- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: International Classification of Headache Disorders.
Displaying page 1 of 3.
EudraCT Number: 2020-001968-28 | Sponsor Protocol Number: 19385A | Start Date*: 2022-02-24 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, open-label, fixed-dose multiple administration study to evaluate long-term treatment with eptinezumab in patients with chronic cluster headache | |||||||||||||
Medical condition: Chronic cluster headache | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) NL (Completed) FI (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003729-62 | Sponsor Protocol Number: R-Verapamil-001 | Start Date*: 2013-01-16 | |||||||||||
Sponsor Name:CENTER LABORATORIES, INC | |||||||||||||
Full Title: A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Phase 2 Study to Evaluate the Safety and Efficacy of R-Verapamil in the Prophylaxis of Episodic Cluster Headache | |||||||||||||
Medical condition: Episodic Cluster Headache | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004835-23 | Sponsor Protocol Number: TON/01/05-CLIN | Start Date*: 2006-01-26 |
Sponsor Name:Minster Pharmaceuticals Ltd | ||
Full Title: Multi-centre, parallel group, double-blind, placebo controlled study of the efficacy and tolerability of TONABERSAT in prophylaxis of migraine headache | ||
Medical condition: Migraine with or without aura meeting the diagnostic criteria of the International Classification of Headache Disorders (Edition 2). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) DK (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003148-21 | Sponsor Protocol Number: BASICstudy | Start Date*: 2019-01-25 |
Sponsor Name:NTNU- Norwegian University of Science and Technology | ||
Full Title: BASIC - Botulinum toxin type A blockade of the sphenopalatine ganglion in treatment-refractory chronic cluster headache | ||
Medical condition: Chronic cluster headache | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006687-25 | Sponsor Protocol Number: 79665 | Start Date*: 2022-07-21 |
Sponsor Name:Leiden University Medical Centre | ||
Full Title: Repeated corticosteroid injections around the Greater Occipital Nerve (GON) as prophylactic treatment in chronic cluster headache | ||
Medical condition: Chronic Cluster headache | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001882-17 | Sponsor Protocol Number: I5Q-MC-CGAH | 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 Episodic Migraine - the EVOLVE-2 Study | |||||||||||||
Medical condition: Episodic Migraine Headache | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) CZ (Completed) DE (Completed) ES (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: 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: 2019-002331-28 | Sponsor Protocol Number: 20190006 | Start Date*: 2020-03-10 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: Biomarker and Genetic Predictors of Erenumab Treatment Response, a Phase 4 Investigational Open-label Study (INTERROGATE) | |||||||||||||
Medical condition: Episodic or chronic migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) IS (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: 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: 2006-000210-21 | Sponsor Protocol Number: TON/02/05-CLIN | Start Date*: 2006-03-27 |
Sponsor Name:Prof Jes Olesen | ||
Full Title: A single centre, double-blind, randomised, placebo controlled cross-over study to evaluate the efficacy and tolerability of tonabersat in the prophylaxis of migraine in patients presenting with mig... | ||
Medical condition: Migraine with aura meeting the diagnostic criteria of the International Classification of Headache Disorders (Edition 2) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001771-36 | Sponsor Protocol Number: CHDR1755 | Start Date*: 2019-07-16 | |||||||||||
Sponsor Name:Centre for Human Drug Research | |||||||||||||
Full Title: Assessment of Neublastin-Induced Skin and Sensory Alterations and Headache in Healthy Subjects and Migraine Patients | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (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: 2019-004378-24 | 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) |
EudraCT Number: 2017-002866-38 | Sponsor Protocol Number: FM-BOEM | Start Date*: 2018-01-25 | |||||||||||
Sponsor Name:IRCCS FONDAZIONE ISTITUTO NEUROLOGICO NAZIONALE C. MONDINO | |||||||||||||
Full Title: Pilot study for the evaluation of the efficacy of OnabotulinumtoxinA in high frequency migraine | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2022-001175-14 | Sponsor Protocol Number: BHV3000-406 | Start Date*: 2023-04-17 | |||||||||||
Sponsor Name:Biohaven Pharmaceuticals, Inc. | |||||||||||||
Full Title: BHV3000-406: A Phase 4, Randomized, Double-blind Placebo-Controlled, Efficacy and Tolerability Trial of Rimegepant for the Acute Treatment of Migraine in Adults Unsuitable for Triptan Use | |||||||||||||
Medical condition: migraine attacks with or without aura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) IT (Trial now transitioned) SE (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001884-38 | Sponsor Protocol Number: I5Q-MC-CGAJ | Start Date*: 2015-12-07 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: A Phase 3, Long-Term, Open-Label Safety Study of LY2951742 in Patients with Migraine. | ||
Medical condition: Episodic or chronic migraine headache | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) BE (Completed) FR (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 |
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