- Trials with a EudraCT protocol (177)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
177 result(s) found for: Migraine Headache.
Displaying page 3 of 9.
EudraCT Number: 2007-002667-28 | Sponsor Protocol Number: 0974-031 | Start Date*: 2008-05-29 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A Multicenter, Double-Blind, Placebo-Controlled, Parallel Group Multiple Attacks Study to Compare the Efficacy and Safety of Oral MK-0974 With Placebo for the Acute Treatment of Migraine With or Wi... | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) CZ (Completed) ES (Completed) AT (Completed) DK (Completed) FR (Completed) NL (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003736-38 | Sponsor Protocol Number: BIA-2093-209 | Start Date*: 2009-02-17 | |||||||||||
Sponsor Name:BIAL-Portela & Ca, S.A. | |||||||||||||
Full Title: Efficacy and safety of Eslicarbazepine acetate as preventive therapy for patients with migraine: a double-blind, randomised, placebo-controlled, parallel-group, multicentre clinical trial | |||||||||||||
Medical condition: Adult patients with migraine with or without aura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) DE (Completed) AT (Completed) ES (Completed) PT (Completed) SK (Completed) CZ (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004497-25 | Sponsor Protocol Number: 18898A | Start Date*: 2020-10-27 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, randomized, double-blind, parallel-group, placebo-controlled study with an extension period to evaluate the efficacy and safety of eptinezumab for the prevention of migraine in pati... | |||||||||||||
Medical condition: Migraine in patients with unsuccessful prior preventive treatments | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) DK (Completed) FI (Completed) BE (Completed) PL (Completed) GB (GB - no longer in EU/EEA) SK (Completed) HU (Completed) SE (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000923-15 | Sponsor Protocol Number: 20160172 | Start Date*: 2018-06-14 | |||||||||||
Sponsor Name:Amgen | |||||||||||||
Full Title: A Phase I, Randomized, Open-label, Multiple-dose Study to Evaluate Safety, Tolerability, and Pharmacokinetics of AMG 334 in Children and Adolescents With Migraine | |||||||||||||
Medical condition: Migraine prevention | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001883-21 | Sponsor Protocol Number: I5Q-MC-CGAI | Start Date*: 2016-01-18 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of LY2951742 in Patients with Chronic Migraine - the REGAIN Study | |||||||||||||
Medical condition: Chronic Migraine Headache | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003761-18 | Sponsor Protocol Number: BHV3000-312 | Start Date*: 2022-01-20 | |||||||||||||||||||||||||||||||
Sponsor Name:Biohaven Pharmaceuticals Inc. | |||||||||||||||||||||||||||||||||
Full Title: Phase 3, multicenter, open-label study to assess the long-term safety and tolerability of rimegepant for the acute treatment of migraine (with or without aura) in children and adolescents ≥ 6 to < ... | |||||||||||||||||||||||||||||||||
Medical condition: Acute Migraine (with or without aura) | |||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) PL (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003049-40 | Sponsor Protocol Number: 20007A | Start Date*: 2022-07-22 | ||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||
Full Title: Interventional, randomized, double-blind, parallel-group, placebo-controlled study of add-on eptinezumab treatment to brief educational intervention for the preventive treatment of migraine in pati... | ||||||||||||||||||
Medical condition: Migraine and medication overuse headache | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) SE (Trial now transitioned) NO (Trial now transitioned) DE (Trial now transitioned) DK (Trial now transitioned) NL (Ongoing) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001604-23 | Sponsor Protocol Number: CLOP01 | Start Date*: 2008-12-03 | |||||||||||
Sponsor Name:Guy's & St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: A double blind placebo controlled trial investigating the efficacy of Clopidogrel as prophylactic treatment for migrane. | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004509-30 | Sponsor Protocol Number: 012020 | Start Date*: 2021-05-13 | |||||||||||
Sponsor Name:INSTITUTO DE ESTUDIOS DE CIENCIAS DE LA SALUD DE CASTILLA Y LEON | |||||||||||||
Full Title: A prospective structural, diffusion and connectomics MRI study on migraine patients treated with Fremanezumab | |||||||||||||
Medical condition: MIGRAINE | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000805-42 | Sponsor Protocol Number: MeIn/06/Fro-pp/001 | Start Date*: 2007-06-12 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg S.A., Avenue de la Gare, 1611 Luxembourg, Luxembourg | |||||||||||||
Full Title: A double-blind, cross-over patient preference study of frovatriptan versus zolmitriptan for the acute treatment of migraine | |||||||||||||
Medical condition: Migraine with or without aura according to the IHS criteria | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) DK (Completed) ES (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002348-28 | Sponsor Protocol Number: 0462-083 | Start Date*: 2011-06-30 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess Safety, Tolerability, and Single-Dose Pharmacokinetics of MK-0462 in Migraineurs Aged 6 to 17 Years | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003386-18 | Sponsor Protocol Number: CandMigIII | Start Date*: 2019-12-18 | |||||||||||
Sponsor Name:Department of Neurology and Clinical Neurophysiology, St Olavs Hospital, Trondheim University hospital | |||||||||||||
Full Title: CandMig III study Candesartan for migraine prevention: A multicentre, binational, triple blind, placebo controlled, parallel group study of two doses of candesartan (8 and 16 mg) | |||||||||||||
Medical condition: Episodic migraine with and without aura | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) EE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005107-34 | Sponsor Protocol Number: 07161 | Start Date*: 2009-05-28 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: A double blind parallel group randomised placebo controlled trial of Propranolol and Pizotifen in preventing migraine in children. | |||||||||||||
Medical condition: Children and young people aged 5 years-16 years with Migraine with Out aura (MO), Migraine with Aura (MA), or Probable Migraine (PM) as defined by the International Headache Society (IHS) with 2 to... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000600-42 | Sponsor Protocol Number: I5Q-MC-CGAW | Start Date*: 2018-06-26 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of Galcanezumab in Adults with Treatment-Resistant Migraine - The CONQUER Study | |||||||||||||
Medical condition: Treatment-resistant Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) CZ (Completed) BE (Completed) NL (Completed) HU (Completed) DK (Prematurely Ended) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004257-14 | Sponsor Protocol Number: 0974-011 | Start Date*: 2007-02-21 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (MSD) | |||||||||||||
Full Title: A Multicenter, Double-Blind, Placebo and Active-Controlled, Parallel Group Study to Compare the Efficacy and Safety of Oral MK-0974 With Placebo and Zolmitriptan for the Acute Treatment of Migraine... | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002349-36 | Sponsor Protocol Number: 0462-107 | Start Date*: 2011-06-30 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: An Open-Label Single-Dose Study to Evaluate the Pediatric Palatability of Maxalt Oral Disintegrating Tablets | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004379-38 | Sponsor Protocol Number: H8H-MC-LAHW | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, 12-Month, Open-Label Study of Lasmiditan in Pediatric Patients with Migraine | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001306-41 | Sponsor Protocol Number: ALD403-CLIN-011 | Start Date*: 2017-04-27 | |||||||||||
Sponsor Name:Alder BioPharmaceuticals, Inc. | |||||||||||||
Full Title: A Parallel Group, Double-Blind, Randomized, Placebo Controlled Phase 3 Trial to Evaluate the Efficacy and Safety of ALD403 Administered Intravenously in Patients with Chronic Migraine | |||||||||||||
Medical condition: Chronic Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) DK (Completed) DE (Completed) BE (Completed) SK (Completed) HU (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002086-31 | Sponsor Protocol Number: RC 32\07 | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:ISTITUTO PER L'INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Randomized controlled Trial on the effectiveness of metoclopramide alone or in combination with ketoprofene, versus ketoprofene in acute migraine of child | |||||||||||||
Medical condition: Acute Migraine in childhood | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002201-22 | Sponsor Protocol Number: CAMG334ADE03 | Start Date*: 2019-08-28 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Assessment of Prolonged safety and tOLerability of erenumab in migraine patients in a Long-term OpeN-label study (APOLLON) | |||||||||||||
Medical condition: Migraine prophylaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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