- ICH GCP
- Registro delle prove cliniche dell'UE
Ultime prove
EudraCT Number: 2017-005129-18 | Sponsor Protocol Number: PROMISE | Start Date: | |||||||||||
Sponsor Name: Università degli Studi Aldo Moro | |||||||||||||
Full Title: Multi-centre, randomised, open label pragmatic trial to compare the effectiveness and safety of interferon beta-1a (IFN-beta-1a) weekly i.m. and glatiramer-acetate (GA) in paediatric patients affec... | |||||||||||||
Medical condition: Relapsing-remitting multiple sclerosis with paediatric onset | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022273-34 | Sponsor Protocol Number: CRAD001KDE37 | Start Date: | |||||||||||
Sponsor Name: Novartis Pharma GmbH | |||||||||||||
Full Title: A multi-centric, open-label, phase II study investigating the combination of Afinitor with paclitaxel and carboplatin in first line treatment of patients with advanced (stage IV) large cell lung c... | |||||||||||||
Medical condition: large-cell neuroendocrine carcinoma of the lung | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013792-22 | Sponsor Protocol Number: LEO 29102-C21 | Start Date: | |||||||||||
Sponsor Name: LEO Pharma A/S | |||||||||||||
Full Title: A Phase 2, proof of concept and dose finding study, investigating treatment efficacy of LEO 29102 cream (2.5 mg/g, 1.0 mg/g, 0.3 mg/g, 0.1 mg/g, 0.03 mg/g), LEO 29102 cream vehicle, and Elidel (Pim... | |||||||||||||
Medical condition: Diagnosis of atopic dermatitis graded as mild to moderate according to the Rajka and Langeland system. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004878-29 | Sponsor Protocol Number: NA | Start Date: | |||||||||||
Sponsor Name: St. Antonius Hospital | |||||||||||||
Full Title: Perioperative antibiotic use in the treatment of acute calculous cholecystitis | |||||||||||||
Medical condition: Acute calculous cholecystitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021134-66 | Sponsor Protocol Number: IJL-AFHT-TH10 | Start Date: | ||||||||||||||||
Sponsor Name: Institut Jerome Lejeune | ||||||||||||||||||
Full Title: Efficacy assessment of systematic treatment with folinic acid and thyroid hormone on psychomotor development of Down Syndrome young children | ||||||||||||||||||
Medical condition: Down syndrome | ||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001866-14 | Sponsor Protocol Number: 3150-303-008 | Start Date: | |||||||||||
Sponsor Name: AstraZeneca AB | |||||||||||||
Full Title: An Open-label, Long-term Extension Study of Brazikumab in Participants with Moderately to Severely Active Crohn’s Disease | |||||||||||||
Medical condition: Moderately to Severely Active Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) DE (Completed) CZ (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) IT (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002255-37 | Sponsor Protocol Number: MGT-RPGR-022 | Start Date: | |||||||||||
Sponsor Name: MeiraGTx UK II Limited | |||||||||||||
Full Title: Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene | |||||||||||||
Medical condition: X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004966-34 | Sponsor Protocol Number: 38825 | Start Date: | |||||||||||
Sponsor Name: NV Organon | |||||||||||||
Full Title: A phase III, uncontrolled trial to assess the non-immunogenicity and safety of Org 36286 in patients undergoing repeated controlled ovarian stimulation cycles using a multiple dose GnRH antagonist ... | |||||||||||||
Medical condition: Controlled Ovarian Stimulation (COS) to induce the development of multiple follicles in patients participating in an Assisted Reproductive Technology (ART) program | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) SE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003816-47 | Sponsor Protocol Number: Met-ADI-01 | Start Date: | ||||||
Sponsor Name: Pädiatrische Endokrinologie, Universitätsmedizin Berlin, Charité | ||||||||
Full Title: Clinical pilot study on the effect of Metformin in adipose children and adolescents with insulin-resistance Klinische Pilotstudie zur Untersuchung der Wirkung von Metformin bei adipösen Kindern un... | ||||||||
Medical condition: Insuline-resistance in adipose children and adolescents | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2010-021139-15 | Sponsor Protocol Number: ESC-928-MOL-0000-I | Start Date: | |||||||||||
Sponsor Name: Technische Universität München Fakultät für Medizin | |||||||||||||
Full Title: Do Selective Radiation Dose Escalation and Tumor Hypoxia Status Impact the Locoregional Tumor Control after Radiochemotherapy of Head & Neck Tumors? | |||||||||||||
Medical condition: This study tests the hypothesis that the Radiation dose escalation to the macroscopic Tumor improves the locoregional control survival after concomitant chemoradiation over 2 years. As a transla... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |