- Trials with a EudraCT protocol (727)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
727 result(s) found for: Biochemistry.
Displaying page 1 of 37.
EudraCT Number: 2021-005629-25 | Sponsor Protocol Number: 215301 | Start Date*: 2022-08-25 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals SA | |||||||||||||
Full Title: A Phase 1/2a, open-label, randomised, controlled, multi-country, dose-escalation study to assess the safety and immunogenicity of AS37 in combination with the Hepatitis B surface antigen (HBsAg), a... | |||||||||||||
Medical condition: Healthy volunteers (Hepatitis B Virus infection) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001561-88 | Sponsor Protocol Number: CICL670ATRO4 | Start Date*: 2016-04-14 |
Sponsor Name:Novartis Pharmaceuticals | ||
Full Title: A Phase II, Multi-center, Single-arm, Prospective Study to Evaluate the Safety and Efficacy of Deferasirox in Beta-thalassemia Major Patients After Hematopoietic Stem Cell Transplantation | ||
Medical condition: -Iron overload | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-001005-16 | Sponsor Protocol Number: CL2-44819-004 | Start Date*: 2016-09-21 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Randomized Efficacy and Safety Trial with Oral S 44819 after Recent ischemic cerebral Event. International, multi-centre, randomized, double-blind placebo-controlled phase II study. | |||||||||||||
Medical condition: Post stroke recovery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) SE (Completed) DE (Completed) BE (Completed) NL (Completed) ES (Completed) PL (Completed) CZ (Completed) SI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004199-12 | Sponsor Protocol Number: RG_11-139vitd | Start Date*: 2012-01-04 |
Sponsor Name:University of Birmingham | ||
Full Title: An open label dose ranging study to optimise vitamin D levels prior to oesophagectomy | ||
Medical condition: perioperative inflammation in patients undergoing oesophagectomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004610-29 | Sponsor Protocol Number: 2014.001 | Start Date*: 2015-02-18 |
Sponsor Name:Skanes University Hospital | ||
Full Title: Ciclosporin to Protect Renal function In Cardiac Surgery. CiPRICS. A Phase II Double Blind Randomized Placebo Controlled Study. | ||
Medical condition: Renal dysfunction after CABG surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003367-40 | Sponsor Protocol Number: 2007/049/HP | Start Date*: 2009-03-03 |
Sponsor Name:CHU de Rouen | ||
Full Title: Pilot study of the effect of a substance P antagonist, aprepitant, on aldosterone and cortisol secretions in healthy volunteers | ||
Medical condition: The aim is to measure plasma aldosterone and cortisol concentrations in basal conditions and in response to different stimulation tests of the adrenal function | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-003885-14 | Sponsor Protocol Number: XRP6976J/3502 | Start Date*: 2005-03-30 |
Sponsor Name:Aventis Pharma, S.A. | ||
Full Title: Multidisciplinar, multicenter, randomized phase III clinical trial comparing taxotere plus estramustine phosphate plus prednisone, versus taxotere prednisone, in advanced prostate carcinoma patient... | ||
Medical condition: Acvanced prostate carcinoma | ||
Disease: | ||
Population Age: Adults | Gender: | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002828-85 | Sponsor Protocol Number: RG_15-114 | Start Date*: 2017-04-28 | |||||||||||||||||||||
Sponsor Name:University of Birmingham | |||||||||||||||||||||||
Full Title: Paediatric Hepatic International Tumour Trial | |||||||||||||||||||||||
Medical condition: Hepatoblastoma and Hepatocellular Carcinoma. | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Trial now transitioned) ES (Ongoing) NO (Trial now transitioned) DE (Ongoing) CZ (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) AT (Trial now transitioned) SE (Completed) FI (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002425-30 | Sponsor Protocol Number: 0171 | Start Date*: 2020-03-17 |
Sponsor Name:Theravance Biopharma Ireland Limited | ||
Full Title: A Phase 3, 182-week, Open-Label, Extension Study to Investigate the Safety and Tolerability Study of TD-9855 in Treating Symptomatic Neurogenic Orthostatic Hypotension (symptomatic nOH) in Subjects... | ||
Medical condition: Symptomatic Neurogenic Orthostatic Hypotension in Subjects with Primary Autonomic Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) ES (Prematurely Ended) PL (Completed) EE (Completed) FR (Completed) PT (Prematurely Ended) AT (Prematurely Ended) BG (Prematurely Ended) DE (Prematurely Ended) HU (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-002741-21 | Sponsor Protocol Number: AAA-Ga-TOC-EU-01 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Advanced Accelerator Applications SA | |||||||||||||
Full Title: Safety and tolerability of 68Ga-DOTATOC for injection in patients with proven gastro-entero-pancreatic neuroendocrine tumors (GEP-NETs). | |||||||||||||
Medical condition: Patients with proven gastro-entero-pancreatic neuroendocrine tumours (GEP-NETs) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001157-32 | Sponsor Protocol Number: A4250-003 | Start Date*: 2015-05-13 |
Sponsor Name:Albireo AB | ||
Full Title: An exploratory Phase II Study to demonstrate the Safety and Efficacy of A4250 in Children with Cholestatic Pruritus | ||
Medical condition: Patients wih Cholestatic Pruritus | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) DK (Completed) DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002864-24 | Sponsor Protocol Number: UMCN-AKF 06.02 | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:Dept. of Clinical Pharmacy, Radboud UMC Nijmegen, The Netherlands | |||||||||||||
Full Title: Drug interactions between ATOvaquone used in MAlaria prophylaxis and antiretroviral agents in HIV-1 infected patients (ATOMA) | |||||||||||||
Medical condition: malaria prophylaxis in HIV patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005165-49 | Sponsor Protocol Number: PLX-HF-01 | Start Date*: 2018-09-24 | |||||||||||
Sponsor Name:Pluristem Ltd. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study, Designed to Determine the Efficacy, Safety, and Tolerability of Intramuscular Administration of Allogeneic PLX-PAD Cell... | |||||||||||||
Medical condition: Muscle Injury Following Arthroplasty for Hip Fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (GB - no longer in EU/EEA) DK (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004987-91 | Sponsor Protocol Number: 2020/ABM/01/00098 | Start Date*: 2021-11-17 | |||||||||||
Sponsor Name:Uniwersytet Medyczny im. Piastów Śląskich we Wrocławiu | |||||||||||||
Full Title: Effects of calcium electroporation, electrochemotherapy, and irreversible electroporation (IRE-CaCl2, ECT and IRE) on quality of life and progression – free survival in patients with pancreatic can... | |||||||||||||
Medical condition: Unresectable pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020233-56 | Sponsor Protocol Number: DC-006 | Start Date*: 2011-03-24 |
Sponsor Name:Oslo University Hospital | ||
Full Title: PHASE I/II TRIAL OF VACCINE THERAPY IN RELAPSED AND PLATINUM RESISTANT EPITHELIAL OVARIAN CANCER PATIENTS USING AUTOLOGOUS DENDRITIC CELLS LOADED WITH AMPLIFIED OVARIAN CANCER STEM CELL mRNA, hTE... | ||
Medical condition: Relapsed and platinum resistant epithelial ovarian carcinoma patients that have received one line of non-platinum chemotherapy in resistance disease setting. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000985-12 | Sponsor Protocol Number: 1719-B | Start Date*: 2018-11-26 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Near-infrared fluorescence imaging in kidney transplantations using ZW800-1 for perfusion assessment: a pilot study | ||
Medical condition: Patients undergoing a living-donor kidney transplantation (living kidney donor and kidney recipient) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001620-31 | Sponsor Protocol Number: CZB/4/622 | Start Date*: 2009-09-14 |
Sponsor Name:NHS Highland | ||
Full Title: Glutathione Status in Platelets From Patients With Type 2 Diabetes: Therapeutic Potential of N-acetylcysteine to Help Prevent Platelet Hyperaggregability | ||
Medical condition: Platelet Aggregation in type 2 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018584-41 | Sponsor Protocol Number: P10.YYY | Start Date*: 2010-07-23 | |||||||||||
Sponsor Name:LUMC | |||||||||||||
Full Title: A phase II study of ARA290 as therapeutic strategy in no-option critical limb ischemia patients. | |||||||||||||
Medical condition: Critical Limb Ischemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004357-13 | Sponsor Protocol Number: CTH201401 | Start Date*: 2015-03-18 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Coagaulation in patients with atrial fibrillation: The effect of dabigatran | |||||||||||||
Medical condition: Atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004305-25 | Sponsor Protocol Number: EPU P25 | Start Date*: 2006-09-15 |
Sponsor Name:Maastricht University | ||
Full Title: Residual effects of zopiclone 7.5 mg and temazepam 20 mg on cognition and actual driving performance in healthy elderly | ||
Medical condition: Healthy elderly volunteers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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