- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Seizures AND Petit Mal Epilepsy AND Epilepsy.
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EudraCT Number: 2016-002313-22 | Sponsor Protocol Number: ADV6770-A11CS | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:ADVICENNE PHARMA SA | ||||||||||||||||||
Full Title: A randomised, active controlled, open-label, 2-way cross-over, multicentre study to investigate the palatability, acceptability, pharmacokinetics, safety and tolerability, and treatment compliance ... | ||||||||||||||||||
Medical condition: Children with chilhood absence epilepsy. | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001514-29 | Sponsor Protocol Number: LAM115377 | Start Date*: 2017-08-11 | |||||||||||
Sponsor Name:GlaxoSmithKline KK | |||||||||||||
Full Title: A multi-center, uncontrolled, open-label, evaluation of Lamotrigine monotherapy on newly diagnosed typical absence seizures in children and adolescents | |||||||||||||
Medical condition: Typical absence seizure | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002750-24 | Sponsor Protocol Number: N01269 | Start Date*: 2021-04-16 |
Sponsor Name:UCB Biopharma SRL | ||
Full Title: A Randomized, Dose-Finding and Confirmatory, Double-Blind, Placebo-Controlled, Parallel-Group Multicenter Study With a 2-Stage Adaptive Design and Randomized Withdrawal to Evaluate the Efficacy, Sa... | ||
Medical condition: Childhood absence epilepsy and juvenile absence epilepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: PL (Completed) BE (Completed) IT (Trial now transitioned) SK (Trial now transitioned) Outside EU/EEA ES (Trial now transitioned) RO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001318-32 | Sponsor Protocol Number: P261-401 | Start Date*: 2011-11-17 | |||||||||||
Sponsor Name:Upsher-Smith Laboratories, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of Intranasal Midazolam (USL261) in the Outpatient Treatment of Subjects with Seizure Clusters ARTEMIS-1: Acute Rescu... | |||||||||||||
Medical condition: epilepsy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
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 | |||||||||||||
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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: 2016-002879-96 | Sponsor Protocol Number: N01361 | Start Date*: 2016-07-25 | ||||||||||||||||
Sponsor Name:UCB Japan Co. Ltd. | ||||||||||||||||||
Full Title: An open-label, multicenter, long-term, follow-up study in Japan to evaluate the safety, tolerability, and efficacy of adjunctive treatment with oral L059 (levetiracetam) in epilepsy subjects with g... | ||||||||||||||||||
Medical condition: Epilepsy Generalized Tonic-Clonic Seizures | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003557-91 | Sponsor Protocol Number: E2090-E044-315 | Start Date*: 2008-07-09 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled, multicentre study to assess the efficacy and safety of adjunctive zonisamide in primary generalised tonic clonic seizures | |||||||||||||
Medical condition: Primary generalised tonic-clonic seizures (PGTCS) in idiopathic generalised epilepsy (IGE) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Prematurely Ended) LT (Prematurely Ended) FI (Prematurely Ended) CZ (Prematurely Ended) EE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006695-10 | Sponsor Protocol Number: E2090-E044-316 | Start Date*: 2008-09-23 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: Open Label Extension Study Following Double-blind, Randomized, Placebo-controlled, Multicenter Study to Assess Efficacy and Safety of Adjunctive Zonisamide in Primary Generalized Tonic-Clonic Seizures | |||||||||||||
Medical condition: Primary generalised tonic-clonic seizures (PGTCS) in idiopathic generalised epilepsy (IGE) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2018-001337-41 | Sponsor Protocol Number: YKP3089C025 | Start Date*: 2018-12-17 | |||||||||||
Sponsor Name:SK Life Science, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Cenobamate Adjunctive Therapy in Subjects with Primary Generalized Tonic-Clonic Seizures | |||||||||||||
Medical condition: Primary Generalized Tonic-Clonic Seizures | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) BG (Completed) CZ (Completed) SK (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2015-002142-31 | Sponsor Protocol Number: 547-SSE-301 | Start Date*: 2016-11-16 | |||||||||||
Sponsor Name:Sage Therapeutics | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF SAGE-547 INJECTION IN THE TREATMENT OF SUBJECTS WITH SUPER-REFRACTORY STATUS EPILEPTICUS | |||||||||||||
Medical condition: SUPER-REFRACTORY STATUS EPILEPTICUS (SRSE) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) SE (Completed) DK (Completed) ES (Completed) NL (Completed) FI (Completed) HU (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003392-34 | Sponsor Protocol Number: FAST-trail | Start Date*: 2021-10-19 | |||||||||||
Sponsor Name:Odense Universitetshospital | |||||||||||||
Full Title: “FAST ACUTE SEDATION AT INTENSIVE CARE VS. HIGH-DOSE I.V. ANTI-SEIZURE MEDICATION FOR TREATMENT OF NON-CONVULSIVE STATUS EPILEPTICUS - A RANDOMIZED, MULTICENTER TRIAL (FAST TRIAL)” | |||||||||||||
Medical condition: Verfied non convulsive status epilepticus refractory to standard treatment with benzodiazepines and at least one first line drug | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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