Found 48 matching trials
Efficacy, Immunogenicity and Safety of V503 in Chinese Women Aged 20-45 Years (V503-023)
PHASE3This study will evaluate the efficacy, immunogenicity and safety of 9-valen...
Status
Active Not Recruiting
Location
Lingchuan Center for Disease Control and Prevention ( Site 0002)
Safety, Tolerability and Immunogenicity of a Plant-made Seasonal Quadrivalent VLP Influenza Vaccine in Adults
PHASE1A phase I/II trial conducted in a single centre, observer-blind, randomized...
Location
Miami Research Associates
Dose-Ranging Study of Quadrivalent Human Papillomavirus (HPV) (Types 6,11,16,18) L1 Virus-Like Particle (VLP) Vaccine (V501-007)(COMPLETED)
PHASE2This study was conducted in 2 parts. Part A was a randomized, double-blind,...
Location
Multiple Locations
Safety of and Immune Response to a Novel Human Papillomavirus Vaccine in HIV Infected Children
PHASE2The purpose of this study is to determine the safety of and immune response...
Study of an Investigational Vaccine in Pre-Adolescents and Adolescents (Gardasil)(V501-016)
PHASE3The primary purpose of the study is to determine if an investigational vacc...
Location
Multiple Locations
Effectiveness and B-memory Cell Response to QHPV Vaccine 9-years Post-vaccination Among HIV-infected Boys and Girls
N/AIn 2013, the Investigators enrolled a cohort of 180 HIV-1 infected adolesce...
Location
Multiple Locations
Immunogenicity and Tolerability of V503 Versus GARDASIL (V503-009)
PHASE3Primary objective:
• To demonstrate that administration of V503 induces no...
Location
Multiple Locations
Safety and Tolerability Study of V501 in Japanese Boys (V501-200)
PHASE3This is a study of V501 \[quadrivalent Human Papillomavirus (HPV) (Type 6, ...
Study to Test the Safety of HPV Vaccine in Women (V501-011)(COMPLETED)
PHASE3The primary purpose of the study is to test the safety of HPV Vaccine in Wo...
Location
Multiple Locations
Immunogenicity, Safety and Tolerability of a Plant-Derived Seasonal VLP Quadrivalent Influenza Vaccine in the Elderly Population
PHASE2This is a multiple sites phase II trial, randomized, observer-blind, dose r...
Location
MUHC-Vaccine Study Centre