- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
11 result(s) found for: Pyoderma.
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EudraCT Number: 2008-008291-14 | Sponsor Protocol Number: UKDCTN0901 | Start Date*: 2009-05-14 | ||||||||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | ||||||||||||||||||
Full Title: Study of treatments in Pyoderma Gangrenosum patients | ||||||||||||||||||
Medical condition: pyoderma gangrenosum | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000762-65 | Sponsor Protocol Number: CAIN457ADE01T | Start Date*: 2015-07-09 | |||||||||||
Sponsor Name:Technische Universität München, School of Medicine, represented by Dean | |||||||||||||
Full Title: Single-arm study to assess a potential effect of anti-IL-17 (Secukinumab) in the treatment of pyoderma gangrenosum | |||||||||||||
Medical condition: Pyoderma gangrenosum is an autoinflammatory disease, characterized by relapsing, painful ulcers of the skin. Treatment of PG is difficult. Patients suffer from long hospitalization, pain and redu... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003273-21 | Sponsor Protocol Number: IFX-1-P2.7 | Start Date*: 2020-11-09 | |||||||||||
Sponsor Name:InflaRx GmbH | |||||||||||||
Full Title: Open label exploratory phase IIa trial to investigate the safety and efficacy of IFX-1 in treating subjects with Pyoderma Gangrenosum (OPTIMA). | |||||||||||||
Medical condition: Pyoderma gangrenosum | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002920-41 | Sponsor Protocol Number: StelaraPG01 | Start Date*: 2012-01-04 | |||||||||||
Sponsor Name:University Hospital Tübingen | |||||||||||||
Full Title: Open-label Trial of Stelara® (Ustekinumab) In Patients with Pyoderma gangrenosum – an open, non-placebo controlled pilot study with 10 patients. | |||||||||||||
Medical condition: Patients with a clinical diagnosis of Pyoderma gangrenosum | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006013-11 | Sponsor Protocol Number: HOTPANTS | Start Date*: 2022-08-29 |
Sponsor Name:Erasmus MC, department of dermatology | ||
Full Title: Hyperbaric Oxygen Therapy for Pyoderma gangrenosum As a New Treatment Strategy | ||
Medical condition: Pyoderma gangrenosum | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002249-53 | Sponsor Protocol Number: P150924 | Start Date*: 2023-02-16 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux de Paris (AP-HP) | |||||||||||||
Full Title: Comparing short to standard amoxicillin course for eRysipElas: a non-inferiority randomized controlled trial | |||||||||||||
Medical condition: Adults diagnosed with lower limbs erysipelas/ cellulitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005754-28 | Sponsor Protocol Number: PAPA-Can | Start Date*: 2023-07-10 | ||||||||||||||||||||||||||
Sponsor Name:IRCCS ISTITUTO GIANNINA GASLINI | ||||||||||||||||||||||||||||
Full Title: A double-blind, placebo-controlled, randomized withdrawal study of canakinumab in pyogenic sterile arthritis pyoderma gangrenosum and acne (PAPA) syndrome | ||||||||||||||||||||||||||||
Medical condition: PAPA syndrome (Pyogenic Arthritis, Pyoderma gangrenosum and Acne) | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001276-56 | Sponsor Protocol Number: AIDA | Start Date*: 2014-07-11 |
Sponsor Name:North Bristol NHS - Southmead Hospital | ||
Full Title: A prospective, open label, randomised controlled clinical trial, with pharmacokinetic-pharmacodynamic validation, to compare antimicrobial treatment with oral minocycline plus rifampicin to treatme... | ||
Medical condition: Complicated Skin and Skin Structure infections caused by Methicillin Resistant Staphylococcus Aureus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004860-78 | Sponsor Protocol Number: P1209NY | Start Date*: 2014-05-09 | |||||||||||
Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
Full Title: A randomised, active-controlled, observer-blind, non-inferiority study to investigate the efficacy, safety and tolerability of a local treatment with dimeticone-based pediculicides in head lice inf... | |||||||||||||
Medical condition: Pediculosis capitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005281-30 | Sponsor Protocol Number: DUR001-306 | Start Date*: 2016-11-03 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Allergan Ltd. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin versus Active Comparator in Pediatric Subjects with Acute Bacterial Skin and Sk... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute bacterial skin and skin structure infection. For Cohort 5 (from birth to less than 3 months) also patients with sepsis are allowed. | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) ES (Prematurely Ended) BG (Completed) GR (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003797-40 | Sponsor Protocol Number: APD334-006 | Start Date*: 2017-02-23 |
Sponsor Name:Arena Pharmaceuticals, Inc. | ||
Full Title: A Phase 2a, Proof of Concept, Open-label Study Evaluating the Efficacy and Safety of Etrasimod (APD334) in Inflammatory Bowel Disease Patients with active Skin Extra-intestinal Manifestations | ||
Medical condition: Active Skin Extra-Intestinal Manifestations in Inflammatory Bowel Disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DE (Completed) | ||
Trial results: View results |
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