- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: Vulva.
Displaying page 1 of 3.
EudraCT Number: 2006-004052-20 | Sponsor Protocol Number: CKTO 2005-25R | Start Date*: 2006-11-01 | |||||||||||
Sponsor Name:Koningin Wilhelmina Fonds | |||||||||||||
Full Title: Phase II study of definitive radiochemotherapy for locally advanced squamous cell cancer of the vulva: an efficacy study | |||||||||||||
Medical condition: advanced stage squamous cell cancer of the vulva | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002052-17 | Sponsor Protocol Number: PITVIN | Start Date*: 2012-09-21 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Univ. Frauenklinik, Abteilung für Gynäkologie | |||||||||||||
Full Title: Primary Imiquimod Treatment versus Surgery for Vulvar Intraepithelial Neoplasia: A Prospective Randomized Controlled Trial | |||||||||||||
Medical condition: Vulvar intraepithelial neoplasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006761-32 | Sponsor Protocol Number: A 091152 | Start Date*: 2008-04-15 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
Full Title: Vulval intraepithelial neoplasia: immune responses to human papillpmavirus. | |||||||||||||
Medical condition: Vulval intraepithelial neoplasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005230-37 | Sponsor Protocol Number: HPV01/01 | Start Date*: 2008-04-02 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Randomised Controlled Study on the Effects of Imiquimod, a TLR 7 Activating Agent, on the HPV16-Specific Immune Response Following HPV16 E6/E7 Synthetic Long Peptides Vaccination in Women with HPV1... | |||||||||||||
Medical condition: Adult female patients, with histological evidence of Vulvar intraepithelial neoplasia (VIN) grade III lesions of the squamous cell type, positive for HPV (Human Papilloma Virus)16. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003134-13 | Sponsor Protocol Number: A551109 | Start Date*: 2012-02-13 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: 5-Aminolevulinic Acid PhotoDynamic Therapy for the treatment of premalignant disorders of the vulva. | |||||||||||||
Medical condition: Premalignant vulvar disorders (usual type Vulvar Intraepithelial Neoplasia) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2014-000547-32 | Sponsor Protocol Number: 13123 | Start Date*: 2014-04-02 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: A Randomised Controlled Trial of Adjunctive Systemic Therapy for Vulval Erosive Lichen Planus | |||||||||||||
Medical condition: Vulval erosive lichen planus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002724-16 | Sponsor Protocol Number: CLS001-CO-PR-010;CHDR1508 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:Cutanea Life Sciences | |||||||||||||
Full Title: A phase 2, randomized, double-blind, parallel-group study to assess the pharmacodynamics, safety/tolerability and efficacy of topical omiganan in patients with usual type vulvar intraepithelial neo... | |||||||||||||
Medical condition: Patients with usual type vulvar intraepithelial neoplasia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008251-42 | Sponsor Protocol Number: 26014 | Start Date*: 2009-09-07 | ||||||||||||||||||||||||||
Sponsor Name:Erasmus MC | ||||||||||||||||||||||||||||
Full Title: Clinical and immunological effects of imiquimod and HPV-vaccination compared to imiquimod alone in female patients with Usual type VIN | ||||||||||||||||||||||||||||
Medical condition: In this trial, the efficacy of Gardasil combined with imiquimod in women with usual type Vulvar Intraepithelial Neoplasia is investigated. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005475-34 | Sponsor Protocol Number: Ovar-protect2007 | Start Date*: 2008-06-12 | |||||||||||||||||||||||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||||||||||||||||||||||
Full Title: Prospektive Studie zur potentiellen Protektion der Ovarfunktion von Frauen mit gynäkologischen Malignomen unter Chemotherapie mittels GnRH-Analoga-Applikation | |||||||||||||||||||||||||||||||||
Medical condition: Primärdiagnose eines histologisch gesicherten gynäkologischen Malignoms: Zervixkarzinom, rezeptornegatives Mammakarzinom, Ovarialkarzinom, Vaginalkarzinom, Vulvakarzinom mit Ovarerhalt und fehlende... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004277-31 | Sponsor Protocol Number: E012-HPV | Start Date*: 2021-12-23 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:eTheRNA immunotherapies NV | ||||||||||||||||||||||||||||||||||||||
Full Title: A phase I/IIa open label study to assess the safety, tolerability, immunogenicity and clinical activity of EI-201 mRNA immunotherapy given intravenously in subjects with recurrent or metastatic HPV... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Incurable recurrent or metastatic (R/M) HPV16-positive (HPV16+) tumors (e.g. oropharyngeal cancer, cervical, vulvar, vaginal, anal, penile cancer, etc.) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) NL (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001191-30 | Sponsor Protocol Number: IISR-2015-101127 | Start Date*: 2017-04-25 | |||||||||||
Sponsor Name:Department of Obstetrics & Gynecology, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: Use of TachoSil® for the prevention of postoperative complications after groin dissection in vulva cancer patients | |||||||||||||
Medical condition: Vulva cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002247-23 | Sponsor Protocol Number: MITOCERV4 | Start Date*: 2020-01-29 | ||||||||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | ||||||||||||||||||
Full Title: Single arm phase II study on Pembrolizumab in preneoplastic high grade HPV-related vulvar and cervical lesions | ||||||||||||||||||
Medical condition: Patients with pre neoplastic high grade HPV-related vulvar and cervical lesions | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003107-19 | Sponsor Protocol Number: 13-0288 | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:University of Birmingham [...] | |||||||||||||
Full Title: Phase II clinical trial investigating the use of epigallocatechin-3-gallate (Veregen) in the treatment of vulval intraepithelial neoplasia | |||||||||||||
Medical condition: Vulval intraepithelial neoplasia (VIN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004638-99 | Sponsor Protocol Number: 2105xx1 | Start Date*: 2017-11-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine and PET | |||||||||||||||||||||||||||||||||
Full Title: Phase II trial: uPAR PET/CT and FDG PET/CT for preoperative staging of gynecological cancers | |||||||||||||||||||||||||||||||||
Medical condition: gynecological cancers: Vulvar cancer endometrial cancer (uterine cancer) cervical cancer ovarian cancer | |||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004327-11 | Sponsor Protocol Number: SPON 245-06 | Start Date*: 2008-10-23 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: A randomised phase II multi-centre trial of topical treatment in women with vulval intraepithelial neoplasia | |||||||||||||
Medical condition: Vulval Intraepithelial Neoplasia grade 3 (VIN 3) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000230-29 | Sponsor Protocol Number: CA209-358 | Start Date*: 2015-09-29 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Non-Comparative, Open-Label, Multiple Cohort, Phase 1/2 Study of Nivolumab and Nivolumab plus Ipilimumab in Subjects with Virus-Positive and Virus-Negative Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Virus-associated tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000907-34 | Sponsor Protocol Number: H-200-001 | Start Date*: 2021-11-11 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Hookipa Biotech GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase I/II Study of TheraT® Vector(s) Expressing Human Papillomavirus 16 Positive (HPV 16+) Specific Antigens in Patients with HPV 16+ Confirmed Cancers | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) FR (Ongoing) NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002614-13 | Sponsor Protocol Number: ElechtraPlatinum | Start Date*: 2022-03-07 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: Electrochemotherapy with Carboplatinum plus Bleomycin versus Bleomycin alone in vulvar cancer: the ElechtraPlatinum Study. A Randomized Controlled Trial | |||||||||||||
Medical condition: relapsing vulvar carcinoma already subjected to multiple treatments | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004168-36 | Sponsor Protocol Number: UCL/17/0672 | Start Date*: 2018-10-16 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University College London | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase II study of pembrolizumab in patients with advanced gynaecological clear cell cancer | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced Gynaecological Clear Cell Cancer | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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