- Trials with a EudraCT protocol (205)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (49)
205 result(s) found for: Migraine.
Displaying page 1 of 11.
EudraCT Number: 2020-002470-27 | Sponsor Protocol Number: 3101-312-002 | Start Date*: 2021-05-12 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Allergan Limited | ||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE 3, MULTICENTER, OPEN-LABEL 52-WEEK EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY AND TOLERABILITY OF ORAL ATOGEPANT FOR THE PREVENTION OF MIGRAINE IN PARTICIPANTS WITH CHRONIC OR EPISODI... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chronic or Episodic Migraine (Migraine without aura, migraine with aura, or chronic migraine) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) CZ (Trial now transitioned) SE (Completed) HU (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005689-40 | Sponsor Protocol Number: COL-MIG-302 | Start Date*: 2016-10-18 | |||||||||||||||||||||||||||||||
Sponsor Name:CoLucid Pharmaceuticals, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Study of Three Doses of Lasmiditan (50 mg, 100 mg and 200 mg) Compared to Placebo in the Acute TReaTment of MigrAiNe: A randomized, double-blind, placebo-controlled parallel group study (SPARTAN) | |||||||||||||||||||||||||||||||||
Medical condition: acute migraine | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019288-13 | Sponsor Protocol Number: MK0974-065 | Start Date*: 2010-06-24 | |||||||||||
Sponsor Name:Merck, Sharp & Dohme B.V. | |||||||||||||
Full Title: A Six Month Phase II/III, Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Evaluate the Safety, Tolerability, and Efficacy of Telcagepant (MK-0974) for Prevention of Menstrually Relat... | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) SE (Completed) DE (Completed) FI (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000244-90 | Sponsor Protocol Number: IT/ALMO/01 | Start Date*: 2005-03-08 | |||||||||||
Sponsor Name:ALMIRALL PRODESFARMA | |||||||||||||
Full Title: A randomized, prospective, cross-over, double blind, placebo-controlled multicentre study to assess the efficacy and tolerability of almotriptan 12.5 mg in the mild pain phase of Mestrual Migraine ... | |||||||||||||
Medical condition: Treatment of migraine | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000866-38 | Sponsor Protocol Number: MeFi/05/Dex-Mig/01 | Start Date*: 2005-08-05 | |||||||||||
Sponsor Name:A. MENARINI I.F.R. | |||||||||||||
Full Title: DEXKETOPROFEN TROMETAMOL IN ATTACK THERAPY OF MIGRAINE. | |||||||||||||
Medical condition: ATTACK THERAPY OF MIGRAINE. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001707-36 | Sponsor Protocol Number: 20120295 | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of AMG 334 in Chronic Migraine Prevention | |||||||||||||
Medical condition: Prevention of chronic migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) NO (Completed) FI (Completed) DK (Completed) PL (Completed) CZ (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005316-28 | Sponsor Protocol Number: CBGG492A2214 | Start Date*: 2012-07-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, parallel group, placebo controlled, study in patients with non-chronic migraine to assess the efficacy, safety and tolerability of BID oral doses of BGG492... | |||||||||||||
Medical condition: Non-chronic migraine with or without aura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002211-18 | Sponsor Protocol Number: CAMG334A2301 | Start Date*: 2016-10-31 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-week double-blind, randomized, multicenter study comparing the efficacy and safety of once monthly subcutaneous 140 mg AMG 334 against placebo in adult episodic migraine patients who have fail... | |||||||||||||
Medical condition: Migraine Prevention | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) SE (Completed) DE (Completed) FI (Completed) ES (Completed) AT (Completed) DK (Completed) BE (Completed) GR (Completed) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004095-43 | Sponsor Protocol Number: 0974-046 | Start Date*: 2008-12-29 | |||||||||||
Sponsor Name:MSD Finland Oy | |||||||||||||
Full Title: A Phase IIa Randomized, Double-Blind, Parallel-Group, Placebo and Active-Controlled, Clinical Trial to Study the Efficacy and Safety of MK-0974 Co-administered with Ibuprofen or Acetaminophen in Pa... | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) CZ (Completed) DE (Completed) FR (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005674-37 | Sponsor Protocol Number: COL-MIG-305(H8H-CD-LAHL) | Start Date*: 2016-11-01 | |||||||||||||||||||||||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||||||||||||||||||||||
Full Title: An Open-label, LonG-term, Safety Study of LAsmiDItan (100 mg and 200 mg) in the Acute Treatment Of MigRaine (GLADIATOR) | |||||||||||||||||||||||||||||||||
Medical condition: acute migraine | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004464-38 | Sponsor Protocol Number: 20120296 | Start Date*: 2015-06-25 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of AMG 334 in Migraine Prevention | |||||||||||||
Medical condition: Migraine Prevention | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) CZ (Completed) DE (Completed) SK (Completed) AT (Completed) PL (Completed) HU (Prematurely Ended) BE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004463-20 | Sponsor Protocol Number: 20120297 | Start Date*: 2015-10-02 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of AMG 334 in Migraine Prevention | |||||||||||||
Medical condition: Migraine Prevention | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) GR (Completed) DK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000785-36 | Sponsor Protocol Number: MeIn/06/Fro-pp/002 | Start Date*: 2007-04-26 | |||||||||||
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 rizatriptan 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: FI (Completed) GB (Completed) GR (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004259-40 | Sponsor Protocol Number: 0974-012-07 | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:Merck & Co Inc., | |||||||||||||
Full Title: A Multicenter, Double-Blind, Active-Controlled, Parallel Group Study to Examine the Safety, Tolerability and Efficacy of Oral MK-0974 for the Long Term Treatment of Acute Migraine With or Without Aura | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) FR (Completed) IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000079-31 | Sponsor Protocol Number: 1246.4 | Start Date*: 2008-07-16 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A randomised, double-blind, placebo- and active comparator-controlled, five parallel groups study to investigate the efficacy and safety of BI 44370 TA (50 mg, 200 mg, and 400 mg) administered oral... | |||||||||||||
Medical condition: migraine headache with and without aura | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) FR (Completed) BE (Completed) SE (Completed) ES (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003646-33 | Sponsor Protocol Number: 20190008 | Start Date*: 2020-06-24 | |||||||||||
Sponsor Name:Amgen, Inc. | |||||||||||||
Full Title: Comprehensive Assessment of Erenumab Efficacy in Subjects With High Frequency Episodic Migraine With at Least 1 Previously Failed Preventive Treatment: a Global, Double-blind, Placebo-controlled Ph... | |||||||||||||
Medical condition: High frequency episodic migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) PT (Completed) HU (Completed) BG (Completed) CZ (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004351-23 | Sponsor Protocol Number: I5Q-MC-CGAS | Start Date*: 2021-02-22 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of Galcanezumab in Patients 6 to 17 Years of Age with Episodic Migraine – the REBUILD-1 Study | |||||||||||||
Medical condition: Episodic Migraine | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) DE (Completed) IT (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005311-27 | Sponsor Protocol Number: 20130255 | Start Date*: 2015-04-08 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: An Open-label Extension (OLE) Study to Assess the Long-term Safety and Efficacy of AMG 334 | |||||||||||||
Medical condition: Prevention of chronic migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) DK (Completed) NO (Completed) PL (Completed) CZ (Completed) FI (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001649-38 | Sponsor Protocol Number: 19379A | Start Date*: 2022-06-24 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Long-term, open-label (dose-blinded), extension study of eptinezumab in children and adolescents with chronic or episodic migraine | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PT (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004378-24 | Sponsor Protocol Number: H8H-MC-LAHV | Start Date*: 2020-09-07 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Pediatric Options for Migraine Relief: A randomized, double-blind, placebo-controlled study of lasmiditan for acute treatment of 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) NL (Trial now transitioned) BE (Trial now transitioned) IT (Prematurely Ended) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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