- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
6 result(s) found for: Photochemotherapy.
Displaying page 1 of 1.
EudraCT Number: 2007-001302-25 | Sponsor Protocol Number: 2008-0312-08 | Start Date*: 2009-11-05 | |||||||||||
Sponsor Name:Lab for pharmaceutical biology [...] | |||||||||||||
Full Title: Evaluation of the benefits and effects of hypericin Photodynamic therapy (PDT) in the clinical treatment of superficial bladder carcinoma. | |||||||||||||
Medical condition: the study population consists of 10 patients with anatomopathologically proven muscle invasive TCC without metastasis. These patients require a cystoscopy. Before the planned cystoscopy, the bladde... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006982-17 | Sponsor Protocol Number: 05.09.2006 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:Division of Special and Environmental Dermatology | |||||||||||||
Full Title: UVA 1 therapy versus 5-MOP UVA photochemotherapy for patients with severe generalized atopic dermatitis | |||||||||||||
Medical condition: Severe generalized atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001243-28 | Sponsor Protocol Number: P04320 | Start Date*: 2005-08-03 | |||||||||||
Sponsor Name:essex pharma GmbH | |||||||||||||
Full Title: Study to determine the non inferiority of GROUP I (“high need”) compared to GROUP II (“low need”) concerning the efficacy of infliximab with respect to safety and tolerability in patients suffering... | |||||||||||||
Medical condition: Moderate to severe plaque-type psoriaris (psoriasis vulgaris). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001531-12 | Sponsor Protocol Number: LRP/LNP1955/2016/003 | Start Date*: 2016-08-16 | |||||||||||
Sponsor Name:Lupin Limited | |||||||||||||
Full Title: A Phase II, Dose Ranging, Exploratory Clinical Study to Assess the Efficacy, Pharmacodynamics, and Safety of LNP1955 in Patients with Moderate-to-Severe Plaque Psoriasis | |||||||||||||
Medical condition: Moderate to severe plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002141-39 | Sponsor Protocol Number: CDP870-040 | Start Date*: 2005-10-25 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: Multicenter, dose response, randomized, double blin, parallel, 3 arms, placebo controlled clinical trial to evaluate the efficacy and the safety of subcutaneous CDP870 (certolizumab pegol) at 2 dif... | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004669-16 | Sponsor Protocol Number: C2501004 | Start Date*: 2019-09-23 | |||||||||||
Sponsor Name:Pfizer Inc | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE BLIND, PLACEBO-CONTROLLED, STUDY TO EVALUATE THE SAFETY AND EFFICACY OF PF-06826647 IN PARTICIPANTS WITH MODERATE TO SEVERE PLAQUE PSORIASIS | |||||||||||||
Medical condition: Moderate to severe Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
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