- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Secondary lymphedema.
Displaying page 1 of 1.
| EudraCT Number: 2013-001360-36 | Sponsor Protocol Number: LF-DML-MS | Start Date*: 2013-09-30 |
| Sponsor Name:ULB - Unité de Recherche en Lymphologie - Faculté des Sciences de la motricité | ||
| Full Title: Evaluation of the benefit of lymphofluoroscopy in the validation of the manual drainage techniques on lymphedema | ||
| Medical condition: upper limb lymphedema | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004443-20 | Sponsor Protocol Number: HP-LY-CL-2063 | Start Date*: 2018-05-07 | |||||||||||||||||||||
| Sponsor Name:Herantis Pharma Plc | |||||||||||||||||||||||
| Full Title: A Phase II, double-blind, placebo-controlled, randomized study to assess the efficacy, safety and tolerability of Lymfactin® (AdAptVEGF-C Adenoviral Vector) in combination with a surgical lymph nod... | |||||||||||||||||||||||
| Medical condition: Secondary lymphedema associated with the treatment of breast cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FI (Prematurely Ended) SE (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2019-004403-12 | Sponsor Protocol Number: APHP190871 | Start Date*: 2020-10-26 |
| Sponsor Name:ASSISTANCE PUBLIQUE DES HOPITAUX DE PARIS | ||
| Full Title: Phase II multicenter study of talimogene laherparepvec in classic or endemic Kaposi sarcoma Kapvec Study | ||
| Medical condition: The study will provide an overview of efficacy and safety of talimogene laherparepvec in classic and endemic KS | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004501-24 | Sponsor Protocol Number: CT-2011-01 | Start Date*: 2012-03-06 | |||||||||||
| Sponsor Name:CureTech Ltd. | |||||||||||||
| Full Title: Phase II study to evaluate the safety, tolerability and efficacy of CT-011 administered intravenously to patients with metastatic melanoma | |||||||||||||
| Medical condition: Metastatic melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005846-39 | Sponsor Protocol Number: GISG-06 | Start Date*: 2014-07-22 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University of Heidelberg | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Phase II, multicenter, open-label, single-arm trial in advanced and relapsed Angiosarcomas, to evaluate the efficacy of pazopanib (Votrient) in combination with standard of care treatment paclitaxe... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Advanced and relapsed angiosarcoma | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) AT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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