- Trials with a EudraCT protocol (138)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
138 result(s) found for: Human Papillomavirus.
Displaying page 1 of 7.
EudraCT Number: 2019-003486-17 | Sponsor Protocol Number: 9-VPH-MVIH | Start Date*: 2020-02-11 |
Sponsor Name:CARMEN HIDALGO TENORIO | ||
Full Title: Immunogenicity and safety of a 9-valent human papillomavirus vaccine in HIV-positive women | ||
Medical condition: New infection and lesions of papillomavirus in HIV-infected women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000108-42 | Sponsor Protocol Number: V505-001 | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase IIa Randomized, Double-Blinded, Controlled With GARDASIL™ Clinical Trial to Study the Tolerability and Immunogenicity of V505 (A Multivalent Human Papillomavirus [HPV] L1 Virus-Like-Particl... | |||||||||||||
Medical condition: vaccination against HPV infection/related disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003399-10 | Sponsor Protocol Number: GDS07C | Start Date*: 2014-03-24 | |||||||||||
Sponsor Name:Sanofi Pasteur MSD S.N.C. | |||||||||||||
Full Title: A Randomized, Double-Blinded, Controlled with GARDASIL® (Human Papillomavirus Vaccine [Types 6, 11, 16, 18] (Recombinant, adsorbed)), Phase 3 Clinical Trial to Study the Immunogenicity and Tolerabi... | |||||||||||||
Medical condition: Prevention of premalignant genital lesions (cervical, vulvar and vaginal) and cervical cancer and genital warts (condyloma acuminata) causally related to Human Papillomavirus (HPV) Types 6, 11, 16,... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000215-24 | Sponsor Protocol Number: GeSIDA10017 | Start Date*: 2018-06-05 |
Sponsor Name:Fundacion SEIMC-GESIDA | ||
Full Title: A single-arm, open-label and multicentre phase IV trial to evaluate the immunogenicity of the nonavalent vaccine against human papillomavirus in HIV-infected men who have sex with men. GESIDA 10017... | ||
Medical condition: AIDS | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000109-19 | Sponsor Protocol Number: V502-001 | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Randomized, International, Double-Blinded (With In-House Blinding), Controlled With GARDASIL™, Dose-Ranging Study of Octavalent Human Papillomavirus (HPV) (Types 6, 11, 16, 18, 31, 45, 52, and 58... | |||||||||||||
Medical condition: vaccination against HPV infection/related disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000333-13 | Sponsor Protocol Number: APHP200046 | Start Date*: Information not available in EudraCT |
Sponsor Name:APHP DRCI | ||
Full Title: Efficacy of the nonavalent HPV vaccine in the treatment of difficult-to-treat palmo-plantar warts | ||
Medical condition: Vaccination by nonavalent vaccine against HPV could lead to a complete resolution of difficult-to-treat palmo-plantar warts in patients of more than 15 years and 3 months of age | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005093-38 | Sponsor Protocol Number: V503-004 | Start Date*: 2016-07-05 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck Co., Inc | |||||||||||||
Full Title: An Open-Label Phase III Clinical Trial to Study the Immunogenicity and Tolerability of GARDASIL®9 (A Multivalent Human Papillomavirus [HPV] L1 Virus-Like Particle [VLP] Vaccine) in Adult Women (27-... | |||||||||||||
Medical condition: Prevention of cervical,vulvar,vaginal, and anal cancers and related precancers, external genital lesions, Pap test abnormalities, and persistent infection caused by HPV Types 6,11,16,18,31,33,45,52,58 | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) AT (Completed) ES (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000228-33 | Sponsor Protocol Number: CE/17-12-06 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU Saint-Pierre | |||||||||||||
Full Title: Prospective longitudinal study on immunogenicity, induction of cellular immune responses and safety of vaccination against HPV with the 9valent vaccine in HIV-positive women | |||||||||||||
Medical condition: Immune responses to administration of 9valent vaccine against HPV in HIV-positive women | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006773-32 | Sponsor Protocol Number: HPV_CSP01 | Start Date*: 2009-05-20 | |||||||||||
Sponsor Name:Health Protection Agency | |||||||||||||
Full Title: A Phase IV, randomised study to evaluate the immune responses of UK adolescent girls receiving Cervarix(TM) or Gardasil(TM) Human Papillomavirus vaccines | |||||||||||||
Medical condition: This study will investigate vaccines that prevent premalignant cervical lesions and cervical cancer causally related to Human Papillomavirus (HPV) types 16 and 18. This study will investigate wheth... | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000164-24 | Sponsor Protocol Number: 109836 | Start Date*: 2007-05-21 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase I/II, partially-blind, randomized multicentre study to assess the safety and immunogenicity of an HPV-16/18/33/58 L1 VLP vaccine formulated with different adjuvant systems when administered... | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003591-13 | Sponsor Protocol Number: V503-076 | Start Date*: 2024-05-06 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label Study to Evaluate the Safety and Immunogenicity of 2-dose Regimens of 9vHPV and mRNA-1273 SARS-CoV-2 Vaccines Where the First Dose of Each Vaccine Are Given Conco... | |||||||||||||
Medical condition: Papilloma viral infection | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003236-23 | Sponsor Protocol Number: V503-049 | Start Date*: 2020-03-11 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | |||||||||||||
Full Title: A Phase 3, International, Multi-center, Randomized, Double-blind, Placebo-controlled Clinical Trial to Study the Efficacy, Immunogenicity, and Safety of the 9vHPV Vaccine, a Multivalent L1 Virus-li... | |||||||||||||
Medical condition: Oral persistent infection caused by any of the human papillomavirus types 16, 18, 31, 33, 45, 52, and 58 | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000090-15 | Sponsor Protocol Number: 213749 | Start Date*: 2022-12-19 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals SA | |||||||||||||
Full Title: A Phase 1/2 randomized, observer-blinded, multi-country study to evaluate safety and immunogenicity of investigational adjuvanted human papillomavirus vaccine in females (16 to 26 years of age) | |||||||||||||
Medical condition: Active immunisation for the prevention of human papillomavirus infection | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) FR (Completed) BG (Completed) EE (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003528-39 | Sponsor Protocol Number: V503-001 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Merck & Co. Inc. | |||||||||||||
Full Title: A Randomized, International, Double-Blinded (With In-House Blinding), Controlled With GARDASIL™, Dose-Ranging, Tolerability, Immunogenicity, and Efficacy Study of a Multivalent Human Papillomavi... | |||||||||||||
Medical condition: Prevention of cervical, vulvar, and vaginal cancers and related precancers, external genital lesions, Pap test abnormalities, and persistent infection caused by Human Papillomavirus (HPV) 6, 11, ... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) DE (Completed) AT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005569-38 | Sponsor Protocol Number: CLS003-CO-PR-001 | Start Date*: 2014-02-17 | |||||||||||
Sponsor Name:Cutanea Life Sciences | |||||||||||||
Full Title: A phase I/IIa open-label First-in-Human study to assess safety and pharmacokinetics and explore biomarker effects of topical ionic contra-viral therapy (ICVT) comprised of digoxin and furosemide in... | |||||||||||||
Medical condition: Cutaneous warts | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004581-16 | Sponsor Protocol Number: V501-030 | Start Date*: 2015-04-02 |
Sponsor Name:Merck Sharp & Dohme (China) Ltd. | ||
Full Title: An Immunogenicity and Safety Study of GARDASIL™ in Chinese Female Subjects Aged 9 to 45 Years and Male Subjects Aged 9 to 15 Years | ||
Medical condition: Prevention of HPV types 6, 11, 16 and 18 related cervical cancer, vulvar, vaginal pre-cancers, low-grade, pre-cancerous lesions, and genital warts in Chinese female subjects aged 9 to 45 years and ... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-003177-42 | Sponsor Protocol Number: COHEAHR-WP4 | Start Date*: 2014-10-10 | ||||||||||||||||
Sponsor Name:Catalan Institute of Oncology | ||||||||||||||||||
Full Title: Multinational study assessing the acceptability and determinants of compliance to HPV vaccination to women in screening ages 30 to 45 years | ||||||||||||||||||
Medical condition: Cervical cancer | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) ES (Completed) BE (Completed) FI (Completed) SI (Completed) NL (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008605-22 | Sponsor Protocol Number: 1.0 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Univ.Klinik für Dermatologie | |||||||||||||
Full Title: Determination of the human papillomavirus (HPV)-specific antibody status in oral fluids of individuals vaccinated with a quadrivalent HPV vaccine | |||||||||||||
Medical condition: Healthy women aged 18-26 | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000458-20 | Sponsor Protocol Number: 108160 | Start Date*: 2017-11-14 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A post-marketing surveillance (PMS) study to monitor the safety and reactogenicity of GlaxoSmithKline (GSK) Biologicals’ human papillo-mavirus (HPV) vaccine (Cervarix) in 3,000 healthy female Filip... | ||
Medical condition: Healthy volunteers (active immunization against Human papillomavirus infection in female subjects for the prevention of cervical cancer). | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-004662-33 | Sponsor Protocol Number: C/39/2018 | Start Date*: 2019-07-12 |
Sponsor Name:Imperial College London | ||
Full Title: NOVEL: Nonavalent HPV vaccine after local conservative treatment for cervical pre-invasive disease - a randomised controlled trial | ||
Medical condition: Cervical intra-epithelial neoplasia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) FI (Completed) | ||
Trial results: (No results available) |
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