- Trials with a EudraCT protocol (265)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
265 result(s) found for: Adalimumab (Humira).
Displaying page 2 of 14.
EudraCT Number: 2019-000717-37 | Sponsor Protocol Number: AMGEVITA-HVM2019 | Start Date*: 2019-06-27 |
Sponsor Name:Fundación Publica Andaluza para la Gestión de Salud en Sevilla (FISEVI) | ||
Full Title: LOSS OF RESPONSE OF THE ADALIMUMAB BIOSIMILAR COMPARED WITH THE LOSS OF RESPONSE OF THE ADALIMUMAB ORIGINAL: CONTROLLED, RANDOMIZED, NON-INFERIORITY OPEN STUDY. "ADA-SWITCH Study" | ||
Medical condition: Inflammatory Bowel Disease: Crohn's Disease and Ulcerative Colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003053-21 | Sponsor Protocol Number: M16-560 | Start Date*: 2019-06-27 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: Randomized, Double-Blind, Double-Dummy, Active Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of ABBV-3373 in Subjects with Moderate to Severe Rheumatoid Arth... | |||||||||||||
Medical condition: Moderate to Severe Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001918-42 | Sponsor Protocol Number: TDM-ADA2019 | Start Date*: 2020-04-22 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: A non-inferiority study on dose reduction of adalimumab in psoriasis patients who are overtreated. | |||||||||||||
Medical condition: Patients with moderate-to-severe psoriasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000632-15 | Sponsor Protocol Number: CHS-1420-02 | Start Date*: 2015-09-25 | |||||||||||
Sponsor Name:Coherus BioSciences, Inc. | |||||||||||||
Full Title: A Double-Blind, Randomized, Parallel-Group, Active-Control Study to Compare the Efficacy and Safety of CHS-1420 Versus Humira® in Subjects With Chronic Plaque Psoriasis (PsOsim) | |||||||||||||
Medical condition: Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) IT (Completed) SK (Completed) EE (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001919-39 | Sponsor Protocol Number: 48890 | Start Date*: 2014-08-27 |
Sponsor Name:Erasmus MC | ||
Full Title: Lengthening Adalimumab Dosing Interval in IBD patients in long term remission, the LADI study | ||
Medical condition: Inflammatory bowel disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014348-12 | Sponsor Protocol Number: ASIM (IMM 08-0061) | Start Date*: 2009-10-13 | |||||||||||
Sponsor Name:Mikkel Østergaard | |||||||||||||
Full Title: Helkrops MR, MR af sacroiliacaled og columna totalis og cirkulerende biomarkører hos patienter med spondylartritis i behandling med adalimumab (ASIM) | |||||||||||||
Medical condition: Spondyloartritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000352-29 | Sponsor Protocol Number: B5381002 | Start Date*: 2014-10-27 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A PHASE 3 RANDOMIZED, DOUBLE-BLIND STUDY ASSESSING THE EFFICACY AND SAFETY OF PF-06410293 AND ADALIMUMAB IN COMBINATION WITH METHOTREXATE IN SUBJECTS WITH MODERATELY TO SEVERELY ACTIVE RHEUMATOID ... | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) EE (Completed) LT (Completed) HU (Completed) GB (Completed) DE (Completed) ES (Completed) FR (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003420-46 | Sponsor Protocol Number: MYL-1410A-3001 | Start Date*: 2015-07-22 | |||||||||||
Sponsor Name:Mylan GmbH (Mylan) | |||||||||||||
Full Title: Multicenter, Double-Blind, Randomized, 2-Arm, Parallel-Group, Equivalence Study Evaluating Efficacy and Safety Similarity of Mylan Adalimumab (MYL-1401A) Compared With Humira® in Subjects With Mode... | |||||||||||||
Medical condition: Chronic Plaque-Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) EE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004971-37 | Sponsor Protocol Number: STRU-09-06 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Adalimumab for psoriasis patients who are non-responders to etanercept: An open-label study | |||||||||||||
Medical condition: psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005809-53 | Sponsor Protocol Number: 10041986 | Start Date*: 2013-05-23 |
Sponsor Name: | ||
Full Title: A prospective study to determine the minimal biologic drug serum trough concentration required to maintain stable disease activity in psoriasis. | ||
Medical condition: Psoriasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002911-25 | Sponsor Protocol Number: AVT02-GL-302 | Start Date*: 2020-06-02 | |||||||||||
Sponsor Name:Alvotech Swiss AG | |||||||||||||
Full Title: Multicenter, Double-blind, Randomized, Parallel-group, Study Evaluating Pharmacokinetic, Efficacy, Safety, and Immunogenicity Between Patients with Moderate to Severe Chronic Plaque Psoriasis Recei... | |||||||||||||
Medical condition: Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) IS (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003073-97 | Sponsor Protocol Number: M10-060 | Start Date*: 2007-11-19 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Multi-center, Randomized, Vehicle-Controlled Study to Assess the Efficacy and Safety of Adalimumab in Combination with Topical Treatment (Calcipotriol/Betamethasone) in Subjects with Moderate to ... | |||||||||||||
Medical condition: Moderate to Severe Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) NL (Completed) DE (Completed) CZ (Completed) GR (Completed) DK (Completed) GB (Completed) BE (Completed) SE (Completed) ES (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002934-20 | Sponsor Protocol Number: M04-691 | Start Date*: 2005-02-22 |
Sponsor Name:Abbott GmbH & Co. KG | ||
Full Title: A Multi-Centre, Randomized, Double-Blind, Placebo-Controlled Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of Clinical Remission in Subjects with Moderate to Severe C... | ||
Medical condition: Crohn's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006885-27 | Sponsor Protocol Number: ADA-periSPA2008 | Start Date*: 2009-04-21 | |||||||||||
Sponsor Name:Clinical Immunology and Rheumatology | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ADALIMUMAB (HUMIRA®) IN PATIENTS WITH PERIPHERAL SPONDYLOARTHRITIS WITHOUT ANKYLOSING SPONDYLITIS OR PSORIATIC ARTHRITIS | |||||||||||||
Medical condition: PERIPHERAL SPONDYLOARTHRITIS WITHOUT ANKYLOSING SPONDYLITIS OR PSORIATIC ARTHRITIS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004826-21 | Sponsor Protocol Number: M05-760 | Start Date*: 2006-01-20 |
Sponsor Name:Abbott GmbH & Co. KG | ||
Full Title: Review of Safety and Efficacy With Adalimumab in Patients With Active Ankylosing Spondylitis – An Open-Label Study to Evaluate the Response to Adalimumab in Patients Who Have Failed Standard Therap... | ||
Medical condition: Active Ankylosing Spondylitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) NO (Completed) DE (Completed) GB (Completed) SE (Completed) DK (Completed) IE (Completed) ES (Completed) BE (Completed) AT (Completed) IT (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004814-41 | Sponsor Protocol Number: M06-806 | Start Date*: 2007-08-07 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Double-Blind Study to Evaluate the Safety, Efficacy and Pharmacokinetics of the Human Anti-TNF Monoclonal Antibody Adalimumab in Pediatric Subjects with Moderate to Severe Crohn's Di... | |||||||||||||
Medical condition: Moderate to Severe Crohn's Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) BE (Completed) NL (Completed) GB (Completed) IT (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003433-10 | Sponsor Protocol Number: GP17-302 | Start Date*: 2016-06-08 | |||||||||||
Sponsor Name:Hexal, AG | |||||||||||||
Full Title: GP17-302 A randomized, double-blind, parallel-group, multicenter study to demonstrate similar efficacy and to compare safety and immunogenicity of GP2017 and Humira® in patients with moderate t... | |||||||||||||
Medical condition: rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) DE (Completed) HU (Completed) RO (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003321-42 | Sponsor Protocol Number: NL58948.091.16 | Start Date*: 2017-01-18 |
Sponsor Name:Radboud University Medical Centre | ||
Full Title: Lengthening Adalimumab Dosing Interval in quiescent Crohn’s disease patients: the LADI study. | ||
Medical condition: Crohn's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001554-25 | Sponsor Protocol Number: 371 | Start Date*: 2019-10-29 |
Sponsor Name:Reade | ||
Full Title: Adalimumab dose optimization in rheumatoid arthritis using therapeutic drug monitoring (ADDORA): multi-center single blinded randomized controlled trail | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003199-11 | Sponsor Protocol Number: 2013-1 | Start Date*: 2015-09-25 |
Sponsor Name:GETAID - Groupe d'Etude Thérapeutique des Affections Inflammatoires Digestives | ||
Full Title: Changing the coUrse of cRohn's disease with an Early use of adalimumab: The CURE study. | ||
Medical condition: Crohn's disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) FR (Ongoing) | ||
Trial results: (No results available) |
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