- ICH GCP
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Laatste proeven
EudraCT Number: 2020-001211-24 | Sponsor Protocol Number: DRM06-AD07/J2T-DM-KGAA | Start Date: | |||||||||||
Sponsor Name: Dermira, Inc., a wholly-owned subsidiary of Eli Lilly and Company | |||||||||||||
Full Title: A LONG-TERM STUDY TO ASSESS THE SAFETY AND EFFICACY OF LEBRIKIZUMAB IN PATIENTS WITH MODERATE-TO-SEVERE ATOPIC DERMATITIS | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Ongoing) DE (Completed) LV (Ongoing) LT (Ongoing) EE (Ongoing) FR (Completed) BG (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003643-10 | Sponsor Protocol Number: NAM | Start Date: | ||||||
Sponsor Name: UMC Utrecht | ||||||||
Full Title: Modulating regulatory T cell function in JIA with Vitamin B3 (nicotinamide) treatment | ||||||||
Medical condition: Juvenile idiopathic arthritis (JIA) | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: NL (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008254-23 | Sponsor Protocol Number: SIG112851 | Start Date: | |||||||||||
Sponsor Name: GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, 2-way crossover study to determine the efficacy of repeat inhaled doses of GW870086X on FEV1 in mild to moderate asthmatics | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001589-17 | Sponsor Protocol Number: KN 38-7271-001 | Start Date: | ||||||
Sponsor Name: KeyNeurotek Pharmaceuticals AG | ||||||||
Full Title: A doubel-blind, parallel-group, Phase IIa study to investigate the efficacy, safety and pharmacokinetics of two dose levels of KN 38-7271 versus placebo in comatose patients with severe traumatic b... | ||||||||
Medical condition: Comatose patients with traumatic brain injury (TBI). | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) BE (Completed) CZ (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011152-22 | Sponsor Protocol Number: GTG003.08 | Start Date: | ||||||
Sponsor Name: GENETHON | ||||||||
Full Title: Phase 1/2 clinical trial of haematopoietic stem cell gene therapy for the Wiskott-Aldrich Syndrome | ||||||||
Medical condition: Phase 1/2 clinical trial of haematopoietic stem cell gene therapy for the Wiskott-Aldrich Syndrome. An open labelled, non-randomised, phase I/II, cohort study involving a single infusion of autolo... | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | |||||||
Trial protocol: FR (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2016-003673-18 | Sponsor Protocol Number: 1062016 | Start Date: | ||||||
Sponsor Name: UZ Brussel | ||||||||
Full Title: Can we with vitamin D3, improve the innate immune system? | ||||||||
Medical condition: Immunological problems such as hypogammaglobulinemia with clinical recurrent infections such as sinusitis , pneumonia , otitis , skin infections and gastrointestinal infections. | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: BE (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022844-19 | Sponsor Protocol Number: | Start Date: | |||||||||||
Sponsor Name: CHU de Dijon | |||||||||||||
Full Title: Randomized phase III study of a treatment driven by early PET response compared to a treatment not monitored by early PET in patients with Ann Arbor Stage III-IV or high risk IIB Hodgkin lymphoma | |||||||||||||
Medical condition: Hodgkin Lymphoma not previously treated | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004154-25 | Sponsor Protocol Number: CLCZ696B2319E1 | Start Date: | |||||||||||
Sponsor Name: Novartis Pharma AG | |||||||||||||
Full Title: A multicenter study to evaluate long-term safety and tolerability of open label sacubitril/valsartan in pediatric patients with heart failure due to systemic left ventricle systolic dysfunction wh... | |||||||||||||
Medical condition: Pediatric heart failure : Patients (≥ 13 months) with HF due to systemic left ventricular systolic dysfunction. [Note: All patients per protocol for the core study CLCZ696B2319 (PANORAMA-HF) ... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Ongoing) FR (Ongoing) BG (Ongoing) PT (Ongoing) CZ (Completed) ES (Ongoing) HU (Ongoing) HR (Ongoing) DE (Completed) AT (Completed) IT (Ongoing) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000497-28 | Sponsor Protocol Number: PTC923-MD-004-PKU | Start Date: | |||||||||||
Sponsor Name: PTC Therapeutics, Inc. | |||||||||||||
Full Title: Phase 3 Open-Label Study of PTC923 (Sepiapterin) in Phenylketonuria | |||||||||||||
Medical condition: Metabolic Disorders - Phenylketonuria | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) PT (Ongoing) DK (Ongoing) NL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003913-15 | Sponsor Protocol Number: ANTRAG01 | Start Date: | ||||||
Sponsor Name: Medical University Innsbruck | ||||||||
Full Title: Wirkung von Oxcarbazepin (Trileptal) auf den Kortikosteroid-Metabolismus - Pilotstudie | ||||||||
Medical condition: Oxcarbazepin, a widely-used antiepileptic treatment is evaluated with respect to Cortisol-degradation. Young adults and adults with oxcarbazepine monotherapy since at least 6 months and temporal lo... | ||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | |||||||
Trial protocol: AT (Ongoing) | ||||||||
Trial results: (No results available) |