- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Bradykinin.
Displaying page 1 of 1.
EudraCT Number: 2004-000333-10 | Sponsor Protocol Number: GEN/231/51/BMcK/JCL | Start Date*: 2004-12-15 |
Sponsor Name:Research & Innovation Services, University of Dundee | ||
Full Title: The inhibitory effect of local anaesthetics on the G-protein-mediated vascular flare response to bradykinin and substance P | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002225-29 | Sponsor Protocol Number: AntagoBrad-Cov | Start Date*: 2020-11-12 | ||||||||||||||||
Sponsor Name:Groupement de Coopération Sanitaire Ramsay Générale de Santé pour l’Enseignement et la Recherche | ||||||||||||||||||
Full Title: Evaluation of the effects of bradykinin antagonists on pulmonary manifestations of COVID-19 infections. | ||||||||||||||||||
Medical condition: COVID positive patients with respiratory impairment | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002339-24 | Sponsor Protocol Number: NA | Start Date*: 2012-05-25 |
Sponsor Name:Barts and the London NHS Trust | ||
Full Title: Open label, single-centre study to evaluate the efficacy of the bradykinin (BK) B2 receptor antagonist, Icatibant, in the relief of symptoms resulting from moderate to severe angioedema unresponsiv... | ||
Medical condition: Idiopathic Angioedema | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014918-99 | Sponsor Protocol Number: BKOS-02 | Start Date*: 2010-01-19 | |||||||||||
Sponsor Name:Menarini Ricerche, S.p.A | |||||||||||||
Full Title: Intra-articular treatment with MEN16132 in patients with symptomatic primary osteoarthritis of the knee: A randomised, multi-centre, double blind, placebo controlled, five parallel group, dose find... | |||||||||||||
Medical condition: patients with symptomatic primary osteoarthritis of the knee | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002805-21 | Sponsor Protocol Number: D2530C00011 | Start Date*: 2005-09-25 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A randomized, double-blind, placebo controlled, three-way crossover study exploring the efficacy of AZD3778 compared with placebo and an oral antihistamine (loratadine) in a model of seasonal aller... | ||
Medical condition: This is a Phase II trial (Proof of Principle) in volunteer rhinitis subjects utilising a seasonal model of rhinitis and challenge agent | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001540-71 | Sponsor Protocol Number: JE049 #2102 | Start Date*: 2005-07-23 |
Sponsor Name:Jerini AG | ||
Full Title: Randomised, double blind, controlled, parallel group, multicentre study of a subcutaneous formulation of Icatibant vs. oral Tranexamic acid for the treatment of hereditary angioedema (HAE). | ||
Medical condition: Hereditary Angioedema (HAE) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) HU (Completed) AT (Completed) LT (Completed) IE (Completed) DE (Completed) GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-019037-10 | Sponsor Protocol Number: INITIAtE | Start Date*: 2010-11-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: IcatibaNt In Treatment of Idiopathic Angio Edema. | |||||||||||||
Medical condition: Idiopathic angioedema. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000757-93 | Sponsor Protocol Number: ISIS721744-CS7 | Start Date*: 2022-09-05 | |||||||||||
Sponsor Name:IONIS PHARMACEUTICALS, INC. | |||||||||||||
Full Title: An Open-Label, Long Term Safety and Efficacy Study of Donidalorsen in the Prophylactic Treatment of Hereditary Angioedema (HAE) | |||||||||||||
Medical condition: Hereditary Angioedema (HAE) | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) IT (Trial now transitioned) DE (Trial now transitioned) NL (Ongoing) DK (Completed) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001670-28 | Sponsor Protocol Number: BER-1272-0058-I | Start Date*: 2013-03-18 | |||||||||||
Sponsor Name:Medizinische Fakultät der Technischen Universität München | |||||||||||||
Full Title: Angiotensin Converting Enzyme Inhibitor (ACE) Induced Angioedema BERINERT Randomized, double-blind, two arms, multicenter, Phase III study of Berinert for treatment of ACE induced Angioedema | |||||||||||||
Medical condition: Angiotensin – Converting – Enzyme – Inhibitors (ACEi) are used in the treatment of several types of cardiovascular and renal diseases. A known side effect of ACEi are angioedema of the head and ... | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001703-20 | Sponsor Protocol Number: SHP643-303 | Start Date*: 2020-08-28 | |||||||||||
Sponsor Name:Dyax Corporation, a Takeda company | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of Lanadelumab for Prevention Against Acute Attacks of Non-histaminergic Angioedema wi... | |||||||||||||
Medical condition: non-histaminergic angioedema with normal C1-INH and acquired angioedema due to C1-INH deficiency | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) HU (Completed) PL (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001739-28 | Sponsor Protocol Number: S63979 | Start Date*: 2020-05-20 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: A randomized, open-label, adaptive, proof-of-concept clinical trial of modulation of host thromboinflammatory response in patients with COVID-19. | |||||||||||||
Medical condition: COVID-19 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
