Completed) PT (Completed) DE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004714-27 | Sponsor Protocol Number: N01258 | Start Date*: 2011-10-05 | |||||||||||
| Sponsor Name:UCB Biosciences, Inc. | |||||||||||||
| Full Title: A Multicenter, Open-label, Four-arm, Randomized trial, Evaluating the Safety and Tolerability of Brivaracetam Intravenous Infusion and Bolus, Administered in BID Regimen as an Adjunctive Antiepilep... | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002461-37 | Sponsor Protocol Number: SP0980 | Start Date*: 2012-04-05 | |||||||||||
| Sponsor Name:UCB BIOSCIENCES Inc | |||||||||||||
| Full Title: A PROSPECTIVE, MULTINATIONAL, OPEN-LABEL, SINGLE-ARM, EXPLORATIVE STUDY TO EVALUATE THE TOLERABILITY AND EFFICACY OF LACOSAMIDE WHEN ADDED TO LEVETIRACETAM WITH WITHDRAWAL OF THE CONCOMITANT SODIUM... | |||||||||||||
| Medical condition: Epilepsy with partial onset seizures | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) AT (Completed) ES (Completed) NL (Prematurely Ended) DK (Completed) BG (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000483-27 | Sponsor Protocol Number: PRA/BIA-2093-302 | Start Date*: 2004-08-19 |
| Sponsor Name:BIAL - Portela & Ca, S.A. | ||
| Full Title: Efficacy and safety of BIA 2-093 as adjunctive therapy for refractory partial seizures in a double-blind, randomised, placebo-controlled, parallel-group, multicentre clinical trial. | ||
| Medical condition: Refractory partial epilepsy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) ES (Completed) DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000144-14 | Sponsor Protocol Number: N01276 | Start Date*: 2008-07-14 | |||||||||||
| Sponsor Name:UCB Inc | |||||||||||||
| Full Title: An international, double-blind, randomized, multi-center, parallel group, historical-control conversion to monotherapy study to evaluate the efficacy and safety of brivaracetam in subjects (≥ 16 to... | |||||||||||||
| Medical condition: Partial onset seizures with or without secondary generalization. | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005606-39 | Sponsor Protocol Number: BIA-2093-208 | Start Date*: 2009-08-24 | |||||||||||
| Sponsor Name:BIAL-Portela & Ca, SA | |||||||||||||
| Full Title: EFFECTS OF ESLICARBAZEPINE ACETATE (BIA 2-093) ON COGNITIVE FUNCTION IN CHILDREN WITH PARTIAL ONSET SEIZURES: AN ADD-ON, DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTICENTRE CL... | |||||||||||||
| Medical condition: Evaluate the effects of ESL on cognition in comparison with placebo as adjunctive therapy in children aged 6 to 16 years old with refractory partial-onset seizures. | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Not Authorised) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002140-10 | Sponsor Protocol Number: N01125 | Start Date*: 2005-08-24 | |||||||||||
| Sponsor Name:UCB Pharma S.A. | |||||||||||||
| Full Title: An open-label, multi-center, follow-up trial to evaluate long-term safety and efficacy of brivaracetam (ucb 34714) used as adjunctive treatment at a flexible dose up to a maximum of 200 mg/day in s... | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) DE (Completed) GB (Completed) FI (Completed) ES (Completed) IT (Completed) SE (Completed) HU (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000145-58 | Sponsor Protocol Number: N01306 | Start Date*: 2008-07-11 | |||||||||||
| Sponsor Name:UCB Pharma S.A. | |||||||||||||
| Full Title: An international, double-blind, randomized, multi-center, parallel group, historical-control conversion to monotherapy study to evaluate the efficacy and safety of brivaracetam in subjects (≥ 16 to... | |||||||||||||
| Medical condition: Partial onset seizures with or without secondary generalization. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Completed) HU (Prematurely Ended) FI (Prematurely Ended) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001449-16 | Sponsor Protocol Number: 802NP301 | Start Date*: 2017-04-11 | |||||||||||
| Sponsor Name:Biogen Idec Research Limited | |||||||||||||
| Full Title: A Phase 3 Placebo-Controlled, Double-Blind Randomized Withdrawal Study to Evaluate the Efficacy and Safety of BIIB074 (Vixotrigine) in Subjects With Trigeminal Neuralgia | |||||||||||||
| Medical condition: Trigeminal Neuralgia | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) GB (GB - no longer in EU/EEA) DK (Prematurely Ended) BE (Prematurely Ended) SK (Prematurely Ended) BG (Prematurely Ended) AT (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000827-42 | Sponsor Protocol Number: N01372 | Start Date*: 2012-09-27 | |||||||||||
| Sponsor Name:UCB Pharma SA | |||||||||||||
| Full Title: AN OPEN-LABEL, MULTICENTER, FOLLOW-UP STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF BRIVARACETAM USED AS ADJUNCTIVE TREATMENT IN SUBJECTS AGED 16 YEARS OR OLDER WITH EPILEPSY | |||||||||||||
| Medical condition: Nonpyschotic Behavioural Side Effects in Subjects With Epilepsy | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005177-23 | Sponsor Protocol Number: N01395 | Start Date*: 2012-09-27 | |||||||||||
| Sponsor Name:UCB Pharma SA | |||||||||||||
| Full Title: An Open-Label, Multicenter, Single-Arm Study to Evaluate the Reduction in Nonpsychotic Behavioral Side Effects in Subjects with Epilepsy Switching from Levetiracetam to Brivaracetam due to Nonpsych... | |||||||||||||
| Medical condition: Nonpyschotic Behavioural Side Effects in Subjects With Epilepsy | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006536-22 | Sponsor Protocol Number: N01263 | Start Date*: 2011-07-05 | |||||||||||
| Sponsor Name:UCB Pharma SA | |||||||||||||
| Full Title: OPEN-LABEL, SINGLE-ARM, MULTICENTER, PHARMACOKINETIC, SAFETY, AND EFFICACY STUDY OF ADJUNCTIVE ADMINISTRATION OF BRIVARACETAM IN SUBJECTS FROM ≥1 MONTH TO <16 YEARS OLD WITH EPILEPSY | |||||||||||||
| Medical condition: Localization-related, generalized or undetermined whether focal or generalized epileptic syndrome, according to ILAE classification | |||||||||||||
|
|||||||||||||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) ES (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.