Efficacy of a quadrivalent prophylactic human papillomavirus (types 6, 11, 16, and 18) L1 virus-like-particle vaccine against high-grade vulval and vaginal lesions: a combined analysis of three randomised clinical trials.

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Published in Lancet on May 19, 2007

Authors

Elmar A Joura1, Sepp Leodolter, Mauricio Hernandez-Avila, Cosette M Wheeler, Gonzalo Perez, Laura A Koutsky, Suzanne M Garland, Diane M Harper, Grace W K Tang, Daron G Ferris, Marc Steben, Ronald W Jones, Janine Bryan, Frank J Taddeo, Oliver M Bautista, Mark T Esser, Heather L Sings, Micki Nelson, John W Boslego, Carlos Sattler, Eliav Barr, Jorma Paavonen

Author Affiliations

1: Department of Gynecology and Obstetrics, Medical University of Vienna, Vienna, Austria.

Associated clinical trials:

Cervical Intraepithelial Neoplasm (CIN) in Women (Gardasil)(V501-015) | NCT00092534

Cervical Intraepithelial Neoplasm (CIN)-Warts Efficacy Trial in Women (Gardasil)(V501-013)(COMPLETED) | NCT00092521

Dose-Ranging Study of Quadrivalent Human Papillomavirus (HPV) (Types 6,11,16,18) L1 Virus-Like Particle (VLP) Vaccine (V501-007)(COMPLETED) | NCT00365716

Evaluation of Long Term Immunity Following HPV Vaccination | NCT02276521

Multicenter Trial Evaluating the Immunogenicity of HPV Vaccination in Girls on Immunosuppressive Therapy. (PRIMAVERA) | NCT01687192

Acceptance of Human Papillomavirus Vaccination in Postpartum Women (HPV Acceptance) | NCT00730704

Immunogenicity of the 9-Valent Human Papillomavirus Recombinant Vaccine in People With Idiopathic CD4 T Cell Lymphocytopenia | NCT03519464

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