- Trials with a EudraCT protocol (195)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (27)
195 result(s) found for: Partial seizures.
Displaying page 1 of 10.
EudraCT Number: 2009-016996-31 | Sponsor Protocol Number: P09-004 | Start Date*: 2010-06-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Randomized, Multicenter, Double-Blind, Placebo–Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-O... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Refractory partial-onset seizures with or without secondary generalization | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) GR (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005440-25 | Sponsor Protocol Number: SP904 | Start Date*: 2009-02-16 | ||||||||||||||||
Sponsor Name:UCB BIOSCIENCES, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Open-label Extension Trial to Assess the Long-term Use of Lacosamide Monotherapy and Safety of Lacosamide Monotherapy and Adjunctive Therapy in Subjects with Partial-onset Seizures | ||||||||||||||||||
Medical condition: Partial-onset seizures (with and 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) Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017904-95 | Sponsor Protocol Number: P09-005 | Start Date*: 2010-06-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: Open-Label Extension Study to Evaluate the Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-Onset Seizures who had Participated in P09-004, a Randomized, Multicenter, Doub... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Refractory partial-onset seizures with or without secondary generalization | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) GR (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000717-20 | Sponsor Protocol Number: SP0967 | Start Date*: 2015-06-03 | |||||||||||
Sponsor Name:UCB Biosciences Inc. | |||||||||||||
Full Title: A MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF LACOSAMIDE AS ADJUNCTIVE THERAPY IN SUBJECTS WITH EPILEPSY ≥1 MONTH TO <4... | |||||||||||||
Medical condition: Epilepsy with partial onset seizures | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) CZ (Completed) LT (Completed) IT (Completed) DE (Prematurely Ended) ES (Prematurely Ended) FR (Completed) PL (Completed) RO (Completed) GR (Completed) BG (Completed) HR (Completed) SK (Completed) BE (Completed) PT (Completed) DK (Prematurely Ended) FI (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001982-33 | Sponsor Protocol Number: E2090-E044-401 | Start Date*: 2005-09-05 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: An open label study of Zonegran (zonisamide) in patients with partial onset seizures. | |||||||||||||
Medical condition: Indicated as adjunctive therapy in the treatment of adult patients with partial seizures, with or without secondary generalisation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) SE (Completed) DK (Completed) FI (Completed) DE (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019035-35 | Sponsor Protocol Number: A0081194 | Start Date*: 2011-02-21 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTI-CENTER TRIAL OF PREGABALIN CONTROLLED RELEASE FORMULATION AS ADJUNCTIVE THERAPY IN ADULTS WITH PARTIAL ONSET SEIZURES - PROTOCO... | |||||||||||||
Medical condition: Adjunctive (add on) therapy for adult subjects with partial onset seizures with or without secondary generalization. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) DE (Completed) BG (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: 2005-004023-19 | Sponsor Protocol Number: A0081046 | Start Date*: 2006-05-25 | |||||||||||
Sponsor Name:Pfizer Ltd, Ramsgate Rd, Sandwich, Kent, United Kingdom | |||||||||||||
Full Title: A RANDOMIZED, COMPARATIVE, DOUBLE-BLIND, PARALLEL-GROUP, MULTICENTER, MONOTHERAPY, STUDY OF PREGABALIN (LYRICA) AND LAMOTRIGINE (LAMICTAL) IN PATIENTS WITH NEWLY DIAGNOSED PARTIAL SEIZURES | |||||||||||||
Medical condition: Epilepsy; Patients with newly diagnosed partial seizures (with or without secondary generalization) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) PT (Completed) ES (Completed) BE (Completed) IE (Completed) CZ (Completed) LT (Completed) DE (Completed) SK (Completed) IT (Completed) HU (Completed) FI (Completed) EE (Completed) BG (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000199-14 | Sponsor Protocol Number: N01009 | Start Date*: 2004-11-25 | |||||||||||
Sponsor Name:UCB Pharma S.A. [...] | |||||||||||||
Full Title: A double-blind, randomized, multicenter, placebo-controlled, in-patients maximum 34 day study of levetiracetam oral solution (20-50 mg/kg/day) as adjunctive treatment of refractory partial onset se... | |||||||||||||
Medical condition: Epilepsy - Refractory Partial Onset Seizures | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) BE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000152-16 | Sponsor Protocol Number: SP774 | Start Date*: 2004-10-13 | |||||||||||
Sponsor Name:SCHWARZ BIOSCIENCES GmbH; A member of the UCB group | |||||||||||||
Full Title: An international open-label extension trial to determine safety and efficacy of long-term oral SPM 927 in patients with partial seizures | |||||||||||||
Medical condition: Partial seizures | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) HU (Completed) CZ (Completed) FI (Completed) SE (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003420-37 | Sponsor Protocol Number: A0081042 | Start Date*: 2014-05-16 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTICENTER STUDY OF THE EFFICACY AND SAFETY OF PREGABALIN AS ADJUNCTIVE THERAPY IN CHILDREN 1 MONTH THROUGH <4 YEARS OF AGE WITH PARTIAL ONSET S... | |||||||||||||
Medical condition: Partial onset seizures | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) NL (Prematurely Ended) ES (Completed) DE (Completed) PL (Completed) SK (Completed) GR (Completed) PT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002322-22 | Sponsor Protocol Number: SP757 | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:SCHWARZ BIOSCIENCES Inc. | |||||||||||||
Full Title: A multi-center, open-label trial to investigate the safety and tolerability of intravenous SPM 927 as replacement for oral SPM 927 in subjects with partial seizures with or without secondary genera... | |||||||||||||
Medical condition: partial seizures with or without secondary generalization | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) SE (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003161-40 | Sponsor Protocol Number: A0081143 | Start Date*: 2007-12-14 | ||||||||||||||||
Sponsor Name:Pfizer Inc,East 42nd street,New york, NY10017, USA | ||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, MULTI-CENTER, COMPARATIVE, FLEXIBLE DOSE TRIAL OF PREGABALIN VERSUS GABAPENTIN AS ADJUNCTIVE THERAPY IN SUBJECTS WITH PARTIAL SEIZURES | ||||||||||||||||||
Medical condition: Adjunctive treatment for subjects with partial seizures, with or without secondary generalization. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Completed) ES (Completed) BG (Completed) SK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005078-55 | Sponsor Protocol Number: N01183 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:UCB PHARMA | |||||||||||||
Full Title: Named Patient Program with Levetiracetam Oral Solution, for Pediatric Patients suffering from Epilepsy having previously participated in study N01148 | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016849-25 | Sponsor Protocol Number: A0081047 | Start Date*: 2010-03-15 | |||||||||||
Sponsor Name:Pfizer Inc | |||||||||||||
Full Title: A DOUBLE-BLIND, RANDOMIZED, MULTICENTER EFFICACY AND SAFETY STUDY OF PREGABALIN (LYRICA) AS MONOTHERAPY IN PATIENTS WITH PARTIAL SEIZURES | |||||||||||||
Medical condition: Partial Seizures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003702-26 | Sponsor Protocol Number: E2007-G000-208 | Start Date*: 2007-01-10 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Explore the Safety And Tolerability of Doses of E2007 up to a Maximum of 12 mg In Patients with Refractory Partial Seizures | |||||||||||||
Medical condition: Refractory Partial Seizures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LV (Completed) EE (Completed) LT (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004265-12 | Sponsor Protocol Number: NBI-921352-FOS2022 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:Neurocrine Biosciences, Inc. | |||||||||||||
Full Title: Prospective, Long-Term, Interventional, Active Extension Study to Evaluate the Safety and Tolerability of NBI-921352 as Adjunctive Therapy in Subjects with Focal Onset Seizures (FOS) | |||||||||||||
Medical condition: Focal Onset Seizures (FOS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) HU (Prematurely Ended) ES (Ongoing) IT (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005344-27 | Sponsor Protocol Number: YKP3089C040 | Start Date*: 2022-02-03 | |||||||||||||||||||||
Sponsor Name:SK Life Science, Inc. | |||||||||||||||||||||||
Full Title: Open-Label Safety and Efficacy Study of Cenobamate (YKP3089) in Pediatric Subjects with Partial-onset (Focal) Seizures | |||||||||||||||||||||||
Medical condition: partial onset (focal) seizures | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020730-26 | Sponsor Protocol Number: A0081074 | Start Date*: 2010-10-08 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PLACEBO-CONTROLLED, ESCALATING DOSE, MULTIPLE DOSE STUDY TO EVALUATE THE SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PREGABALIN IN PEDIATRIC PATIENTS WITH PARTIAL ONSET SEIZURES | |||||||||||||
Medical condition: PARTIAL ONSET SEIZURES | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000987-10 | Sponsor Protocol Number: N01235 | Start Date*: 2006-07-27 | |||||||||||
Sponsor Name:UCB S.A. [...] | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized efficacy and safety study of levetiracetam extended release formulation (LEV XR), administered as 2 x 500 mg LEV XR tablets once daily as add-on thera... | |||||||||||||
Medical condition: Refractory epilepsy suffering from partial onset seizures | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
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