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EudraCT Number: 2007-002586-12 Sponsor Protocol Number: 1160.63 Start Date:
Sponsor Name: Boehringer Ingelheim Pharma GmbH & Co. KG
Full Title: Twice-daily oral direct thrombin inhibitor dabigatran in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary embo...
Medical condition: long-term prevention of recurrent symptomatic venous thromboembolism (VTE) in patients with symptomatic deep-vein thrombosis (DVT) or pulmonary embolism (PE) who completed 6 to 18 months of treatme...
Disease: Version SOC Term Classification Code Term Level
9.1 10049909 Venous thromboembolism prophylaxis LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) SE (Completed) AT (Completed) IT (Completed) PL (Completed) CZ (Completed) NL (Completed) BE (Completed) LT (Completed) LV (Completed) EE (Completed)
Trial results: View results

EudraCT Number: 2007-005865-37 Sponsor Protocol Number: PIL-629-WEB-0128-I Start Date:
Sponsor Name: Medizinische Fakultät der Technischen Universität München, Vertreten durch den Dekan
Full Title: Levofloxacin vs Piperacillin/Sulbactam and Sultamicillin in patients with acute cholecystitis. A double blind, randomized study.
Medical condition: acute cholecystitis
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Prematurely Ended)
Trial results: View results
EudraCT Number: 2017-004554-42 Sponsor Protocol Number: TAMDMD Start Date:
Sponsor Name: University of Basel Children's Hospital, Division of Neuropediatrics
Full Title: Tamoxifen in Duchenne muscular dystrophy: A multicenter, randomised, double-blind, placebo-controlled, phase 3 safety and efficacy 48-week trial Tamoxifen in Duchenne muscular dystrophy: A 48-week...
Medical condition: Duchenne muscular dystrophy
Disease: Version SOC Term Classification Code Term Level
20.0 10010331 - Congenital, familial and genetic disorders 10013801 Duchenne muscular dystrophy PT
Population Age: Children, Adolescents, Under 18 Gender: Male
Trial protocol: DE (Ongoing) GB (GB - no longer in EU/EEA) FR (Ongoing) ES (Ongoing) NL (Ongoing) BE (Ongoing)
Trial results: (No results available)

EudraCT Number: 2016-001767-37 Sponsor Protocol Number: 178-CL-204 Start Date:
Sponsor Name: Astellas Pharma Global Development Inc.
Full Title: A Phase 3, Double blind, Randomized, Multicenter, Parallel Group, Placebo controlled Sequential Dose Titration Study to Evaluate Efficacy, Safety and Pharmacokinetics of Mirabegron in Pediatric Sub...
Medical condition: Overactive bladder (OAB)
Disease: Version SOC Term Classification Code Term Level
23.1 100000004857 10059617 Overactive bladder LLT
Population Age: Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: DE (Completed) NL (Completed) BE (Completed) NO (Completed) FR (Completed) DK (Completed) PL (Completed) IT (Completed) ES (Ongoing)
Trial results: View results
EudraCT Number: 2016-004786-80 Sponsor Protocol Number: ANAKIN Start Date:
Sponsor Name: Ruprecht-Karls-University Heidelberg, Medical Faculty
Full Title: A phase IIa, randomized, placebo-controlled, double-blind, cross-over study to evaluate safety and efficacy of subcutanous administration of anakinra in patients with cystic fibrosis.
Medical condition: Cystic fibrosis
Disease: Version SOC Term Classification Code Term Level
20.0 100000004850 10028141 Mucoviscidosis LLT
Population Age: Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: DE (Ongoing)
Trial results: (No results available)

EudraCT Number: 2016-004479-35 Sponsor Protocol Number: VX16-661-115 Start Date:
Sponsor Name: Vertex Pharmaceuticals Incorporated
Full Title: A Phase 3, Double-blind, Parallel-group Study to Evaluate the Efficacy and Safety of Tezacaftor in Combination With Ivacaftor in Subjects Aged 6 Through 11 Years With Cystic Fibrosis, Homozygous or...
Medical condition: Cystic Fibrosis
Disease: Version SOC Term Classification Code Term Level
20.0 10010331 - Congenital, familial and genetic disorders 10011762 Cystic fibrosis PT
Population Age: Children, Under 18 Gender: Male, Female
Trial protocol: IE (Completed) DK (Completed) BE (Completed) DE (Completed) GB (Completed) PL (Completed) FR (Completed)
Trial results: View results
EudraCT Number: 2015-004139-11 Sponsor Protocol Number: VAC52150EBL4001 Start Date:
Sponsor Name: Janssen Vaccines & Prevention B.V.
Full Title: A Multicountry, Prospective, Clinical Safety Study of Subjects Exposed to the Candidate Ebola Vaccines Ad26.ZEBOV and/or MVA-BN-Filo
Medical condition: Ebola
Disease: Version SOC Term Classification Code Term Level
20.0 10021881 - Infections and infestations 10014071 Ebola disease PT
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly Gender: Male, Female
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed)
Trial results: (No results available)

EudraCT Number: 2006-002847-96 Sponsor Protocol Number: DRI6012 Start Date:
Sponsor Name: Sanofi aventis US Inc.
Full Title: A 13-week Multinational, Randomized, Double-Blind, Placebo-Controlled, Dose-Response Trial Assessing the Safety, Tolerability and Efficacy of AVE0010 in Metformin-Treated Subjects with Type 2 Diabe...
Medical condition: The current study is designed to confirm the already observed clinically meaningful pharmacodynamic effect of AVE0010 on glycemic control, as measured by HbA1c, and to determine the clinically rele...
Disease: Version SOC Term Classification Code Term Level
8.1 10012613 Diabetes mellitus non-insulin-dependent LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: BG (Prematurely Ended)
Trial results: View results
EudraCT Number: 2014-002710-23 Sponsor Protocol Number: P140203 Start Date:
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title:
Medical condition:
Disease: Version SOC Term Classification Code Term Level
18.0 10010331 - Congenital, familial and genetic disorders 10054935 Aicardi's syndrome PT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: FR (Completed)
Trial results: (No results available)

EudraCT Number: 2019-004190-46 Sponsor Protocol Number: D5136C00013 Start Date:
Sponsor Name: AstraZeneca AB
Full Title: A Randomised, Double-Blind, Parallel-Group, Multicentre, Phase III Study to Evaluate the Effect of Ticagrelor versus Placebo in Reducing the Number of Vaso-Occlusive Crises in Paediatric Patients A...
Medical condition: Sickle Cell Disease
Disease: Version SOC Term Classification Code Term Level
21.0 100000004850 10040645 Sickle cell disease NOS LLT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: GB (Prematurely Ended)
Trial results: (No results available)
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