- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Epidermolysis bullosa simplex.
Displaying page 1 of 1.
EudraCT Number: 2017-002332-16 | Sponsor Protocol Number: RC31-16-8917 | Start Date*: 2017-10-03 | |||||||||||
Sponsor Name:Toulouse Hospital | |||||||||||||
Full Title: Evaluation of the efficacy of injections of botulinic toxin in plantar lesions of patients suffering from localized epidermolysis bullosa simplex : double blind randomized controlled study. | |||||||||||||
Medical condition: localized epidermolysis bullosa simplex | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005679-96 | Sponsor Protocol Number: SD-006 | Start Date*: 2015-03-16 | |||||||||||
Sponsor Name:Scioderm, INC | |||||||||||||
Full Title: An Open Label, Multi-center, Extension Study to Evaluate the Long-term Safety of Zorblisa (SD-101-6.0) in Patients with Epidermolysis Bullosa | |||||||||||||
Medical condition: Epidermolysis Bullosa | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) NL (Completed) GB (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) ES (Prematurely Ended) LT (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002288-14 | Sponsor Protocol Number: SD-005 | Start Date*: 2014-08-08 | |||||||||||
Sponsor Name:Scioderm, An Amicus Therapeutics Company | |||||||||||||
Full Title: A Phase 3, Multi-center, Randomized, Double-Blind, Placebo Controlled Study of the Efficacy and Safety of SD-101 Cream in Patients with Epidermolysis Bullosa | |||||||||||||
Medical condition: Epidermolysis Bullosa | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) NL (Completed) GB (Completed) IT (Completed) DE (Completed) PL (Completed) ES (Completed) LT (Completed) BE (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003757-41 | Sponsor Protocol Number: CCP-020-302 | Start Date*: 2018-02-19 | |||||||||||
Sponsor Name:Castle Creek Pharmaceuticals, LLC | |||||||||||||
Full Title: An International, Multicenter, Open-label, Long Term Extension Study Evaluating the Safety of Diacerein 1% Ointment Topical Formulation in Subjects with Epidermolysis Bullosa Simplex (EBS) | |||||||||||||
Medical condition: Epidermolysis Bullosa Simplex (EBS) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) NL (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004427-24 | Sponsor Protocol Number: CCP-020-301 | Start Date*: 2017-08-24 | |||||||||||
Sponsor Name:Castle Creek Pharmaceuticals, LLC | |||||||||||||
Full Title: An International, Multicenter, Randomized, Double-Blind, Parallel-Group Phase 2 Study Evaluating the Safety and Efficacy of Diacerein 1% Ointment Topical Formulation in Subjects with Epidermolysis ... | |||||||||||||
Medical condition: Epidermolysis Bullosa Simplex (EBS) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000214-42 | Sponsor Protocol Number: 755-201-EB | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:InMed Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomised, Double-Blind, Vehicle-Controlled Phase 2 Study of Topically Applied INM-755 (cannabinol) Cream in Patients with Epidermolysis Bullosa. | |||||||||||||
Medical condition: Epidermolysis bullosa | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) AT (Completed) GR (Completed) IT (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002034-21 | Sponsor Protocol Number: Dia2014 | Start Date*: 2013-12-16 |
Sponsor Name:EB House Austria | ||
Full Title: Diacerein for the treatment of Epidermolysis bullosa simplex | ||
Medical condition: Epidermolysis bullosa simplex - type Dowling-Meara | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001542-19 | Sponsor Protocol Number: 20-PP-04 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:CHU NICE | |||||||||||||
Full Title: A 12-Week Multicentre, Randomized, Blinded, Parallel-Group Study Comparing the Efficacy and Safety of Ixekizumab to Placebo in Patients > 6 years of age with EB simplex generalized severe | |||||||||||||
Medical condition: Epidermolysis bullosa simplex | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010763-17 | Sponsor Protocol Number: EBSBTXA09 | Start Date*: 2009-05-26 |
Sponsor Name:Sophiahemmet | ||
Full Title: Botulinumtoxin A Treatment in Epidermolysis Bullosa Simplex and Pachyonychia congenita-a double-blind placebo-controlled phase II proof of concept study | ||
Medical condition: Epidermolysis Bullosa Simplex and Pachyonychia Congenita | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000103-20 | Sponsor Protocol Number: 202000638 | Start Date*: 2021-07-15 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: An explorative randomized, placebo-controlled and double-blind intervention crossover study: Transvamix (100mg/mL THC / 50mg/mL CBD) to treat chronic pain in Epidermolysis Bullosa | ||
Medical condition: Genetic Epidermolysis Bullosa | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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