- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Beta sheets.
Displaying page 1 of 1.
| EudraCT Number: 2017-002126-20 | Sponsor Protocol Number: PID13341 | Start Date*: 2018-08-13 | ||||||||||||||||
| Sponsor Name:University of Oxford | ||||||||||||||||||
| Full Title: Interleukin-2 therapy of Autoimmunity in Diabetes: ITAD | ||||||||||||||||||
| Medical condition: Type 1 Diabetes | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-005668-28 | Sponsor Protocol Number: AGAL06207 | Start Date*: 2008-07-29 | |||||||||||
| Sponsor Name:Genzyme Europe BV | |||||||||||||
| Full Title: A Randomized, Multicenter, Multinational, Phase 3B, Open-Label, Parallel-Group Study of Fabrazyme (agalsidase beta) in Treatment-Naive Male Pediatric Patients with Fabry Disease Without Severe Symp... | |||||||||||||
| Medical condition: Fabry disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) NL (Completed) PT (Prematurely Ended) DE (Prematurely Ended) CZ (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003656-35 | Sponsor Protocol Number: E7389-G000-211 | Start Date*: 2006-03-14 |
| Sponsor Name:Eisai Limited | ||
| Full Title: A phase II open label single-arm study of E7389 in patients with locally advanced or metastatic breast cancer, previously treated with anthracycline, taxane, and capecitabine therapy, refractory to... | ||
| Medical condition: Locally advanced or metastatic breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: BE (Completed) ES (Completed) GB (Completed) AT (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000679-90 | Sponsor Protocol Number: SPD489-325 | Start Date*: 2009-04-08 | |||||||||||
| Sponsor Name:Shire Pharmaceutical Development Limited | |||||||||||||
| Full Title: A Phase III, Randomised, Double-Blind, Multicentre, Parallel-Group, Placebo- and Active-Controlled, Dose-Optimisation Safety and Efficacy Study of Lisdexamfetamine Dimesylate (LDX) in Children and ... | |||||||||||||
| Medical condition: Attention Deficit / Hyperactivity Disorder (ADHD) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) FR (Completed) ES (Completed) NL (Completed) SE (Completed) BE (Completed) IT (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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