- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
16 result(s) found for: Hemangioma.
Displaying page 1 of 1.
EudraCT Number: 2010-023488-16 | Sponsor Protocol Number: V00400SB301 | Start Date*: 2011-02-10 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE represented by INSTITUT DE RECHERCHE PIERRE FABRE | |||||||||||||
Full Title: A multicentre, open-label study of propranolol in infants with proliferating infantile hemangioma requiring systemic therapy | |||||||||||||
Medical condition: Proliferating Infantile Hemangioma | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014571-49 | Sponsor Protocol Number: CDP0901 | Start Date*: 2010-01-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: The use of systemic propranolol in congenital hemangiomas | |||||||||||||
Medical condition: congenital hemangiomas | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018102-22 | Sponsor Protocol Number: V00400SB102 | Start Date*: 2010-03-26 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE | |||||||||||||
Full Title: A multicentre, open-label, repeated-dose, pharmacokinetic study of Propranolol in infants treated for proliferating infantile hemangiomas (IHs) requiring systemic therapy. | |||||||||||||
Medical condition: Proliferating Infantile Hemangioma | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000202-36 | Sponsor Protocol Number: CHUBX 2007/27 | Start Date*: 2008-06-12 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Etude clinique randomisée du propranolol versus placebo dans le traitement des hémangiomes capillaires infantiles. | |||||||||||||
Medical condition: Hémangiomes capillaires | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017241-55 | Sponsor Protocol Number: RC 43/08 | Start Date*: 2009-12-09 | |||||||||||
Sponsor Name:ISTITUTO PER L`INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Open randomized study on propranolol vs prednisone for haemangioma in patients younger than 18 months of age | |||||||||||||
Medical condition: Haemagiomas | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022440-20 | Sponsor Protocol Number: 10-PP-11 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Traitements of angioma plans of the child by laser to pulsed colouring agent and Timolol (Néogel 0,1%). | |||||||||||||
Medical condition: Angioma plans | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019754-41 | Sponsor Protocol Number: PROHÄM | Start Date*: 2010-10-19 | |||||||||||
Sponsor Name:InfectoPharm Arzneimittel und Consilium GmbH | |||||||||||||
Full Title: Multizentrische, prospektive, einarmige Phase III-Studie zur Wirksamkeit und Sicherheit einer oralen Therapie mit Propranolol (ProAngiol Saft; 2 mg/kg KG/d mit fakultativer Dosiserhöhung auf 3 mg/k... | |||||||||||||
Medical condition: Hemangioma in infants and toddlers, requiring systemic therapy | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005555-80 | Sponsor Protocol Number: V00400SB302 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:Pierre Fabre Dermatologie represented by IRPF | |||||||||||||
Full Title: Efficacy and safety of Hemangiol solution in the treatment of high risk infantile hemangioma. A Multinational Single Arm Study | |||||||||||||
Medical condition: High risk infantile haemangioma | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004145-41 | Sponsor Protocol Number: 8638 | Start Date*: 2013-05-22 | |||||||||||
Sponsor Name:UH Montpellier | |||||||||||||
Full Title: Efficacy and safety of acebutolol versus propranolol in the proliferative phase of infantile hemangiomas | |||||||||||||
Medical condition: Infant 0 to 6 months Non-serious hemangioma | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013262-84 | Sponsor Protocol Number: V00400SB201 | Start Date*: 2009-10-28 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE | |||||||||||||
Full Title: A randomised, controlled, multidose, multicentre, adaptive phase II/III study in infants with proliferating infantile hemangiomas requiring systemic therapy to compare four regimens of propranolol ... | |||||||||||||
Medical condition: Proliferating Infantile Hemangioma | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) IT (Completed) HU (Completed) LT (Completed) CZ (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005199-17 | Sponsor Protocol Number: IIBSP-TIM-2013-156 | Start Date*: 2014-07-16 |
Sponsor Name:Institut de Recerca HSCSP | ||
Full Title: Efficacy and safety of topical administration of timolol maleate 0.5% solution in the treatment of Child Proliferative Hemangioma Early Stage Surface. Randomized Controlled Study | ||
Medical condition: Children Superficial Hemangioma | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003144-50 | Sponsor Protocol Number: V00400GL2011A | Start Date*: 2011-11-03 | |||||||||||
Sponsor Name:Pierre Fabre Dermatologie, Represented by Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: A randomised, double blind, controlled, multicentre study in infants with infantile hemangioma to compare propranolol gel to placebo | |||||||||||||
Medical condition: Proliferating localised uncomplicated infantile hemangioma not requiring systemic therapy | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001262-40 | Sponsor Protocol Number: IHA/1 | Start Date*: 2005-03-02 |
Sponsor Name:Investigador del estudio: Dr. Agustín Alomar Muntañola | ||
Full Title: Tratamiento de los hemangiomas de la infancia con imiquimod tópico al 5% | ||
Medical condition: Hemangiomas de la infancia | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012115-18 | Sponsor Protocol Number: IMP13617 | Start Date*: 2010-03-22 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Primovist enhanced MRI for the detection and evaluation of focal liver lesions | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: All benign and malignant focal liver lesions e.g. colorectal liver metastases, HCC, haemangioma, adenoma, cysts, FNH. | |||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017942-30 | Sponsor Protocol Number: 0914M0622 | Start Date*: 2010-06-15 | ||||||||||||||||
Sponsor Name:Shionogi USA, Inc. | ||||||||||||||||||
Full Title: An open-label safety study of S-888711 in adult subjects with relapsed persistent or chronic immune thrombocytopenia with or without prior splenectomy | ||||||||||||||||||
Medical condition: Relapsed persistent or chronic immune thrombocytopenia with or without prior splenectomy | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) GB (Prematurely Ended) DE (Prematurely Ended) HU (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003604-40 | Sponsor Protocol Number: AFT-RAP-01 | Start Date*: 2023-03-21 | |||||||||||
Sponsor Name:AFT Pharmaceuticals Ltd. | |||||||||||||
Full Title: Rapamycin Dose-Ranging Efficacy Study: A Phase II, proof of concept, double-blind, placebo-controlled, randomized, parallel-group, dose-response comparison of the effects of different strengths of ... | |||||||||||||
Medical condition: Subjects diagnosed with port wine stains | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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 . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
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. |
Query did not match any studies.