- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Selection bias.
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EudraCT Number: 2007-007580-24 | Sponsor Protocol Number: EB70 | Start Date*: 2008-02-08 |
Sponsor Name:Emotional Brain | ||
Full Title: A double blind, randomized, 3-arm placebo controlled study to investigate the subjective and physiological efficacy and safety of Lybrido and Lybridos in the domestic setting in healthy female subj... | ||
Medical condition: Hypoactive sexual desire disorder and female sexual arousal disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007704-28 | Sponsor Protocol Number: EB77 | Start Date*: 2009-01-21 | |||||||||||
Sponsor Name:Emotional Brain | |||||||||||||
Full Title: Lybridos PoC: A double blind, randomized, cross-over placebo controlled pilot study to investigate the subjective and physiological efficacy and safety of Lybridos in healthy female subjects with F... | |||||||||||||
Medical condition: Female Sexual Dysfunction, specifically Hypoactive Sexual Desire Disorder, with or without Female Sexual Arousal Disorder. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001816-27 | Sponsor Protocol Number: 62202-655 | Start Date*: 2005-07-28 |
Sponsor Name:Clinical Data Care Spain S.L. | ||
Full Title: Open label randomized phase II, multicentre, pilot study to evaluate safety and efficacy of the combination of cetuximab and concomitant-boost accelerated radiotherapy followed or not by a compleme... | ||
Medical condition: locally advanced oropharynx squamous cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011884-35 | Sponsor Protocol Number: SAKK 77/08 and SASL 29 | Start Date*: 2009-12-19 |
Sponsor Name:Swiss Group for Clinical Cancer Research | ||
Full Title: Sorafenib alone or in combination with everolimus in patients with unresectable hepatocellular carcinoma. A randomized multicenter phase II trial. | ||
Medical condition: Patients with unresectable hepatocellular carcinoma. | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: HU (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002455-97 | Sponsor Protocol Number: 13381 | Start Date*: 2016-10-19 | ||||||||||||||||
Sponsor Name:University of Southampton | ||||||||||||||||||
Full Title: Antibiotics for lower Respiratory Tract Infection in Children presenting in Primary Care | ||||||||||||||||||
Medical condition: Respiratory tract infections in children aged between 6 months and 12 years | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005811-16 | Sponsor Protocol Number: OMB110913 | Start Date*: 2008-12-22 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A Phase III, Open Label, Randomized Trial of Ofatumumab Added to Fludarabine-Cyclophosphamide vs. Fludarabine-Cyclophosphamide Combination in Subjects with Relapsed Chronic Lymphocytic Leukemia | ||
Medical condition: Chronic Lymphocytic Leukaemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) DE (Completed) GR (Completed) IT (Completed) ES (Completed) GB (Completed) BG (Completed) RO (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-004932-19 | Sponsor Protocol Number: OMB110911 | Start Date*: 2009-01-27 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||||||||||||||||||||||||||||||||||||||
Full Title: A phase III, open label, randomized, multicenter trial of Ofatumumab added to Chlorambucil vs. Chlorambucil Monotherapy in previously untreated patients with Chronic Lymphocytic Leukemia | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chronic Lymphocytic Leukaemia | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) IE (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) SE (Completed) BE (Prematurely Ended) CZ (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) GR (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-004331-71 | Sponsor Protocol Number: IB1001-201 | Start Date*: 2019-05-08 | |||||||||||
Sponsor Name:IntraBio Ltd | |||||||||||||
Full Title: Effects of N-Acetyl-L-Leucine on Niemann-Pick type C Disease (NPC): A multinational, multi-center, open-label, rater-blinded Phase II study | |||||||||||||
Medical condition: Niemann-Pick Disease type C (NPC) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004406-25 | Sponsor Protocol Number: IB1001-202 | Start Date*: 2019-05-09 | |||||||||||
Sponsor Name:IntraBio Ltd | |||||||||||||
Full Title: Effects of N-Acetyl-L-Leucine on GM2 Gangliosidosis (Tay-Sachs and Sandhoff Disease): A multinational, multicenter, open-label, rater-blinded Phase II study. | |||||||||||||
Medical condition: GM2 Gangliosidosis (Tay-Sachs and Sandhoff Disease) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020881-53 | Sponsor Protocol Number: 20100008 | Start Date*: 2011-01-18 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Long-term Assessment of Safety and Efficacy of AMG 827 Treatment in Subjects With Crohn’s Disease | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004599-19 | Sponsor Protocol Number: INTERFANT-06 | Start Date*: 2005-11-24 | |||||||||||
Sponsor Name:A.I.E.O.P. - ASSOCIAZIONE ITALIANA EMATOLOGIA ONCOLOGIA PEDIATRICA | |||||||||||||
Full Title: INTERNATIONAL COLLABORATIVE TREATMENT PROTOCOL FOR INFANTS UNDER ONE YEAR WITH ACUTE LYMPHOBLASTIC OR BIPHENOTYPIC LEUKEMIA | |||||||||||||
Medical condition: acute lymphoblastic leukemia (ALL) or biphenotypic leukemia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) BE (Completed) FR (Ongoing) DE (Completed) GB (Completed) AT (Ongoing) PT (Completed) DK (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
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