- Trials with a EudraCT protocol (50)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
50 result(s) found for: Myoclonic epilepsy.
Displaying page 1 of 3.
EudraCT Number: 2007-003556-10 | Sponsor Protocol Number: E2090-E044-317 | Start Date*: 2008-07-09 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled, multi-centre study to assess the efficacy and safety of adjunctive zonisamide in myoclonic seizures associated with idiopathic generalised epilepsy. | |||||||||||||
Medical condition: myoclonic seizures in idiopathic generalised epilepsy (IGE). | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) LT (Prematurely Ended) CZ (Completed) EE (Prematurely Ended) PL (Completed) ES (Completed) FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004355-38 | Sponsor Protocol Number: EpIc 1151 | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:ASSOCIAZIONE S.N.O.- SCIENZE NEUROLOGICHE OSPEDALIERE | |||||||||||||
Full Title: Multicenter, comparative, randomized, open trial to evaluate efficacy and safety of Levetiracetam versus Carbamazepine in post stroke late onset crisis | |||||||||||||
Medical condition: Post stroke late onset epileptic crisis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006696-36 | Sponsor Protocol Number: E2090-E044-318 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: Open label Extension Study Following Double-blind, Randomized, Placebo-controlled, Multicentre Study to Assess Efficacy and Safety of Adjunctive Zonisamide in Myoclonic Seizures associated with Idi... | |||||||||||||
Medical condition: myoclonic seizures in idiopathic generalised epilepsy (IGE). | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002198-30 | Sponsor Protocol Number: EPICURESUB05T02 | Start Date*: 2007-07-03 | |||||||||||
Sponsor Name:Inserm-ISP Pole Recherches cliniques et thérapeutiques | |||||||||||||
Full Title: A MULTICENTRE RANDOMIZED CONTROLLED TRIAL COMPARING TOPIRAMATE, STIRIPENTOL AND CLOBAZAM AT THE MAXIMAL TOLERATED DOSAGE, AS ADJUNCTIVE THERAPY TO VALPROATE AND CLOBAZAM IN PAEDIATRIC PATIENTS WITH... | |||||||||||||
Medical condition: Dravet Syndrome | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003702-95 | Sponsor Protocol Number: EPICURE SUB05T02 | Start Date*: 2007-07-03 | |||||||||||
Sponsor Name:ISTITUTO C. MONDINO | |||||||||||||
Full Title: A MULTICENTRE RANDOMIZED CONTROLLED TRIAL COMPARING TOPIRAMATE, STIRIPENTOL AND CLOBAZAM AS ADJUNCTIVE THERAPY TO VALPROATE AND CLOBAZAM IN PAEDIATRIC PATIENTS WITH DRAVET'S SYNDROME (SMEI) NOT ADE... | |||||||||||||
Medical condition: Dravet Syndrome | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
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) | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003210-33 | Sponsor Protocol Number: ERPME01 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:Department of Neurology, Turku University Hospital | |||||||||||||
Full Title: Effect of ropinirole hydrochloride in progressive myoclonic epilepsy of Unverricht–Lundborg type | |||||||||||||
Medical condition: Progressive myoclonus epilepsy of the Unverricht–Lundborg disease (ULD) type | |||||||||||||
|
|||||||||||||
Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002147-15 | Sponsor Protocol Number: 200200 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DI MANTOVA | |||||||||||||||||||||||
Full Title: Intravenous immunoglobulin for Unverricht–Lundborg disease: single-patient trial. | |||||||||||||||||||||||
Medical condition: Unverricht-Lundborg disease | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001536-46 | Sponsor Protocol Number: N01236 | Start Date*: 2006-11-14 | |||||||||||
Sponsor Name:UCB S.A. | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel study to evaluate the efficacy and safety of brivaracetam used as adjunctive treatment for 12 weeks in adolescent and adult pat... | |||||||||||||
Medical condition: Patients with genetically ascertained Unverricht-Lundborg disease (ULD). | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003094-61 | Sponsor Protocol Number: GWEP20238 | Start Date*: 2022-09-26 | |||||||||||
Sponsor Name:GW RESEARCH LTD. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multisite, Phase 3 study to investigate the efficacy and safety of cannabidiol oral solution (GWP42003-P) in children and adolescents with epilepsy w... | |||||||||||||
Medical condition: Epilepsy with myoclonic-atonic seizures | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000169-12 | Sponsor Protocol Number: N01187 | Start Date*: 2006-09-28 | |||||||||||
Sponsor Name:UCB S.A. | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel study to evaluate the efficacy and safety of brivaracetam used as adjunctive treatment for 12 weeks in adolescent and adult pat... | |||||||||||||
Medical condition: Patients with genetically ascertained Unverricht-Lundborg disease (ULD). | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) FR (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002238-34 | Sponsor Protocol Number: FFA-MAE-EXT | Start Date*: 2021-03-22 | |||||||||||
Sponsor Name:University Hospital Schleswig-Holstein (UKSH) | |||||||||||||
Full Title: Open label extension study for monitoring long-term safety in patients with Myoclonic Astatic Epilepsy (Doose-Syndrome) receiving Fenfluramine as add-on therapy | |||||||||||||
Medical condition: Childhood epilepsy: Myoclonic Astatic Epilepsy (Doose-Syndrome) | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004379-22 | Sponsor Protocol Number: SP0961 | Start Date*: 2015-03-10 | |||||||||||
Sponsor Name:UCB BIOSCIENCES, Inc. | |||||||||||||
Full Title: An Open-Label Pilot Study to Assess the Safety of Oral Lacosamide as Adjunctive Therapy for Uncontrolled Primary Generalized Tonic-Clonic Seizures in Subjects With Idiopathic Generalized Epilepsy | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000185-34 | Sponsor Protocol Number: VAL1221-ITLAFORA-01 | Start Date*: 2023-04-19 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA USL DI BOLOGNA | ||||||||||||||||||||||||||||
Full Title: A SINGLE ARM, OPEN-LABEL, PHASE 2 STUDY TO ASSESS THE SAFETY AND EFFICACY OF VAL-1221 ON SUBJECTS WITH LAFORA DISEASE | ||||||||||||||||||||||||||||
Medical condition: patients with mid- to late stage Lafora Desease | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001446-18 | Sponsor Protocol Number: SP0966 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:UCB Biosciences Inc. | |||||||||||||
Full Title: A MULTI-CENTER, OPEN-LABEL, EXPLORATORY STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF LACOSAMIDE AS ADJUNCTIVE THERAPY IN SUBJECTS ≥1 MONTH TO <18 YEARS WITH EPILEPSY SYNDROMES ASSOCIATED WITH GE... | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) PL (Completed) Outside EU/EEA FR (Completed) | |||||||||||||
Trial results: View results |
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 | |||||||||||||
|
|||||||||||||
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: 2012-001770-29 | Sponsor Protocol Number: EP0012 | Start Date*: 2015-07-06 |
Sponsor Name:UCB BIOSCIENCES, Inc. | ||
Full Title: AN OPEN-LABEL, MULTICENTER EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF LACOSAMIDE AS ADJUNCTIVE THERAPY FOR UNCONTROLLED PRIMARY GENERALIZED TONIC-CLONIC SEIZURES IN SUBJECTS W... | ||
Medical condition: Idiopathic generalized epilepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) HU (Completed) DE (Completed) ES (Ongoing) CZ (Completed) PT (Completed) BE (Completed) PL (Completed) BG (Completed) FR (Completed) RO (Ongoing) Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-000360-17 | Sponsor Protocol Number: TGO-VGB-III-01 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:TARGEON | ||||||||||||||||||
Full Title: Acceptability study of a new paediatric form of vigabatrin in infants and children with infantile spasms or pharmaco-resistant partial epilepsy. Observational, descriptive, open-label, multi-centr... | ||||||||||||||||||
Medical condition: Infantile spasms and pharmaco-resistant partial epilepsy | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004496-12 | Sponsor Protocol Number: 1042-PCDH19-3002 | Start Date*: 2019-09-26 | |||||||||||
Sponsor Name:Marinus Pharmaceuticals, Inc. | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled trial of adjunctive ganaxolone treatment in female children with protocadherin 19 (PCDH19)-related epilepsy followed by long-term open-label treatment | |||||||||||||
Medical condition: protocadherin 19 (PCDH19)-related epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) NL (Prematurely Ended) PL (Completed) HU (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002939-34 | Sponsor Protocol Number: GWEP1424 | Start Date*: 2014-12-29 | |||||||||||
Sponsor Name:GW Research Ltd | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study to investigate the efficacy and safety of cannabidiol (GWP42003-P) in children and young adults with Dravet syndrome. | |||||||||||||
Medical condition: Dravet syndrome | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) NL (Completed) PL (Completed) | |||||||||||||
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

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. |
