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EudraCT Number: 2006-004323-10 | Sponsor Protocol Number: ESAMOX | Start Date: | |||||||||||
Sponsor Name: Technische Universität Dresden | |||||||||||||
Full Title: Effektivität und Verträglichkeit von Esomeprazol, Moxifloxacin und Amoxicillin in der Reservetherapie der Helicobacter pylori Infektion. | |||||||||||||
Medical condition: Reserve Therapie der Helicobacter pylori Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001716-29 | Sponsor Protocol Number: SNX-301-020 | Start Date: | |||||||||||
Sponsor Name: SynOx Therapeutics Ltd | |||||||||||||
Full Title: A Phase III, Multicentre, Randomised, Double-Blind Study to Assess the Safety and Efficacy of Emactuzumab vs. Placebo in Subjects with Tenosynovial Giant Cell Tumour. | |||||||||||||
Medical condition: Tenosynovial Giant Cell Tumour | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000704-14 | Sponsor Protocol Number: S241-GB-07 | Start Date: | ||||||
Sponsor Name: Stiefel Laboratories International Division | ||||||||
Full Title: Human 96 Hour Repeat Open Application Test for Assessment of Skin Irritation | ||||||||
Medical condition: Not applicable (Healthy Volunteer Study) | ||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003882-10 | Sponsor Protocol Number: 2014_21 | Start Date: | |||||||||||
Sponsor Name: CHRU de Lille | |||||||||||||
Full Title: Evaluation of the effectiveness of a treatment involving one (or several ) antibiotic (s) with 14-day tobramycin ( Nebcine® ) by intravenous injection versus the same antibiotic treatment (s ) asso... | |||||||||||||
Medical condition: mucoviscidosis or cystic fibrosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002562-40 | Sponsor Protocol Number: 16-021 | Start Date: | |||||||||||
Sponsor Name: Portola Pharma UK Ltd | |||||||||||||
Full Title: A phase 1, open-label, single dose, non-randomized study to evaluate pharmacokinetics, pharmacodynamics, and safety of Betrixaban in pediatric patients. | |||||||||||||
Medical condition: Pediatric patients who are assessed to be at risk for Venous thromboembolism (VTE) but does not require immediate anticoagulant therapy, for example: a. Has previous thrombosis and completed a cour... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002213-12 | Sponsor Protocol Number: I10 005 | Start Date: | ||||||||||||||||
Sponsor Name: CHU de Limoges | ||||||||||||||||||
Full Title: Paracetamol and setrons : drug interactions in the management of pain after tonsillectomy in children | ||||||||||||||||||
Medical condition: Pain | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003768-29 | Sponsor Protocol Number: DAY101-102 | Start Date: | ||||||
Sponsor Name: Day One Biopharmaceuticals, Inc. (Day One) | ||||||||
Full Title: A Phase 1b/2, Open Label Study of DAY101 Monotherapy or Combination with Other Therapies for Patients with Recurrent, Progressive, or Refractory Solid Tumors Harboring MAPK Pathway Aberrations | ||||||||
Medical condition: Recurrent, Progressive, or Refractory Solid Tumors Harboring MAPK Pathway Aberrations | ||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||
Trial protocol: BE (Ongoing) ES (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001795-34 | Sponsor Protocol Number: CL-N-HTX-Paed-II/10/20 | Start Date: | |||||||||||
Sponsor Name: Dr. Franz Köhler Chemie GmbH | |||||||||||||
Full Title: A prospective randomized single blind multicenter phase II study of organ perfusion with Custodiol-N compared with Custodiol in heart transplantation in children | |||||||||||||
Medical condition: Preservation of hearts prior to heart transplantation in children | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005294-60 | Sponsor Protocol Number: CRAD001C24114 | Start Date: | |||||||||||
Sponsor Name: Novartis Pharma GmbH | |||||||||||||
Full Title: Multicenter, triple-arm, single-stage, phase II trial to determine the preliminary efficacy and safety of RAD001 in patients with histological evidence of progressive or metastatic bone or soft tis... | |||||||||||||
Medical condition: histological evidence of progressive or metastatic bone or soft tissue sarcomas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004526-33 | Sponsor Protocol Number: PDARCT1 | Start Date: | |||||||||||
Sponsor Name: Royal College of Surgeons in Ireland | |||||||||||||
Full Title: A Randomised Controlled Trial of Early Targeted Patent Ductus Arteriosus Treatment Using a Risk Based Severity Score | |||||||||||||
Medical condition: Patent Ductus Arteriosus | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |