- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Condyloma Acuminatum.
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EudraCT Number: 2008-004893-42 | Sponsor Protocol Number: 1.0 | Start Date*: 2008-10-15 | ||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für dermatologie | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: Condyloma accuminata, Vulvar Intraepithelial Neoplasia | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002455-20 | Sponsor Protocol Number: P150957 | Start Date*: 2016-11-18 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Efficacy study of the quadrivalent Human Papilloma Virus (HPV) vaccine to prevent recurrence of External Genital Warts (EGW) in patients who were cured in the first place | |||||||||||||
Medical condition: Patients whose EGW have just disappeared after initial success of classic treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000162-40 | Sponsor Protocol Number: IFN 001 | Start Date*: 2005-09-06 |
Sponsor Name:Helix Product Development (Ireland) Limited | ||
Full Title: Treatment of genital warts with Interferon alpha-2b Cream: a randomized, double blind, placebo-controlled study | ||
Medical condition: Condylomata acuminata (genital warts) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004465-24 | Sponsor Protocol Number: EXP-1167 | Start Date*: 2015-02-18 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Safety and efficacy of repeat use of Picato® 0.05% in the treatment of anogenital warts | |||||||||||||
Medical condition: Anogenital warts | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004007-13 | Sponsor Protocol Number: NCT-2010-1090 | Start Date*: 2013-09-06 | |||||||||||
Sponsor Name:Deutsches Krebsforschungszentrum (DKFZ | |||||||||||||
Full Title: A randomized, placebo-controlled, phase IIIb HPV vaccination trial with Gardasil® in patients with recurrent condylomata acuminata | |||||||||||||
Medical condition: Patients with recurrrent external condylomata acuminata located at the following genital regions: labia minora and majora, introitus vaginae, clitoris, prepuce, glans penis, coronal sulcus and fren... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005553-13 | Sponsor Protocol Number: CLS001-CO-PR-011 | Start Date*: 2016-05-11 | |||||||||||
Sponsor Name:Cutanea Life Sciences | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, VEHICLE-CONTROLLED, DOUBLE-BLIND, PARALLEL-GROUP STUDY TO EXPLORE THE PHARMACODYNAMICS, SAFETY AND EFFICACY OF TOPICAL OMIGANAN IN PATIENTS WITH EXTERNAL GENITAL WARTS | |||||||||||||
Medical condition: Patients with external genital warts | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000870-39 | Sponsor Protocol Number: CHDR1607 | Start Date*: 2017-08-21 | ||||||||||||||||
Sponsor Name:Cutanea Life Sciences | ||||||||||||||||||
Full Title: A phase 2, randomized, vehicle-controlled, double-blind study to explore the efficacy, pharmacodynamics and safety of topical ionic contra-viral therapy (ICVT) comprised of digoxin and furosemide i... | ||||||||||||||||||
Medical condition: HPV-induced genital lesions of immunocompromised and immunocompetent patients | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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