- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
57 result(s) found for: Wilson's disease.
Displaying page 1 of 3.
EudraCT Number: 2020-000963-22 | Sponsor Protocol Number: VTX-801_CLN_001 | Start Date*: 2021-10-18 | |||||||||||
Sponsor Name:Vivet Therapeutics SAS | |||||||||||||
Full Title: A Phase I/II, Multicenter, Non-randomized, Open Label, Adaptive Design, 5-year Follow-up, Single Dose-escalation Study of VTX-801 in Adult Patients with Wilson’s Disease | |||||||||||||
Medical condition: Wilson's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003711-60 | Sponsor Protocol Number: ALXN1840-WD-205 | Start Date*: 2021-01-15 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 2, single-arm, pathologist-blinded study using liver biopsy specimens to assess copper concentration and histopathologic changes in patients with Wilson disease who are treated with ALXN184... | |||||||||||||
Medical condition: Wilson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) DK (Completed) GB (GB - no longer in EU/EEA) FR (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000102-25 | Sponsor Protocol Number: ALXN1840-WD-Cu-Excretion | Start Date*: 2021-04-09 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Efficacy of ALXN1840 on human biliary copper excretion quantified with 64CuCl2 PET/MR-scan | |||||||||||||
Medical condition: Wilson's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004604-33 | Sponsor Protocol Number: TR-004 | Start Date*: 2021-02-23 | |||||||||||
Sponsor Name:Univar Solutions, B.V. | |||||||||||||
Full Title: Open label, Multicenter, Prospective Study to Characterize the Pharmacokinetics and Pharmacodynamics of Cufence (Trientine Dihydrochloride) and to Investigate the Efficacy and Safety in Wilson’s Di... | |||||||||||||
Medical condition: Wilson Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005266-34 | Sponsor Protocol Number: UX701-CL301 | Start Date*: 2022-02-11 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Multicenter, Seamless, Adaptive, Safety, Dose-finding, and Phase 3 Clinical Study of UX701 AAV-mediated Gene Transfer for the Treatment of Wilson Dis... | |||||||||||||
Medical condition: Wilson disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003564-31 | Sponsor Protocol Number: UNV-TRI-002 | Start Date*: 2014-02-27 | |||||||||||
Sponsor Name:Univar B.V. | |||||||||||||
Full Title: Multicentre, Retrospective and Prospective Study to Assess Long Term Outcomes of Chelator-Based Treatment With Trientine in Wilson Disease Patients Withdrawn from Therapy With d-Penicillamine | |||||||||||||
Medical condition: Wilson disease, also known as hepatolenticular degeneration, a rare automsomal, recessively inherited disorder which results in chronic copper intoxication. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001015-82 | Sponsor Protocol Number: ALXN1840-WD-302 | Start Date*: 2021-11-26 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A multicenter, randomized, controlled, open-label, rater-blinded study to evaluate efficacy, safety, pharmacokinetics, and pharmacodynamics of ALXN1840 versus standard of care in pediatric particip... | |||||||||||||
Medical condition: Wilson Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Completed) ES (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005464-21 | Sponsor Protocol Number: DiagnosingWD-PET/MR-pilot | Start Date*: 2022-07-07 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: Diagnosing Wilson’s Disease with 64-Cu PET/MR – A Pilot Study | ||||||||||||||||||
Medical condition: Wilson's disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001104-41 | Sponsor Protocol Number: ALXN1840-WD-204 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, open-label study to assess copper and molybdenum balance in participants with Wilson disease treated with ALXN1840 | |||||||||||||
Medical condition: Wilson Disease (WD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004135-36 | Sponsor Protocol Number: WTX101-301 | Start Date*: 2018-03-23 |
Sponsor Name:Wilson Therapeutics AB | ||
Full Title: A Phase 3, Randomised, Rater-Blinded, Multi-Centre Study to Evaluate the Efficacy and Safety of WTX101 Administered for 48 Weeks Versus Standard of Care in Wilson Disease Subjects Aged 18 and Older... | ||
Medical condition: Wilson Disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) CZ (Prematurely Ended) FR (Completed) AT (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) PT (Completed) SE (Prematurely Ended) BE (Completed) DK (Prematurely Ended) NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-001703-41 | Sponsor Protocol Number: WTX101-201 | Start Date*: 2014-08-18 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, INC. | |||||||||||||
Full Title: A Phase 2, Multi-centre, Open-label, Study to Evaluate the Efficacy and Safety of WTX101 Administered for 24 Weeks in Newly Diagnosed Wilson Disease Patients Aged 18 and Older with an Extension Pha... | |||||||||||||
Medical condition: Wilson Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) PL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003876-29 | Sponsor Protocol Number: GMPO-131-002 | Start Date*: 2017-05-16 | |||||||||||
Sponsor Name:Orphalan | |||||||||||||
Full Title: CHELATE STUDY: Trientine tetrahydrochloride (TETA 4HCl) for the treatment of Wilson’s disease | |||||||||||||
Medical condition: Wilson's disease (WD) is a life-threatening inborn error of copper metabolism leading to an excessive copper accumulation, mainly in the liver or brain, causing hepatic and neurologic severe symptoms. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004445-32 | Sponsor Protocol Number: TR-001PK | Start Date*: 2013-03-06 |
Sponsor Name:Univar BV | ||
Full Title: A Phase I Pharmacokinetic Profiling Study in Patients Receiving Trientine Dihydrochloride for the Treatment of Wilson’s Disease | ||
Medical condition: Wilson disease, also known as hepatolenticular degeneration, a rare autosomal, recessively inherited disorder which results in chronic copper intoxication. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000905-57 | Sponsor Protocol Number: wilson12345 | Start Date*: 2019-04-17 | |||||||||||
Sponsor Name:The Department of Hepatology and Gastroenterology, Aarhus University Hospital | |||||||||||||
Full Title: Efficacy of zinc on human gut copper uptake depending on zinc type and dose regimen quantified with 64CuCl2 PET/CT-scan | |||||||||||||
Medical condition: Healthy volunteers (Wilson's disease) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003588-24 | Sponsor Protocol Number: CAIN457S12201 | Start Date*: 2020-04-22 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A proof of concept study to evaluate the efficacy, safety and tolerability of secukinumab 300 mg over 32 weeks in adult patients with biopsy-proven forms of lichen planus not adequately controlled ... | |||||||||||||
Medical condition: Lichen planus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005832-31 | Sponsor Protocol Number: ALXN1840-HV-Cu-Absorption | Start Date*: 2021-04-13 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals Inc. | |||||||||||||
Full Title: Efficacy of ALXN1840 on human hepatic copper uptake quantified with 64CuCl2 PET/CT-scan. | |||||||||||||
Medical condition: Healthy Volunteers (Wilson's disease) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005083-81 | Sponsor Protocol Number: ALBUCARD | Start Date*: 2006-06-09 |
Sponsor Name:HOSPITAL CLINIC | ||
Full Title: EFECTOS DE LA ADMINISTRACIÓN DE ALBÚMINA INTRAVENOSA SOBRE LA FUNCIÓN DIASTÓLICA DE LOS PACIENTES CON CIRROSIS HEPÁTICA. | ||
Medical condition: Liver cirrhosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002475-34 | Sponsor Protocol Number: REC0559-B-001 | Start Date*: 2020-03-03 | |||||||||||
Sponsor Name:Recordati Rare Diseases | |||||||||||||
Full Title: Efficacy, Safety and Pharmacokinetics of 3 Doses of REC 0/0559 Eye Drops for the Treatment of Stage 2 (Moderate) and 3 (Severe) Neurotrophic Keratitis in Adult Patients | |||||||||||||
Medical condition: Neurotrophic Keratitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) FR (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000936-21 | Sponsor Protocol Number: 2007LF004B | Start Date*: 2007-09-10 | |||||||||||
Sponsor Name:Royal Brompton | |||||||||||||
Full Title: THE EFFECT ON ALVEOLAR NITRIC OXIDE OF SALMETEROL, FLUTICASONE, AND IN COMBINATION, IN STABLE BRONCHIECTASIS. | |||||||||||||
Medical condition: bronchiectasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002984-24 | Sponsor Protocol Number: CYT-C2-001 | Start Date*: 2019-10-25 |
Sponsor Name:RECORDATI Rare Diseases SARL | ||
Full Title: Open-label, Single-arm, Multicenter Study to Assess the Safety of Cystadrops® in Pediatric Cystinosis Patients from 6 Months to Less Than 2 Years Old [SCOB2 Study] | ||
Medical condition: Corneal cystine crystal deposits in pediatric patients with nephropathic cystinosis from 6 months to less than 2 years old | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) FR (Ongoing) DE (Ongoing) BE (Completed) IT (Completed) | ||
Trial results: (No results available) |
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