- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Drug resistant epilepsy.
Displaying page 1 of 2.
EudraCT Number: 2020-004511-27 | Sponsor Protocol Number: S64647 | Start Date*: 2021-08-05 | |||||||||||
Sponsor Name:University Hospital Leuven | |||||||||||||
Full Title: Add-on clioquinol in drug-resistant childhood epilepsy: an exploratory study | |||||||||||||
Medical condition: Drug resistant epilepsy in children | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003241-26 | Sponsor Protocol Number: EP0093 | Start Date*: 2018-09-04 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: An Open-Label, Multicenter, Extension Study to Evaluate the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-Onset Seizures in Adult Subjects with Drug-Resistant Epilepsy | |||||||||||||
Medical condition: Focal-Onset Seizures | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) HU (Prematurely Ended) ES (Prematurely Ended) CZ (Completed) BG (Completed) FR (Completed) LT (Completed) BE (Completed) PT (Prematurely Ended) EE (Completed) NL (Completed) DK (Completed) AT (Completed) GR (Completed) FI (Completed) NO (Completed) SE (Completed) HR (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005954-78 | Sponsor Protocol Number: 100-059 | Start Date*: 2021-10-13 |
Sponsor Name:CEA | ||
Full Title: Exploring P-glycoprotein-mediated efflux transport at the blood-brain barrier as a biomarker of drug-resistance in focal epilepsy | ||
Medical condition: Investigation in healthy volunteers and epilepsy patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004156-19 | Sponsor Protocol Number: VX11-765-402 | Start Date*: 2012-06-21 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 2b, Randomized, Double Blind, Placebo Controlled, Parallel Group, Dose Ranging Study to Evaluate the Efficacy and Safety of VX-765 in Subjects With Treatment Resistant Partial Epilepsy With... | |||||||||||||
Medical condition: Partial epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Prematurely Ended) HU (Completed) GB (Prematurely Ended) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005433-39 | Sponsor Protocol Number: ADFNLE | Start Date*: 2012-03-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
Full Title: PHASE II OPEN STUDY ABOUT THE EFFECTIVENESS OF FENOFIBRATE AS ADD ON THERAPY FOR DRUG RESISTANT NOCTURNAL FRONTAL LOBE EPILEPSY (FNLE) . | |||||||||||||
Medical condition: Drug resistant nocturnal frontal lobe epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001268-20 | Sponsor Protocol Number: EP0073 | Start Date*: 2015-08-13 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: AN OPEN-LABEL, MULTICENTER, EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF UCB0942 WHEN USED AS ADJUNCTIVE THERAPY FOR PARTIAL-ONSET SEIZURES IN ADULT SUBJECTS WITH... | |||||||||||||
Medical condition: highly drug-resistant focal epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) BE (Completed) BG (Completed) HU (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003381-27 | Sponsor Protocol Number: 100045 | Start Date*: 2018-09-24 |
Sponsor Name:CEA | ||
Full Title: Study in 18F-DPA714 PET to better locate preoperatively the epileptic focus to resect in drug-resistant partial epilepsy | ||
Medical condition: Brain imaging on people with partial pharmaco resistant epilepsy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003003-30 | Sponsor Protocol Number: 2014-853 | Start Date*: 2014-10-31 | |||||||||||
Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
Full Title: ENALEPSIE EFFICACY OF NALOXONE IN REDUCING POSTICTAL CENTRAL RESPIRATORY DYSFUNCTION IN PATIENTS WITH EPILEPSY. | |||||||||||||
Medical condition: Sudden unexpected death in epilepsy (SUDEP) primarily affects young adults with drug-resistant epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006702-78 | Sponsor Protocol Number: BraimTOR-NEURO | Start Date*: Information not available in EudraCT |
Sponsor Name:The Children's Memorial Health Institute | ||
Full Title: Open, randomized, IInd phase clinical study evaluating the safety and efficacy of rapamycin in the treatment of drug-resistant epilepsy in children with rare and ultra-rare diseases of the central ... | ||
Medical condition: epilepsy, mTORopathies, focal cortical dysplasia, LEATS | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: PL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002303-33 | Sponsor Protocol Number: EP0092 | Start Date*: 2019-01-03 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Padsevonil as Adjunctive Treatment of Focal-Onset Seizures in Adult Subjects... | |||||||||||||
Medical condition: Focal-Onset Seizures | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) DE (Prematurely Ended) BE (Completed) GB (Completed) HU (Completed) NL (Completed) DK (Completed) SE (Completed) AT (Completed) GR (Completed) BG (Completed) FI (Completed) ES (Prematurely Ended) CZ (Completed) HR (Completed) FR (Completed) PT (Completed) SK (Prematurely Ended) IT (Prematurely Ended) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003200-48 | Sponsor Protocol Number: EP0091 | Start Date*: 2018-04-09 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose Finding Study to Evaluate the Efficacy and Safety of Padsevonil as Adjunctive Treatment of Focal-Onset Seizures in Adult Subjects with Drug- Res... | |||||||||||||
Medical condition: Focal-Onset Seizures | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) HU (Completed) CZ (Completed) BE (Completed) ES (Completed) FR (Completed) BG (Completed) LT (Completed) SK (Completed) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003464-32 | Sponsor Protocol Number: VNS-MIR2018 | Start Date*: 2019-11-05 |
Sponsor Name: | ||
Full Title: Effect of mirtazapine on seizure frequency in medically refractory epileptic patients with vagal nerve stimulation | ||
Medical condition: epilepsy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003330-12 | Sponsor Protocol Number: EP0069 | Start Date*: 2015-08-18 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled study of the efficacy, safety/tolerability, and pharmacokinetic profile of UCB0942 in adult patients with highly drug-resistant focal epilepsy | |||||||||||||
Medical condition: highly drug-resistant focal epilepsy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) NL (Completed) HU (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003137-42 | Sponsor Protocol Number: EPIFLUX | Start Date*: 2020-04-10 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Klinische Pharmakologie | ||
Full Title: Exploring P-glycoprotein-mediated efflux transport at the blood-brain barrier as a biomarker of drug-resistance in focal epilepsy | ||
Medical condition: Investigation in healthy volunteers and epilepsy patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004008-46 | Sponsor Protocol Number: FFA-LGS | Start Date*: 2016-01-07 |
Sponsor Name:UZ Leuven | ||
Full Title: Add-on fenfluramine in Lennox Gastaut epilepsy | ||
Medical condition: Lennox Gastaut Epilepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004548-64 | Sponsor Protocol Number: RaRETS | Start Date*: Information not available in EudraCT |
Sponsor Name:The Children's Memorial Health Institute | ||
Full Title: Multicenter, randomized, double-blind, placebo controlled study to assess the efficacy and safety of Rapamycin in drug Resistant Epilepsy associated with TSC (RaRE-TS) | ||
Medical condition: tuberous sclerosis complex, epilepsy, organ tumors associated with tuberous sclerosis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: PL (Trial now transitioned) | ||
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: 2013-005528-40 | Sponsor Protocol Number: EPISTOP | Start Date*: 2014-12-05 | |||||||||||
Sponsor Name:The Children's Memorial Health Institute | |||||||||||||
Full Title: Long-term, prospective study evaluating clinical and molecular biomarkers of epileptogenesis in a genetic model of epilepsy – Tuberous Sclerosis Complex. | |||||||||||||
Medical condition: Epilepsy in tuberous sclerosis complex (TSC) | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001019-35 | Sponsor Protocol Number: D16-P15 | Start Date*: 2017-12-19 |
Sponsor Name:Centre Hospitalier Sainte-Anne | ||
Full Title: Effect of vitamin D deficiency compensation in the treatment of drug-resistant epilepsy. | ||
Medical condition: Patients suffering from drug-resistant epilepsy. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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. |
