- ICH GCP
- Registre des essais cliniques de l'UE
Derniers essais
EudraCT Number: 2006-003934-14 | Sponsor Protocol Number: 86,1,2006_06_01 | Start Date: | |||||||||||
Sponsor Name: Universitätsmedizin Göttingen | |||||||||||||
Full Title: „Eine randomisierte, placebokontrollierte Doppelblindstudie zur Evaluation der Effektivität oral verabreichten Doxycyclins bei Patienten mit Creutzfeldt-Jakob-Krankheit“ | |||||||||||||
Medical condition: Creutzfeldt-Jakob-Krankheit | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004443-22 | Sponsor Protocol Number: Spirig I 04-05 | Start Date: | |||||||||||
Sponsor Name: Spirig Pharma AG | |||||||||||||
Full Title: Untersuchung der Wirksamkeit einer glycerinhaltigen Creme bei der Behandlung von Atopischer Dermatitis. Kontrolliert, randomisierte Doppel-Blind-Studie. | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001550-34 | Sponsor Protocol Number: TIGEM2-PDH | Start Date: | |||||||||||||||||||||||||||||||
Sponsor Name: FONDAZIONE TELETHON | |||||||||||||||||||||||||||||||||
Full Title: Studio clinico pilota per valutare l’efficacia della terapia con fenilbutirrato in pazienti affetti da deficit di piruvato deidrogenasi | |||||||||||||||||||||||||||||||||
Medical condition: La Sperimentazione verrà eseguita su pazienti affetti da difetto dell’enzima piruvato deidrogenasi.I pazienti affetti da questa malattia manifestano aumento dei livelli di lattato nel sangue e nell... | |||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003199-10 | Sponsor Protocol Number: OLE-NLRC4/XIAP.2016.001 | Start Date: | ||||||
Sponsor Name: AB2 Bio Ltd. | ||||||||
Full Title: Open-label extension study with Tadekinig alfa (r-hIL-18BP) to monitor safety and tolerability in patients with IL-18 driven monogenic autoinflammatory conditions: NLRC4 mutation and XIAP deficiency | ||||||||
Medical condition: NLRC4 mutation XIAP deficiency | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: DE (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000856-33 | Sponsor Protocol Number: 2012-40 | Start Date: | |||||||||||
Sponsor Name: Institut Pasteur | |||||||||||||
Full Title: A phase I/II, open-label, study of intracerebral administration of adeno-associated viral vector containing the human alpha-N-acetylglucosaminidase cDNA in children with Sanfilippo type B syndrome | |||||||||||||
Medical condition: Mucopolysaccharidosis III B | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021474-11 | Sponsor Protocol Number: GE-001-013 | Start Date: | ||||||
Sponsor Name: GE Healthcare Ltd. and its Affiliates | ||||||||
Full Title: A Multicentre, Randomised, Open-label, Comparative Phase IV Trial To Assess Changes in Dementia Diagnostic Category and Diagnostic Confidence After DaTSCAN Imaging in Subjects with an Uncertain Dia... | ||||||||
Medical condition: Subjects with possible Dementia with Lewy Bodies (DLB) who may or may not also fulfil the criteria for Alzheimers Disease (AD) | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) ES (Ongoing) IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-001653-28 | Sponsor Protocol Number: 03/314 | Start Date: | ||||||
Sponsor Name: The Leeds teaching Hospitals NHS trust | ||||||||
Full Title: A comparison of the effects on prostaglandin synthesis and cytokine production of an olive-oil based lipid emulsion (Clinoloeic) with a soya based emulsion (Intralipid) in newborn infnats receiving... | ||||||||
Medical condition: Prematurity Parenteral nutrition | ||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009278-29 | Sponsor Protocol Number: S51477 | Start Date: | ||||||||||||||||||||||||||
Sponsor Name: UZ Leuven | ||||||||||||||||||||||||||||
Full Title: Follow-up studie: Metformin therapie bij kinderen en adolescenten met neurogene of neuromusculaire aandoeningen | ||||||||||||||||||||||||||||
Medical condition: Neuromuscular and neurological diseases, associated with obesity and insulin resistance | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013956-62 | Sponsor Protocol Number: DEMIJO | Start Date: | |||||||||||
Sponsor Name: University Medical Center of the University Ulm | |||||||||||||
Full Title: Preparation of Neuroplant® 300mg N in film-coated tablets (St. John´s wort, SJW) in the treatment of mild to moderate Major Depressive Disorder (MDD) in adolescents from 12 to 17 years (inclusive):... | |||||||||||||
Medical condition: Mild to moderate MDD acc. DSM-IV-TR in adolescents (12−17years inclusive) | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013499-29 | Sponsor Protocol Number: SUNDRO20 | Start Date: | ||||||||||||||||
Sponsor Name: Technische Universität München | ||||||||||||||||||
Full Title: Dosisfindungsstudie für Sugammadex und Neostigmin zur Reversierung einer geringen neuromuskulären Restblockade (train of four ratio 0,2) [Sugammadex and Neostigmine dose finding study for reversal ... | ||||||||||||||||||
Medical condition: Dose finding study for sugammadex and/or neostigmine at residual neuromuscular blockade (whereas residual neuromuscular blockade is defined as a TOF of 0.2 in this study). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |