- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25 result(s) found for: Pemphigoid.
Displaying page 1 of 2.
EudraCT Number: 2012-003370-10 | Sponsor Protocol Number: CQGE031X2202 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, parallel group study evaluating the efficacy, safety, pharmacokinetics and pharmacodynamics of QGE031 in the treatment of patients with bullous pemph... | |||||||||||||
Medical condition: Refractory Bullous Pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006658-24 | Sponsor Protocol Number: 8024 | Start Date*: 2009-03-05 | ||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||
Full Title: A randomised controlled trial to compare the safety and effectiveness of doxycycline (200 mg/day) with prednisolone (0.5 mg/kg/day) for initial treatment of bullous pemphigoid | ||||||||||||||||||
Medical condition: BP is a serious condition with a significant associated morbidity and mortality rate. Widespread tense and haemorrhagic blisters, skin erosions and severe itching cause patients a great deal of dis... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004666-26 | Sponsor Protocol Number: 2015/208/HP | Start Date*: 2017-07-19 | |||||||||||||||||||||
Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||||||||||||
Full Title: Randomised double blind double dummy control trial comparing the safety and efficacy of rituximab versus oral cyclophosphamide in severe forms of mucous membrane pemphigoid | |||||||||||||||||||||||
Medical condition: severe forms of mucous membrane pemphigoid | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000287-32 | Sponsor Protocol Number: D325AC00002 | Start Date*: 2020-12-02 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multinational, Randomized, Double-blind, Parallel-group, Placebo-controlled Study to Investigate the Use of Benralizumab as a Treatment Option for Patients with Bullous Pemphigoid (FJORD) | |||||||||||||
Medical condition: Bullous Pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) DE (Prematurely Ended) FR (Completed) IT (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000756-42 | Sponsor Protocol Number: MEX0111 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Dompé s.p.a. | |||||||||||||
Full Title: A phase 2, multicentre, single arm, pilot study to assess the efficacy and the safety of 150 mg twice a day oral DF2156A in patients with active bullous pemphigoid. | |||||||||||||
Medical condition: active bullous pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001826-23 | Sponsor Protocol Number: MMP-Clob1 | Start Date*: 2023-05-31 | ||||||||||||||||
Sponsor Name:Dipartimento di Scienze della Salute dell'Università degli Studi di Firenze | ||||||||||||||||||
Full Title: A prospective, non controlled, phase 2 pilot study to assess the safety and efficacy of a new topical formulation of clobetasol 0.05% for mucosal use in patients with mucous membrane pemphigoid | ||||||||||||||||||
Medical condition: Mucous membrane pemphigoid | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000060-22 | Sponsor Protocol Number: 2020/0424/HP | Start Date*: 2023-04-03 | |||||||||||||||||||||
Sponsor Name:CHU de Rouen | |||||||||||||||||||||||
Full Title: Comparison of a personalized maintenance therapy based on the evolution of anti-desmoglein antibodies as biomarkers of pemphigus subclinical activity, with the standard treatment (rituximab + corti... | |||||||||||||||||||||||
Medical condition: Pemphigus diseases (Pemphigus Vulgaris - PV and Pemphigus Foliaceus (PF). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001417-32 | Sponsor Protocol Number: 2018/070/HP | Start Date*: 2018-07-13 | |||||||||||
Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||
Full Title: Long-term Follow-up of patients participants with pemphigus From Study RITUXIMAB3. Immunological, clinical and medicoeconomic evaluation | |||||||||||||
Medical condition: Patients with Bullous pemphigoid included in RITUXIMAB3 study | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003063-10 | Sponsor Protocol Number: ARGX-113-2010 | Start Date*: 2023-04-21 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: An Open-label Extension Study of ARGX-113-2009 to Evaluate the Long term Safety, Tolerability, and Efficacy of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid | |||||||||||||
Medical condition: Bullous Pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Trial now transitioned) GR (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) ES (Trial now transitioned) BG (Trial now transitioned) IT (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) HR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003545-32 | Sponsor Protocol Number: I06027 | Start Date*: 2007-09-14 | |||||||||||
Sponsor Name:CHU de Limoges | |||||||||||||
Full Title: Etude prospective ouverte de l'efficacité du leflunomide dans le traitement de la pemphigoïde bulleuse en association aux dermocorticoïdes. | |||||||||||||
Medical condition: Pemphigoïde bulleuse | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005266-31 | Sponsor Protocol Number: 2008/068/HP | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||
Full Title: COMPARAISON D'UN TRAITEMENT PAR L'ANTICORPS MONOCLONAL ANTI-CD 20 : RITUXIMAB (MABTHERA®) ASSOCIE A UNE CORTICOTHERAPIE GENERALE COURTE PAR RAPPORT A UNE CORTICOTHERAPIE GENERALE DE LONGUE DUREE C... | |||||||||||||
Medical condition: Pemphogoide bulleuse | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005987-67 | Sponsor Protocol Number: AK802 | Start Date*: 2021-12-22 | |||||||||||
Sponsor Name:Akari Therapeutics Plc | |||||||||||||
Full Title: A randomized, part A partial blinded and part B double blinded, placebo-controlled 24-week clinical study to evaluate the efficacy and safety of nomacopan therapy in adult patients with bullous pem... | |||||||||||||
Medical condition: moderate to severe bullous pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) NL (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002836-18 | Sponsor Protocol Number: AK801 | Start Date*: 2018-05-07 | |||||||||||
Sponsor Name:Akari Therapeutics Plc. | |||||||||||||
Full Title: A Phase IIa open label single arm study of safety and efficacy of rVA576 in adult mild to moderate Bullous Pemphigoid subjects | |||||||||||||
Medical condition: Mild to Moderate Bullous Pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003520-20 | Sponsor Protocol Number: R668-BP-1902 | Start Date*: 2020-05-19 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients with Bullous Pemphigoid | |||||||||||||
Medical condition: Bullous pemphigoid (BP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001059-37 | Sponsor Protocol Number: AKST4290-221 | Start Date*: 2019-06-21 | |||||||||||
Sponsor Name:Alkahest, Inc. | |||||||||||||
Full Title: Double-Blind, Randomized, Placebo-Controlled Trial of AKST4290 for Adjunctive Treatment of Mild to Moderate Bullous Pemphigoid | |||||||||||||
Medical condition: Mild to Moderate Bullous Pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002391-14 | Sponsor Protocol Number: SAWV1003 | Start Date*: 2005-09-29 |
Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | ||
Full Title: Pulsed Intravenous Methylprednisolone for Ocular Pemphigoid- A Pilot Study | ||
Medical condition: ocular mucous membrane pemphigoid | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004361-32 | Sponsor Protocol Number: KKS-166 | Start Date*: 2013-02-26 |
Sponsor Name:Philipps-Universität Marburg | ||
Full Title: Effect of simvastatin in combination with a superpotent topical corticosteroid in bullous pemphigoid A prospective multi-centre randomised double-blind placebo-controlled pilot study | ||
Medical condition: Bullous pemphigoid (BP) is the most frequent blistering autoimmune disease of the skin. The disease itself is characterized by the development of bullous lesions, frequently following a prodromal p... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-001827-12 | Sponsor Protocol Number: D-IIS-BP-01 | Start Date*: 2005-12-29 |
Sponsor Name:Georg-August-Universität Göttingen, Bereich Humanmedizin | ||
Full Title: Myfortic ® zur Therapie des Bullösen Pemphigoids. Eine offene monozentrische proof-of-concept Studie | ||
Medical condition: Bullous Pemphigoid | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003087-27 | Sponsor Protocol Number: ARGX-113-2009 | Start Date*: 2022-09-26 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 2/3, Randomized, Double-Blinded, Placebo-Controlled, Parallel-Group Study to Investigate the Efficacy and Safety of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid | |||||||||||||
Medical condition: Bullous Pemphigoid | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) HU (Trial now transitioned) ES (Trial now transitioned) GR (Trial now transitioned) BG (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) NL (Trial now transitioned) HR (Trial now transitioned) SK (Trial now transitioned) LV (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000480-41 | Sponsor Protocol Number: FARM6AS8AW | Start Date*: 2008-05-27 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: Multicenter, randomised, double masked, controlled clinical trial on the safety and efficacy of Cyclosporine A eye drop treatment on patients with ocular cicatricial pemphigoid. | |||||||||||||
Medical condition: Ocular cicatricial pemphigoid (OCP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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