- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Fish allergy.
Displaying page 1 of 1.
| EudraCT Number: 2012-005173-32 | Sponsor Protocol Number: K-489DK | Start Date*: 2013-07-09 |
| Sponsor Name:FAST-consortium | ||
| Full Title: FAST-Fish - Food Allergy Specific Treatment for fish allergy | ||
| Medical condition: Fish Allergy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000276-10 | Sponsor Protocol Number: FAST2015 | Start Date*: 2015-07-02 |
| Sponsor Name:FAST Consortium under EU 7. FWP | ||
| Full Title: FAST – Food Allergy Specific ImmunoTherapy A multinational phase IIb study to investigate the efficacy and safety of subcutaneous immunotherapy with a modified fish- parvalbumin given in single ri... | ||
| Medical condition: Food allergy to fish | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IS (Completed) DK (Completed) GR (Ongoing) NL (Completed) PL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003627-30 | Sponsor Protocol Number: 20170367744 | Start Date*: 2018-06-27 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Odense Research Center for Anaphylaxis (ORCA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Protection from food induced anaphylaxis by reducing serum level of specific IgE | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Food Allergy with Anaphylaxis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-004427-37 | Sponsor Protocol Number: 5421234 | Start Date*: 2019-02-20 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Odense Research Centre for Anaphylaxis (ORCA) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Treatment with Omalizumab in food allergic children | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Food Allergy with Anaphylaxis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-000446-34 | Sponsor Protocol Number: MT-18 | Start Date*: 2020-07-14 | |||||||||||
| Sponsor Name:ALK-Abelló A/S | |||||||||||||
| Full Title: A 28-day, single-armed, open-label trial to evaluate safety of the house dust mite (HDM) sublingual allergy immunotherapy (SLIT) tablet in adolescent subjects (12-17 years of age) with HDM allergic... | |||||||||||||
| Medical condition: Allergic rhinitis/rhinoconjunctivitis induced by house dust mite | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) DE (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022260-12 | Sponsor Protocol Number: 1947 | Start Date*: 2011-03-24 | |||||||||||
| Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
| Full Title: A Phase II trial of broad spectrum antibiotic therapy for early stage chronic lymphocytic leukaemia. | |||||||||||||
| Medical condition: Chronic Lymphocytic Leukaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005170-65 | Sponsor Protocol Number: MK-8109-004 | Start Date*: 2014-10-23 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase IIa Open Label, Randomized Clinical Trial to Study the Safety and Efficacy of Vintafolide and the Combination of Vintafolide and Paclitaxel Compared to Paclitaxel in Subjects with Advanced ... | |||||||||||||
| Medical condition: Triple Negative Breast Cancer (advanced breast cancer that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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Query did not match any studies.