- Trials with a EudraCT protocol (163)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (13)
163 result(s) found for: Copper.
Displaying page 1 of 9.
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: 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: 2016-001386-81 | Sponsor Protocol Number: 2016-1-DSF-MBC | Start Date*: 2019-01-11 |
Sponsor Name:Univerzita Palackého v Olomouci | ||
Full Title: PHASE II OPEN LABELED TRIAL OF DISULFIRAM WITH COPPER IN METASTATIC BREAST CANCERS. | ||
Medical condition: Metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) | ||
Trial results: (No results available) |
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: 2020-005832-31 | 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: 2021-000235-30 | Sponsor Protocol Number: GPRI-21001-COV | Start Date*: 2021-02-09 |
Sponsor Name:General Practitioners Research Institute | ||
Full Title: COVID-19 Primary care Platform for Early treatment and Recovery (COPPER) Study: an open-label adaptive platform randomized controlled trial | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
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: 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: 2020-000963-22 | 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: 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: 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: 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: 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: 2019-001972-12 | Sponsor Protocol Number: AA1817 | Start Date*: 2019-09-13 | |||||||||||||||||||||
Sponsor Name:Department of Oncology, Herlev & Gentofte Hospital | |||||||||||||||||||||||
Full Title: A phase 1b/2 open-label, dose-escalating study of safety and efficacy of disulfiram, copper and vinorelbine in advanced solid tumors and advanced breast cancer | |||||||||||||||||||||||
Medical condition: in phase 1b part: advanced and/or treatment refractory solid malignancies in phase 2 part : advanced or metastatic HER2-negative breast cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002748-25 | Sponsor Protocol Number: KFE19.17 | Start Date*: 2019-10-11 | |||||||||||
Sponsor Name:Department of Oncology, Odense Universitetshospital | |||||||||||||
Full Title: Repurposing disulfiram as treatment for metastatic colorectal cancer An investigator initiated clinical phase II trial | |||||||||||||
Medical condition: Metastatic, non-resectable and irinotecan-resistant colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002242-17 | Sponsor Protocol Number: B00844 | Start Date*: 2020-07-30 | |||||||||||
Sponsor Name:Manchester University NHS Foundation Trust | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, phase 2 evaluation of the efficacy and mechanism of trientine in patients with hypertrophic cardiomyopathy. | |||||||||||||
Medical condition: Hypertrophic Cardiomyopathy (HCM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000167-16 | Sponsor Protocol Number: DIRECT-2016 | Start Date*: 2016-05-19 | |||||||||||
Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
Full Title: DIsulfiram REsponse as add-on to ChemoTherapy in recurrent Glioblastoma: A randomized controlled trial | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) NO (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 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: 2019-001957-16 | Sponsor Protocol Number: BREAST-SK-001 | Start Date*: 2019-10-31 | |||||||||||
Sponsor Name:Národný onkologický ústav | |||||||||||||
Full Title: Phase II study of Vinorelbine, cisplatin, disulfiram and copper in CTC_EMT positive refractory metastatic breast cancer. | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SK (Ongoing) | |||||||||||||
Trial results: View results |
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