- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Leukoplakia.
Displaying page 1 of 1.
| EudraCT Number: 2009-014833-26 | Sponsor Protocol Number: IEO S500/409 | Start Date*: 2010-07-29 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: Phase IIB Randomized, Placebo Controlled Trial of Pioglitazone for Oral Premalignant Lesions. An Inter-Consortium Collaborative Study. | |||||||||||||
| Medical condition: oral premalignant lesions | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-018399-25 | Sponsor Protocol Number: MuSH_1.2 | Start Date*: 2011-03-17 | |||||||||||||||||||||
| Sponsor Name:Medizinische Universität Wien, Univ.Klinik für Zahn-,Mund-u.Kieferheilkunde,Klin.Abt.f.orale Chirurg | |||||||||||||||||||||||
| Full Title: A randomized controlled trial: Photodynamic Treatment for the therapy of premalignant mucosal oral lesions. | |||||||||||||||||||||||
| Medical condition: Leukoplakia and oral lichen ruber. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-006011-23 | Sponsor Protocol Number: 130669 | Start Date*: 2021-03-02 |
| Sponsor Name:Petra Pietarinen | ||
| Full Title: Laryngeaalisen leukoplakian mikrobilääkehoito -tutkimusprojekti | ||
| Medical condition: Krooninen laryngiitti | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: | |
| Trial protocol: FI (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002016-28 | Sponsor Protocol Number: 20040118 | Start Date*: 2005-01-04 | |||||||||||
| Sponsor Name:Amgen | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Weekly Doses of Palifermin (Recombinant Human Keratinocyte Growth Factor, rHuKGF) for the Reduct... | |||||||||||||
| Medical condition: Oral mucositis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) AT (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001716-31 | Sponsor Protocol Number: 20040124 | Start Date*: 2015-09-17 | |||||||||||
| Sponsor Name:Swedish Orphan Biovitrum AB (publ.) | |||||||||||||
| Full Title: A Phase 1/2 Study to Evaluate Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of Weekly Doses of Palifermin (Recombinant Human Keratinocyte Growth Factor, rHuKGF) for the Reduct... | |||||||||||||
| Medical condition: Oral Mucositis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000213-35 | Sponsor Protocol Number: 20020402 | Start Date*: 2005-08-05 | |||||||||||
| Sponsor Name:Swedish Orphan Biovitrum AB (publ.) | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Weekly Doses of Palifermin (Recombinant Human Keratinocyte Growth Factor, rHuKGF) for the Reduct... | |||||||||||||
| Medical condition: Oral mucositis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) AT (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001489-41 | Sponsor Protocol Number: P00003466 | Start Date*: 2018-07-02 | |||||||||||
| Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
| Full Title: Radiation- and alkylator-free hematopoietic cell transplantation for bone marrow failure due to dyskeratosis congenita / telomere disease | |||||||||||||
| Medical condition: Dyskeratosis congenita / telomere disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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Query did not match any studies.