- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Progressive Multifocal Leukoencephalopathy.
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EudraCT Number: 2008-001314-24 | Sponsor Protocol Number: 111JC101 | Start Date*: 2009-01-02 | |||||||||||
Sponsor Name:Biogen Idec Ltd | |||||||||||||
Full Title: A Randomized, Rater-Blinded Study to Explore the Effect of Mefloquine in Subjects with Progressive Multifocal Leukoencephalopathy (PML) | |||||||||||||
Medical condition: Progressive Multifocal Leukoencephalopathy (PML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000725-41 | Sponsor Protocol Number: CLI-107-15 | Start Date*: 2013-01-22 | |||||||||||
Sponsor Name:Cytheris S.A. | |||||||||||||
Full Title: A randomized, placebo controlled, multicenter phase IIb study of human recombinant Interleukin-7 (CYT107) in HIV-related Progressive Multifocal Leukoencephalopathy. | |||||||||||||
Medical condition: HIV-infected patients with Progressive Multifocal Leukoencephalopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Ongoing) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002566-13 | Sponsor Protocol Number: NEXT-MS | Start Date*: 2019-12-19 | |||||||||||
Sponsor Name:Amsterdam University Medical Center | |||||||||||||
Full Title: Personalized extended interval dosing of natalizumab in relapsing remitting multiple sclerosis | |||||||||||||
Medical condition: Relapsing remitting multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020369-26 | Sponsor Protocol Number: 101JC404 | Start Date*: 2010-11-29 | |||||||||||
Sponsor Name:Biogen Idec | |||||||||||||
Full Title: High-Dose Corticosteroids for Immune Reconstitution Inflammatory Syndrome in Patients Who Develop Progressive Multifocal Leukoencephalopathy on Natalizumab | |||||||||||||
Medical condition: Immune Reconstitution Inflammatory Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004435-72 | Sponsor Protocol Number: GA28951 | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: AN OPEN LABEL EXTENSION AND SAFETY MONITORING STUDY OF MODERATE TO SEVERE ULCERATIVE COLITIS PATIENTS PREVIOUSLY ENROLLED IN ETROLIZUMAB PHASE II/III STUDIES | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Prematurely Ended) DE (Ongoing) CZ (Prematurely Ended) DK (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended) AT (Completed) PT (Prematurely Ended) EE (Prematurely Ended) NL (Prematurely Ended) NO (Prematurely Ended) ES (Prematurely Ended) GR (Prematurely Ended) BE (Prematurely Ended) HR (Completed) IT (Prematurely Ended) SK (Prematurely Ended) HU (Prematurely Ended) BG (Completed) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003855-76 | Sponsor Protocol Number: GA29145 | Start Date*: 2015-08-12 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: AN OPEN-LABEL EXTENSION AND SAFETY MONITORING STUDY OF PATIENTS WITH MODERATELY TO SEVERELY ACTIVE CROHN’S DISEASE PREVIOUSLY ENROLLED IN THE ETROLIZUMAB PHASE III PROTOCOL GA29144 | |||||||||||||
Medical condition: Crohn`s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) EE (Ongoing) LT (Prematurely Ended) LV (Prematurely Ended) HU (Ongoing) DE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) SK (Prematurely Ended) CZ (Prematurely Ended) BE (Prematurely Ended) AT (Completed) FR (Ongoing) HR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003409-36 | Sponsor Protocol Number: GA27927 | Start Date*: 2011-11-14 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A Phase II Open-Label Extension Study to Evaluate the Long-Term Safety of rhuMAb Beta7 in Patients with Moderate to Severe Ulcerative Colitis | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) CZ (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000018-16 | Sponsor Protocol Number: OZA22/IM047-048 | Start Date*: 2023-04-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Effect of ozanimod on meningeal inflammation and glial activation in Multiple Sclerosis: one year phase 4 experimental study | |||||||||||||
Medical condition: Relapsing Multiple Sclerosis (relapsing-remitting, relapsing-progressive) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002765-34 | Sponsor Protocol Number: MabionCD20-003RA | Start Date*: 2021-10-21 | |||||||||||
Sponsor Name:Mabion S.A. | |||||||||||||
Full Title: A Double-Blind, Randomized, Parallel-Group Study to Investigate the Pharmacokinetic and Clinical Similarity Between MabionCD20 (manufactured in commercial scale), EU-approved MabThera® and US-licen... | |||||||||||||
Medical condition: Moderate-to-severe rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003649-10 | Sponsor Protocol Number: CA40192 | Start Date*: 2018-03-13 | ||||||||||||||||
Sponsor Name:Roche Farma S.A. (Soc unipersonal) que realiza el ensayo en España y que actúa como represntante de FHoffmann-La Roche | ||||||||||||||||||
Full Title: A PHASE I, OPEN–LABEL, RANDOMIZED, PHARMACOKINETIC, PHARMACODYNAMIC, AND SAFETY STUDY OF ETROLIZUMAB FOLLOWED BY OPEN–LABEL EXTENSION AND SAFETY MONITORING IN PEDIATRIC PATIENTS FROM 4 YEARS TO LES... | ||||||||||||||||||
Medical condition: Moderate to severe ulcerative colitis (UC); moderate to severe Crohn’s disease (CD) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) GB (GB - no longer in EU/EEA) PL (Ongoing) DE (Completed) BE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000441-38 | Sponsor Protocol Number: CPCRA 065 | Start Date*: 2005-04-26 |
Sponsor Name:National Institute of Allergy and Infectious Diseases, National Institutes of Health | ||
Full Title: Large, Simple Trial Comparing Two Strategies for Management of Anti-Retroviral Therapy (The SMART Study) | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) IT (Prematurely Ended) IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004061-41 | Sponsor Protocol Number: 101-MS-321 | Start Date*: 2006-06-01 | |||||||||||
Sponsor Name:BIOGEN IDEC LTD | |||||||||||||
Full Title: An Open-label, Multicenter, Extension Study to Evaluate the Safety and Tolerability of Natalizumab Following Re-Initiation of Dosing in Multiple Sclerosis Subjects Who Have Completed Study C-1801 o... | |||||||||||||
Medical condition: Multiple sclerosis (MS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Prematurely Ended) FI (Prematurely Ended) IE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) HU (Prematurely Ended) DK (Prematurely Ended) CZ (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000630-34 | Sponsor Protocol Number: MLN0002-3029 | Start Date*: 2022-12-09 |
Sponsor Name:Takeda Development Center Americas, Inc. | ||
Full Title: A Phase 3b Extension Study to Evaluate the Long-term Safety of Vedolizumab Intravenous in Pediatric Patients With Ulcerative Colitis or Crohn’s Disease | ||
Medical condition: Active Ulcerative Colitis (UC) or Crohn's disease (CD) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Ongoing) PL (Ongoing) CZ (Ongoing) ES (Prematurely Ended) SK (Prematurely Ended) GR (Ongoing) BE (Ongoing) LT (Completed) HR (Ongoing) Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2013-003884-71 | Sponsor Protocol Number: LPS13649 | Start Date*: 2015-02-05 | |||||||||||
Sponsor Name:Genzyme Corporation | |||||||||||||
Full Title: A long-term follow-up study for Multiple Sclerosis patients who have completed the alemtuzumab Extension Study (CAMMS03409) | |||||||||||||
Medical condition: Relapsing-remitting multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) CZ (Completed) ES (Completed) DE (Completed) IT (Completed) DK (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
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