- Trials with a EudraCT protocol (120)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
120 result(s) found for: Migraines.
Displaying page 1 of 6.
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: 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: 2004-003973-10 | Sponsor Protocol Number: EU-2004-04 | Start Date*: 2005-07-21 | |||||||||||
Sponsor Name:Capnia, Inc. | |||||||||||||
Full Title: Multi-Center, Randomized Double-Blind Study to Evaluate the Efficacy and Safety of CAP3 in the Treatment of Acute Migraine | |||||||||||||
Medical condition: Acute migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2008-004095-43 | 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: 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: 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: 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: 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: 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: 2006-006187-35 | Sponsor Protocol Number: 0974-016 | Start Date*: 2007-04-10 | |||||||||||
Sponsor Name:Laboratoires Merck Sharp & Dohme - Chibret | |||||||||||||
Full Title: A phase III, Multicenter, Randomized, Placebo-Controlled Clinical Trial to Study the Safety and Efficacy of Oral MK-0974 in the Acute Treatment of Migraine with or Without Aura. | |||||||||||||
Medical condition: Acute treatment of Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005285-20 | Sponsor Protocol Number: M/31416/50 | Start Date*: 2005-12-28 | |||||||||||
Sponsor Name:Almirall Prodesfarma, S.A. | |||||||||||||
Full Title: Treatment of Acute Migraine when Pain is Mild versus when Pain is Moderate to Severe: an Almotriptan Parallel, Placebo Controlled Clinical Trial “Act when mild?” | |||||||||||||
Medical condition: Acute treatment of the headache phase of migraine attacks with or without aura | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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: 2020-005924-12 | Sponsor Protocol Number: 19678A | Start Date*: 2021-12-04 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, randomized, double-blind, parallel-group, placebo-controlled study of Lu AG09222 for the prevention of migraine in patients with unsuccessful prior preventive treatments | |||||||||||||
Medical condition: Prevention of migraine in patients with unsuccessful prior preventive treatments | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) CZ (Completed) DK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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: 2006-001488-51 | Sponsor Protocol Number: ADX10059-201 | Start Date*: 2006-08-01 | |||||||||||
Sponsor Name:Addex Pharmaceuticals S.A. | |||||||||||||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY, TO INVESTIGATE THE EFFICACY, SAFETY AND TOLERABILITY OF THE MGLUR5 NEGATIVE ALLOSTERIC MODULATOR ADX10059 IN THE ACUTE TREATMENT OF MIGRAINE | |||||||||||||
Medical condition: Migraine with or without aura | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001431-58 | Sponsor Protocol Number: ROX-2007-01 | Start Date*: 2007-09-10 | |||||||||||
Sponsor Name:ROXRO PHARMA, Inc. | |||||||||||||
Full Title: A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study of the Safety, Tolerability, and Analgesic Efficacy of Ketorolac Tromethamine Administered Intranasally for the Acute Treatment of Mig... | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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 |
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